Sample records for created on-line biology

  1. Professor Created On-line Biology Laboratory Course

    NASA Technical Reports Server (NTRS)

    Bowman, Arthur W.

    2010-01-01

    This paper will share the creation, implementation, and modification of an online college level general biology laboratory course offered for non-science majors as a part of a General Education Curriculum. The ability of professors to develop quality online laboratories will address a growing need in Higher Education as more institutions combine course sections and look for suitable alternative course delivery formats due to declining departmental budgets requiring reductions in staffing, equipment, and supplies. Also, there is an equal or greater need for more professors to develop the ability to create online laboratory experiences because many of the currently available online laboratory course packages from publishers do not always adequately parallel on-campus laboratory courses, or are not as aligned with the companion lecture sections. From a variety of scientific simulation and animation web sites, professors can easily identify material that closely fit the specific needs of their courses, instructional environment, and students that they serve. All too often, on-campus laboratory courses in the sciences provide what are termed confirmation experiences that do NOT allow students to experience science as would be carried out by scientists. Creatively developed online laboratory experiences can often provide the type of authentic investigative experiences that are not possible on-campus due to the time constraints of a typical two-hour, once-per-week-meeting laboratory course. In addition, online laboratory courses can address issues related to the need for students to more easily complete missing laboratory assignments, and to have opportunities to extend introductory exercises into more advanced undertakings where a greater sense of scientific discovery can be experienced. Professors are strongly encourages to begin creating online laboratory exercises for their courses, and to consider issues regarding assessment, copyrights, and Intellectual Property

  2. Creating biological nanomaterials using synthetic biology.

    PubMed

    Rice, MaryJoe K; Ruder, Warren C

    2014-02-01

    Synthetic biology is a new discipline that combines science and engineering approaches to precisely control biological networks. These signaling networks are especially important in fields such as biomedicine and biochemical engineering. Additionally, biological networks can also be critical to the production of naturally occurring biological nanomaterials, and as a result, synthetic biology holds tremendous potential in creating new materials. This review introduces the field of synthetic biology, discusses how biological systems naturally produce materials, and then presents examples and strategies for incorporating synthetic biology approaches in the development of new materials. In particular, strategies for using synthetic biology to produce both organic and inorganic nanomaterials are discussed. Ultimately, synthetic biology holds the potential to dramatically impact biological materials science with significant potential applications in medical systems.

  3. Plant biology: From on-campus to on-line development and implementation

    NASA Astrophysics Data System (ADS)

    Bradley, Lucy K.

    The lecture content of the Plant Biology class for non-majors was transformed from a traditional on-campus lecture to an asynchronous website that could be used both as a stand-alone course and as an adjunct to the on campus course sections. In addition, an interactive, on-line website with home laboratory experiments was developed and implemented by the Plant Biology Department in collaboration with design specialists from the Information Technology and Instructional Support Department of the Arizona State University. The 259-page lecture website included 134 interactive animations, as well as 11 videos. The lab website included 176 pages, with 187 graphics and 36 separate animations. Convenience was identified by most students as the key benefit of taking the course on-line. Website construction was rated highly by all of the students; however, website audio was problematic for 50% of them; video, for 71%. Students, staff, and faculty all agreed that to benefit fully from the website, adequate hardware, software, and internet connection speed were vital. Challenges with the web-based lab were either technological (inadequate equipment or skills), logistical (dissatisfaction with having to pick up home lab kits from campus), or motivational (student survey responses added to the growing literature that suggests that mature, focused, self-motivated students benefit more from distance learning).

  4. Creating stimuli for the study of biological-motion perception.

    PubMed

    Dekeyser, Mathias; Verfaillie, Karl; Vanrie, Jan

    2002-08-01

    In the perception of biological motion, the stimulus information is confined to a small number of lights attached to the major joints of a moving person. Despite this drastic degradation of the stimulus information, the human visual apparatus organizes the swarm of moving dots into a vivid percept of a moving biological creature. Several techniques have been proposed to create point-light stimuli: placing dots at strategic locations on photographs or films, video recording a person with markers attached to the body, computer animation based on artificial synthesis, and computer animation based on motion-capture data. A description is given of the technique we are currently using in our laboratory to produce animated point-light figures. The technique is based on a combination of motion capture and three-dimensional animation software (Character Studio, Autodesk, Inc., 1998). Some of the advantages of our approach are that the same actions can be shown from any viewpoint, that point-light versions, as well as versions with a full-fleshed character, can be created of the same actions, and that point lights can indicate the center of a joint (thereby eliminating several disadvantages associated with other techniques).

  5. Learning through Creating Robotic Models of Biological Systems

    ERIC Educational Resources Information Center

    Cuperman, Dan; Verner, Igor M.

    2013-01-01

    This paper considers an approach to studying issues in technology and science, which integrates design and inquiry activities towards creating and exploring technological models of scientific phenomena. We implemented this approach in a context where the learner inquires into a biological phenomenon and develops its representation in the form of a…

  6. Creating Successful Campus Partnerships for Teaching Communication in Biology Courses and Labs.

    PubMed

    Hall, Susanne E; Birch, Christina

    2018-01-01

    Creating and teaching successful writing and communication assignments for biology undergraduate students can be challenging for faculty trying to balance the teaching of technical content. The growing body of published research and scholarship on effective teaching of writing and communication in biology can help inform such work, but there are also local resources available to support writing within biology courses that may be unfamiliar to science faculty and instructors. In this article, we discuss common on-campus resources biology faculty can make use of when incorporating writing and communication into their teaching. We present the missions, histories, and potential collaboration outcomes of three major on-campus writing resources: writing across the curriculum and writing in the disciplines initiatives (WAC/WID), writing programs, and writing centers. We explain some of the common misconceptions about these resources in order to help biology faculty understand their uses and limits, and we offer guiding questions faculty might ask the directors of these resources to start productive conversations. Collaboration with these resources will likely save faculty time and effort on curriculum development and, more importantly, will help biology students develop and improve their critical reading, writing, and communication skills.

  7. Creating Successful Campus Partnerships for Teaching Communication in Biology Courses and Labs

    PubMed Central

    Hall, Susanne E.; Birch, Christina

    2018-01-01

    Creating and teaching successful writing and communication assignments for biology undergraduate students can be challenging for faculty trying to balance the teaching of technical content. The growing body of published research and scholarship on effective teaching of writing and communication in biology can help inform such work, but there are also local resources available to support writing within biology courses that may be unfamiliar to science faculty and instructors. In this article, we discuss common on-campus resources biology faculty can make use of when incorporating writing and communication into their teaching. We present the missions, histories, and potential collaboration outcomes of three major on-campus writing resources: writing across the curriculum and writing in the disciplines initiatives (WAC/WID), writing programs, and writing centers. We explain some of the common misconceptions about these resources in order to help biology faculty understand their uses and limits, and we offer guiding questions faculty might ask the directors of these resources to start productive conversations. Collaboration with these resources will likely save faculty time and effort on curriculum development and, more importantly, will help biology students develop and improve their critical reading, writing, and communication skills. PMID:29904537

  8. Using photoshop filters to create anatomic line-art medical images.

    PubMed

    Kirsch, Jacobo; Geller, Brian S

    2006-08-01

    There are multiple ways to obtain anatomic drawings suitable for publication or presentations. This article demonstrates how to use Photoshop to alter digital radiologic images to create line-art illustrations in a quick and easy way. We present two simple to use methods; however, not every image can adequately be transformed and personal preferences and specific changes need to be applied to each image to obtain the desired result. There are multiple ways to obtain anatomic drawings suitable for publication or to prepare presentations. Medical illustrators have always played a major role in the radiology and medical education process. Whether used to teach a complex surgical or radiologic procedure, to define typical or atypical patterns of the spread of disease, or to illustrate normal or aberrant anatomy, medical illustration significantly affects learning (). However, if you are not an accomplished illustrator, the alternatives can be expensive (contacting a professional medical illustrator or buying an already existing stock of digital images) or simply not necessarily applicable to what you are trying to communicate. The purpose of this article is to demonstrate how using Photoshop (Adobe Systems, San Jose, CA) to alter digital radiologic images we can create line-art illustrations in a quick, inexpensive, and easy way in preparation for electronic presentations and publication.

  9. fgui: A Method for Automatically Creating Graphical User Interfaces for Command-Line R Packages

    PubMed Central

    Hoffmann, Thomas J.; Laird, Nan M.

    2009-01-01

    The fgui R package is designed for developers of R packages, to help rapidly, and sometimes fully automatically, create a graphical user interface for a command line R package. The interface is built upon the Tcl/Tk graphical interface included in R. The package further facilitates the developer by loading in the help files from the command line functions to provide context sensitive help to the user with no additional effort from the developer. Passing a function as the argument to the routines in the fgui package creates a graphical interface for the function, and further options are available to tweak this interface for those who want more flexibility. PMID:21625291

  10. Comparable Efficacy of Abatacept Used as First-line or Second-line Biological Agent for Severe Juvenile Idiopathic Arthritis-related Uveitis.

    PubMed

    Birolo, Carolina; Zannin, Maria Elisabetta; Arsenyeva, Svetlana; Cimaz, Rolando; Miserocchi, Elisabetta; Dubko, Margarita; Deslandre, Chantal Job; Falcini, Fernanda; Alessio, Maria; La Torre, Francesco; Denisova, Ekaterina; Martini, Giorgia; Nikishina, Irina; Zulian, Francesco

    2016-11-01

    Abatacept (ABA) has recently been proposed as second-line treatment in patients with juvenile idiopathic arthritis (JIA)-associated uveitis refractory to anti-tumor necrosis factor-α (anti-TNF) agents, but little is known about its efficacy as a first-line approach. The aim of the present study was to compare the safety and efficacy of ABA as a first-line biological agent (ABA-1) with that of ABA as a second-line treatment after 1 or more anti-TNF agents (ABA-2), in patients with severe JIA-related uveitis. In this multicenter study, we collected data on patients with severe JIA-related uveitis treated with ABA as a first-line or second-line biological agent. Changes in frequency of uveitis flares/year and ocular complications before and after ABA treatment, clinical remission, and side effects were recorded. Thirty-five patients with a mean age of 10.8 years were treated with ABA for a mean period of 19.6 months. In 4 patients, ABA administration was discontinued, owing to inefficacy on arthritis in 3 cases and allergic reaction in 1. Thirty-one patients, 14 in the ABA-1 group and 17 in the ABA-2 group, completed the 12-month followup period; of these, 17 (54.8%) had clinical remission. The mean frequency of uveitis flares decreased from 4.1 to 1.2 in the ABA-1 group (p = 0.002) and from 3.7 to 1.2 in the ABA-2 group (p = 0.004). Preexisting ocular complications improved or remained stable in all but 5 patients, all in the ABA-2 group. No significant difference was found between the efficacy of the 2 treatment modalities. ABA confirmed its good safety profile. ABA, used as first-line biological treatment or after 1 or more anti-TNF agents, induces a comparable improvement in severe refractory JIA-related uveitis.

  11. Description of Patients Treated with Biologic Drugs as First-Line Systemic Therapy in the BIOBADADERM Registry Between 2008 and 2016.

    PubMed

    Carretero Hernández, G; Ferrándiz, C; Rivera Díaz, R; Daudén Tello, E; de la Cueva-Dobao, P; Gómez-García, F J; Herrera-Ceballos, E; Belinchón Romero, I; López-Estebaranz, J L; Alsina Gibert, M; Sánchez-Carazo, J L; Ferrán Farrés, M; González Quesada, A; Carrascosa Carrillo, J M; Llamas-Velasco, M; Mendiola Fernández, M V; Ruiz Genao, D; Muñoz Santos, C; García-Doval, I; Descalzo, M A

    2018-06-07

    Biologic drugs are usually prescribed as second-line treatment for psoriasis, that is, after the patient has first been treated with a conventional psoriasis drug. There are, however, cases where, depending on the characteristics of the patient or the judgement of the physician, biologics may be chosen as first-line therapy. No studies to date have analyzed the demographics or clinical characteristics of patients in this setting or the safety profile of the agents used. The main aim of this study was to characterize these aspects of first-line biologic therapy and compare them to those observed for patients receiving biologics as second-line therapy. We conducted an observational study of 181 patients treated in various centers with a systemic biologic drug as first-line treatment for moderate to severe psoriasis between January 2008 and November 2016. All the patients were registered in the Spanish Registry of Adverse Events Associated with Biologic Drugs in Dermatology. The characteristics of the first- and second-line groups were very similar, although the patients receiving a biologic as first-line treatment for their psoriasis were older. No differences were observed for disease severity (assessed using the PASI) or time to diagnosis. Hypertension, diabetes, and liver disease were all more common in the first-line group. There were no differences between the groups in terms of reasons for drug withdrawal or occurrence of adverse effects. No major differences were found between patients with psoriasis receiving biologic drugs as first- or second-line therapy, a finding that provides further evidence of the safety of biologic therapy in patients with psoriasis. Publicado por Elsevier España, S.L.U.

  12. The HepaRG cell line: biological properties and relevance as a tool for cell biology, drug metabolism, and virology studies.

    PubMed

    Marion, Marie-Jeanne; Hantz, Olivier; Durantel, David

    2010-01-01

    Liver progenitor cells may play an important role in carcinogenesis in vivo and represent therefore useful cellular materials for in vitro studies. The HepaRG cell line, which is a human bipotent progenitor cell line capable to differentiate toward two different cell phenotypes (i.e., biliary-like and hepatocyte-like cells), has been established from a liver tumor associated with chronic hepatitis C. This cell line represents a valuable alternative to ex vivo cultivated primary human hepatocytes (PHH), as HepaRG cells share some features and properties with adult hepatocytes. The cell line is particularly useful to evaluate drugs and perform drug metabolism studies, as many detoxifying enzymes are expressed and functional. It is also an interesting tool to study some aspect of progenitor biology (e.g., differentiation process), carcinogenesis, and the infection by some pathogens for which the cell line is permissive (e.g., HBV infection). Overall, this chapter gives a concise overview of the biological properties and potential applications of this cell line.

  13. Supplementing Introductory Biology with On-Line Curriculum

    ERIC Educational Resources Information Center

    McGroarty, Estelle; Parker, Joyce; Heidemann, Merle; Lim, Heejun; Olson, Mark; Long, Tammy; Merrill, John; Riffell, Samuel; Smith, James; Batzli, Janet; Kirschtel, David

    2004-01-01

    We developed web-based modules addressing fundamental concepts of introductory biology delivered through the LON-CAPA course management system. These modules were designed and used to supplement large, lecture-based introductory biology classes. Incorporating educational principles and the strength of web-based instructional technology, choices…

  14. 9 CFR 113.52 - Requirements for cell lines used for production of biologics.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 9 Animals and Animal Products 1 2012-01-01 2012-01-01 false Requirements for cell lines used for... STANDARD REQUIREMENTS Ingredient Requirements § 113.52 Requirements for cell lines used for production of... cell line used to prepare a biological product shall be tested as prescribed in this section. A cell...

  15. 9 CFR 113.52 - Requirements for cell lines used for production of biologics.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 9 Animals and Animal Products 1 2011-01-01 2011-01-01 false Requirements for cell lines used for... STANDARD REQUIREMENTS Ingredient Requirements § 113.52 Requirements for cell lines used for production of... cell line used to prepare a biological product shall be tested as prescribed in this section. A cell...

  16. 9 CFR 113.52 - Requirements for cell lines used for production of biologics.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 9 Animals and Animal Products 1 2013-01-01 2013-01-01 false Requirements for cell lines used for... STANDARD REQUIREMENTS Ingredient Requirements § 113.52 Requirements for cell lines used for production of... cell line used to prepare a biological product shall be tested as prescribed in this section. A cell...

  17. 9 CFR 113.52 - Requirements for cell lines used for production of biologics.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 9 Animals and Animal Products 1 2014-01-01 2014-01-01 false Requirements for cell lines used for... STANDARD REQUIREMENTS Ingredient Requirements § 113.52 Requirements for cell lines used for production of... cell line used to prepare a biological product shall be tested as prescribed in this section. A cell...

  18. 9 CFR 113.52 - Requirements for cell lines used for production of biologics.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 9 Animals and Animal Products 1 2010-01-01 2010-01-01 false Requirements for cell lines used for... STANDARD REQUIREMENTS Ingredient Requirements § 113.52 Requirements for cell lines used for production of... cell line used to prepare a biological product shall be tested as prescribed in this section. A cell...

  19. Differential biological effects of dehydroepiandrosterone (DHEA) between mouse (B16F10) and human melanoma (BLM) cell lines.

    PubMed

    Joshi, Kumud; Hassan, Sherif S; Ramaraj, Pandurangan

    2017-01-01

    Dehydroepiandrosterone (DHEA) is a weak androgen and had been shown to have anti-cancer, anti-adipogenic and anti-inflammatory effects on mouse and other rodent models, but not on humans, suggesting a systemic level difference between mouse and human. Our previous study on DHEA biological functions involving a variety of cell lines, suggested that the functional differences between mouse and human existed even at the cellular level. Hence, using mouse and human melanoma cell models, in-vitro effects of DHEA on cell growth, mechanism of cell death and mechanism of DHEA action were studied. Results indicated a differential biological effects of DHEA between mouse and human melanoma cell lines. These in-vitro studies also suggested that the differential biological effects observed between these two cell lines could be due to the difference in the way DHEA was processed or metabolized inside the cell.

  20. Differential Drug Survival of Second-Line Biologic Therapies in Patients with Psoriasis: Observational Cohort Study from the British Association of Dermatologists Biologic Interventions Register (BADBIR).

    PubMed

    Iskandar, Ireny Y K; Warren, Richard B; Lunt, Mark; Mason, Kayleigh J; Evans, Ian; McElhone, Kathleen; Smith, Catherine H; Reynolds, Nick J; Ashcroft, Darren M; Griffiths, Christopher E M

    2018-04-01

    Little is known about the drug survival of second-line biologic therapies for psoriasis in routine clinical practice. We assessed drug survival of second-line biologic therapies and estimated the risk of recurrent discontinuation due to adverse events or ineffectiveness in patients with psoriasis who had failed a first biologic therapy and switched to a second in a large, multicenter pharmacovigilance registry (n = 1,239; adalimumab, n = 538; etanercept, n = 104; ustekinumab, n = 597). The overall drug survival rate in the first year after switching was 77% (95% confidence interval = 74-79%), falling to 58% (55-61%) in the third year. Female sex, multiple comorbidities, concomitant therapy with cyclosporine, and a high Psoriasis Area and Severity Index at switching to the second-line biologic therapy were predictors of overall discontinuation (multivariable Cox proportional hazard model). Compared to adalimumab, patients receiving etanercept were more likely to discontinue therapy (hazard ratio = 1.87, 95% confidence interval = 1.24-2.83), whereas patients receiving ustekinumab were more likely to persist (hazard ratio = 0.46; 95% confidence interval = 0.33-0.64). Discontinuation of the first biologic therapy because of adverse events was associated with an increased rate of second drug discontinuation because of adverse events (hazard ratio = 2.55; 95% confidence interval = 1.50-4.32). In conclusion, drug survival rates differed among biologic therapies and decreased over time; second-line discontinuation because of adverse events was more common among those who discontinued first-line treatment for this reason. The results of this study should support clinical decision making when choosing second-line biologic therapy for patients with psoriasis. Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

  1. Effects of high-voltage transmission lines on honeybees

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Greenberg, B.; Bindokas, V.P.; Gauger, J.R.

    When shielded and exposed colonies were placed at incremental distances at a right angle from a 760-kV transmission line different thresholds for biologic effects were obtained. Hive exposures were controlled (E-field: 7, 5.5, 4.1, 1.8, and 0.65 to 0.85 kV/m) by variable height current collectors; shielded hives under the line behave normally. Exposure to 7 kV/m can produce the following sequence of events: (1) increased motor activity and transient hive temperature increase; (2) abnormal propolization; (3) retarded hive weight gain; (4) excess queen cell production with queen loss; (5) reduction of sealed brood area; and (6) poor winter survival. Nomore » biological effects were detected below 4.1 kV/m, thus the ''biological effects corridor'' is limited to approximately 23 m beyond a ground projection of each outer phase wire. Hive architecture enhances E-fields and creates shock hazards for bees. Intra-hive E-fields (15 to 100+ kV/m) were measured with a displacement current sensor and fiber optic telemetry link. Step-potential-induced currents up to 0.5 uA were measured with a bee model in hives at 7 kV/m. To investigate further the role of shock versus electric field exposure the study was continued to develop hive entrance extensions (porches), which produce controlled bee exposure to E-field or shock, and to test the feasibility of using these porches in such a study. Biological effects (e.g., abnormal propolization, retarded hive weight, queen loss) found in colonies with total-hive exposure were produced by entrance-only exposure of adult bees. We now have an exposure system in which E-field and shock can be separately controlled to reproduce the biological effects. 10 refs.« less

  2. The application of vector concepts on two skew lines

    NASA Astrophysics Data System (ADS)

    Alghadari, F.; Turmudi; Herman, T.

    2018-01-01

    The purpose of this study is knowing how to apply vector concepts on two skew lines in three-dimensional (3D) coordinate and its utilization. Several mathematical concepts have a related function for the other, but the related between the concept of vector and 3D have not applied in learning classroom. In fact, there are studies show that female students have difficulties in learning of 3D than male. It is because of personal spatial intelligence. The relevance of vector concepts creates both learning achievement and mathematical ability of male and female students enables to be balanced. The distance like on a cube, cuboid, or pyramid whose are drawn on the rectangular coordinates of a point in space. Two coordinate points of the lines can be created a vector. The vector of two skew lines has the shortest distance and the angle. Calculating of the shortest distance is started to create two vectors as a representation of line by vector position concept, next to determining a norm-vector of two vector which was obtained by cross-product, and then to create a vector from two combination of pair-points which was passed by two skew line, the shortest distance is scalar orthogonal projection of norm-vector on a vector which is a combination of pair-points. While calculating the angle are used two vectors as a representation of line to dot-product, and the inverse of cosine is yield. The utilization of its application on mathematics learning and orthographic projection method.

  3. The Line-drawing Problem in Disease Definition.

    PubMed

    Rogers, Wendy A; Walker, Mary Jean

    2017-08-01

    Biological dysfunction is regarded, in many accounts, as necessary and perhaps sufficient for disease. But although disease is conceptualized as all-or-nothing, biological functions often differ by degree. A tension is created by attempting to use a continuous variable as the basis for a categorical definition, raising questions about how we are to pinpoint the boundary between health and disease. This is the line-drawing problem. In this paper, we show how the line-drawing problem arises within "dysfunction-requiring" accounts of disease, such as those of Christopher Boorse and Jerome Wakefield. We then provide several detailed examples to establish that biological dysfunction cannot provide a boundary. We examine potential ways of resolving the line-drawing problem, either by dropping one of the claims that generates it, or by appealing to additional criteria. We argue that two of these options are plausible, and that each of these can be applied with regard to different diseases. © The Author 2017. Published by Oxford University Press, on behalf of the Journal of Medicine and Philosophy Inc. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

  4. Creating an Excellent Patient Experience Through Service Education: Content and Methods for Engaging and Motivating Front-Line Staff.

    PubMed

    Kennedy, Denise M

    2017-12-01

    Service quality and patient satisfaction affect an organization's value-based payments. This new value paradigm calls for a new approach to service education and training for front-line staff. Thoughtfully conceived, department-specific content, infused with patient feedback, value creation, and science of service quality principles, was developed to give front-line staff a deeper understanding of the impact of their performance on patient experience, value creation, and value-based revenue. Feedback from nearly 1500 trainees in 60 educational sessions delivered over 7 years indicates good understanding of the content and appreciation of the targeted approach. On a 5-point scale ranging from 1 (least effective) to 5 (most effective), trainees' ratings of their understanding of service quality concepts and impact on value ranged from 4.7 to 4.9. Verbatim comments showed a positive impact on staff. Employee feedback suggests that value-based service education may be useful in motivating front-line staff, improving service quality, and creating value.

  5. Discovery of HeLa Cell Contamination in HES Cells: Call for Cell Line Authentication in Reproductive Biology Research.

    PubMed

    Kniss, Douglas A; Summerfield, Taryn L

    2014-08-01

    Continuous cell lines are used frequently in reproductive biology research to study problems in early pregnancy events and parturition. It has been recognized for 50 years that many mammalian cell lines contain inter- or intraspecies contaminations with other cells. However, most investigators do not routinely test their culture systems for cross-contamination. The most frequent contributor to cross-contamination of cell lines is the HeLa cell isolated from an aggressive cervical adenocarcinoma. We report on the discovery of HeLa cell contamination of the human endometrial epithelial cell line HES isolated in our laboratory. Short tandem repeat analysis of 9 unique genetic loci demonstrated molecular identity between HES and HeLa cells. In addition, we verified that WISH cells, isolated originally from human amnion epithelium, were also contaminated with HeLa cells. Inasmuch as our laboratory did not culture HeLa cells at the time of HES cell derivations, the source of contamination was the WISH cell line. These data highlight the need for continued diligence in authenticating cell lines used in reproductive biology research. © The Author(s) 2014.

  6. Comparative morphology, biology and histology of reproductive development in three lines of Manihot esculenta Crantz (Euphorbiaceae: Crotonoideae).

    PubMed

    Perera, P I P; Quintero, M; Dedicova, B; Kularatne, J D J S; Ceballos, H

    2013-01-01

    Cassava (Manihot esculenta), a major food staple in the tropics and subtropics, thrives even in environments undergoing threatening climate change. To satisfy the increasing demand for crop improvement and overcome the limitations of conventional breeding, the introduction of inbreeding techniques such as the production of doubled haploid lines via androgenesis or gynogenesis offers advantages. However, comprehensive studies on cassava flower bud biology or structural development are lacking and precise structural and biological information is a prerequisite to enhance the efficiency of these techniques. The floral biology of three selected cassava lines was studied, focusing on morphology, phenology and pollen biology (quantity, viability and dimorphism). Histological studies were also conducted on microsporogenesis/microgametogenesis and megasporogenesis/megagameto-genesis to generate precise developmental data for these lines. Male and female cyathia have distinct developmental phases. Pollen viability was high during immature stages of plant development; however, pollen mortality was common at later stages. Pollen trimorphism in male gametophytes towards the larger or smaller pollen size, as compared with normal size, was observed. Ten characteristic events were identified in male gametogenesis and six in female gametogenesis that were correlated with flower bud diameter. Male gametophyte diameter at different developmental stages was also determined. Results indicate that the three lines did not differ significantly, except regarding a few morphological aspects such as plant height, flower colour and number of male cyathia. Pollen grains were initially viable, but viability decreased drastically at later stages of growth. Abnormal meiosis or mitosis triggered pollen trimorphism. The demonstrated sequential events of reproductive development generated valuable information at the cellular level, which will help close the current information gap for cassava

  7. On-Line Course Development: Engaging and Retaining Students

    ERIC Educational Resources Information Center

    Bruster, Benita G.

    2015-01-01

    As the number of on-line classes and the demand for on-line education continues to sky-rocket, it is critical that course developers and university faculty have the skills to effectively design curricula, to develop engaging learning opportunities, and to create responsive courses that meet individual student needs. This paper details three…

  8. Biological pacemaker created by minimally invasive somatic reprogramming in pigs with complete heart block

    PubMed Central

    Hu, Yu-Feng; Dawkins, James Frederick; Cho, Hee Cheol; Marbán, Eduardo; Cingolani, Eugenio

    2016-01-01

    Somatic reprogramming by reexpression of the embryonic transcription factor T-box 18 (TBX18) converts cardiomyocytes into pacemaker cells. We hypothesized that this could be a viable therapeutic avenue for pacemaker-dependent patients afflicted with device-related complications, and therefore tested whether adenoviral TBX18 gene transfer could create biological pacemaker activity in vivo in a large-animal model of complete heart block. Biological pacemaker activity, originating from the intramyocardial injection site, was evident in TBX18-transduced animals starting at day 2 and persisted for the duration of the study (14 days) with minimal backup electronic pacemaker use. Relative to controls transduced with a reporter gene, TBX18-transduced animals exhibited enhanced autonomic responses and physiologically superior chronotropic support of physical activity. Induced sinoatrial node cells could be identified by their distinctive morphology at the site of injection in TBX18-transduced animals, but not in controls. No local or systemic safety concerns arose. Thus, minimally invasive TBX18 gene transfer creates physiologically relevant pacemaker activity in complete heart block, providing evidence for therapeutic somatic reprogramming in a clinically relevant disease model. PMID:25031269

  9. Biological sample evaluation using a line-scan based SWIR hyperspectral imaging system

    USDA-ARS?s Scientific Manuscript database

    A new line-scan hyperspectral imaging system was developed to enable short wavelength infrared (SWIR) imagery for biological sample evaluation. Critical sensing components include a SWIR imaging spectrograph and an HgCdTe (MCT) focal plane array detector. To date, agricultural applications of infra...

  10. Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response.

    PubMed

    Nickerson, M L; Witte, N; Im, K M; Turan, S; Owens, C; Misner, K; Tsang, S X; Cai, Z; Wu, S; Dean, M; Costello, J C; Theodorescu, D

    2017-01-05

    The utility of tumor-derived cell lines is dependent on their ability to recapitulate underlying genomic aberrations and primary tumor biology. Here, we sequenced the exomes of 25 bladder cancer (BCa) cell lines and compared mutations, copy number alterations (CNAs), gene expression and drug response to BCa patient profiles in The Cancer Genome Atlas (TCGA). We observed a mutation pattern associated with altered CpGs and APOBEC-family cytosine deaminases similar to mutation signatures derived from somatic alterations in muscle-invasive (MI) primary tumors, highlighting a major mechanism(s) contributing to cancer-associated alterations in the BCa cell line exomes. Non-silent sequence alterations were confirmed in 76 cancer-associated genes, including mutations that likely activate oncogenes TERT and PIK3CA, and alter chromatin-associated proteins (MLL3, ARID1A, CHD6 and KDM6A) and established BCa genes (TP53, RB1, CDKN2A and TSC1). We identified alterations in signaling pathways and proteins with related functions, including the PI3K/mTOR pathway, altered in 60% of lines; BRCA DNA repair, 44%; and SYNE1-SYNE2, 60%. Homozygous deletions of chromosome 9p21 are known to target the cell cycle regulators CDKN2A and CDKN2B. This loci was commonly lost in BCa cell lines and we show the deletions extended to the polyamine enzyme methylthioadenosine (MTA) phosphorylase (MTAP) in 36% of lines, transcription factor DMRTA1 (27%) and antiviral interferon epsilon (IFNE, 19%). Overall, the BCa cell line genomic aberrations were concordant with those found in BCa patient tumors. We used gene expression and copy number data to infer pathway activities for cell lines, then used the inferred pathway activities to build a predictive model of cisplatin response. When applied to platinum-treated patients gathered from TCGA, the model predicted treatment-specific response. Together, these data and analysis represent a valuable community resource to model basic tumor biology and to study

  11. Students Reflecting on Test Performance and Feedback: An On-Line Approach

    ERIC Educational Resources Information Center

    Fyfe, Georgina; Fyfe, Sue; Meyer, Jan; Ziman, Mel; Sanders, Kathy; Hill, Julie

    2014-01-01

    Undergraduate students accessing on-line tests in Human Biology in three Western Australian universities were asked to complete an on-line post-test reflective survey about their perceptions of their test performance in light of automated feedback. The survey allowed pre-determined choices and comment text boxes relating to students' perceptions…

  12. Tailored first-line biologic therapy in patients with rheumatoid arthritis, spondyloarthritis, and psoriatic arthritis.

    PubMed

    Cantini, Fabrizio; Niccoli, Laura; Nannini, Carlotta; Cassarà, Emanuele; Kaloudi, Olga; Giulio Favalli, Ennio; Becciolini, Andrea; Biggioggero, Martina; Benucci, Maurizio; Li Gobbi, Francesca; Grossi, Valentina; Infantino, Maria; Meacci, Francesca; Manfredi, Mariangela; Guiducci, Serena; Bellando-Randone, Silvia; Matucci-Cerinic, Marco; Foti, Rosario; Di Gangi, Marcella; Mosca, Marta; Tani, Chiara; Palmieri, Fabrizio; Goletti, Delia

    2016-04-01

    A multidisciplinary expert panel, the Italian board for the TAilored BIOlogic therapy (ITABIO), was constituted to formulate evidence-based decisional statements for the first-line tailored biologic therapy in patient with rheumatoid arthritis (RA), spondyloarthritis (SpA), and psoriatic arthritis (PsA). Systematic review of the literature to identify English-language articles on the variables influencing the first-line biologic choice, including the efficacy and safety of the drug, the route of administration, the availability of response predictor biomarkers, the need of monotherapy, the patient socio-economic status, lifestyle, cultural level, personality, fertility and childbearing potential in women, the presence of comorbidities, the host-related risk factors for infection and latent tuberculosis infection (LTBI) reactivation, the cardiovascular (CV) risk, and costs. Some variables, including the patients' preference, the indication for anti-TNF monotherapy in potential childbearing women, and the intravenous route with dose titration in obese subjects resulted valid for all the three rheumatic conditions. Further, evidence of a better cost-effectiveness profile for etanercept (ETN) and biosimilar infliximab (IFX) in RA was found. Any biologic may be employed in absence of choice driving factors in RA. Otherwise, a high infection risk or LTBI positivity drive the choice toward abatacept (ABA), tocilizumab (TCZ), or ETN. TCZ should be the first choice if monotherapy is required. High rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPA) titers should drive the choice toward TCZ or ABA, while in patients at high CVD risk anti-TNF choice, with preference for ETN, seems appropriate. Presence of anterior uveitis or inflammatory bowel disease drives the choice to monoclonal antibody anti-TNFs (MoAb anti-TNFs). In PsA, ustekinumab (UTK), and to a lesser extent ETN, represents the first choice in patients at high infection and TB risk. Anti-TNFs or

  13. On Designing Multicore-Aware Simulators for Systems Biology Endowed with OnLine Statistics

    PubMed Central

    Calcagno, Cristina; Coppo, Mario

    2014-01-01

    The paper arguments are on enabling methodologies for the design of a fully parallel, online, interactive tool aiming to support the bioinformatics scientists .In particular, the features of these methodologies, supported by the FastFlow parallel programming framework, are shown on a simulation tool to perform the modeling, the tuning, and the sensitivity analysis of stochastic biological models. A stochastic simulation needs thousands of independent simulation trajectories turning into big data that should be analysed by statistic and data mining tools. In the considered approach the two stages are pipelined in such a way that the simulation stage streams out the partial results of all simulation trajectories to the analysis stage that immediately produces a partial result. The simulation-analysis workflow is validated for performance and effectiveness of the online analysis in capturing biological systems behavior on a multicore platform and representative proof-of-concept biological systems. The exploited methodologies include pattern-based parallel programming and data streaming that provide key features to the software designers such as performance portability and efficient in-memory (big) data management and movement. Two paradigmatic classes of biological systems exhibiting multistable and oscillatory behavior are used as a testbed. PMID:25050327

  14. On designing multicore-aware simulators for systems biology endowed with OnLine statistics.

    PubMed

    Aldinucci, Marco; Calcagno, Cristina; Coppo, Mario; Damiani, Ferruccio; Drocco, Maurizio; Sciacca, Eva; Spinella, Salvatore; Torquati, Massimo; Troina, Angelo

    2014-01-01

    The paper arguments are on enabling methodologies for the design of a fully parallel, online, interactive tool aiming to support the bioinformatics scientists .In particular, the features of these methodologies, supported by the FastFlow parallel programming framework, are shown on a simulation tool to perform the modeling, the tuning, and the sensitivity analysis of stochastic biological models. A stochastic simulation needs thousands of independent simulation trajectories turning into big data that should be analysed by statistic and data mining tools. In the considered approach the two stages are pipelined in such a way that the simulation stage streams out the partial results of all simulation trajectories to the analysis stage that immediately produces a partial result. The simulation-analysis workflow is validated for performance and effectiveness of the online analysis in capturing biological systems behavior on a multicore platform and representative proof-of-concept biological systems. The exploited methodologies include pattern-based parallel programming and data streaming that provide key features to the software designers such as performance portability and efficient in-memory (big) data management and movement. Two paradigmatic classes of biological systems exhibiting multistable and oscillatory behavior are used as a testbed.

  15. Synthesis and biological evaluation of Fotemustine analogues on human melanoma cell lines.

    PubMed

    Winum, Jean Yves; Bouissière, Jean Luc; Passagne, Isabelle; Evrard, Alexandre; Montero, Véronique; Cuq, Pierre; Montero, Jean Louis

    2003-03-01

    Two new analogues of Fotemustine have been synthesized and tested on two melanoma cell lines. Compounds 4 and 8 proved to be more potent than the reference compound on A375 cell line which express the MGMT enzyme involved in the chemoresistance of tumoral cells.

  16. The implementation of an integrated on-line health education system at RMIT.

    PubMed

    Zylinski, J; Allan, G L; Jamieson, P; Maher, K P; Green, R; Hislop, J

    1998-06-01

    The Faculty of Biomedical and Health Sciences at RMIT has been developing an on-line health education system using a systems thinking approach, to create a learning environment whose basis is supported by Information Technology (IT). The centre-piece of this system is the Faculty Learning Centre, which has been created, both in space and layout, to promote collaborative learning between the students, so that the educator is physically assimilated with the student body. This facility is supplemented by the Faculty WWW server, which has been the main vehicle for course material dissemination to students. To ensure an effective on-line teaching environment, the position of an on-line facilitator has been created, whose responsibilities include both the continual evaluation of the system and the implementation of appropriate system changes. Aspects have included the production of a staff development training program and extensive user documentation. This paper discusses the systems thinking approach used to implement this integrated on-line system, and the establishment of explicit educational rationales in the use of IT to support learning strategies. Some examples of the on-line educational programs are also presented.

  17. Assessment of biological effectiveness of boron neutron capture therapy in primary and metastatic melanoma cell lines.

    PubMed

    Rossini, Andrés E; Dagrosa, Maria A; Portu, Agustina; Saint Martin, Giselle; Thorp, Silvia; Casal, Mariana; Navarro, Aimé; Juvenal, Guillermo J; Pisarev, Mario A

    2015-01-01

    In order to optimize the effectiveness of Boron Neutron Capture Therapy (BNCT), Relative Biological Effectiveness (RBE) and Compound Biological Effectiveness (CBE) were determined in two human melanoma cell lines, M8 and Mel-J cells, using the amino acid p-boronophenylalanine (BPA) as boron carrier. The effects of BNCT on the primary amelanotic cell line M8 and on the metastatic pigmented melanoma cell line Mel-J were studied using colony formation assay. The RBE values were determined using both a gamma ray source, and the neutron beam from the Nuclear Reactor of the National Atomic Energy Commission (RA-3). For the determination of the RBE, cells were irradiated with increasing doses of both sources, between 1 and 8 Gy; and for the determination of CBE factors, the cells were pre-incubated with BPA before irradiation. Afterwards, the cell surviving fraction (SF) was determined for each treatment. Marked differences were observed between both cell lines. Mel-J cells were more radioresistant than the M8 cell line. The clonogenic assays showed that for a SF of 1%, the RBE values were 1.3 for M8 cells and 1.5 for Mel-J cells. Similarly, the CBE values for a 1% SF were 2.1 for M8 and 3 for Mel-J cell lines. For the endpoint of 0.1% of SF the RBE values obtained were 1.2 for M8 and 1.4 for Mel-J cells. Finally, CBE values calculated for a 0.1% were 2 and 2.6 for M8 and Mel-J cell lines respectively. In order to estimate the uptake of the non-radioactive isotope Boron 10 ((10)B), a neutron induced autoradiographic technique was performed showing discrepancies in (10)B uptake between both cell lines. These obtained in vitro results are the first effectiveness factors determined for human melanoma at the RA-3 nuclear reactor and show that BNCT dosimetry planning for patients could be successfully performed using these new factors.

  18. Inhibition of Survivin Influences the Biological Activities of Canine Histiocytic Sarcoma Cell Lines

    PubMed Central

    Hoshino, Yuki; Hosoya, Kenji; Okumura, Masahiro

    2013-01-01

    Canine histiocytic sarcoma (CHS) is an aggressive malignant neoplasm that originates from histiocytic lineage cells, including dendritic cells and macrophages, and is characterized by progressive local infiltration and a very high metastatic potential. Survivin is as an apoptotic inhibitory factor that has major functions in cell proliferation, including inhibition of apoptosis and regulation of cell division, and is expressed in most types of human and canine malignant neoplasms, including melanoma and osteosarcoma. To investigate whether survivin was expressed at high levels in CHS and whether its expression was correlated with the aggressive biological behavior of CHS, we assessed relation between survivin expression and CHS progression, as well as the effects of survivin inhibition on the biological activities of CHS cells. We comparatively analyzed the expression of 6 selected anti-apoptotic genes, including survivin, in specimens from 30 dogs with histiocytic sarcoma and performed annexin V staining to evaluate apoptosis, methylthiazole tetrazolium assays to assess cell viability and chemosensitivity, and latex bead assays to measure changes in phagocytic activities in 4 CHS cell lines and normal canine fibroblasts transfected with survivin siRNA. Survivin gene expression levels in 30 specimens were significantly higher than those of the other 6 genes. After transfection with survivin siRNA, apoptosis, cell growth inhibition, enhanced chemosensitivity, and weakened phagocytic activities were observed in all CHS cell lines. In contrast, normal canine fibroblasts were not significantly affected by survivin knockdown. These results suggested that survivin expression may mediate the aggressive biological activities of CHS and that survivin may be an effective therapeutic target for the treatment of CHS. PMID:24260303

  19. Characterization of Relative Biological Effectiveness for Proton Therapy in Human Cancer Cell Lines

    NASA Astrophysics Data System (ADS)

    Howard, Michelle Erin

    Purpose: Relative biological effectiveness (RBE) is utilized to account for the differences in biological effect from different radiation types. The RBE for proton therapy remains uncertain as it has been shown to vary from the clinically used value of 1.1. The purpose of this thesis was to investigate the RBE of protons as compared to X-rays and correlate the biological differences with the underlying physics. Methods: Three cell lines were irradiated (CHO, Chinese hamster ovary; A549, human lung adenocarcinoma; and T98, human glioma) and assessed for cell survival using clonogenic assay. Cells were irradiated with 71 and 160 MeV protons at depths along the Bragg curve and 6 MV X-rays to various doses. To correlate the underlying physics to RBE, both the dose averaged lineal energy (y¯D) and dose averaged LET (LETd) investigated. The microdosimetric quantity y¯D was measured under similar conditions as the cells using a solid state microdosimeter and LETd calculated using Monte Carlo (MC) simulations. Survival data were fit using the linear quadratic model. RBE values were calculated by comparing the physical dose (D6MV/Dp) that results in 50% (RBE0.5), 10% (RBE0.1) cell survival, and survival after 2Gy (RBE2 Gy).. Results: For 10% and 50% survival, the RBE for all three cell lines increased with decreasing proton energy (or increased depth). The RBE at 2Gy also increased with a decrease in proton energy in all cases, within experimental error. Results also showed the experimental end point proved to influence the measured proton RBE as well with larger values corresponding to 50% cell survival. Cell type had the least influence on proton RBE compared to proton energy and end point. Results from this study showed an increase in RBE corresponded to an increase in both LETd and y¯ D. Additionally, the measured y¯D and calculated LET d values did not match for all the points of measurement along the curve for the 71 and 160 MeV proton beams. Conclusion: Proton

  20. Magnetic Field Lines on the Sun

    NASA Image and Video Library

    2015-01-28

    Scientists have developed a way to produce models of where the magnetic field lines are several times each day. Here we have created a time-lapse version of these models over four days (2-3 each day) to give you a peek at how these change over time. The spiraling arcs of magnetic field lines emerge from active regions and connect back to areas with the opposite polarity. The field lines are more concentrated where regions are more magnetically intense. And of course, they rotate with the rotation of the Sun. Credit: NASA/Solar Dynamics Observatory NASA image use policy. NASA Goddard Space Flight Center enables NASA’s mission through four scientific endeavors: Earth Science, Heliophysics, Solar System Exploration, and Astrophysics. Goddard plays a leading role in NASA’s accomplishments by contributing compelling scientific knowledge to advance the Agency’s mission. Follow us on Twitter Like us on Facebook Find us on Instagram

  1. A Theoretical Approach to Selection of a Biologically Active Substance in Ultra-Low Doses for Effective Action on a Biological System.

    PubMed

    Boldyreva, Liudmila Borisovna

    2018-05-01

     An approach is offered to selecting a biologically active substance (BAS) in ultra-low dose for effective action on a biological system (BS). The technique is based on the assumption that BAS in ultra-low doses exerts action on BS by means of spin supercurrent emerging between the spin structure created by BAS, on the one hand, and the spin structure created by BS, on the other hand. According to modern quantum-mechanical concepts, these spin structures may be virtual particles pairs having precessing spin (that is, be essentially spin vortices in the physical vacuum) and created by the quantum entities that BAS and BS consist of. The action is effective provided there is equality of precession frequencies of spins in these spin structures.  In this work, some methods are considered for determining the precession frequencies of spins in virtual particles pairs: (1) determination of energy levels of quantum entities that BS and BAS consist of; (2) the use of spin-flip effect of the virtual particles pair spin, the effect being initiated by action of magnetic vector potential (the spin-flip effect takes place when the varied frequency of the magnetic vector potential equals the precession frequency of the spin); (3) determining the frequencies of photons effectively acting on BS.  It is shown that the effect of BAS in ultra-low doses on BS can be replaced by the effect of a beam of low-intensity photons, if the frequency of photons equals the precession frequency of spin in spin structures created by BS. Consequently, the color of bodies placed near a biological system is able to exert an effective action on the biological system: that is "color therapy" is possible. It is also supposed that the spin-flip effect may be used not only for determining the precession frequency of spin in spin structures created by BS but also for therapeutic action on biological systems. The Faculty of Homeopathy.

  2. Expanding biological data standards development processes for US IOOS: visual line transect observing community for mammal, bird, and turtle data

    USGS Publications Warehouse

    Fornwall, M.; Gisiner, R.; Simmons, S. E.; Moustahfid, Hassan; Canonico, G.; Halpin, P.; Goldstein, P.; Fitch, R.; Weise, M.; Cyr, N.; Palka, D.; Price, J.; Collins, D.

    2012-01-01

    The US Integrated Ocean Observing System (IOOS) has recently adopted standards for biological core variables in collaboration with the US Geological Survey/Ocean Biogeographic Information System (USGS/OBIS-USA) and other federal and non-federal partners. In this Community White Paper (CWP) we provide a process to bring into IOOS a rich new source of biological observing data, visual line transect surveys, and to establish quality data standards for visual line transect observations, an important source of at-sea bird, turtle and marine mammal observation data. The processes developed through this exercise will be useful for other similar biogeographic observing efforts, such as passive acoustic point and line transect observations, tagged animal data, and mark-recapture (photo-identification) methods. Furthermore, we suggest that the processes developed through this exercise will serve as a catalyst for broadening involvement by the larger marine biological data community within the goals and processes of IOOS.

  3. Relative biological effectiveness of light ions in human tumoural cell lines: role of protein p53

    NASA Technical Reports Server (NTRS)

    Baggio, L.; Cavinato, M.; Cherubini, R.; Conzato, M.; Cucinotta, F.; Favaretto, S.; Gerardi, S.; Lora, S.; Stoppa, P.; Williams, J. R.

    2002-01-01

    Protons and alpha particles of high linear energy transfer (LET) have shown an increased relative biological effectiveness (RBE) with respect to X/gamma rays for several cellular and molecular endpoints in different in vitro cell systems. To contribute to understanding the biochemical mechanisms involved in the increased effectiveness of high LET radiation, an extensive study has been designed. The present work reports the preliminary result of this study on two human tumoural cell lines, DLD1 and HCT116, (with different p53 status), which indicate that for these cell lines, p53 does not appear to take a part in the response to radiation induced DNA damage, suggesting an alternative p53-independent pathway and a cell biochemical mechanism dependent on the cell type.

  4. Immortal hepatic stellate cell lines: useful tools to study hepatic stellate cell biology and function?

    PubMed Central

    Herrmann, Jens; Gressner, Axel M; Weiskirchen, Ralf

    2007-01-01

    Abstract At the cellular level, the activation and transdifferentiation of quiescent hepatic stellate cells (HSC) into myofibroblasts is the key process involved in hepatic fibrogenesis that is associated with an increased and altered deposition of extracellular matrix components in the liver. The temporal sequence of molecular events associated with stellate cell activation turned out to be appropriately mimicked when HSC isolated from normal livers are cultured on uncoated plastic surface. Therefore, cultured primary cells isolated from rodents and human beings are common in vitro models in investigations addressing these issues of hepatic stellate biology and function. However, the limited supply, cost-effective isolation procedure and the ever growing need have resulted in efforts to establish immortalized stellate cell lines having the advantage of virtually unlimited access. They allow rapid screening for disease-associated factors and restrict the necessary number of animal experiments. From the first description of an immortal HSC line in 1986, a huge number of studies were conducted with these established cell lines. However, differences in morphology, growth characteristics and anomalies of chromosome number and structure make the applications of these models questionable. Here, we summarize the history and cellular characteristics of respective cell lines and discuss the differences of continuous HSC lines and their primary counterparts. PMID:17760834

  5. Immortal hepatic stellate cell lines: useful tools to study hepatic stellate cell biology and function?

    PubMed

    Herrmann, Jens; Gressner, Axel M; Weiskirchen, Ralf

    2007-01-01

    At the cellular level, the activation and transdifferentiation of quiescent hepatic stellate cells (HSC) into myofibroblasts is the key process involved in hepatic fibrogenesis that is associated with an increased and altered deposition of extracellular matrix components in the liver. The temporal sequence of molecular events associated with stellate cell activation turned out to be appropriately mimicked when HSC isolated from normal livers are cultured on uncoated plastic surface. Therefore, cultured primary cells isolated from rodents and human beings are common in vitro models in investigations addressing these issues of hepatic stellate biology and function. However, the limited supply, cost-effective isolation procedure and the ever growing need have resulted in efforts to establish immortalized stellate cell lines having the advantage of virtually unlimited access. They allow rapid screening for disease-associated factors and restrict the necessary number of animal experiments. From the first description of an immortal HSC line in 1986, a huge number of studies were conducted with these established cell lines. However, differences in morphology, growth characteristics and anomalies of chromosome number and structure make the applications of these models questionable. Here, we summarize the history and cellular characteristics of respective cell lines and discuss the differences of continuous HSC lines and their primary counterparts.

  6. [History of the Montpellier Society of Biology].

    PubMed

    Bali, Jean-Pierre

    2017-01-01

    The provincial branch of Montpellier was officially created in April, 1956, that is to say if the gestation was long since the birth of the Society of Biology of Paris in 1848. During this long period, famous personalities of Montpellier in the field of biology and physiology came to Paris to present their work, published in the "Comptes Rendus des Séances de la Société de Biologie et de ses Filiales". Following its creation as a 1901 law public association, the provincial branch organized communication sessions, followed by thematic meetings on various topics, always in the spirit of Claude Bernard on the transversality of knowledge. Through the visit of a portrait gallery of famous personalities, the main lines of the life of this provincial branch of Montpellier will be presented. © Société de Biologie, 2017.

  7. The Biology of the Germ line in Echinoderms

    PubMed Central

    Wessel, Gary M.; Brayboy, Lynae; Fresques, Tara; Gustafson, Eric A.; Oulhen, Nathalie; Ramos, Isabela; Reich, Adrian; Swartz, S. Zachary; Yajima, Mamiko; Zazueta, Vanessa

    2014-01-01

    SUMMARY The formation of the germ line in an embryo marks a fresh round of reproductive potential. The developmental stage and location within the embryo where the primordial germ cells (PGCs) form, however, differs markedly among species. In many animals, the germ line is formed by an inherited mechanism, in which molecules made and selectively partitioned within the oocyte drive the early development of cells that acquire this material to a germ-line fate. In contrast, the germ line of other animals is fated by an inductive mechanism that involves signaling between cells that directs this specialized fate. In this review, we explore the mechanisms of germ-line determination in echinoderms, an early-branching sister group to the chordates. One member of the phylum, sea urchins, appears to use an inherited mechanism of germ-line formation, whereas their relatives, the sea stars, appear to use an inductive mechanism. We first integrate the experimental results currently available for germ line determination in the sea urchin, for which considerable new information is available, and then broaden the investigation to the lesser-known mechanisms in sea stars and other echinoderms. Even with this limited insight, it appears that sea stars, and perhaps the majority of the echinoderm taxon, rely on inductive mechanisms for germ-line fate determination. This enables a strongly contrasted picture for germ-line determination in this phylum, but one for which transitions between different modes of germ-line determination might now be experimentally addressed. PMID:23900765

  8. Graduate student training and creating new physics labs for biology students, killing two birds with one stone.

    NASA Astrophysics Data System (ADS)

    Jones, Barbara

    2001-03-01

    At UCSD biology majors are required to take 3 quarters of a calculus based physics course. This is taught in a standard format large lecture class partly by faculty and partly by freeway flyers. We are working with physics graduate students who are also participating in our PFPF (Preparing Future Physics Faculty) program to write, review, and teach new weekly labs for these biology students. This provides an experience for the grad student that is both rewarding to them and useful to the department. The grad students participate in curriculum development, they observe the students behaviour in the labs, and assess the effectiveness of different lab formats. The labs are intended to provide an interactive, hands on experience with a wide variety of equipment which is mostly both simple and inexpensive. Both students and grads find the labs to be engaging and fun. Based on group discussions the labs are modified to try to try to create the best teaching environment. The biology students benefit from the improvements both in the quality of the labs they do, and from the enthusiasm of the TAs who take an active interest in their learning. The ability to make significant changes to the material taught maintains the interest of the grad students and helps to make the labs a stable and robust environment.

  9. The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes.

    PubMed

    Richardson, Sandra R; Doucet, Aurélien J; Kopera, Huira C; Moldovan, John B; Garcia-Perez, José Luis; Moran, John V

    2015-04-01

    Transposable elements have had a profound impact on the structure and function of mammalian genomes. The retrotransposon Long INterspersed Element-1 (LINE-1 or L1), by virtue of its replicative mobilization mechanism, comprises ∼17% of the human genome. Although the vast majority of human LINE-1 sequences are inactive molecular fossils, an estimated 80-100 copies per individual retain the ability to mobilize by a process termed retrotransposition. Indeed, LINE-1 is the only active, autonomous retrotransposon in humans and its retrotransposition continues to generate both intra-individual and inter-individual genetic diversity. Here, we briefly review the types of transposable elements that reside in mammalian genomes. We will focus our discussion on LINE-1 retrotransposons and the non-autonomous Short INterspersed Elements (SINEs) that rely on the proteins encoded by LINE-1 for their mobilization. We review cases where LINE-1-mediated retrotransposition events have resulted in genetic disease and discuss how the characterization of these mutagenic insertions led to the identification of retrotransposition-competent LINE-1s in the human and mouse genomes. We then discuss how the integration of molecular genetic, biochemical, and modern genomic technologies have yielded insight into the mechanism of LINE-1 retrotransposition, the impact of LINE-1-mediated retrotransposition events on mammalian genomes, and the host cellular mechanisms that protect the genome from unabated LINE-1-mediated retrotransposition events. Throughout this review, we highlight unanswered questions in LINE-1 biology that provide exciting opportunities for future research. Clearly, much has been learned about LINE-1 and SINE biology since the publication of Mobile DNA II thirteen years ago. Future studies should continue to yield exciting discoveries about how these retrotransposons contribute to genetic diversity in mammalian genomes.

  10. Electrical and Biological Effects of Transmission Lines: A Review.

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Lee, Jack M.

    1989-06-01

    This review describes the electrical properties of a-c and d-c transmission lines and the resulting effects on plants, animals, and people. Methods used by BPA to mitigate undesirable effects are also discussed. Although much of the information in this review pertains to high-voltage transmission lines, information on distribution lines and electrical appliances is included. The electrical properties discussed are electric and magnetic fields and corona: first for alternating-current (a-c) lines, then for direct current (d-c).

  11. Hydrology or biology? Modeling simplistic physical constraints on lake carbon biogeochemistry to identify when and where biology is likely to matter

    NASA Astrophysics Data System (ADS)

    Jones, S.; Zwart, J. A.; Solomon, C.; Kelly, P. T.

    2017-12-01

    Current efforts to scale lake carbon biogeochemistry rely heavily on empirical observations and rarely consider physical or biological inter-lake heterogeneity that is likely to regulate terrestrial dissolved organic carbon (tDOC) decomposition in lakes. This may in part result from a traditional focus of lake ecologists on in-lake biological processes OR physical-chemical pattern across lake regions, rather than on process AND pattern across scales. To explore the relative importance of local biological processes and physical processes driven by lake hydrologic setting, we created a simple, analytical model of tDOC decomposition in lakes that focuses on the regulating roles of lake size and catchment hydrologic export. Our simplistic model can generally recreate patterns consistent with both local- and regional-scale patterns in tDOC concentration and decomposition. We also see that variation in lake hydrologic setting, including the importance of evaporation as a hydrologic export, generates significant, emergent variation in tDOC decomposition at a given hydrologic residence time, and creates patterns that have been historically attributed to variation in tDOC quality. Comparing predictions of this `biologically null model' to field observations and more biologically complex models could indicate when and where biology is likely to matter most.

  12. Creating Perfused Functional Vascular Channels Using 3D Bio-Printing Technology

    PubMed Central

    Lee, Vivian K.; Kim, Diana Y.; Ngo, Haygan; Lee, Young; Seo, Lan; Yoo, Seung-Schik; Vincent, Peter A.; Dai, Guohao

    2014-01-01

    We developed a methodology using 3D bio-printing technology to create a functional in vitro vascular channel with perfused open lumen using only cells and biological matrices. The fabricated vasculature has a tight, confluent endothelium lining, presenting barrier function for both plasma protein and high-molecular weight dextran molecule. The fluidic vascular channel is capable of supporting the viability of tissue up to 5mm in distance at 5 million cells/mL density under the physiological flow condition. In static-cultured vascular channels, active angiogenic sprouting from the vessel surface was observed whereas physiological flow strongly suppressed this process. Gene expression analysis were reported in this study to show the potential of this vessel model in vascular biology research. The methods have great potential in vascularized tissue fabrication using 3D bio-printing technology as the vascular channel is simultaneously created while cells and matrix are printed around the channel in desired 3D patterns. It can also serve as a unique experimental tool for investigating fundamental mechanisms of vascular remodeling with extracellular matrix and maturation process under 3D flow condition. PMID:24965886

  13. The Lesson Observation On-Line (Evidence Portfolio) Platform

    ERIC Educational Resources Information Center

    Cooper, David G.

    2015-01-01

    At a time when teacher training is being moved to school-based programmes it is important to engage in a research-informed dialogue about creating more distinctive, and cost-effective 21st century models of teacher training. Three years ago I began feasibility field testing the Lesson Observation On-line (Evidence Portfolio) Platform [LOOP]…

  14. Generation of Rab-based transgenic lines for in vivo studies of endosome biology in zebrafish

    PubMed Central

    Clark, Brian S.; Winter, Mark; Cohen, Andrew R.; Link, Brian A.

    2011-01-01

    The Rab family of small GTPases function as molecular switches regulating membrane and protein trafficking. Individual Rab isoforms define and are required for specific endosomal compartments. To facilitate in vivo investigation of specific Rab proteins, and endosome biology in general, we have generated transgenic zebrafish lines to mark and manipulate Rab proteins. We also developed software to track and quantify endosome dynamics within time-lapse movies. The established transgenic lines ubiquitously express EGFP fusions of Rab5c (early endosomes), Rab11a (recycling endosomes), and Rab7 (late endosomes) to study localization and dynamics during development. Additionally, we generated UAS-based transgenic lines expressing constitutive active (CA) and dominant negative (DN) versions for each of these Rab proteins. Predicted localization and functional consequences for each line were verified through a variety of assays, including lipophilic dye uptake and Crumbs2a localization. In summary, we have established a toolset for in vivo analyses of endosome dynamics and functions. PMID:21976318

  15. Polymer monolithic capillary microextraction on-line coupled with inductively coupled plasma-mass spectrometry for the determination of trace Au and Pd in biological samples

    NASA Astrophysics Data System (ADS)

    Liu, Xiaolan; He, Man; Chen, Beibei; Hu, Bin

    2014-11-01

    A novel method based on on-line polymer monolithic capillary microextraction (CME)-inductively coupled plasma mass spectrometry (ICP-MS) was developed for the determination of trace Au and Pd in biological samples. For this purpose, poly(glycidyl methacrylate-ethylene dimethacrylate) monolith was prepared and functionalized with mercapto groups. The prepared monolith exhibited good selectivity to Au and Pd, and good resistance to strong acid with a long life span. Factors affecting the extraction efficiency of CME, such as sample acidity, sample flow rate, eluent conditions and coexisting ion interference were investigated in detail. Under the optimal conditions, the limits of detection (LODs, 3σ) were 5.9 ng L- 1 for Au and 8.3 ng L- 1 for Pd, and the relative standard deviations (RSDs, c = 50 ng L-1, n = 7) were 6.5% for Au and 1.1% for Pd, respectively. The developed method was successfully applied to the determination of Au and Pd in human urine and serum samples with the recovery in the range of 84-118% for spiked samples. The developed on-line polymer monolithic CME-ICP-MS method has the advantages of rapidity, simplicity, low sample/reagent consumption, high sensitivity and is suitable for the determination of trace Au and Pd in biological samples with limited amount available and complex matrix.

  16. Number Sense on the Number Line

    ERIC Educational Resources Information Center

    Woods, Dawn Marie; Ketterlin Geller, Leanne; Basaraba, Deni

    2018-01-01

    A strong foundation in early number concepts is critical for students' future success in mathematics. Research suggests that visual representations, like a number line, support students' development of number sense by helping them create a mental representation of the order and magnitude of numbers. In addition, explicitly sequencing instruction…

  17. Automated high performance liquid chromatography with on-line reduction of disulfides and chemiluminescence detection for determination of thiols and disulfides in biological fluids.

    PubMed

    Bai, Shouli; Chen, Qingshuo; Lu, Chao; Lin, Jin-Ming

    2013-03-20

    In general, the reduction of disulfide bonds with tris(2-carboxyethyl)phosphine (TCEP) is performed using off-line operation, which is not only time-consuming but also vulnerable to the spontaneous re-oxidation of thiols during sample preparation and subsequent analysis procedures. To the best of our knowledge, there has been not any case on the on-line reduction for biological disulfides coupled with high performance liquid chromatography (HPLC). In this study, these obstacles are overcome by packing Zn(II)-TCEP complexes into a home-made column. The as-synthesized Zn(II)-TCEP complexes enable efficient reduction of disulfide bonds at pH 3.0. This acidic pH value was compatible with that of the mobile phase for HPLC separation of thiols and disulfides. Therefore, using fluorosurfactant-prepared triangular gold nanoparticles as HPLC postcolumn specific chemiluminescence (CL) reagents for thiols, the feasibility of the established on-line reduction column has been confirmed for the direct identification of both thiols and disulfides by incorporating this reduction column into a single chromatographic separation. Detection limits for these analytes range from 8.3 to 25.4 nM and the linear range in a log-log plot can comprise three orders of magnitude. Finally, the utility of this automated on-line reduction of disulfides-HPLC-CL system has been demonstrated for the reliable determination of thiols and disulfides in human urine and plasma samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  18. Effect of quantum dots on the biological behavior of the EJ human bladder urothelial carcinoma cell line.

    PubMed

    Yuan, Run; Yu, Wei-Min; Cheng, Fan; Zhang, Xiao-Bin; Ruan, Yuan; Cao, Zhi-Xiu; Larré, Stéphane

    2015-10-01

    Quantum dots (QDs) are a type of fluorescent label with applications in biological molecules, cells and in vivo imaging. The current study investigated the effect of QDs on the toxicity, proliferation, migration and invasion of the EJ human bladder cancer cell line in vitro. The cell counting kit‑8 test was used to measure the survival rate of EJ cells following incubation with varying concentrations of QDs. Additionally, the effect of QDs on tumor cell migration and invasion was evaluated using the Transwell chamber assay, and cell proliferation rate was assessed using a hemocytometer. Data from the current study demonstrated no significant differences in survival rate between the experimental and control groups with the conventionally used concentrations (5, 10 and 20 nM) of QD605 (P>0.05). However, with high concentrations of QD605 (40 and 80 nM), significant differences were observed (P<0.001). The survival rate of EJ cells, however, remained at 92.6%. In addition, no significant differences were observed between the EJ cells labeled with transactivator of transcription (TAT)‑QD605 and the unlabeled EJ cells with regard to proliferation, migration and invasion (P>0.05). Thus, the results of the current study indicate that QDs exhibit a certain degree of influence on the activity of the EJ bladder cancer cell line at high concentrations. However, at the concentrations that QDs are conventionally used, there was little impact on the survival of the EJ cells. In addition, the proliferation, migration and invasion abilities of the EJ cells were not affected by TAT‑QDs. Therefore, the peptide‑conjugated QDs have potential to be applied in the imaging and tracking of live cells in vitro and of animals in vivo. Notably, QDs may provide the foundation for a novel, non‑invasive imaging strategy for the early diagnosis of tumors.

  19. On-line estimation of suspended solids in biological reactors of WWTPs using a Kalman observer.

    PubMed

    Beltrán, S; Irizar, I; Monclús, H; Rodríguez-Roda, I; Ayesa, E

    2009-01-01

    The total amount of solids in Wastewater Treatment Plants (WWTPs) and their distribution among the different elements and lines play a crucial role in the stability, performance and operational costs of the process. However, an accurate prediction of the evolution of solids concentration in the different elements of a WWTP is not a straightforward task. This paper presents the design, development and validation of a generic Kalman observer for the on-line estimation of solids concentration in the tank reactors of WWTPs. The proposed observer is based on the fact that the information about the evolution of the total amount of solids in the plant can be supplied by the available on-line Suspended Solids (SS) analysers, while their distribution can be simultaneously estimated from the hydraulic pattern of the plant. The proposed observer has been applied to the on-line estimation of SS in the reactors of a pilot-scale Membrane Bio-Reactor (MBR). The results obtained have shown that the experimental information supplied by a sole on-line SS analyser located in the first reactor of the pilot plant, in combination with updated information about internal flow rates data, has been able to give a reasonable estimation of the evolution of the SS concentration in all the tanks.

  20. Graphitic and oxidised high pressure high temperature (HPHT) nanodiamonds induce differential biological responses in breast cancer cell lines.

    PubMed

    Woodhams, Benjamin; Ansel-Bollepalli, Laura; Surmacki, Jakub; Knowles, Helena; Maggini, Laura; de Volder, Michael; Atatüre, Mete; Bohndiek, Sarah

    2018-06-19

    Nanodiamonds have demonstrated potential as powerful sensors in biomedicine, however, their translation into routine use requires a comprehensive understanding of their effect on the biological system being interrogated. Under normal fabrication processes, nanodiamonds are produced with a graphitic carbon shell, but are often oxidized in order to modify their surface chemistry for targeting to specific cellular compartments. Here, we assessed the biological impact of this purification process, considering cellular proliferation, uptake, and oxidative stress for graphitic and oxidized nanodiamond surfaces. We show for the first time that oxidized nanodiamonds possess improved biocompatibility compared to graphitic nanodiamonds in breast cancer cell lines, with graphitic nanodiamonds inducing higher levels of oxidative stress despite lower uptake.

  1. The Design of a Molecular Assembly Line Based on Biological Molecules

    DTIC Science & Technology

    2003-06-01

    and will demonstrate how one can construct a purely synthetic analogue of a polyketide synthase . 15. SUBJECT TERMS 16. SECURITY CLASSIFICATION OF...scaffold in programmed assembly and molecular electronics. It is based on the principles of the biological molecules polyketide synthase and kinesin, and in...stereoselective centers) with any reasonable yield, not including the R&D and process development time. Figure 1.6 shows how a polyketide synthase

  2. Ab initio study of boron nitride lines on graphene

    NASA Astrophysics Data System (ADS)

    Mata-Carrizal, Berenice; Sanginés-Mendoza, Raúl; Martinez, Edgar

    2013-03-01

    Graphene has unusual electronic properties which make it a promising material for electronic devices. Neverthless, the absence of a band gap sets limitations on its practical applications. Thus, it is crucial to find methods to create and tune the band gap of systems based on graphene. In this way, we explore the modulation of the electronic properties of graphene through doping with boron nitride lines. In particular, we studied the electronic structure of graphene sheets doped with boron nitride lines armchair and zigzag type. The calculations were performed using the pseudopotential LCAO method with a Generalized Gradient Approximation (GGA) for the exchange-correlation energy functional. We found that both doping lines type induce a bandgap and that the energy gap increases as the length of doping lines increases. Accordingly to our DFT calculations, we found that the energy gap on graphene doped with armchair and zigzag lines is due to a two different mechanisms to drain charge from pi- to sigma- orbitals. Thus, we found that doping graphene with boron nitride lines is a useful way to induce and modulate the bandgap on graphene. This research was supported by Consejo Nacional de Ciencia y Tecnología (Conacyt) under Grant No. 133022.

  3. Tumor-specific delivery of biologics by a novel T-cell line HOZOT

    PubMed Central

    Onishi, Teppei; Tazawa, Hiroshi; Hashimoto, Yuuri; Takeuchi, Makoto; Otani, Takeshi; Nakamura, Shuji; Sakurai, Fuminori; Mizuguchi, Hiroyuki; Kishimoto, Hiroyuki; Umeda, Yuzo; Shirakawa, Yasuhiro; Urata, Yasuo; Kagawa, Shunsuke; Fujiwara, Toshiyoshi

    2016-01-01

    “Cell-in-cell” denotes an invasive phenotype in which one cell actively internalizes in another. The novel human T-cell line HOZOT, established from human umbilical cord blood, was shown to penetrate a variety of human cancer cells but not normal cells. Oncolytic viruses are emerging as biological therapies for human cancers; however, efficient viral delivery is limited by a lack of tumor-specific homing and presence of pre-existing or therapy-induced neutralizing antibodies. Here, we report a new, intriguing approach using HOZOT cells to transmit biologics such as oncolytic viruses into human cancer cells by cell-in-cell invasion. HOZOT cells were successfully loaded via human CD46 antigen with an attenuated adenovirus containing the fiber protein of adenovirus serotype 35 (OBP-401/F35), in which the telomerase promoter regulates viral replication. OBP-401/F35–loaded HOZOT cells were efficiently internalized into human cancer cells and exhibited tumor-specific killing by release of viruses, even in the presence of anti-viral neutralizing antibodies. Moreover, intraperitoneal administration of HOZOT cells loaded with OBP-401/F35 significantly suppressed peritoneally disseminated tumor growth in mice. This unique cell-in-cell property provides a platform for selective delivery of biologics into human cancer cells, which has important implications for the treatment of human cancers. PMID:27901098

  4. On-line soft sensing in upstream bioprocessing.

    PubMed

    Randek, Judit; Mandenius, Carl-Fredrik

    2018-02-01

    This review provides an overview and a critical discussion of novel possibilities of applying soft sensors for on-line monitoring and control of industrial bioprocesses. Focus is on bio-product formation in the upstream process but also the integration with other parts of the process is addressed. The term soft sensor is used for the combination of analytical hardware data (from sensors, analytical devices, instruments and actuators) with mathematical models that create new real-time information about the process. In particular, the review assesses these possibilities from an industrial perspective, including sensor performance, information value and production economy. The capabilities of existing analytical on-line techniques are scrutinized in view of their usefulness in soft sensor setups and in relation to typical needs in bioprocessing in general. The review concludes with specific recommendations for further development of soft sensors for the monitoring and control of upstream bioprocessing.

  5. Agroterrorism, Biological Crimes, and Biological Warfare Targeting Animal Agriculture

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Wilson, Terry M.; Logan-Henfrey, Linda; Weller, Richard E.

    2000-04-12

    There is a rising level of concern that agriculture might be targeted for economic sabotage by terrorists. Knowledge gathered about the Soviet Union biological weapons program and Iraq following the Gulf War, confirmed that animals and agricultural crops were targets of bioweapon development. These revelations are particularly disturbing in light of the fact that both countries are States Parties to the Biological and Toxin Weapons Convention that entered into force in 1975. The potential for misusing biotechnology to create more virulent pathogens and the lack of international means to detect unethical uses of new technologies to create destructive bioweapons ismore » of increasing concern. Disease outbreaks, whether naturally occurring or intentionally, involving agricultural pathogens that destroy livestock and crops would have a profound impact on a country's infrastructure, economy and export markets. This chapter deals with the history of agroterrorism, biological crimes and biological warfare directed toward animal agriculture, specifically, horses, cattle, swine, sheep, goats, and poultry.« less

  6. Extra-high voltage transmission lines: mechanisms of biological effects on honeybees. Final report

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Greenberg, B.; Bindokas, V.

    1985-08-01

    The authors confirmed that bee exposure to E fields, including 100 kV/m, under the dry conditions cause no detectable effect on colony behavior. If, however, exposure occurs when moisture is present, or if bees are on a conductive surface, they become visibly disturbed, mortality is increased, abnormal propolization occurs, and colony development may be impaired. It seems plausible that bees on conductive surfaces within a hive under a 765-kV/m transmission line can perceive shocks from body currents induced by enhanced intra-hive E fields. Hives exposed under a 765-kV/m transmission line to an ambient E field of 7 kV/m have internalmore » step-potential-induced currents and interchamber chort-circuit currents which range from one-half to several microamperes. Total hive currents can exceed 100 ..mu..A. Thus, induced hive currents exceed the empirical sting threshold by up to a factor of 100 and the E-field-induced body current by up to a factor of 1000. The degree of disturbance which could be produced by these intra-hive currents will eclipse that produced by perception of E-field-induced body currents. The authors therefore attribute the disturbance of colonies under a transmission line primarily to electric shock from induced hive currents. 10 refs., 51 figs., 18 tabs. (DT)« less

  7. Rapid micropatterning of cell lines and human pluripotent stem cells on elastomeric membranes.

    PubMed

    Paik, Isha; Scurr, David J; Morris, Bryan; Hall, Graham; Denning, Chris; Alexander, Morgan R; Shakesheff, Kevin M; Dixon, James E

    2012-10-01

    Tissue function during development and in regenerative medicine completely relies on correct cell organization and patterning at micro and macro scales. We describe a rapid method for patterning mammalian cells including human embryonic stem cells (HESCs) and induced pluripotent stem cells (iPSCs) on elastomeric membranes such that micron-scale control of cell position can be achieved over centimeter-length scales. Our method employs surface engineering of hydrophobic polydimethylsiloxane (PDMS) membranes by plasma polymerization of allylamine. Deposition of plasma polymerized allylamine (ppAAm) using our methods may be spatially restricted using a micro-stencil leaving faithful hydrophilic ppAAm patterns. We employed airbrushing to create aerosols which deposit extracellular matrix (ECM) proteins (such as fibronectin and Matrigel™) onto the same patterned ppAAm rich regions. Cell patterns were created with a variety of well characterized cell lines (e.g., NIH-3T3, C2C12, HL1, BJ6, HESC line HUES7, and HiPSC line IPS2). Individual and multiple cell line patterning were also achieved. Patterning remains faithful for several days and cells are viable and proliferate. To demonstrate the utility of our technique we have patterned cells in a variety of configurations. The ability to rapidly pattern cells at high resolution over macro scales should aid future tissue engineering efforts for regenerative medicine applications and in creating in vitro stem cell niches. Copyright © 2012 Wiley Periodicals, Inc.

  8. Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines

    PubMed Central

    Romano, Paolo; Manniello, Assunta; Aresu, Ottavia; Armento, Massimiliano; Cesaro, Michela; Parodi, Barbara

    2009-01-01

    The Cell Line Data Base (CLDB) is a well-known reference information source on human and animal cell lines including information on more than 6000 cell lines. Main biological features are coded according to controlled vocabularies derived from international lists and taxonomies. HyperCLDB (http://bioinformatics.istge.it/hypercldb/) is a hypertext version of CLDB that improves data accessibility by also allowing information retrieval through web spiders. Access to HyperCLDB is provided through indexes of biological characteristics and navigation in the hypertext is granted by many internal links. HyperCLDB also includes links to external resources. Recently, an interest was raised for a reference nomenclature for cell lines and CLDB was seen as an authoritative system. Furthermore, to overcome the cell line misidentification problem, molecular authentication methods, such as fingerprinting, single-locus short tandem repeat (STR) profile and single nucleotide polymorphisms validation, were proposed. Since this data is distributed, a reference portal on authentication of human cell lines is needed. We present here the architecture and contents of CLDB, its recent enhancements and perspectives. We also present a new related database, the Cell Line Integrated Molecular Authentication (CLIMA) database (http://bioinformatics.istge.it/clima/), that allows to link authentication data to actual cell lines. PMID:18927105

  9. Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.

    PubMed

    Romano, Paolo; Manniello, Assunta; Aresu, Ottavia; Armento, Massimiliano; Cesaro, Michela; Parodi, Barbara

    2009-01-01

    The Cell Line Data Base (CLDB) is a well-known reference information source on human and animal cell lines including information on more than 6000 cell lines. Main biological features are coded according to controlled vocabularies derived from international lists and taxonomies. HyperCLDB (http://bioinformatics.istge.it/hypercldb/) is a hypertext version of CLDB that improves data accessibility by also allowing information retrieval through web spiders. Access to HyperCLDB is provided through indexes of biological characteristics and navigation in the hypertext is granted by many internal links. HyperCLDB also includes links to external resources. Recently, an interest was raised for a reference nomenclature for cell lines and CLDB was seen as an authoritative system. Furthermore, to overcome the cell line misidentification problem, molecular authentication methods, such as fingerprinting, single-locus short tandem repeat (STR) profile and single nucleotide polymorphisms validation, were proposed. Since this data is distributed, a reference portal on authentication of human cell lines is needed. We present here the architecture and contents of CLDB, its recent enhancements and perspectives. We also present a new related database, the Cell Line Integrated Molecular Authentication (CLIMA) database (http://bioinformatics.istge.it/clima/), that allows to link authentication data to actual cell lines.

  10. Follow-on biologics: data exclusivity and the balance between innovation and competition.

    PubMed

    Grabowski, Henry

    2008-06-01

    Legislation to create a regulatory pathway for follow-on biologics is currently being considered by the United States Congress. A critical issue in this respect is the period of data exclusivity for innovator companies before a follow-on competitor can rely in part on data obtained for an original biologic for an abbreviated approval. Given the nature of patents on biologics, the period of data exclusivity is anticipated to have a key role in determining how quickly follow-on competitors emerge, and consequently also on the time available for originator companies to recoup their investment. With this issue in mind, this article discusses factors influencing return on investment on biologic research and development. A break-even analysis for a representative portfolio of biologics provides support for a substantial data exclusivity period.

  11. Fludarabine plus alemtuzumab (FA) front-line treatment in young patients with chronic lymphocytic leukemia (CLL) and an adverse biologic profile.

    PubMed

    Mauro, Francesca R; Molica, Stefano; Laurenti, Luca; Cortelezzi, Agostino; Carella, Angelo M; Zaja, Francesco; Chiarenza, Annalisa; Angrilli, Francesco; Nobile, Francesco; Marasca, Roberto; Musolino, Caterina; Brugiatelli, Maura; Piciocchi, Alfonso; Vignetti, Marco; Fazi, Paola; Gentile, Giuseppe; De Propris, Maria S; Della Starza, Irene; Marinelli, Marilisa; Chiaretti, Sabina; Del Giudice, Ilaria; Nanni, Mauro; Albano, Francesco; Cuneo, Antonio; Guarini, Anna; Foà, Robin

    2014-02-01

    In 45, ≤ 60 years old patients with CLL and an adverse biologic profile, a front-line treatment with Fludarabine and Campath (Alemtuzumab(®)) was given. The overall response rate was 75.5%, the complete response rate (CR) 24.4% with the lowest CR rates, 16.7% and 8.3%, in 11q and 17p deleted cases. The 3-year progression-free survival (PFS) and overall survival were 42.5% and 79.9%, respectively. PFS was significantly influenced by CLL duration, beta2-microglobulin, and improved by post-remissional stem cell transplantation. Front-line fludarabine and alemtuzumab showed a manageable safety profile and evidence of a benefit in a small series of CLL patients with adverse biologic features. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. Establishment and Biological Characterization of a Panel of Glioblastoma Multiforme (GBM) and GBM Variant Oncosphere Cell Lines.

    PubMed

    Binder, Zev A; Wilson, Kelli M; Salmasi, Vafi; Orr, Brent A; Eberhart, Charles G; Siu, I-Mei; Lim, Michael; Weingart, Jon D; Quinones-Hinojosa, Alfredo; Bettegowda, Chetan; Kassam, Amin B; Olivi, Alessandro; Brem, Henry; Riggins, Gregory J; Gallia, Gary L

    2016-01-01

    Human tumor cell lines form the basis of the majority of present day laboratory cancer research. These models are vital to studying the molecular biology of tumors and preclinical testing of new therapies. When compared to traditional adherent cell lines, suspension cell lines recapitulate the genetic profiles and histologic features of glioblastoma multiforme (GBM) with higher fidelity. Using a modified neural stem cell culture technique, here we report the characterization of GBM cell lines including GBM variants. Tumor tissue samples were obtained intra-operatively and cultured in neural stem cell conditions containing growth factors. Tumor lines were characterized in vitro using differentiation assays followed by immunostaining for lineage-specific markers. In vivo tumor formation was assayed by orthotopic injection in nude mice. Genetic uniqueness was confirmed via short tandem repeat (STR) DNA profiling. Thirteen oncosphere lines derived from GBM and GBM variants, including a GBM with PNET features and a GBM with oligodendroglioma component, were established. All unique lines showed distinct genetic profiles by STR profiling. The lines assayed demonstrated a range of in vitro growth rates. Multipotency was confirmed using in vitro differentiation. Tumor formation demonstrated histologic features consistent with high grade gliomas, including invasion, necrosis, abnormal vascularization, and high mitotic rate. Xenografts derived from the GBM variants maintained histopathological features of the primary tumors. We have generated and characterized GBM suspension lines derived from patients with GBMs and GBM variants. These oncosphere cell lines will expand the resources available for preclinical study.

  13. [Establishment of a new human glioma cell line and analysis of its biological characteristics].

    PubMed

    Chen, Guilin; Li, Yanyan; Xie, Xueshun; Chen, Jinming; Wu, Tingfeng; Li, Xuetao; Wang, Hangzhou; Zhou, Youxin; Du, Ziwei

    2015-02-01

    To establish a new glioma cell line and analyze its biological characteristics, and to provide a useful cellular tool with new features for cancer research. Glioma tissue was taken from surgical specimen clinical of a clinical patient. Primary culture was carried out, and a cell line (SHG139) was established after 10 passages. Immunofluorescence staining was performed to detect the expression of proteins, and cell proliferation and cycle were detected by flow cytometry method (FCM). The biological characteristics of SHG139 cells were detected by chromosome karyotype analysis. SHG139s glioma cells derived from SHG139 glioma cell line were cultured with neural stem cell medium. Then stem cell markers were determined. SHG139s cells were induced with serum-containing medium, and their expression of A2B5, GFAP, β-III tubulin, and GalC was detected. Intracranial xenograft tumor of both SHG139 glioma cells and SHG139s glioma stem cell spheres was generated in rats. The expressions of A2B5, GalC, GFAP, S-100, and vimentin in the 20 and 60 passages of SHG139 cells were positive, consistent with the immunohistochemical results and pathological features. SHG139 cells proliferated significantly within 24 h after subculture, and their total number of chromosomes was 68 and mostly multiploid. They were positive for A2B5 (84.12±9.96)%, nestin (73.86±5.01)%, and NG2 (73.37±2.09)%. SHG139s cells were induced, and the ratio of positive cells of GFAP, β-III tubulin and GalC was (92.89±2.24)%, (64.85±4.09)% and (33.57±4.14)%, respectively. SHG139 is an astroglioma cell line, from which SHG139s cells can be successfully obtained by culture with NSCM. SHG139s cells are of A2B5(+)/CD133(-) GSCs subgroup cells, with potentials of self-renewal and multi-directional differentiation. Compared with the intracranial SHG139 xenograft tumor, the intracranial SHG139s xenograft tumor is more malignant and aggressive.

  14. Mitigating the risk of Zika virus contamination of raw materials and cell lines in the manufacture of biologicals.

    PubMed

    Zmurko, Joanna; Vasey, Douglas B; Donald, Claire L; Armstrong, Alison A; McKee, Marian L; Kohl, Alain; Clayton, Reginald F

    2018-02-01

    Ensuring the virological safety of biologicals is challenging due to the risk of viral contamination of raw materials and cell banks, and exposure during in-process handling to known and/or emerging viral pathogens. Viruses may contaminate raw materials and biologicals intended for human or veterinary use and remain undetected until appropriate testing measures are employed. The outbreak and expansive spread of the mosquito-borne flavivirus Zika virus (ZIKV) poses challenges to screening human- and animal -derived products used in the manufacture of biologicals. Here, we report the results of an in vitro study where detector cell lines were challenged with African and Asian lineages of ZIKV. We demonstrate that this pathogen is robustly detectable by in vitro assay, thereby providing assurance of detection of ZIKV, and in turn underpinning the robustness of in vitro virology assays in safety testing of biologicals.

  15. Going below the line: creating transportable brands for Australia's dark market.

    PubMed

    Carter, S M

    2003-12-01

    To investigate non-point-of-sale cigarette marketing in Australia, one of the "darkest" markets in the world. Analysis of 172 tobacco industry documents. The tobacco industry has continued to market their products despite severe restrictions on legal marketing activity. They made careful plans to circumvent regulation well in advance. In preparation for bans, they chose and strengthened existing brands to enable their continued success in a dark market and prepared the consumer for bans by increasing their spending on below the line activities. Bans reduced the industry's effectiveness and efficiency. After bans new brand launches stopped: instead key existing brands were strengthened via alterations to the product, line extensions, and stretching loopholes in the legislation as far as possible. In line with the general trend towards integrated marketing, a range of activities have been used in combination, including guerrilla marketing, advertising in imported international magazines, altering the pack, sponsorships, brand stretching, event promotions, lifestyle premiums, and the development of corporate websites. The tobacco industry acknowledges that marketing restrictions have an impact, validating their continued use in tobacco control. The industry is extremely creative in circumventing these marketing restrictions, requiring tobacco marketing regulations to be informed by marketing expertise, regularly updated, and to adopt the broadest possible scope. Tobacco control advocates, particularly those communicating with young people, could learn from the creativity of the tobacco industry.

  16. The Relative Biological Effectiveness for Carbon and Oxygen Ion Beams Using the Raster-Scanning Technique in Hepatocellular Carcinoma Cell Lines

    PubMed Central

    Habermehl, Daniel; Ilicic, Katarina; Dehne, Sarah; Rieken, Stefan; Orschiedt, Lena; Brons, Stephan; Haberer, Thomas; Weber, Klaus-Josef; Debus, Jürgen; Combs, Stephanie E.

    2014-01-01

    Background Aim of this study was to evaluate the relative biological effectiveness (RBE) of carbon (12C) and oxygen ion (16O)-irradiation applied in the raster-scanning technique at the Heidelberg Ion beam Therapy center (HIT) based on clonogenic survival in hepatocellular carcinoma cell lines compared to photon irradiation. Methods Four human HCC lines Hep3B, PLC, HepG2 and HUH7 were irradiated with photons, 12C and 16O using a customized experimental setting at HIT for in-vitro trials. Cells were irradiated with increasing physical photon single doses of 0, 2, 4 and 6 Gy and heavy ionsingle doses of 0, 0.125, 0.5, 1, 2, 3 Gy (12C and 16O). SOBP-penetration depth and extension was 35 mm +/−4 mm and 36 mm +/−5 mm for carbon ions and oxygen ions respectively. Mean energy level and mean linear energy transfer (LET) were 130 MeV/u and 112 keV/um for 12C, and 154 MeV/u and 146 keV/um for 16O. Clonogenic survival was computated and realtive biological effectiveness (RBE) values were defined. Results For all cell lines and both particle modalities α- and β-values were determined. As expected, α-values were significantly higher for 12C and 16O than for photons, reflecting a steeper decline of the initial slope of the survival curves for high-LET beams. RBE-values were in the range of 2.1–3.3 and 1.9–3.1 for 12C and 16O, respectively. Conclusion Both irradiation with 12C and 16O using the rasterscanning technique leads to an enhanced RBE in HCC cell lines. No relevant differences between achieved RBE-values for 12C and 16O were found. Results of this work will further influence biological-adapted treatment planning for HCC patients that will undergo particle therapy with 12C or 16O. PMID:25460352

  17. Digital in-line holography: 4-D imaging and tracking of micro-structures and organisms in microfluidics and biology

    NASA Astrophysics Data System (ADS)

    Garcia-Sucerquia, J.; Xu, W.; Jericho, S. K.; Jericho, M. H.; Tamblyn, I.; Kreuzer, H. J.

    2006-01-01

    In recent years, in-line holography as originally proposed by Gabor, supplemented with numerical reconstruction, has been perfected to the point at which wavelength resolution both laterally and in depth is routinely achieved with light by using digital in-line holographic microscopy (DIHM). The advantages of DIHM are: (1) simplicity of the hardware (laser- pinhole-CCD camera), (2) magnification is obtained in the numerical reconstruction, (3) maximum information of the 3-D structure with a depth of field of millimeters, (4) changes in the specimen and the simultaneous motion of many species, can be followed in 4-D at the camera frame rate. We present results obtained with DIHM in biological and microfluidic applications. By taking advantage of the large depth of field and the plane-to-plane reconstruction capability of DIHM, we can produce 3D representations of the paths followed by micron-sized objects such as suspensions of microspheres and biological samples (cells, algae, protozoa, bacteria). Examples from biology include a study of the motion of bacteria in a diatom and the track of algae and paramecium. In microfluidic applications we observe micro-channel flow, motion of bubbles in water and evolution in electrolysis. The paper finishes with new results from an underwater version of DIHM.

  18. Virtual, on-line, frog dissection vs. conventional laboratory dissection: A comparison of student achievement and teacher perceptions among honors, general ability, and foundations-level high school biology classes

    NASA Astrophysics Data System (ADS)

    Kopec, Ronald H.

    2002-09-01

    Dissecting animal specimens has long been a tradition in biology classes. Objections by students, based on religious or ethical grounds, have been raised regarding the dissections of animals in classroom laboratories. A number of states now have legal proceedings or statewide policies requiring that alternatives to the actual dissection of laboratory animal specimens be permitted in their school districts. Alternatives to actual dissections have been developed in recent years. For a variety of reasons, performing an actual or conventional animal dissection may not be a desirable option. The purpose of this study was to investigate how a virtual On-line frog dissection compares with an actual laboratory dissection. What were the perceptions of the teacher's using it? How does student achievement compare among three the different ability levels on a pre and posttest regarding basic frog anatomy? Is a virtual On-line dissection a suitable alternative for students who, for whatever reason, do not participate in the actual laboratory experience? The subjects consisted of 218 biology students among three different ability levels, in a Northeastern suburban high school. Approximately half of the student groups participated in a virtual On-line dissection, the other half in an actual laboratory dissection. A pretest of basic frog anatomy was administered to the students two days before and the posttest one day after their dissection experience. Data were analyzed using matched pairs t-Tests, Analysis of Variance, Tukey HSD, and Squared Curvilinear Coefficients. Survey questionnaires were administered to the teachers after the dissection experiences were completed. There were no significant differences found in achievement between the virtual and conventional dissection groups. There were significant differences found in achievement score means among the three ability levels. There was no significant interaction between gender and achievement. Perceptions of the teacher

  19. On-line Determination of Zinc in Water and Biological Samples after Its Preconcentration onto Zincon Anchored Polyurethane Foam.

    PubMed

    Azeem, Sami M Abdel; Hanafi, Hassan A; El-Shahat, M F

    2015-01-01

    A fast and sensitive on-line procedure for the determination of zinc in water and biological samples was developed. Zinc was preconcentrated in a mini-column packed with polyurethane foam (PUF) chemically modified with zincon via -N=N- bonding. The optimal conditions for preconcentration were pH 8.5 and sample flow rate of 4.0 mL min(-1). Quantitative desorption of Zn(II) was obtained by 0.1 mol L(-1) hydrochloric acid and subsequent spectrophotmetric determination using 4-(2-pyridylazo)-resorcinol at 498 nm. The obtained detection limit was found to be 3.0 ng mL(-1), precision (RSD) was 4.8 and 6.7% at 20 and 110 ng mL(-1), respectively, for 60 s preconcentration time and enrichment factor was 31. The linearity range was from 10 to 120 ng mL(-1) and maximum sample throughput was 20 h(-1). Finally, the method was successfully applied to the determination of zinc in tap water, Nile River water and human urine samples with RSD in the range of 1.1 - 8.3%.

  20. Going below the line: creating transportable brands for Australia's dark market

    PubMed Central

    Carter, S

    2003-01-01

    Objective: To investigate non-point-of-sale cigarette marketing in Australia, one of the "darkest" markets in the world. Design: Analysis of 172 tobacco industry documents. Results: The tobacco industry has continued to market their products despite severe restrictions on legal marketing activity. They made careful plans to circumvent regulation well in advance. In preparation for bans, they chose and strengthened existing brands to enable their continued success in a dark market and prepared the consumer for bans by increasing their spending on below the line activities. Bans reduced the industry's effectiveness and efficiency. After bans new brand launches stopped: instead key existing brands were strengthened via alterations to the product, line extensions, and stretching loopholes in the legislation as far as possible. In line with the general trend towards integrated marketing, a range of activities have been used in combination, including guerrilla marketing, advertising in imported international magazines, altering the pack, sponsorships, brand stretching, event promotions, lifestyle premiums, and the development of corporate websites. Conclusions: The tobacco industry acknowledges that marketing restrictions have an impact, validating their continued use in tobacco control. The industry is extremely creative in circumventing these marketing restrictions, requiring tobacco marketing regulations to be informed by marketing expertise, regularly updated, and to adopt the broadest possible scope. Tobacco control advocates, particularly those communicating with young people, could learn from the creativity of the tobacco industry. PMID:14645953

  1. On-Line and Off-Line Assessment of Metacognition

    ERIC Educational Resources Information Center

    Saraç, Seda; Karakelle, Sema

    2012-01-01

    The study investigates the interrelationships between different on-line and off-line measures for assessing metacognition. The participants were 47 fifth grade elementary students. Metacognition was assessed through two off-line and two on-line measures. The off-line measures consisted of a teacher rating scale and a self-report questionnaire. The…

  2. Fully On-line Introductory Physics with a Lab

    NASA Astrophysics Data System (ADS)

    Schatz, Michael

    We describe the development and implementation of a college-level introductory physics (mechanics) course and laboratory that is suited for both on-campus and on-line environments. The course emphasizes a ``Your World is Your Lab'' approach whereby students first examine and capture on video (using cellphones) motion in their immediate surroundings, and then use free, open-source software both to extract data from the video and to apply physics principles to build models that describe, predict, and visualize the observations. Each student reports findings by creating a video lab report and posting it online; these video lab reports are then distributed to the rest of the class for peer review. In this talk, we will discuss the student and instructor experiences in courses offered to three distinct audiences in different venues: (1) a Massively Open On-line Course (MOOC) for off-campus participants, (2) a flipped/blended course for on-campus students, and, most recently, (3) a fully-online course for off-campus students.

  3. Identification of line-specific strategies for improving carotenoid production in synthetic maize through data-driven mathematical modeling.

    PubMed

    Comas, Jorge; Benfeitas, Rui; Vilaprinyo, Ester; Sorribas, Albert; Solsona, Francesc; Farré, Gemma; Berman, Judit; Zorrilla, Uxue; Capell, Teresa; Sandmann, Gerhard; Zhu, Changfu; Christou, Paul; Alves, Rui

    2016-09-01

    Plant synthetic biology is still in its infancy. However, synthetic biology approaches have been used to manipulate and improve the nutritional and health value of staple food crops such as rice, potato and maize. With current technologies, production yields of the synthetic nutrients are a result of trial and error, and systematic rational strategies to optimize those yields are still lacking. Here, we present a workflow that combines gene expression and quantitative metabolomics with mathematical modeling to identify strategies for increasing production yields of nutritionally important carotenoids in the seed endosperm synthesized through alternative biosynthetic pathways in synthetic lines of white maize, which is normally devoid of carotenoids. Quantitative metabolomics and gene expression data are used to create and fit parameters of mathematical models that are specific to four independent maize lines. Sensitivity analysis and simulation of each model is used to predict which gene activities should be further engineered in order to increase production yields for carotenoid accumulation in each line. Some of these predictions (e.g. increasing Zmlycb/Gllycb will increase accumulated β-carotenes) are valid across the four maize lines and consistent with experimental observations in other systems. Other predictions are line specific. The workflow is adaptable to any other biological system for which appropriate quantitative information is available. Furthermore, we validate some of the predictions using experimental data from additional synthetic maize lines for which no models were developed. © 2016 The Authors The Plant Journal © 2016 John Wiley & Sons Ltd.

  4. Students' Reaction to WebCT: Implications for Designing On-Line Learning Environments

    ERIC Educational Resources Information Center

    Osman, Mohamed Eltahir

    2005-01-01

    There is a growing number of web-based and web-assisted course development tools and products that can be used to create on-line learning environment. The utility of these products, however, varies greatly depending on their feasibility, prerequisite infrastructure, technical features, interface, and course development and management tools. WebCT…

  5. Improving off-line accelerated tryptic digestion. Towards fast-lane proteolysis of complex biological samples.

    PubMed

    Vukovic, Jadranka; Loftheim, Håvard; Winther, Bjørn; Reubsaet, J Léon E

    2008-06-27

    Off-line digestion of proteins using immobilized trypsin beads is studied with respect to the format of the digestion reactor, the digestion conditions, the comparison with in-solution digestion and its use in complex biological samples. The use of the filter vial as the most appropriate digestion reactor enables simple, efficient and easy-to-handle off-line digestion of the proteins on trypsin beads. It was shown that complex proteins like bovine serum albumin (BSA) need much longer time (89 min) and elevated temperature (37 degrees C) to be digested to an acceptable level compared to smaller proteins like cytochrome c (5 min, room temperature). Comparing the BSA digestion using immobilized trypsin beads with conventional in-solution digestion (overnight at 37 degrees C), it was shown that comparable results were obtained with respect to sequence coverage (>90%) and amount of missed cleavages (in both cases around 20 peptides with 1 or 2 missed cleavages were detected). However, the digestion using immobilized trypsin beads was considerable less time consuming. Good reproducibility and signal intensities were obtained for the digestion products of BSA in a complex urine sample. In addition to this, peptide products of proteins typically present in urine were identified.

  6. Genomic deletions created upon LINE-1 retrotransposition.

    PubMed

    Gilbert, Nicolas; Lutz-Prigge, Sheila; Moran, John V

    2002-08-09

    LINE-1 (L1) retrotransposition continues to impact the human genome, yet little is known about how L1 integrates into DNA. Here, we developed a plasmid-based rescue system and have used it to recover 37 new L1 retrotransposition events from cultured human cells. Sequencing of the insertions revealed the usual L1 structural hallmarks; however, in four instances, retrotransposition generated large target site deletions. Remarkably, three of those resulted in the formation of chimeric L1s, containing the 5' end of an endogenous L1 fused precisely to our engineered L1. Thus, our data demonstrate multiple pathways for L1 integration in cultured cells, and show that L1 is not simply an insertional mutagen, but that its retrotransposition can result in significant deletions of genomic sequence.

  7. Creating Alien Life Forms: Problem Solving in Biology.

    ERIC Educational Resources Information Center

    Grimnes, Karin A.

    1996-01-01

    Describes a project that helps students integrate biological concepts using both creativity and higher-order problem-solving skills. Involves students playing the roles of junior scientists aboard a starship in orbit around a class M planet and using a description of habitats, seasonal details, and a surface map of prominent geographic features to…

  8. Combined influence of Bt rice and rice dwarf virus on biological parameters of a non-target herbivore, Nephotettix cincticeps (Uhler) (Hemiptera: Cicadellidae)

    PubMed Central

    Wang, Qianjin; Han, Naishun; Dang, Cong; Lu, Zengbin; Wang, Fang; Yao, Hongwei; Peng, Yufa; Stanley, David

    2017-01-01

    The advent of genetically modified (GM) Bt rice creates the possibility of interactions among Bt crops, crop pathogens and non-target herbivores. In particular, information on how pathogen-infected Bt-expressing plants will influence non-target herbivores is necessary to predict the sustainability of GM cropping systems. Laboratory bioassays were conducted to evaluate the potential combined impacts of rice dwarf virus (RDV) and two Bt rice lines, T1C-19 (Cry1C) and T2A-1 (Cry2A), on non-target green rice leafhopper (GRLH), Nephotettix cincticeps (Uhler) (Hemiptera: Cicadellidae). In the first experiment, GRLHs feeding preference tests on Bt rice lines compared to a parental control rice line, MH63, were conducted. As rice plants were uninfected with RDV, GRLHs generally preferred the control MH63 line over the two Bt lines during the initial 8 h, with no significant preference during the following 64 h. As rice plants were infected with RDV, there were no clear preferences between the Bt rice lines and the control MH63 line. In the second experiment, we assessed the combined influence of RDV-infection status and Bt rice lines on GRLH biological parameters. Egg duration, adult weights, and male adult longevity were significantly affected on RDV-infected Bt rice. Other parameters, egg hatching rate, nymph survival and fecundity were not significantly influenced. We infer that interaction effect among two testing Bt rice lines and RDV will not lead to enlarged pest populations, thus demonstrating that growing these two Bt rice lines will poses negligible risk to GRLH in sustainable rice agroecosystems. Long-term field experiments to monitor the population dynamics of GRLHs at large scale need to be carried out to confirm the current results. PMID:28753622

  9. Combined influence of Bt rice and rice dwarf virus on biological parameters of a non-target herbivore, Nephotettix cincticeps (Uhler) (Hemiptera: Cicadellidae).

    PubMed

    Wang, Qianjin; Han, Naishun; Dang, Cong; Lu, Zengbin; Wang, Fang; Yao, Hongwei; Peng, Yufa; Stanley, David; Ye, Gongyin

    2017-01-01

    The advent of genetically modified (GM) Bt rice creates the possibility of interactions among Bt crops, crop pathogens and non-target herbivores. In particular, information on how pathogen-infected Bt-expressing plants will influence non-target herbivores is necessary to predict the sustainability of GM cropping systems. Laboratory bioassays were conducted to evaluate the potential combined impacts of rice dwarf virus (RDV) and two Bt rice lines, T1C-19 (Cry1C) and T2A-1 (Cry2A), on non-target green rice leafhopper (GRLH), Nephotettix cincticeps (Uhler) (Hemiptera: Cicadellidae). In the first experiment, GRLHs feeding preference tests on Bt rice lines compared to a parental control rice line, MH63, were conducted. As rice plants were uninfected with RDV, GRLHs generally preferred the control MH63 line over the two Bt lines during the initial 8 h, with no significant preference during the following 64 h. As rice plants were infected with RDV, there were no clear preferences between the Bt rice lines and the control MH63 line. In the second experiment, we assessed the combined influence of RDV-infection status and Bt rice lines on GRLH biological parameters. Egg duration, adult weights, and male adult longevity were significantly affected on RDV-infected Bt rice. Other parameters, egg hatching rate, nymph survival and fecundity were not significantly influenced. We infer that interaction effect among two testing Bt rice lines and RDV will not lead to enlarged pest populations, thus demonstrating that growing these two Bt rice lines will poses negligible risk to GRLH in sustainable rice agroecosystems. Long-term field experiments to monitor the population dynamics of GRLHs at large scale need to be carried out to confirm the current results.

  10. Comparative study of biological and technological characters in three generations of silkworm Bombyx mori L. ameiotic, parthenogenetically cloned lines.

    PubMed

    Greiss, H; Vassilieva, J; Petkov, N; Petkov, Z

    2004-11-01

    Detect any deviation in biologic and technologic characters of eight ameiotic-parthenogenetically cloned lines of Bombyx mori L. from different origins from a normal sexually reproduced control line in three generations. Comparative study of the three generations was conducted in SES, Vratza, unit of the National Center for Agrarian Sciences of Bulgaria after fixing all environmental rearing conditions. The ameiotic-parthen-clones displayed good parthenogenetic development, although total hatchability was significantly less than the sexually reproducing control populations. Survival rates between clones and control were not significantly different. All clones displayed significantly longer larval periods. Slight decline in second generation, and a steeper one in the third generation were observed for all eight cloned lines in cocoon weight, shell weight, and shell ratio and these differences were statistically significant. Cocoon yield was significantly lower than the control throughout the three generations. Our parthen-cloning method has a high rate of success in comparison to other cloning methods, the cloned progeny populations although were weaker technologically (cocoon weight, shell weight, and shell ratio), the biological characters (parthenogenetic development and survival rate) were not compromised. Further study is needed to determine the thermal needs of the cloned embryos and metabolic rate of all stages.

  11. Many Ways to Make A Line

    ERIC Educational Resources Information Center

    Ferrell, Holly

    2006-01-01

    This article describes a middle school introductory art lesson that encourages experimentation as an essential part of the creative process. In this lesson, students experiment with different types of media and tools to create an abstract piece that focuses on the most basic element of art--line. Students focus on line quality, focal points,…

  12. The use of selective adsorbents in capillary electrophoresis-mass spectrometry for analyte preconcentration and microreactions: a powerful three-dimensional tool for multiple chemical and biological applications.

    PubMed

    Guzman, N A; Stubbs, R J

    2001-10-01

    Much attention has recently been directed to the development and application of online sample preconcentration and microreactions in capillary electrophoresis using selective adsorbents based on chemical or biological specificity. The basic principle involves two interacting chemical or biological systems with high selectivity and affinity for each other. These molecular interactions in nature usually involve noncovalent and reversible chemical processes. Properly bound to a solid support, an "affinity ligand" can selectively adsorb a "target analyte" found in a simple or complex mixture at a wide range of concentrations. As a result, the isolated analyte is enriched and highly purified. When this affinity technique, allowing noncovalent chemical interactions and biochemical reactions to occur, is coupled on-line to high-resolution capillary electrophoresis and mass spectrometry, a powerful tool of chemical and biological information is created. This paper describes the concept of biological recognition and affinity interaction on-line with high-resolution separation, the fabrication of an "analyte concentrator-microreactor", optimization conditions of adsorption and desorption, the coupling to mass spectrometry, and various applications of clinical and pharmaceutical interest.

  13. Colony, hanging drop, and methylcellulose three dimensional hypoxic growth optimization of renal cell carcinoma cell lines.

    PubMed

    Matak, Damian; Brodaczewska, Klaudia K; Lipiec, Monika; Szymanski, Łukasz; Szczylik, Cezary; Czarnecka, Anna M

    2017-08-01

    Renal cell carcinoma (RCC) is the most lethal of the common urologic malignancies, comprising 3% of all human neoplasms, and the incidence of kidney cancer is rising annually. We need new approaches to target tumor cells that are resistant to current therapies and that give rise to recurrence and treatment failure. In this study, we focused on low oxygen tension and three-dimensional (3D) cell culture incorporation to develop a new RCC growth model. We used the hanging drop and colony formation methods, which are common in 3D culture, as well as a unique methylcellulose (MC) method. For the experiments, we used human primary RCC cell lines, metastatic RCC cell lines, human kidney cancer stem cells, and human healthy epithelial cells. In the hanging drop assay, we verified the potential of various cell lines to create solid aggregates in hypoxic and normoxic conditions. With the semi-soft agar method, we also determined the ability of various cell lines to create colonies under different oxygen conditions. Different cell behavior observed in the MC method versus the hanging drop and colony formation assays suggests that these three assays may be useful to test various cell properties. However, MC seems to be a particularly valuable alternative for 3D cell culture, as its higher efficiency of aggregate formation and serum independency are of interest in different areas of cancer biology.

  14. A Corpus Approach for Autonomous Teachers and Learners: Implementing an On-Line Concordancer on Teachers' Laptops

    ERIC Educational Resources Information Center

    Lee, Jang Ho; Lee, Hansol; Sert, Cetin

    2015-01-01

    The present article deals with the issue of how to create and operate a customizable on-line concordancer from viewpoints of language teachers and with their own laptops. It aims to introduce how to use and manage this application without relying on computer engineers for various pedagogical purposes, focusing on the four beneficial dimensions of…

  15. Third international congress of plant molecular biology: Molecular biology of plant growth and development

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Hallick, R.B.

    The Congress was held October 6-11, 1991 in Tucson with approximately 3000 scientists attending and over 300 oral presentations and 1800 posters. Plant molecular biology is one of the most rapidly developing areas of the biological sciences. Recent advances in the ability to isolate genes, to study their expression, and to create transgenic plants have had a major impact on our understanding of the many fundamental plant processes. In addition, new approaches have been created to improve plants for agricultural purposes. This is a book of presentation and posters from the conference.

  16. Hands-on-Entropy, Energy Balance with Biological Relevance

    NASA Astrophysics Data System (ADS)

    Reeves, Mark

    2015-03-01

    Entropy changes underlie the physics that dominates biological interactions. Indeed, introductory biology courses often begin with an exploration of the qualities of water that are important to living systems. However, one idea that is not explicitly addressed in most introductory physics or biology textbooks is important contribution of the entropy in driving fundamental biological processes towards equilibrium. From diffusion to cell-membrane formation, to electrostatic binding in protein folding, to the functioning of nerve cells, entropic effects often act to counterbalance deterministic forces such as electrostatic attraction and in so doing, allow for effective molecular signaling. A small group of biology, biophysics and computer science faculty have worked together for the past five years to develop curricular modules (based on SCALEUP pedagogy). This has enabled students to create models of stochastic and deterministic processes. Our students are first-year engineering and science students in the calculus-based physics course and they are not expected to know biology beyond the high-school level. In our class, they learn to reduce complex biological processes and structures in order model them mathematically to account for both deterministic and probabilistic processes. The students test these models in simulations and in laboratory experiments that are biologically relevant such as diffusion, ionic transport, and ligand-receptor binding. Moreover, the students confront random forces and traditional forces in problems, simulations, and in laboratory exploration throughout the year-long course as they move from traditional kinematics through thermodynamics to electrostatic interactions. This talk will present a number of these exercises, with particular focus on the hands-on experiments done by the students, and will give examples of the tangible material that our students work with throughout the two-semester sequence of their course on introductory

  17. Polymer monolithic capillary microextraction combined on-line with inductively coupled plasma MS for the determination of trace rare earth elements in biological samples.

    PubMed

    Zhang, Lin; Chen, Beibei; He, Man; Hu, Bin

    2013-07-01

    A rapid and sensitive method based on polymer monolithic capillary microextraction combined on-line with microconcentric nebulization inductively coupled plasma MS has been developed for the determination of trace/ultratrace rare earth elements in biological samples. For this purpose, the iminodiacetic acid modified poly(glycidyl methacrylate-trimethylolpropane trimethacrylate) monolithic capillary was prepared and characterized by SEM and FTIR spectroscopy. Factors affecting the extraction efficiency, such as sample pH, sample flow rate, sample/eluent volume, and coexisting ions were investigated in detail. Under the optimal conditions, the LODs for rare earth elements were in the range of 0.08 (Er) to 0.97 ng/L (Nd) with a sampling frequency of 8.5 h(-1), and the RSDs were between 1.5% (Sm) and 7.4% (Nd) (c = 20 ng/L, n = 7). The proposed method was successfully applied to the analysis of trace/ultratrace rare earth elements in human urine and serum samples, and the recoveries for the spiked samples were in the range of 82-105%. The developed method was simple, rapid, sensitive, and favorable for the analysis of trace/ultratrace rare earth elements in biological samples with limited sample volume. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Creating breakthroughs at 3M.

    PubMed

    von Hippel, E; Thomke, S; Sonnack, M

    1999-01-01

    Most senior managers want their product development teams to create break-throughs--new products that will allow their companies to grow rapidly and maintain high margins. But more often they get incremental improvements to existing products. That's partly because companies must compete in the short term. Searching for breakthroughs is expensive and time consuming; line extensions can help the bottom line immediately. In addition, developers simply don't know how to achieve breakthroughs, and there is usually no system in place to guide them. By the mid-1990s, the lack of such a system was a problem even for an innovative company like 3M. Then a project team in 3M's Medical-Surgical Markets Division became acquainted with a method for developing breakthrough products: the lead user process. The process is based on the fact that many commercially important products are initially thought of and even prototyped by "lead users"--companies, organizations, or individuals that are well ahead of market trends. Their needs are so far beyond those of the average user that lead users create innovations on their own that may later contribute to commercially attractive breakthroughs. The lead user process transforms the job of inventing breakthroughs into a systematic task of identifying lead users and learning from them. The authors explain the process and how the 3M project team successfully navigated through it. In the end, the team proposed three major new product lines and a change in the division's strategy that has led to the development of breakthrough products. And now several more divisions are using the process to break away from incrementalism.

  19. Advances in 3D cell culture technologies enabling tissue-like structures to be created in vitro.

    PubMed

    Knight, Eleanor; Przyborski, Stefan

    2015-12-01

    Research in mammalian cell biology often relies on developing in vitro models to enable the growth of cells in the laboratory to investigate a specific biological mechanism or process under different test conditions. The quality of such models and how they represent the behavior of cells in real tissues plays a critical role in the value of the data produced and how it is used. It is particularly important to recognize how the structure of a cell influences its function and how co-culture models can be used to more closely represent the structure of real tissue. In recent years, technologies have been developed to enhance the way in which researchers can grow cells and more readily create tissue-like structures. Here we identify the limitations of culturing mammalian cells by conventional methods on two-dimensional (2D) substrates and review the popular approaches currently available that enable the development of three-dimensional (3D) tissue models in vitro. There are now many ways in which the growth environment for cultured cells can be altered to encourage 3D cell growth. Approaches to 3D culture can be broadly categorized into scaffold-free or scaffold-based culture systems, with scaffolds made from either natural or synthetic materials. There is no one particular solution that currently satisfies all requirements and researchers must select the appropriate method in line with their needs. Using such technology in conjunction with other modern resources in cell biology (e.g. human stem cells) will provide new opportunities to create robust human tissue mimetics for use in basic research and drug discovery. Application of such models will contribute to advancing basic research, increasing the predictive accuracy of compounds, and reducing animal usage in biomedical science. © 2014 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society.

  20. Plan for a Statewide On-Line Information System for Libraries (MnLINK).

    ERIC Educational Resources Information Center

    Minnesota State Dept. of Education, St. Paul.

    The 1996 Legislature directed the Minnesota Higher Education Services Office (HESO), in cooperation with the Library Planning Task Force to, "create a plan and process to develop a statewide on-line information system for libraries"; this memo with attached information was submitted in fulfillment of that request. The name chosen for the…

  1. Reflecting on Graphs: Attributes of Graph Choice and Construction Practices in Biology

    ERIC Educational Resources Information Center

    Angra, Aakanksha; Gardner, Stephanie M.

    2017-01-01

    Undergraduate biology education reform aims to engage students in scientific practices such as experimental design, experimentation, and data analysis and communication. Graphs are ubiquitous in the biological sciences, and creating effective graphical representations involves quantitative and disciplinary concepts and skills. Past studies…

  2. Is there anything unique in the ethics of synthetic biology?

    PubMed

    Heyd, David

    2012-01-01

    Synthetic biology does not create any ethical dilemmas that have not already been raised in the development of practices such as genetic screening, genetic engineering, and other interventions in the evolutionary processes. The issue is, nevertheless, ethically serious. Two different angles are examined: the philosophical legitimacy of human intervention in the shaping of human nature, and the more pragmatic (though by no means less important) question of the risks involved in such a novel line of research. As for the first, the claim made here is that in principle there is no constraint in human intervention in the world, since ultimately the source of any value lies in human interests, welfare, and values. This is an approach that is opposite to Habermas's. As for the practical problem of risk, research in synthetic biology calls for particular caution, since in at least the first stages of a new research or program, there is no social regulation, and society is wholly dependent on the scientist's ethical integrity.

  3. Adventitious viruses in insect cell lines used for recombinant protein expression.

    PubMed

    Geisler, Christoph; Jarvis, Donald L

    2018-04-01

    Insect cells are widely used for recombinant protein expression, typically as hosts for recombinant baculovirus vectors, but also for plasmid-mediated transient transfection or stable genetic transformation. Insect cells are used to express proteins for research, as well as to manufacture biologicals for human and veterinary medicine. Recently, several insect cell lines used for recombinant protein expression were found to be persistently infected with adventitious viruses. This has raised questions about how these infections might affect research performed using those cell lines. Furthermore, these findings raised serious concerns about the safety of biologicals produced using those cell lines. In response, new insect cell lines lacking adventitious viruses have been isolated for use as improved research tools and safer biological manufacturing platforms. Here, we review the scientific and patent literature on adventitious viruses found in insect cell lines, affected cell lines, and new virus-free cell lines. Copyright © 2017 Elsevier Inc. All rights reserved.

  4. Creating FGDC and NBII metadata with Metavist 2005.

    Treesearch

    David J. Rugg

    2004-01-01

    This report documents a computer program for creating metadata compliant with the Federal Geographic Data Committee (FGDC) 1998 metadata standard or the National Biological Information Infrastructure (NBII) 1999 Biological Data Profile for the FGDC standard. The software runs under the Microsoft Windows 2000 and XP operating systems, and requires the presence of...

  5. The iPlant Collaborative: Cyberinfrastructure for Plant Biology.

    PubMed

    Goff, Stephen A; Vaughn, Matthew; McKay, Sheldon; Lyons, Eric; Stapleton, Ann E; Gessler, Damian; Matasci, Naim; Wang, Liya; Hanlon, Matthew; Lenards, Andrew; Muir, Andy; Merchant, Nirav; Lowry, Sonya; Mock, Stephen; Helmke, Matthew; Kubach, Adam; Narro, Martha; Hopkins, Nicole; Micklos, David; Hilgert, Uwe; Gonzales, Michael; Jordan, Chris; Skidmore, Edwin; Dooley, Rion; Cazes, John; McLay, Robert; Lu, Zhenyuan; Pasternak, Shiran; Koesterke, Lars; Piel, William H; Grene, Ruth; Noutsos, Christos; Gendler, Karla; Feng, Xin; Tang, Chunlao; Lent, Monica; Kim, Seung-Jin; Kvilekval, Kristian; Manjunath, B S; Tannen, Val; Stamatakis, Alexandros; Sanderson, Michael; Welch, Stephen M; Cranston, Karen A; Soltis, Pamela; Soltis, Doug; O'Meara, Brian; Ane, Cecile; Brutnell, Tom; Kleibenstein, Daniel J; White, Jeffery W; Leebens-Mack, James; Donoghue, Michael J; Spalding, Edgar P; Vision, Todd J; Myers, Christopher R; Lowenthal, David; Enquist, Brian J; Boyle, Brad; Akoglu, Ali; Andrews, Greg; Ram, Sudha; Ware, Doreen; Stein, Lincoln; Stanzione, Dan

    2011-01-01

    The iPlant Collaborative (iPlant) is a United States National Science Foundation (NSF) funded project that aims to create an innovative, comprehensive, and foundational cyberinfrastructure in support of plant biology research (PSCIC, 2006). iPlant is developing cyberinfrastructure that uniquely enables scientists throughout the diverse fields that comprise plant biology to address Grand Challenges in new ways, to stimulate and facilitate cross-disciplinary research, to promote biology and computer science research interactions, and to train the next generation of scientists on the use of cyberinfrastructure in research and education. Meeting humanity's projected demands for agricultural and forest products and the expectation that natural ecosystems be managed sustainably will require synergies from the application of information technologies. The iPlant cyberinfrastructure design is based on an unprecedented period of research community input, and leverages developments in high-performance computing, data storage, and cyberinfrastructure for the physical sciences. iPlant is an open-source project with application programming interfaces that allow the community to extend the infrastructure to meet its needs. iPlant is sponsoring community-driven workshops addressing specific scientific questions via analysis tool integration and hypothesis testing. These workshops teach researchers how to add bioinformatics tools and/or datasets into the iPlant cyberinfrastructure enabling plant scientists to perform complex analyses on large datasets without the need to master the command-line or high-performance computational services.

  6. The iPlant Collaborative: Cyberinfrastructure for Plant Biology

    PubMed Central

    Goff, Stephen A.; Vaughn, Matthew; McKay, Sheldon; Lyons, Eric; Stapleton, Ann E.; Gessler, Damian; Matasci, Naim; Wang, Liya; Hanlon, Matthew; Lenards, Andrew; Muir, Andy; Merchant, Nirav; Lowry, Sonya; Mock, Stephen; Helmke, Matthew; Kubach, Adam; Narro, Martha; Hopkins, Nicole; Micklos, David; Hilgert, Uwe; Gonzales, Michael; Jordan, Chris; Skidmore, Edwin; Dooley, Rion; Cazes, John; McLay, Robert; Lu, Zhenyuan; Pasternak, Shiran; Koesterke, Lars; Piel, William H.; Grene, Ruth; Noutsos, Christos; Gendler, Karla; Feng, Xin; Tang, Chunlao; Lent, Monica; Kim, Seung-Jin; Kvilekval, Kristian; Manjunath, B. S.; Tannen, Val; Stamatakis, Alexandros; Sanderson, Michael; Welch, Stephen M.; Cranston, Karen A.; Soltis, Pamela; Soltis, Doug; O'Meara, Brian; Ane, Cecile; Brutnell, Tom; Kleibenstein, Daniel J.; White, Jeffery W.; Leebens-Mack, James; Donoghue, Michael J.; Spalding, Edgar P.; Vision, Todd J.; Myers, Christopher R.; Lowenthal, David; Enquist, Brian J.; Boyle, Brad; Akoglu, Ali; Andrews, Greg; Ram, Sudha; Ware, Doreen; Stein, Lincoln; Stanzione, Dan

    2011-01-01

    The iPlant Collaborative (iPlant) is a United States National Science Foundation (NSF) funded project that aims to create an innovative, comprehensive, and foundational cyberinfrastructure in support of plant biology research (PSCIC, 2006). iPlant is developing cyberinfrastructure that uniquely enables scientists throughout the diverse fields that comprise plant biology to address Grand Challenges in new ways, to stimulate and facilitate cross-disciplinary research, to promote biology and computer science research interactions, and to train the next generation of scientists on the use of cyberinfrastructure in research and education. Meeting humanity's projected demands for agricultural and forest products and the expectation that natural ecosystems be managed sustainably will require synergies from the application of information technologies. The iPlant cyberinfrastructure design is based on an unprecedented period of research community input, and leverages developments in high-performance computing, data storage, and cyberinfrastructure for the physical sciences. iPlant is an open-source project with application programming interfaces that allow the community to extend the infrastructure to meet its needs. iPlant is sponsoring community-driven workshops addressing specific scientific questions via analysis tool integration and hypothesis testing. These workshops teach researchers how to add bioinformatics tools and/or datasets into the iPlant cyberinfrastructure enabling plant scientists to perform complex analyses on large datasets without the need to master the command-line or high-performance computational services. PMID:22645531

  7. The Effect Analysis of Strain Rate on Power Transmission Tower-Line System under Seismic Excitation

    PubMed Central

    Wang, Wenming

    2014-01-01

    The effect analysis of strain rate on power transmission tower-line system under seismic excitation is studied in this paper. A three-dimensional finite element model of a transmission tower-line system is created based on a real project. Using theoretical analysis and numerical simulation, incremental dynamic analysis of the power transmission tower-line system is conducted to investigate the effect of strain rate on the nonlinear responses of the transmission tower and line. The results show that the effect of strain rate on the transmission tower generally decreases the maximum top displacements, but it would increase the maximum base shear forces, and thus it is necessary to consider the effect of strain rate on the seismic analysis of the transmission tower. The effect of strain rate could be ignored for the seismic analysis of the conductors and ground lines, but the responses of the ground lines considering strain rate effect are larger than those of the conductors. The results could provide a reference for the seismic design of the transmission tower-line system. PMID:25105157

  8. Creating Science Picture Books for an Authentic Audience

    ERIC Educational Resources Information Center

    DeFauw, Danielle L.; Saad, Klodia

    2014-01-01

    This article presents an authentic writing opportunity to help ninth-grade students use the writing process in a science classroom to write and illustrate picture books for fourth-grade students to demonstrate and share their understanding of a biology unit on cells. By creating a picture book, students experience the writing process, understand…

  9. Systems interface biology

    PubMed Central

    Doyle, Francis J; Stelling, Jörg

    2006-01-01

    The field of systems biology has attracted the attention of biologists, engineers, mathematicians, physicists, chemists and others in an endeavour to create systems-level understanding of complex biological networks. In particular, systems engineering methods are finding unique opportunities in characterizing the rich behaviour exhibited by biological systems. In the same manner, these new classes of biological problems are motivating novel developments in theoretical systems approaches. Hence, the interface between systems and biology is of mutual benefit to both disciplines. PMID:16971329

  10. The effect of cosmic rays on biological systems - an investigation during GLE events

    NASA Astrophysics Data System (ADS)

    Belisheva, N. K.; Lammer, H.; Biernat, H. K.; Vashenuyk, E. V.

    2012-01-01

    In this study, first direct and circumstantial evidences of the effects of cosmic rays (CR) on biological systems are presented. A direct evidence of biological effects of CR is demonstrated in experiments with three cellular lines growing in culture during three events of Ground Level Enhancement (GLEs) in the neutron count rate detected by ground-based neutron monitor in October 1989. Various phenomena associated with DNA lesion on the cellular level demonstrate coherent dynamics of radiation effects in all cellular lines coincident with the time of arrival of high-energy solar particles to the near-Earth space and with the main peak in GLE. These results were obtained in the course of six separate experiments, with partial overlapping of the time of previous and subsequent experiments, which started and finished in the quiet period of solar activity (SA). A significant difference between the values of multinuclear cells in all cellular lines in the quiet period and during GLE events indicates that the cause of radiation effects in the cell cultures is an exposure of cells to the secondary solar CR near the Earth's surface. The circumstantial evidence was obtained by statistical analysis of cases of congenital malformations (CM) at two sites in the Murmansk region. The number of cases of all classes of CM reveals a significant correlation with the number of GLE events. The number of cases of CM with pronounced chromosomal abnormalities clearly correlates with the GLE events that occurred a year before the birth of a child. We have found a significant correlation between modulations of the water properties and daily background variations of CR intensity. We believe that the effects of CR on biological systems can be also mediated by fluctuations in water properties, considered as one of possible mechanisms controlling the effects of CRs on biological systems.

  11. Synthetic biology as red herring.

    PubMed

    Preston, Beth

    2013-12-01

    It has become commonplace to say that with the advent of technologies like synthetic biology the line between artifacts and living organisms, policed by metaphysicians since antiquity, is beginning to blur. But that line began to blur 10,000 years ago when plants and animals were first domesticated; and has been thoroughly blurred at least since agriculture became the dominant human subsistence pattern many millennia ago. Synthetic biology is ultimately only a late and unexceptional offshoot of this prehistoric development. From this perspective, then, synthetic biology is a red herring, distracting us from more thorough philosophical consideration of the most truly revolutionary human practice-agriculture. In the first section of this paper I will make this case with regard to ontology, arguing that synthetic biology crosses no ontological lines that were not crossed already in the Neolithic. In the second section I will construct a parallel case with regard to cognition, arguing that synthetic biology as biological engineering represents no cognitive advance over what was required for domestication and the new agricultural subsistence pattern it grounds. In the final section I will make the case with regard to human existence, arguing that synthetic biology, even if wildly successful, is not in a position to cause significant existential change in what it is to be human over and above the massive existential change caused by the transition to agriculture. I conclude that a longer historical perspective casts new light on some important issues in philosophy of technology and environmental philosophy. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. The impact of an introductory college-level biology class on biology self-efficacy and attitude towards science

    NASA Astrophysics Data System (ADS)

    Thomas, Megan Elizabeth

    Self-efficacy theory was first introduced in a seminal article by Albert Bandura in 1977 entitled "Self-efficacy: Toward a unifying theory of behavioral change". Since its original introduction, self-efficacy has been a major focus of academic performance, anxiety, career development, and teacher retention research. Self-efficacy can be defined as the belief an individual possesses about their ability to perform a given task. Bandura proposed that self-efficacy should be measured at the highest level of specificity due to the fact that different people are efficacious in different areas. Interested in students' efficacy toward biology, Ebert-May, Baldwin, & Allred (1997) created and validated a survey to measure students' biology self-efficacy. Their survey was modeled after the guidelines for science literacy, and loaded to three sub-factors; methods of biology, generalization to other science courses, and application of the concepts. As self-efficacy theory has been related to effort expenditure and persistence (Bandura, 1977; 1997), one might think it would have some effect on students' attitudes toward the topic at hand. The current research investigated what changes in biology self-efficacy occurred after an introductory biology course with an inquiry based laboratory learning environment. In addition, changes in students' attitudes towards science were explored and how self-efficacy might affect them.

  13. Racing of the biological pacemaker.

    PubMed

    Yu, Han-Gang

    2009-01-01

    Over the past decade, rapid progress in the molecular studies of cardiac ion channels and stem cells biology has led to efforts to create a biological pacemaker to supplement the widely-used electronic pacemaker. We will review the main concepts of cardiac pacemaker activities in different heart regions and the approaches to design a working biological pacemaker. We will focus on how to use the gene- and cell-based approaches to meet the requirements of a working biological pacemaker. Possible future development and precautions for creation of an effective biological pacemaker superior to the electronic counterpart are also discussed along with recent patents.

  14. Pancreatic cancer cell lines as patient-derived avatars: genetic characterisation and functional utility.

    PubMed

    Knudsen, Erik S; Balaji, Uthra; Mannakee, Brian; Vail, Paris; Eslinger, Cody; Moxom, Christopher; Mansour, John; Witkiewicz, Agnieszka K

    2018-03-01

    Pancreatic ductal adenocarcinoma (PDAC) is a therapy recalcitrant disease with the worst survival rate of common solid tumours. Preclinical models that accurately reflect the genetic and biological diversity of PDAC will be important for delineating features of tumour biology and therapeutic vulnerabilities. 27 primary PDAC tumours were employed for genetic analysis and development of tumour models. Tumour tissue was used for derivation of xenografts and cell lines. Exome sequencing was performed on the originating tumour and developed models. RNA sequencing, histological and functional analyses were employed to determine the relationship of the patient-derived models to clinical presentation of PDAC. The cohort employed captured the genetic diversity of PDAC. From most cases, both cell lines and xenograft models were developed. Exome sequencing confirmed preservation of the primary tumour mutations in developed cell lines, which remained stable with extended passaging. The level of genetic conservation in the cell lines was comparable to that observed with patient-derived xenograft (PDX) models. Unlike historically established PDAC cancer cell lines, patient-derived models recapitulated the histological architecture of the primary tumour and exhibited metastatic spread similar to that observed clinically. Detailed genetic analyses of tumours and derived models revealed features of ex vivo evolution and the clonal architecture of PDAC. Functional analysis was used to elucidate therapeutic vulnerabilities of relevance to treatment of PDAC. These data illustrate that with the appropriate methods it is possible to develop cell lines that maintain genetic features of PDAC. Such models serve as important substrates for analysing the significance of genetic variants and create a unique biorepository of annotated cell lines and xenografts that were established simultaneously from same primary tumour. These models can be used to infer genetic and empirically determined

  15. Superresolved digital in-line holographic microscopy for high-resolution lensless biological imaging

    NASA Astrophysics Data System (ADS)

    Micó, Vicente; Zalevsky, Zeev

    2010-07-01

    Digital in-line holographic microscopy (DIHM) is a modern approach capable of achieving micron-range lateral and depth resolutions in three-dimensional imaging. DIHM in combination with numerical imaging reconstruction uses an extremely simplified setup while retaining the advantages provided by holography with enhanced capabilities derived from algorithmic digital processing. We introduce superresolved DIHM incoming from time and angular multiplexing of the sample spatial frequency information and yielding in the generation of a synthetic aperture (SA). The SA expands the cutoff frequency of the imaging system, allowing submicron resolutions in both transversal and axial directions. The proposed approach can be applied when imaging essentially transparent (low-concentration dilutions) and static (slow dynamics) samples. Validation of the method for both a synthetic object (U.S. Air Force resolution test) to quantify the resolution improvement and a biological specimen (sperm cells biosample) are reported showing the generation of high synthetic numerical aperture values working without lenses.

  16. Problem-based learning in an on-line biotechnology course

    NASA Astrophysics Data System (ADS)

    Cheaney, James Daniel

    Problem-based learning (PBL) is a pedagogical tool that uses a "real world" problem or situation as a context for learning. PBL encourages student development of critical thinking skills, a high professional competency, problem-solving ability, knowledge acquisition, the ability to work productively as a team member and make decisions in unfamiliar situations, and the acquisition of skills that support self-directed life-long learning, metacognition, and adaptation to change. However, little research has focused on the use of PBL in on-line "virtual" classes. We conducted two studies exploring the use of PBL in an on-line biotechnology course. In the first study, ethical, legal, social, and human issues were used as a motivation for learning about DNA testing technologies, applications, and bioethical issues. In the second study, we combined PBL pedagogy with a rich multimedia environment of streaming video interviews, physical artifacts, and extensive links to articles and databases to create a multidimensional immersive PBL environment called "Robert's World". In "Robert's World", a man is determining whether to undergo a pre-symptomatic DNA test for an untreatable, incurable, fatal genetic disease for which he has a family history. In both studies, design and implementation issues of the on-line PBL environment are discussed, as are differences between on-line PBL and face-to-face PBL. Both studies provide evidence to suggest that PBL stimulates higher-order learning in students. However, in both studies, student performance on an exam testing acquisition of lower-order factual learning was lower for PBL students than for students who learned the same material through a traditional lecture-based approach. Possible reasons for this lower level of performance are explored. Student feedback expressed engagement with the issues and material covered, with reservations about some aspects of the PBL format, such as the lack of flexibility provided in cooperative

  17. Structuring a service line.

    PubMed

    Zablocki, E

    1997-05-01

    In 1993, Community Hospitals Indianapolis created 10 service lines--each unique to the needs of the patients it serves. Two service line leaders talk about the factors critical to successful restructuring, the working relationships established, and the importance of clear communication to ensure understanding and get buy-in to the process.

  18. Synthetic Biology: Knowledge Accessed by Everyone (Open Sources)

    ERIC Educational Resources Information Center

    Sánchez Reyes, Patricia Margarita

    2016-01-01

    Using the principles of biology, along with engineering and with the help of computer, scientists manage to copy. DNA sequences from nature and use them to create new organisms. DNA is created through engineering and computer science managing to create life inside a laboratory. We cannot dismiss the role that synthetic biology could lead in…

  19. Effect of graphene oxide on undifferentiated and retinoic acid-differentiated SH-SY5Y cells line

    NASA Astrophysics Data System (ADS)

    Lv, Min; Zhang, Yujie; Liang, Le; Wei, Min; Hu, Wenbing; Li, Xiaoming; Huang, Qing

    2012-06-01

    Graphene oxide (GO), has created an unprecedented opportunity for development and application in biology, due to its abundant functional groups and well water solubility. Recently, the potential toxicity of GO in the environment and in humans has garnered more and more attention. In this paper, we systematically studied the cytotoxicity of GO nanosheets via examining the effect of GO on the morphology, viability and differentiation of a human neuroblastoma SH-SY5Y cell line, which was an ideal model used to study neuronal disease in vitro. The results suggested that GO had no obvious cytotoxicity at low concentration (<80 μg mL-1) for 96 h, but the viability of cells exhibited dose- and time-dependent decreases at high concentration (>=80 μg mL-1). Moreover, GO did not induce apoptosis. Very interestingly, GO significantly enhanced the differentiation of SH-SY5Y induced-retinoic acid (RA) by evaluating neurite length and the expression of neuronal marker MAP2. These data provide a promising application for neurodegenerative diseases.

  20. Single-cell lineage tracking analysis reveals that an established cell line comprises putative cancer stem cells and their heterogeneous progeny

    PubMed Central

    Sato, Sachiko; Rancourt, Ann; Sato, Yukiko; Satoh, Masahiko S.

    2016-01-01

    Mammalian cell culture has been used in many biological studies on the assumption that a cell line comprises putatively homogeneous clonal cells, thereby sharing similar phenotypic features. This fundamental assumption has not yet been fully tested; therefore, we developed a method for the chronological analysis of individual HeLa cells. The analysis was performed by live cell imaging, tracking of every single cell recorded on imaging videos, and determining the fates of individual cells. We found that cell fate varied significantly, indicating that, in contrast to the assumption, the HeLa cell line is composed of highly heterogeneous cells. Furthermore, our results reveal that only a limited number of cells are immortal and renew themselves, giving rise to the remaining cells. These cells have reduced reproductive ability, creating a functionally heterogeneous cell population. Hence, the HeLa cell line is maintained by the limited number of immortal cells, which could be putative cancer stem cells. PMID:27003384

  1. From the front line to the bottom line: building revenue integrity.

    PubMed

    Britt, John; Adams, Shawn; Snow, Trevor

    2015-07-01

    To improve trends in accounts receivable and a hospital's bottom line without fear of penalty or repayment, organizations should expand the definition of the revenue cycle team by: Engaging front-line clinical and business personnel. Training personnel to understand the roles they play in revenue integrity. Creating scorecards with measurable goals to promote accountability. Monitoring the outcomes and defining real-time, actionable responses to negative variances.

  2. Unconscious-thought effects take place off-line, not on-line.

    PubMed

    Strick, Madelijn; Dijksterhuis, Ap; van Baaren, Rick B

    2010-04-01

    The unconscious-thought effect refers to an improvement in decision making following distraction from the decision context for a period of time. The dominant explanation for this effect is that unconscious processes continue to deal with the problem during the distraction period. Recently, however, some researchers have proposed that unconscious thinkers may be merely recalling a judgment that was formed on-line (i.e., during information acquisition). We present two experiments that rule out the latter interpretation. In the unconscious-thought condition of the first experiment, participants who reported making their decision after unconscious thought made better decisions than those who reported making their decision on-line. In the second experiment, all participants judged the choice alternatives both on-line and off-line. On-line judgments were predictive of off-line judgments only in the immediate-decision condition, but not in the conscious- and unconscious-thought conditions. These results demonstrate that a period of unconscious thought does improve judgments that were formed earlier on-line.

  3. Studies on the treatment of urine by the biological purification-UV photocatalytic oxidation

    NASA Astrophysics Data System (ADS)

    Liu, Ch. Ch; Liu, R. D.; Liu, X. S.; Chen, M.; Bian, Z. L.; Hu, J. Ch.

    The water-consuming amount in a long-term astro-navigation is large In order to reduce the burden of water supply from Earth ground the space station needs to resolve the problems of water supply For this reason the recovery and regeneration of urine solution of spacemen and its utilization possess a key importance Many investigations on this aspect have been reported Our research based on biological absorption-purification-UV photocatalytic oxidation techniques with a relevant treating equipment that for a comprehensive treatment to fresh urine of spacemen has been created In this equipment the urine solution was used as the nutrient solution for the biological parts in ecological life ensurant system after absorbing the nutrient it was decomposed metabolized and purified in some distance and created a favorable condition for the follow-up oxidation treatment by UV-Photocatalytic Oxidation After these two processes the treated urine solution reached the GB5749-85 standard of water quality

  4. Studies on urine treatment by biological purification using Azolla and UV photocatalytic oxidation

    NASA Astrophysics Data System (ADS)

    Liu, Xiaofeng; Chen, Min; Bian, Zuliang; Liu, Chung-Chu

    The amount of water consumed in space station operations is very large. In order to reduce the amount of water which must be resupplied from Earth, the space station needs to resolve the problems of water supply. For this reason, the recovery, regeneration and utilization of urine of astronauts are of key importance. Many investigations on this subject have been reported. Our research is based on biological absorption and, purification using UV photocatalytic oxidation techniques to achieve comprehensive treatment for urine. In the treatment apparatus we created, the urine solution is used as part of the nutrient solution for the biological components in our bioregenerative life support system. After being absorbed, the nutrients from the urine were then decomposed, metabolized and purified which creates a favorable condition for the follow-up oxidation treatment by UV photocatalytic oxidation. After these two processes, the treated urine solution reached Chinese national standards for drinking water quality (GB5749-1985).

  5. Creating an Excellent Patient Experience Through Service Education

    PubMed Central

    2017-01-01

    Service quality and patient satisfaction affect an organization’s value-based payments. This new value paradigm calls for a new approach to service education and training for front-line staff. Thoughtfully conceived, department-specific content, infused with patient feedback, value creation, and science of service quality principles, was developed to give front-line staff a deeper understanding of the impact of their performance on patient experience, value creation, and value-based revenue. Feedback from nearly 1500 trainees in 60 educational sessions delivered over 7 years indicates good understanding of the content and appreciation of the targeted approach. On a 5-point scale ranging from 1 (least effective) to 5 (most effective), trainees’ ratings of their understanding of service quality concepts and impact on value ranged from 4.7 to 4.9. Verbatim comments showed a positive impact on staff. Employee feedback suggests that value-based service education may be useful in motivating front-line staff, improving service quality, and creating value. PMID:29276761

  6. Creating, generating and comparing random network models with NetworkRandomizer.

    PubMed

    Tosadori, Gabriele; Bestvina, Ivan; Spoto, Fausto; Laudanna, Carlo; Scardoni, Giovanni

    2016-01-01

    Biological networks are becoming a fundamental tool for the investigation of high-throughput data in several fields of biology and biotechnology. With the increasing amount of information, network-based models are gaining more and more interest and new techniques are required in order to mine the information and to validate the results. To fill the validation gap we present an app, for the Cytoscape platform, which aims at creating randomised networks and randomising existing, real networks. Since there is a lack of tools that allow performing such operations, our app aims at enabling researchers to exploit different, well known random network models that could be used as a benchmark for validating real, biological datasets. We also propose a novel methodology for creating random weighted networks, i.e. the multiplication algorithm, starting from real, quantitative data. Finally, the app provides a statistical tool that compares real versus randomly computed attributes, in order to validate the numerical findings. In summary, our app aims at creating a standardised methodology for the validation of the results in the context of the Cytoscape platform.

  7. Microfluidic Technologies for Synthetic Biology

    PubMed Central

    Vinuselvi, Parisutham; Park, Seongyong; Kim, Minseok; Park, Jung Min; Kim, Taesung; Lee, Sung Kuk

    2011-01-01

    Microfluidic technologies have shown powerful abilities for reducing cost, time, and labor, and at the same time, for increasing accuracy, throughput, and performance in the analysis of biological and biochemical samples compared with the conventional, macroscale instruments. Synthetic biology is an emerging field of biology and has drawn much attraction due to its potential to create novel, functional biological parts and systems for special purposes. Since it is believed that the development of synthetic biology can be accelerated through the use of microfluidic technology, in this review work we focus our discussion on the latest microfluidic technologies that can provide unprecedented means in synthetic biology for dynamic profiling of gene expression/regulation with high resolution, highly sensitive on-chip and off-chip detection of metabolites, and whole-cell analysis. PMID:21747695

  8. Microfluidic technologies for synthetic biology.

    PubMed

    Vinuselvi, Parisutham; Park, Seongyong; Kim, Minseok; Park, Jung Min; Kim, Taesung; Lee, Sung Kuk

    2011-01-01

    Microfluidic technologies have shown powerful abilities for reducing cost, time, and labor, and at the same time, for increasing accuracy, throughput, and performance in the analysis of biological and biochemical samples compared with the conventional, macroscale instruments. Synthetic biology is an emerging field of biology and has drawn much attraction due to its potential to create novel, functional biological parts and systems for special purposes. Since it is believed that the development of synthetic biology can be accelerated through the use of microfluidic technology, in this review work we focus our discussion on the latest microfluidic technologies that can provide unprecedented means in synthetic biology for dynamic profiling of gene expression/regulation with high resolution, highly sensitive on-chip and off-chip detection of metabolites, and whole-cell analysis.

  9. Biological activity of Xanthium strumarium seed extracts on different cancer cell lines and Aedes caspius, Culex pipiens (Diptera: Culicidae).

    PubMed

    Al-Mekhlafi, Fahd A; Abutaha, Nael; Mashaly, Ashraf M A; Nasr, Fahd A; Ibrahim, Khalid E; Wadaan, Mohamed A

    2017-05-01

    Effects of methanol extracts of Xanthium strumarium on different cancer cell lines and on the mortality rates of Aedes caspius, Culex pipiens (Diptera: Culicidae) were investigated. Among the cell lines tested, the Jurkat cell line was the most sensitive to the methanol extract and ethyl acetate fraction, with reported LC 50 values of 50.18 and 48.73 μg/ml respectively. Conversely, methanol extracts were not that toxic to the A549 cell line though the toxicity increased on further purification. The percentage of growth inhibition was dose dependent for the methanol extract and ethyl acetate fraction. The ethyl acetate fraction showed higher toxicity to all cell lines tested when compared to the methanol extract. The results showed that methanol extracts of plant seeds caused 100% mortality of mosquito larvae at a concentration of 1000 μg/ml after 24 h of treatment. The LC 50 and LC 90 values of X. strumarium were found to be 531.07 and 905.95 μg/ml against Ae. caspius and 502.32 and 867.63 μg/ml against Cx. Pipiens, respectively. From the investigations, it was concluded that the crude extract of X. strumarium showed a weak potential for controlling the larval instars of Ae. caspius and Cx. pipiens . However, on further purification the extract lost the larvicidal activity. The ethyl acetate fraction showed higher toxicity to all cell lines tested when compared to the methanol extract. The ethyl acetate fraction investigated in this study appears to have a weak larvicidal activity but a promising cytotoxic activity. Future studies will include purification and investigation in further detail of the action of X. strumarium on Cancer Cell Lines and mosquitoes.

  10. [Effects of fasudil on bleomycin-induced pulmonary fibrosis in mice and on the biological behaviors in NIH3T3 mouse fibroblast cell line].

    PubMed

    Jiang, Chunguo; Huang, Hui; Liu, Jia; Wang, Yanxun; Zhao, Yuyue; Xu, Zuojun

    2014-09-01

    To determine the beneficial effects and mechanisms of fasudil, a selective ROCK inhibitor, on bleomycin-induced pulmonary fibrosis in mice and to determine the effects and mechanisms of fasudil on the biological behaviors in NIH3T3 mouse fibroblast cell line. The BPF model was induced by a single dosage of 2.5 mg/kg bleomycin intratracheal injection in mice and fasudil intraperitoneal injection was given to the mice. The fibrosis degree was determined pathologically by using the Ashcroft scoring method and biochemically by hydroxyproline assay in lung tissue. NIH3T3 mouse fibroblast cell line was cultured in vitro and fasudil was given to the cell. The proliferation activity in NIH3T3 cells were detected by MTT assay and flat colony forming experiment. The migration activity in NIH3T3 cells were detected by scratch test and transwell chamber experiment. The expression of CyclinD1, MMP2 and TIMP1 mRNA in NIH3T3 cells was detected by RT-PCR. The expression of CyclinD1, MMP2 and TIMP1 protein and the level of MYPT1 phosphorylation in NIH3T3 cells was detected by Western blot. Compare to the mice administrated by bleomycin, the Ashcroft score and hydroxyproline content were significantly decreased in the mice administered fasudil. Administration of fasudil can reduce the ability of proliferation and migration in a dose-dependent manner in NIH3T3 cells. The effect of fasudil was possibly related to increase the production of TIMP1 and decrease the production of CyclinD1 and MMP2. Administration of fasudil can attenuate pulmonary fibrosis both in vivo and in vitro. These findings suggest that fasudil may be a potential therapeutic candidate for the treatment of pulmonary fibrosis.

  11. Synthetic biology: navigating the challenges ahead.

    PubMed

    Bhutkar, Arjun

    2005-01-01

    The emerging field of synthetic biology is broadly defined as the area of intersection of biology and engineering that focuses on the modification or creation of novel biological systems that do not have a counterpart in nature. Potential applications of this technology range from creating systems for environmental cleanup tasks, for medical diagnosis and treatment, to economical generation of hydrogen fuel. This technology is in tis nascent state and there are a number of concerns surrounding its potential applications and the nature of research being performed. With the potential to create hitherto unknown "living organisms", it raises a number of challenges along different dimensions. This article reviews the current state of the technology and analyzes synthetic biology using different lenses: patentability, ethics, and regulation. It proposes a classification system for the products of synthetic biology and provides recommendations in each of the above areas (patentability, ethics, and regulation) in the context of this classification system. These recommendations include an improved framework for patentability testing, ethical principles to guide work in this area, a controlled approval process, and reference frameworks for regulation.

  12. On Line Disaster Response Community: People as Sensors of High Magnitude Disasters Using Internet GIS

    PubMed Central

    Laituri, Melinda; Kodrich, Kris

    2008-01-01

    The Indian Ocean tsunami (2004) and Hurricane Katrina (2005) reveal the coming of age of the on-line disaster response community. Due to the integration of key geospatial technologies (remote sensing - RS, geographic information systems - GIS, global positioning systems – GPS) and the Internet, on-line disaster response communities have grown. They include the traditional aspects of disaster preparedness, response, recovery, mitigation, and policy as facilitated by governmental agencies and relief response organizations. However, the contribution from the public via the Internet has changed significantly. The on-line disaster response community includes several key characteristics: the ability to donate money quickly and efficiently due to improved Internet security and reliable donation sites; a computer-savvy segment of the public that creates blogs, uploads pictures, and disseminates information – oftentimes faster than government agencies, and message boards to create interactive information exchange in seeking family members and identifying shelters. A critical and novel occurrence is the development of “people as sensors” - networks of government, NGOs, private companies, and the public - to build rapid response databases of the disaster area for various aspects of disaster relief and response using geospatial technologies. This paper examines these networks, their products, and their future potential. PMID:27879864

  13. A bridge from physics to biology.

    PubMed

    Preparata, Giuliano

    2010-01-01

    Through molecular biology, the 'atomistic paradigm' tries to remove from the analysis of living matter every element of what appears as the distinguishing character of the chain of the biological processes: their cooperative, collective aspects. Living matter appears, on the contrary, governed by Quantum Field Theory (QFT), spontaneously creating order when the thermodynamical conditions are right. 'Electrodynamical coherence' (EC) is the most promising hint for the existence of a bridge between Physics and Biology.

  14. e-Biologics: Fabrication of Sustainable Electronics with "Green" Biological Materials.

    PubMed

    Lovley, Derek R

    2017-06-27

    The growing ubiquity of electronic devices is increasingly consuming substantial energy and rare resources for materials fabrication, as well as creating expansive volumes of toxic waste. This is not sustainable. Electronic biological materials (e-biologics) that are produced with microbes, or designed with microbial components as the guide for synthesis, are a potential green solution. Some e-biologics can be fabricated from renewable feedstocks with relatively low energy inputs, often while avoiding the harsh chemicals used for synthesizing more traditional electronic materials. Several are completely free of toxic components, can be readily recycled, and offer unique features not found in traditional electronic materials in terms of size, performance, and opportunities for diverse functionalization. An appropriate investment in the concerted multidisciplinary collaborative research required to identify and characterize e-biologics and to engineer materials and devices based on e-biologics could be rewarded with a new "green age" of sustainable electronic materials and devices. Copyright © 2017 Lovley.

  15. Nature and Consequences of Biological Reductionism for the Immunological Study of Infectious Diseases

    DOE PAGES

    Rivas, Ariel L.; Leitner, Gabriel; Jankowski, Mark D.; ...

    2017-05-31

    Evolution has conserved “economic” systems that perform many functions, faster or better, with less. For example, three to five leukocyte types protect from thousands of pathogens. In order to achieve so much with so little, biological systems combine their limited elements, creating complex structures. Yet, the prevalent research paradigm is reductionist. Focusing on infectious diseases, reductionist and non-reductionist views are here described. Furthermore, the literature indicates that reductionism is associated with information loss and errors, while non-reductionist operations can extract more information from the same data. When designed to capture one-to-many/many-to-one interactions—including the use of arrows that connect pairs ofmore » consecutive observations—non-reductionist (spatial–temporal) constructs eliminate data variability from all dimensions, except along one line, while arrows describe the directionality of temporal changes that occur along the line. To validate the patterns detected by non-reductionist operations, reductionist procedures are needed. Integrated (non-reductionist and reductionist) methods can (i) distinguish data subsets that differ immunologically and statistically; (ii) differentiate false-negative from -positive errors; (iii) discriminate disease stages; (iv) capture in vivo, multilevel interactions that consider the patient, the microbe, and antibiotic-mediated responses; and (v) assess dynamics. Integrated methods provide repeatable and biologically interpretable information.« less

  16. Nature and Consequences of Biological Reductionism for the Immunological Study of Infectious Diseases.

    PubMed

    Rivas, Ariel L; Leitner, Gabriel; Jankowski, Mark D; Hoogesteijn, Almira L; Iandiorio, Michelle J; Chatzipanagiotou, Stylianos; Ioannidis, Anastasios; Blum, Shlomo E; Piccinini, Renata; Antoniades, Athos; Fazio, Jane C; Apidianakis, Yiorgos; Fair, Jeanne M; Van Regenmortel, Marc H V

    2017-01-01

    Evolution has conserved "economic" systems that perform many functions, faster or better, with less. For example, three to five leukocyte types protect from thousands of pathogens. To achieve so much with so little, biological systems combine their limited elements, creating complex structures. Yet, the prevalent research paradigm is reductionist. Focusing on infectious diseases, reductionist and non-reductionist views are here described. The literature indicates that reductionism is associated with information loss and errors, while non-reductionist operations can extract more information from the same data. When designed to capture one-to-many/many-to-one interactions-including the use of arrows that connect pairs of consecutive observations-non-reductionist (spatial-temporal) constructs eliminate data variability from all dimensions, except along one line, while arrows describe the directionality of temporal changes that occur along the line. To validate the patterns detected by non-reductionist operations, reductionist procedures are needed. Integrated (non-reductionist and reductionist) methods can (i) distinguish data subsets that differ immunologically and statistically; (ii) differentiate false-negative from -positive errors; (iii) discriminate disease stages; (iv) capture in vivo , multilevel interactions that consider the patient, the microbe, and antibiotic-mediated responses; and (v) assess dynamics. Integrated methods provide repeatable and biologically interpretable information.

  17. Nature and Consequences of Biological Reductionism for the Immunological Study of Infectious Diseases

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Rivas, Ariel L.; Leitner, Gabriel; Jankowski, Mark D.

    Evolution has conserved “economic” systems that perform many functions, faster or better, with less. For example, three to five leukocyte types protect from thousands of pathogens. In order to achieve so much with so little, biological systems combine their limited elements, creating complex structures. Yet, the prevalent research paradigm is reductionist. Focusing on infectious diseases, reductionist and non-reductionist views are here described. Furthermore, the literature indicates that reductionism is associated with information loss and errors, while non-reductionist operations can extract more information from the same data. When designed to capture one-to-many/many-to-one interactions—including the use of arrows that connect pairs ofmore » consecutive observations—non-reductionist (spatial–temporal) constructs eliminate data variability from all dimensions, except along one line, while arrows describe the directionality of temporal changes that occur along the line. To validate the patterns detected by non-reductionist operations, reductionist procedures are needed. Integrated (non-reductionist and reductionist) methods can (i) distinguish data subsets that differ immunologically and statistically; (ii) differentiate false-negative from -positive errors; (iii) discriminate disease stages; (iv) capture in vivo, multilevel interactions that consider the patient, the microbe, and antibiotic-mediated responses; and (v) assess dynamics. Integrated methods provide repeatable and biologically interpretable information.« less

  18. Nature and Consequences of Biological Reductionism for the Immunological Study of Infectious Diseases

    PubMed Central

    Rivas, Ariel L.; Leitner, Gabriel; Jankowski, Mark D.; Hoogesteijn, Almira L.; Iandiorio, Michelle J.; Chatzipanagiotou, Stylianos; Ioannidis, Anastasios; Blum, Shlomo E.; Piccinini, Renata; Antoniades, Athos; Fazio, Jane C.; Apidianakis, Yiorgos; Fair, Jeanne M.; Van Regenmortel, Marc H. V.

    2017-01-01

    Evolution has conserved “economic” systems that perform many functions, faster or better, with less. For example, three to five leukocyte types protect from thousands of pathogens. To achieve so much with so little, biological systems combine their limited elements, creating complex structures. Yet, the prevalent research paradigm is reductionist. Focusing on infectious diseases, reductionist and non-reductionist views are here described. The literature indicates that reductionism is associated with information loss and errors, while non-reductionist operations can extract more information from the same data. When designed to capture one-to-many/many-to-one interactions—including the use of arrows that connect pairs of consecutive observations—non-reductionist (spatial–temporal) constructs eliminate data variability from all dimensions, except along one line, while arrows describe the directionality of temporal changes that occur along the line. To validate the patterns detected by non-reductionist operations, reductionist procedures are needed. Integrated (non-reductionist and reductionist) methods can (i) distinguish data subsets that differ immunologically and statistically; (ii) differentiate false-negative from -positive errors; (iii) discriminate disease stages; (iv) capture in vivo, multilevel interactions that consider the patient, the microbe, and antibiotic-mediated responses; and (v) assess dynamics. Integrated methods provide repeatable and biologically interpretable information. PMID:28620378

  19. Towards a Unified Understanding of Lithium Action in Basic Biology and its Significance for Applied Biology.

    PubMed

    Jakobsson, Eric; Argüello-Miranda, Orlando; Chiu, See-Wing; Fazal, Zeeshan; Kruczek, James; Nunez-Corrales, Santiago; Pandit, Sagar; Pritchet, Laura

    2017-12-01

    Lithium has literally been everywhere forever, since it is one of the three elements created in the Big Bang. Lithium concentration in rocks, soil, and fresh water is highly variable from place to place, and has varied widely in specific regions over evolutionary and geologic time. The biological effects of lithium are many and varied. Based on experiments in which animals are deprived of lithium, lithium is an essential nutrient. At the other extreme, at lithium ingestion sufficient to raise blood concentration significantly over 1 mM/, lithium is acutely toxic. There is no consensus regarding optimum levels of lithium intake for populations or individuals-with the single exception that lithium is a generally accepted first-line therapy for bipolar disorder, and specific dosage guidelines for sufferers of that condition are generally agreed on. Epidemiological evidence correlating various markers of social dysfunction and disease vs. lithium level in drinking water suggest benefits of moderately elevated lithium compared to average levels of lithium intake. In contrast to other biologically significant ions, lithium is unusual in not having its concentration in fluids of multicellular animals closely regulated. For hydrogen ions, sodium ions, potassium ions, calcium ions, chloride ions, and magnesium ions, blood and extracellular fluid concentrations are closely and necessarily regulated by systems of highly selective channels, and primary and secondary active transporters. Lithium, while having strong biological activity, is tolerated over body fluid concentrations ranging over many orders of magnitude. The lack of biological regulation of lithium appears due to lack of lithium-specific binding sites and selectivity filters. Rather lithium exerts its myriad physiological and biochemical effects by competing for macromolecular sites that are relatively specific for other cations, most especially for sodium and magnesium. This review will consider what is known

  20. Designing Health Care Risk Management On-Line: Meeting Regulators' Concerns for Fixed-Hour Curriculum

    ERIC Educational Resources Information Center

    Hyer, Kathryn; Taylor, Heidi H.; Nanni, Kenneth

    2004-01-01

    This paper describes the experience of creating a continuing professional education on-line risk management program that is designed to meet Florida's educational requirements for licensure as a risk manager in health-care settings and details the challenges faced when the in-class didactic program of 15 eight-hour sessions is reformatted as an…

  1. Synthetic biology: exploring and exploiting genetic modularity through the design of novel biological networks.

    PubMed

    Agapakis, Christina M; Silver, Pamela A

    2009-07-01

    Synthetic biology has been used to describe many biological endeavors over the past thirty years--from designing enzymes and in vitro systems, to manipulating existing metabolisms and gene expression, to creating entirely synthetic replicating life forms. What separates the current incarnation of synthetic biology from the recombinant DNA technology or metabolic engineering of the past is an emphasis on principles from engineering such as modularity, standardization, and rigorously predictive models. As such, synthetic biology represents a new paradigm for learning about and using biological molecules and data, with applications in basic science, biotechnology, and medicine. This review covers the canonical examples as well as some recent advances in synthetic biology in terms of what we know and what we can learn about the networks underlying biology, and how this endeavor may shape our understanding of living systems.

  2. Nanoparticle-based biologic mimetics

    PubMed Central

    Cliffel, David E.; Turner, Brian N.; Huffman, Brian J.

    2009-01-01

    Centered on solid chemistry foundations, biology and materials science have reached a crossroad where bottom-up designs of new biologically important nanomaterials are a reality. The topics discussed here present the interdisciplinary field of creating biological mimics. Specifically, this discussion focuses on mimics that are developed using various types of metal nanoparticles (particularly gold) through facile synthetic methods. These methods conjugate biologically relevant molecules, e.g., small molecules, peptides, proteins, and carbohydrates, in conformationally favorable orientations on the particle surface. These new products provide stable, safe, and effective substitutes for working with potentially hazardous biologicals for applications such as drug targeting, immunological studies, biosensor development, and biocatalysis. Many standard bioanalytical techniques can be used to characterize and validate the efficacy of these new materials, including quartz crystal microbalance (QCM), surface plasmon resonance (SPR), and enzyme-linked immunosorbent assay (ELISA). Metal nanoparticle–based biomimetics continue to be developed as potential replacements for the native biomolecule in applications of immunoassays and catalysis. PMID:20049778

  3. Line, Shape, Color.

    ERIC Educational Resources Information Center

    Greenman, Geri

    2002-01-01

    Describes an art project used with beginning high school art students that teaches them about continuous line drawing. Explains that the students create portraits of themselves, or another student, using glue, black construction paper, and chalk. (CMK)

  4. On the three-dimensional magnetic structure of the plasmoid created in the magnetotail at substorm onset

    NASA Technical Reports Server (NTRS)

    Hones, E. W., Jr.; Bame, S. J.; Birn, J.; Paschmann, G.; Russell, C. T.

    1982-01-01

    The magnetic field in the plasmoid which is created by the reconnection of magnetic field lines at a neutral line formed in the near-earth region of the plasma sheet at substorm onset, and which flows out of the magnetotail into the magnetosphere's wake, displays a strong positive or negative Y(SM) component that has been difficult to reconcile with the standard, two-dimensional reconnection geometry. It is shown that this deviation of the magnetic field is a manifestation of the newly-reconnected field line loop's draping toward the tail's central or midnight meridian, and that the draping is a consequence of the three-dimensional plasma flow associated with the reconnection process.

  5. Influence of damage and basal friction on the grounding line dynamics

    NASA Astrophysics Data System (ADS)

    Brondex, Julien; Gagliardini, Olivier; Gillet-Chaulet, Fabien; Durand, Gael

    2016-04-01

    The understanding of grounding line dynamics is a major issue in the prediction of future sea level rise due to ice released from polar ice sheets into the ocean. This dynamics is complex and significantly affected by several physical processes not always adequately accounted for in current ice flow models. Among those processes, our study focuses on ice damage and evolving basal friction conditions. Softening of the ice due to damaging processes is known to have a strong impact on its rheology by reducing its viscosity and therefore promoting flow acceleration. Damage creates where shear stresses are high enough which is usually the case at shear margins and in the vicinity of pinning points in contact with ice-shelves. Those areas are known to have a buttressing effect on ice shelves contributing to stabilize the grounding line. We aim at evaluating the extent to which this stabilizing effect is hampered by damaging processes. Several friction laws have been proposed by various author to model the contact between grounded-ice and bedrock. Among them, Coulomb-type friction laws enable to account for reduced friction related to low effective pressure (the ice pressure minus the water pressure). Combining such a friction law to a parametrization of the effective pressure accounting for the fact that the area upstream the grounded line is connected to the ocean, is expected to have a significant impact on the grounding line dynamics. Using the finite-element code Elmer/Ice within which both the Coulomb-type friction law, the effective pressure parametrization and the damage model have been implemented, the goal of this study is to investigate the sensitivity of the grounding line dynamics to damage and to an evolving basal friction. The relative importance between those two processes on the grounding line dynamics is addressed as well.

  6. The effect of fast created inbreeding on litter size and body weights in mice

    PubMed Central

    Holt, Marte; Meuwissen, Theo; Vangen, Odd

    2005-01-01

    This study was designed to reveal any differences in effects of fast created versus total inbreeding on reproduction and body weights in mice. A line selected for large litter size for 124 generations (H) and a control line (K) maintained without selection for the same number of generations were crossed (HK) and used as a basis for the experiment. Within the HK cross, full sib, cousin or random mating were practised for two generations in order to create new inbreeding (IBF) at a fast rate. In the first generation of systematic mating, old inbreeding was regenerated in addition to creation of new inbreeding from the mating design giving total inbreeding (IBT). The number of pups born alive (NBA) and body weights of the animals were then analysed by a model including both IBT and IBF. The IBT of the dam was in the present study found to reduce the mean NBA with -0.48 (± 0.22) (p < 0.05) pups per 10% increase in the inbreeding coefficient, while the additional effect of IBF was -0.42 (± 0.27). For the trait NBA per female mated, the effect of IBT was estimated to be -0.45 (± 0.29) per 10% increase in the inbreeding coefficient and the effect of IBF was -0.90 (± 0.37) (p < 0.05) pups. In the present study, only small or non-significant effects of IBF of the dam could be found on sex-ratio and body weights at three and six weeks of age in a population already adjusted for IBT. PMID:16093013

  7. Line-by-line spectroscopic simulations on graphics processing units

    NASA Astrophysics Data System (ADS)

    Collange, Sylvain; Daumas, Marc; Defour, David

    2008-01-01

    We report here on software that performs line-by-line spectroscopic simulations on gases. Elaborate models (such as narrow band and correlated-K) are accurate and efficient for bands where various components are not simultaneously and significantly active. Line-by-line is probably the most accurate model in the infrared for blends of gases that contain high proportions of H 2O and CO 2 as this was the case for our prototype simulation. Our implementation on graphics processing units sustains a speedup close to 330 on computation-intensive tasks and 12 on memory intensive tasks compared to implementations on one core of high-end processors. This speedup is due to data parallelism, efficient memory access for specific patterns and some dedicated hardware operators only available in graphics processing units. It is obtained leaving most of processor resources available and it would scale linearly with the number of graphics processing units in parallel machines. Line-by-line simulation coupled with simulation of fluid dynamics was long believed to be economically intractable but our work shows that it could be done with some affordable additional resources compared to what is necessary to perform simulations on fluid dynamics alone. Program summaryProgram title: GPU4RE Catalogue identifier: ADZY_v1_0 Program summary URL:http://cpc.cs.qub.ac.uk/summaries/ADZY_v1_0.html Program obtainable from: CPC Program Library, Queen's University, Belfast, N. Ireland Licensing provisions: Standard CPC licence, http://cpc.cs.qub.ac.uk/licence/licence.html No. of lines in distributed program, including test data, etc.: 62 776 No. of bytes in distributed program, including test data, etc.: 1 513 247 Distribution format: tar.gz Programming language: C++ Computer: x86 PC Operating system: Linux, Microsoft Windows. Compilation requires either gcc/g++ under Linux or Visual C++ 2003/2005 and Cygwin under Windows. It has been tested using gcc 4.1.2 under Ubuntu Linux 7.04 and using Visual C

  8. Switching of biologics in psoriasis: Reasons and results.

    PubMed

    Honda, Hiromi; Umezawa, Yoshinori; Kikuchi, Sota; Yanaba, Koichi; Fukuchi, Osamu; Ito, Toshihiro; Nobeyama, Yoshimasa; Asahina, Akihiko; Nakagawa, Hidemi

    2017-09-01

    Efficacy and safety profiles of biologics have been established for moderate to severe psoriasis. However, inefficacy or adverse events sometimes require changing the treatment to other biologics. Here, we examine the effectiveness of this strategy. We retrospectively investigated cases requiring switching biologics. We enrolled 275 psoriatic patients treated with biologics between January 2010 and December 2014 in our hospital. Of these, 51 required a switch to another biologic. First-line therapies were infliximab (IFX, n = 26), adalimumab (ADA, n = 18) and ustekinumab (UST, n = 7), and second-line therapies were IFX (n = 5), ADA (n = 21) and UST (n = 25). Reasons for switching were inefficacy (n = 38), adverse events (n = 11) and others (n = 2). The details were primary failure (n = 15), secondary failure (n = 23) and infusion reactions (n = 8). In 49 patients who switched biologics due to inefficacy and adverse events, the mean Psoriasis Area and Severity Index (PASI) score at week 16 was 4.3 for first-line therapies and 2.9 for second-line therapies (P < 0.05). Switching to a second biologic therapy to address the first's inefficacy or adverse events often results in significant improvement in moderate to severe psoriasis. © 2017 Japanese Dermatological Association.

  9. Firing up the front line.

    PubMed

    Katzenbach, J R; Santamaria, J A

    1999-01-01

    For many organizations, achieving competitive advantage means eliciting superior performance from employees on the front line--the burger flippers, hotel room cleaners, and baggage handlers whose work has an enormous effect on customers. That's no easy task. Front line workers are paid low wages, have scant hope of advancement, and--not surprisingly--often care little about the company's performance. But then how do some companies succeed in engaging the emotional energy of rank-and-file workers? A team of researchers at McKinsey & Company and the Conference Board recently explored that question and discovered that one highly effective route is demonstrated by the U.S. Marine Corps. The Marines' approach to motivation follows the "mission, values, and pride" path, which researchers say is practical and relevant for the business world. More specifically, the authors say the Marines follow five practices: they over-invest in cultivating core value; prepare every person to lead, including front line supervisors; learn when to create teams and when to create single-leader work groups; attend to all employees, not just the top half; and encourage self-discipline as a way of building pride. The authors admit there are critical differences between the Marines and most businesses. But using vivid examples from companies such as KFC and Marriott International, the authors illustrate how the Marines' approach can be translated for corporate use. Sometimes, the authors maintain, minor changes in a company's standard operating procedure can have a powerful effect on front line pride and can result in substantial payoffs in company performance.

  10. e-Biologics: Fabrication of Sustainable Electronics with “Green” Biological Materials

    PubMed Central

    2017-01-01

    ABSTRACT The growing ubiquity of electronic devices is increasingly consuming substantial energy and rare resources for materials fabrication, as well as creating expansive volumes of toxic waste. This is not sustainable. Electronic biological materials (e-biologics) that are produced with microbes, or designed with microbial components as the guide for synthesis, are a potential green solution. Some e-biologics can be fabricated from renewable feedstocks with relatively low energy inputs, often while avoiding the harsh chemicals used for synthesizing more traditional electronic materials. Several are completely free of toxic components, can be readily recycled, and offer unique features not found in traditional electronic materials in terms of size, performance, and opportunities for diverse functionalization. An appropriate investment in the concerted multidisciplinary collaborative research required to identify and characterize e-biologics and to engineer materials and devices based on e-biologics could be rewarded with a new “green age” of sustainable electronic materials and devices. PMID:28655820

  11. Microfluidic chambers using fluid walls for cell biology.

    PubMed

    Soitu, Cristian; Feuerborn, Alexander; Tan, Ann Na; Walker, Henry; Walsh, Pat A; Castrejón-Pita, Alfonso A; Cook, Peter R; Walsh, Edmond J

    2018-06-12

    Many proofs of concept have demonstrated the potential of microfluidics in cell biology. However, the technology remains inaccessible to many biologists, as it often requires complex manufacturing facilities (such as soft lithography) and uses materials foreign to cell biology (such as polydimethylsiloxane). Here, we present a method for creating microfluidic environments by simply reshaping fluids on a substrate. For applications in cell biology, we use cell media on a virgin Petri dish overlaid with an immiscible fluorocarbon. A hydrophobic/fluorophilic stylus then reshapes the media into any pattern by creating liquid walls of fluorocarbon. Microfluidic arrangements suitable for cell culture are made in minutes using materials familiar to biologists. The versatility of the method is demonstrated by creating analogs of a common platform in cell biology, the microtiter plate. Using this vehicle, we demonstrate many manipulations required for cell culture and downstream analysis, including feeding, replating, cloning, cryopreservation, lysis plus RT-PCR, transfection plus genome editing, and fixation plus immunolabeling (when fluid walls are reconfigured during use). We also show that mammalian cells grow and respond to stimuli normally, and worm eggs develop into adults. This simple approach provides biologists with an entrée into microfluidics. Copyright © 2018 the Author(s). Published by PNAS.

  12. The Time-Limited Hot Line.

    ERIC Educational Resources Information Center

    Loring, Marti Tamm; Wimberley, Edward T.

    1993-01-01

    Notes that media have become involved in creating programs and addressing issues that have been historically exclusive purview of mental health and human services agencies. Explains how time-limited hot line has been used to address specific issues raised by these programs. Provides overview of this type of hot line, offering triangular model of…

  13. [Establishment of fibroblast cell line and its biological characteristics in Matou goat].

    PubMed

    Li, Tianda; Liu, Chousheng; Wang, Zhigang; Zhang, Liping; Sun, Xiuzhu; Zhao, Junjin; Meng, Fei; Luo, Guihe; Zhu, Jinqing

    2008-12-01

    Taking Matou goat ear margin as the study material, we succeeded in established a fibroblast cell line by the method of explant culture directly. Observations on morphology, dynamic growth, determination of viability, analysis of karyotype, test of microorganism and other characteristics were detected. Results showed: Population Doubling Time (PDT) of cells was approximately 36 h; Cell viability was 96.7% after thawing; The status of cell After passage was constant; Analysis of chromosomal karyotyps indicated that diploid (2n=60) account for 98% in the cell line. Every index in the cell line met all the standard quality controls of ATCC in USA. The established of Matou goat ear fibroblast cell line has not only important genetic resources preserved at the cell level, but also valuable material for genome, postgenome and somatic cell nuclear transfer research.

  14. Generation of stable PDX derived cell lines using conditional reprogramming.

    PubMed

    Borodovsky, Alexandra; McQuiston, Travis J; Stetson, Daniel; Ahmed, Ambar; Whitston, David; Zhang, Jingwen; Grondine, Michael; Lawson, Deborah; Challberg, Sharon S; Zinda, Michael; Pollok, Brian A; Dougherty, Brian A; D'Cruz, Celina M

    2017-12-06

    Efforts to develop effective cancer therapeutics have been hindered by a lack of clinically predictive preclinical models which recapitulate this complex disease. Patient derived xenograft (PDX) models have emerged as valuable tools for translational research but have several practical limitations including lack of sustained growth in vitro. In this study, we utilized Conditional Reprogramming (CR) cell technology- a novel cell culture system facilitating the generation of stable cultures from patient biopsies- to establish PDX-derived cell lines which maintain the characteristics of the parental PDX tumor. Human lung and ovarian PDX tumors were successfully propagated using CR technology to create stable explant cell lines (CR-PDX). These CR-PDX cell lines maintained parental driver mutations and allele frequency without clonal drift. Purified CR-PDX cell lines were amenable to high throughput chemosensitivity screening and in vitro genetic knockdown studies. Additionally, re-implanted CR-PDX cells proliferated to form tumors that retained the growth kinetics, histology, and drug responses of the parental PDX tumor. CR technology can be used to generate and expand stable cell lines from PDX tumors without compromising fundamental biological properties of the model. It offers the ability to expand PDX cells in vitro for subsequent 2D screening assays as well as for use in vivo to reduce variability, animal usage and study costs. The methods and data detailed here provide a platform to generate physiologically relevant and predictive preclinical models to enhance drug discovery efforts.

  15. Creating Cross-disciplinary Courses.

    PubMed

    Reynolds, Elaine R

    2012-01-01

    Because of its focus on the biological underpinnings of action and behavior, neuroscience intersects with many fields of human endeavor. Some of these cross-disciplinary intersections have been long standing, while others, such as neurotheology or neuroeconomics, are more recently formed fields. Many undergraduate institutions have sought to include cross-disciplinary courses in their curriculum because this style of pedagogy is often seen as applicable to real world problems. However, it can be difficult for faculty with specialized training within their discipline to expand beyond their own fields to offer cross-disciplinary courses. I have been creating a series of multi- or cross-disciplinary courses and have found some strategies that have helped me successfully teach these classes. I will discuss general strategies and tools in developing these types of courses including: 1) creating mixed experience classrooms of students and contributing faculty 2) finding the right tools that will allow you to teach to a mixed population without prerequisites 3) examining the topic using multiple disciplinary perspectives 4) feeding off student experience and interest 5) assessing the impact of these courses on student outcomes and your neuroscience program. This last tool in particular is important in establishing the validity of this type of teaching for neuroscience students and the general student population.

  16. Creating Cross-disciplinary Courses

    PubMed Central

    Reynolds, Elaine R.

    2012-01-01

    Because of its focus on the biological underpinnings of action and behavior, neuroscience intersects with many fields of human endeavor. Some of these cross-disciplinary intersections have been long standing, while others, such as neurotheology or neuroeconomics, are more recently formed fields. Many undergraduate institutions have sought to include cross-disciplinary courses in their curriculum because this style of pedagogy is often seen as applicable to real world problems. However, it can be difficult for faculty with specialized training within their discipline to expand beyond their own fields to offer cross-disciplinary courses. I have been creating a series of multi- or cross-disciplinary courses and have found some strategies that have helped me successfully teach these classes. I will discuss general strategies and tools in developing these types of courses including: 1) creating mixed experience classrooms of students and contributing faculty 2) finding the right tools that will allow you to teach to a mixed population without prerequisites 3) examining the topic using multiple disciplinary perspectives 4) feeding off student experience and interest 5) assessing the impact of these courses on student outcomes and your neuroscience program. This last tool in particular is important in establishing the validity of this type of teaching for neuroscience students and the general student population. PMID:23494491

  17. Fabrication of a highly oriented line structure on an aluminum surface and the nanoscale patterning on the nanoscale structure using highly functional molecules

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Watanabe, Y.; Kato, H.; Takemura, S.

    2009-07-15

    The surface of an Al plate was treated with a combination of chemical and electrochemical processes for fabrication of surface nanoscale structures on Al plates. Chemical treatments by using acetone and pure water under supersonic waves were conducted on an Al surface. Additional electrochemical process in H{sub 2}SO{sub 4} solution created a finer and oriented nanoscale structure on the Al surface. Dynamic force microscopy (DFM) measurement clarified that the nanoscale highly oriented line structure was successfully created on the Al surface. The line distance was estimated approximately 30-40 nm. At the next stage, molecular patterning on the highly oriented linemore » structure by functional molecules such as copper phthalocyanine (CuPc) and fullerene C{sub 60} was also conducted. CuPc or C{sub 60} molecules were deposited on the highly oriented line structure on Al. A toluene droplet containing CuPc molecules was cast on the nanostructured Al plate and was extended on the surface. CuPc or C{sub 60} deposition on the nanostructured Al surface proceeded by evaporation of toluene. DFM and x-ray photoemission spectroscopy measurements demonstrated that a unique molecular pattern was fabricated so that the highly oriented groove channels were filled with the functional molecules.« less

  18. [Experimental analysis of finishing lines in ceramometal restorations].

    PubMed

    Gascón, F; Gil, J A; Fons, A; Badal, R

    1990-11-01

    The preparation is the first step of any tooth reconstruction. The biological integration of the protesis is depending on the marginal adaptation (finish line of the preparation), occlusal adaptation (occlusal reduction), longevity of the restoration (retention and luting) and esthetics. The effect the two finish line of the preparation is studied using experimental design. In porcelain-fused-to-metal the finish line of the preparation in chanfer is superior at the beveled shoulder, because proportioning better marginal adaptation.

  19. Synthetic Biology: Putting Synthesis into Biology

    PubMed Central

    Liang, Jing; Luo, Yunzi; Zhao, Huimin

    2010-01-01

    The ability to manipulate living organisms is at the heart of a range of emerging technologies that serve to address important and current problems in environment, energy, and health. However, with all its complexity and interconnectivity, biology has for many years been recalcitrant to engineering manipulations. The recent advances in synthesis, analysis, and modeling methods have finally provided the tools necessary to manipulate living systems in meaningful ways, and have led to the coining of a field named synthetic biology. The scope of synthetic biology is as complicated as life itself – encompassing many branches of science, and across many scales of application. New DNA synthesis and assembly techniques have made routine the customization of very large DNA molecules. This in turn has allowed the incorporation of multiple genes and pathways. By coupling these with techniques that allow for the modeling and design of protein functions, scientists have now gained the tools to create completely novel biological machineries. Even the ultimate biological machinery – a self-replicating organism – is being pursued at this moment. It is the purpose of this review to dissect and organize these various components of synthetic biology into a coherent picture. PMID:21064036

  20. Biological synthesis of silver nanoparticles using the fungus Humicola sp. and evaluation of their cytoxicity using normal and cancer cell lines.

    PubMed

    Syed, Asad; Saraswati, Supriya; Kundu, Gopal C; Ahmad, Absar

    2013-10-01

    Nanoscience is a new born science of the modern era and taps into the potential of particles at nanoscale. Bulk materials reduced to nanoscale dimensions thus obtain unique properties such as electronic, optical, magnetic and chemical. As far as synthesis of nanoparticles is concerned, biological synthesis has recently sparked a great interest as compared to other available chemical and physical methods on account of its eco-friendliness and cost-effectiveness. Here we report, for the first time, the biosynthesis of silver nanoparticles by the thermophilic fungus Humicola sp. The fungus when reacted with Ag(+) ions reduces the precursor solution and leads to the formation of extracellular nanoparticles as monitored by ultra violet visible spectroscopy (UV-Vis). The morphology of nanoparticles is found to be spherical with good dispersity as revealed by transmission electron microscopy (TEM). Cell viability assays were carried out to assess the cytotoxicity of silver nanoparticles on NIH3T3 mouse embryonic fibroblast cell line and MDA-MB-231 human breast carcinoma cell line. Copyright © 2013 Elsevier B.V. All rights reserved.

  1. The Biological Reference Repository (BioR): a rapid and flexible system for genomics annotation.

    PubMed

    Kocher, Jean-Pierre A; Quest, Daniel J; Duffy, Patrick; Meiners, Michael A; Moore, Raymond M; Rider, David; Hossain, Asif; Hart, Steven N; Dinu, Valentin

    2014-07-01

    The Biological Reference Repository (BioR) is a toolkit for annotating variants. BioR stores public and user-specific annotation sources in indexed JSON-encoded flat files (catalogs). The BioR toolkit provides the functionality to combine and retrieve annotation from these catalogs via the command-line interface. Several catalogs from commonly used annotation sources and instructions for creating user-specific catalogs are provided. Commands from the toolkit can be combined with other UNIX commands for advanced annotation processing. We also provide instructions for the development of custom annotation pipelines. The package is implemented in Java and makes use of external tools written in Java and Perl. The toolkit can be executed on Mac OS X 10.5 and above or any Linux distribution. The BioR application, quickstart, and user guide documents and many biological examples are available at http://bioinformaticstools.mayo.edu. © The Author 2014. Published by Oxford University Press.

  2. Skills Associated with Line Breaks in Elite Rugby Union

    PubMed Central

    den Hollander, Steve; Brown, James; Lambert, Michael; Treu, Paul; Hendricks, Sharief

    2016-01-01

    The ability of the attacking team to break through the defensive line is a key indicator of success as it creates opportunities to score tries. The aim of this study was to analyse line breaks and identify the associated skills and playing characteristics. The 2013 Super Rugby season (125 games) was analysed, in which 362 line breaks were identified and coded using variables that assessed team patterns and non-contact attacking skills in the phases preceding the line break. There was an average of 3 line breaks per game, with 39% of line breaks resulting in a try. Line breaks occurred when the ball-carrier was running fast [61%, x2(4) = 25.784, p = 0.000, Cramer’s v = 0.1922, weak]. At a moderate distance, short lateral passes (19%) and skip passes (15%) attributed to the highest percentage of line breaks [x2(26) = 50.899, p = 0.036, Cramer’s v = 0.2484, moderate]. Faster defensive line speeds resulted in more line breaks [x2(12) = 61.703, p < 0.001, Cramer’s v = 0.3026, moderate]. Line breaks are associated with overall team success and try scoring opportunities. Awareness of the defenders line speed and depth, fast running speed when receiving the ball and quick passing between attackers to the outside backs creates line break opportunities. During training, coaches should emphasise the movement speed of the ball between attackers and manipulate the speed and distance of the defenders. Key points Line breaks are associated with overall team success and try scoring opportunities. Awareness of the defenders line speed and depth, fast running speed when receiving the ball and quick passing between attackers to the outside backs creates line break opportunities During training, coaches should emphasise the movement speed of the ball between attackers and manipulate the speed and distance of the defenders. PMID:27803629

  3. Engineering a Biological Revolution.

    PubMed

    Matheson, Susan

    2017-01-26

    The new field of synthetic biology promises to change health care, computer technology, the production of biofuels, and more. Students participating in the International Genetically Engineered Machine (iGEM) competition are on the front lines of this revolution. Copyright © 2017 Elsevier Inc. All rights reserved.

  4. CellLineNavigator: a workbench for cancer cell line analysis

    PubMed Central

    Krupp, Markus; Itzel, Timo; Maass, Thorsten; Hildebrandt, Andreas; Galle, Peter R.; Teufel, Andreas

    2013-01-01

    The CellLineNavigator database, freely available at http://www.medicalgenomics.org/celllinenavigator, is a web-based workbench for large scale comparisons of a large collection of diverse cell lines. It aims to support experimental design in the fields of genomics, systems biology and translational biomedical research. Currently, this compendium holds genome wide expression profiles of 317 different cancer cell lines, categorized into 57 different pathological states and 28 individual tissues. To enlarge the scope of CellLineNavigator, the database was furthermore closely linked to commonly used bioinformatics databases and knowledge repositories. To ensure easy data access and search ability, a simple data and an intuitive querying interface were implemented. It allows the user to explore and filter gene expression, focusing on pathological or physiological conditions. For a more complex search, the advanced query interface may be used to query for (i) differentially expressed genes; (ii) pathological or physiological conditions; or (iii) gene names or functional attributes, such as Kyoto Encyclopaedia of Genes and Genomes pathway maps. These queries may also be combined. Finally, CellLineNavigator allows additional advanced analysis of differentially regulated genes by a direct link to the Database for Annotation, Visualization and Integrated Discovery (DAVID) Bioinformatics Resources. PMID:23118487

  5. Team-Teaching a Current Events-Based Biology Course for Nonmajors

    ERIC Educational Resources Information Center

    Bondos, Sarah E.; Phillips, Dereth

    2008-01-01

    Rice University has created a team-taught interactive biology course for nonmajors with a focus on cutting edge biology in the news--advances in biotechnology, medicine, and science policy, along with the biological principles and methodology upon which these advances are based. The challenges inherent to teaching current topics were minimized by…

  6. Creating to understand - developmental biology meets engineering in Paris.

    PubMed

    Kicheva, Anna; Rivron, Nicolas C

    2017-03-01

    In November 2016, developmental biologists, synthetic biologists and engineers gathered in Paris for a meeting called 'Engineering the embryo'. The participants shared an interest in exploring how synthetic systems can reveal new principles of embryonic development, and how the in vitro manipulation and modeling of development using stem cells can be used to integrate ideas and expertise from physics, developmental biology and tissue engineering. As we review here, the conference pinpointed some of the challenges arising at the intersection of these fields, along with great enthusiasm for finding new approaches and collaborations. © 2017. Published by The Company of Biologists Ltd.

  7. Can sterile and pyrogen-free on-line substitution fluid be routinely delivered? A multicentric study on the microbiological safety of on-line haemodiafiltration.

    PubMed

    Vaslaki, L; Karátson, A; Vörös, P; Major, L; Pethö, F; Ladányi, E; Weber, C; Mitteregger, R; Falkenhagen, D

    2000-01-01

    Microbial contamination is characterized not only by the presence of bacteria, but also by high concentrations of biologically active by-products. They are potentially able to cross ultrafiltration and dialysis membranes and stimulate immunocompetent blood cells to synthesize cytokines. In turn, cytokine induction causes acute symptoms and has been incriminated in the long-term complications of haemodialysis patients. Infusion of large volumes of substitution fluids following ultrafiltration of microbially contaminated dialysis fluids may place patients on on-line therapies at particular risk. In this study we evaluated 30 machines with a two-stage ultrafiltration system in routine clinical haemodiafiltration settings in six centres for 6 months. Microbiological safety was assessed monthly and at the last use of the filters by determining microbial counts, endotoxin concentration and cytokine-inducing activity. No pyrogenic episodes were observed during the study period. Double-filtration of standard dialysis fluid (range, <1-895 cfu/ml, 0.0028-4.6822 IU/ml) resulted in sterile substitution fluids with endotoxin concentrations well below the Ph.Eur. standard for haemofiltration solutions (range, 0.0014-0.0281 vs 0.25 IU/ml). Moreover, they did not differ from commercial haemofiltration solutions and depyrogenated saline. Likewise, there was no difference in the cytokine-inducing activity between the solutions tested. The high microbiological quality of the ultrafiltered dialysis fluid, which was in the same range as substitution fluid, translates into both the absence of cytokine induction by dialyser back-transport and a redundant safety mode of the on-line system by a second filtration step. On-line HDF treatment can routinely be provided with ultra-pure dialysis fluids and sterile substitution fluids at pyrogen-free levels. The online preparation of substitution fluids thus can be considered microbiologically safe.

  8. Adaptive filtering in biological signal processing.

    PubMed

    Iyer, V K; Ploysongsang, Y; Ramamoorthy, P A

    1990-01-01

    The high dependence of conventional optimal filtering methods on the a priori knowledge of the signal and noise statistics render them ineffective in dealing with signals whose statistics cannot be predetermined accurately. Adaptive filtering methods offer a better alternative, since the a priori knowledge of statistics is less critical, real time processing is possible, and the computations are less expensive for this approach. Adaptive filtering methods compute the filter coefficients "on-line", converging to the optimal values in the least-mean square (LMS) error sense. Adaptive filtering is therefore apt for dealing with the "unknown" statistics situation and has been applied extensively in areas like communication, speech, radar, sonar, seismology, and biological signal processing and analysis for channel equalization, interference and echo canceling, line enhancement, signal detection, system identification, spectral analysis, beamforming, modeling, control, etc. In this review article adaptive filtering in the context of biological signals is reviewed. An intuitive approach to the underlying theory of adaptive filters and its applicability are presented. Applications of the principles in biological signal processing are discussed in a manner that brings out the key ideas involved. Current and potential future directions in adaptive biological signal processing are also discussed.

  9. Synchronization as a biological, psychological and social mechanism to create common time: A theoretical frame and a single case study.

    PubMed

    Bao, Yan; Pöppel, Ernst; Wang, Lingyan; Lin, Xiaoxiong; Yang, Taoxi; Avram, Mihai; Blautzik, Janusch; Paolini, Marco; Silveira, Sarita; Vedder, Aline; Zaytseva, Yuliya; Zhou, Bin

    2015-12-01

    Synchronizing neural processes, mental activities, and social interactions is considered to be fundamental for the creation of temporal order on the personal and interpersonal level. Several different types of synchronization are distinguished, and for each of them examples are given: self-organized synchronizations on the neural level giving rise to pre-semantically defined time windows of some tens of milliseconds and of approximately 3 s; time windows that are created by synchronizing different neural representations, as for instance in aesthetic appreciations or moral judgments; and synchronization of biological rhythms with geophysical cycles, like the circadian clock with the 24-hr rhythm of day and night. For the latter type of synchronization, an experiment is described that shows the importance of social interactions for sharing or avoiding common time. In a group study with four subjects being completely isolated together for 3 weeks from the external world, social interactions resulted both in intra- and interindividual circadian synchronization and desynchronization. A unique phenomenon in circadian regulation is described, the "beat phenomenon," which has been made visible by the interaction of two circadian rhythms with different frequencies in one body. The separation of the two physiological rhythms was the consequence of social interactions, that is, by the desire of a subject to share and to escape common time during different phases of the long-term experiment. The theoretical arguments on synchronization are summarized with the general statement: "Nothing in cognitive science makes sense except in the light of time windows." The hypothesis is forwarded that time windows that express discrete timing mechanisms in behavioral control and on the level of conscious experiences are the necessary bases to create cognitive order, and it is suggested that time windows are implemented by neural oscillations in different frequency domains. © 2015 The

  10. Use of Internet Resources in the Biology Lecture Classroom.

    ERIC Educational Resources Information Center

    Francis, Joseph W.

    2000-01-01

    Introduces internet resources that are available for instructional use in biology classrooms. Provides information on video-based technologies to create and capture video sequences, interactive web sites that allow interaction with biology simulations, online texts, and interactive videos that display animated video sequences. (YDS)

  11. A historical discourse analysis of the cancerous and non-cancerous body in secondary biology textbooks

    NASA Astrophysics Data System (ADS)

    Bowers, Neil Thomas

    This dissertation applies the archeological concepts developed by Michel Foucault to a study of thirteen biology textbooks (1993-2004) in order to develop an understanding of 'purchased truths' concerning cancer. This study focuses on the construction of the health/illness dialogue concerning cancer within the textbooks and not the meaning that the individual makes from reading the text; as such this study concerns itself with social truths rather than the search for an individual awareness of names, dates, or places. This study investigates the practices that allow the creation of dialogues that are inserted into a biology textbook and looks at how discursive formations create the 'truth regime' from which the biology textbook is said to speak. Using the Foucaultian themes of 'event', 'emergence', 'enunciation', and 'exteriority' a new reading of topics concerning cancer emerge from biology textbooks. Cancer is a disease that will impact the lives of countless individuals but coverage devoted to the pathology of cancer in secondary biology textbooks is very limited and no study textbook devoted a whole chapter to the discussion of cancer. There is an identified reduction in the number of pages and depth of coverage devoted to cancer in the newer biology texts compared to the older texts. Humans are pictured more than plants or animals in presentations concerning cancer with emphasis being placed on the digitalization of human cells via the scanning electron microscope. When the whole body is presented it is seldom located within the technology of disease diagnosis and treatment but rather is posed for specific social control. Just as each digitized picture of the cancerous cell in the texts is used to create a story so too are the pictures of the whole body in action. Possible story lines offered by the publishing houses concerning the reaction of the body to cancer are shown to intermingle with risk factor analysis to project a sense of Foucaultian

  12. Quantitative biology of single neurons

    PubMed Central

    Eberwine, James; Lovatt, Ditte; Buckley, Peter; Dueck, Hannah; Francis, Chantal; Kim, Tae Kyung; Lee, Jaehee; Lee, Miler; Miyashiro, Kevin; Morris, Jacqueline; Peritz, Tiina; Schochet, Terri; Spaethling, Jennifer; Sul, Jai-Yoon; Kim, Junhyong

    2012-01-01

    The building blocks of complex biological systems are single cells. Fundamental insights gained from single-cell analysis promise to provide the framework for understanding normal biological systems development as well as the limits on systems/cellular ability to respond to disease. The interplay of cells to create functional systems is not well understood. Until recently, the study of single cells has concentrated primarily on morphological and physiological characterization. With the application of new highly sensitive molecular and genomic technologies, the quantitative biochemistry of single cells is now accessible. PMID:22915636

  13. Physical constraints on biological integral control design for homeostasis and sensory adaptation.

    PubMed

    Ang, Jordan; McMillen, David R

    2013-01-22

    Synthetic biology includes an effort to use design-based approaches to create novel controllers, biological systems aimed at regulating the output of other biological processes. The design of such controllers can be guided by results from control theory, including the strategy of integral feedback control, which is central to regulation, sensory adaptation, and long-term robustness. Realization of integral control in a synthetic network is an attractive prospect, but the nature of biochemical networks can make the implementation of even basic control structures challenging. Here we present a study of the general challenges and important constraints that will arise in efforts to engineer biological integral feedback controllers or to analyze existing natural systems. Constraints arise from the need to identify target output values that the combined process-plus-controller system can reach, and to ensure that the controller implements a good approximation of integral feedback control. These constraints depend on mild assumptions about the shape of input-output relationships in the biological components, and thus will apply to a variety of biochemical systems. We summarize our results as a set of variable constraints intended to provide guidance for the design or analysis of a working biological integral feedback controller. Copyright © 2013 Biophysical Society. Published by Elsevier Inc. All rights reserved.

  14. Skylign: a tool for creating informative, interactive logos representing sequence alignments and profile hidden Markov models

    PubMed Central

    2014-01-01

    Background Logos are commonly used in molecular biology to provide a compact graphical representation of the conservation pattern of a set of sequences. They render the information contained in sequence alignments or profile hidden Markov models by drawing a stack of letters for each position, where the height of the stack corresponds to the conservation at that position, and the height of each letter within a stack depends on the frequency of that letter at that position. Results We present a new tool and web server, called Skylign, which provides a unified framework for creating logos for both sequence alignments and profile hidden Markov models. In addition to static image files, Skylign creates a novel interactive logo plot for inclusion in web pages. These interactive logos enable scrolling, zooming, and inspection of underlying values. Skylign can avoid sampling bias in sequence alignments by down-weighting redundant sequences and by combining observed counts with informed priors. It also simplifies the representation of gap parameters, and can optionally scale letter heights based on alternate calculations of the conservation of a position. Conclusion Skylign is available as a website, a scriptable web service with a RESTful interface, and as a software package for download. Skylign’s interactive logos are easily incorporated into a web page with just a few lines of HTML markup. Skylign may be found at http://skylign.org. PMID:24410852

  15. Molecular Imaging in Synthetic Biology, and Synthetic Biology in Molecular Imaging.

    PubMed

    Gilad, Assaf A; Shapiro, Mikhail G

    2017-06-01

    Biomedical synthetic biology is an emerging field in which cells are engineered at the genetic level to carry out novel functions with relevance to biomedical and industrial applications. This approach promises new treatments, imaging tools, and diagnostics for diseases ranging from gastrointestinal inflammatory syndromes to cancer, diabetes, and neurodegeneration. As these cellular technologies undergo pre-clinical and clinical development, it is becoming essential to monitor their location and function in vivo, necessitating appropriate molecular imaging strategies, and therefore, we have created an interest group within the World Molecular Imaging Society focusing on synthetic biology and reporter gene technologies. Here, we highlight recent advances in biomedical synthetic biology, including bacterial therapy, immunotherapy, and regenerative medicine. We then discuss emerging molecular imaging approaches to facilitate in vivo applications, focusing on reporter genes for noninvasive modalities such as magnetic resonance, ultrasound, photoacoustic imaging, bioluminescence, and radionuclear imaging. Because reporter genes can be incorporated directly into engineered genetic circuits, they are particularly well suited to imaging synthetic biological constructs, and developing them provides opportunities for creative molecular and genetic engineering.

  16. [Fundamental biological model for trials of wound ballistics].

    PubMed

    Krajsa, J; Hirt, M

    2006-10-01

    The aim of our experiment was the testing of effects of common ammunition on usable and slightly accessible biological tissue thereby to create fundamental simple biological model for trials of wounded ballistic. Like objective tissue was elected biological material - pork and beef hind-limbs, pork head, pork bodily cavity. It was discovered that objective tissue is able to react to singles types of shots in all spectrum results namely simple smooth penetration wound as well as splintery fracture in dependence on kind of using ammunition. Pork hind-limb was evaluated like the most suitable biological material for given object.

  17. Integrating Multiple On-line Knowledge Bases for Disease-Lab Test Relation Extraction.

    PubMed

    Zhang, Yaoyun; Soysal, Ergin; Moon, Sungrim; Wang, Jingqi; Tao, Cui; Xu, Hua

    2015-01-01

    A computable knowledge base containing relations between diseases and lab tests would be a great resource for many biomedical informatics applications. This paper describes our initial step towards establishing a comprehensive knowledge base of disease and lab tests relations utilizing three public on-line resources. LabTestsOnline, MedlinePlus and Wikipedia are integrated to create a freely available, computable disease-lab test knowledgebase. Disease and lab test concepts are identified using MetaMap and relations between diseases and lab tests are determined based on source-specific rules. Experimental results demonstrate a high precision for relation extraction, with Wikipedia achieving the highest precision of 87%. Combining the three sources reached a recall of 51.40%, when compared with a subset of disease-lab test relations extracted from a reference book. Moreover, we found additional disease-lab test relations from on-line resources, indicating they are complementary to existing reference books for building a comprehensive disease and lab test relation knowledge base.

  18. Integrating interactive computational modeling in biology curricula.

    PubMed

    Helikar, Tomáš; Cutucache, Christine E; Dahlquist, Lauren M; Herek, Tyler A; Larson, Joshua J; Rogers, Jim A

    2015-03-01

    While the use of computer tools to simulate complex processes such as computer circuits is normal practice in fields like engineering, the majority of life sciences/biological sciences courses continue to rely on the traditional textbook and memorization approach. To address this issue, we explored the use of the Cell Collective platform as a novel, interactive, and evolving pedagogical tool to foster student engagement, creativity, and higher-level thinking. Cell Collective is a Web-based platform used to create and simulate dynamical models of various biological processes. Students can create models of cells, diseases, or pathways themselves or explore existing models. This technology was implemented in both undergraduate and graduate courses as a pilot study to determine the feasibility of such software at the university level. First, a new (In Silico Biology) class was developed to enable students to learn biology by "building and breaking it" via computer models and their simulations. This class and technology also provide a non-intimidating way to incorporate mathematical and computational concepts into a class with students who have a limited mathematical background. Second, we used the technology to mediate the use of simulations and modeling modules as a learning tool for traditional biological concepts, such as T cell differentiation or cell cycle regulation, in existing biology courses. Results of this pilot application suggest that there is promise in the use of computational modeling and software tools such as Cell Collective to provide new teaching methods in biology and contribute to the implementation of the "Vision and Change" call to action in undergraduate biology education by providing a hands-on approach to biology.

  19. Creating a pipeline of talent for informatics: STEM initiative for high school students in computer science, biology, and biomedical informatics

    PubMed Central

    Dutta-Moscato, Joyeeta; Gopalakrishnan, Vanathi; Lotze, Michael T.; Becich, Michael J.

    2014-01-01

    This editorial provides insights into how informatics can attract highly trained students by involving them in science, technology, engineering, and math (STEM) training at the high school level and continuing to provide mentorship and research opportunities through the formative years of their education. Our central premise is that the trajectory necessary to be expert in the emergent fields in front of them requires acceleration at an early time point. Both pathology (and biomedical) informatics are new disciplines which would benefit from involvement by students at an early stage of their education. In 2009, Michael T Lotze MD, Kirsten Livesey (then a medical student, now a medical resident at University of Pittsburgh Medical Center (UPMC)), Richard Hersheberger, PhD (Currently, Dean at Roswell Park), and Megan Seippel, MS (the administrator) launched the University of Pittsburgh Cancer Institute (UPCI) Summer Academy to bring high school students for an 8 week summer academy focused on Cancer Biology. Initially, pathology and biomedical informatics were involved only in the classroom component of the UPCI Summer Academy. In 2011, due to popular interest, an informatics track called Computer Science, Biology and Biomedical Informatics (CoSBBI) was launched. CoSBBI currently acts as a feeder program for the undergraduate degree program in bioinformatics at the University of Pittsburgh, which is a joint degree offered by the Departments of Biology and Computer Science. We believe training in bioinformatics is the best foundation for students interested in future careers in pathology informatics or biomedical informatics. We describe our approach to the recruitment, training and research mentoring of high school students to create a pipeline of exceptionally well-trained applicants for both the disciplines of pathology informatics and biomedical informatics. We emphasize here how mentoring of high school students in pathology informatics and biomedical informatics

  20. Creating a pipeline of talent for informatics: STEM initiative for high school students in computer science, biology, and biomedical informatics.

    PubMed

    Dutta-Moscato, Joyeeta; Gopalakrishnan, Vanathi; Lotze, Michael T; Becich, Michael J

    2014-01-01

    This editorial provides insights into how informatics can attract highly trained students by involving them in science, technology, engineering, and math (STEM) training at the high school level and continuing to provide mentorship and research opportunities through the formative years of their education. Our central premise is that the trajectory necessary to be expert in the emergent fields in front of them requires acceleration at an early time point. Both pathology (and biomedical) informatics are new disciplines which would benefit from involvement by students at an early stage of their education. In 2009, Michael T Lotze MD, Kirsten Livesey (then a medical student, now a medical resident at University of Pittsburgh Medical Center (UPMC)), Richard Hersheberger, PhD (Currently, Dean at Roswell Park), and Megan Seippel, MS (the administrator) launched the University of Pittsburgh Cancer Institute (UPCI) Summer Academy to bring high school students for an 8 week summer academy focused on Cancer Biology. Initially, pathology and biomedical informatics were involved only in the classroom component of the UPCI Summer Academy. In 2011, due to popular interest, an informatics track called Computer Science, Biology and Biomedical Informatics (CoSBBI) was launched. CoSBBI currently acts as a feeder program for the undergraduate degree program in bioinformatics at the University of Pittsburgh, which is a joint degree offered by the Departments of Biology and Computer Science. We believe training in bioinformatics is the best foundation for students interested in future careers in pathology informatics or biomedical informatics. We describe our approach to the recruitment, training and research mentoring of high school students to create a pipeline of exceptionally well-trained applicants for both the disciplines of pathology informatics and biomedical informatics. We emphasize here how mentoring of high school students in pathology informatics and biomedical informatics

  1. Frontiers of optofluidics in synthetic biology.

    PubMed

    Tan, Cheemeng; Lo, Shih-Jie; LeDuc, Philip R; Cheng, Chao-Min

    2012-10-07

    The development of optofluidic-based technology has ushered in a new era of lab-on-a-chip functionality, including miniaturization of biomedical devices, enhanced sensitivity for molecular detection, and multiplexing of optical measurements. While having great potential, optofluidic devices have only begun to be exploited in many biotechnological applications. Here, we highlight the potential of integrating optofluidic devices with synthetic biological systems, which is a field focusing on creating novel cellular systems by engineering synthetic gene and protein networks. First, we review the development of synthetic biology at different length scales, ranging from single-molecule, single-cell, to cellular population. We emphasize light-sensitive synthetic biological systems that would be relevant for the integration with optofluidic devices. Next, we propose several areas for potential applications of optofluidics in synthetic biology. The integration of optofluidics and synthetic biology would have a broad impact on point-of-care diagnostics and biotechnology.

  2. Four Novel Splice-Switch Reporter Cell Lines: Distinct Impact of Oligonucleotide Chemistry and Delivery Vector on Biological Activity.

    PubMed

    Rocha, Cristina S J; Lundin, Karin E; Behlke, Mark A; Zain, Rula; El Andaloussi, Samir; Smith, C I Edvard

    2016-12-01

    New advances in oligonucleotide (ON) chemistry emerge continuously, and over the last few years, several aspects of ON delivery have been improved. However, clear knowledge regarding how certain chemistries behave alone, or in combination with various delivery vectors, is limited. Moreover, characterization is frequently limited to a single reporter cell line and, when different cell types are studied, experiments are commonly not carried out under similar conditions, hampering comparative analysis. To address this, we have developed a small "tissue" library of new, stable, pLuc/705 splice-switching reporter cell lines (named HuH7_705, U-2 OS_705, C2C12_705, and Neuro-2a_705). Our data show that, indeed, the cell type used in activity screenings influences the efficiency of ONs of different chemistry (phosphorothioate with locked nucleic acid or 2'-O-methyl with or without N,N-diethyl-4-(4-nitronaphthalen-1-ylazo)-phenylamine). Likewise, the delivery method, Lipofectamine ® 2000, PepFect14 nanoparticles, or "naked" uptake, also demonstrates cell-type-dependent outcomes. Taken together, these cell lines can potentially become useful tools for future in vitro evaluation of new nucleic acid-based oligomers as well as delivery compounds for splice-switching approaches and cell-specific therapies.

  3. Regional seismic lines reprocessed using post-stack processing techniques; National Petroleum Reserve, Alaska

    USGS Publications Warehouse

    Miller, John J.; Agena, W.F.; Lee, M.W.; Zihlman, F.N.; Grow, J.A.; Taylor, D.J.; Killgore, Michele; Oliver, H.L.

    2000-01-01

    This CD-ROM contains stacked, migrated, 2-Dimensional seismic reflection data and associated support information for 22 regional seismic lines (3,470 line-miles) recorded in the National Petroleum Reserve ? Alaska (NPRA) from 1974 through 1981. Together, these lines constitute about one-quarter of the seismic data collected as part of the Federal Government?s program to evaluate the petroleum potential of the Reserve. The regional lines, which form a grid covering the entire NPRA, were created by combining various individual lines recorded in different years using different recording parameters. These data were reprocessed by the USGS using modern, post-stack processing techniques, to create a data set suitable for interpretation on interactive seismic interpretation computer workstations. Reprocessing was done in support of ongoing petroleum resource studies by the USGS Energy Program. The CD-ROM contains the following files: 1) 22 files containing the digital seismic data in standard, SEG-Y format; 2) 1 file containing navigation data for the 22 lines in standard SEG-P1 format; 3) 22 small scale graphic images of each seismic line in Adobe Acrobat? PDF format; 4) a graphic image of the location map, generated from the navigation file, with hyperlinks to the graphic images of the seismic lines; 5) an ASCII text file with cross-reference information for relating the sequential trace numbers on each regional line to the line number and shotpoint number of the original component lines; and 6) an explanation of the processing used to create the final seismic sections (this document). The SEG-Y format seismic files and SEG-P1 format navigation file contain all the information necessary for loading the data onto a seismic interpretation workstation.

  4. Leukemia-lymphoma cell lines as model systems for hematopoietic research.

    PubMed

    Drexler, Hans G; MacLeod, Roderick A F

    2003-01-01

    Continuous human leukemia-lymphoma (LL) cell lines comprise a rich self-renewing resource of accessible and manipulable living cells which has illuminated the pathophysiology of hematopoietic tumors as well as basic cell biology. The major key advantages of continuous cell lines are the unlimited supply and worldwide availability of identical cell material and their cryopreservation. LL cell lines are characterized generally by monoclonal origin and differentiation arrest, sustained proliferation in vitro with preservation of most cellular features, and specific genetic alterations. The most practical classification of LL cell lines assigns them to one of the physiologically occurring cell lineages, based on their immunophenotype, genotype and functional features. Truly malignant cell lines may be distinguished from Epstein-Barr virus (EBV)-immortalized normal cells, using various operational and conceptual parameters. The characterization and publication of new LL cell lines provides important and informative core data which, by opening new avenues for investigation, have become ubiquitous powerful research tools that are available to every investigator by reference cell repositories. There is a need in the scientific community for clean and authenticated LL cell lines to which every scientist has access as offered by these institutionalized public cell line banks. A list of the most useful, robust and freely available reference cell lines is proposed in this review. Clearly, studies of LL cell lines have provided seminal insights into the biology of hematopoietic neoplasia.

  5. Development and Evaluation of an On-Line Educational Module for Volunteer Leaders on Bio-Security in Washington State 4-H Livestock Projects

    ERIC Educational Resources Information Center

    Stevenson, Jill L.; Moore, Dale A.; Newman, Jerry; Schmidt, Janet L.; Smith, Sarah M.; Smith, Jean; Kerr, Susan; Wallace, Michael; BoyEs, Pat

    2011-01-01

    An on-line module on disease prevention was created for 4-H volunteer leaders who work with livestock projects in Washington to better prepare them to teach youth about bio-security and its importance in 4-H livestock projects. Evaluation of the module and usage statistics since the module's debut were collected and evaluated. The module increases…

  6. Beyond the Biology: A Systematic Investigation of Noncontent Instructor Talk in an Introductory Biology Course.

    PubMed

    Seidel, Shannon B; Reggi, Amanda L; Schinske, Jeffrey N; Burrus, Laura W; Tanner, Kimberly D

    2015-01-01

    Instructors create classroom environments that have the potential to impact learning by affecting student motivation, resistance, and self-efficacy. However, despite the critical importance of the learning environment in increasing conceptual understanding, little research has investigated what instructors say and do to create learning environments in college biology classrooms. We systematically investigated the language used by instructors that does not directly relate to course content and defined the construct of Instructor Talk. Transcripts were generated from a semester-long, cotaught introductory biology course (n = 270 students). Transcripts were analyzed using a grounded theory approach to identify emergent categories of Instructor Talk. The five emergent categories from analysis of more than 600 quotes were, in order of prevalence, 1) Building the Instructor/Student Relationship, 2) Establishing Classroom Culture, 3) Explaining Pedagogical Choices, 4) Sharing Personal Experiences, and 5) Unmasking Science. Instances of Instructor Talk were present in every class session analyzed and ranged from six to 68 quotes per session. The Instructor Talk framework is a novel research variable that could yield insights into instructor effectiveness, origins of student resistance, and methods for overcoming stereotype threat. Additionally, it holds promise in professional development settings to assist instructors in reflecting on the learning environments they create. © 2015 S. B. Seidel et al. CBE—Life Sciences Education © 2015 The American Society for Cell Biology. This article is distributed by The American Society for Cell Biology under license from the author(s). It is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

  7. Emerging biomedical applications of synthetic biology.

    PubMed

    Weber, Wilfried; Fussenegger, Martin

    2011-11-29

    Synthetic biology aims to create functional devices, systems and organisms with novel and useful functions on the basis of catalogued and standardized biological building blocks. Although they were initially constructed to elucidate the dynamics of simple processes, designed devices now contribute to the understanding of disease mechanisms, provide novel diagnostic tools, enable economic production of therapeutics and allow the design of novel strategies for the treatment of cancer, immune diseases and metabolic disorders, such as diabetes and gout, as well as a range of infectious diseases. In this Review, we cover the impact and potential of synthetic biology for biomedical applications.

  8. Biological Effects of Nonionizing Electromagnetic Radiation. Volume IV. Number 3.

    DTIC Science & Technology

    1980-03-01

    lines that produce EMR. perimental evidence on human health effects due to electromagnetic field exposures from high-voltage transmission lines is...1311, Mrch YOW that a permissible occupational exposure level to The biologic effects of electromagnetic fields on MW and RF radiation of 500 PW/cm 2...along with the principal physical param- eters of exposure . 6402 REGULATING POSSIBLE HEALTH EFFECTS FROM AC TRANSMISSION LINE ELECTROMAGNETIC FIELDS

  9. Creating new growth platforms.

    PubMed

    Laurie, Donald L; Doz, Yves L; Sheer, Claude P

    2006-05-01

    Sooner or later, most companies can't attain the growth rates expected by their boards and CEOs and demanded by investors. To some extent, such businesses are victims of their own successes. Many were able to sustain high growth rates for a long time because they were in high-growth industries. But once those industries slowed down, the businesses could no longer deliver the performance that investors had come to take for granted. Often, companies have resorted to acquisition, though this strategy has a discouraging track record. Over time, 65% of acquisitions destroy more value than they create. So where does real growth come from? For the past 12 years, the authors have been researching and advising companies on this issue. With the support of researchers at Harvard Business School and Insead, they instituted a project titled "The CEO Agenda and Growth". They identified and approached 24 companies that had achieved significant organic growth and interviewed their CEOs, chief strategists, heads of R&D, CFOs, and top-line managers. They asked, "Where does your growth come from?" and found a consistent pattern in the answers. All the businesses grew by creating new growth platforms (NGPs) on which they could build families of products and services and extend their capabilities into multiple new domains. Identifying NGP opportunities calls for executives to challenge conventional wisdom. In all the companies studied, top management believed that NGP innovation differed significantly from traditional product or service innovation. They had independent, senior-level units with a standing responsibility to create NGPs, and their CEOs spent as much as 50% of their time working with these units. The payoff has been spectacular and lasting. For example, from 1985 to 2004, the medical devices company Medtronic grew revenues at 18% per year, earnings at 20%, and market capitalization at 30%.

  10. Designing health care risk management on-line:meeting regulators' concerns for fixed-hour curriculum.

    PubMed

    Hyer, Kathryn; Taylor, Heidi H; Nanni, Kennith

    2004-01-01

    This paper describes the experience of creating a continuing professional education on-line risk management program that is designed to meet Florida's educational requirements for licensure as a risk manager in health-care settings and details the challenges faced when the in-class didactic program of 15 eight-hour sessions is reformatted as an on-line program. Structuring instructor/learner interactivity remains a challenge, especially if the program allows learner control and is a key feature in marketing the program. The article presents the dilemmas for state regulators as they work to determine if the on-line program meets legislative intent and statutory requirements because the learning platform does not have a clock function that accumulates time for each learner. While some details reflect the uniqueness of the 120-hour educational requirements for risk managers in Florida, the experience of the authors provides insight into the development of continuing professional education distance learning programs that are multidisciplinary and move primarily from a time-based format into a curriculum that uses time as only one dimension of the evaluation of learning.

  11. Selecting islands and shoals for conservation based on biological and aesthetic criteria

    USGS Publications Warehouse

    Knutson, M.G.; Leopold, D.J.; Smardon, R.C.

    1993-01-01

    Consideration of biological quality has long been an important component of rating areas for conservation. Often these same areas are highly valued by people for aesthetic reasons, creating demands for housing and recreation that may conflict with protection plans for these habitats. Most methods of selecting land for conservation purposes use biological factors alone. For some land areas, analysis of aesthetic qualities is also important in describing the scenic value of undisturbed land. A method for prioritizing small islands and shoals based on both biological and visual quality factors is presented here. The study included 169 undeveloped islands and shoals a??0.8 ha in the Thousand Islands Region of the St. Lawrence River, New York. Criteria such as critical habitat for uncommon plant and animal species were considered together with visual quality and incorporated into a rating system that ranked the islands and shoals according to their priority for conservation management and protection from development. Biological factors were determined based on previous research and a field survey. Visual quality was determined by visual diagnostic criteria developed from public responses to photographs of a sample of islands. Variables such as elevation, soil depth, and type of plant community can be used to classify islands into different categories of visual quality but are unsuccessful in classifying islands into categories of overall biological quality.

  12. Integration of Bioinformatics into an Undergraduate Biology Curriculum and the Impact on Development of Mathematical Skills

    ERIC Educational Resources Information Center

    Wightman, Bruce; Hark, Amy T.

    2012-01-01

    The development of fields such as bioinformatics and genomics has created new challenges and opportunities for undergraduate biology curricula. Students preparing for careers in science, technology, and medicine need more intensive study of bioinformatics and more sophisticated training in the mathematics on which this field is based. In this…

  13. Using Computer Technology to Create a Revolutionary New Style of Biology.

    ERIC Educational Resources Information Center

    Monaghan, Peter

    1993-01-01

    A $13-million gift of William Gates III to the University of Washington has enabled establishment of the country's first department in molecular biotechnology, a combination of medicine and molecular biology to be practiced by researchers versed in a variety of fields, including computer science, computation, applied physics, and engineering. (MSE)

  14. A Bayesian-Based System to Assess Wave-Driven Flooding Hazards on Coral Reef-Lined Coasts

    NASA Astrophysics Data System (ADS)

    Pearson, S. G.; Storlazzi, C. D.; van Dongeren, A. R.; Tissier, M. F. S.; Reniers, A. J. H. M.

    2017-12-01

    Many low-elevation, coral reef-lined, tropical coasts are vulnerable to the effects of climate change, sea level rise, and wave-induced flooding. The considerable morphological diversity of these coasts and the variability of the hydrodynamic forcing that they are exposed to make predicting wave-induced flooding a challenge. A process-based wave-resolving hydrodynamic model (XBeach Non-Hydrostatic, "XBNH") was used to create a large synthetic database for use in a "Bayesian Estimator for Wave Attack in Reef Environments" (BEWARE), relating incident hydrodynamics and coral reef geomorphology to coastal flooding hazards on reef-lined coasts. Building on previous work, BEWARE improves system understanding of reef hydrodynamics by examining the intrinsic reef and extrinsic forcing factors controlling runup and flooding on reef-lined coasts. The Bayesian estimator has high predictive skill for the XBNH model outputs that are flooding indicators, and was validated for a number of available field cases. It was found that, in order to accurately predict flooding hazards, water depth over the reef flat, incident wave conditions, and reef flat width are the most essential factors, whereas other factors such as beach slope and bed friction due to the presence or absence of corals are less important. BEWARE is a potentially powerful tool for use in early warning systems or risk assessment studies, and can be used to make projections about how wave-induced flooding on coral reef-lined coasts may change due to climate change.Plain Language SummaryLow-lying tropical coasts fronted by coral reefs are threatened by the effects of climate change, sea level rise, and flooding caused by waves. However, the reefs <span class="hlt">on</span> these coasts differ widely in their shape, size, and physical characteristics; the wave and water level conditions affecting these coastlines also vary in space and time. These factors make it difficult to predict flooding caused</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4960624','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4960624"><span>Subwavelength grating enabled <span class="hlt">on</span>-chip ultra-compact optical true time delay <span class="hlt">line</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Wang, Junjia; Ashrafi, Reza; Adams, Rhys; Glesk, Ivan; Gasulla, Ivana; Capmany, José; Chen, Lawrence R.</p> <p>2016-01-01</p> <p>An optical true time delay <span class="hlt">line</span> (OTTDL) is a basic photonic building block that enables many microwave photonic and optical processing operations. The conventional design for an integrated OTTDL that is based <span class="hlt">on</span> spatial diversity uses a length-variable waveguide array to <span class="hlt">create</span> the optical time delays, which can introduce complexities in the integrated circuit design. Here we report the first ever demonstration of an integrated index-variable OTTDL that exploits spatial diversity in an equal length waveguide array. The approach uses subwavelength grating waveguides in silicon-<span class="hlt">on</span>-insulator (SOI), which enables the realization of OTTDLs having a simple geometry and that occupy a compact chip area. Moreover, compared to conventional wavelength-variable delay <span class="hlt">lines</span> with a few THz operation bandwidth, our index-variable OTTDL has an extremely broad operation bandwidth practically exceeding several tens of THz, which supports operation for various input optical signals with broad ranges of central wavelength and bandwidth. PMID:27457024</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27457024','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27457024"><span>Subwavelength grating enabled <span class="hlt">on</span>-chip ultra-compact optical true time delay <span class="hlt">line</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Junjia; Ashrafi, Reza; Adams, Rhys; Glesk, Ivan; Gasulla, Ivana; Capmany, José; Chen, Lawrence R</p> <p>2016-07-26</p> <p>An optical true time delay <span class="hlt">line</span> (OTTDL) is a basic photonic building block that enables many microwave photonic and optical processing operations. The conventional design for an integrated OTTDL that is based <span class="hlt">on</span> spatial diversity uses a length-variable waveguide array to <span class="hlt">create</span> the optical time delays, which can introduce complexities in the integrated circuit design. Here we report the first ever demonstration of an integrated index-variable OTTDL that exploits spatial diversity in an equal length waveguide array. The approach uses subwavelength grating waveguides in silicon-<span class="hlt">on</span>-insulator (SOI), which enables the realization of OTTDLs having a simple geometry and that occupy a compact chip area. Moreover, compared to conventional wavelength-variable delay <span class="hlt">lines</span> with a few THz operation bandwidth, our index-variable OTTDL has an extremely broad operation bandwidth practically exceeding several tens of THz, which supports operation for various input optical signals with broad ranges of central wavelength and bandwidth.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28602761','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28602761"><span>Joining Forces: The Chemical <span class="hlt">Biology</span>-Medicinal Chemistry Continuum.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Plowright, Alleyn T; Ottmann, Christian; Arkin, Michelle; Auberson, Yves P; Timmerman, Henk; Waldmann, Herbert</p> <p>2017-09-21</p> <p>The scientific advances being made across all disciplines are <span class="hlt">creating</span> ever-increasing opportunities to enhance our knowledge of <span class="hlt">biological</span> systems and how they relate to human disease. One of the central driving forces in discovering new medicines is medicinal chemistry, where the design and synthesis of novel compounds has led to multiple drugs. Chemical <span class="hlt">biology</span>, sitting at the interface of many disciplines, has now emerged as a major contributor to the understanding of <span class="hlt">biological</span> systems and is becoming an integral part of drug discovery. Bringing chemistry and <span class="hlt">biology</span> much closer and blurring the boundaries between disciplines is <span class="hlt">creating</span> new opportunities to probe and understand <span class="hlt">biology</span>; both disciplines play key roles and need to join forces and work together effectively to synergize their impact. The power of chemical <span class="hlt">biology</span> will then reach its full potential and drive innovation, leading to the discovery of transformative medicines to treat patients. Advances in cancer <span class="hlt">biology</span> and drug discovery highlight this potential. Copyright © 2017 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4900751','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4900751"><span>WISB: Warwick Integrative Synthetic <span class="hlt">Biology</span> Centre</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>McCarthy, John</p> <p>2016-01-01</p> <p>Synthetic <span class="hlt">biology</span> promises to <span class="hlt">create</span> high-impact solutions to challenges in the areas of biotechnology, human/animal health, the environment, energy, materials and food security. Equally, synthetic biologists <span class="hlt">create</span> tools and strategies that have the potential to help us answer important fundamental questions in <span class="hlt">biology</span>. Warwick Integrative Synthetic <span class="hlt">Biology</span> (WISB) pursues both of these mutually complementary ‘build to apply’ and ‘build to understand’ approaches. This is reflected in our research structure, in which a core theme <span class="hlt">on</span> predictive biosystems engineering develops underpinning understanding as well as next-generation experimental/theoretical tools, and these are then incorporated into three applied themes in which we engineer biosynthetic pathways, microbial communities and microbial effector systems in plants. WISB takes a comprehensive approach to training, education and outreach. For example, WISB is a partner in the EPSRC/BBSRC-funded U.K. Doctoral Training Centre in synthetic <span class="hlt">biology</span>, we have developed a new undergraduate module in the subject, and we have established five WISB Research Career Development Fellowships to support young group leaders. Research in Ethical, Legal and Societal Aspects (ELSA) of synthetic <span class="hlt">biology</span> is embedded in our centre activities. WISB has been highly proactive in building an international research and training network that includes partners in Barcelona, Boston, Copenhagen, Madrid, Marburg, São Paulo, Tartu and Valencia. PMID:27284024</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27284024','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27284024"><span>WISB: Warwick Integrative Synthetic <span class="hlt">Biology</span> Centre.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>McCarthy, John</p> <p>2016-06-15</p> <p>Synthetic <span class="hlt">biology</span> promises to <span class="hlt">create</span> high-impact solutions to challenges in the areas of biotechnology, human/animal health, the environment, energy, materials and food security. Equally, synthetic biologists <span class="hlt">create</span> tools and strategies that have the potential to help us answer important fundamental questions in <span class="hlt">biology</span>. Warwick Integrative Synthetic <span class="hlt">Biology</span> (WISB) pursues both of these mutually complementary 'build to apply' and 'build to understand' approaches. This is reflected in our research structure, in which a core theme <span class="hlt">on</span> predictive biosystems engineering develops underpinning understanding as well as next-generation experimental/theoretical tools, and these are then incorporated into three applied themes in which we engineer biosynthetic pathways, microbial communities and microbial effector systems in plants. WISB takes a comprehensive approach to training, education and outreach. For example, WISB is a partner in the EPSRC/BBSRC-funded U.K. Doctoral Training Centre in synthetic <span class="hlt">biology</span>, we have developed a new undergraduate module in the subject, and we have established five WISB Research Career Development Fellowships to support young group leaders. Research in Ethical, Legal and Societal Aspects (ELSA) of synthetic <span class="hlt">biology</span> is embedded in our centre activities. WISB has been highly proactive in building an international research and training network that includes partners in Barcelona, Boston, Copenhagen, Madrid, Marburg, São Paulo, Tartu and Valencia. © 2016 The Author(s).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AcSpe..64..549D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AcSpe..64..549D"><span>Determination of Se in <span class="hlt">biological</span> samples by axial view inductively coupled plasma optical emission spectrometry after digestion with aqua regia and <span class="hlt">on-line</span> chemical vapor generation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>dos Santos, Éder José; Herrmann, Amanda Beatriz; de Caires, Suzete Kulik; Frescura, Vera Lúcia Azzolin; Curtius, Adilson José</p> <p>2009-06-01</p> <p>A simple and fast method for the determination of Se in <span class="hlt">biological</span> samples, including food, by axial view inductively coupled plasma optical emission spectrometry using <span class="hlt">on-line</span> chemical vapor generation (CVG-ICP OES) is proposed. The concentrations of HCl and NaBH 4, used in the chemical vapor generation were optimized by factorial analysis. Six certified materials (non-fat milk powder, lobster hepatopancreas, human hair, whole egg powder, oyster tissue, and lyophilised pig kidney) were treated with 10 mL of aqua regia in a microwave system under reflux for 15 min followed by additional 15 min in an ultrasonic bath. The solutions were transferred to a 100 mL volumetric flask and the final volume was made up with water. The Se was determined directly in these solutions by CVG-ICP OES, using the analytical <span class="hlt">line</span> at 196.026 nm. Calibration against aqueous standards in 10% v/v aqua regia in the concentration range of 0.5-10.0 µg L - 1 Se(IV) was used for the analysis. The quantification limit, considering a 0.5 g sample weight in a final volume of 100 mL - 1 was 0.10 µg g - 1. The obtained concentration values were in agreement with the total certified concentrations, according to the t-test for a 95% confidence level.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_10 --> <div id="page_11" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="201"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5070806','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5070806"><span><span class="hlt">LINE</span>-1 Cultured Cell Retrotransposition Assay</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Kopera, Huira C.; Larson, Peter A.; Moldovan, John B.; Richardson, Sandra R.; Liu, Ying; Moran, John V.</p> <p>2016-01-01</p> <p>Summary The Long INterspersed Element-1 (<span class="hlt">LINE</span>-1 or L1) retrotransposition assay has facilitated the discovery and characterization of active (i.e., retrotransposition-competent) <span class="hlt">LINE</span>-1 sequences from mammalian genomes. In this assay, an engineered <span class="hlt">LINE</span>-1 containing a retrotransposition reporter cassette is transiently transfected into a cultured cell <span class="hlt">line</span>. Expression of the reporter cassette, which occurs only after a successful round of retrotransposition, allows the detection and quantification of the <span class="hlt">LINE</span>-1 retrotransposition efficiency. This assay has yielded insight into the mechanism of <span class="hlt">LINE</span>-1 retrotransposition. It also has provided a greater understanding of how the cell regulates <span class="hlt">LINE</span>-1 retrotransposition and how <span class="hlt">LINE</span>-1 retrotransposition impacts the structure of mammalian genomes. Below, we provide a brief introduction to <span class="hlt">LINE</span>-1 <span class="hlt">biology</span> and then detail how the <span class="hlt">LINE</span>-1 retrotransposition assay is performed in cultured mammalian cells. PMID:26895052</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5589433','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5589433"><span>Reflecting <span class="hlt">on</span> Graphs: Attributes of Graph Choice and Construction Practices in <span class="hlt">Biology</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Angra, Aakanksha; Gardner, Stephanie M.</p> <p>2017-01-01</p> <p>Undergraduate <span class="hlt">biology</span> education reform aims to engage students in scientific practices such as experimental design, experimentation, and data analysis and communication. Graphs are ubiquitous in the <span class="hlt">biological</span> sciences, and <span class="hlt">creating</span> effective graphical representations involves quantitative and disciplinary concepts and skills. Past studies document student difficulties with graphing within the contexts of classroom or national assessments without evaluating student reasoning. Operating under the metarepresentational competence framework, we conducted think-aloud interviews to reveal differences in reasoning and graph quality between undergraduate <span class="hlt">biology</span> students, graduate students, and professors in a pen-and-paper graphing task. All professors planned and thought about data before graph construction. When reflecting <span class="hlt">on</span> their graphs, professors and graduate students focused <span class="hlt">on</span> the function of graphs and experimental design, while most undergraduate students relied <span class="hlt">on</span> intuition and data provided in the task. Most undergraduate students meticulously plotted all data with scaled axes, while professors and some graduate students transformed the data, aligned the graph with the research question, and reflected <span class="hlt">on</span> statistics and sample size. Differences in reasoning and approaches taken in graph choice and construction corroborate and extend previous findings and provide rich targets for undergraduate and graduate instruction. PMID:28821538</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/909148','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/909148"><span>Sixth International Conference <span class="hlt">on</span> Systems <span class="hlt">Biology</span> (ICSB 2005)</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Professor Andrew Murray</p> <p>2005-10-22</p> <p>. Our aim in selecting these contributors showcased work that is “hot off the bench” (or computer) at the time of the conference, and also <span class="hlt">created</span> additional opportunities for younger investigators to present their work. The main conference was preceded by a day of tutorials, and followed by two days of workshops, <span class="hlt">on</span> a range of topics in quantitative, computational and systems <span class="hlt">biology</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27936283','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27936283"><span>Purity, adulteration and price of drugs bought <span class="hlt">on-line</span> versus off-<span class="hlt">line</span> in the Netherlands.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>van der Gouwe, Daan; Brunt, Tibor M; van Laar, Margriet; van der Pol, Peggy</p> <p>2017-04-01</p> <p><span class="hlt">On-line</span> drug markets flourish and consumers have high expectations of <span class="hlt">on-line</span> quality and drug value. The aim of this study was to (i) describe <span class="hlt">on-line</span> drug purchases and (ii) compare <span class="hlt">on-line</span> with off-<span class="hlt">line</span> purchased drugs regarding purity, adulteration and price. Comparison of laboratory analyses of 32 663 drug consumer samples (stimulants and hallucinogens) purchased between January 2013 and January 2016, 928 of which were bought <span class="hlt">on-line</span>. The Netherlands. Primary outcome measures were (i) the percentage of samples purchased <span class="hlt">on-line</span> and (ii) the chemical purity of powders (or dosage per tablet); adulteration; and the price per gram, blotter or tablet of drugs bought <span class="hlt">on-line</span> compared with drugs bought off-<span class="hlt">line</span>. The proportion of drug samples purchased <span class="hlt">on-line</span> increased from 1.4% in 2013 to 4.1% in 2015. The frequency varied widely, from a maximum of 6% for controlled, traditional substances [ecstasy tablets, 3,4-methylenedioxy-methamphetamine (MDMA) powder, amphetamine powder, cocaine powder, 4-bromo-2,5-dimethoxyphenethylamine (2C-B) and lysergic acid diethylamide (LSD)] to more than a third for new psychoactive substances (NPS) [4-fluoroamphetamine (4-FA), 5/6-(2-aminopropyl)benzofuran (5/6-APB) and methoxetamine (MXE)]. There were no large differences in drug purity, yet small but statistically significant differences were found for 4-FA (<span class="hlt">on-line</span> 59% versus off-<span class="hlt">line</span> 52% purity for 4-FA <span class="hlt">on</span> average, P = 0.001), MDMA powders (45 versus 61% purity for MDMA, P = 0.02), 2C-B tablets (21 versus 10 mg 2C-B/tablet dosage, P = 0.49) and ecstasy tablets (131 versus 121 mg MDMA/tablet dosage, P = 0.05). The proportion of adulterated samples purchased <span class="hlt">on-line</span> and off-<span class="hlt">line</span> did not differ, except for 4-FA powder, being less adulterated <span class="hlt">on-line</span> (χ 2  = 8.3; P < 0.02). Drug prices were mainly higher <span class="hlt">on-line</span>, ranging for various drugs from 10 to 23% higher than that of drugs purchased off-<span class="hlt">line</span> (six of 10 substances: P < 0.05). Dutch drug users increasingly</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27346524','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27346524"><span>Wiring Together Synthetic Bacterial Consortia to <span class="hlt">Create</span> a <span class="hlt">Biological</span> Integrated Circuit.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Perry, Nicolas; Nelson, Edward M; Timp, Gregory</p> <p>2016-12-16</p> <p>The promise of adapting <span class="hlt">biology</span> to information processing will not be realized until engineered gene circuits, operating in different cell populations, can be wired together to express a predictable function. Here, elementary <span class="hlt">biological</span> integrated circuits (BICs), consisting of two sets of transmitter and receiver gene circuit modules with embedded memory placed in separate cell populations, were meticulously assembled using live cell lithography and wired together by the mass transport of quorum-sensing (QS) signal molecules to form two isolated communication links (comlinks). The comlink dynamics were tested by broadcasting "clock" pulses of inducers into the networks and measuring the responses of functionally linked fluorescent reporters, and then modeled through simulations that realistically captured the protein production and molecular transport. These results show that the comlinks were isolated and each mimicked aspects of the synchronous, sequential networks used in digital computing. The observations about the flow conditions, derived from numerical simulations, and the biofilm architectures that foster or silence cell-to-cell communications have implications for everything from decontamination of drinking water to bacterial virulence.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3740588','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3740588"><span>Understanding pathogenetic aspects and clinical presentation of primary effusion lymphoma (PEL) through its derived cell <span class="hlt">lines</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Carbone, Antonino; Cesarman, Ethel; Gloghini, Annunziata; Drexler, Hans G.</p> <p>2013-01-01</p> <p>Primary effusion lymphoma (PEL) is a very rare subgroup of B-cell lymphomas presenting as pleural, peritoneal and pericardial neoplastic effusions in the absence of a solid tumor mass or recognizable nodal involvement. There is strong evidence that Kaposi’s sarcoma associated herpesvirus (KSHV) is a causal agent of PEL. PEL tumor cells are latently infected by KSHV with consistent expression of several viral proteins and microRNAs that can affect cellular proliferation, differentiation and survival. The most relevant data <span class="hlt">on</span> pathogenesis and <span class="hlt">biology</span> of KSHV have been provided by studies <span class="hlt">on</span> PEL derived cell <span class="hlt">lines</span>. Fourteen continuous cell <span class="hlt">lines</span> have been established from the malignant effusions of patients with AIDS-and non-AIDS-associated PEL. These KSHV+ EBV+/− cell <span class="hlt">lines</span> are wellcharacterized, authenticated and mostly available from public <span class="hlt">biological</span> ressource centers. The PEL cell <span class="hlt">lines</span> display unique features and are clearly distinct from other lymphoma cell <span class="hlt">lines</span>. PEL cell <span class="hlt">lines</span> represent an indispensable tool for the understanding of KSHV <span class="hlt">biology</span> and its impact <span class="hlt">on</span> the clinical manifestation of PEL. Studies <span class="hlt">on</span> PEL cell <span class="hlt">lines</span> have shown that a number of viral genes, expressed during latency or lytic life cycle, have effects <span class="hlt">on</span> cell binding, proliferation, angiogenesis and inflammation. Also PEL cell <span class="hlt">lines</span> are important model systems for the study of the pathology of PEL including the lack of invasive or destructive growth patterns and the peculiar propensity of PEL to involve body cavity surfaces. PMID:20051807</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26931399','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26931399"><span>Testing <span class="hlt">CREATE</span> at Community Colleges: An Examination of Faculty Perspectives and Diverse Student Gains.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kenyon, Kristy L; Onorato, Morgan E; Gottesman, Alan J; Hoque, Jamila; Hoskins, Sally G</p> <p>2016-01-01</p> <p><span class="hlt">CREATE</span> (Consider, Read, Elucidate the hypotheses, Analyze and interpret the data, and Think of the next Experiment) is an innovative pedagogy for teaching science through the intensive analysis of scientific literature. Initiated at the City College of New York, a minority-serving institution, and regionally expanded in the New York/New Jersey/Pennsylvania area, this methodology has had multiple positive impacts <span class="hlt">on</span> faculty and students in science, technology, engineering, and mathematics courses. To determine whether the <span class="hlt">CREATE</span> strategy is effective at the community college (2-yr) level, we prepared 2-yr faculty to use <span class="hlt">CREATE</span> methodologies and investigated <span class="hlt">CREATE</span> implementation at community colleges in seven regions of the United States. We used outside evaluation combined with pre/postcourse assessments of students to test related hypotheses: 1) workshop-trained 2-yr faculty teach effectively with the <span class="hlt">CREATE</span> strategy in their first attempt, and 2) 2-yr students in <span class="hlt">CREATE</span> courses make cognitive and affective gains during their <span class="hlt">CREATE</span> quarter or semester. Community college students demonstrated positive shifts in experimental design and critical-thinking ability concurrent with gains in attitudes/self-rated learning and maturation of epistemological beliefs about science. © 2016 K. L. Kenyon et al. CBE—Life Sciences Education © 2016 The American Society for Cell <span class="hlt">Biology</span>. This article is distributed by The American Society for Cell <span class="hlt">Biology</span> under license from the author(s). It is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24065964','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24065964"><span>Chemical synthetic <span class="hlt">biology</span>: a mini-review.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chiarabelli, Cristiano; Stano, Pasquale; Luisi, Pier Luigi</p> <p>2013-01-01</p> <p>Chemical synthetic <span class="hlt">biology</span> (CSB) is a branch of synthetic <span class="hlt">biology</span> (SB) oriented toward the synthesis of chemical structures alternative to those present in nature. Whereas SB combines <span class="hlt">biology</span> and engineering with the aim of synthesizing <span class="hlt">biological</span> structures or life forms that do not exist in nature - often based <span class="hlt">on</span> genome manipulation, CSB uses and assembles <span class="hlt">biological</span> parts, synthetic or not, to <span class="hlt">create</span> new and alternative structures. A short epistemological note will introduce the theoretical concepts related to these fields, whereas the text will be largely devoted to introduce and comment two main projects of CSB, carried out in our laboratory in the recent years. The "Never Born Biopolymers" project deals with the construction and the screening of RNA and peptide sequences that are not present in nature, whereas the "Minimal Cell" project focuses <span class="hlt">on</span> the construction of semi-synthetic compartments (usually liposomes) containing the minimal and sufficient number of components to perform the basic function of a <span class="hlt">biological</span> cell. These two topics are extremely important for both the general understanding of <span class="hlt">biology</span> in terms of function, organization, and development, and for applied biotechnology.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003JGRE..108.5022Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003JGRE..108.5022Z"><span>Energy for <span class="hlt">biologic</span> sulfate reduction in a hydrothermally formed ocean <span class="hlt">on</span> Europa</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zolotov, Mikhail Y.; Shock, Everett L.</p> <p>2003-04-01</p> <p>Formation of a sulfate-bearing ocean <span class="hlt">on</span> Jupiter's satellite Europa by quenched hydrothermal fluids provides a source of metabolic energy for low-temperature sulfate-reducing organisms that use dissolved H2 as an electron donor. Inhibition of thermodynamically favorable sulfate reduction in cooled hydrothermal fluids <span class="hlt">creates</span> the potential for <span class="hlt">biologic</span> reduction. Both high temperature and reduced conditions of ocean-forming hydrothermal solutions favor sulfate reduction in quenched fluids. The maximum amount of energy available to support autotrophic sulfate reduction is <span class="hlt">on</span> the order of a few kilojoules per kilogram of water and is limited by the low abundances of either H2 or sulfate in ocean-forming fluids. Although this irreplaceable energy source might have supported early life <span class="hlt">on</span> Europa, maintenance of <span class="hlt">biologic</span> sulfate reduction throughout the ocean's history would require a supply of organic compounds from endogenic sources or from the satellite's surface.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27759334','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27759334"><span><span class="hlt">On-line</span> approaches for the determination of residues and contaminants in complex samples.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fumes, Bruno Henrique; Andrade, Mariane Aissa; Franco, Maraíssa Silva; Lanças, Fernando Mauro</p> <p>2017-01-01</p> <p>The determination of residues and contaminants in complex matrices such as in the case of food, environmental, and <span class="hlt">biological</span> samples requires a combination of several steps to succeed in the aimed goal. At least three independent steps are integrated to provide the best available situation to deal with such matrices: (1) a sample preparation technique is employed to isolate the target compounds from the rest of the matrix; (2) a chromatographic (second) step further "purifies" the isolated compounds from the co-extracted matrix interferences; (3) a spectroscopy-based device acts as chromatographic detector (ideally containing a tandem high-resolution mass analyzer) for the qualitative and quantitative analysis. These techniques can be operated in different modes including the off-<span class="hlt">line</span> and the <span class="hlt">on-line</span> modes. The present report focus the <span class="hlt">on-line</span> coupling techniques aiming the determination of analytes present in complex matrices. The fundamentals of these approaches as well as the most common set ups are presented and discussed, as well as a review <span class="hlt">on</span> the recent applications of these two approaches to the fields of bioanalytical, environmental, and food analysis are critically discussed. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/9038077','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/9038077"><span>[<span class="hlt">Biological</span> behavior of hypopharyngeal carcinoma].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhou, L X</p> <p>1997-01-01</p> <p>Hypopharyngeal squamous cell carcinomas (HPC) has an extremely poor prognosis. Characteristics of cell <span class="hlt">lines</span> of head and neck squamous cell carcinomas including HPC were studied by various methods, e.g., chemosensitivity test and the immunohistochemistry staining method, to determine whether this poor prognosis is due to the <span class="hlt">biological</span> behavior of this cancer. An HPC cell <span class="hlt">line</span> was found to be resistant to anti tumor drugs, i.e., PEP, MTX and CPM and moderately sensitive to CDDP, 5-FU and ADM. Thermoresistance to hyperthermatic treatment and weak expression of ICAM-1 <span class="hlt">on</span> the HPC cell <span class="hlt">line</span> were observed. DNA synthesis by the HPC cell <span class="hlt">line</span> was induced by stimulation with a low concentration of EGF and the amount of EGFR <span class="hlt">on</span> these HPC cells was very high. In addition, cyclinD1 overexpression was found in the HPC cell <span class="hlt">line</span>. Based <span class="hlt">on</span> the above findings, further analysis of hypopharyngeal carcinoma cells and the development of a new treatment modality to control tumor growth and metastatic factors influencing the poor outcome are necessary to improve the prognosis of this cancer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1541411','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1541411"><span>Surface receptors <span class="hlt">on</span> human haematopoietic cell <span class="hlt">lines</span>.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Huber, C; Sundström, C; Nilsson, K; Wigzell, H</p> <p>1976-01-01</p> <p>The expression of complement receptors, of Fc receptors, of SRBC receptors and of S-Ig was investigated <span class="hlt">on</span> human haematopoietic cell <span class="hlt">lines</span> of proved malignant derivation. According to their origin and to a panel of phenotypic markers these <span class="hlt">lines</span> have been classified into lymphoma <span class="hlt">lines</span>, myeloma <span class="hlt">lines</span> and leukemia <span class="hlt">lines</span>. Results were compared with those obtained <span class="hlt">on</span> non-malignant EBV carrying lymphoblastoid cell <span class="hlt">lines</span> (LCL). Among the lymphoid cell <span class="hlt">lines</span> the LCL showed a pattern of B-lymphocyte surface markers, i.e. surface immunoglobulins, C3 receptors but low density of Fc receptors. The non-Burkitt lymphoma <span class="hlt">lines</span> bore in varying degree these B-lymphocyte markers. The <span class="hlt">lines</span> U-698 M and DG-75 were exceptional in having only surface immunoglobulin. The Burkitt lymphoma <span class="hlt">lines</span> had all B-lymphocyte markers. The myeloma <span class="hlt">lines</span> differed from the lymphoid <span class="hlt">lines</span> in lacking C3 and Fc receptors and showed only trace amounts of surface immunoglobulins. In contrast to lymphoid and myeloma <span class="hlt">lines</span>, the leukaemia <span class="hlt">lines</span> were completely lacking surface immunoglobulins, but showed C3 and Fc receptors in variable densities. <span class="hlt">On</span> <span class="hlt">line</span>, the ALL derived <span class="hlt">line</span> MOLT-3 showed the capacity to spontaneous rosette formation with SRBC. The findings that LCL presented a homogeneous pattern of B-lymphocyte surface markers may be of value in order to discriminate between these <span class="hlt">lines</span> and <span class="hlt">lines</span> derived from haematopoietic malignancies other than Burkitt lymphomas. PMID:963908</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26302176','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26302176"><span>Finding mouse models of human lymphomas and leukemia's using the Jackson laboratory mouse tumor <span class="hlt">biology</span> database.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Begley, Dale A; Sundberg, John P; Krupke, Debra M; Neuhauser, Steven B; Bult, Carol J; Eppig, Janan T; Morse, Herbert C; Ward, Jerrold M</p> <p>2015-12-01</p> <p>Many mouse models have been <span class="hlt">created</span> to study hematopoietic cancer types. There are over thirty hematopoietic tumor types and subtypes, both human and mouse, with various origins, characteristics and clinical prognoses. Determining the specific type of hematopoietic lesion produced in a mouse model and identifying mouse models that correspond to the human subtypes of these lesions has been a continuing challenge for the scientific community. The Mouse Tumor <span class="hlt">Biology</span> Database (MTB; http://tumor.informatics.jax.org) is designed to facilitate use of mouse models of human cancer by providing detailed histopathologic and molecular information <span class="hlt">on</span> lymphoma subtypes, including expertly annotated, <span class="hlt">on</span> <span class="hlt">line</span>, whole slide scans, and providing a repository for storing information <span class="hlt">on</span> and querying these data for specific lymphoma models. Copyright © 2015 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29686393','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29686393"><span>Characterizing Cancer Drug Response and <span class="hlt">Biological</span> Correlates: A Geometric Network Approach.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Pouryahya, Maryam; Oh, Jung Hun; Mathews, James C; Deasy, Joseph O; Tannenbaum, Allen R</p> <p>2018-04-23</p> <p>In the present work, we apply a geometric network approach to study common <span class="hlt">biological</span> features of anticancer drug response. We use for this purpose the panel of 60 human cell <span class="hlt">lines</span> (NCI-60) provided by the National Cancer Institute. Our study suggests that mathematical tools for network-based analysis can provide novel insights into drug response and cancer <span class="hlt">biology</span>. We adopted a discrete notion of Ricci curvature to measure, via a link between Ricci curvature and network robustness established by the theory of optimal mass transport, the robustness of <span class="hlt">biological</span> networks constructed with a pre-treatment gene expression dataset and coupled the results with the GI50 response of the cell <span class="hlt">lines</span> to the drugs. Based <span class="hlt">on</span> the resulting drug response ranking, we assessed the impact of genes that are likely associated with individual drug response. For genes identified as important, we performed a gene ontology enrichment analysis using a curated bioinformatics database which resulted in <span class="hlt">biological</span> processes associated with drug response across cell <span class="hlt">lines</span> and tissue types which are plausible from the point of view of the <span class="hlt">biological</span> literature. These results demonstrate the potential of using the mathematical network analysis in assessing drug response and in identifying relevant genomic biomarkers and <span class="hlt">biological</span> processes for precision medicine.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018NatCh..10..245M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018NatCh..10..245M"><span>Biosynthesis: Reprogramming assembly <span class="hlt">lines</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Menon, Binuraj R. K.; Jenner, Matthew</p> <p>2018-03-01</p> <p>Rational engineering of biosynthetic assembly <span class="hlt">lines</span> for production of new compounds is an attractive prospect, yet it presents many challenges. Learning from <span class="hlt">biology</span>, some of the rules for expanding the chemical diversity of non-ribosomal peptides have been uncovered in two recent studies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015PhDT........22R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015PhDT........22R"><span><span class="hlt">Biology</span>, literacy, and the African American voice: A case study of meaningful learning in the <span class="hlt">biology</span> classroom</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Reese, Keturah</p> <p></p> <p>Under the direction of Sharon Murphy Augustine, Ph.D./Ph.D Curriculum and Instruction There was a substantial performance gap among African Americans and other ethnic groups. Additionally, African American students in a Title I school were at a significantly high risk of not meeting or exceeding <span class="hlt">on</span> performance tests in science. Past reports have shown average gains in some subject areas, and declines in others (NCES, 2011; GADOE, 2012). Current instructional strategies and the lack of literacy within the <span class="hlt">biology</span> classroom <span class="hlt">created</span> a problem for African American high school students <span class="hlt">on</span> national and state assessments. The purpose of this study was to examine the perceptions of African American students and teachers in the context of literacy and <span class="hlt">biology</span> through the incorporation of an interactive notebook and other literacy strategies. The data was collected three ways: field notes for a two week observation period within the <span class="hlt">biology</span> classroom, student and teacher interviews, and student work samples. During the observations, student work collection, and interviews, I looked for the following codes: active learning, constructive learning, collaborative learning, authentic learning, and intentional learning. In the process of coding for the pre-determined codes, three more codes emerged. The three codes that emerged were organization, studying/student ownership, and student teacher relationships. Students and teachers both solidified the notion that literacy and <span class="hlt">biology</span> worked well together. The implemented literacy strategies were something that both teachers and students appreciated in their learning of <span class="hlt">biology</span>. Overall students and teachers perceived that the interactive notebook along Cornell notes, Thinking maps, close reads, writing, lab experiments, and group work <span class="hlt">created</span> meaningful learning experiences within the <span class="hlt">biology</span> classroom.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=biology&id=EJ1098017','ERIC'); return false;" href="https://eric.ed.gov/?q=biology&id=EJ1098017"><span>Grades and Withdrawal Rates in Cell <span class="hlt">Biology</span> and Genetics Based upon Institution Type for General <span class="hlt">Biology</span> and Implications for Transfer Articulation Agreements</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Regier, Kimberly Fayette</p> <p>2016-01-01</p> <p>General <span class="hlt">biology</span> courses (for majors) are often transferred from one institution to another. These courses must prepare students for upper division courses in <span class="hlt">biology</span>. In Colorado, a <span class="hlt">Biology</span> Transfer Articulation Agreement that includes general <span class="hlt">biology</span> has been <span class="hlt">created</span> across the state. An evaluation was conducted of course grades in two upper…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28821538','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28821538"><span>Reflecting <span class="hlt">on</span> Graphs: Attributes of Graph Choice and Construction Practices in <span class="hlt">Biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Angra, Aakanksha; Gardner, Stephanie M</p> <p>2017-01-01</p> <p>Undergraduate <span class="hlt">biology</span> education reform aims to engage students in scientific practices such as experimental design, experimentation, and data analysis and communication. Graphs are ubiquitous in the <span class="hlt">biological</span> sciences, and <span class="hlt">creating</span> effective graphical representations involves quantitative and disciplinary concepts and skills. Past studies document student difficulties with graphing within the contexts of classroom or national assessments without evaluating student reasoning. Operating under the metarepresentational competence framework, we conducted think-aloud interviews to reveal differences in reasoning and graph quality between undergraduate <span class="hlt">biology</span> students, graduate students, and professors in a pen-and-paper graphing task. All professors planned and thought about data before graph construction. When reflecting <span class="hlt">on</span> their graphs, professors and graduate students focused <span class="hlt">on</span> the function of graphs and experimental design, while most undergraduate students relied <span class="hlt">on</span> intuition and data provided in the task. Most undergraduate students meticulously plotted all data with scaled axes, while professors and some graduate students transformed the data, aligned the graph with the research question, and reflected <span class="hlt">on</span> statistics and sample size. Differences in reasoning and approaches taken in graph choice and construction corroborate and extend previous findings and provide rich targets for undergraduate and graduate instruction. © 2017 A. Angra and S. M. Gardner. CBE—Life Sciences Education © 2017 The American Society for Cell <span class="hlt">Biology</span>. This article is distributed by The American Society for Cell <span class="hlt">Biology</span> under license from the author(s). It is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23464376','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23464376"><span>Detection of oral streptococci in dental unit water <span class="hlt">lines</span> after therapy with air turbine handpiece: <span class="hlt">biological</span> fluid retraction more frequent than expected.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Petti, Stefano; Moroni, Catia; Messano, Giuseppe Alessio; Polimeni, Antonella</p> <p>2013-03-01</p> <p>Oral streptococci detected in water from dental unit water <span class="hlt">lines</span> (DUWLs) are a surrogate marker of patients' <span class="hlt">biological</span> fluid retraction during therapy. We investigated oral streptococci detection rate in DUWLs in a representative sample of private offices in real-life conditions. Samples of nondisinfected water (100 ml) were collected from the DUWL designated for the air turbine handpiece in 81 dental units, immediately after dental treatment of patients with extensive air turbine handpiece use. Water was filtered and plated <span class="hlt">on</span> a selective medium for oral streptococci and, morphologically, typical colonies of oral streptococci were counted. The lowest detection limit was 0.01 CFU/ml. The oral streptococci detection rate was 72% (95% CI: 62-81%), with a mean level of 0.7 CFU/ml. Oral streptococci detection was not affected by handpiece age or dental treatment type, but was associated with dental unit age. <span class="hlt">Biological</span> fluid retraction into DUWLs during patient treatment and, possibly, the risk for patient-to-patient blood- or air-borne pathogen transmission are more frequent than expected.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23737624','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23737624"><span>Competency-based reforms of the undergraduate <span class="hlt">biology</span> curriculum: integrating the physical and <span class="hlt">biological</span> sciences.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Thompson, Katerina V; Chmielewski, Jean; Gaines, Michael S; Hrycyna, Christine A; LaCourse, William R</p> <p>2013-06-01</p> <p>The National Experiment in Undergraduate Science Education project funded by the Howard Hughes Medical Institute is a direct response to the Scientific Foundations for Future Physicians report, which urged a shift in premedical student preparation from a narrow list of specific course work to a more flexible curriculum that helps students develop broad scientific competencies. A consortium of four universities is working to <span class="hlt">create</span>, pilot, and assess modular, competency-based curricular units that require students to use higher-order cognitive skills and reason across traditional disciplinary boundaries. Purdue University; the University of Maryland, Baltimore County; and the University of Miami are each developing modules and case studies that integrate the <span class="hlt">biological</span>, chemical, physical, and mathematical sciences. The University of Maryland, College Park, is leading the effort to <span class="hlt">create</span> an introductory physics for life sciences course that is reformed in both content and pedagogy. This course has prerequisites of <span class="hlt">biology</span>, chemistry, and calculus, allowing students to apply strategies from the physical sciences to solving authentic <span class="hlt">biological</span> problems. A comprehensive assessment plan is examining students' conceptual knowledge of physics, their attitudes toward interdisciplinary approaches, and the development of specific scientific competencies. Teaching modules developed during this initial phase will be tested <span class="hlt">on</span> multiple partner campuses in preparation for eventual broad dissemination.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_11 --> <div id="page_12" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="221"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20070031718','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20070031718"><span>Integration of <span class="hlt">On-Line</span> and Off-<span class="hlt">Line</span> Diagnostic Algorithms for Aircraft Engine Health Management</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Kobayashi, Takahisa; Simon, Donald L.</p> <p>2007-01-01</p> <p>This paper investigates the integration of <span class="hlt">on-line</span> and off-<span class="hlt">line</span> diagnostic algorithms for aircraft gas turbine engines. The <span class="hlt">on-line</span> diagnostic algorithm is designed for in-flight fault detection. It continuously monitors engine outputs for anomalous signatures induced by faults. The off-<span class="hlt">line</span> diagnostic algorithm is designed to track engine health degradation over the lifetime of an engine. It estimates engine health degradation periodically over the course of the engine s life. The estimate generated by the off-<span class="hlt">line</span> algorithm is used to update the <span class="hlt">on-line</span> algorithm. Through this integration, the <span class="hlt">on-line</span> algorithm becomes aware of engine health degradation, and its effectiveness to detect faults can be maintained while the engine continues to degrade. The benefit of this integration is investigated in a simulation environment using a nonlinear engine model.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014SPIE.9090E..0KL','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014SPIE.9090E..0KL"><span><span class="hlt">Line</span> fitting based feature extraction for object recognition</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Bing</p> <p>2014-06-01</p> <p>Image feature extraction plays a significant role in image based pattern applications. In this paper, we propose a new approach to generate hierarchical features. This new approach applies <span class="hlt">line</span> fitting to adaptively divide regions based upon the amount of information and <span class="hlt">creates</span> <span class="hlt">line</span> fitting features for each subsequent region. It overcomes the feature wasting drawback of the wavelet based approach and demonstrates high performance in real applications. For gray scale images, we propose a diffusion equation approach to map information-rich pixels (pixels near edges and ridge pixels) into high values, and pixels in homogeneous regions into small values near zero that form energy map images. After the energy map images are generated, we propose a <span class="hlt">line</span> fitting approach to divide regions recursively and <span class="hlt">create</span> features for each region simultaneously. This new feature extraction approach is similar to wavelet based hierarchical feature extraction in which high layer features represent global characteristics and low layer features represent local characteristics. However, the new approach uses <span class="hlt">line</span> fitting to adaptively focus <span class="hlt">on</span> information-rich regions so that we avoid the feature waste problems of the wavelet approach in homogeneous regions. Finally, the experiments for handwriting word recognition show that the new method provides higher performance than the regular handwriting word recognition approach.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26608109','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26608109"><span>A high-content platform to characterise human induced pluripotent stem cell <span class="hlt">lines</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Leha, Andreas; Moens, Nathalie; Meleckyte, Ruta; Culley, Oliver J; Gervasio, Mia K; Kerz, Maximilian; Reimer, Andreas; Cain, Stuart A; Streeter, Ian; Folarin, Amos; Stegle, Oliver; Kielty, Cay M; Durbin, Richard; Watt, Fiona M; Danovi, Davide</p> <p>2016-03-01</p> <p>Induced pluripotent stem cells (iPSCs) provide invaluable opportunities for future cell therapies as well as for studying human development, modelling diseases and discovering therapeutics. In order to realise the potential of iPSCs, it is crucial to comprehensively characterise cells generated from large cohorts of healthy and diseased individuals. The human iPSC initiative (HipSci) is assessing a large panel of cell <span class="hlt">lines</span> to define cell phenotypes, dissect inter- and intra-<span class="hlt">line</span> and donor variability and identify its key determinant components. Here we report the establishment of a high-content platform for phenotypic analysis of human iPSC <span class="hlt">lines</span>. In the described assay, cells are dissociated and seeded as single cells onto 96-well plates coated with fibronectin at three different concentrations. This method allows assessment of cell number, proliferation, morphology and intercellular adhesion. Altogether, our strategy delivers robust quantification of phenotypic diversity within complex cell populations facilitating future identification of the genetic, <span class="hlt">biological</span> and technical determinants of variance. Approaches such as the one described can be used to benchmark iPSCs from multiple donors and <span class="hlt">create</span> novel platforms that can readily be tailored for disease modelling and drug discovery. Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22035709','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22035709"><span>Life <span class="hlt">lines</span>: An art history of <span class="hlt">biological</span> research around 1800.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bruhn, Matthias</p> <p>2011-12-01</p> <p>Around 1800, the scientific "illustrator" emerged as a new artistic profession in Europe. Artists were increasingly sought after in order to picture anatomical dissections and microscopic observations and to translate drawings into artworks for books and journals. By training and technical expertise, they introduced a particular kind of knowledge into scientific perception that also shaped the common image of nature. Illustrations of scientific publications, often undervalued as a biased interpretation of facts and subordinate to logic and description, thus convey an 'art history' of science in its own right, relevant both for the understanding of <span class="hlt">biological</span> thought around 1800 as well as for the development of the arts and their historiography. The article is based <span class="hlt">on</span> an analysis of botanical treatises produced for the Göttingen Society of Sciences in 1803, during an early phase of microscopic cell research, in order to determine the constitutive role of artistic knowledge and the media employed for the visualization and conceptualization of <span class="hlt">biological</span> issues. Copyright © 2011 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26079404','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26079404"><span>Dental Age Estimation Helps <span class="hlt">Create</span> a New Identity.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>De Angelis, Danilo; Gibelli, Daniele; Fabbri, Paolo; Cattaneo, Cristina</p> <p>2015-09-01</p> <p>Age estimation involves the reconstruction of age by <span class="hlt">biological</span> parameters such as skeletal and dental development in minors, or reduction of pulp chamber in adults, to gain indications concerning the chronological age of the person. In most cases, it is needed in forensic scenarios to verify if the supposed age of an individual is correct; in exceptional cases, age estimation is instead required by judicial authorities to <span class="hlt">create</span> a new identity usually in persons who do not remember who they are.This article aims at reporting the case of J. who was found in 2005 with signs of amnesia because he did not remember his name and age. After several unsuccessful attempts at identifying him, the judicial authority decided to assign a new identity, which was to be constructed according to the real <span class="hlt">biological</span> data of the individual. The help of a forensic pathologist and a forensic odontologist was then requested, and age estimation was reached by applying methods for adults based <span class="hlt">on</span> the physiological reduction of pulp chamber. Dental age estimation yielded a final result of approximately 31 years, which was the new age assigned to the person.This article shows a peculiar application of dental age estimation, which can be used not only to ascertain or deny supposed age, but is sometimes needed to <span class="hlt">create</span> a new identity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26677427','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26677427"><span>Current dichotomy between traditional molecular <span class="hlt">biological</span> and omic research in cancer <span class="hlt">biology</span> and pharmacology.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Reinhold, William C</p> <p>2015-12-10</p> <p>There is currently a split within the cancer research community between traditional molecular <span class="hlt">biological</span> hypothesis-driven and the more recent "omic" forms or research. While the molecular <span class="hlt">biological</span> approach employs the tried and true single alteration-single response formulations of experimentation, the omic employs broad-based assay or sample collection approaches that generate large volumes of data. How to integrate the benefits of these two approaches in an efficient and productive fashion remains an outstanding issue. Ideally, one would merge the understandability, exactness, simplicity, and testability of the molecular <span class="hlt">biological</span> approach, with the larger amounts of data, simultaneous consideration of multiple alterations, consideration of genes both of known interest along with the novel, cross-sample comparisons among cell <span class="hlt">lines</span> and patient samples, and consideration of directed questions while simultaneously gaining exposure to the novel provided by the omic approach. While at the current time integration of the two disciplines remains problematic, attempts to do so are ongoing, and will be necessary for the understanding of the large cell <span class="hlt">line</span> screens including the Developmental Therapeutics Program's NCI-60, the Broad Institute's Cancer Cell <span class="hlt">Line</span> Encyclopedia, and the Wellcome Trust Sanger Institute's Cancer Genome Project, as well as the the Cancer Genome Atlas clinical samples project. Going forward there is significant benefit to be had from the integration of the molecular <span class="hlt">biological</span> and the omic forms or research, with the desired goal being improved translational understanding and application.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ1118304.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ1118304.pdf"><span>Creation of a Unified Educational Space within a SLA University Classroom Using Cloud Storage and <span class="hlt">On-Line</span> Applications</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Karabayeva, Kamilya Zhumartovna</p> <p>2016-01-01</p> <p>In the present article the author gives evidence of effective application of cloud storage and <span class="hlt">on-line</span> applications in the educational process of the higher education institution, as well as considers the problems and prospects of using cloud technologies in the educational process, when <span class="hlt">creating</span> a unified educational space in the foreign language…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27638202','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27638202"><span>Leveraging premalignant <span class="hlt">biology</span> for immune-based cancer prevention.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Spira, Avrum; Disis, Mary L; Schiller, John T; Vilar, Eduardo; Rebbeck, Timothy R; Bejar, Rafael; Ideker, Trey; Arts, Janine; Yurgelun, Matthew B; Mesirov, Jill P; Rao, Anjana; Garber, Judy; Jaffee, Elizabeth M; Lippman, Scott M</p> <p>2016-09-27</p> <p>Prevention is an essential component of cancer eradication. Next-generation sequencing of cancer genomes and epigenomes has defined large numbers of driver mutations and molecular subgroups, leading to therapeutic advances. By comparison, there is a relative paucity of such knowledge in premalignant neoplasia, which inherently limits the potential to develop precision prevention strategies. Studies <span class="hlt">on</span> the interplay between germ-<span class="hlt">line</span> and somatic events have elucidated genetic processes underlying premalignant progression and preventive targets. Emerging data hint at the immune system's ability to intercept premalignancy and prevent cancer. Genetically engineered mouse models have identified mechanisms by which genetic drivers and other somatic alterations recruit inflammatory cells and induce changes in normal cells to <span class="hlt">create</span> and interact with the premalignant tumor microenvironment to promote oncogenesis and immune evasion. These studies are currently limited to only a few lesion types and patients. In this Perspective, we advocate a large-scale collaborative effort to systematically map the <span class="hlt">biology</span> of premalignancy and the surrounding cellular response. By bringing together scientists from diverse disciplines (e.g., biochemistry, omics, and computational <span class="hlt">biology</span>; microbiology, immunology, and medical genetics; engineering, imaging, and synthetic chemistry; and implementation science), we can drive a concerted effort focused <span class="hlt">on</span> cancer vaccines to reprogram the immune response to prevent, detect, and reject premalignancy. Lynch syndrome, clonal hematopoiesis, and cervical intraepithelial neoplasia which also serve as models for inherited syndromes, blood, and viral premalignancies, are ideal scenarios in which to launch this initiative.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28103762','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28103762"><span>Cultural and <span class="hlt">biological</span> factors modulate spatial biases over development.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Girelli, Luisa; Marinelli, Chiara Valeria; Grossi, Giuseppe; Arduino, Lisa S</p> <p>2017-11-01</p> <p>Increasing evidence supports the contribution of both <span class="hlt">biological</span> and cultural factors to visuospatial processing. The present study adds to the literature by exploring the interplay of perceptual and linguistic mechanisms in determining visuospatial asymmetries in adults (Experiment 1) and children (Experiment 2). In particular, pre-schoolers (3 and 5 year-olds), school-aged children (8 year-old), and adult participants were required to bisect different types of stimuli, that is, <span class="hlt">lines</span>, words, and figure strings. In accordance with the literature, results yielded a leftward bias for <span class="hlt">lines</span> and words and a rightward bias for figure strings, in adult participants. More critically, different biases were found for <span class="hlt">lines</span>, words, and figure strings in children as a function of age, reflecting the impact of both cultural and <span class="hlt">biological</span> factors <span class="hlt">on</span> the processing of different visuospatial materials. Specifically, an adult-like pattern of results emerged only in the older group of children (8 year-old), but not in pre-schoolers. Results are discussed in terms of literacy, reading habits exposure, and <span class="hlt">biological</span> maturation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/866416','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/866416"><span>Methods and apparatus for reducing corrosion in refractory <span class="hlt">linings</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Poeppel, Roger B.; Greenberg, Sherman; Diercks, Dwight R.</p> <p>1987-01-01</p> <p>Methods and apparatus are provided for reducing corrosion in a refractory <span class="hlt">lining</span> of a liquid-containing vessel used in direct steelmaking processes. The vessel operates at between about 1600.degree. C. and about 1800.degree. C. and an oxygen partial pressure of about 10.sup.-12 atmospheres, <span class="hlt">creating</span> slag which is rich in FeO. The refractory <span class="hlt">lining</span> includes a significant level of chromium oxide (Cr.sub.2 O.sub.3), and has small interconnected pores which may be filled with a gas mixture having a higher total pressure and oxygen partial pressure than the total pressure and oxygen partial pressure associted with the liquid against the <span class="hlt">lining</span> of the vessel. The gas mixture is forced through the pores of the <span class="hlt">lining</span> so that the pores are continuously filled with the mixture. In this manner, the gas mixture <span class="hlt">creates</span> a blanket which increases the oxygen partial pressure at the <span class="hlt">lining</span> enough to maintain the chromium in the <span class="hlt">lining</span> in a selected valence state in which the chromium has decreased solubility in the FeO slag, thereby reducing corrosion by the FeO and increasing the useful life of the refractory <span class="hlt">lining</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28682233','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28682233"><span>[History of the Strasbourg Society of <span class="hlt">Biology</span>].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Antony, Pierre; Romier, Christophe; Mantz, Jean-Marie</p> <p>2017-01-01</p> <p>The Society of <span class="hlt">Biology</span> of Strasbourg (SBS) is a learned society that was <span class="hlt">created</span> in 1919 based <span class="hlt">on</span> the model of the Society of <span class="hlt">Biology</span> of which it is a subsidiary. Like its Parisian colleague, SBS aims at diffusing and promoting scientific knowledge in <span class="hlt">biology</span>. To achieve this goal, SBS initiated since its creation a dialogue interface between researchers in <span class="hlt">biology</span> and physicians, and more recently with other scientific disciplines, industry and the civil society. At the dawn of its first century, the Society of <span class="hlt">Biology</span> of Strasbourg must continue to reinvent itself to pursue its development and to fulfil its mission of sharing scientific knowledge. This work continues in strong collaboration with our partners that share with SBS the willingness to foster excellence in <span class="hlt">biological</span> research in Strasbourg, its region and beyond. © Société de Biologie, 2017.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20150022292','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20150022292"><span>Software Development: 3D Animations and <span class="hlt">Creating</span> User Interfaces for Realistic Simulations</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Gordillo, Orlando Enrique</p> <p>2015-01-01</p> <p>My fall 2015 semester was spent at the Lyndon B. Johnson Space Center working in the Integrated Graphics, Operations, and Analysis Laboratory (IGOAL). My first project was to <span class="hlt">create</span> a video animation that could tell the story of OMICS. OMICS is a term being used in the field of biomedical science to describe the collective technologies that study <span class="hlt">biological</span> systems, such as what makes up a cell and how it functions with other systems. In the IGOAL I used a large 23 inch Wacom monitor to draw storyboards, graphics, and <span class="hlt">line</span> art animations. I used Blender as the 3D environment to sculpt, shape, cut or modify the several scenes and models for the video. A challenge <span class="hlt">creating</span> this video was to take a term used in biomedical science and describe it in such a way that an 8th grade student can understand. I used a <span class="hlt">line</span> art style because it would visually set the tone for what we thought was an educational style. In order to get a handle <span class="hlt">on</span> the perspective and overall feel for the animation without overloading my workspace, I split up the 2 minute animation into several scenes. I used Blender's python scripting capabilities which allowed for the addition of plugins to add or modify tools. The scripts can also directly interact with the objects to <span class="hlt">create</span> naturalistic patterns or movements. After collecting the rendered scenes, I used Blender's built-in video editing workspace to output the animation. My second project was to write software that emulates a physical system's interface. The interface was to simulate a boat, ROV, and winch system. Simulations are a time and cost effective way to test complicated data and provide training for operators without having to use expensive hardware. We <span class="hlt">created</span> the virtual controls with 3-D Blender models and 2-D graphics, and then add functionality in C# using the Unity game engine. The Unity engine provides several essential behaviors of a simulator, such as the start and update functions. A framework for Unity, which was developed in</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21601677','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21601677"><span>The Eugene language for synthetic <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bilitchenko, Lesia; Liu, Adam; Densmore, Douglas</p> <p>2011-01-01</p> <p>Synthetic <span class="hlt">biological</span> systems are currently <span class="hlt">created</span> by an ad hoc, iterative process of design, simulation, and assembly. These systems would greatly benefit from the introduction of a more formalized and rigorous specification of the desired system components as well as constraints <span class="hlt">on</span> their composition. In order to do so, the creation of robust and efficient design flows and tools is imperative. We present a human readable language (Eugene) which allows for both the specification of synthetic <span class="hlt">biological</span> designs based <span class="hlt">on</span> <span class="hlt">biological</span> parts as well as providing a very expressive constraint system to drive the creation of composite devices from collection of parts. This chapter provides an overview of the language primitives as well as instructions <span class="hlt">on</span> installation and use of Eugene v0.03b. Copyright © 2011 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19930013436','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19930013436"><span>Gravitational <span class="hlt">Biology</span> Facility <span class="hlt">on</span> Space Station: Meeting the needs of space <span class="hlt">biology</span></span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Allen, Katherine; Wade, Charles</p> <p>1992-01-01</p> <p>The Gravitational <span class="hlt">Biology</span> Facility (GBF) is a set of generic laboratory equipment needed to conduct research <span class="hlt">on</span> Space Station Freedom (SSF), focusing <span class="hlt">on</span> Space <span class="hlt">Biology</span> Program science (Cell and Developmental <span class="hlt">Biology</span> and Plant <span class="hlt">Biology</span>). The GBF will be functional from the earliest utilization flights through the permanent manned phase. Gravitational <span class="hlt">biology</span> research will also make use of other Life Sciences equipment <span class="hlt">on</span> the space station as well as existing equipment developed for the space shuttle. The facility equipment will be developed based <span class="hlt">on</span> requirements derived from experiments proposed by the scientific community to address critical questions in the Space <span class="hlt">Biology</span> Program. This requires that the facility have the ability to house a wide variety of species, various methods of observation, and numerous methods of sample collection, preservation, and storage. The selection of the equipment will be done by the members of a scientific working group (5 members representing cell <span class="hlt">biology</span>, 6 developmental <span class="hlt">biology</span>, and 6 plant <span class="hlt">biology</span>) who also provide requirements to design engineers to ensure that the equipment will meet scientific needs. All equipment will undergo extensive ground based experimental validation studies by various investigators addressing a variety of experimental questions. Equipment will be designed to be adaptable to other space platforms. The theme of the Gravitational <span class="hlt">Biology</span> Facility effort is to provide optimal and reliable equipment to answer the critical questions in Space <span class="hlt">Biology</span> as to the effects of gravity <span class="hlt">on</span> living systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3598413','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3598413"><span><span class="hlt">Creating</span> Objects and Object Categories for Studying Perception and Perceptual Learning</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Hauffen, Karin; Bart, Eugene; Brady, Mark; Kersten, Daniel; Hegdé, Jay</p> <p>2012-01-01</p> <p>In order to quantitatively study object perception, be it perception by <span class="hlt">biological</span> systems or by machines, one needs to <span class="hlt">create</span> objects and object categories with precisely definable, preferably naturalistic, properties1. Furthermore, for studies <span class="hlt">on</span> perceptual learning, it is useful to <span class="hlt">create</span> novel objects and object categories (or object classes) with such properties2. Many innovative and useful methods currently exist for <span class="hlt">creating</span> novel objects and object categories3-6 (also see refs. 7,8). However, generally speaking, the existing methods have three broad types of shortcomings. First, shape variations are generally imposed by the experimenter5,9,10, and may therefore be different from the variability in natural categories, and optimized for a particular recognition algorithm. It would be desirable to have the variations arise independently of the externally imposed constraints. Second, the existing methods have difficulty capturing the shape complexity of natural objects11-13. If the goal is to study natural object perception, it is desirable for objects and object categories to be naturalistic, so as to avoid possible confounds and special cases. Third, it is generally hard to quantitatively measure the available information in the stimuli <span class="hlt">created</span> by conventional methods. It would be desirable to <span class="hlt">create</span> objects and object categories where the available information can be precisely measured and, where necessary, systematically manipulated (or 'tuned'). This allows one to formulate the underlying object recognition tasks in quantitative terms. Here we describe a set of algorithms, or methods, that meet all three of the above criteria. Virtual morphogenesis (VM) <span class="hlt">creates</span> novel, naturalistic virtual 3-D objects called 'digital embryos' by simulating the <span class="hlt">biological</span> process of embryogenesis14. Virtual phylogenesis (VP) <span class="hlt">creates</span> novel, naturalistic object categories by simulating the evolutionary process of natural selection9,12,13. Objects and object categories <span class="hlt">created</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23149420','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23149420"><span><span class="hlt">Creating</span> objects and object categories for studying perception and perceptual learning.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hauffen, Karin; Bart, Eugene; Brady, Mark; Kersten, Daniel; Hegdé, Jay</p> <p>2012-11-02</p> <p>In order to quantitatively study object perception, be it perception by <span class="hlt">biological</span> systems or by machines, one needs to <span class="hlt">create</span> objects and object categories with precisely definable, preferably naturalistic, properties. Furthermore, for studies <span class="hlt">on</span> perceptual learning, it is useful to <span class="hlt">create</span> novel objects and object categories (or object classes) with such properties. Many innovative and useful methods currently exist for <span class="hlt">creating</span> novel objects and object categories (also see refs. 7,8). However, generally speaking, the existing methods have three broad types of shortcomings. First, shape variations are generally imposed by the experimenter, and may therefore be different from the variability in natural categories, and optimized for a particular recognition algorithm. It would be desirable to have the variations arise independently of the externally imposed constraints. Second, the existing methods have difficulty capturing the shape complexity of natural objects. If the goal is to study natural object perception, it is desirable for objects and object categories to be naturalistic, so as to avoid possible confounds and special cases. Third, it is generally hard to quantitatively measure the available information in the stimuli <span class="hlt">created</span> by conventional methods. It would be desirable to <span class="hlt">create</span> objects and object categories where the available information can be precisely measured and, where necessary, systematically manipulated (or 'tuned'). This allows one to formulate the underlying object recognition tasks in quantitative terms. Here we describe a set of algorithms, or methods, that meet all three of the above criteria. Virtual morphogenesis (VM) <span class="hlt">creates</span> novel, naturalistic virtual 3-D objects called 'digital embryos' by simulating the <span class="hlt">biological</span> process of embryogenesis. Virtual phylogenesis (VP) <span class="hlt">creates</span> novel, naturalistic object categories by simulating the evolutionary process of natural selection. Objects and object categories <span class="hlt">created</span> by these simulations can</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23691473','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23691473"><span>Effect of coriolus versicolor polysaccharide-B <span class="hlt">on</span> the <span class="hlt">biological</span> characteristics of human esophageal carcinoma cell <span class="hlt">line</span> eca109.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Dao-Feng; Lou, Ning; Li, Xiao-Dong</p> <p>2012-09-01</p> <p>To investigate the effect of Coriolus versicolor polysaccharide-B (CVPs-B) <span class="hlt">on</span> the <span class="hlt">biological</span> characteristics of human esophageal carcinoma cell <span class="hlt">line</span> Eca109 in vitro. The cells of experimental group (EG) were cultured in DMEM with 10% FCS and 150µg/mL CVPs-B, the cells of control group (CG) were cultured in DMEM with 10% FCS without CVPs-B. MTT reduction assay was performed to detect the effect of CVPs-B <span class="hlt">on</span> the proliferation of Eca109 cells after the compound was administrated in varying concentrations. The living conditions of the Eca109 cells were determined using trypan blue exclusion. Then, cell growth curves were drawn. Flow cytometry was performed to detect the effect of CVPs-B <span class="hlt">on</span> the apoptosis and cell cycle of Eca109. In comparison with the CG, a marked decrease in the proliferation of Eca09 cells was observed in the EG, after incubation with CVPs-B. The survival rate of Eca09 cells decreased as the time of CVPs-B incubation prolonged. Comparing the cell cycles and apoptotic rates between the two groups, the proportions of cells in the G0/G1, S, and G2/M phases in the EG were found to be (68.4±3.7)%, (13.9±2.1)%, and (17.7±1.4)%, respectively, after 24 h incubation with CVPs-B. The cells had an apoptotic rate of (9.7±0.7)%. <span class="hlt">On</span> the other hand, the proportions of the G0/G1, S, and G2/M cells of the CG were found to be (53.9±3.6)%, (26.6±2.8)%, and (19.5±2.3)%, respectively, with an apoptotic rate of (5.7±1.4)%. In comparison with the CG cells, significant cell growth in the G0/G1 phase was observed in the EG (P<0.05). Furthermore, a significant decrease in the number of cells in the S phase was observed (P<0.05) in the EG. CVPs-B can inhibit proliferation and enhance apoptosis of Eca109 cells and may be useful in the treatment of esophageal carcinoma.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3643661','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3643661"><span>Effect of Coriolus Versicolor Polysaccharide-B <span class="hlt">on</span> the <span class="hlt">Biological</span> Characteristics of Human Esophageal Carcinoma Cell <span class="hlt">Line</span> Eca109</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Wang, Dao-feng; Lou, Ning; Li, Xiao-dong</p> <p>2012-01-01</p> <p>Objective To investigate the effect of Coriolus versicolor polysaccharide-B (CVPs-B) <span class="hlt">on</span> the <span class="hlt">biological</span> characteristics of human esophageal carcinoma cell <span class="hlt">line</span> Eca109 in vitro. Methods The cells of experimental group (EG) were cultured in DMEM with 10% FCS and 150µg/mL CVPs-B, the cells of control group (CG) were cultured in DMEM with 10% FCS without CVPs-B. MTT reduction assay was performed to detect the effect of CVPs-B <span class="hlt">on</span> the proliferation of Eca109 cells after the compound was administrated in varying concentrations. The living conditions of the Eca109 cells were determined using trypan blue exclusion. Then, cell growth curves were drawn. Flow cytometry was performed to detect the effect of CVPs-B <span class="hlt">on</span> the apoptosis and cell cycle of Eca109. Results In comparison with the CG, a marked decrease in the proliferation of Eca09 cells was observed in the EG, after incubation with CVPs-B. The survival rate of Eca09 cells decreased as the time of CVPs-B incubation prolonged. Comparing the cell cycles and apoptotic rates between the two groups, the proportions of cells in the G0/G1, S, and G2/M phases in the EG were found to be (68.4±3.7)%, (13.9±2.1)%, and (17.7±1.4)%, respectively, after 24 h incubation with CVPs-B. The cells had an apoptotic rate of (9.7±0.7)%. <span class="hlt">On</span> the other hand, the proportions of the G0/G1, S, and G2/M cells of the CG were found to be (53.9±3.6)%, (26.6±2.8)%, and (19.5±2.3)%, respectively, with an apoptotic rate of (5.7±1.4)%. In comparison with the CG cells, significant cell growth in the G0/G1 phase was observed in the EG (P<0.05). Furthermore, a significant decrease in the number of cells in the S phase was observed (P<0.05) in the EG. Conclusions CVPs-B can inhibit proliferation and enhance apoptosis of Eca109 cells and may be useful in the treatment of esophageal carcinoma. PMID:23691473</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/911257','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/911257"><span>Monitoring <span class="hlt">Biological</span> Activity at Geothermal Power Plants</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Peter Pryfogle</p> <p>2005-09-01</p> <p>The economic impact of microbial growth in geothermal power plants has been estimated to be as high as $500,000 annually for a 100 MWe plant. Many methods are available to monitor <span class="hlt">biological</span> activity at these facilities; however, very few plants have any <span class="hlt">on-line</span> monitoring program in place. Metal coupon, selective culturing (MPN), total organic carbon (TOC), adenosine triphosphate (ATP), respirometry, phospholipid fatty acid (PLFA), and denaturing gradient gel electrophoresis (DGGE) characterizations have been conducted using water samples collected from geothermal plants located in California and Utah. In addition, the <span class="hlt">on-line</span> performance of a commercial electrochemical monitor, the BIoGEORGE?, has beenmore » evaluated during extended deployments at geothermal facilities. This report provides a review of these techniques, presents data <span class="hlt">on</span> their application from laboratory and field studies, and discusses their value in characterizing and monitoring <span class="hlt">biological</span> activities at geothermal power plants.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4942245','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4942245"><span>Cell <span class="hlt">Line</span> Modeling to Study Biomarker Panel in Prostate Cancer</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>NickKholgh, Bita; Fang, Xiaolan; Winters, Shira M.; Raina, Anvi; Pandya, Komal S.; Gyabaah, Kenneth; Fino, Nora; Balaji, K.C.</p> <p>2016-01-01</p> <p>BACKGROUND African–American men with prostate cancer (PCa) present with higher-grade and -stage tumors compared to Caucasians. While the disparity may result from multiple factors, a <span class="hlt">biological</span> basis is often strongly suspected. Currently, few well-characterized experimental model systems are available to study the <span class="hlt">biological</span> basis of racial disparity in PCa. We report a validated in vitro cell <span class="hlt">line</span> model system that could be used for the purpose. METHODS We assembled a PCa cell <span class="hlt">line</span> model that included currently available African–American PCa cell <span class="hlt">lines</span> and LNCaP (androgen-dependent) and C4-2 (castration-resistant) Caucasian PCa cells. The utility of the cell <span class="hlt">lines</span> in studying the <span class="hlt">biological</span> basis of variance in a malignant phenotype was explored using a multiplex biomarker panel consisting of proteins that have been proven to play a role in the progression of PCa. The panel expression was evaluated by Western blot and RT-PCR in cell <span class="hlt">lines</span> and validated in human PCa tissues by RT-PCR. As proof-of-principle to demonstrate the utility of our model in functional studies, we performed MTS viability assays and molecular studies. RESULTS The dysregulation of the multiplex biomarker panel in primary African–American cell <span class="hlt">line</span> (E006AA) was similar to metastatic Caucasian cell <span class="hlt">lines</span>, which would suggest that the cell <span class="hlt">line</span> model could be used to study an inherent aggressive phenotype in African–American men with PCa. We had previously demonstrated that Protein kinase D1 (PKD1) is a novel kinase that is down regulated in advanced prostate cancer. We established the functional relevance by over expressing PKD1, which resulted in decreased proliferation and epithelial mesenchymal transition (EMT) in PCa cells. Moreover, we established the feasibility of studying the expression of the multiplex biomarker panel in archived human PCa tissue from African–Americans and Caucasians as a prelude to future translational studies. CONCLUSION We have characterized a novel in</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_12 --> <div id="page_13" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="241"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4123686','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4123686"><span>Adhesive micro-<span class="hlt">line</span> periodicity determines guidance of axonal outgrowth†</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Huang, Yu; Fothergill, Thomas; Lumbard, Derek C.; Dent, Erik W.; Williams, Justin C.</p> <p>2014-01-01</p> <p>Adhesive micro-<span class="hlt">lines</span> of various sub-cellular geometries were <span class="hlt">created</span> using a non-traditional micro stamping technique. This technique employed the use of commercially available diffraction gratings as the molds for the micro stamps, a method which is quick and inexpensive, and which could easily be adopted as a patterning tool in a variety of research efforts. The atypical saw-tooth profile of the micro stamps enabled a unique degree of control and flexibility over patterned <span class="hlt">line</span> and gap widths. Cortical neurons cultured <span class="hlt">on</span> patterned poly-lysine micro-<span class="hlt">lines</span> <span class="hlt">on</span> PDMS exhibit a startling transition in axonal guidance: From the expected parallel guidance to an unexpected perpendicular guidance that becomes dominant as patterned <span class="hlt">lines</span> and gaps become sufficiently narrow. This transition is most obvious when the <span class="hlt">lines</span> are narrow relative to gaps, while the periodicity of the pattern is reduced. Axons growing perpendicular to micro-<span class="hlt">lines</span> exhibited ‘vinculated’ growth, a unique morphological phenotype consisting of periodic orthogonal extensions along the axon. PMID:23250489</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28804177','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28804177"><span>Tracking the emergence of synthetic <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shapira, Philip; Kwon, Seokbeom; Youtie, Jan</p> <p>2017-01-01</p> <p>Synthetic <span class="hlt">biology</span> is an emerging domain that combines <span class="hlt">biological</span> and engineering concepts and which has seen rapid growth in research, innovation, and policy interest in recent years. This paper contributes to efforts to delineate this emerging domain by presenting a newly constructed bibliometric definition of synthetic <span class="hlt">biology</span>. Our approach is dimensioned from a core set of papers in synthetic <span class="hlt">biology</span>, using procedures to obtain benchmark synthetic <span class="hlt">biology</span> publication records, extract keywords from these benchmark records, and refine the keywords, supplemented with articles published in dedicated synthetic <span class="hlt">biology</span> journals. We compare our search strategy with other recent bibliometric approaches to define synthetic <span class="hlt">biology</span>, using a common source of publication data for the period from 2000 to 2015. The paper details the rapid growth and international spread of research in synthetic <span class="hlt">biology</span> in recent years, demonstrates that diverse research disciplines are contributing to the multidisciplinary development of synthetic <span class="hlt">biology</span> research, and visualizes this by profiling synthetic <span class="hlt">biology</span> research <span class="hlt">on</span> the map of science. We further show the roles of a relatively concentrated set of research sponsors in funding the growth and trajectories of synthetic <span class="hlt">biology</span>. In addition to discussing these analyses, the paper notes limitations and suggests <span class="hlt">lines</span> for further work.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20160005035','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20160005035"><span>A <span class="hlt">Biological</span> Perspective <span class="hlt">on</span> the Meaning of Time</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Rothschild, Lynn J.</p> <p>2014-01-01</p> <p>We have become impatient waiting for a web page to load, but the first member of our species evolved about 150,000 years ago - a geological instant as brief and as transitory as a text message. The shortest generation time of a bacterium is a sprint at under ten minutes, whereas a 200-year old whale, turtle or tree is not unknown. Life is a phenomenon that integrates processes ranging from the near instantaneous reactions of photosynthesis to the more stately pace of evolution. Here I will elucidate these processes with radically different time scales that go to <span class="hlt">creating</span> and maintaining the diversity of life <span class="hlt">on</span> earth, the clocks that nature uses to time them, and how modern <span class="hlt">biology</span> is being used to alter the natural time scales.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20951646','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20951646"><span>The quality of <span class="hlt">on-line</span> communication in a national learning programme for newly qualified nurses, midwives and allied health professionals.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lauder, W; Roxburgh, M; Atkinson, John; Banks, Pauline; Kane, Helen</p> <p>2011-05-01</p> <p>Asynchronous communication has become the dominant mode of <span class="hlt">on-line</span> instruction and has been incorporated into Flying Start NHS, an <span class="hlt">on-line</span> programme for newly qualified NMAHPs in the transition phase from student to registered practitioner. <span class="hlt">On-line</span> programmes have a number of objectives including the delivery of educational materials and the development of <span class="hlt">on-line</span> communities. This study sought to provide a direct and objective understanding of the quality of the <span class="hlt">on-line</span> community within Flying Start NHS and give an indication of areas of strength and weakness. The study used mixed methods including a Gricean analysis of <span class="hlt">on-line</span> communication focusing <span class="hlt">on</span> quantity, quality, relevance, and manner, and a thematic analysis of communication content. There was little evidence that students engaged in the type of interactive communication essential for <span class="hlt">creating</span> <span class="hlt">on-line</span> learning communities. The majority of postings related to progression through Flying Start. The small number of communications which did begin to engage with the learning materials were limited with little evidence of the development of critical debate. Analysis of the qualitative data indicates that the period of transition continues to be stressful with Flying Start NHS being undertaken concurrently with local CPD being seen as duplication of effort. Copyright © 2010 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26056745','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26056745"><span>The diversification of developmental <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Crowe, Nathan; Dietrich, Michael R; Alomepe, Beverly S; Antrim, Amelia F; ByrneSim, Bay Lauris; He, Yi</p> <p>2015-10-01</p> <p>In the 1960s, "developmental <span class="hlt">biology</span>" became the dominant term to describe some of the research that had previously been included under the rubrics of embryology, growth, morphology, and physiology. As scientific societies formed under this new label, a new discipline took shape. Historians, however, have a number of different perspectives <span class="hlt">on</span> what changes led to this new field of developmental <span class="hlt">biology</span> and how the field itself was constituted during this period. Using the General Embryological Information Service, a global index of post-World War II development-related research, we have documented and visualized significant changes in the kinds of research that occurred as this new field formed. In particular, our analysis supports the claim that the transition toward developmental <span class="hlt">biology</span> was marked by a growth in new topics and forms of research. Although many historians privilege the role of molecular <span class="hlt">biology</span> and/or the molecularization of <span class="hlt">biology</span> in general during this formative period, we have found that the influence of molecular <span class="hlt">biology</span> is not sufficient to account for the wide range of new research that constituted developmental <span class="hlt">biology</span> at the time. Overall, our work <span class="hlt">creates</span> a robust characterization of the changes that occurred with regard to research <span class="hlt">on</span> growth and development in the decades following World War II and provides a context for future work <span class="hlt">on</span> the specific drivers of those changes. Copyright © 2015 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4710404','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4710404"><span>Beyond the <span class="hlt">Biology</span>: A Systematic Investigation of Noncontent Instructor Talk in an Introductory <span class="hlt">Biology</span> Course</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Seidel, Shannon B.; Reggi, Amanda L.; Schinske, Jeffrey N.; Burrus, Laura W.; Tanner, Kimberly D.</p> <p>2015-01-01</p> <p>Instructors <span class="hlt">create</span> classroom environments that have the potential to impact learning by affecting student motivation, resistance, and self-efficacy. However, despite the critical importance of the learning environment in increasing conceptual understanding, little research has investigated what instructors say and do to <span class="hlt">create</span> learning environments in college <span class="hlt">biology</span> classrooms. We systematically investigated the language used by instructors that does not directly relate to course content and defined the construct of Instructor Talk. Transcripts were generated from a semester-long, cotaught introductory <span class="hlt">biology</span> course (n = 270 students). Transcripts were analyzed using a grounded theory approach to identify emergent categories of Instructor Talk. The five emergent categories from analysis of more than 600 quotes were, in order of prevalence, 1) Building the Instructor/Student Relationship, 2) Establishing Classroom Culture, 3) Explaining Pedagogical Choices, 4) Sharing Personal Experiences, and 5) Unmasking Science. Instances of Instructor Talk were present in every class session analyzed and ranged from six to 68 quotes per session. The Instructor Talk framework is a novel research variable that could yield insights into instructor effectiveness, origins of student resistance, and methods for overcoming stereotype threat. Additionally, it holds promise in professional development settings to assist instructors in reflecting <span class="hlt">on</span> the learning environments they <span class="hlt">create</span>. PMID:26582237</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/AD1033539','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/AD1033539"><span>EMERGE: Engineered Materials that <span class="hlt">Create</span> Environments for ReGeneration via Electric Field</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2016-10-01</p> <p>Recruitment of multiple cell <span class="hlt">lines</span> by collagen-synthetic copolymer matrices in corneal regeneration ,” Biomaterials (2004). A) B) REDD-2016-537...AWARD NUMBER: W81XWH-14-1-0542 TITLE: EMERGE: Engineered Materials that <span class="hlt">Create</span> Environments for ReGeneration via Electric Field PRINCIPAL...23 Sep 2016 4. TITLE AND SUBTITLE 5a. CONTRACT NUMBER EMERGE: Engineered Materials that <span class="hlt">Create</span> Environments for ReGeneration via Electric Field</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2592046','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2592046"><span><span class="hlt">Biology</span> in Bloom: Implementing Bloom's Taxonomy to Enhance Student Learning in <span class="hlt">Biology</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Dirks, Clarissa; Wenderoth, Mary Pat</p> <p>2008-01-01</p> <p>We developed the Blooming <span class="hlt">Biology</span> Tool (BBT), an assessment tool based <span class="hlt">on</span> Bloom's Taxonomy, to assist science faculty in better aligning their assessments with their teaching activities and to help students enhance their study skills and metacognition. The work presented here shows how assessment tools, such as the BBT, can be used to guide and enhance teaching and student learning in a discipline-specific manner in postsecondary education. The BBT was first designed and extensively tested for a study in which we ranked almost 600 science questions from college life science exams and standardized tests. The BBT was then implemented in three different collegiate settings. Implementation of the BBT helped us to adjust our teaching to better enhance our students' current mastery of the material, design questions at higher cognitive skills levels, and assist students in studying for college-level exams and in writing study questions at higher levels of Bloom's Taxonomy. From this work we also <span class="hlt">created</span> a suite of complementary tools that can assist <span class="hlt">biology</span> faculty in <span class="hlt">creating</span> classroom materials and exams at the appropriate level of Bloom's Taxonomy and students to successfully develop and answer questions that require higher-order cognitive skills. PMID:19047424</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26998488','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26998488"><span>Establishment and Characterization of a Telomerase-Immortalized Sheep Trophoblast Cell <span class="hlt">Line</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Yufei; Shi, Jing; Liu, Shuying</p> <p>2016-01-01</p> <p>The primary sheep trophoblast cells (STCs) have a finite lifespan in culture. This feature limits the scope for long-term in vitro studies with STCs. This study was an attempt to establish and characterize a telomerase-immortalized sheep trophoblast cell <span class="hlt">line</span>. STCs were isolated and purified by using Percoll and specific immunoaffinity purification, respectively. The purified STCs were transfected with a plasmid carrying sequences of human telomerase reverse transcriptase (hTERT) to <span class="hlt">create</span> immortalized sheep trophoblast cell <span class="hlt">line</span> (hTERT-STCs). hTERT-STCs showed a stable expression of hTERT gene, serially passaged for a year, and showed active proliferation without signs of senescence. Cytokeratin 7 (CK-7), secreted human chorionic gonadotrophin subunit β (CG-β), placental lactogen (PL), and endogenous jaagsiekte sheep retrovirus (enJSRV) envelope genes were expressed in hTERT-STCs. Transwell cell invasion assay indicated that hTERT-STCs still possessed the same invasive characteristics as normal primary sheep trophoblast cells. hTERT-STCs could not grow in soft agar and did not develop into tumors in nude mice. In this study, we established a strain of immortalized sheep trophoblast cell <span class="hlt">line</span> which could be gainfully employed in the future as an experimental model to study trophoblast cells with secretory function, invasive features, and probable <span class="hlt">biological</span> function of enJSRV envelope genes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11600898','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11600898"><span>Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Babinet, C; Cohen-Tannoudji, M</p> <p>2001-09-01</p> <p>The ability to introduce genetic modifications in the germ <span class="hlt">line</span> of complex organisms has been a long-standing goal of those who study developmental <span class="hlt">biology</span>. In this regard, the mouse, a favorite model for the study of the mammals, is unique: indeed not only is it possible since the late seventies, to add genes to the mouse genome like in several other complex organisms but also to perform gene replacement and modification. This has been made possible via two technological breakthroughs: 1) the isolation and culture of embryonic stem cells (ES), which have the unique ability to colonize all the tissues of an host embryo including its germ <span class="hlt">line</span>; 2) the development of methods allowing homologous recombination between an incoming DNA and its cognate chromosomal sequence (gene "targeting"). As a result, it has become possible to <span class="hlt">create</span> mice bearing null mutations in any cloned gene (knock-out mice). Such a possibility has revolutionized the genetic approach of almost all aspects of the <span class="hlt">biology</span> of the mouse. In recent years, the scope of gene targeting has been widened even more, due to the refinement of the knock-out technology: other types of genetic modifications may now be <span class="hlt">created</span>, including subtle mutations (point mutations, micro deletions or insertions, etc.) and chromosomal rearrangements such as large deletions, duplications and translocations. Finally, methods have been devised which permit the creation of conditional mutations, allowing the study of gene function throughout the life of an animal, when gene inactivation entails embryonic lethality. In this paper, we present an overview of the methods and scenarios used for the programmed modification of mouse genome, and we underline their enormous interest for the study of mammalian <span class="hlt">biology</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017APS..DPPJ11039L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017APS..DPPJ11039L"><span>Ross filter development for absolute measurement of Al <span class="hlt">line</span> radiation <span class="hlt">on</span> MST</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lauersdorf, N.; Reusch, L. M.; den Hartog, D. J.; Goetz, J. A.; Franz, P.; Vanmeter, P.</p> <p>2017-10-01</p> <p>The MST has a two-color soft x-ray tomography (SXT) diagnostic that, using the double-filter technique, measures electron temperature (Te) from the slope of the soft x-ray (SXR) continuum. Because MST has an aluminum plasma-facing surface, bright Al <span class="hlt">line</span> radiation occurs in the SXR spectrum. In past application of the double-filter technique, these <span class="hlt">lines</span> have been filtered out using thick Be filters ( 400 μm and 800 μm), restricting the measurement temperature range to >=1 keV due to the signal strength having a positive correlation with Te. Another way to deal with the <span class="hlt">line</span> radiation is to explicitly include it into the SXR spectrum analysis from which Te is derived. A Ross filter set has been designed to measure this <span class="hlt">line</span> radiation, and will enable the absolute intensities of the aluminum <span class="hlt">lines</span> to be quantified and incorporated into the analysis. The Ross filter will be used to measure Al+11 and Al+12 <span class="hlt">lines</span>, occurring between 1.59 and 2.04 keV. By using multiple detectors with filters made of varying element concentrations, we <span class="hlt">create</span> spectral bins in which the dominant transmission is the <span class="hlt">line</span> radiation. Absolute measurement of Al <span class="hlt">line</span> intensities will enable use of thinner filters in the SXT diagnostic and accurate measurement of Te < 1 keV. This material is based upon work supported by the U.S. Department of Energy Office of Science, Office of Fusion Energy Sciences program under Award Numbers DE-FC02-05ER54814 and DE-SC0015474.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23270154','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23270154"><span>Influence of Orientia tsutsugamushi infection <span class="hlt">on</span> the developmental <span class="hlt">biology</span> of Leptotrombidium imphalum and Leptotrombidium chiangraiensis (Acari: Trombiculidae).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Phasomkusolsil, Siriporn; Tanskul, Panita; Ratanatham, Supaporn; Watcharapichat, Pochaman; Phulsuksombati, Duangporn; Frances, Stephen P; Lerdthusnee, Kriangkrai; Linthicum, Kenneth J</p> <p>2012-11-01</p> <p>Leptotrombidium chiangraiensis Tanskul & Linthicum, and Leptotrombidium imphalum Vercammen-Grandjean are important vectors of scrub typhus in rice field habitats in northern Thailand. The developmental <span class="hlt">biology</span> of all stages of the life cycle of two generations of these species of mites infected with Orientia tsutsugamushi (Hayashi) and uninfected mites is reported. The development of the infected <span class="hlt">lines</span> of both F1 and F2 L. chiangraiensis were significantly longer than their respective uninfected <span class="hlt">lines</span> (P < 0.05). The developmental times of uninfected and infected F1 <span class="hlt">lines</span> of L. imphalum were not significantly different; however, F2 infected <span class="hlt">lines</span> took significantly longer to develop (P < 0.05). Both F1 and F2 generations of infected L. imphalum and L. chiangraiensis oviposited <span class="hlt">on</span> average >150 fewer eggs than uninfected mites.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AcSpe.125...25R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AcSpe.125...25R"><span>Utilizing the ratio and the summation of two spectral <span class="hlt">lines</span> for estimation of optical depth: Focus <span class="hlt">on</span> thick plasmas</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rezaei, Fatemeh; Tavassoli, Seyed Hassan</p> <p>2016-11-01</p> <p>In this paper, a study is performed <span class="hlt">on</span> the spectral <span class="hlt">lines</span> of plasma radiations <span class="hlt">created</span> from focusing of the Nd:YAG laser <span class="hlt">on</span> Al standard alloys at atmospheric air pressure. A new theoretical method is presented to investigate the evolution of the optical depth of the plasma based <span class="hlt">on</span> the radiative transfer equation, in LTE condition. This work relies <span class="hlt">on</span> the Boltzmann distribution, <span class="hlt">lines</span> broadening equations, and as well as the self-absorption relation. Then, an experimental set-up is devised to extract some of plasma parameters such as temperature from modified <span class="hlt">line</span> ratio analysis, electron density from Stark broadening mechanism, <span class="hlt">line</span> intensities of two spectral <span class="hlt">lines</span> in the same order of ionization from similar species, and the plasma length from the shadowgraphy section. In this method, the summation and the ratio of two spectral <span class="hlt">lines</span> are considered for evaluation of the temporal variations of the plasma parameters in a LIBS homogeneous plasma. The main advantage of this method is that it comprises the both of thin and thick laser induced plasmas without straight calculation of self-absorption coefficient. Moreover, the presented model can also be utilized for evaluation the transition of plasma from the thin condition to the thick one. The results illustrated that by measuring the <span class="hlt">line</span> intensities of two spectral <span class="hlt">lines</span> at different evolution times, the plasma cooling and the growth of the optical depth can be followed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24877076','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24877076"><span>OWL reasoning framework over big <span class="hlt">biological</span> knowledge network.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chen, Huajun; Chen, Xi; Gu, Peiqin; Wu, Zhaohui; Yu, Tong</p> <p>2014-01-01</p> <p>Recently, huge amounts of data are generated in the domain of <span class="hlt">biology</span>. Embedded with domain knowledge from different disciplines, the isolated <span class="hlt">biological</span> resources are implicitly connected. Thus it has shaped a big network of versatile <span class="hlt">biological</span> knowledge. Faced with such massive, disparate, and interlinked <span class="hlt">biological</span> data, providing an efficient way to model, integrate, and analyze the big <span class="hlt">biological</span> network becomes a challenge. In this paper, we present a general OWL (web ontology language) reasoning framework to study the implicit relationships among <span class="hlt">biological</span> entities. A comprehensive <span class="hlt">biological</span> ontology across traditional Chinese medicine (TCM) and western medicine (WM) is used to <span class="hlt">create</span> a conceptual model for the <span class="hlt">biological</span> network. Then corresponding <span class="hlt">biological</span> data is integrated into a <span class="hlt">biological</span> knowledge network as the data model. Based <span class="hlt">on</span> the conceptual model and data model, a scalable OWL reasoning method is utilized to infer the potential associations between <span class="hlt">biological</span> entities from the <span class="hlt">biological</span> network. In our experiment, we focus <span class="hlt">on</span> the association discovery between TCM and WM. The derived associations are quite useful for biologists to promote the development of novel drugs and TCM modernization. The experimental results show that the system achieves high efficiency, accuracy, scalability, and effectivity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4022201','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4022201"><span>OWL Reasoning Framework over Big <span class="hlt">Biological</span> Knowledge Network</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Chen, Huajun; Chen, Xi; Gu, Peiqin; Wu, Zhaohui; Yu, Tong</p> <p>2014-01-01</p> <p>Recently, huge amounts of data are generated in the domain of <span class="hlt">biology</span>. Embedded with domain knowledge from different disciplines, the isolated <span class="hlt">biological</span> resources are implicitly connected. Thus it has shaped a big network of versatile <span class="hlt">biological</span> knowledge. Faced with such massive, disparate, and interlinked <span class="hlt">biological</span> data, providing an efficient way to model, integrate, and analyze the big <span class="hlt">biological</span> network becomes a challenge. In this paper, we present a general OWL (web ontology language) reasoning framework to study the implicit relationships among <span class="hlt">biological</span> entities. A comprehensive <span class="hlt">biological</span> ontology across traditional Chinese medicine (TCM) and western medicine (WM) is used to <span class="hlt">create</span> a conceptual model for the <span class="hlt">biological</span> network. Then corresponding <span class="hlt">biological</span> data is integrated into a <span class="hlt">biological</span> knowledge network as the data model. Based <span class="hlt">on</span> the conceptual model and data model, a scalable OWL reasoning method is utilized to infer the potential associations between <span class="hlt">biological</span> entities from the <span class="hlt">biological</span> network. In our experiment, we focus <span class="hlt">on</span> the association discovery between TCM and WM. The derived associations are quite useful for biologists to promote the development of novel drugs and TCM modernization. The experimental results show that the system achieves high efficiency, accuracy, scalability, and effectivity. PMID:24877076</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA496344','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA496344"><span>FDA Regulation of Follow-<span class="hlt">On</span> <span class="hlt">Biologics</span></span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2009-02-24</p> <p>opening a pathway for the approval of follow-<span class="hlt">on</span> <span class="hlt">biologics</span>. A <span class="hlt">biologic</span> is a preparation, such as a drug or a vaccine , that is made from living...2006 Drug Trend Report, April 2006, p. 38. C <span class="hlt">Biologic</span> vs. Follow-<span class="hlt">on</span> <span class="hlt">Biologic</span> A <span class="hlt">biologic</span> is a preparation, such as a drug or a vaccine , that is...doc9496/s1695.pdf. 19 Thijs J. Giezen, Aukje K. Mantel-Teeuwisse, and Sabine M. J. M. Straus, et al., “Safety-related regulatory actions for <span class="hlt">biologicals</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25108565','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25108565"><span>How chemistry supports cell <span class="hlt">biology</span>: the chemical toolbox at your service.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wijdeven, Ruud H; Neefjes, Jacques; Ovaa, Huib</p> <p>2014-12-01</p> <p>Chemical <span class="hlt">biology</span> is a young and rapidly developing scientific field. In this field, chemistry is inspired by <span class="hlt">biology</span> to <span class="hlt">create</span> various tools to monitor and modulate biochemical and cell <span class="hlt">biological</span> processes. Chemical contributions such as small-molecule inhibitors and activity-based probes (ABPs) can provide new and unique insights into previously unexplored cellular processes. This review provides an overview of recent breakthroughs in chemical <span class="hlt">biology</span> that are likely to have a significant impact <span class="hlt">on</span> cell <span class="hlt">biology</span>. We also discuss the application of several chemical tools in cell <span class="hlt">biology</span> research. Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=existence+AND+business&id=EJ792336','ERIC'); return false;" href="https://eric.ed.gov/?q=existence+AND+business&id=EJ792336"><span>Developing New <span class="hlt">Lines</span> of Business: A Case Study</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Clegg, Judith; Smart, Dawn Hanson</p> <p>2006-01-01</p> <p>Developing a new <span class="hlt">line</span> of business in an independent consulting firm provides an excellent way to expand, increase income for the company, and <span class="hlt">create</span> cross-marketing opportunities. If it is not done correctly, however, this potential opportunity can imperil the existence of the business. This chapter's case highlights the benefits new <span class="hlt">lines</span> of…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=310620','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=310620"><span>Measure of mechanical impacts in commercial blueberry packing <span class="hlt">lines</span> and potential damage to blueberry fruit</span></a></p> <p><a target="_blank" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>Modern blueberry packing <span class="hlt">lines</span> <span class="hlt">create</span> impact damage to blueberries which will result in fruit bruising. In this study, impacts <span class="hlt">created</span> by commercial blueberry packing <span class="hlt">lines</span> were measured quantitatively using a miniature instrumented sphere. Impacts were recorded at transfer points. Average peakG ...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28849556','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28849556"><span>sbv IMPROVER: Modern Approach to Systems <span class="hlt">Biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Guryanova, Svetlana; Guryanova, Anna</p> <p>2017-01-01</p> <p>The increasing amount and variety of data in biosciences call for innovative methods of visualization, scientific verification, and pathway analysis. Novel approaches to <span class="hlt">biological</span> networks and research quality control are important because of their role in development of new products, improvement, and acceleration of existing health policies and research for novel ways of solving scientific challenges. One such approach is sbv IMPROVER. It is a platform that uses crowdsourcing and verification to <span class="hlt">create</span> <span class="hlt">biological</span> networks with easy public access. It contains 120 networks built in <span class="hlt">Biological</span> Expression Language (BEL) to interpret data from PubMed articles with high-quality verification available for free <span class="hlt">on</span> the CBN database. Computable, human-readable <span class="hlt">biological</span> networks with a structured syntax are a powerful way of representing <span class="hlt">biological</span> information generated from high-density data. This article presents sbv IMPROVER, a crowd-verification approach for the visualization and expansion of <span class="hlt">biological</span> networks.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_13 --> <div id="page_14" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="261"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3597627','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3597627"><span>Phenotypes and Karyotypes of Human Malignant Mesothelioma Cell <span class="hlt">Lines</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Relan, Vandana; Morrison, Leanne; Parsonson, Kylie; Clarke, Belinda E.; Duhig, Edwina E.; Windsor, Morgan N.; Matar, Kevin S.; Naidoo, Rishendran; Passmore, Linda; McCaul, Elizabeth; Courtney, Deborah; Yang, Ian A.; Fong, Kwun M.; Bowman, Rayleen V.</p> <p>2013-01-01</p> <p>Background Malignant mesothelioma is an aggressive tumour of serosal surfaces most commonly pleura. Characterised cell <span class="hlt">lines</span> represent a valuable tool to study the <span class="hlt">biology</span> of mesothelioma. The aim of this study was to develop and <span class="hlt">biologically</span> characterise six malignant mesothelioma cell <span class="hlt">lines</span> to evaluate their potential as models of human malignant mesothelioma. Methods Five <span class="hlt">lines</span> were initiated from pleural biopsies, and one from pleural effusion of patients with histologically proven malignant mesothelioma. Mesothelial origin was assessed by standard morphology, Transmission Electron Microscopy (TEM) and immunocytochemistry. Growth characteristics were assayed using population doubling times. Spectral karyotyping was performed to assess chromosomal abnormalities. Authentication of donor specific derivation was undertaken by DNA fingerprinting using a panel of SNPs. Results Most of cell <span class="hlt">lines</span> exhibited spindle cell shape, with some retaining stellate shapes. At passage 2 to 6 all <span class="hlt">lines</span> stained positively for calretinin and cytokeratin 19, and demonstrated capacity for anchorage-independent growth. At passage 4 to 16, doubling times ranged from 30–72 hours, and <span class="hlt">on</span> spectral karyotyping all <span class="hlt">lines</span> exhibited numerical chromosomal abnormalities ranging from 41 to 113. Monosomy of chromosomes 8, 14, 22 or 17 was observed in three <span class="hlt">lines</span>. One <span class="hlt">line</span> displayed four different karyotypes at passage 8, but only one karyotype at passage 42, and another displayed polyploidy at passage 40 which was not present at early passages. At passages 5–17, TEM showed characteristic features of mesothelioma ultrastructure in all <span class="hlt">lines</span> including microvilli and tight intercellular junctions. Conclusion These six cell <span class="hlt">lines</span> exhibit varying cell morphology, a range of doubling times, and show diverse passage-dependent structural chromosomal changes observed in malignant tumours. However they retain characteristic immunocytochemical protein expression profiles of mesothelioma during</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012PhDT.......425B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012PhDT.......425B"><span>The use of <span class="hlt">on-line</span> characterization technologies during the manufacture of nanostructured materials</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Barbas, Joana Margarida de Oliveira</p> <p></p> <p>Since their potential has become widely recognized, one of the major research <span class="hlt">lines</span> <span class="hlt">on</span> polymer-clay nanocomposites has focused <span class="hlt">on</span> the preparation of well dispersed systems, which involves investigating their compounding (including their structural and morphological characterization) and the determination of their physical and mechanical performances. Currently, there is an understanding that a high degree of dispersion, particularly exfoliation, of the nanoclay is required to improve the overall performance. Although the influencing parameters are known - interfacial adhesion, chemical affinity and operating conditions - the effect of each <span class="hlt">on</span> the onset and extent of the organoclay dispersion are still subject of debate. Twin screw extrusion allows for control of the main variables (shear, stress and time), but also, due to the typical modular construction, offers a high degree of freedom in <span class="hlt">creating</span> the adequate screw design and enables knowledgeable alteration of the barrel. These features offer a solid basis for the development and implementation of apt <span class="hlt">on-line/in-line</span> monitoring techniques, able to follow up the evolution of dispersion of polymer-clay nanocomposites during processing. This research included the validation, implementation and application of a methodology based <span class="hlt">on</span> inline Near-Infrared (NIR) Spectroscopy for the characterization of the dispersion along the extruder axis. The results showed that the operating conditions have great impact <span class="hlt">on</span> the dispersion level, but also that degradation may affect the interfacial chemistry of the system, altering the dispersion pathways. Overall the results obtained confirm that NIR is a valid tool for the <span class="hlt">on-line</span> characterization of these materials, offering the possibility of assessing in real time the clay dispersion, enabling proper corrective and optimization actions over the material characteristics in a timely manner.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3044748','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3044748"><span>Standard <span class="hlt">Biological</span> Parts Knowledgebase</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Galdzicki, Michal; Rodriguez, Cesar; Chandran, Deepak; Sauro, Herbert M.; Gennari, John H.</p> <p>2011-01-01</p> <p>We have <span class="hlt">created</span> the Knowledgebase of Standard <span class="hlt">Biological</span> Parts (SBPkb) as a publically accessible Semantic Web resource for synthetic <span class="hlt">biology</span> (sbolstandard.org). The SBPkb allows researchers to query and retrieve standard <span class="hlt">biological</span> parts for research and use in synthetic <span class="hlt">biology</span>. Its initial version includes all of the information about parts stored in the Registry of Standard <span class="hlt">Biological</span> Parts (partsregistry.org). SBPkb transforms this information so that it is computable, using our semantic framework for synthetic <span class="hlt">biology</span> parts. This framework, known as SBOL-semantic, was built as part of the Synthetic <span class="hlt">Biology</span> Open Language (SBOL), a project of the Synthetic <span class="hlt">Biology</span> Data Exchange Group. SBOL-semantic represents commonly used synthetic <span class="hlt">biology</span> entities, and its purpose is to improve the distribution and exchange of descriptions of <span class="hlt">biological</span> parts. In this paper, we describe the data, our methods for transformation to SBPkb, and finally, we demonstrate the value of our knowledgebase with a set of sample queries. We use RDF technology and SPARQL queries to retrieve candidate “promoter” parts that are known to be both negatively and positively regulated. This method provides new web based data access to perform searches for parts that are not currently possible. PMID:21390321</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21390321','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21390321"><span>Standard <span class="hlt">biological</span> parts knowledgebase.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Galdzicki, Michal; Rodriguez, Cesar; Chandran, Deepak; Sauro, Herbert M; Gennari, John H</p> <p>2011-02-24</p> <p>We have <span class="hlt">created</span> the Knowledgebase of Standard <span class="hlt">Biological</span> Parts (SBPkb) as a publically accessible Semantic Web resource for synthetic <span class="hlt">biology</span> (sbolstandard.org). The SBPkb allows researchers to query and retrieve standard <span class="hlt">biological</span> parts for research and use in synthetic <span class="hlt">biology</span>. Its initial version includes all of the information about parts stored in the Registry of Standard <span class="hlt">Biological</span> Parts (partsregistry.org). SBPkb transforms this information so that it is computable, using our semantic framework for synthetic <span class="hlt">biology</span> parts. This framework, known as SBOL-semantic, was built as part of the Synthetic <span class="hlt">Biology</span> Open Language (SBOL), a project of the Synthetic <span class="hlt">Biology</span> Data Exchange Group. SBOL-semantic represents commonly used synthetic <span class="hlt">biology</span> entities, and its purpose is to improve the distribution and exchange of descriptions of <span class="hlt">biological</span> parts. In this paper, we describe the data, our methods for transformation to SBPkb, and finally, we demonstrate the value of our knowledgebase with a set of sample queries. We use RDF technology and SPARQL queries to retrieve candidate "promoter" parts that are known to be both negatively and positively regulated. This method provides new web based data access to perform searches for parts that are not currently possible.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMIN21D0064C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMIN21D0064C"><span><span class="hlt">CREATE</span>-IP and <span class="hlt">CREATE</span>-V: Data and Services Update</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Carriere, L.; Potter, G. L.; Hertz, J.; Peters, J.; Maxwell, T. P.; Strong, S.; Shute, J.; Shen, Y.; Duffy, D.</p> <p>2017-12-01</p> <p>The NASA Center for Climate Simulation (NCCS) at the Goddard Space Flight Center and the Earth System Grid Federation (ESGF) are working together to build a uniform environment for the comparative study and use of a group of reanalysis datasets of particular importance to the research community. This effort is called the Collaborative REAnalysis Technical Environment (<span class="hlt">CREATE</span>) and it contains two components: the <span class="hlt">CREATE</span>-Intercomparison Project (<span class="hlt">CREATE</span>-IP) and <span class="hlt">CREATE</span>-V. This year's efforts included generating and publishing an atmospheric reanalysis ensemble mean and spread and improving the analytics available through <span class="hlt">CREATE</span>-V. Related activities included adding access to subsets of the reanalysis data through ArcGIS and expanding the visualization tool to GMAO forecast data. This poster will present the access mechanisms to this data and use cases including example Jupyter Notebook code. The reanalysis ensemble was generated using two methods, first using standard Python tools for regridding, extracting levels and <span class="hlt">creating</span> the ensemble mean and spread <span class="hlt">on</span> a virtual server in the NCCS environment. The second was using a new analytics software suite, the Earth Data Analytics Services (EDAS), coupled with a high-performance Data Analytics and Storage System (DASS) developed at the NCCS. Results were compared to validate the EDAS methodologies, and the results, including time to process, will be presented. The ensemble includes selected 6 hourly and monthly variables, regridded to 1.25 degrees, with 24 common levels used for the 3D variables. Use cases for the new data and services will be presented, including the use of EDAS for the backend analytics <span class="hlt">on</span> <span class="hlt">CREATE</span>-V, the use of the GMAO forecast aerosol and cloud data in <span class="hlt">CREATE</span>-V, and the ability to connect <span class="hlt">CREATE</span>-V data to NCCS ArcGIS services.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28981255','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28981255"><span><span class="hlt">On-Line</span> Ion Exchange Liquid Chromatography as a Process Analytical Technology for Monoclonal Antibody Characterization in Continuous Bioprocessing.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Patel, Bhumit A; Pinto, Nuno D S; Gospodarek, Adrian; Kilgore, Bruce; Goswami, Kudrat; Napoli, William N; Desai, Jayesh; Heo, Jun H; Panzera, Dominick; Pollard, David; Richardson, Daisy; Brower, Mark; Richardson, Douglas D</p> <p>2017-11-07</p> <p>Combining process analytical technology (PAT) with continuous production provides a powerful tool to observe and control monoclonal antibody (mAb) fermentation and purification processes. This work demonstrates <span class="hlt">on-line</span> liquid chromatography (<span class="hlt">on-line</span> LC) as a PAT tool for monitoring a continuous <span class="hlt">biologics</span> process and forced degradation studies. Specifically, this work focused <span class="hlt">on</span> ion exchange chromatography (IEX), which is a critical separation technique to detect charge variants. Product-related impurities, including charge variants, that impact function are classified as critical quality attributes (CQAs). First, we confirmed no significant differences were observed in the charge heterogeneity profile of a mAb through both at-<span class="hlt">line</span> and <span class="hlt">on-line</span> sampling and that the <span class="hlt">on-line</span> method has the ability to rapidly detect changes in protein quality over time. The robustness and versatility of the PAT methods were tested by sampling from two purification locations in a continuous mAb process. The PAT IEX methods used with <span class="hlt">on-line</span> LC were a weak cation exchange (WCX) separation and a newly developed shorter strong cation exchange (SCX) assay. Both methods provided similar results with the distribution of percent acidic, main, and basic species remaining unchanged over a 2 week period. Second, a forced degradation study showed an increase in acidic species and a decrease in basic species when sampled <span class="hlt">on-line</span> over 7 days. These applications further strengthen the use of <span class="hlt">on-line</span> LC to monitor CQAs of a mAb continuously with various PAT IEX analytical methods. Implementation of <span class="hlt">on-line</span> IEX will enable faster decision making during process development and could potentially be applied to control in biomanufacturing.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/12101956','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/12101956"><span><span class="hlt">On-line</span> hemodiafiltration. Gold standard or top therapy?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Passlick-Deetjen, Jutta; Pohlmeier, Robert</p> <p>2002-01-01</p> <p>In summary, <span class="hlt">on-line</span> HDF is an extracorporeal blood purification therapy with increased convective removal of uremic toxins as compared to the most frequently used low- or high-flux HD therapy. The clinical advantages of <span class="hlt">on-line</span> HDF have shown to be dose dependent, which makes <span class="hlt">on-line</span> HDF superior to other therapies with less convective solute removal. Among the therapies with high convective solute removal, i.e. <span class="hlt">on-line</span> HDF, <span class="hlt">on-line</span> HF and double high-flux dialysis, it is difficult to finally decide <span class="hlt">on</span> the best therapy, as direct comparisons of these therapies are not performed. Theoretical considerations like the relative to <span class="hlt">on-line</span> HDF lower achievable Kt/Vurea with <span class="hlt">on-line</span> HF, allow to state that <span class="hlt">on-line</span> HDF is the top therapy now available for patients with ESRD. A gold standard may be defined as something with which everything else is compared if one tries to establish it in the respective field. In order to declare <span class="hlt">on-line</span> HDF as the gold standard in renal replacement therapy, we need more direct comparisons of <span class="hlt">on-line</span> HDF with other therapies, including mortality as an outcome parameter. However, based <span class="hlt">on</span> our current knowledge, it does not seem to be too speculative that high-quality clinical studies will establish <span class="hlt">on-line</span> HDF in the next years as the new gold standard in renal replacement therapy.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25821530','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25821530"><span>Convergent <span class="hlt">Lines</span> of Descent: Symptoms, Patterns, Constellations, and the Emergent Interface of Systems <span class="hlt">Biology</span> and Chinese Medicine.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Scheid, Volker</p> <p>2014-03-01</p> <p>During the first decade of the twenty-first century, a network composed of politicians, regulators, bioscientists, clinical researchers, and Chinese medicine specialists has emerged that seeks to bridge an imagined gulf between the modern West and ancient China in order to <span class="hlt">create</span> a new type of personalized medicine. The central building block of this bridge is the Chinese medical concept of zheng /, variously translated into English as syndrome, pattern, or type. My paper places side by side two different genealogies of how zheng assumed this central role. The first genealogy examines the process by means of which zheng came to be considered as something shared by both ancient China and cutting-edge <span class="hlt">biological</span> science and, by extension, how it manages to hold together the entire institutional, political, and economic framework into which this bridge is embedded and which it co-<span class="hlt">creates</span>. The second genealogy shows zheng to be central to a much older series of redefinitions of Chinese medicine and Chinese medical practice that extend from the eleventh century to the present. Read together, these two genealogies-neither of which should be seen as exhaustive-raise three important issues that are further discussed in the conclusion of the paper. First, I explore how the concept of zheng has come to tie a medical tradition derided by its adversaries for being a pseudoscience to one of the most cutting-edge fields of bioscience research. I ask what is at stake in this synthesis, for whom, and why, and how it transforms Chinese medicine and/or systems <span class="hlt">biology</span> along the way. Second, I am interested in finding out how and why the very same concept can be at the heart of two apparently agonistic visions of Chinese medicine's future as it is popularly imagined in China today. Finally, I insist that the medical humanities need to become actively involved in the construction of emergent articulations such as the ones I am exploring. Merely writing a history of the present will</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4374107','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4374107"><span>Convergent <span class="hlt">Lines</span> of Descent: Symptoms, Patterns, Constellations, and the Emergent Interface of Systems <span class="hlt">Biology</span> and Chinese Medicine</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Scheid, Volker</p> <p>2015-01-01</p> <p>During the first decade of the twenty-first century, a network composed of politicians, regulators, bioscientists, clinical researchers, and Chinese medicine specialists has emerged that seeks to bridge an imagined gulf between the modern West and ancient China in order to <span class="hlt">create</span> a new type of personalized medicine. The central building block of this bridge is the Chinese medical concept of zheng 證/証, variously translated into English as syndrome, pattern, or type. My paper places side by side two different genealogies of how zheng assumed this central role. The first genealogy examines the process by means of which zheng came to be considered as something shared by both ancient China and cutting-edge <span class="hlt">biological</span> science and, by extension, how it manages to hold together the entire institutional, political, and economic framework into which this bridge is embedded and which it co-<span class="hlt">creates</span>. The second genealogy shows zheng to be central to a much older series of redefinitions of Chinese medicine and Chinese medical practice that extend from the eleventh century to the present. Read together, these two genealogies—neither of which should be seen as exhaustive—raise three important issues that are further discussed in the conclusion of the paper. First, I explore how the concept of zheng has come to tie a medical tradition derided by its adversaries for being a pseudoscience to one of the most cutting-edge fields of bioscience research. I ask what is at stake in this synthesis, for whom, and why, and how it transforms Chinese medicine and/or systems <span class="hlt">biology</span> along the way. Second, I am interested in finding out how and why the very same concept can be at the heart of two apparently agonistic visions of Chinese medicine’s future as it is popularly imagined in China today. Finally, I insist that the medical humanities need to become actively involved in the construction of emergent articulations such as the ones I am exploring. Merely writing a history of the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18205066','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18205066"><span>Synthesis and <span class="hlt">biological</span> activity of chloroethyl pyrimidine nucleosides.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Colombeau, Ludovic; Teste, Karine; Hadj-Bouazza, Amel; Chaleix, Vincent; Zerrouki, Rachida; Kraemer, Michel; Catherine, Odile Sainte</p> <p>2008-02-01</p> <p>The synthesis and <span class="hlt">biological</span> activity of chloroethyl pyrimidine nucleosides is presented. One of these new nucleosides analogues significantly inhibited cell proliferation, migration and invasion as tested in vitro <span class="hlt">on</span> the A431 vulvar epidermal carcinoma cell <span class="hlt">line</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ1102793.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ1102793.pdf"><span>Effects of Web Based Inquiry Science Environment <span class="hlt">on</span> Cognitive Outcomes in <span class="hlt">Biological</span> Science in Correlation to Emotional Intelligence</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Manoj, T. I.; Devanathan, S.</p> <p>2010-01-01</p> <p>This research study is the report of an experiment conducted to find out the effects of web based inquiry science environment <span class="hlt">on</span> cognitive outcomes in <span class="hlt">Biological</span> science in correlation to Emotional intelligence. Web based inquiry science environment (WISE) provides a platform for <span class="hlt">creating</span> inquiry-based science projects for students to work…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20160008946','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20160008946"><span>Where Synthetic <span class="hlt">Biology</span> Meets ET</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Rothschild, Lynn J.</p> <p>2016-01-01</p> <p>Synthetic <span class="hlt">biology</span> - the design and construction of new <span class="hlt">biological</span> parts and systems and the redesign of existing ones for useful purposes - has the potential to transform fields from pharmaceuticals to fuels. Our lab has focused <span class="hlt">on</span> the potential of synthetic <span class="hlt">biology</span> to revolutionize all three major parts of astrobiology: Where do we come from? Where are we going? and Are we alone? For the first and third, synthetic <span class="hlt">biology</span> is allowing us to answer whether the evolutionary narrative that has played out <span class="hlt">on</span> planet earth is likely to have been unique or universal. For example, in our lab we are re-evolving the biosynthetic pathways of amino acids in order to understand potential capabilities of an early organism with a limited repertoire of amino acids and developing techniques for the recovery of metals from spent electronics <span class="hlt">on</span> other planetary bodies. And what about the limits for life? Can we <span class="hlt">create</span> organisms that expand the envelope for life? In the future synthetic <span class="hlt">biology</span> will play an increasing role in human activities both <span class="hlt">on</span> earth, in fields as diverse as human health and the industrial production of novel bio-composites. Beyond earth, we will rely increasingly <span class="hlt">on</span> <span class="hlt">biologically</span>-provided life support, as we have throughout our evolutionary history. In order to do this, the field will build <span class="hlt">on</span> two of the great contributions of astrobiology: studies of the origin of life and life in extreme environments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1999JPFR...75..672I','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1999JPFR...75..672I"><span><span class="hlt">Biological</span> and Agricultural Studies <span class="hlt">on</span> Application of Discharge Plasma and Electromagnetic Fields 5. Effects of High Electric Fields <span class="hlt">on</span> Animals</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Isaka, Katsuo</p> <p></p> <p>The <span class="hlt">biological</span> effects of extremely low frequency electric fields <span class="hlt">on</span> animals are reviewed with emphasis <span class="hlt">on</span> studies of the nervous system, behavior, endocrinology, and blood chemistry. First, this paper provides a histrical overview of studies <span class="hlt">on</span> the electric field effects initiated in Russia and the United States mainly regarding electric utility workers in high voltage substations and transmission <span class="hlt">lines</span>. Then, the possible mechanisms of electric field effects are explained using the functions of surface electric fields and induced currents in <span class="hlt">biological</span> objects. The real mechanisms have not yet been identified. The thresholds of electric field perception levels for rats, baboons, and humans are introduced and compared. The experimental results concerning the depression of melatonin secretion in rats exposed to electric fields are described.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20000032105','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20000032105"><span>RF Transmission <span class="hlt">Lines</span> <span class="hlt">on</span> Silicon Substrates</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Ponchak, George E.</p> <p>1999-01-01</p> <p>A review of RF transmission <span class="hlt">lines</span> <span class="hlt">on</span> silicon substrates is presented. Through measurements and calculated results, it is shown that attenuation is dominated by conductor loss if silicon substrates with a resistivity greater than 2500 Ohm-cm are used. Si passivation layers affect the transmission <span class="hlt">line</span> attenuation; however, measured results demonstrate that passivation layers do not necessarily increase attenuation. If standard, low resistivity Si wafers must be used, alternative transmission <span class="hlt">lines</span> such as thin film microstrip and Co-Planar Waveguide (CPW) <span class="hlt">on</span> thick polyimide layers must be used. Measured results presented here show that low loss per unit length is achievable with these transmission <span class="hlt">lines</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29358079','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29358079"><span>Bacterial RNA <span class="hlt">Biology</span> <span class="hlt">on</span> a Genome Scale.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hör, Jens; Gorski, Stanislaw A; Vogel, Jörg</p> <p>2018-06-07</p> <p>Bacteria are an exceedingly diverse group of organisms whose molecular exploration is experiencing a renaissance. While the classical view of bacterial gene expression was relatively simple, the emerging view is more complex, encompassing extensive post-transcriptional control involving riboswitches, RNA thermometers, and regulatory small RNAs (sRNAs) associated with the RNA-binding proteins CsrA, Hfq, and ProQ, as well as CRISPR/Cas systems that are programmed by RNAs. Moreover, increasing interest in members of the human microbiota and environmental microbial communities has highlighted the importance of understudied bacterial species with largely unknown transcriptome structures and RNA-based control mechanisms. Collectively, this <span class="hlt">creates</span> a need for global RNA <span class="hlt">biology</span> approaches that can rapidly and comprehensively analyze the RNA composition of a bacterium of interest. We review such approaches with a focus <span class="hlt">on</span> RNA-seq as a versatile tool to investigate the different layers of gene expression in which RNA is made, processed, regulated, modified, translated, and turned over. Copyright © 2017 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28765873','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28765873"><span>Classification of cancer cell <span class="hlt">lines</span> using matrix-assisted laser desorption/ionization time‑of‑flight mass spectrometry and statistical analysis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Serafim, Vlad; Shah, Ajit; Puiu, Maria; Andreescu, Nicoleta; Coricovac, Dorina; Nosyrev, Alexander; Spandidos, Demetrios A; Tsatsakis, Aristides M; Dehelean, Cristina; Pinzaru, Iulia</p> <p>2017-10-01</p> <p>Over the past decade, matrix-assisted laser desorption/ionization time‑of‑flight mass spectrometry (MALDI‑TOF MS) has been established as a valuable platform for microbial identification, and it is also frequently applied in <span class="hlt">biology</span> and clinical studies to identify new markers expressed in pathological conditions. The aim of the present study was to assess the potential of using this approach for the classification of cancer cell <span class="hlt">lines</span> as a quantifiable method for the proteomic profiling of cellular organelles. Intact protein extracts isolated from different tumor cell <span class="hlt">lines</span> (human and murine) were analyzed using MALDI‑TOF MS and the obtained mass lists were processed using principle component analysis (PCA) within Bruker Biotyper® software. Furthermore, reference spectra were <span class="hlt">created</span> for each cell <span class="hlt">line</span> and were used for classification. Based <span class="hlt">on</span> the intact protein profiles, we were able to differentiate and classify six cancer cell <span class="hlt">lines</span>: two murine melanoma (B16‑F0 and B164A5), one human melanoma (A375), two human breast carcinoma (MCF7 and MDA‑MB‑231) and one human liver carcinoma (HepG2). The cell <span class="hlt">lines</span> were classified according to cancer type and the species they originated from, as well as by their metastatic potential, offering the possibility to differentiate non‑invasive from invasive cells. The obtained results pave the way for developing a broad‑based strategy for the identification and classification of cancer cells.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24456507','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24456507"><span>The TRANSPLANTA collection of Arabidopsis <span class="hlt">lines</span>: a resource for functional analysis of transcription factors based <span class="hlt">on</span> their conditional overexpression.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Coego, Alberto; Brizuela, Esther; Castillejo, Pablo; Ruíz, Sandra; Koncz, Csaba; del Pozo, Juan C; Piñeiro, Manuel; Jarillo, José A; Paz-Ares, Javier; León, José</p> <p>2014-03-01</p> <p>Transcription factors (TFs) are key regulators of gene expression in all organisms. In eukaryotes, TFs are often represented by functionally redundant members of large gene families. Overexpression might prove a means to unveil the <span class="hlt">biological</span> functions of redundant TFs; however, constitutive overexpression of TFs frequently causes severe developmental defects, preventing their functional characterization. Conditional overexpression strategies help to overcome this problem. Here, we report <span class="hlt">on</span> the TRANSPLANTA collection of Arabidopsis <span class="hlt">lines</span>, each expressing one of 949 TFs under the control of a β-estradiol-inducible promoter. Thus far, 1636 independent homozygous <span class="hlt">lines</span>, representing an average of 2.6 <span class="hlt">lines</span> for every TF, have been produced for the inducible expression of 634 TFs. Along with a GUS-GFP reporter, randomly selected TRANSPLANTA <span class="hlt">lines</span> were tested and confirmed for conditional transgene expression upon β-estradiol treatment. As a proof of concept for the exploitation of this resource, β-estradiol-induced proliferation of root hairs, dark-induced senescence, anthocyanin accumulation and dwarfism were observed in <span class="hlt">lines</span> conditionally expressing full-length cDNAs encoding RHD6, WRKY22, MYB123/TT2 and MYB26, respectively, in agreement with previously reported phenotypes conferred by these TFs. Further screening performed with other TRANSPLANTA <span class="hlt">lines</span> allowed the identification of TFs involved in different plant <span class="hlt">biological</span> processes, illustrating that the collection is a powerful resource for the functional characterization of TFs. For instance, ANAC058 and a TINY/AP2 TF were identified as modulators of ABA-mediated germination potential, and RAP2.10/DEAR4 was identified as a regulator of cell death in the hypocotyl-root transition zone. Seeds of TRANSPLANTA <span class="hlt">lines</span> have been deposited at the Nottingham Arabidopsis Stock Centre for further distribution. © 2014 The Authors The Plant Journal © 2014 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ1044649.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ1044649.pdf"><span><span class="hlt">Creating</span> Better Library Information Systems: The Road to FRBR-Land</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Mercun, Tanja; Švab, Katarina; Harej, Viktor; Žumer, Maja</p> <p>2013-01-01</p> <p>Introduction: To provide valuable services in the future, libraries will need to <span class="hlt">create</span> better information systems and set up an infrastructure more in <span class="hlt">line</span> with the current technologies. The "Functional Requirements for Bibliographic Records" conceptual model provides a basis for this transformation, but there are still a number of…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016SPIE.9703E..0FC','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016SPIE.9703E..0FC"><span><span class="hlt">Line</span>-scanning, stage scanning confocal microscope</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Carucci, John A.; Stevenson, Mary; Gareau, Daniel</p> <p>2016-03-01</p> <p>We <span class="hlt">created</span> a <span class="hlt">line</span>-scanning, stage scanning confocal microscope as part of a new procedure: video assisted micrographic surgery (VAMS). The need for rapid pathological assessment of the tissue <span class="hlt">on</span> the surface of skin excisions very large since there are 3.5 million new skin cancers diagnosed annually in the United States. The new design presented here is a confocal microscope without any scanning optics. Instead, a <span class="hlt">line</span> is focused in space and the sample, which is flattened, is physically translated such that the <span class="hlt">line</span> scans across its face in a direction perpendicular to the <span class="hlt">line</span> its self. The <span class="hlt">line</span> is 6mm long and the stage is capable of scanning 50 mm, hence the field of view is quite large. The theoretical diffraction-limited resolution is 0.7um lateral and 3.7um axial. However, in this preliminary report, we present initial results that are a factor of 5-7 poorer in resolution. The results are encouraging because they demonstrate that the linear array detector measures sufficient signal from fluorescently labeled tissue and also demonstrate the large field of view achievable with VAMS.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29477650','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29477650"><span>A comparison of <span class="hlt">on-line</span> and off-<span class="hlt">line</span> bioaerosol measurements at a biowaste site.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Feeney, Patrick; Rodríguez, Santiago Fernández; Molina, Rafael; McGillicuddy, Eoin; Hellebust, Stig; Quirke, Michael; Daly, Shane; O'Connor, David; Sodeau, John</p> <p>2018-06-01</p> <p>An air measurement campaign was carried out at a green-waste composting site in the South of Ireland during Spring 2016. The aim was to quantify and identify the levels of Primary <span class="hlt">Biological</span> Aerosol Particles (PBAP) that were present using the traditional off-<span class="hlt">line</span>, impaction/optical microscopy method alongside an <span class="hlt">on-line</span>, spectroscopic approach termed WIBS (Wideband Integrated Bioaerosol Sensor), which can provide number concentrations, sizes and "shapes" of airborne PBAP in real-time by use of Light Induced Fluorescence (LIF). The results from the two techniques were compared in order to validate the use of the spectroscopic method for determining the releases of the wide-range of PBAP present there as a function of site activity and meteorological conditions. The seven-day monitoring period undertaken was much longer than any real-time studies that have been previously performed and allowed due comparison between weekday (working) activities at the site and weekend (closed) releases. The time-span also allowed relationships between site activities like turning, agitation or waste delivery and the WIBS data to be determined in a quantitative manner. This information cannot be obtained with the Andersen Sampling methods generally employed at green-waste management sites. Furthermore, few specific bioaerosol types other than Aspergillus fumigatus, are identified using the traditional protocols employed for site licensing purposes. Here though the co-location of WIBS with the impaction instrument made it possible to identify the real-time release behaviour of a specific plant pathogenic spore, Ustilago maydis, present after green-waste deliveries were made by a local distillery. Copyright © 2018 Elsevier Ltd. All rights reserved.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_14 --> <div id="page_15" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="281"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008SPIE.7019E..1LL','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008SPIE.7019E..1LL"><span>A first-generation software product <span class="hlt">line</span> for data acquisition systems in astronomy</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>López-Ruiz, J. C.; Heradio, Rubén; Cerrada Somolinos, José Antonio; Coz Fernandez, José Ramón; López Ramos, Pablo</p> <p>2008-07-01</p> <p>This article presents a case study <span class="hlt">on</span> developing a software product <span class="hlt">line</span> for data acquisition systems in astronomy based <span class="hlt">on</span> the Exemplar Driven Development methodology and the Exemplar Flexibilization Language tool. The main strategies to build the software product <span class="hlt">line</span> are based <span class="hlt">on</span> the domain commonality and variability, the incremental scope and the use of existing artifacts. It consists <span class="hlt">on</span> a lean methodology with little impact <span class="hlt">on</span> the organization, suitable for small projects, which reduces product <span class="hlt">line</span> start-up time. Software Product <span class="hlt">Lines</span> focuses <span class="hlt">on</span> <span class="hlt">creating</span> a family of products instead of individual products. This approach has spectacular benefits <span class="hlt">on</span> reducing the time to market, maintaining the know-how, reducing the development costs and increasing the quality of new products. The maintenance of the products is also enhanced since all the data acquisition systems share the same product <span class="hlt">line</span> architecture.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19216932','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19216932"><span>Desegregating undergraduate mathematics and <span class="hlt">biology</span>--interdisciplinary instruction with emphasis <span class="hlt">on</span> ongoing biomedical research.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Robeva, Raina</p> <p>2009-01-01</p> <p>The remarkable advances in the field of <span class="hlt">biology</span> in the last decade, specifically in the areas of biochemistry, genetics, genomics, proteomics, and systems <span class="hlt">biology</span>, have demonstrated how critically important mathematical models and methods are in addressing questions of vital importance for these disciplines. There is little doubt that the need for utilizing and developing mathematical methods for <span class="hlt">biology</span> research will only grow in the future. The rapidly increasing demand for scientists with appropriate interdisciplinary skills and knowledge, however, is not being reflected in the way undergraduate mathematics and <span class="hlt">biology</span> courses are structured and taught in most colleges and universities nationwide. While a number of institutions have stepped forward and addressed this need by <span class="hlt">creating</span> and offering interdisciplinary courses at the juncture of mathematics and <span class="hlt">biology</span>, there are still many others at which there is little, if any, interdisciplinary interaction between the curricula. This chapter describes an interdisciplinary course and a textbook in mathematical <span class="hlt">biology</span> developed collaboratively by faculty from Sweet Briar College and the University of Virginia School of Medicine. The course and textbook are designed to provide a bridge between the mathematical and <span class="hlt">biological</span> sciences at the lower undergraduate level. The course is developed for and is being taught in a liberal arts setting at Sweet Briar College, Virginia, but some of the advanced modules are used in a course at the University of Virginia for advanced undergraduate and beginning graduate students. The individual modules are relatively independent and can be used as stand-alone projects in conventional mathematics and <span class="hlt">biology</span> courses. Except for the introductory material, the course and textbook topics are based <span class="hlt">on</span> current biomedical research.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=biological+AND+control&pg=5&id=EJ746189','ERIC'); return false;" href="https://eric.ed.gov/?q=biological+AND+control&pg=5&id=EJ746189"><span><span class="hlt">On</span> Feeling in Control: A <span class="hlt">Biological</span> Theory for Individual Differences in Control Perception</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Declerck, Carolyn H.; Boone, Christophe; De Brabander, Bert</p> <p>2006-01-01</p> <p>This review aims to <span class="hlt">create</span> a cross-disciplinary framework for understanding the perception of control. Although, the personality trait locus of control, the most common measure of control perception, has traditionally been regarded as a product of social learning, it may have <span class="hlt">biological</span> antecedents as well. It is suggested that control perception…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29792156','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29792156"><span>Design, synthesis and <span class="hlt">biological</span> evaluation of 1H-1,2,3-Triazole-Linked-1H‑Dibenzo[b,h]xanthenes as Inductors of ROS-Mediated Apoptosis in the Breast Cancer Cell <span class="hlt">Line</span> MCF-7.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bortolot, Carolina S; da S M Forezi, Luana; Marra, Roberta K F; Reis, Marcelo I P; Sa, Barbara V F E; Filho, Ricardo Imbroisi; Ghasemishahrestani, Zeinab; Sola-Penna, Mauro; Zancan, Patricia; Ferreira, Vitor F; de C da Silva, Fernando</p> <p>2018-05-23</p> <p>Low molecular weight 1,2,3-triazoles and naphthoquinones are endowed with various types of <span class="hlt">biological</span> activity, such as against cancer, HIV and bacteria. However, in some cases, the conjugation of these two nuclei considerably increases their <span class="hlt">biological</span> activities Objective: In this work, we decided to study the synthesis and screening of bis-naphthoquinones and xanthenes tethered to 1,2,3-triazoles against cancer cell <span class="hlt">lines</span>, specifically the human breast cancer cell <span class="hlt">line</span> MCF-7. Starting from lawsone and aryl-1H-1,2,3-triazole-4-carbaldehydes (10a-h) several new 7-(1-aryl-1H-1,2,3-triazol-4-yl)-6H-dibenzo[b,h]xanthene-5,6,8,13(7H)-tetraones (12a-h) and 3,3'-((1-aryl-1H-1,2,3-triazol-4-yl)methylene)bis(2-hydroxynaphthalene-1,4-diones) 11a-h were synthesized and evaluated for their cytotoxic activities using the human breast cancer cell <span class="hlt">line</span> MCF-7 and the non-tumor cell <span class="hlt">line</span> MCF10A as control. We performed test of cell viability, cell proliferation, intracellular ATP content and cell cytometry to determine reactive oxygen species (ROS) formation. Based <span class="hlt">on</span> these results, we found that compound 12a promote ROS production, interfering with energy metabolism, cell viability and proliferation, and thus promoting an whole cell damage. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=case+AND+catalonia&pg=2&id=EJ973376','ERIC'); return false;" href="https://eric.ed.gov/?q=case+AND+catalonia&pg=2&id=EJ973376"><span>Does <span class="hlt">On-Line</span> Distance Higher Education Pay off for Adult Learners? The Case of the Open University of Catalonia</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Carnoy, Martin; Rabling, Brenda Jarillo; Castano-Munoz, Jonatan; Montoliu, Josep Maria Duart; Sancho-Vinuesa, Teresa</p> <p>2012-01-01</p> <p>The increasing opportunities <span class="hlt">created</span> for adults by <span class="hlt">on-line</span> distance universities raise important issues about the payoff to such education. This study uses a unique set of survey data gathered by the Open University of Catalonia (UOC) in 2009 to estimate the earnings gains of the 2000-2003 cohorts of UOC students in six programmes of study over an…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2547828','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2547828"><span>State of the art in <span class="hlt">on-line</span> techniques coupled to flow injection analysis FIA/<span class="hlt">on-line</span>- a critical review</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Puchades, R.; Maquieira, A.; Atienza, J.; Herrero, M. A.</p> <p>1990-01-01</p> <p>Flow injection analysis (FIA) has emerged as an increasingly used laboratory tool in chemical analysis. Employment of the technique for <span class="hlt">on-line</span> sample treatment and <span class="hlt">on-line</span> measurement in chemical process control is a growing trend. This article reviews the recent applications of FlA. Most papers refer to <span class="hlt">on-line</span> sample treatment. Although FIA is very well suited to continuous <span class="hlt">on-line</span> process monitoring, few examples have been found in this areamost of them have been applied to water treatment or fermentation processes. PMID:18925271</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017APS..DFDQ11008S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017APS..DFDQ11008S"><span>Moving contact <span class="hlt">lines</span> <span class="hlt">on</span> vibrating surfaces</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Solomenko, Zlatko; Spelt, Peter; Scott, Julian</p> <p>2017-11-01</p> <p>Large-scale simulations of flows with moving contact <span class="hlt">lines</span> for realistic conditions generally requires a subgrid scale model (analyses based <span class="hlt">on</span> matched asymptotics) to account for the unresolved part of the flow, given the large range of length scales involved near contact <span class="hlt">lines</span>. Existing models for the interface shape in the contact-<span class="hlt">line</span> region are primarily for steady flows <span class="hlt">on</span> homogeneous substrates, with encouraging results in 3D simulations. Introduction of complexities would require further investigation of the contact-<span class="hlt">line</span> region, however. Here we study flows with moving contact <span class="hlt">lines</span> <span class="hlt">on</span> planar substrates subject to vibrations, with applications in controlling wetting/dewetting. The challenge here is to determine the change in interface shape near contact <span class="hlt">lines</span> due to vibrations. To develop further insight, 2D direct numerical simulations (wherein the flow is resolved down to an imposed slip length) have been performed to enable comparison with asymptotic theory, which is also developed further. Perspectives will also be presented <span class="hlt">on</span> the final objective of the work, which is to develop a subgrid scale model that can be utilized in large-scale simulations. The authors gratefully acknowledge the ANR for financial support (ANR-15-CE08-0031) and the meso-centre FLMSN for use of computational resources. This work was Granted access to the HPC resources of CINES under the allocation A0012B06893 made by GENCI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19780003228','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19780003228"><span>Scientific experiments in the flight of the 1977 <span class="hlt">biological</span> satellite (draft plan)</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p></p> <p>1977-01-01</p> <p>The physiological, <span class="hlt">biological</span>, radiobiological and radiophysical experiments planned for the 1977 <span class="hlt">biological</span> satellite are described. The <span class="hlt">biological</span> experiments will involve rats, higher and lower plants, insects and other <span class="hlt">biological</span> specimens carried <span class="hlt">on</span> the biosatellite. The responses of these organisms to weightlessness, artificial gravity, cosmic radiation particles and general flight factors will be studied. The radiophysical experiments will investigate certain properties of cosmic radiation as well as the possibility of <span class="hlt">creating</span> electrostatic and dielectric radiation shields under actual space-flight conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3690854','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3690854"><span>Marital satisfaction and break-ups differ across <span class="hlt">on-line</span> and off-<span class="hlt">line</span> meeting venues</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Cacioppo, John T.; Cacioppo, Stephanie; Gonzaga, Gian C.; Ogburn, Elizabeth L.; VanderWeele, Tyler J.</p> <p>2013-01-01</p> <p>Marital discord is costly to children, families, and communities. The advent of the Internet, social networking, and <span class="hlt">on-line</span> dating has affected how people meet future spouses, but little is known about the prevalence or outcomes of these marriages or the demographics of those involved. We addressed these questions in a nationally representative sample of 19,131 respondents who married between 2005 and 2012. Results indicate that more than one-third of marriages in America now begin <span class="hlt">on-line</span>. In addition, marriages that began <span class="hlt">on-line</span>, when compared with those that began through traditional off-<span class="hlt">line</span> venues, were slightly less likely to result in a marital break-up (separation or divorce) and were associated with slightly higher marital satisfaction among those respondents who remained married. Demographic differences were identified between respondents who met their spouse through <span class="hlt">on-line</span> vs. traditional off-<span class="hlt">line</span> venues, but the findings for marital break-up and marital satisfaction remained significant after statistically controlling for these differences. These data suggest that the Internet may be altering the dynamics and outcomes of marriage itself. PMID:23733955</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16078857','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16078857"><span>Towards molecular medicine: a case for a <span class="hlt">biological</span> periodic table.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gawad, Charles</p> <p>2005-01-01</p> <p>The recently amplified pace of development in the technologies to study both normal and aberrant cellular physiology has allowed for a transition from the traditional reductionist approaches to global interrogations of human <span class="hlt">biology</span>. This transformation has <span class="hlt">created</span> the anticipation that we will soon more effectively treat or contain most types of diseases through a 'systems-based' approach to understanding and correcting the underlying etiology of these processes. However, to accomplish these goals, we must first have a more comprehensive understanding of all the elements involved in human cellular physiology, as well as why and how they interact. With the vast number of <span class="hlt">biological</span> components that have and are being discovered, <span class="hlt">creating</span> methods with modern computational techniques to better organize <span class="hlt">biological</span> elements is the next requisite step in this process. This article aims to articulate the importance of the organization of chemical elements into a periodic table had <span class="hlt">on</span> the conversion of chemistry into a quantitative, translatable science, as well as how we can apply the lessons learned in that transition to the current transformation taking place in <span class="hlt">biology</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16967621','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16967621"><span>10 ways to <span class="hlt">create</span> shareholder value.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rappaport, Alfred</p> <p>2006-09-01</p> <p>Executives have developed tunnel vision in their pursuit of shareholder value, focusing <span class="hlt">on</span> short-term performance at the expense of investing in long-term growth. It's time to broaden that perspective and begin shaping business strategies in light of the competitive landscape, not the shareholder list. In this article, Alfred Rappaport offers ten basic principles to help executives <span class="hlt">create</span> lasting shareholder value. For starters, companies should not manage earnings or provide earnings guidance; those that fail to embrace this first principle of shareholder value will almost certainly be unable to follow the rest. Additionally, leaders should make strategic decisions and acquisitions and carry assets that maximize expected value, even if near-term earnings are negatively affected as a result. During times when there are no credible value-<span class="hlt">creating</span> opportunities to invest in the business, companies should avoid using excess cash to make investments that look good <span class="hlt">on</span> the surface but might end up destroying value, such as ill-advised, overpriced acquisitions. It would be better to return the cash to shareholders in the form of dividends and buybacks. Rappaport also offers guidelines for establishing effective pay incentives at every level of management; emphasizes that senior executives need to lay their wealth <span class="hlt">on</span> the <span class="hlt">line</span> just as shareholders do; and urges companies to embrace full disclosure, an antidote to short-term earnings obsession that serves to lessen investor uncertainty, which could reduce the cost of capital and increase the share price. The author notes that a few types of companies--high-tech start-ups, for example, and severely capital-constrained organizations--cannot afford to ignore market pressures for short-term performance. Most companies with a sound, well-executed business model, however, could better realize their potential for <span class="hlt">creating</span> shareholder value by adopting the ten principles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19850007253&hterms=ionized+atoms&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dionized%2Batoms','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19850007253&hterms=ionized+atoms&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dionized%2Batoms"><span>Observations of Absorption <span class="hlt">Lines</span> from Highly Ionized Atoms</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Jenkins, E. B.</p> <p>1984-01-01</p> <p>In the ultraviolet spectra of hot stars, absorption <span class="hlt">lines</span> can be seen from highly ionized species in the interstellar medium. Observations of these features which have been very influential in revising the perception of the medium's various physical states, are discussed. The pervasiveness of O 6 absorption <span class="hlt">lines</span>, coupled with complementary observations of a diffuse background in soft X-rays and EUV radiation, shows that there is an extensive network of low density gas (n approx. fewX 0.001/cucm) existing at coronal temperatures, 5.3 or = log T or = 6.3. Shocks <span class="hlt">created</span> by supernova explosions or mass loss from early-type stars can propagate freely through space and eventually transfer a large amount of energy to the medium. To <span class="hlt">create</span> the coronal temperatures, the shocks must have velocities in excess of 150 km/sec; shocks at somewhat lower velocity 9v or = 100 km/sec) can be directly observed in the <span class="hlt">lines</span> of Si3. Observations of other <span class="hlt">lines</span> in the ultraviolet, such as Si 4V and C 5, may highlight the widespread presence of energetic uv radiation from very hot, dward stars. More advanced techniques in visible and X-ray astronomical spectroscopy may open up for inspection selected <span class="hlt">lines</span> from atoms in much higher stages of ionization.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014EGUGA..1611570S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014EGUGA..1611570S"><span>Earth is speaking: listen her! <span class="hlt">On-line</span> questionnaire about anomalous geological and <span class="hlt">biological</span> phenomena</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sciarra, Alessandra; Quattrocchi, Fedora; Cantucci, Barbara; Mazzarini, Francesco</p> <p>2014-05-01</p> <p>Earthquakes can be associated with non-seismic phenomena which may manifest many weeks before and after the main shock. These phenomena are characterized by ground fractures and soil liquefactions at surface often coupled with degassing events, chemical alterations of water and soils, changes in temperature and/or waters level in the epicentral area. Further manifestations include radio disturbances and light emissions. <span class="hlt">On</span> the other hand, anomalous behavior of animals has been reported to occur before environmental changes. The co-occurrence of several phenomena may be considered as a signal of subsurface changes, and their analysis may be used as possible forecast indicators for seismic events, landslides, damages in infrastructure (e.g., dam) and groundwaters contamination. In order to obtain an accurate statistical analysis of these factors, a pre-crisis large database over a prolonged period of time is a pre-requisite. To this end, we elaborated a questionnaire for the population to pick up signs about anomalous phenomena like as: animal behavior, geological manifestations, effect <span class="hlt">on</span> vegetation, degassing, changes <span class="hlt">on</span> aquifers, wells and springs. After the January 25, 2013, mainshock (ML 4.8) in the Garfagnana seismic district, the Bagni di Lucca Municipality was selected as pilot site for testing this questionnaire. The complexity, variety and extension of this territory (165 kmq) sound suitable for this project. Bagni di Lucca is located in the southern border of the Garfagnana seismogenic source, characterized by the carbonate Mesozoic sequences and the Tertiary terrigenous sedimentary deposits of the Tuscan Nappe. The questionnaire was published <span class="hlt">on</span> Bagni di Lucca web site (https://docs.google.com/file/d/0Bzw3vOYX47XoTGltTVJRbkJuajA/edit) in collaboration with Municipal Commitee, Local Civil Protection and Local Red Cross, and sent by ordinary mail to the citizenry. It is possible to answer to the questionnaire, also anonymously, direct <span class="hlt">on</span> <span class="hlt">line</span> (https</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20110005676','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20110005676"><span><span class="hlt">Creating</span> Synthetic Coronal Observational Data From MHD Models: The Forward Technique</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Rachmeler, Laurel A.; Gibson, Sarah E.; Dove, James; Kucera, Therese Ann</p> <p>2010-01-01</p> <p>We present a generalized forward code for <span class="hlt">creating</span> simulated corona) observables off the limb from numerical and analytical MHD models. This generalized forward model is capable of <span class="hlt">creating</span> emission maps in various wavelengths for instruments such as SXT, EIT, EIS, and coronagraphs, as well as spectropolari metric images and <span class="hlt">line</span> profiles. The inputs to our code can be analytic models (of which four come with the code) or 2.5D and 3D numerical datacubes. We present some examples of the observable data <span class="hlt">created</span> with our code as well as its functional capabilities. This code is currently available for beta-testing (contact authors), with the ultimate goal of release as a SolarSoft package</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AIPC.1882b0074S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AIPC.1882b0074S"><span><span class="hlt">Biological</span>-based and physical-based optimization for <span class="hlt">biological</span> evaluation of prostate patient's plans</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sukhikh, E.; Sheino, I.; Vertinsky, A.</p> <p>2017-09-01</p> <p>Modern modalities of radiation treatment therapy allow irradiation of the tumor to high dose values and irradiation of organs at risk (OARs) to low dose values at the same time. In this paper we study optimal radiation treatment plans made in Monaco system. The first aim of this study was to evaluate dosimetric features of Monaco treatment planning system using <span class="hlt">biological</span> versus dose-based cost functions for the OARs and irradiation targets (namely tumors) when the full potential of built-in <span class="hlt">biological</span> cost functions is utilized. The second aim was to develop criteria for the evaluation of radiation dosimetry plans for patients based <span class="hlt">on</span> the macroscopic radiobiological criteria - TCP/NTCP. In the framework of the study four dosimetric plans were <span class="hlt">created</span> utilizing the full extent of <span class="hlt">biological</span> and physical cost functions using dose calculation-based treatment planning for IMRT Step-and-Shoot delivery of stereotactic body radiation therapy (SBRT) in prostate case (5 fractions per 7 Gy).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1996AIPC..381..197S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1996AIPC..381..197S"><span><span class="hlt">On-line</span> atomic data access</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schultz, David R.; Nash, Jeffrey K.</p> <p>1996-07-01</p> <p>The need for atomic data is one which continues to expand in a wide variety of applications including fusion energy, astrophysics, laser-produced plasma research, and plasma processing. Modern computer database and communications technology enables this data to be placed <span class="hlt">on-line</span> and obtained by users over the INTERNET. Presented here is a summary of the observations and conclusions regarding such <span class="hlt">on-line</span> atomic data access derived from a forum held at the Tenth APS Topical Conference <span class="hlt">on</span> Atomic Processes in Plasmas.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24730317','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24730317"><span><span class="hlt">Biological</span> applications of nanobiotechnology.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>de Morais, Michele Greque; Martins, Vilásia Guimarães; Steffens, Daniela; Pranke, Patricia; da Costa, Jorge Alberto Vieira</p> <p>2014-01-01</p> <p>Nanotechnology is a multidisciplinary field that covers a vast and diverse array of devices derived from engineering, physics, chemistry, and <span class="hlt">biology</span>. Nanotechnology has opened up by rapid advances in science and technology, <span class="hlt">creating</span> new opportunities for advances in the fields of medicine, electronics, foods, and the environment. Nanoscale structures and materials (nanoparticles, nanowires, nanofibers, nanotubes) have been explored in many <span class="hlt">biological</span> applications (biosensing, <span class="hlt">biological</span> separation, molecular imaging, anticancer therapy) because their novel properties and functions differ drastically from their bulk counterparts. Their high volume/surface ratio, improved solubility, and multifunctionality open many new possibilities. The objective of this review is to describe the potential benefits and impacts of the nanobiotechnology in different areas.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24462322','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24462322"><span>Appropriateness and long-term discontinuation rate of <span class="hlt">biological</span> therapies in ulcerative colitis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Maillard, Michel H; Bortolotti, Murielle; Vader, John-Paul; Mottet, Christian; Schoepfer, Alain; Gonvers, Jean-Jacques; Burnand, Bernard; Froehlich, Florian; Michetti, Pierre; Pittet, Valérie</p> <p>2014-08-01</p> <p>Anti-TNFα agents are commonly used for ulcerative colitis (UC) therapy in the event of non-response to conventional strategies or as colon-salvaging therapy. The objectives were to assess the appropriateness of <span class="hlt">biological</span> therapies for UC patients and to study treatment discontinuation over time, according to appropriateness of treatment, as a measure of outcome. We selected adult ulcerative colitis patients from the Swiss IBD cohort who had been treated with anti-TNFα agents. Appropriateness of the first-<span class="hlt">line</span> anti-TNFα treatment was assessed using detailed criteria developed during the European Panel <span class="hlt">on</span> the Appropriateness of Therapy for UC. Treatment discontinuation as an outcome was assessed for categories of appropriateness. Appropriateness of the first-<span class="hlt">line</span> <span class="hlt">biological</span> treatment was determined in 186 UC patients. For 64% of them, this treatment was considered appropriate. During follow-up, 37% of all patients discontinued <span class="hlt">biological</span> treatment, 17% specifically because of failure. Time-to-failure of treatment was significantly different among patients <span class="hlt">on</span> an appropriate <span class="hlt">biological</span> treatment compared to those for whom the treatment was considered not appropriate (p=0.0007). Discontinuation rate after 2years was 26% compared to 54% between those two groups. Patients <span class="hlt">on</span> inappropriate <span class="hlt">biological</span> treatment were more likely to have severe disease, concomitant steroids and/or immunomodulators. They were also consistently more likely to suffer a failure of efficacy and to stop therapy during follow-up. Appropriateness of first-<span class="hlt">line</span> anti-TNFα therapy results in a greater likelihood of continuing with the therapy. In situations where <span class="hlt">biological</span> treatment is uncertain or inappropriate, physicians should consider other options instead of prescribing anti-TNFα agents. Copyright © 2014 European Crohn's and Colitis Organisation. Published by Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5874048','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5874048"><span>Versatile approach for functional analysis of human proteins and efficient stable cell <span class="hlt">line</span> generation using FLP-mediated recombination system</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Szczesny, Roman J.; Kowalska, Katarzyna; Klosowska-Kosicka, Kamila; Chlebowski, Aleksander; Owczarek, Ewelina P.; Warkocki, Zbigniew; Kulinski, Tomasz M.; Adamska, Dorota; Affek, Kamila; Jedroszkowiak, Agata; Kotrys, Anna V.; Tomecki, Rafal; Krawczyk, Pawel S.; Borowski, Lukasz S.; Dziembowski, Andrzej</p> <p>2018-01-01</p> <p>Deciphering a function of a given protein requires investigating various <span class="hlt">biological</span> aspects. Usually, the protein of interest is expressed with a fusion tag that aids or allows subsequent analyses. Additionally, downregulation or inactivation of the studied gene enables functional studies. Development of the CRISPR/Cas9 methodology opened many possibilities but in many cases it is restricted to non-essential genes. Recombinase-dependent gene integration methods, like the Flp-In system, are very good alternatives. The system is widely used in different research areas, which calls for the existence of compatible vectors and efficient protocols that ensure straightforward DNA cloning and generation of stable cell <span class="hlt">lines</span>. We have <span class="hlt">created</span> and validated a robust series of 52 vectors for streamlined generation of stable mammalian cell <span class="hlt">lines</span> using the FLP recombinase-based methodology. Using the sequence-independent DNA cloning method all constructs for a given coding-sequence can be made with just three universal PCR primers. Our collection allows tetracycline-inducible expression of proteins with various tags suitable for protein localization, FRET, bimolecular fluorescence complementation (BiFC), protein dynamics studies (FRAP), co-immunoprecipitation, the RNA tethering assay and cell sorting. Some of the vectors contain a bidirectional promoter for concomitant expression of miRNA and mRNA, so that a gene can be silenced and its product replaced by a mutated miRNA-insensitive version. Our toolkit and protocols have allowed us to <span class="hlt">create</span> more than 500 constructs with ease. We demonstrate the efficacy of our vectors by <span class="hlt">creating</span> stable cell <span class="hlt">lines</span> with various tagged proteins (numatrin, fibrillarin, coilin, centrin, THOC5, PCNA). We have analysed transgene expression over time to provide a guideline for future experiments and compared the effectiveness of commonly used inducers for tetracycline-responsive promoters. As proof of concept we examined the role of the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1347507','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1347507"><span>The Genomes <span class="hlt">On</span> <span class="hlt">Line</span> Database (GOLD) v.2: a monitor of genome projects worldwide</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Liolios, Konstantinos; Tavernarakis, Nektarios; Hugenholtz, Philip; Kyrpides, Nikos C.</p> <p>2006-01-01</p> <p>The Genomes <span class="hlt">On</span> <span class="hlt">Line</span> Database (GOLD) is a web resource for comprehensive access to information regarding complete and ongoing genome sequencing projects worldwide. The database currently incorporates information <span class="hlt">on</span> over 1500 sequencing projects, of which 294 have been completed and the data deposited in the public databases. GOLD v.2 has been expanded to provide information related to organism properties such as phenotype, ecotype and disease. Furthermore, project relevance and availability information is now included. GOLD is available at . It is also mirrored at the Institute of Molecular <span class="hlt">Biology</span> and Biotechnology, Crete, Greece at PMID:16381880</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_15 --> <div id="page_16" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="301"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23769313','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23769313"><span>Microbial-enzymatic-hybrid <span class="hlt">biological</span> fuel cell with optimized growth conditions for Shewanella oneidensis DSP-10.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Roy, Jared N; Luckarift, Heather R; Sizemore, Susan R; Farrington, Karen E; Lau, Carolin; Johnson, Glenn R; Atanassov, Plamen</p> <p>2013-07-10</p> <p>In this work we present a <span class="hlt">biological</span> fuel cell fabricated by combining a Shewanella oneidensis microbial anode and a laccase-modified air-breathing cathode. This concept is devised as an extension to traditional biochemical methods by incorporating diverse <span class="hlt">biological</span> catalysts with the aim of powering small devices. In preparing the <span class="hlt">biological</span> fuel cell anode, novel hierarchical-structured architectures and biofilm configurations were investigated. A method for <span class="hlt">creating</span> an artificial biofilm based <span class="hlt">on</span> encapsulating microorganisms in a porous, thin film of silica was compared with S. oneidensis biofilms that were allowed to colonize naturally. Results indicate comparable current and power densities for artificial and natural biofilm formations, based <span class="hlt">on</span> growth characteristics. As a result, this work describes methods for <span class="hlt">creating</span> controllable and reproducible bio-anodes and demonstrates the versatility of hybrid <span class="hlt">biological</span> fuel cells. Copyright © 2013 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005MHD....41..317S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005MHD....41..317S"><span>Ferromagnetic nanoparticles containing <span class="hlt">biologically</span> active alkanolamines: preparation and properties</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Segal, I.; Zablotskaya, A.; Lukevics, E.; Maiorov, M.; Zablotsky, D.</p> <p>2005-12-01</p> <p>The objective of the present study is to investigate the possibility of sorption <span class="hlt">on</span> ultrafine magnetic particles of some model <span class="hlt">biologically</span> active organosilicon alkanolamines, structural analogs of natural <span class="hlt">biologically</span> active substances, choline and colamine, with increased lipophilicity. Double-coated ferromagnetic samples containing oleic acid, as a first layer, and organosilicon alcanolamines, as a second layer, were obtained and characterized by their physical/chemical (sorption and magnetisation) and <span class="hlt">biological</span> (toxicity and cytotoxicity) properties. The present results clearly reveal the sorption of the <span class="hlt">biologically</span> active alkanolamines <span class="hlt">on</span> the surface of magnetic particles and a principal possibility to coat magnetite directly with <span class="hlt">biologically</span> active alkanolamines, <span class="hlt">creating</span> a mono-layer cover. The data presented in the study of cytotoxic properties of the newly obtained ferromagnetic nanoparticles show that it is reasonable to investigate such systems as potential cytotoxic agents. Tables 3, Figs 3, Refs 16.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70195114','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70195114"><span>A Bayesian-based system to assess wave-driven flooding hazards <span class="hlt">on</span> coral reef-<span class="hlt">lined</span> coasts</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Pearson, S. G.; Storlazzi, Curt; van Dongeren, A. R.; Tissier, M. F. S.; Reniers, A. J. H. M.</p> <p>2017-01-01</p> <p>Many low-elevation, coral reef-<span class="hlt">lined</span>, tropical coasts are vulnerable to the effects of climate change, sea level rise, and wave-induced flooding. The considerable morphological diversity of these coasts and the variability of the hydrodynamic forcing that they are exposed to make predicting wave-induced flooding a challenge. A process-based wave-resolving hydrodynamic model (XBeach Non-Hydrostatic, “XBNH”) was used to <span class="hlt">create</span> a large synthetic database for use in a “Bayesian Estimator for Wave Attack in Reef Environments” (BEWARE), relating incident hydrodynamics and coral reef geomorphology to coastal flooding hazards <span class="hlt">on</span> reef-<span class="hlt">lined</span> coasts. Building <span class="hlt">on</span> previous work, BEWARE improves system understanding of reef hydrodynamics by examining the intrinsic reef and extrinsic forcing factors controlling runup and flooding <span class="hlt">on</span> reef-<span class="hlt">lined</span> coasts. The Bayesian estimator has high predictive skill for the XBNH model outputs that are flooding indicators, and was validated for a number of available field cases. It was found that, in order to accurately predict flooding hazards, water depth over the reef flat, incident wave conditions, and reef flat width are the most essential factors, whereas other factors such as beach slope and bed friction due to the presence or absence of corals are less important. BEWARE is a potentially powerful tool for use in early warning systems or risk assessment studies, and can be used to make projections about how wave-induced flooding <span class="hlt">on</span> coral reef-<span class="hlt">lined</span> coasts may change due to climate change.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ835415.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ835415.pdf"><span><span class="hlt">Creating</span> Partnerships <span class="hlt">on</span> Campus to Facilitate Practical Experiences</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Becker, Craig M.; Johnson, Hans; McNeil, Michael P.; Warren, Karen</p> <p>2006-01-01</p> <p>College campuses <span class="hlt">create</span> small communities where mutually beneficial partnerships can be used to <span class="hlt">create</span> practical work experiences for students. The procedure outlined in this article outlines how to <span class="hlt">create</span> a partnership between the campus health and recreation center and an academic department to evaluate the implementation of a new smoking…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70128757','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70128757"><span>Managing <span class="hlt">biological</span> diversity</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Samson, Fred B.; Knopf, Fritz L.</p> <p>1993-01-01</p> <p><span class="hlt">Biological</span> diversity is the variety of life and accompanying ecological processes (Off. Technol. Assess. 1987, Wilcove and Samson 1987, Keystone 1991). Conservation of <span class="hlt">biological</span> diversity is a major environmental issue (Wilson 1988, Counc. Environ. Quality 1991). The health and future of the earth's ecological systems (Lubchenco et al. 1991), global climate change (Botkin 1990), and an ever-increasing rate in loss of species, communities, and ecological systems (Myers 1990) are among issues drawing <span class="hlt">biological</span> diversity to the mainstream of conservation worldwide (Int. Union Conserv. Nat. and Nat. Resour. [IUCN] et al. 1991). The legal mandate for conserving <span class="hlt">biological</span> diversity is now in place (Carlson 1988, Doremus 1991). More than 19 federal laws govern the use of <span class="hlt">biological</span> resources in the United States (Rein 1991). The proposed National <span class="hlt">Biological</span> Diversity Conservation and Environmental Research Act (H.R. 585 and S.58) notes the need for a national <span class="hlt">biological</span> diversity policy, would <span class="hlt">create</span> a national center for <span class="hlt">biological</span> diversity research, and recommends a federal interagency strategy for ecosystem conservation. There are, however, hard choices ahead for the conservation of <span class="hlt">biological</span> diversity, and biologists are grappling with how to set priorities in research and management (Roberts 1988). We sense disillusion among field biologists and managers relative to how to operationally approach the seemingly overwhelming charge of conserving <span class="hlt">biological</span> diversity. Biologists also need to respond to critics like Hunt (1991) who suggest a tree farm has more <span class="hlt">biological</span> diversity than an equal area of old-growth forest. At present, science has played only a minor role in the conservation of <span class="hlt">biological</span> diversity (Weston 1992) with no unified approach available to evaluate strategies and programs that address the quality and quantity of <span class="hlt">biological</span> diversity (Murphy 1990, Erwin 1992). Although actions to conserve <span class="hlt">biological</span> diversity need to be clearly defined by</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4566270','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4566270"><span>Multiple-<span class="hlt">Line</span> Inference of Selection <span class="hlt">on</span> Quantitative Traits</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Riedel, Nico; Khatri, Bhavin S.; Lässig, Michael; Berg, Johannes</p> <p>2015-01-01</p> <p>Trait differences between species may be attributable to natural selection. However, quantifying the strength of evidence for selection acting <span class="hlt">on</span> a particular trait is a difficult task. Here we develop a population genetics test for selection acting <span class="hlt">on</span> a quantitative trait that is based <span class="hlt">on</span> multiple-<span class="hlt">line</span> crosses. We show that using multiple <span class="hlt">lines</span> increases both the power and the scope of selection inferences. First, a test based <span class="hlt">on</span> three or more <span class="hlt">lines</span> detects selection with strongly increased statistical significance, and we show explicitly how the sensitivity of the test depends <span class="hlt">on</span> the number of <span class="hlt">lines</span>. Second, a multiple-<span class="hlt">line</span> test can distinguish between different lineage-specific selection scenarios. Our analytical results are complemented by extensive numerical simulations. We then apply the multiple-<span class="hlt">line</span> test to QTL data <span class="hlt">on</span> floral character traits in plant species of the Mimulus genus and <span class="hlt">on</span> photoperiodic traits in different maize strains, where we find a signature of lineage-specific selection not seen in two-<span class="hlt">line</span> tests. PMID:26139839</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18929406','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18929406"><span>The development of peptide-based interfacial biomaterials for generating <span class="hlt">biological</span> functionality <span class="hlt">on</span> the surface of bioinert materials.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Meyers, Steven R; Khoo, Xiaojuan; Huang, Xin; Walsh, Elisabeth B; Grinstaff, Mark W; Kenan, Daniel J</p> <p>2009-01-01</p> <p>Biomaterials used in implants have traditionally been selected based <span class="hlt">on</span> their mechanical properties, chemical stability, and biocompatibility. However, the durability and clinical efficacy of implantable biomedical devices remain limited in part due to the absence of appropriate <span class="hlt">biological</span> interactions at the implant interface and the lack of integration into adjacent tissues. Herein, we describe a robust peptide-based coating technology capable of modifying the surface of existing biomaterials and medical devices through the non-covalent binding of modular biofunctional peptides. These peptides contain at least one material binding sequence and at least one <span class="hlt">biologically</span> active sequence and thus are termed, "Interfacial Biomaterials" (IFBMs). IFBMs can simultaneously bind the biomaterial surface while endowing it with desired <span class="hlt">biological</span> functionalities at the interface between the material and <span class="hlt">biological</span> realms. We demonstrate the capabilities of model IFBMs to convert native polystyrene, a bioinert surface, into a bioactive surface that can support a range of cell activities. We further distinguish between simple cell attachment with insufficient integrin interactions, which in some cases can adversely impact downstream <span class="hlt">biology</span>, versus <span class="hlt">biologically</span> appropriate adhesion, cell spreading, and cell survival mediated by IFBMs. Moreover, we show that we can use the coating technology to <span class="hlt">create</span> spatially resolved patterns of fluorophores and cells <span class="hlt">on</span> substrates and that these patterns retain their borders in culture.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5825909','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5825909"><span>Low-Latency <span class="hlt">Line</span> Tracking Using Event-Based Dynamic Vision Sensors</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Everding, Lukas; Conradt, Jörg</p> <p>2018-01-01</p> <p>In order to safely navigate and orient in their local surroundings autonomous systems need to rapidly extract and persistently track visual features from the environment. While there are many algorithms tackling those tasks for traditional frame-based cameras, these have to deal with the fact that conventional cameras sample their environment with a fixed frequency. Most prominently, the same features have to be found in consecutive frames and corresponding features then need to be matched using elaborate techniques as any information between the two frames is lost. We introduce a novel method to detect and track <span class="hlt">line</span> structures in data streams of event-based silicon retinae [also known as dynamic vision sensors (DVS)]. In contrast to conventional cameras, these <span class="hlt">biologically</span> inspired sensors generate a quasicontinuous stream of vision information analogous to the information stream <span class="hlt">created</span> by the ganglion cells in mammal retinae. All pixels of DVS operate asynchronously without a periodic sampling rate and emit a so-called DVS address event as soon as they perceive a luminance change exceeding an adjustable threshold. We use the high temporal resolution achieved by the DVS to track features continuously through time instead of only at fixed points in time. The focus of this work lies <span class="hlt">on</span> tracking <span class="hlt">lines</span> in a mostly static environment which is observed by a moving camera, a typical setting in mobile robotics. Since DVS events are mostly generated at object boundaries and edges which in man-made environments often form <span class="hlt">lines</span> they were chosen as feature to track. Our method is based <span class="hlt">on</span> detecting planes of DVS address events in x-y-t-space and tracing these planes through time. It is robust against noise and runs in real time <span class="hlt">on</span> a standard computer, hence it is suitable for low latency robotics. The efficacy and performance are evaluated <span class="hlt">on</span> real-world data sets which show artificial structures in an office-building using event data for tracking and frame data for ground</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4984445','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4984445"><span>Selection platforms for directed evolution in synthetic <span class="hlt">biology</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Tizei, Pedro A.G.; Csibra, Eszter; Torres, Leticia; Pinheiro, Vitor B.</p> <p>2016-01-01</p> <p>Life <span class="hlt">on</span> Earth is incredibly diverse. Yet, underneath that diversity, there are a number of constants and highly conserved processes: all life is based <span class="hlt">on</span> DNA and RNA; the genetic code is universal; <span class="hlt">biology</span> is limited to a small subset of potential chemistries. A vast amount of knowledge has been accrued through describing and characterizing enzymes, <span class="hlt">biological</span> processes and organisms. Nevertheless, much remains to be understood about the natural world. One of the goals in Synthetic <span class="hlt">Biology</span> is to recapitulate <span class="hlt">biological</span> complexity from simple systems made from <span class="hlt">biological</span> molecules–gaining a deeper understanding of life in the process. Directed evolution is a powerful tool in Synthetic <span class="hlt">Biology</span>, able to bypass gaps in knowledge and capable of engineering even the most highly conserved <span class="hlt">biological</span> processes. It encompasses a range of methodologies to <span class="hlt">create</span> variation in a population and to select individual variants with the desired function–be it a ligand, enzyme, pathway or even whole organisms. Here, we present some of the basic frameworks that underpin all evolution platforms and review some of the recent contributions from directed evolution to synthetic <span class="hlt">biology</span>, in particular methods that have been used to engineer the Central Dogma and the genetic code. PMID:27528765</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4685481','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4685481"><span>US Competitiveness in Synthetic <span class="hlt">Biology</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p></p> <p>2015-01-01</p> <p>Synthetic <span class="hlt">biology</span> is an emerging technical field that aims to make <span class="hlt">biology</span> easier to engineer; the field has applications in strategically important sectors for the US economy. While the United States currently leads in synthetic <span class="hlt">biology</span> R&D, other nations are heavily investing in order to boost their economies, which will inevitably diminish the US leadership position. This outcome is not entirely negative—additional investments will expand markets—but it is critical that the US government take steps to remain competitive: There are applications from which the US population and economy may benefit; there are specific applications with importance for national defense; and US technical leadership will ensure that US experts have a leading role in synthetic <span class="hlt">biology</span> governance, regulation, and oversight. Measures to increase competitiveness in S&T generally are broadly applicable for synthetic <span class="hlt">biology</span> and should be pursued. However, the US government will also need to take action <span class="hlt">on</span> fundamental issues that will affect the field's development, such as countering anti-GMO (genetically modified organism) sentiments and anti-GMO legislation. The United States should maintain its regulatory approach so that it is the product that is regulated, not the method used to <span class="hlt">create</span> a product. At the same time, the United States needs to ensure that the regulatory framework is updated so that synthetic <span class="hlt">biology</span> products do not fall into regulatory gaps. Finally, the United States needs to pay close attention to how synthetic <span class="hlt">biology</span> applications may be governed internationally, such as through the Nagoya Protocol of the Convention <span class="hlt">on</span> <span class="hlt">Biological</span> Diversity, so that beneficial applications may be realized. PMID:26690379</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26690379','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26690379"><span>US Competitiveness in Synthetic <span class="hlt">Biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gronvall, Gigi Kwik</p> <p>2015-01-01</p> <p>Synthetic <span class="hlt">biology</span> is an emerging technical field that aims to make <span class="hlt">biology</span> easier to engineer; the field has applications in strategically important sectors for the US economy. While the United States currently leads in synthetic <span class="hlt">biology</span> R&D, other nations are heavily investing in order to boost their economies, which will inevitably diminish the US leadership position. This outcome is not entirely negative--additional investments will expand markets--but it is critical that the US government take steps to remain competitive: There are applications from which the US population and economy may benefit; there are specific applications with importance for national defense; and US technical leadership will ensure that US experts have a leading role in synthetic <span class="hlt">biology</span> governance, regulation, and oversight. Measures to increase competitiveness in S&T generally are broadly applicable for synthetic <span class="hlt">biology</span> and should be pursued. However, the US government will also need to take action <span class="hlt">on</span> fundamental issues that will affect the field's development, such as countering anti-GMO (genetically modified organism) sentiments and anti-GMO legislation. The United States should maintain its regulatory approach so that it is the product that is regulated, not the method used to <span class="hlt">create</span> a product. At the same time, the United States needs to ensure that the regulatory framework is updated so that synthetic <span class="hlt">biology</span> products do not fall into regulatory gaps. Finally, the United States needs to pay close attention to how synthetic <span class="hlt">biology</span> applications may be governed internationally, such as through the Nagoya Protocol of the Convention <span class="hlt">on</span> <span class="hlt">Biological</span> Diversity, so that beneficial applications may be realized.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=principles+AND+accounting&pg=4&id=EJ967650','ERIC'); return false;" href="https://eric.ed.gov/?q=principles+AND+accounting&pg=4&id=EJ967650"><span>Evidence <span class="hlt">on</span> the Effectiveness of <span class="hlt">On-Line</span> Homework</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Dillard-Eggers, Jane; Wooten, Tommy; Childs, Brad; Coker, John</p> <p>2008-01-01</p> <p>The purpose of this research is to evaluate the impact and effectiveness of <span class="hlt">on-line</span> homework in principles of accounting classes. We surveyed students to determine their degree of satisfaction with <span class="hlt">on-line</span> homework and their perceptions about its effectiveness in enhancing their learning. We also gathered data to determine the extent of online…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28159623','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28159623"><span>Synthetic <span class="hlt">biology</span> era: Improving antibiotic's world.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Guzmán-Trampe, Silvia; Ceapa, Corina D; Manzo-Ruiz, Monserrat; Sánchez, Sergio</p> <p>2017-06-15</p> <p>The emergence of antibiotic-resistant pathogen microorganisms is problematic in the context of the current spectrum of available medication. The poor specificity and the high toxicity of some available molecules have made imperative the search for new strategies to improve the specificity and to pursue the discovery of novel compounds with increased bioactivity. Using living cells as platforms, synthetic <span class="hlt">biology</span> has counteracted this problem by offering novel pathways to <span class="hlt">create</span> synthetic systems with improved and desired functions. Among many other biotechnological approaches, the advances in synthetic <span class="hlt">biology</span> have made it possible to design and construct novel <span class="hlt">biological</span> systems in order to look for new drugs with increased bioactivity. Advancements have also been made in the redesigning of RNA and DNA molecules in order to engineer antibiotic clusters for antibiotic overexpression. As for the production of these antibacterial compounds, yeasts and filamentous fungi as well as gene therapy are utilized to enhance protein solubility. Specific delivery is achieved by <span class="hlt">creating</span> chimeras using plant genes into bacterial hosts. Some of these synthetic systems are currently in clinical trials, proving the proficiency of synthetic <span class="hlt">biology</span> in terms of both pharmacological activities as well as an increase in the biosafety of treatments. It is possible that we may just be seeing the tip of the iceberg, and synthetic <span class="hlt">biology</span> applications will overpass expectations beyond our present knowledge. Copyright © 2017. Published by Elsevier Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16615800','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16615800"><span>Automated <span class="hlt">on-line</span> renewable solid-phase extraction-liquid chromatography exploiting multisyringe flow injection-bead injection lab-<span class="hlt">on</span>-valve analysis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Quintana, José Benito; Miró, Manuel; Estela, José Manuel; Cerdà, Víctor</p> <p>2006-04-15</p> <p>In this paper, the third generation of flow injection analysis, also named the lab-<span class="hlt">on</span>-valve (LOV) approach, is proposed for the first time as a front end to high-performance liquid chromatography (HPLC) for <span class="hlt">on-line</span> solid-phase extraction (SPE) sample processing by exploiting the bead injection (BI) concept. The proposed microanalytical system based <span class="hlt">on</span> discontinuous programmable flow features automated packing (and withdrawal after single use) of a small amount of sorbent (<5 mg) into the microconduits of the flow network and quantitative elution of sorbed species into a narrow band (150 microL of 95% MeOH). The hyphenation of multisyringe flow injection analysis (MSFIA) with BI-LOV prior to HPLC analysis is utilized for <span class="hlt">on-line</span> postextraction treatment to ensure chemical compatibility between the eluate medium and the initial HPLC gradient conditions. This circumvents the band-broadening effect commonly observed in conventional <span class="hlt">on-line</span> SPE-based sample processors due to the low eluting strength of the mobile phase. The potential of the novel MSFI-BI-LOV hyphenation for <span class="hlt">on-line</span> handling of complex environmental and <span class="hlt">biological</span> samples prior to reversed-phase chromatographic separations was assessed for the expeditious determination of five acidic pharmaceutical residues (viz., ketoprofen, naproxen, bezafibrate, diclofenac, and ibuprofen) and one metabolite (viz., salicylic acid) in surface water, urban wastewater, and urine. To this end, the copolymeric divinylbenzene-co-n-vinylpyrrolidone beads (Oasis HLB) were utilized as renewable sorptive entities in the micromachined unit. The automated analytical method features relative recovery percentages of >88%, limits of detection within the range 0.02-0.67 ng mL(-1), and coefficients of variation <11% for the column renewable mode and gives rise to a drastic reduction in operation costs ( approximately 25-fold) as compared to <span class="hlt">on-line</span> column switching systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19940020623','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19940020623"><span><span class="hlt">On-line</span> evaluation of multiloop digital controller performance</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Wieseman, Carol D.</p> <p>1993-01-01</p> <p>The purpose of this presentation is to inform the Guidance and Control community of capabilities which were developed by the Aeroservoelasticity Branch to evaluate the performance of multivariable control laws, <span class="hlt">on-line</span>, during wind-tunnel testing. The capabilities are generic enough to be useful for all kinds of <span class="hlt">on-line</span> analyses involving multivariable control in experimental testing. Consequently, it was decided to present this material at this workshop even though it has been presented elsewhere. Topics covered include: essential <span class="hlt">on-line</span> analysis requirements; <span class="hlt">on-line</span> analysis capabilities; <span class="hlt">on-line</span> analysis software; frequency domain procedures; controller performance evaluation frequency-domain flutter suppression; and plant determination.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/6578297-mechanism-biological-effects-observed-honey-bees-apis-mellifera-hived-under-extra-high-voltage-transmission-lines-implications-derived-from-bee-exposure-simulated-intense-electric-fields-shocks','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/6578297-mechanism-biological-effects-observed-honey-bees-apis-mellifera-hived-under-extra-high-voltage-transmission-lines-implications-derived-from-bee-exposure-simulated-intense-electric-fields-shocks"><span>Mechanism of <span class="hlt">biological</span> effects observed in honey bees (Apis mellifera, L. ) hived under extra-high-voltage transmission <span class="hlt">lines</span>: implications derived from bee exposure to simulated intense electric fields and shocks</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Bindokas, V.P.; Gauger, J.R.; Greenberg, B.</p> <p></p> <p>This work explores mechanisms for disturbance of honey bee colonies under a 765 kV, 60-Hz transmission <span class="hlt">line</span> (electric (E) field = 7 kV/m) observed in previous studies. Proposed mechanisms fell into two categories: direct bee perception of enhanced in-hive E fields and perception of shock from induced currents. The adverse <span class="hlt">biological</span> effects could be reproduced in simulations where only the worker bees were exposed to shock or to E field in elongated hive entranceways (= tunnels). We now report the results of full-scale experiments using the tunnel exposure scheme, which assesses the contribution of shock and intense E field tomore » colony disturbance. Exposure of worker bees (1400 h) to 60-Hz E fields including 100 kV/m under moisture-free conditions within a nonconductive tunnel causes no deleterious affect <span class="hlt">on</span> colony behavior. Exposure of bees in conductive (e.g., wet) tunnels produces bee disturbance, increased mortality, abnormal propolization, and possible impairment of colony growth. We propose that this substrate dependence of bee disturbance is the result of perception of shock from coupled body currents and enhanced current densities postulated to exist in the legs and thorax of bees <span class="hlt">on</span> conductors. Similarly, disturbance occurs when bees are exposed to step-potential-induced currents. At 275-350 nA single bees are disturbed; at 600 nA bees begin abnormal propolization behavior; and stinging occurs at 900 nA. We conclude that <span class="hlt">biological</span> effects seen in bee colonies under a transmission <span class="hlt">line</span> are primarily the result of electric shock from induced hive currents. This evaluation is based <span class="hlt">on</span> the limited effects of E-field exposure in tunnels, the observed disturbance thresholds caused by shocks in tunnels, and the ability of hives exposed under a transmission <span class="hlt">line</span> to source currents 100-1,000 times the shock thresholds.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18569783','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18569783"><span>Synthesis and <span class="hlt">biological</span> activity of mustard derivatives of thymine.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hadj-Bouazza, Amel; Teste, Karine; Colombeau, Ludovic; Chaleix, Vincent; Zerrouki, Rachida; Kraemer, Michel; Sainte Catherine, Odile</p> <p>2008-05-01</p> <p>The synthesis and <span class="hlt">biological</span> activity of a novel DNA cross-linking antitumor agent is presented. The new alkylating agent significantly inhibited cell proliferation, migration and invasion as tested in vitro <span class="hlt">on</span> the A431 vulvar epidermal carcinoma cell <span class="hlt">line</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=conversion+AND+rate+AND+online&id=ED083996','ERIC'); return false;" href="https://eric.ed.gov/?q=conversion+AND+rate+AND+online&id=ED083996"><span><span class="hlt">On-Line</span> Cataloging.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>OCLC Online Computer Library Center, Inc., Dublin, OH.</p> <p></p> <p>The principal objective of the Ohio College Library Center is to lower the rate of rise of per-unit library costs while increasing the availability of library resources for use by patrons of participating libraries. A major procedural goal of the <span class="hlt">on-line</span> cataloging system is to furnish cataloging personnel in individual libraries with…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17487085','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17487085"><span><span class="hlt">Line</span> width determination using a biomimetic fly eye vision system.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Benson, John B; Wright, Cameron H G; Barrett, Steven F</p> <p>2007-01-01</p> <p>Developing a new vision system based <span class="hlt">on</span> the vision of the common house fly, Musca domestica, has <span class="hlt">created</span> many interesting design challenges. One of those problems is <span class="hlt">line</span> width determination, which is the topic of this paper. It has been discovered that <span class="hlt">line</span> width can be determined with a single sensor as long as either the sensor, or the object in question, has a constant, known velocity. This is an important first step for determining the width of any arbitrary object, with unknown velocity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28240207','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28240207"><span>[Application of microelectronics CAD tools to synthetic <span class="hlt">biology</span>].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Madec, Morgan; Haiech, Jacques; Rosati, Élise; Rezgui, Abir; Gendrault, Yves; Lallement, Christophe</p> <p>2017-02-01</p> <p>Synthetic <span class="hlt">biology</span> is an emerging science that aims to <span class="hlt">create</span> new <span class="hlt">biological</span> functions that do not exist in nature, based <span class="hlt">on</span> the knowledge acquired in life science over the last century. Since the beginning of this century, several projects in synthetic <span class="hlt">biology</span> have emerged. The complexity of the developed artificial bio-functions is relatively low so that empirical design methods could be used for the design process. Nevertheless, with the increasing complexity of <span class="hlt">biological</span> circuits, this is no longer the case and a large number of computer aided design softwares have been developed in the past few years. These tools include languages for the behavioral description and the mathematical modelling of <span class="hlt">biological</span> systems, simulators at different levels of abstraction, libraries of <span class="hlt">biological</span> devices and circuit design automation algorithms. All of these tools already exist in other fields of engineering sciences, particularly in microelectronics. This is the approach that is put forward in this paper. © 2017 médecine/sciences – Inserm.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_16 --> <div id="page_17" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="321"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ1093162.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ1093162.pdf"><span>Locating Fractions <span class="hlt">on</span> a Number <span class="hlt">Line</span></span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Wong, Monica</p> <p>2013-01-01</p> <p>Understanding fractions remains problematic for many students. The use of the number <span class="hlt">line</span> aids in this understanding, but requires students to recognise that a fraction represents the distance from zero to a dot or arrow marked <span class="hlt">on</span> a number <span class="hlt">line</span> which is a linear scale. This article continues the discussion from "Identifying Fractions <span class="hlt">on</span> a…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/ED419552.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/ED419552.pdf"><span><span class="hlt">On-Line</span> Assessment: What, Why, How.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Natal, Dottie</p> <p></p> <p>Recent increases in the speed and accessibility of computers and networks have made it possible to administer tests <span class="hlt">on-line</span>. <span class="hlt">On-line</span> assessment can be conducted in a controlled setting, such as a testing center, or distributed over local area networks or the Internet to libraries and student homes, allowing students the flexibility to complete…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19740005768','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19740005768"><span><span class="hlt">On-line</span> diagnosis of sequential systems</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Sundstrom, R. J.</p> <p>1973-01-01</p> <p>A model for <span class="hlt">on-line</span> diagnosis was investigated for discrete-time systems, and resettable sequential systems. Generalized notions of a realization are discussed along with fault tolerance and errors. Further investigation into the theory of <span class="hlt">on-line</span> diagnosis is recommended for three levels: binary state-assigned level, logical circuit level, and the subsystem-network level.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27110921','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27110921"><span>Data Integration and Mining for Synthetic <span class="hlt">Biology</span> Design.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mısırlı, Göksel; Hallinan, Jennifer; Pocock, Matthew; Lord, Phillip; McLaughlin, James Alastair; Sauro, Herbert; Wipat, Anil</p> <p>2016-10-21</p> <p>One aim of synthetic biologists is to <span class="hlt">create</span> novel and predictable <span class="hlt">biological</span> systems from simpler modular parts. This approach is currently hampered by a lack of well-defined and characterized parts and devices. However, there is a wealth of existing <span class="hlt">biological</span> information, which can be used to identify and characterize <span class="hlt">biological</span> parts, and their design constraints in the literature and numerous <span class="hlt">biological</span> databases. However, this information is spread among these databases in many different formats. New computational approaches are required to make this information available in an integrated format that is more amenable to data mining. A tried and tested approach to this problem is to map disparate data sources into a single data set, with common syntax and semantics, to produce a data warehouse or knowledge base. Ontologies have been used extensively in the life sciences, providing this common syntax and semantics as a model for a given <span class="hlt">biological</span> domain, in a fashion that is amenable to computational analysis and reasoning. Here, we present an ontology for applications in synthetic <span class="hlt">biology</span> design, SyBiOnt, which facilitates the modeling of information about <span class="hlt">biological</span> parts and their relationships. SyBiOnt was used to <span class="hlt">create</span> the SyBiOntKB knowledge base, incorporating and building upon existing life sciences ontologies and standards. The reasoning capabilities of ontologies were then applied to automate the mining of <span class="hlt">biological</span> parts from this knowledge base. We propose that this approach will be useful to speed up synthetic <span class="hlt">biology</span> design and ultimately help facilitate the automation of the <span class="hlt">biological</span> engineering life cycle.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18361520','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18361520"><span>Electrospray micromixer chip for <span class="hlt">on-line</span> derivatization and kinetic studies.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Abonnenc, Mélanie; Dayon, Loïc; Perruche, Brice; Lion, Niels; Girault, Hubert H</p> <p>2008-05-01</p> <p>An electrospray microchip for mass spectrometry comprising an integrated passive mixer to carry out <span class="hlt">on</span>-chip chemical derivatizations is described. The microchip fabricated using UV-photoablation is composed of two microchannels linked together by a liquid junction. Downstream of this liquid junction, a mixing unit made of parallel oblique grooves is integrated to the microchannel in order to <span class="hlt">create</span> flow perturbations. Several mixer designs are evaluated. The mixer efficiency is investigated both by fluorescence study and mass spectrometric monitoring of the tagging reaction of cysteinyl peptides with 1,4-benzoquinone. The comparisons with a microchip without a mixing unit and a kinetic model are used to assess the efficiency of the mixer showing tagging kinetics close to that of bulk reactions in an ideally mixed reactor. As an ultimate application, the electrospray micromixer is implemented in a LC-MS workflow. <span class="hlt">On-line</span> derivatization of albumin tryptic peptides after a reversed-phase separation and counting of their cysteines drastically enhance the protein identification.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22458684-lung-cancer-cell-line-screen-links-fanconi-anemia-brca-pathway-defects-increased-relative-biological-effectiveness-proton-radiation','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22458684-lung-cancer-cell-line-screen-links-fanconi-anemia-brca-pathway-defects-increased-relative-biological-effectiveness-proton-radiation"><span>Lung Cancer Cell <span class="hlt">Line</span> Screen Links Fanconi Anemia/BRCA Pathway Defects to Increased Relative <span class="hlt">Biological</span> Effectiveness of Proton Radiation</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Liu, Qi; Ghosh, Priyanjali; Magpayo, Nicole</p> <p>2015-04-01</p> <p>Purpose: Growing knowledge of genomic heterogeneity in cancer, especially when it results in altered DNA damage responses, requires re-examination of the generic relative <span class="hlt">biological</span> effectiveness (RBE) of 1.1 of protons. Methods and Materials: For determination of cellular radiosensitivity, we irradiated 17 lung cancer cell <span class="hlt">lines</span> at the mid-spread-out Bragg peak of a clinical proton beam (linear energy transfer, 2.5 keV/μm). For comparison, 250-kVp X rays and {sup 137}Cs γ-rays were used. To estimate the RBE of protons relative to {sup 60}Co (Co60eq), we assigned an RBE(Co60Eq) of 1.1 to X rays to correct the physical dose measured. Standard DNA repair foci assaysmore » were used to monitor damage responses. FANCD2 was depleted using RNA interference. Results: Five lung cancer cell <span class="hlt">lines</span> (29.4%) exhibited reduced clonogenic survival after proton irradiation compared with X-irradiation with the same physical doses. This was confirmed in a 3-dimensional sphere assay. Corresponding proton RBE(Co60Eq) estimates were statistically significantly different from 1.1 (P≤.05): 1.31 to 1.77 (for a survival fraction of 0.5). In 3 of these <span class="hlt">lines</span>, increased RBE was correlated with alterations in the Fanconi anemia (FA)/BRCA pathway of DNA repair. In Calu-6 cells, the data pointed toward an FA pathway defect, leading to a previously unreported persistence of proton-induced RAD51 foci. The FA/BRCA-defective cells displayed a 25% increase in the size of subnuclear 53BP1 foci 18 hours after proton irradiation. Conclusions: Our cell <span class="hlt">line</span> screen has revealed variations in proton RBE that are partly due to FA/BRCA pathway defects, suggesting that the use of a generic RBE for cancers should be revisited. We propose that functional biomarkers, such as size of residual 53BP1 foci, may be used to identify cancers with increased sensitivity to proton radiation.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1559726','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1559726"><span>Automatic document classification of <span class="hlt">biological</span> literature</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Chen, David; Müller, Hans-Michael; Sternberg, Paul W</p> <p>2006-01-01</p> <p>Background Document classification is a wide-spread problem with many applications, from organizing search engine snippets to spam filtering. We previously described Textpresso, a text-mining system for <span class="hlt">biological</span> literature, which marks up full text according to a shallow ontology that includes terms of <span class="hlt">biological</span> interest. This project investigates document classification in the context of <span class="hlt">biological</span> literature, making use of the Textpresso markup of a corpus of Caenorhabditis elegans literature. Results We present a two-step text categorization algorithm to classify a corpus of C. elegans papers. Our classification method first uses a support vector machine-trained classifier, followed by a novel, phrase-based clustering algorithm. This clustering step autonomously <span class="hlt">creates</span> cluster labels that are descriptive and understandable by humans. This clustering engine performed better <span class="hlt">on</span> a standard test-set (Reuters 21578) compared to previously published results (F-value of 0.55 vs. 0.49), while producing cluster descriptions that appear more useful. A web interface allows researchers to quickly navigate through the hierarchy and look for documents that belong to a specific concept. Conclusion We have demonstrated a simple method to classify <span class="hlt">biological</span> documents that embodies an improvement over current methods. While the classification results are currently optimized for Caenorhabditis elegans papers by human-<span class="hlt">created</span> rules, the classification engine can be adapted to different types of documents. We have demonstrated this by presenting a web interface that allows researchers to quickly navigate through the hierarchy and look for documents that belong to a specific concept. PMID:16893465</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26049713','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26049713"><span>Robust and automated three-dimensional segmentation of densely packed cell nuclei in different <span class="hlt">biological</span> specimens with <span class="hlt">Lines</span>-of-Sight decomposition.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mathew, B; Schmitz, A; Muñoz-Descalzo, S; Ansari, N; Pampaloni, F; Stelzer, E H K; Fischer, S C</p> <p>2015-06-08</p> <p>Due to the large amount of data produced by advanced microscopy, automated image analysis is crucial in modern <span class="hlt">biology</span>. Most applications require reliable cell nuclei segmentation. However, in many <span class="hlt">biological</span> specimens cell nuclei are densely packed and appear to touch one another in the images. Therefore, a major difficulty of three-dimensional cell nuclei segmentation is the decomposition of cell nuclei that apparently touch each other. Current methods are highly adapted to a certain <span class="hlt">biological</span> specimen or a specific microscope. They do not ensure similarly accurate segmentation performance, i.e. their robustness for different datasets is not guaranteed. Hence, these methods require elaborate adjustments to each dataset. We present an advanced three-dimensional cell nuclei segmentation algorithm that is accurate and robust. Our approach combines local adaptive pre-processing with decomposition based <span class="hlt">on</span> <span class="hlt">Lines</span>-of-Sight (LoS) to separate apparently touching cell nuclei into approximately convex parts. We demonstrate the superior performance of our algorithm using data from different specimens recorded with different microscopes. The three-dimensional images were recorded with confocal and light sheet-based fluorescence microscopes. The specimens are an early mouse embryo and two different cellular spheroids. We compared the segmentation accuracy of our algorithm with ground truth data for the test images and results from state-of-the-art methods. The analysis shows that our method is accurate throughout all test datasets (mean F-measure: 91%) whereas the other methods each failed for at least one dataset (F-measure≤69%). Furthermore, nuclei volume measurements are improved for LoS decomposition. The state-of-the-art methods required laborious adjustments of parameter values to achieve these results. Our LoS algorithm did not require parameter value adjustments. The accurate performance was achieved with one fixed set of parameter values. We developed a novel and</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3872726','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3872726"><span>IBES: a tool for <span class="hlt">creating</span> instructions based <span class="hlt">on</span> event segmentation</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mura, Katharina; Petersen, Nils; Huff, Markus; Ghose, Tandra</p> <p>2013-01-01</p> <p>Receiving informative, well-structured, and well-designed instructions supports performance and memory in assembly tasks. We describe IBES, a tool with which users can quickly and easily <span class="hlt">create</span> multimedia, step-by-step instructions by segmenting a video of a task into segments. In a validation study we demonstrate that the step-by-step structure of the visual instructions <span class="hlt">created</span> by the tool corresponds to the natural event boundaries, which are assessed by event segmentation and are known to play an important role in memory processes. In one part of the study, 20 participants <span class="hlt">created</span> instructions based <span class="hlt">on</span> videos of two different scenarios by using the proposed tool. In the other part of the study, 10 and 12 participants respectively segmented videos of the same scenarios yielding event boundaries for coarse and fine events. We found that the visual steps chosen by the participants for <span class="hlt">creating</span> the instruction manual had corresponding events in the event segmentation. The number of instructional steps was a compromise between the number of fine and coarse events. Our interpretation of results is that the tool picks up <span class="hlt">on</span> natural human event perception processes of segmenting an ongoing activity into events and enables the convenient transfer into meaningful multimedia instructions for assembly tasks. We discuss the practical application of IBES, for example, <span class="hlt">creating</span> manuals for differing expertise levels, and give suggestions for research <span class="hlt">on</span> user-oriented instructional design based <span class="hlt">on</span> this tool. PMID:24454296</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24454296','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24454296"><span>IBES: a tool for <span class="hlt">creating</span> instructions based <span class="hlt">on</span> event segmentation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mura, Katharina; Petersen, Nils; Huff, Markus; Ghose, Tandra</p> <p>2013-12-26</p> <p>Receiving informative, well-structured, and well-designed instructions supports performance and memory in assembly tasks. We describe IBES, a tool with which users can quickly and easily <span class="hlt">create</span> multimedia, step-by-step instructions by segmenting a video of a task into segments. In a validation study we demonstrate that the step-by-step structure of the visual instructions <span class="hlt">created</span> by the tool corresponds to the natural event boundaries, which are assessed by event segmentation and are known to play an important role in memory processes. In one part of the study, 20 participants <span class="hlt">created</span> instructions based <span class="hlt">on</span> videos of two different scenarios by using the proposed tool. In the other part of the study, 10 and 12 participants respectively segmented videos of the same scenarios yielding event boundaries for coarse and fine events. We found that the visual steps chosen by the participants for <span class="hlt">creating</span> the instruction manual had corresponding events in the event segmentation. The number of instructional steps was a compromise between the number of fine and coarse events. Our interpretation of results is that the tool picks up <span class="hlt">on</span> natural human event perception processes of segmenting an ongoing activity into events and enables the convenient transfer into meaningful multimedia instructions for assembly tasks. We discuss the practical application of IBES, for example, <span class="hlt">creating</span> manuals for differing expertise levels, and give suggestions for research <span class="hlt">on</span> user-oriented instructional design based <span class="hlt">on</span> this tool.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22624302-su-irradiation-human-cell-lines-using-various-ions','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22624302-su-irradiation-human-cell-lines-using-various-ions"><span>SU-C-204-04: Irradiation of Human Cell <span class="hlt">Lines</span> Using Various Ions</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Lin, Y; McMahon, S; Kaminuma, T</p> <p>2016-06-15</p> <p>Purpose: The purpose of this study is to investigate and quantify the <span class="hlt">biological</span> effects of ion radiation using several human cell <span class="hlt">lines</span>. We aim to answer the question of whether carbon ion the most ideal ion species for heavy ion radiotherapy. Methods: The cells were irradiated at different positions along the pristine Bragg peak of several ions with different atomic number. The <span class="hlt">biological</span> effectiveness was evaluated using the clonogenic cell survival assay. Irradiation of three human lung cancer cell <span class="hlt">lines</span> and a fibroblast cell <span class="hlt">line</span> were undertaken using the charged particle beam at the NASA Space Radiation Laboratory at Brookhavenmore » National Lab. Four mono-energetic ion beams (carbon, oxygen, helium and lithium) were used to irradiate the cells. Water or media-filled T25 flasks were <span class="hlt">lined</span> up along the beam <span class="hlt">line</span> so that the cell-containing surfaces of the flasks were placed at a specific depth along the pristine Bragg curve. Four depths along the curve, representing entrance point, rising peak, peak and distal fall off, were selected to determine <span class="hlt">biological</span> effectiveness. Gaf-chromic films were placed between the flasks to monitor the irradiation as soon as it was finished. Results: For all ion radiations, the maximum cell killing effect occurs at either peak or distal fall off, depending <span class="hlt">on</span> the cell <span class="hlt">lines</span>. For instance, for the fibroblast cell <span class="hlt">line</span> AGO1522, RBEs of 1.4, 1.2, 1.4 and 1.9 were observed at the Bragg peak for Helium, Lithium, Carbon and Oxygen ions. Comparing positions, RBEs of 0.9, 1.2, 1.4 and 1.8 were observed for carbon irradiation of AGO-1522 cells positions corresponding to entrance, rising peak, peak and distal fall off. Conclusion: RBE values differ with position in the Bragg peak, ion species and cell <span class="hlt">line</span>. Ions other than carbon may prove more effective in certain irradiation conditions and may contribute to optimized heavy ion therapy.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006PhDT........55M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006PhDT........55M"><span>Rethinking <span class="hlt">biology</span> instruction: The application of DNR-based instruction to the learning and teaching of <span class="hlt">biology</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Maskiewicz, April Lee</p> <p></p> <p> that <span class="hlt">create</span> cognitive disequilibrium-equilibrium phases and thus lead to modification or refinement of existing schemes. Elements that contributed to <span class="hlt">creating</span> intellectual need include (a) problem tasks that built <span class="hlt">on</span> students' existing knowledge; (b) problem tasks that challenged students; (c) a routine in which students presented their group's solution to the class; and (d) the didactical contract (Brousseau, 1997) established in the classroom.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27417148','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27417148"><span>Predictors of chronic pulmonary vein reconnections after contact force-guided ablation: importance of completing electrical isolation with circumferential <span class="hlt">lines</span> and <span class="hlt">creating</span> sufficient ablation lesion densities.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Nakamura, Kohki; Naito, Shigeto; Sasaki, Takehito; Minami, Kentaro; Take, Yutaka; Shimizu, Satoru; Yamaguchi, Yoshiaki; Yano, Toshiaki; Senga, Michiharu; Yamashita, Eiji; Sugai, Yoshinao; Kumagai, Koji; Funabashi, Nobusada; Oshima, Shigeru</p> <p>2016-12-01</p> <p>We aimed to identify the predictors of chronic pulmonary vein reconnections (CPVRs) after contact force (CF)-guided circumferential PV isolation (CPVI) of atrial fibrillation (AF). Forty-nine consecutive patients undergoing second ablation procedures for recurrent AF after CF-guided ablation were retrospectively studied. The CPVI was performed by point-by-point ablation with a target CF of 15-20 g. The incidence of CPVRs was evaluated along the right- and left-sided anterior and posterior CPVI regions (Ant-RPVs, Post-RPVs, Ant-LPVs, and Post-LPVs). CPVRs were observed in 30.6, 22.4, 20.4, and 32.7 % of patients along the Ant-RPVs, Post-RPVs, Ant-LPVs, and Post-LPVs, respectively (P = 0.436). In the multivariate logistic analyses, completing a left atrium-PV conduction block with touch-up ablation inside the initially estimated CPVI <span class="hlt">lines</span> (Ant-RPVs, Post-RPVs, Ant-LPVs, Post-LPVs; odds ratio [OR] 5.747, 15.000, 207.619, 7.940; P = 0.032, 0.004, 0.034, 0.021) and region length (Post-LPVs; OR 3.183, P = 0.027) were positive predictors of CPVRs, while the mean CF (Ant-RPVs; OR 0.861, P = 0.045) and number of radiofrequency applications per unit length (Ant-LPVs, Post-LPVs; OR 0.038, 0.122; P = 0.034, 0.029) were negative predictors. At optimal cutoffs of 5.8 cm for the region length, 14.2 g for the mean CF, and 1.97/cm (Ant-LPVs) and 2.01/cm (Post-LPVs) for the radiofrequency application density, the sensitivity and specificity were 93.8 and 63.6 %, 60.0 and 76.5 %, 90.0 and 64.1 %, and 75.0 and 63.6 %, respectively. Completing PVI with circumferential <span class="hlt">lines</span> without touch-up ablation and <span class="hlt">creating</span> a sufficient density of radiofrequency ablation lesions <span class="hlt">on</span> the <span class="hlt">lines</span> with a sufficient CF may be necessary to prevent CPVRs after a CF-guided CPVI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28585435','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28585435"><span><span class="hlt">Creating</span> animal models, why not use the Chinese tree shrew (Tupaia belangeri chinensis)?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yao, Yong-Gang</p> <p>2017-05-18</p> <p>The Chinese tree shrew ( Tupaia belangeri chinensis ), a squirrel-like and rat-sized mammal, has a wide distribution in Southeast Asia, South and Southwest China and has many unique characteristics that make it suitable for use as an experimental animal. There have been many studies using the tree shrew ( Tupaia belangeri ) aimed at increasing our understanding of fundamental <span class="hlt">biological</span> mechanisms and for the modeling of human diseases and therapeutic responses. The recent release of a publicly available annotated genome sequence of the Chinese tree shrew and its genome database (www.treeshrewdb.org) has offered a solid base from which it is possible to elucidate the basic <span class="hlt">biological</span> properties and <span class="hlt">create</span> animal models using this species. The extensive characterization of key factors and signaling pathways in the immune and nervous systems has shown that tree shrews possess both conserved and unique features relative to primates. Hitherto, the tree shrew has been successfully used to <span class="hlt">create</span> animal models for myopia, depression, breast cancer, alcohol-induced or non-alcoholic fatty liver diseases, herpes simplex virus type 1 (HSV-1) and hepatitis C virus (HCV) infections, to name a few. The recent successful genetic manipulation of the tree shrew has opened a new avenue for the wider usage of this animal in biomedical research. In this opinion paper, I attempt to summarize the recent research advances that have used the Chinese tree shrew, with a focus <span class="hlt">on</span> the new knowledge obtained by using the <span class="hlt">biological</span> properties identified using the tree shrew genome, a proposal for the genome-based approach for <span class="hlt">creating</span> animal models, and the genetic manipulation of the tree shrew. With more studies using this species and the application of cutting-edge gene editing techniques, the tree shrew will continue to be under the spot light as a viable animal model for investigating the basis of many different human diseases.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18983935','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18983935"><span>Toward scalable parts families for predictable design of <span class="hlt">biological</span> circuits.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lucks, Julius B; Qi, Lei; Whitaker, Weston R; Arkin, Adam P</p> <p>2008-12-01</p> <p>Our current ability to engineer <span class="hlt">biological</span> circuits is hindered by design cycles that are costly in terms of time and money, with constructs failing to operate as desired, or evolving away from the desired function once deployed. Synthetic biologists seek to understand <span class="hlt">biological</span> design principles and use them to <span class="hlt">create</span> technologies that increase the efficiency of the genetic engineering design cycle. Central to the approach is the creation of <span class="hlt">biological</span> parts--encapsulated functions that can be composited together to <span class="hlt">create</span> new pathways with predictable behaviors. We define five desirable characteristics of <span class="hlt">biological</span> parts--independence, reliability, tunability, orthogonality and composability, and review studies of small natural and synthetic <span class="hlt">biological</span> circuits that provide insights into each of these characteristics. We propose that the creation of appropriate sets of families of parts with these properties is a prerequisite for efficient, predictable engineering of new function in cells and will enable a large increase in the sophistication of genetic engineering applications.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29636378','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29636378"><span>Cardiac c-Kit <span class="hlt">Biology</span> Revealed by Inducible Transgenesis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gude, Natalie A; Firouzi, Fareheh; Broughton, Kathleen M; Ilves, Kelli; Nguyen, Kristine P; Payne, Christina R; Sacchi, Veronica; Monsanto, Megan M; Casillas, Alexandria R; Khalafalla, Farid G; Wang, Bingyan J; Ebeid, David E; Alvarez, Roberto; Dembitsky, Walter P; Bailey, Barbara A; van Berlo, Jop; Sussman, Mark A</p> <p>2018-06-22</p> <p><span class="hlt">Biological</span> significance of c-Kit as a cardiac stem cell marker and role(s) of c-Kit+ cells in myocardial development or response to pathological injury remain unresolved because of varied and discrepant findings. Alternative experimental models are required to contextualize and reconcile discordant published observations of cardiac c-Kit myocardial <span class="hlt">biology</span> and provide meaningful insights regarding clinical relevance of c-Kit signaling for translational cell therapy. The main objectives of this study are as follows: demonstrating c-Kit myocardial <span class="hlt">biology</span> through combined studies of both human and murine cardiac cells; advancing understanding of c-Kit myocardial <span class="hlt">biology</span> through creation and characterization of a novel, inducible transgenic c-Kit reporter mouse model that overcomes limitations inherent to knock-in reporter models; and providing perspective to reconcile disparate viewpoints <span class="hlt">on</span> c-Kit <span class="hlt">biology</span> in the myocardium. In vitro studies confirm a critical role for c-Kit signaling in both cardiomyocytes and cardiac stem cells. Activation of c-Kit receptor promotes cell survival and proliferation in stem cells and cardiomyocytes of either human or murine origin. For creation of the mouse model, the cloned mouse c-Kit promoter drives Histone2B-EGFP (enhanced green fluorescent protein; H2BEGFP) expression in a doxycycline-inducible transgenic reporter <span class="hlt">line</span>. The combination of c-Kit transgenesis coupled to H2BEGFP readout provides sensitive, specific, inducible, and persistent tracking of c-Kit promoter activation. Tagging efficiency for EGFP+/c-Kit+ cells is similar between our transgenic versus a c-Kit knock-in mouse <span class="hlt">line</span>, but frequency of c-Kit+ cells in cardiac tissue from the knock-in model is 55% lower than that from our transgenic <span class="hlt">line</span>. The c-Kit transgenic reporter model reveals intimate association of c-Kit expression with adult myocardial <span class="hlt">biology</span>. Both cardiac stem cells and a subpopulation of cardiomyocytes express c-Kit in uninjured adult heart</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22081222','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22081222"><span>Simbios: an NIH national center for physics-based simulation of <span class="hlt">biological</span> structures.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Delp, Scott L; Ku, Joy P; Pande, Vijay S; Sherman, Michael A; Altman, Russ B</p> <p>2012-01-01</p> <p>Physics-based simulation provides a powerful framework for understanding <span class="hlt">biological</span> form and function. Simulations can be used by biologists to study macromolecular assemblies and by clinicians to design treatments for diseases. Simulations help biomedical researchers understand the physical constraints <span class="hlt">on</span> <span class="hlt">biological</span> systems as they engineer novel drugs, synthetic tissues, medical devices, and surgical interventions. Although individual biomedical investigators make outstanding contributions to physics-based simulation, the field has been fragmented. Applications are typically limited to a single physical scale, and individual investigators usually must <span class="hlt">create</span> their own software. These conditions <span class="hlt">created</span> a major barrier to advancing simulation capabilities. In 2004, we established a National Center for Physics-Based Simulation of <span class="hlt">Biological</span> Structures (Simbios) to help integrate the field and accelerate biomedical research. In 6 years, Simbios has become a vibrant national center, with collaborators in 16 states and eight countries. Simbios focuses <span class="hlt">on</span> problems at both the molecular scale and the organismal level, with a long-term goal of uniting these in accurate multiscale simulations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015LSSR....4...35C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015LSSR....4...35C"><span>Constitutive expression of tdTomato protein as a cytotoxicity and proliferation marker for space radiation <span class="hlt">biology</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chishti, Arif A.; Hellweg, Christine E.; Berger, Thomas; Baumstark-Khan, Christa; Feles, Sebastian; Kätzel, Thorben; Reitz, Günther</p> <p>2015-01-01</p> <p>The radiation risk assessment for long-term space missions requires knowledge <span class="hlt">on</span> the <span class="hlt">biological</span> effectiveness of different space radiation components, e.g. heavy ions, <span class="hlt">on</span> the interaction of radiation and other space environmental factors such as microgravity, and <span class="hlt">on</span> the physical and <span class="hlt">biological</span> dose distribution in the human body. Space experiments and ground-based experiments at heavy ion accelerators require fast and reliable test systems with an easy readout for different endpoints. In order to determine the effect of different radiation qualities <span class="hlt">on</span> cellular proliferation and the <span class="hlt">biological</span> depth dose distribution after heavy ion exposure, a stable human cell <span class="hlt">line</span> expressing a novel fluorescent protein was established and characterized. tdTomato, a red fluorescent protein of the new generation with fast maturation and high fluorescence intensity, was selected as reporter of cell proliferation. Human embryonic kidney (HEK/293) cells were stably transfected with a plasmid encoding tdTomato under the control of the constitutively active cytomegalovirus (CMV) promoter (ptdTomato-N1). The stably transfected cell <span class="hlt">line</span> was named HEK-ptdTomato-N1 8. This cytotoxicity biosensor was tested by ionizing radiation (X-rays and accelerated heavy ions) exposure. As <span class="hlt">biological</span> endpoints, the proliferation kinetics and the cell density reached 100 h after irradiation reflected by constitutive expression of the tdTomato were investigated. Both were reduced dose-dependently after radiation exposure. Finally, the cell <span class="hlt">line</span> was used for <span class="hlt">biological</span> weighting of heavy ions of different linear energy transfer (LET) as space-relevant radiation quality. The relative <span class="hlt">biological</span> effectiveness of accelerated heavy ions in reducing cellular proliferation peaked at an LET of 91 keV/μm. The results of this study demonstrate that the HEK-ptdTomato-N1 reporter cell <span class="hlt">line</span> can be used as a fast and reliable biosensor system for detection of cytotoxic damage caused by ionizing radiation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/EJ1018798.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/EJ1018798.pdf"><span>Landlabs: An Integrated Approach to <span class="hlt">Creating</span> Agricultural Enterprises that Meet the Triple Bottom <span class="hlt">Line</span></span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Jordan, Nicholas; Schulte, Lisa A.; Williams, Carol; Mulla, David; Pitt, David; Slotterback, Carissa Schively; Jackson, Randall; Landis, Douglas; Dale, Bruce; Becker, Dennis; Rickenbach, Mark; Helmers, Matt; Bringi, Bobby</p> <p>2013-01-01</p> <p>Global demand is increasing for food, feed, and fiber; for additional agricultural outputs, such as biofuels; and for ecosystem services, such as clean water and outdoor recreation. In response, new agricultural enterprises are needed that produce more outputs from existing lands while meeting the "triple bottom <span class="hlt">line</span>" of high performance…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5455923','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5455923"><span><span class="hlt">Biological</span> Activation of Inert Ceramics: Recent Advances Using Tailored Self-Assembled Monolayers <span class="hlt">on</span> Implant Ceramic Surfaces</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Böke, Frederik; Schickle, Karolina; Fischer, Horst</p> <p>2014-01-01</p> <p>High-strength ceramics as materials for medical implants have a long, research-intensive history. Yet, especially <span class="hlt">on</span> applications where the ceramic components are in direct contact with the surrounding tissue, an unresolved issue is its inherent property of <span class="hlt">biological</span> inertness. To combat this, several strategies have been investigated over the last couple of years. One promising approach investigates the technique of Self-Assembled Monolayers (SAM) and subsequent chemical functionalization to <span class="hlt">create</span> a <span class="hlt">biologically</span> active tissue-facing surface layer. Implementation of this would have a beneficial impact <span class="hlt">on</span> several fields in modern implant medicine such as hip and knee arthroplasty, dental applications and related fields. This review aims to give a summarizing overview of the latest advances in this recently emerging field, along with thorough introductions of the underlying mechanism of SAMs and surface cell attachment mechanics <span class="hlt">on</span> the cell side. PMID:28788687</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_17 --> <div id="page_18" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="341"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26284562','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26284562"><span><span class="hlt">Biologic</span> agents for IBD: practical insights.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Danese, Silvio; Vuitton, Lucine; Peyrin-Biroulet, Laurent</p> <p>2015-09-01</p> <p>Six <span class="hlt">biologic</span> agents are currently approved for the treatment of IBD: four anti-TNF agents (infliximab, adalimumab, golimumab and certolizumab pegol) and two anti-integrin agents (natalizumab and vedolizumab). In Crohn's disease and ulcerative colitis refractory to standard medications, treatment choice among available <span class="hlt">biologic</span> agents can be challenging. Several parameters should be taken into account to help physicians through the decision-making process, including the comparative effectiveness and long-term safety profile, availability and labelling in the prescriber's country, international guidelines, and cost, as well as patient preferences (such as the route of administration). Herein, we provide practical insights <span class="hlt">on</span> the use of <span class="hlt">biologic</span> agents in IBD. The results of head-to-head trials between <span class="hlt">biologic</span> agents are eagerly awaited to guide decision-making regarding the choice of first-<span class="hlt">line</span> <span class="hlt">biologic</span> agents and to determine whether switching within the same drug class or swapping (switching out of the drug class) is preferable after primary or secondary loss of response to the first <span class="hlt">biologic</span> agent. In the near future, treatment algorithms might evolve with the launch of new drugs (such as ustekinumab, tofacitinib and etrolizumab) and the increased use of biosimilars.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4171059','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4171059"><span>Comparative Study <span class="hlt">on</span> Interaction of Form and Motion Processing Streams by Applying Two Different Classifiers in Mechanism for Recognition of <span class="hlt">Biological</span> Movement</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p></p> <p>2014-01-01</p> <p>Research <span class="hlt">on</span> psychophysics, neurophysiology, and functional imaging shows particular representation of <span class="hlt">biological</span> movements which contains two pathways. The visual perception of <span class="hlt">biological</span> movements formed through the visual system called dorsal and ventral processing streams. Ventral processing stream is associated with the form information extraction; <span class="hlt">on</span> the other hand, dorsal processing stream provides motion information. Active basic model (ABM) as hierarchical representation of the human object had revealed novelty in form pathway due to applying Gabor based supervised object recognition method. It <span class="hlt">creates</span> more <span class="hlt">biological</span> plausibility along with similarity with original model. Fuzzy inference system is used for motion pattern information in motion pathway <span class="hlt">creating</span> more robustness in recognition process. Besides, interaction of these paths is intriguing and many studies in various fields considered it. Here, the interaction of the pathways to get more appropriated results has been investigated. Extreme learning machine (ELM) has been implied for classification unit of this model, due to having the main properties of artificial neural networks, but crosses from the difficulty of training time substantially diminished in it. Here, there will be a comparison between two different configurations, interactions using synergetic neural network and ELM, in terms of accuracy and compatibility. PMID:25276860</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20160011208','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20160011208"><span>Misconceptions of Synthetic <span class="hlt">Biology</span>: Lessons from an Interdisciplinary Summer School</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Verseux, Cyprien; Acevedo-Rocha, Carlos G.; Chizzolini, Fabio; Rothschild, Lynn J.</p> <p>2016-01-01</p> <p>In 2014, an international group of scholars from various fields analysed the "societal dimensions" of synthetic <span class="hlt">biology</span> in an interdisciplinary summer school. Here, we report and discuss the biologists' observations <span class="hlt">on</span> the general perception of synthetic <span class="hlt">biology</span> by non-biologists who took part in this event. Most attendees mainly associated synthetic <span class="hlt">biology</span> with contributions from the best-known public figures of the field, rarely mentioning other scientists. Media extrapolations of those contributions appeared to have <span class="hlt">created</span> unrealistic expectations and irrelevant fears that were widely disconnected from the current research in synthetic <span class="hlt">biology</span>. Another observation was that when debating developments in synthetic <span class="hlt">biology</span>, semantics strongly mattered: depending <span class="hlt">on</span> the terms used to present an application of synthetic <span class="hlt">biology</span>, attendees reacted in radically different ways. For example, using the term "GMOs" (genetically modified organisms) rather than the term "genetic engineering" led to very different reactions. Stimulating debates also happened with participants having unanticipated points of view, for instance biocentrist ethicists who argued that engineered microbes should not be used for human purposes. Another communication challenge emerged from the connotations and inaccuracies surrounding the word "life", which impaired constructive debates, thus leading to misconceptions about the abilities of scientists to engineer or even <span class="hlt">create</span> living organisms. Finally, it appeared that synthetic biologists tend to overestimate the knowledge of non-biologists, further affecting communication. The motivation and ability of synthetic biologists to communicate their work outside their research field needs to be fostered, notably towards policymakers who need a more accurate and technical understanding of the field to make informed decisions. Interdisciplinary events gathering scholars working in and around synthetic <span class="hlt">biology</span> are an effective tool in addressing those</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22680022-relativistic-iron-lines-accretion-disks-contribution-higher-order-images-strong-deflection-limit','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22680022-relativistic-iron-lines-accretion-disks-contribution-higher-order-images-strong-deflection-limit"><span>Relativistic iron <span class="hlt">lines</span> in accretion disks: the contribution of higher order images in the strong deflection limit</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Aldi, Giulio Francesco; Bozza, Valerio, E-mail: giuliofrancesco.aldi@sa.infn.it, E-mail: valboz@sa.infn.it</p> <p></p> <p>The shapes of relativistic iron <span class="hlt">lines</span> observed in spectra of candidate black holes carry the signatures of the strong gravitational fields in which the accretion disks lie. These <span class="hlt">lines</span> result from the sum of the contributions of all images of the disk <span class="hlt">created</span> by gravitational lensing, with the direct and first-order images largely dominating the overall shapes. Higher order images <span class="hlt">created</span> by photons tightly winding around the black holes are often neglected in the modeling of these <span class="hlt">lines</span>, since they require a substantially higher computational effort. With the help of the strong deflection limit, we present the most accurate semi-analyticalmore » calculation of these higher order contributions to the iron <span class="hlt">lines</span> for Schwarzschild black holes. We show that two regimes exist depending <span class="hlt">on</span> the inclination of the disk with respect to the <span class="hlt">line</span> of sight. Many useful analytical formulae can be also derived in this framework.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006JMiMi..16.1571S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006JMiMi..16.1571S"><span><span class="hlt">Creating</span> micro-scale surface topology to achieve anisotropic wettability <span class="hlt">on</span> an aluminum surface</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sommers, Andrew D.; Jacobi, Anthony M.</p> <p>2006-08-01</p> <p>A technique for fabricating micropatterned aluminum surfaces with parallel grooves 30 µm wide and tens of microns in depth is described. Standard photolithographic techniques are used to obtain this precise surface-feature patterning. Positive photoresists, S1813 and AZ4620, are selected to mask the surface, and a mixture of BCl3 and Cl2 gases is used to perform the etching. Experimental data show that a droplet placed <span class="hlt">on</span> the micro-grooved aluminum surface using a micro-syringe exhibits an increased apparent contact angle, and for droplets condensed <span class="hlt">on</span> these etched surfaces, more than a 50% reduction in the volume needed for the onset of droplet sliding is manifest. No chemical surface treatment is necessary to achieve this water repellency; it is accomplished solely by an anisotropic surface morphology that manipulates droplet geometry and <span class="hlt">creates</span> and exploits discontinuities in the three-phase contact <span class="hlt">line</span>. These micro-structured surfaces are proposed for use in a broad range of air-cooling applications, where the management of condensate and defrost liquid <span class="hlt">on</span> the heat transfer surface is essential to the energy-efficient operation of the machine.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11086173','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11086173"><span>Continuous hematopoietic cell <span class="hlt">lines</span> as model systems for leukemia-lymphoma research.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Drexler, H G; Matsuo, A Y; MacLeod, R A</p> <p>2000-11-01</p> <p>Along with other improvements, the advent of continuous human leukemia-lymphoma (LL) cell <span class="hlt">lines</span> as a rich resource of abundant, accessible and manipulable living cells has contributed significantly to a better understanding of the pathophysiology of hematopoietic tumors. The first LL cell <span class="hlt">lines</span>, Burkitt's lymphoma-derived <span class="hlt">lines</span>, were established in 1963. Since then, more than 1000 cell <span class="hlt">lines</span> have been described, although not all of them in full detail. The major advantages of continuous cell <span class="hlt">lines</span> is the unlimited supply and worldwide availability of identical cell material, and the infinite viable storability in liquid nitrogen. LL cell <span class="hlt">lines</span> are characterized generally by monoclonal origin and differentiation arrest, sustained proliferation in vitro under preservation of most cellular features, and specific genetic alterations. The most practical classification of LL cell <span class="hlt">lines</span> assigns them to one of the physiologically occurring cell lineages, based <span class="hlt">on</span> their immunophenotype, genotype and functional features. Truly malignant cell <span class="hlt">lines</span> must be discerned from Epstein-Barr virus (EBV)-immortalized normal cells, using various distinguishing parameters. However, the picture is not quite so straightforward, as some types of LL cell <span class="hlt">lines</span> are indeed EBV+, and some EBV+ normal cell <span class="hlt">lines</span> carry also genetic aberrations and may mimic malignancy-associated features. Apart from EBV and human T-cell leukemia virus in some <span class="hlt">lines</span>, the majority of wild-type LL cell <span class="hlt">lines</span> are virus-negative. The efficiency of cell <span class="hlt">line</span> establishment is rather low and the deliberate establishment of new LL cell <span class="hlt">lines</span> remains by and large an unpredictable random process. Difficulties in establishing continuous cell <span class="hlt">lines</span> may be caused by the inappropriate selection of nutrients and growth factors for these cells. Clearly, a generally suitable microenvironment for hematopoietic cells, either malignant or normal, cannot yet be <span class="hlt">created</span> in vitro. The characterization and publication of new LL cell</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011PhDT.........7L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011PhDT.........7L"><span>The impact of a scheduling change <span class="hlt">on</span> ninth grade high school performance <span class="hlt">on</span> <span class="hlt">biology</span> benchmark exams and the California Standards Test</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Leonardi, Marcelo</p> <p></p> <p>The primary purpose of this study was to examine the impact of a scheduling change from a trimester 4x4 block schedule to a modified hybrid schedule <span class="hlt">on</span> student achievement in ninth grade <span class="hlt">biology</span> courses. This study examined the impact of the scheduling change <span class="hlt">on</span> student achievement through teacher <span class="hlt">created</span> benchmark assessments in Genetics, DNA, and Evolution and <span class="hlt">on</span> the California Standardized Test in <span class="hlt">Biology</span>. The secondary purpose of this study examined the ninth grade <span class="hlt">biology</span> teacher perceptions of ninth grade <span class="hlt">biology</span> student achievement. Using a mixed methods research approach, data was collected both quantitatively and qualitatively as aligned to research questions. Quantitative methods included gathering data from departmental benchmark exams and California Standardized Test in <span class="hlt">Biology</span> and conducting multiple analysis of covariance and analysis of covariance to determine significance differences. Qualitative methods include journal entries questions and focus group interviews. The results revealed a statistically significant increase in scores <span class="hlt">on</span> both the DNA and Evolution benchmark exams. DNA and Evolution benchmark exams showed significant improvements from a change in scheduling format. The scheduling change was responsible for 1.5% of the increase in DNA benchmark scores and 2% of the increase in Evolution benchmark scores. The results revealed a statistically significant decrease in scores <span class="hlt">on</span> the Genetics Benchmark exam as a result of the scheduling change. The scheduling change was responsible for 1% of the decrease in Genetics benchmark scores. The results also revealed a statistically significant increase in scores <span class="hlt">on</span> the CST <span class="hlt">Biology</span> exam. The scheduling change was responsible for .7% of the increase in CST <span class="hlt">Biology</span> scores. Results of the focus group discussions indicated that all teachers preferred the modified hybrid schedule over the trimester schedule and that it improved student achievement.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5967446','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5967446"><span>Publishing activities improves undergraduate <span class="hlt">biology</span> education</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Smith, Michelle K</p> <p>2018-01-01</p> <p>Abstract To improve undergraduate <span class="hlt">biology</span> education, there is an urgent need for <span class="hlt">biology</span> instructors to publish their innovative active-learning instructional materials in peer-reviewed journals. To do this, instructors can measure student knowledge about a variety of <span class="hlt">biology</span> concepts, iteratively design activities, explore student learning outcomes and publish the results. <span class="hlt">Creating</span> a set of well-vetted activities, searchable through a journal interface, saves other instructors time and encourages the use of active-learning instructional practices. For authors, these publications offer new opportunities to collaborate and can provide evidence of a commitment to using active-learning instructional techniques in the classroom. PMID:29672697</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29672697','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29672697"><span>Publishing activities improves undergraduate <span class="hlt">biology</span> education.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Smith, Michelle K</p> <p>2018-06-01</p> <p>To improve undergraduate <span class="hlt">biology</span> education, there is an urgent need for <span class="hlt">biology</span> instructors to publish their innovative active-learning instructional materials in peer-reviewed journals. To do this, instructors can measure student knowledge about a variety of <span class="hlt">biology</span> concepts, iteratively design activities, explore student learning outcomes and publish the results. <span class="hlt">Creating</span> a set of well-vetted activities, searchable through a journal interface, saves other instructors time and encourages the use of active-learning instructional practices. For authors, these publications offer new opportunities to collaborate and can provide evidence of a commitment to using active-learning instructional techniques in the classroom.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3878816','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3878816"><span>The development of peptide-based interfacial biomaterials for generating <span class="hlt">biological</span> functionality <span class="hlt">on</span> the surface of bioinert materials</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Meyers, Steven R.; Khoo, Xiaojuan; Huang, Xin; Walsh, Elisabeth B.; Grinstaff, Mark W.; Kenan, Daniel J.</p> <p>2013-01-01</p> <p>Biomaterials used in implants have traditionally been selected based <span class="hlt">on</span> their mechanical properties, chemical stability, and biocompatibility. However, the durability and clinical efficacy of implantable biomedical devices remains limited in part due to the absence of appropriate <span class="hlt">biological</span> interactions at the implant interface and the lack of integration into adjacent tissues. Herein, we describe a robust peptide-based coating technology capable of modifying the surface of existing biomaterials and medical devices through the non-covalent binding of modular biofunctional peptides. These peptides contain at least one material binding sequence and at least one <span class="hlt">biologically</span> active sequence and thus are termed, “Interfacial Biomaterials” (IFBMs). IFBMs can simultaneously bind the biomaterial surface while endowing it with desired <span class="hlt">biological</span> functionalities at the interface between the material and <span class="hlt">biological</span> realms. We demonstrate the capabilities of model IFBMs to convert native polystyrene, a bioinert surface, into a bioactive surface that can support a range of cell activities. We further distinguish between simple cell attachment with insufficient integrin interactions, which in some cases can adversely impact downstream <span class="hlt">biology</span>, versus <span class="hlt">biologically</span> appropriate adhesion, cell spreading, and cell survival mediated by IFBMs. Moreover, we show that we can use the coating technology to <span class="hlt">create</span> spatially resolved patterns of fluorophores and cells <span class="hlt">on</span> substrates and that these patterns retain their borders in culture. PMID:18929406</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2768596','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2768596"><span>Slowed Speech Input has a Differential Impact <span class="hlt">on</span> <span class="hlt">On-line</span> and Off-<span class="hlt">line</span> Processing in Children’s Comprehension of Pronouns</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Walenski, Matthew; Swinney, David</p> <p>2009-01-01</p> <p>The central question underlying this study revolves around how children process co-reference relationships—such as those evidenced by pronouns (him) and reflexives (himself)—and how a slowed rate of speech input may critically affect this process. Previous studies of child language processing have demonstrated that typical language developing (TLD) children as young as 4 years of age process co-reference relations in a manner similar to adults <span class="hlt">on-line</span>. In contrast, off-<span class="hlt">line</span> measures of pronoun comprehension suggest a developmental delay for pronouns (relative to reflexives). The present study examines dependency relations in TLD children (ages 5–13) and investigates how a slowed rate of speech input affects the unconscious (<span class="hlt">on-line</span>) and conscious (off-<span class="hlt">line</span>) parsing of these constructions. For the <span class="hlt">on-line</span> investigations (using a cross-modal picture priming paradigm), results indicate that at a normal rate of speech TLD children demonstrate adult-like syntactic reflexes. At a slowed rate of speech the typical language developing children displayed a breakdown in automatic syntactic parsing (again, similar to the pattern seen in unimpaired adults). As demonstrated in the literature, our off-<span class="hlt">line</span> investigations (sentence/picture matching task) revealed that these children performed much better <span class="hlt">on</span> reflexives than <span class="hlt">on</span> pronouns at a regular speech rate. However, at the slow speech rate, performance <span class="hlt">on</span> pronouns was substantially improved, whereas performance <span class="hlt">on</span> reflexives was not different than at the regular speech rate. We interpret these results in light of a distinction between fast automatic processes (relied upon for <span class="hlt">on-line</span> processing in real time) and conscious reflective processes (relied upon for off-<span class="hlt">line</span> processing), such that slowed speech input disrupts the former, yet improves the latter. PMID:19343495</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22270477','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22270477"><span>Impact of graphic format <span class="hlt">on</span> perception of change in <span class="hlt">biological</span> data: implications for health monitoring in conditions such as asthma.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jansen, Jesse; McCaffery, Kirsten J; Hayen, Andrew; Ma, David; Reddel, Helen K</p> <p>2012-03-01</p> <p>Variation in graphic format can substantially influence interpretation of data. Despite a large body of literature <span class="hlt">on</span> the optimal design of graphs, little attention has been paid to the format of charts for health monitoring. This study assessed the effect of aspect ratio (x:y ratio) and interconnecting <span class="hlt">lines</span> <span class="hlt">on</span> visual identification of change in <span class="hlt">biological</span> data, such as during asthma exacerbations. Eighty volunteers viewed 72 sets of six consecutive blocks of unidentified <span class="hlt">biological</span> data, recording if each block of data was increasing, decreasing, or the same as the previous block. Three chart aspect ratios were examined (A, 5.2:1; B, 3.0:1; C, 1.1:1), with or without <span class="hlt">lines</span> between data points. Datasets from lung function monitoring by asthma patients included a mild/moderate/severe fall ('exacerbation') or no exacerbation. False negative (missing true exacerbations) and false positive (identifying non-existent exacerbations) responses were calculated. 84% of exacerbation blocks were correctly identified. There was a significant interaction between exacerbation severity and aspect ratio (p=0.0048). The most compressed chart (C) had the fewest false negative responses. Moderate falls were missed in 24%, 12%, and 5% of trials <span class="hlt">on</span> charts A, B, and C, respectively (C vs A: adjusted relative risk 0.19 (95% CI 0.12 to 0.30)). False positive responses were infrequent (A, 2.5%; B, 3.8%; C, 8.3%), increasing slightly if data points were joined with <span class="hlt">lines</span> (4.3% vs 5.1%, p=0.004) . Compressed charts can improve the visual detection of change in <span class="hlt">biological</span> data by up to 80%. The aspect ratio of charts should be standardised to facilitate clinical pattern recognition.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27528765','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27528765"><span>Selection platforms for directed evolution in synthetic <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tizei, Pedro A G; Csibra, Eszter; Torres, Leticia; Pinheiro, Vitor B</p> <p>2016-08-15</p> <p>Life <span class="hlt">on</span> Earth is incredibly diverse. Yet, underneath that diversity, there are a number of constants and highly conserved processes: all life is based <span class="hlt">on</span> DNA and RNA; the genetic code is universal; <span class="hlt">biology</span> is limited to a small subset of potential chemistries. A vast amount of knowledge has been accrued through describing and characterizing enzymes, <span class="hlt">biological</span> processes and organisms. Nevertheless, much remains to be understood about the natural world. One of the goals in Synthetic <span class="hlt">Biology</span> is to recapitulate <span class="hlt">biological</span> complexity from simple systems made from <span class="hlt">biological</span> molecules-gaining a deeper understanding of life in the process. Directed evolution is a powerful tool in Synthetic <span class="hlt">Biology</span>, able to bypass gaps in knowledge and capable of engineering even the most highly conserved <span class="hlt">biological</span> processes. It encompasses a range of methodologies to <span class="hlt">create</span> variation in a population and to select individual variants with the desired function-be it a ligand, enzyme, pathway or even whole organisms. Here, we present some of the basic frameworks that underpin all evolution platforms and review some of the recent contributions from directed evolution to synthetic <span class="hlt">biology</span>, in particular methods that have been used to engineer the Central Dogma and the genetic code. © 2016 The Author(s).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018PhyS...93d3001K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018PhyS...93d3001K"><span>Towards physical principles of <span class="hlt">biological</span> evolution</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Katsnelson, Mikhail I.; Wolf, Yuri I.; Koonin, Eugene V.</p> <p>2018-03-01</p> <p><span class="hlt">Biological</span> systems reach organizational complexity that far exceeds the complexity of any known inanimate objects. <span class="hlt">Biological</span> entities undoubtedly obey the laws of quantum physics and statistical mechanics. However, is modern physics sufficient to adequately describe, model and explain the evolution of <span class="hlt">biological</span> complexity? Detailed parallels have been drawn between statistical thermodynamics and the population-genetic theory of <span class="hlt">biological</span> evolution. Based <span class="hlt">on</span> these parallels, we outline new perspectives <span class="hlt">on</span> <span class="hlt">biological</span> innovation and major transitions in evolution, and introduce a <span class="hlt">biological</span> equivalent of thermodynamic potential that reflects the innovation propensity of an evolving population. Deep analogies have been suggested to also exist between the properties of <span class="hlt">biological</span> entities and processes, and those of frustrated states in physics, such as glasses. Such systems are characterized by frustration whereby local state with minimal free energy conflict with the global minimum, resulting in ‘emergent phenomena’. We extend such analogies by examining frustration-type phenomena, such as conflicts between different levels of selection, in <span class="hlt">biological</span> evolution. These frustration effects appear to drive the evolution of <span class="hlt">biological</span> complexity. We further address evolution in multidimensional fitness landscapes from the point of view of percolation theory and suggest that percolation at level above the critical threshold dictates the tree-like evolution of complex organisms. Taken together, these multiple connections between fundamental processes in physics and <span class="hlt">biology</span> imply that construction of a meaningful physical theory of <span class="hlt">biological</span> evolution might not be a futile effort. However, it is unrealistic to expect that such a theory can be <span class="hlt">created</span> in one scoop; if it ever comes to being, this can only happen through integration of multiple physical models of evolutionary processes. Furthermore, the existing framework of theoretical physics is unlikely to suffice</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://prevention.cancer.gov/news-and-events/news/consortium-molecular','NCI'); return false;" href="https://prevention.cancer.gov/news-and-events/news/consortium-molecular"><span>Consortium for Molecular Characterization of Screen-Detected Lesions <span class="hlt">Created</span>: Eight Grants Awarded | Division of Cancer Prevention</span></a></p> <p><a target="_blank" href="http://www.cancer.gov">Cancer.gov</a></p> <p></p> <p></p> <p>The NCI has awarded eight grants to <span class="hlt">create</span> the Consortium for Molecular Characterization of Screen-Detected Lesions. The consortium has seven molecular characterization laboratories (MCLs) and a coordinating center, and is supported by the Division of Cancer Prevention and the Division of Cancer <span class="hlt">Biology</span>. | 7 laboratories and a coordinating center focused <span class="hlt">on</span> identifying</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29536444','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29536444"><span>Revisit of Machine Learning Supported <span class="hlt">Biological</span> and Biomedical Studies.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yu, Xiang-Tian; Wang, Lu; Zeng, Tao</p> <p>2018-01-01</p> <p>Generally, machine learning includes many in silico methods to transform the principles underlying natural phenomenon to human understanding information, which aim to save human labor, to assist human judge, and to <span class="hlt">create</span> human knowledge. It should have wide application potential in <span class="hlt">biological</span> and biomedical studies, especially in the era of big <span class="hlt">biological</span> data. To look through the application of machine learning along with <span class="hlt">biological</span> development, this review provides wide cases to introduce the selection of machine learning methods in different practice scenarios involved in the whole <span class="hlt">biological</span> and biomedical study cycle and further discusses the machine learning strategies for analyzing omics data in some cutting-edge <span class="hlt">biological</span> studies. Finally, the notes <span class="hlt">on</span> new challenges for machine learning due to small-sample high-dimension are summarized from the key points of sample unbalance, white box, and causality.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1997SPIE.3214...13K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1997SPIE.3214...13K"><span><span class="hlt">Line</span> length dependencies in interconnect optimization</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kadoch, Daniel; Duane, Michael; Lee, Yohan</p> <p>1997-09-01</p> <p>Metal <span class="hlt">line</span> delay has become increasingly important for ULSI devices. Numerous expressions and software tools have been developed to describe interconnect delay as a function of the geometry and layout. Although many of these formulas have <span class="hlt">line</span> length effects, this has not been explored in depth. Most software tools are either geared towards circuit designers, or involve more complex and CPU-intensive 3D modeling. In this work, PISCES (a 2D device simulator) was used to extract metal capacitance per unit length. We extend this approach for various lengths by <span class="hlt">creating</span> a ladder network of the RC components and simulating in SPICE, or using simple closed-form Elmore delay equations. A new key result is that there are optimum metal <span class="hlt">line</span> width/space for a fixed pitch and height/space ratios that are metal length dependent. For metal <span class="hlt">lines</span> shorter than about 1500 micrometers , it is better to have narrower metal <span class="hlt">lines</span>, and for lengths less than 500 micrometers , shrinking metal height is desirable because the penalty in resistance is more than compensated by the decrease in capacitance. For longer <span class="hlt">lines</span>, the time delay is dominated by resistance, and wider, taller <span class="hlt">lines</span> are better. Increasing metal spacing or reducing dielectric constant were beneficial for both long and short metal <span class="hlt">lines</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28719221','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28719221"><span>Biosimilars: <span class="hlt">biologics</span> that meet patients' needs and healthcare economics.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>McCamish, Mark; Yoon, William; McKay, James</p> <p>2016-09-01</p> <p><span class="hlt">Biologics</span> have revolutionized medical care, yet uniform access to these effective medicines remains difficult due to the increasing costs of healthcare. As patent exclusivity <span class="hlt">on</span> the early <span class="hlt">biologics</span> wanes, regulatory and legal systems are adapting to bring competition to the field in the form of biosimilars. Biosimilars are <span class="hlt">biologics</span> that offer the same clinical benefit in one or more of the same indications as the reference <span class="hlt">biologic</span> drug and bring competition to the <span class="hlt">biologics</span> space. Legislation <span class="hlt">creating</span> a pathway resulting in the first US approvals of biosimilars has been in place since 2010, but the regulatory methodology and science of evaluating the sameness of two <span class="hlt">biologics</span> has been in use for decades. The demonstration of biosimilarity is based <span class="hlt">on</span> the "totality of the evidence" concept, in which all structural, functional, nonclinical, and clinical data for a biosimilar product are evaluated to show high similarity to the reference product. Clinical trials for biosimilars, therefore, are designed to confirm similarity, or discover clinically relevant differences between the reference product and the biosimilar, should differences exist. It is hoped that competition from biosimilars will drive <span class="hlt">biologic</span> innovation and increase patient access to <span class="hlt">biologics</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11246921','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11246921"><span>Making the most of <span class="hlt">on-line</span> recruiting.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cappelli, P</p> <p>2001-03-01</p> <p>Ninety percent of large U.S. companies are already recruiting via the Internet. By simply logging <span class="hlt">on</span> to the Web, company recruiters can locate vast numbers of qualified candidates for jobs at every level, screen them in minutes, and contact the most promising ones immediately. The payoffs can be enormous: it costs substantially less to hire someone <span class="hlt">on-line</span>, and the time saved is equally great. In this article, Peter Cappelli examines some of the emerging service providers and technologies--matchmakers, job boards, hiring management systems software, and applicant-screening mechanisms that test skills and record interests. He also looks at some of the strategies companies are adopting as they enter <span class="hlt">on-line</span> labor markets. Recruiting needs to be refashioned to resemble marketing, he stresses. Accordingly, smart companies are designing Web pages, and even product ads, with potential recruits in mind. They're giving <span class="hlt">line</span> managers authority to hire so that candidates in cyberspace aren't lost. They're building internal <span class="hlt">on-line</span> job networks to retain talent. Integrating recruiting efforts with overall marketing campaigns, especially through coordination and identification with the company's brand, is the most important thing companies can do to ensure success in <span class="hlt">on-line</span> hiring. Along the way, Cappelli sounds two cautionary notes. First, a human touch, not electronic contact, is vital in the last steps of a successful hiring process. Second, companies must make sure that <span class="hlt">on-line</span> testing and hiring criteria do not discriminate against women, disabled people, workers over 40, or members of minority groups. When competition for talent is fierce, companies that master the art and science of <span class="hlt">on-line</span> recruiting will be the ones that attract and keep the best people.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21559524','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21559524"><span>Eugene--a domain specific language for specifying and constraining synthetic <span class="hlt">biological</span> parts, devices, and systems.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bilitchenko, Lesia; Liu, Adam; Cheung, Sherine; Weeding, Emma; Xia, Bing; Leguia, Mariana; Anderson, J Christopher; Densmore, Douglas</p> <p>2011-04-29</p> <p>Synthetic <span class="hlt">biological</span> systems are currently <span class="hlt">created</span> by an ad-hoc, iterative process of specification, design, and assembly. These systems would greatly benefit from a more formalized and rigorous specification of the desired system components as well as constraints <span class="hlt">on</span> their composition. Therefore, the creation of robust and efficient design flows and tools is imperative. We present a human readable language (Eugene) that allows for the specification of synthetic <span class="hlt">biological</span> designs based <span class="hlt">on</span> <span class="hlt">biological</span> parts, as well as provides a very expressive constraint system to drive the automatic creation of composite Parts (Devices) from a collection of individual Parts. We illustrate Eugene's capabilities in three different areas: Device specification, design space exploration, and assembly and simulation integration. These results highlight Eugene's ability to <span class="hlt">create</span> combinatorial design spaces and prune these spaces for simulation or physical assembly. Eugene <span class="hlt">creates</span> functional designs quickly and cost-effectively. Eugene is intended for forward engineering of DNA-based devices, and through its data types and execution semantics, reflects the desired abstraction hierarchy in synthetic <span class="hlt">biology</span>. Eugene provides a powerful constraint system which can be used to drive the creation of new devices at runtime. It accomplishes all of this while being part of a larger tool chain which includes support for design, simulation, and physical device assembly.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_18 --> <div id="page_19" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="361"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25404324','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25404324"><span>Evolutionary cell <span class="hlt">biology</span>: two origins, one objective.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lynch, Michael; Field, Mark C; Goodson, Holly V; Malik, Harmit S; Pereira-Leal, José B; Roos, David S; Turkewitz, Aaron P; Sazer, Shelley</p> <p>2014-12-02</p> <p>All aspects of <span class="hlt">biological</span> diversification ultimately trace to evolutionary modifications at the cellular level. This central role of cells frames the basic questions as to how cells work and how cells come to be the way they are. Although these two <span class="hlt">lines</span> of inquiry lie respectively within the traditional provenance of cell <span class="hlt">biology</span> and evolutionary <span class="hlt">biology</span>, a comprehensive synthesis of evolutionary and cell-<span class="hlt">biological</span> thinking is lacking. We define evolutionary cell <span class="hlt">biology</span> as the fusion of these two eponymous fields with the theoretical and quantitative branches of biochemistry, biophysics, and population genetics. The key goals are to develop a mechanistic understanding of general evolutionary processes, while specifically infusing cell <span class="hlt">biology</span> with an evolutionary perspective. The full development of this interdisciplinary field has the potential to solve numerous problems in diverse areas of <span class="hlt">biology</span>, including the degree to which selection, effectively neutral processes, historical contingencies, and/or constraints at the chemical and biophysical levels dictate patterns of variation for intracellular features. These problems can now be examined at both the within- and among-species levels, with single-cell methodologies even allowing quantification of variation within genotypes. Some results from this emerging field have already had a substantial impact <span class="hlt">on</span> cell <span class="hlt">biology</span>, and future findings will significantly influence applications in agriculture, medicine, environmental science, and synthetic <span class="hlt">biology</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EPJD...71..317C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EPJD...71..317C"><span>Simultaneous influence of Stark effect and excessive <span class="hlt">line</span> broadening <span class="hlt">on</span> the Hα <span class="hlt">line</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cvetanović, Nikola; Ivković, Saša S.; Obradović, Bratislav M.; Kuraica, Milorad M.</p> <p>2017-12-01</p> <p>The aim of this paper is to study the combined influence of the Stark effect and the excessive Doppler broadening <span class="hlt">on</span> the Balmer alpha <span class="hlt">line</span> in hydrogen discharges. Since this <span class="hlt">line</span> is a good candidate for measuring electric field in various types of discharges with different gas compositions, a simple method for field measurement based <span class="hlt">on</span> polarization spectroscopy is developed, that includes all the excitation mechanisms. To simultaneously test the flexibility of the fitting procedure and investigate the excessive broadening, we applied the fitting procedure <span class="hlt">on</span> <span class="hlt">line</span> profiles obtained at a range of conditions from two different discharges. The range of pressures and voltages was examined in an abnormal glow and in dielectric barrier discharge operating with hydrogen gas. The model fitting function was able to respond and follow the change in the <span class="hlt">line</span> profile caused by the change of conditions. This procedure can therefore be recommended for electric field measurement. Contribution to the "Topical Issue: Physics of Ionized Gases (SPIG 2016)", edited by Goran Poparic, Bratislav Obradovic, Dragana Maric and Aleksandar Milosavljevic.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=DISTRIBUTED+AND+SYSTEMS&pg=2&id=EJ947418','ERIC'); return false;" href="https://eric.ed.gov/?q=DISTRIBUTED+AND+SYSTEMS&pg=2&id=EJ947418"><span>A Distributed System for Learning Programming <span class="hlt">On-Line</span></span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Verdu, Elena; Regueras, Luisa M.; Verdu, Maria J.; Leal, Jose P.; de Castro, Juan P.; Queiros, Ricardo</p> <p>2012-01-01</p> <p>Several Web-based <span class="hlt">on-line</span> judges or <span class="hlt">on-line</span> programming trainers have been developed in order to allow students to train their programming skills. However, their pedagogical functionalities in the learning of programming have not been clearly defined. EduJudge is a project which aims to integrate the "UVA <span class="hlt">On-line</span> Judge", an existing…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28321783','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28321783"><span><span class="hlt">Biological</span> and Mechanical Effects of Micro-Nanostructured Titanium Surface <span class="hlt">on</span> an Osteoblastic Cell <span class="hlt">Line</span> In vitro and Osteointegration In vivo.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hao, Jingzu; Li, Ying; Li, Baoe; Wang, Xiaolin; Li, Haipeng; Liu, Shimin; Liang, Chunyong; Wang, Hongshui</p> <p>2017-09-01</p> <p>Hybrid micro-nanostructure implant surface was produced <span class="hlt">on</span> titanium (Ti) surface by acid etching and anodic oxidation to improve the <span class="hlt">biological</span> and mechanical properties. The <span class="hlt">biological</span> properties of the micro-nanostructure were investigated by simulated body fluid (SBF) soaking test and MC3T3-E1 cell co-culture experiment. The cell proliferation, spreading, and bone sialoprotein (BSP) gene expression were examined by MTT, SEM, and reverse transcription-polymerase chain reaction (RT-PCR), respectively. In addition, the mechanical properties were evaluated by instrumented nanoindentation test and friction-wear test. Furthermore, the effect of the micro-nanostructure surface <span class="hlt">on</span> implant osteointegration was examined by in vivo experiment. The results showed that the formation of bone-like apatite was accelerated <span class="hlt">on</span> the micro-nanostructured Ti surface after immersion in simulated body fluid, and the proliferation, spreading, and BSP gene expression of the MC3T3-E1 cells were also upregulated <span class="hlt">on</span> the modified surface. The micro-nanostructured Ti surface displayed decreased friction coefficient, stiffness value, and Young's modulus which were much closer to those of the cortical bone, compared to the polished Ti surface. This suggested much better mechanical match to the surrounding bone tissue of the micro-nanostructured Ti surface. Furthermore, the in vivo animal experiment showed that after implantation in the rat femora, the micro-nanostructure surface displayed higher bonding strength between bone tissues and implant; hematoxylin and eosin (H&E) staining suggested that much compact osteoid tissue was observed at the interface of Micro-nano-Ti-bone than polished Ti-bone interface after implantation. Based <span class="hlt">on</span> these results mentioned above, it was concluded that the improved <span class="hlt">biological</span> and mechanical properties of the micro-nanostructure endowed Ti surface with good biocompatibility and better osteointegration, implying the enlarged application of the micro</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27860239','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27860239"><span>Chemiluminescence of off-<span class="hlt">line</span> and <span class="hlt">on-line</span> gold nanoparticle-catalyzed luminol system in the presence of flavonoid.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wu, Dong; Zhang, Xiaoyue; Liu, Yong; Ma, Yan; Wang, Xiaowu; Wang, Xiaojuan; Xu, Liuxin</p> <p>2017-06-01</p> <p>It was found that flavonoids could remarkably inhibit the chemiluminescence (CL) intensity of an off-<span class="hlt">line</span> gold nanoparticle (AuNP)-catalyzed luminol-H 2 O 2 CL system. By contrast, flavonoids enhanced the CL intensity of an <span class="hlt">on-line</span> AuNP-catalyzed luminol-H 2 O 2 CL system. In the off-<span class="hlt">line</span> system, the AuNPs were prepared beforehand, whereas in the <span class="hlt">on-line</span> system, AuNPs were produced by <span class="hlt">on-line</span> mixing of luminol prepared in a buffer solution of NaHCO 3  - Na 2 CO 3 and HAuCl 4 with no need for the preliminary preparation of AuNPs. The <span class="hlt">on-line</span> system had prominent advantages over the off-<span class="hlt">line</span> system, namely a lowering of the background noise and improvements in the stability of the CL system. The results show that differences in the signal suppression effect of flavonoids <span class="hlt">on</span> the off-<span class="hlt">line</span> AuNP-catalyzed CL system are influenced by the combined action of a free radical scavenging effect and occupy-sites function; the latter was proved to be predominant using controlled experiments. Enhancement of the <span class="hlt">on-line</span> system was ascribed to the presence of flavonoids promoting the <span class="hlt">on-line</span> formation of AuNPs, which better catalyzed the luminol-H 2 O 2 CL reaction, and the enhancement activity of the six flavonoids increased with the increase in reducibility. This work broadens the scope of practical applications of an AuNP-catalyzed CL system. Copyright © 2016 John Wiley & Sons, Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27017908','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27017908"><span>Establishment and characterization of a novel osteosarcoma cell <span class="hlt">line</span>: CHOS.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Yunlu; Feng, Xiaobo; Zhang, Yukun; Jiang, Hongyan; Cai, Xianyi; Yan, Xinxin; Huang, Zengfa; Mo, Fengbo; Yang, Wen; Yang, Cao; Yang, Shuhua; Liu, Xianzhe</p> <p>2016-12-01</p> <p>Osteosarcoma has a well-recognized bimodal distribution, with the first peak in adolescence and another in the elderly age-group. The elderly patients have different clinical features and a poorer prognosis as compared to adolescents. To better understand the <span class="hlt">biological</span> features of osteosarcoma in the elderly population, we established a new human osteosarcoma cell <span class="hlt">line</span> from a 58-year-old man with primary chondroblastic osteosarcoma. After 6 months of continuous culture in vitro for over 50 passages, an immortalized cell <span class="hlt">line</span> CHOS was established. The cell <span class="hlt">line</span> was well-characterized by cytogenetic, biomarker, functional, and histological analyses. The CHOS cells exhibited a spindle-shaped morphology and a doubling time of 36 h. Cytogenetic analysis of CHOS cells revealed the loss of chromosome Y and the gain of chromosome 12. Quantitative real-time polymerase chain reaction (RT-PCR), Western blotting and/or immunofluorescence revealed the expression of chondroblastic, mesenchymal and tumor metastasis markers in the CHOS cells. Compared with the osteosarcoma cell <span class="hlt">line</span>, the CHOS cells were found to be more sensitive to cisplatin and doxorubicin, but were resistant to methotrexate. The cell <span class="hlt">line</span> was highly tumorigenic and maintained the histological characteristics and invasive nature of the original tumor. Furthermore, <span class="hlt">on</span> immunohistochemical analysis, the xenografts and metastases were found to co-express collagen II, aggrecan, vimentin and S100A4 that resembled the original tumor cells. Our results indicate, the potential of CHOS cell <span class="hlt">line</span> to serve as a useful tool for further studies <span class="hlt">on</span> the molecular <span class="hlt">biology</span> of osteosarcoma, especially in the elderly patients. © 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:2116-2125, 2016. © 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26362842','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26362842"><span>Cost analysis of <span class="hlt">biologic</span> drugs in rheumatoid arthritis first <span class="hlt">line</span> treatment after methotrexate failure according to patients' body weight.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Román Ivorra, José Andrés; Ivorra, José; Monte-Boquet, Emilio; Canal, Cristina; Oyagüez, Itziar; Gómez-Barrera, Manuel</p> <p>2016-01-01</p> <p>The objective was to assess the influence of patients' weight in the cost of rheumatoid arthritis treatment with <span class="hlt">biologic</span> drugs used in first <span class="hlt">line</span> after non-adequate response to methotrexate. Pharmaceutical and administration costs were calculated in two scenarios: non-optimization and optimization of intravenous (IV) vials. The retrospective analysis of 66 patients from a Spanish 1,000 beds-hospital Rheumatology Clinic Service was used to obtain posology and weight data. The study time horizon was two years. Costs were expressed in 2013 euros. For an average 69kg-weighted patient the lowest cost corresponded to abatacept subcutaneous (SC ABA) (€21,028.09) in the scenario without IV vials optimization and infliximab (IFX) (€20,779.29) with optimization. Considering patients' weight in the scenario without IV vials optimization infliximab (IFX) was the least expensive drug in patients ranged 45-49kg, IV ABA in 50-59kg and SC ABA in patients over 60kg. With IV vials optimization IFX was the least expensive drug in patients under 69kg and SC ABA over 70kg. Assuming comparable effectiveness of <span class="hlt">biological</span> drugs, patient's weight is a variable to consider, potentials savings could reach €20,000 in two years. Copyright © 2015 Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de Reumatología. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21374979','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21374979"><span>[<span class="hlt">Biological</span> activity evaluation of porous HA ceramics using NH4 HCO3/PVA as pore-<span class="hlt">creating</span> agents].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Songquan; Zhang, Dekun</p> <p>2010-12-01</p> <p>Porous HA ceramics were prepared by using NH4 HCO3/PVA as pore-formed material along with <span class="hlt">biological</span> glass as intensifier, and these ceramics were immersed in Locke's Physiological Saline and Simulate Body Fluid (SBF). The changes of phase composition, grain size and crystallinity of porous HA ceramics before and after immersion were investigated by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The <span class="hlt">biological</span> activity was evaluated. The porous HA ceramics showed various degrees of decomposition after immersion in the two solution systems, but there was no evident change in respect to crystallinity. Besides, the impact of different degrees of solution systems <span class="hlt">on</span> the change of grain size and planar preferred orientation was observed. The TCP phase of the ceramics immersed in Locke's Physiological Saline decomposed and there was no crystal growth <span class="hlt">on</span> the surface of ceramics; however, the grain size of ceramics immersed in SBF became refined in certain degree and the surface of ceramics took <span class="hlt">on</span> the new crystal growth.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3737162','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3737162"><span>The Genomic and Transcriptomic Landscape of a HeLa Cell <span class="hlt">Line</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Landry, Jonathan J. M.; Pyl, Paul Theodor; Rausch, Tobias; Zichner, Thomas; Tekkedil, Manu M.; Stütz, Adrian M.; Jauch, Anna; Aiyar, Raeka S.; Pau, Gregoire; Delhomme, Nicolas; Gagneur, Julien; Korbel, Jan O.; Huber, Wolfgang; Steinmetz, Lars M.</p> <p>2013-01-01</p> <p>HeLa is the most widely used model cell <span class="hlt">line</span> for studying human cellular and molecular <span class="hlt">biology</span>. To date, no genomic reference for this cell <span class="hlt">line</span> has been released, and experiments have relied <span class="hlt">on</span> the human reference genome. Effective design and interpretation of molecular genetic studies performed using HeLa cells require accurate genomic information. Here we present a detailed genomic and transcriptomic characterization of a HeLa cell <span class="hlt">line</span>. We performed DNA and RNA sequencing of a HeLa Kyoto cell <span class="hlt">line</span> and analyzed its mutational portfolio and gene expression profile. Segmentation of the genome according to copy number revealed a remarkably high level of aneuploidy and numerous large structural variants at unprecedented resolution. Some of the extensive genomic rearrangements are indicative of catastrophic chromosome shattering, known as chromothripsis. Our analysis of the HeLa gene expression profile revealed that several pathways, including cell cycle and DNA repair, exhibit significantly different expression patterns from those in normal human tissues. Our results provide the first detailed account of genomic variants in the HeLa genome, yielding insight into their impact <span class="hlt">on</span> gene expression and cellular function as well as their origins. This study underscores the importance of accounting for the strikingly aberrant characteristics of HeLa cells when designing and interpreting experiments, and has implications for the use of HeLa as a model of human <span class="hlt">biology</span>. PMID:23550136</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25365334','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25365334"><span>Synthetic <span class="hlt">Biology</span>: Applications in the Food Sector.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tyagi, Ashish; Kumar, Ashwani; Aparna, S V; Mallappa, Rashmi H; Grover, Sunita; Batish, Virender Kumar</p> <p>2016-08-17</p> <p>Synthetic <span class="hlt">biology</span> also termed as "genomic alchemy" represents a powerful area of science that is based <span class="hlt">on</span> the convergence of <span class="hlt">biological</span> sciences with systems engineering. It has been fittingly described as "moving from reading the genetic code to writing it" as it focuses <span class="hlt">on</span> building, modeling, designing and fabricating novel <span class="hlt">biological</span> systems using customized gene components that result in artificially <span class="hlt">created</span> genetic circuitry. The scientifically compelling idea of the technological manipulation of life has been advocated since long time. Realization of this idea has gained momentum with development of high speed automation and the falling cost of gene sequencing and synthesis following the completion of the human genome project. Synthetic <span class="hlt">biology</span> will certainly be instrumental in shaping the development of varying areas ranging from biomedicine, biopharmaceuticals, chemical production, food and dairy quality monitoring, packaging, and storage of food and dairy products, bioremediation and bioenergy production, etc. However, potential dangers of using synthetic life forms have to be acknowledged and adoption of policies by the scientific community to ensure safe practice while making important advancements in the ever expanding field of synthetic <span class="hlt">biology</span> is to be fully supported and implemented.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25127889','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25127889"><span>SPARQLGraph: a web-based platform for graphically querying <span class="hlt">biological</span> Semantic Web databases.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Schweiger, Dominik; Trajanoski, Zlatko; Pabinger, Stephan</p> <p>2014-08-15</p> <p>Semantic Web has established itself as a framework for using and sharing data across applications and database boundaries. Here, we present a web-based platform for querying <span class="hlt">biological</span> Semantic Web databases in a graphical way. SPARQLGraph offers an intuitive drag & drop query builder, which converts the visual graph into a query and executes it <span class="hlt">on</span> a public endpoint. The tool integrates several publicly available Semantic Web databases, including the databases of the just recently released EBI RDF platform. Furthermore, it provides several predefined template queries for answering <span class="hlt">biological</span> questions. Users can easily <span class="hlt">create</span> and save new query graphs, which can also be shared with other researchers. This new graphical way of <span class="hlt">creating</span> queries for <span class="hlt">biological</span> Semantic Web databases considerably facilitates usability as it removes the requirement of knowing specific query languages and database structures. The system is freely available at http://sparqlgraph.i-med.ac.at.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016IJSEd..38.1882N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016IJSEd..38.1882N"><span>Influence of using challenging tasks in <span class="hlt">biology</span> classrooms <span class="hlt">on</span> students' cognitive knowledge structure: an empirical video study</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Nawani, Jigna; Rixius, Julia; Neuhaus, Birgit J.</p> <p>2016-08-01</p> <p>Empirical analysis of secondary <span class="hlt">biology</span> classrooms revealed that, <span class="hlt">on</span> average, 68% of teaching time in Germany revolved around processing tasks. Quality of instruction can thus be assessed by analyzing the quality of tasks used in classroom discourse. This quasi-experimental study analyzed how teachers used tasks in 38 videotaped <span class="hlt">biology</span> lessons pertaining to the topic 'blood and circulatory system'. Two fundamental characteristics used to analyze tasks include: (1) required cognitive level of processing (e.g. low level information processing: repetiition, summary, define, classify and high level information processing: interpret-analyze data, formulate hypothesis, etc.) and (2) complexity of task content (e.g. if tasks require use of factual, linking or concept level content). Additionally, students' cognitive knowledge structure about the topic 'blood and circulatory system' was measured using student-drawn concept maps (N = 970 students). Finally, linear multilevel models were <span class="hlt">created</span> with high-level cognitive processing tasks and higher content complexity tasks as class-level predictors and students' prior knowledge, students' interest in <span class="hlt">biology</span>, and students' interest in <span class="hlt">biology</span> activities as control covariates. Results showed a positive influence of high-level cognitive processing tasks (β = 0.07; p < .01) <span class="hlt">on</span> students' cognitive knowledge structure. However, there was no observed effect of higher content complexity tasks <span class="hlt">on</span> students' cognitive knowledge structure. Presented findings encourage the use of high-level cognitive processing tasks in <span class="hlt">biology</span> instruction.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=297914','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=297914"><span>Effects of Fuzzless Cottonseed Phenotype <span class="hlt">on</span> Cottonseed Nutrient Composition in near Isogenic Cotton (Gossypium hirsutum L.) Mutant <span class="hlt">Lines</span> under Well-Watered and Water Stress Conditions</span></a></p> <p><a target="_blank" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>Cotton mutant near isogenic <span class="hlt">lines</span> (NILs) for fuzzless seed trait has been used to investigate cell <span class="hlt">biology</span>, genetic, and molecular processes of fiber initiation, development, fiber yield and quality. However, there is no information available <span class="hlt">on</span> the effect of fuzzless seed trait <span class="hlt">on</span> cottonseed nutrie...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=theory+AND+Logistics&pg=7&id=EJ1006859','ERIC'); return false;" href="https://eric.ed.gov/?q=theory+AND+Logistics&pg=7&id=EJ1006859"><span>Using Logistic Approximations of Marginal Trace <span class="hlt">Lines</span> to Develop Short Assessments</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Stucky, Brian D.; Thissen, David; Edelen, Maria Orlando</p> <p>2013-01-01</p> <p>Test developers often need to <span class="hlt">create</span> unidimensional scales from multidimensional data. For item analysis, "marginal trace <span class="hlt">lines</span>" capture the relation with the general dimension while accounting for nuisance dimensions and may prove to be a useful technique for <span class="hlt">creating</span> short-form tests. This article describes the computations needed to obtain…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23715992','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23715992"><span>Bioinformatics workflows and web services in systems <span class="hlt">biology</span> made easy for experimentalists.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jimenez, Rafael C; Corpas, Manuel</p> <p>2013-01-01</p> <p>Workflows are useful to perform data analysis and integration in systems <span class="hlt">biology</span>. Workflow management systems can help users <span class="hlt">create</span> workflows without any previous knowledge in programming and web services. However the computational skills required to build such workflows are usually above the level most <span class="hlt">biological</span> experimentalists are comfortable with. In this chapter we introduce workflow management systems that reuse existing workflows instead of <span class="hlt">creating</span> them, making it easier for experimentalists to perform computational tasks.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=real+AND+time+AND+operation+AND+system&pg=3&id=EJ049228','ERIC'); return false;" href="https://eric.ed.gov/?q=real+AND+time+AND+operation+AND+system&pg=3&id=EJ049228"><span><span class="hlt">On-Line</span> Library Housekeeping Systems. A Survey</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>McAllister, Caryl</p> <p>1971-01-01</p> <p>A general discussion of <span class="hlt">on-line</span> procedures, batch and real-time updating, types of files and indexes, terminals, and the use of a general-purpose data management system as a vehicle for <span class="hlt">on-line</span> operation is followed by an Appendix giving detailed information <span class="hlt">on</span> each <span class="hlt">on</span> the known systems. (14 references) (Author/NH)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29192757','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29192757"><span>Innovations in Undergraduate Chemical <span class="hlt">Biology</span> Education.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Van Dyke, Aaron R; Gatazka, Daniel H; Hanania, Mariah M</p> <p>2018-01-19</p> <p>Chemical <span class="hlt">biology</span> derives intellectual vitality from its scientific interface: applying chemical strategies and perspectives to <span class="hlt">biological</span> questions. There is a growing need for chemical biologists to synergistically integrate their research programs with their educational activities to become holistic teacher-scholars. This review examines how course-based undergraduate research experiences (CUREs) are an innovative method to achieve this integration. Because CUREs are course-based, the review first offers strategies for <span class="hlt">creating</span> a student-centered learning environment, which can improve students' outcomes. Exemplars of CUREs in chemical <span class="hlt">biology</span> are then presented and organized to illustrate the five defining characteristics of CUREs: significance, scientific practices, discovery, collaboration, and iteration. Finally, strategies to overcome common barriers in CUREs are considered as well as future innovations in chemical <span class="hlt">biology</span> education.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19770055101&hterms=biology+cell&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3DThe%2Bbiology%2BThe%2Bcell','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19770055101&hterms=biology+cell&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3DThe%2Bbiology%2BThe%2Bcell"><span>Cell <span class="hlt">biology</span> experiments conducted in space</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Taylor, G. R.</p> <p>1977-01-01</p> <p>A review of cell <span class="hlt">biology</span> experiments conducted during the first two decades of space flight is provided. References are tabulated for work done with six types of living test system: isolated viruses, bacteriophage-host, bacteria, yeasts and filamentous fungi, protozoans, and small groups of cells (such as hamster cell tissue and fertilized frog eggs). The general results of studies involving the survival of cells in space, the effect of space flight <span class="hlt">on</span> growing cultures, the <span class="hlt">biological</span> effects of multicharged high-energy particles, and the effects of space flight <span class="hlt">on</span> the genetic apparatus of microorganisms are summarized. It is concluded that cell systems remain sufficiently stable during space flight to permit experimentation with models requiring a fixed cell <span class="hlt">line</span> during the space shuttle era.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22213327','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22213327"><span>Influence of calcitriol <span class="hlt">on</span> prostaglandin- and vitamin D-metabolising enzymes in benign and malignant breast cell <span class="hlt">lines</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Thill, Marc; Cordes, Tim; Hoellen, Friederike; Becker, Steffi; Dittmer, Christine; Kümmel, Sherko; Salehin, Darius; Friedrich, Michael; Diedrich, Klaus; Köster, Frank</p> <p>2012-01-01</p> <p>Cyclooxygenase-2 (COX-2) is a potential molecular prognostic factor for breast cancer, and calcitriol [1,25(OH)(2)D(3)], the <span class="hlt">biologically</span> active form of vitamin D, is a promising target in breast cancer therapy. The influence of calcitriol <span class="hlt">on</span> the proliferation and the effects of calcitriol <span class="hlt">on</span> the expression of prostaglandin- and vitamin D-metabolising enzymes were examined in benign and malignant breast cells. Calcitriol inhibited the proliferation of MCF-10F and MCF-7 cells but not of invasive MDA-MB-231 cells and reduced the expression of COX-2 and 15-hydroxyprostaglandin dehydrogenase (15-PGDH) in the benign breast cell <span class="hlt">line</span> MCF-10F. Furthermore, dysregulation in vitamin D-metabolising proteins was detected, especially in MDA-MB-231 cells. These results suggest dysregulation of vitamin D metabolism and a lack of a possible influence of calcitriol <span class="hlt">on</span> the metabolism of prostaglandins in the malignant breast cell <span class="hlt">lines</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/50709-computer-aided-statistical-process-control-line-instrumentation','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/50709-computer-aided-statistical-process-control-line-instrumentation"><span>Computer aided statistical process control for <span class="hlt">on-line</span> instrumentation</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Meils, D.E.</p> <p>1995-01-01</p> <p><span class="hlt">On-line</span> chemical process instrumentation historically has been used for trending. Recent technological advances in <span class="hlt">on-line</span> instrumentation have improved the accuracy and reliability of <span class="hlt">on-line</span> instrumentation. However, little attention has been given to validating and verifying <span class="hlt">on-line</span> instrumentation. This paper presents two practical approaches for validating instrument performance by comparison of <span class="hlt">on-line</span> instrument response to either another portable instrument or another bench instrument. Because the comparison of two instruments` performance to each other requires somewhat complex statistical calculations, a computer code (Lab Stats Pack{reg_sign}) is used to simplify the calculations. Lab Stats Pack{reg_sign} also develops control charts that may be usedmore » for continuous verification of <span class="hlt">on-line</span> instrument performance.« less</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_19 --> <div id="page_20" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="381"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26570998','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26570998"><span>Pharmacogenomic agreement between two cancer cell <span class="hlt">line</span> data sets.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p></p> <p>2015-12-03</p> <p>Large cancer cell <span class="hlt">line</span> collections broadly capture the genomic diversity of human cancers and provide valuable insight into anti-cancer drug response. Here we show substantial agreement and <span class="hlt">biological</span> consilience between drug sensitivity measurements and their associated genomic predictors from two publicly available large-scale pharmacogenomics resources: The Cancer Cell <span class="hlt">Line</span> Encyclopedia and the Genomics of Drug Sensitivity in Cancer databases.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27312181','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27312181"><span>Mobility as an emergent property of <span class="hlt">biological</span> organization: Insights from experimental evolution.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wallace, Ian J; Garland, Theodore</p> <p>2016-05-06</p> <p>Anthropologists accept that mobility is a critical dimension of human culture, one that links economy, technology, and social relations. Less often acknowledged is that mobility depends <span class="hlt">on</span> complex and dynamic interactions between multiple levels of our <span class="hlt">biological</span> organization, including anatomy, physiology, neurobiology, and genetics. Here, we describe a novel experimental approach to examining the <span class="hlt">biological</span> foundations of mobility, using mice from a long-term artificial selection experiment for high levels of voluntary exercise <span class="hlt">on</span> wheels. In this experiment, mice from selectively bred <span class="hlt">lines</span> have evolved to run roughly three times as far per day as those from nonselected control <span class="hlt">lines</span>. We consider three insights gleaned from this experiment as foundational principles for the study of mobility from the perspective of <span class="hlt">biological</span> evolution. First, an evolutionary change in mobility will necessarily be associated with alterations in <span class="hlt">biological</span> traits both directly and indirectly connected to mobility. Second, changing mobility will result in trade-offs and constraints among some of the affected traits. Third, multiple solutions exist to altering mobility, so that various combinations of adjustments to traits linked with mobility can achieve the same overall behavioral outcome. We suggest that anthropological knowledge of variation in human mobility might be improved by greater research attention to its <span class="hlt">biological</span> dimensions. © 2016 Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25723667','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25723667"><span>Unilateral microform cleft lip repair: application of muscle tension <span class="hlt">line</span> group theory.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yin, Ningbei; Song, Tao; Wu, Jiajun; Chen, Bo; Ma, Hengyuan; Zhao, Zhenmin; Wang, Yongqian; Li, Haidong; Wu, Di</p> <p>2015-03-01</p> <p>In microform cleft lip repair, reconstructing the elaborate structures is difficult. We describe a new technique of unilateral microform cleft lip repair that is based <span class="hlt">on</span> the muscle tension <span class="hlt">line</span> group theory. According to the shape of Cupid bow, a different small incision is used without <span class="hlt">creating</span> an obvious cutaneous scar. First, the nasolabial muscle around the nasal floor (the first auxiliary tension <span class="hlt">line</span> group) is reconstructed, and then the orbicularis oris muscle around the philtrum (the second auxiliary tension <span class="hlt">line</span> group) is reconstructed based <span class="hlt">on</span> the muscle tension <span class="hlt">line</span> group theory. From June 2006 to June 2012, the technique was used in 263 unilateral microform cleft lip repairs. For 18 months, 212 patients were followed up. The appearance of the nasal alar, nasal sill, philtrum, and Cupid bow peak improved. Most patients had a satisfactory appearance. Based <span class="hlt">on</span> the muscle tension <span class="hlt">line</span> group theory, using this technique offers the ability to adduct the nasal alar effectively to form a good nasal sill and philtrum.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19740021422','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19740021422"><span><span class="hlt">On-line</span> diagnosis of sequential systems, 2</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Sundstrom, R. J.</p> <p>1974-01-01</p> <p>The theory and techniques applicable to the <span class="hlt">on-line</span> diagnosis of sequential systems, were investigated. A complete model for the study of <span class="hlt">on-line</span> diagnosis is developed. First an appropriate class of system models is formulated which can serve as a basis for a theoretical study of <span class="hlt">on-line</span> diagnosis. Then notions of realization, fault, fault-tolerance and diagnosability are formalized which have meaningful interpretations in the the context of <span class="hlt">on-line</span> diagnosis. The diagnosis of systems which are structurally decomposed and are represented as a network of smaller systems is studied. The fault set considered is the set of faults which only affect one component system is the network. A characterization of those networks which can be diagnosed using a purely combinational detector is achieved. A technique is given which can be used to realize any network by a network which is diagnosable in the above sense. Limits are found <span class="hlt">on</span> the amount of redundancy involved in any such technique.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25583299','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25583299"><span><span class="hlt">Biologically</span> inspired dynamic material systems.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Studart, André R</p> <p>2015-03-09</p> <p>Numerous examples of material systems that dynamically interact with and adapt to the surrounding environment are found in nature, from hair-based mechanoreceptors in animals to self-shaping seed dispersal units in plants to remodeling bone in vertebrates. Inspired by such fascinating <span class="hlt">biological</span> structures, a wide range of synthetic material systems have been <span class="hlt">created</span> to replicate the design concepts of dynamic natural architectures. Examples of <span class="hlt">biological</span> structures and their man-made counterparts are herein revisited to illustrate how dynamic and adaptive responses emerge from the intimate microscale combination of building blocks with intrinsic nanoscale properties. By using top-down photolithographic methods and bottom-up assembly approaches, <span class="hlt">biologically</span> inspired dynamic material systems have been <span class="hlt">created</span> 1) to sense liquid flow with hair-inspired microelectromechanical systems, 2) to autonomously change shape by utilizing plantlike heterogeneous architectures, 3) to homeostatically influence the surrounding environment through self-regulating adaptive surfaces, and 4) to spatially concentrate chemical species by using synthetic microcompartments. The ever-increasing complexity and remarkable functionalities of such synthetic systems offer an encouraging perspective to the rich set of dynamic and adaptive properties that can potentially be implemented in future man-made material systems. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5948912','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5948912"><span>Improved Seam-<span class="hlt">Line</span> Searching Algorithm for UAV Image Mosaic with Optical Flow</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Zhang, Weilong; Guo, Bingxuan; Liao, Xuan; Li, Wenzhuo</p> <p>2018-01-01</p> <p>Ghosting and seams are two major challenges in <span class="hlt">creating</span> unmanned aerial vehicle (UAV) image mosaic. In response to these problems, this paper proposes an improved method for UAV image seam-<span class="hlt">line</span> searching. First, an image matching algorithm is used to extract and match the features of adjacent images, so that they can be transformed into the same coordinate system. Then, the gray scale difference, the gradient minimum, and the optical flow value of pixels in adjacent image overlapped area in a neighborhood are calculated, which can be applied to <span class="hlt">creating</span> an energy function for seam-<span class="hlt">line</span> searching. Based <span class="hlt">on</span> that, an improved dynamic programming algorithm is proposed to search the optimal seam-<span class="hlt">lines</span> to complete the UAV image mosaic. This algorithm adopts a more adaptive energy aggregation and traversal strategy, which can find a more ideal splicing path for adjacent UAV images and avoid the ground objects better. The experimental results show that the proposed method can effectively solve the problems of ghosting and seams in the panoramic UAV images. PMID:29659526</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29659526','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29659526"><span>Improved Seam-<span class="hlt">Line</span> Searching Algorithm for UAV Image Mosaic with Optical Flow.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Weilong; Guo, Bingxuan; Li, Ming; Liao, Xuan; Li, Wenzhuo</p> <p>2018-04-16</p> <p>Ghosting and seams are two major challenges in <span class="hlt">creating</span> unmanned aerial vehicle (UAV) image mosaic. In response to these problems, this paper proposes an improved method for UAV image seam-<span class="hlt">line</span> searching. First, an image matching algorithm is used to extract and match the features of adjacent images, so that they can be transformed into the same coordinate system. Then, the gray scale difference, the gradient minimum, and the optical flow value of pixels in adjacent image overlapped area in a neighborhood are calculated, which can be applied to <span class="hlt">creating</span> an energy function for seam-<span class="hlt">line</span> searching. Based <span class="hlt">on</span> that, an improved dynamic programming algorithm is proposed to search the optimal seam-<span class="hlt">lines</span> to complete the UAV image mosaic. This algorithm adopts a more adaptive energy aggregation and traversal strategy, which can find a more ideal splicing path for adjacent UAV images and avoid the ground objects better. The experimental results show that the proposed method can effectively solve the problems of ghosting and seams in the panoramic UAV images.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3798292','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3798292"><span><span class="hlt">On</span> Crowd-verification of <span class="hlt">Biological</span> Networks</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Ansari, Sam; Binder, Jean; Boue, Stephanie; Di Fabio, Anselmo; Hayes, William; Hoeng, Julia; Iskandar, Anita; Kleiman, Robin; Norel, Raquel; O’Neel, Bruce; Peitsch, Manuel C.; Poussin, Carine; Pratt, Dexter; Rhrissorrakrai, Kahn; Schlage, Walter K.; Stolovitzky, Gustavo; Talikka, Marja</p> <p>2013-01-01</p> <p><span class="hlt">Biological</span> networks with a structured syntax are a powerful way of representing <span class="hlt">biological</span> information generated from high density data; however, they can become unwieldy to manage as their size and complexity increase. This article presents a crowd-verification approach for the visualization and expansion of <span class="hlt">biological</span> networks. Web-based graphical interfaces allow visualization of causal and correlative <span class="hlt">biological</span> relationships represented using <span class="hlt">Biological</span> Expression Language (BEL). Crowdsourcing principles enable participants to communally annotate these relationships based <span class="hlt">on</span> literature evidences. Gamification principles are incorporated to further engage domain experts throughout <span class="hlt">biology</span> to gather robust peer-reviewed information from which relationships can be identified and verified. The resulting network models will represent the current status of <span class="hlt">biological</span> knowledge within the defined boundaries, here processes related to human lung disease. These models are amenable to computational analysis. For some period following conclusion of the challenge, the published models will remain available for continuous use and expansion by the scientific community. PMID:24151423</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24875418','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24875418"><span>Cytoplasmic effects <span class="hlt">on</span> DNA methylation between male sterile <span class="hlt">lines</span> and the maintainer in wheat (Triticum aestivum L.).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ba, Qingsong; Zhang, Gaisheng; Niu, Na; Ma, Shoucai; Wang, Junwei</p> <p>2014-10-01</p> <p>Male sterile cytoplasm plays an important role in hybrid wheat, and three-<span class="hlt">line</span> system including male sterile (A <span class="hlt">line</span>), its maintainer (B <span class="hlt">line</span>) and restoring (R <span class="hlt">line</span>) has played a major role in wheat hybrid production. It is well known that DNA methylation plays an important role in gene expression regulation during <span class="hlt">biological</span> development in wheat. However, no reports are available <span class="hlt">on</span> DNA methylation affected by different male sterile cytoplasms in hybrid wheat. We employed a methylation-sensitive amplified polymorphism technique to characterize nuclear DNA methylation in three male sterile cytoplasms. A and B <span class="hlt">lines</span> share the same nucleus, but have different cytoplasms which is male sterile for the A and fertile for the B. The results revealed a relationship of DNA methylation at these sites specifically with male sterile cytoplasms, as well as male sterility, since the only difference between the A <span class="hlt">lines</span> and B <span class="hlt">line</span> was the cytoplasm. The DNA methylation was markedly affected by male sterile cytoplasms. K-type cytoplasm affected the methylation to a much greater degree than T-type and S-type cytoplasms, as indicated by the ratio of methylated sites, ratio of fully methylated sites, and polymorphism between A <span class="hlt">lines</span> and B <span class="hlt">line</span> for these cytoplasms. The genetic distance between the cytoplasm and nucleus for the K-type is much greater than for the T- and S-types because the former is between Aegilops genus and Triticum genus and the latter is within Triticum genus between Triticum spelta and Triticum timopheevii species. Thus, this difference in genetic distance may be responsible for the variation in methylation that we observed. Copyright © 2014. Published by Elsevier B.V.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17608077','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17608077"><span>The re-emergence of clinical service <span class="hlt">line</span> management.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Litch, Bonnie K</p> <p>2007-01-01</p> <p>As healthcare leaders are positioning their organizations for a more competitive environment characterized by expanding consumer choice models, they are renewing their attention <span class="hlt">on</span> organizing along clinical service <span class="hlt">lines</span>. Bringing together clinical services in ways meaningful to patients can improve quality b better integrating care, while at the same time strengthening an organization's market position and <span class="hlt">creating</span> new opportunities for increased physician collaboration--from collaborative planning to management to economic participation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27174935','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27174935"><span>tRNAscan-SE <span class="hlt">On-line</span>: integrating search and context for analysis of transfer RNA genes.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lowe, Todd M; Chan, Patricia P</p> <p>2016-07-08</p> <p>High-throughput genome sequencing continues to grow the need for rapid, accurate genome annotation and tRNA genes constitute the largest family of essential, ever-present non-coding RNA genes. Newly developed tRNAscan-SE 2.0 has advanced the state-of-the-art methodology in tRNA gene detection and functional prediction, captured by rich new content of the companion Genomic tRNA Database. Previously, web-server tRNA detection was isolated from knowledge of existing tRNAs and their annotation. In this update of the tRNAscan-SE <span class="hlt">On-line</span> resource, we tie together improvements in tRNA classification with greatly enhanced <span class="hlt">biological</span> context via dynamically generated links between web server search results, the most relevant genes in the GtRNAdb and interactive, rich genome context provided by UCSC genome browsers. The tRNAscan-SE <span class="hlt">On-line</span> web server can be accessed at http://trna.ucsc.edu/tRNAscan-SE/. © The Author(s) 2016. Published by Oxford University Press <span class="hlt">on</span> behalf of Nucleic Acids Research.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018MS%26E..317a2002N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018MS%26E..317a2002N"><span>Investigation of the Effect of Small Hardening Spots <span class="hlt">Created</span> <span class="hlt">on</span> the Sample Surface by Laser Complex with Solid-State Laser</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Nozdrina, O.; Zykov, I.; Melnikov, A.; Tsipilev, V.; Turanov, S.</p> <p>2018-03-01</p> <p>This paper describes the results of an investigation of the effect of small hardening spots (about 1 mm) <span class="hlt">created</span> <span class="hlt">on</span> the surface of a sample by laser complex with solid-state laser. The melted area of the steel sample is not exceed 5%. Steel microhardness change in the region subjected to laser treatment is studied. Also there is a graph of the deformation of samples dependence <span class="hlt">on</span> the tension. As a result, the yield plateau and plastic properties changes were detected. The flow <span class="hlt">line</span> was tracked in the series of speckle photographs. As a result we can see how mm surface inhomogeneity can influence <span class="hlt">on</span> the deformation and strength properties of steel.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1996eso..pres...14.','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1996eso..pres...14."><span>Astronomy <span class="hlt">On-Line</span> Programme Enters "hot Week"</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p></p> <p>1996-11-01</p> <p>World's Biggest Astronomy WWW-Event Attracts Thousands of Students The Astronomy <span class="hlt">On-line</span> Programme (See ESO Press Release 09/96 of 18 June 1996) began officially <span class="hlt">on</span> 1 October and is now about to enter its most intense phase, known as the Hot Week . <span class="hlt">On</span> 18 - 22 November, an estimated 4000 astronomy-interested, mostly young people in Europe and <span class="hlt">on</span> four other continents will get together during five days in what - not unexpected - has become the world's biggest astronomy event ever organised <span class="hlt">on</span> the World Wide Web. This carefully structured Programme is carried out in collaboration between the European Association for Astronomy Education (EAAE), the European Southern Observatory and the European Commission, under the auspices of the Fourth European Week for Scientific and Technological Culture. The Programme has already had a most visible impact <span class="hlt">on</span> the school education of natural sciences in various countries; for instance, the Internet-connection of schools has been advanced in some, in order to allow groups to participate. There have been numerous contacts among the groups across the borders and there are clear signs that many Astronomy <span class="hlt">On-line</span> participants have progressed to use the impressive possibilities of the Web in an efficient and structured way. There has been a lively media interest in Astronomy <span class="hlt">On-line</span> all over Europe and it is expected to increase during the next week. The current status of Astronomy <span class="hlt">On-line</span> It is obvious that the pilot function of the Astronomy <span class="hlt">On-line</span> Programme in the use of the Web has been very effective and that the associated dissemination of astronomical knowledge has been successful. At this time, more than 650 groups have registered with Astronomy <span class="hlt">On-line</span>. Most come from 31 different European countries and a few dozen groups are located in North and South America as well as in Asia and Australia. Together they have experienced the steady build-up of Astronomy <span class="hlt">On-line</span> over the past weeks, by means of numerous contributions from a</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11122491','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11122491"><span>Review of russian literature <span class="hlt">on</span> <span class="hlt">biological</span> action of DC and low-frequency AC magnetic fields.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhadin, M N</p> <p>2001-01-01</p> <p>This review considers the Russian scientific literature <span class="hlt">on</span> the influence of weak static and of low-frequency alternating magnetic fields <span class="hlt">on</span> <span class="hlt">biological</span> systems. The review covers the most interesting works and the main <span class="hlt">lines</span> of investigation during the period 1900 to the present. Shown here are the historical roots, beginning with the ideas of V. Vernadsky and A. Chizhevsky, which led in the field of Russian <span class="hlt">biology</span> to an increasing interest in magnetic fields, based <span class="hlt">on</span> an intimate connection between solar activity and life <span class="hlt">on</span> the Earth, and which determined the peculiar development of Russian magnetobiology. The variety of studies <span class="hlt">on</span> the effects of magnetic storms and extremely low-frequency, periodic variations of the geomagnetic field <span class="hlt">on</span> human beings and animals as well as <span class="hlt">on</span> social phenomena are described. The diverse experiments involving artificial laboratory magnetic fields acting <span class="hlt">on</span> different <span class="hlt">biological</span> entities under different conditions are also considered. A series of theoretical advances are reviewed that have paved the way for a step-by-step understanding of the mechanisms of magnetic field effects <span class="hlt">on</span> <span class="hlt">biological</span> systems. The predominantly unfavorable influence of magnetic fields <span class="hlt">on</span> living beings is shown, but the cases of favorable influence of magnetic fields <span class="hlt">on</span> human beings and lower animals are demonstrated as well. The majority of Russian investigations in this area of science has been unknown among the non-Russian speaking audience for many reasons, primarily because of a language barrier. Therefore, it is hoped that this review may be of interest to the international scientific community. Copyright 2001 Wiley-Liss, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20050000870&hterms=Biomedicine&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3DBiomedicine','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20050000870&hterms=Biomedicine&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3DBiomedicine"><span>Parallel <span class="hlt">line</span> analysis: multifunctional software for the biomedical sciences</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Swank, P. R.; Lewis, M. L.; Damron, K. L.; Morrison, D. R.</p> <p>1990-01-01</p> <p>An easy to use, interactive FORTRAN program for analyzing the results of parallel <span class="hlt">line</span> assays is described. The program is menu driven and consists of five major components: data entry, data editing, manual analysis, manual plotting, and automatic analysis and plotting. Data can be entered from the terminal or from previously <span class="hlt">created</span> data files. The data editing portion of the program is used to inspect and modify data and to statistically identify outliers. The manual analysis component is used to test the assumptions necessary for parallel <span class="hlt">line</span> assays using analysis of covariance techniques and to determine potency ratios with confidence limits. The manual plotting component provides a graphic display of the data <span class="hlt">on</span> the terminal screen or <span class="hlt">on</span> a standard <span class="hlt">line</span> printer. The automatic portion runs through multiple analyses without operator input. Data may be saved in a special file to expedite input at a future time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3293987','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3293987"><span>Parts plus pipes: synthetic <span class="hlt">biology</span> approaches to metabolic engineering</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Boyle, Patrick M.; Silver, Pamela A.</p> <p>2011-01-01</p> <p>Synthetic biologists combine modular <span class="hlt">biological</span> “parts” to <span class="hlt">create</span> higher-order devices. Metabolic engineers construct <span class="hlt">biological</span> “pipes” by optimizing the microbial conversion of basic substrates to desired compounds. Many scientists work at the intersection of these two philosophies, employing synthetic devices to enhance metabolic engineering efforts. These integrated approaches promise to do more than simply improve product yields; they can expand the array of products that are tractable to produce <span class="hlt">biologically</span>. In this review, we explore the application of synthetic <span class="hlt">biology</span> techniques to next-generation metabolic engineering challenges, as well as the emerging engineering principles for <span class="hlt">biological</span> design. PMID:22037345</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3317705','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3317705"><span>Development of <span class="hlt">On-Line</span> High Performance Liquid Chromatography (HPLC)-Biochemical Detection Methods as Tools in the Identification of Bioactives</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Malherbe, Christiaan J.; de Beer, Dalene; Joubert, Elizabeth</p> <p>2012-01-01</p> <p>Biochemical detection (BCD) methods are commonly used to screen plant extracts for specific <span class="hlt">biological</span> activities in batch assays. Traditionally, bioactives in the most active extracts were identified through time-consuming bio-assay guided fractionation until single active compounds could be isolated. Not only are isolation procedures often tedious, but they could also lead to artifact formation. <span class="hlt">On-line</span> coupling of BCD assays to high performance liquid chromatography (HPLC) is gaining ground as a high resolution screening technique to overcome problems associated with pre-isolation by measuring the effects of compounds post-column directly after separation. To date, several <span class="hlt">on-line</span> HPLC-BCD assays, applied to whole plant extracts and mixtures, have been published. In this review the focus will fall <span class="hlt">on</span> enzyme-based, receptor-based and antioxidant assays. PMID:22489144</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22527514','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22527514"><span>The Protein Structure Initiative Structural <span class="hlt">Biology</span> Knowledgebase Technology Portal: a structural <span class="hlt">biology</span> web resource.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gifford, Lida K; Carter, Lester G; Gabanyi, Margaret J; Berman, Helen M; Adams, Paul D</p> <p>2012-06-01</p> <p>The Technology Portal of the Protein Structure Initiative Structural <span class="hlt">Biology</span> Knowledgebase (PSI SBKB; http://technology.sbkb.org/portal/ ) is a web resource providing information about methods and tools that can be used to relieve bottlenecks in many areas of protein production and structural <span class="hlt">biology</span> research. Several useful features are available <span class="hlt">on</span> the web site, including multiple ways to search the database of over 250 technological advances, a link to videos of methods <span class="hlt">on</span> YouTube, and access to a technology forum where scientists can connect, ask questions, get news, and develop collaborations. The Technology Portal is a component of the PSI SBKB ( http://sbkb.org ), which presents integrated genomic, structural, and functional information for all protein sequence targets selected by the Protein Structure Initiative. <span class="hlt">Created</span> in collaboration with the Nature Publishing Group, the SBKB offers an array of resources for structural biologists, such as a research library, editorials about new research advances, a featured <span class="hlt">biological</span> system each month, and a functional sleuth for searching protein structures of unknown function. An overview of the various features and examples of user searches highlight the information, tools, and avenues for scientific interaction available through the Technology Portal.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/AD1005694','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/AD1005694"><span>2011 Chemical, <span class="hlt">Biological</span>, Radiological, and Nuclear Survivability Conference</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2011-05-18</p> <p>Protection (barrier, sorptive and reactive material technologies) o Top surface antimicrobial treatments (kills spores, bacteria, fungi, viruses ) o...Warning System (TWS) CDD - Countermeasure Anti-Torpedo ( CAT ) CDD UNCLASSIFIED Joint Program Executive Office for Chemical and <span class="hlt">Biological</span> Defense May...<span class="hlt">Creating</span> viruses de novo <span class="hlt">Biological</span> Threats UNCLASSIFIED JPEO-CBD Radiological/Nuclear (RN) Status and Path Forward • Issue: No identified DoD</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/6721','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/6721"><span>Proceedings of the California Forest Soils Council Conference <span class="hlt">on</span> Forest Soils <span class="hlt">Biology</span> and Forest Management</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Robert F. Powers; Donald L. Hauxwell; Gary M. Nakamura</p> <p>2000-01-01</p> <p>Biotic properties of forest soil are the linkages connecting forest vegetation with an inert rooting medium to <span class="hlt">create</span> a dynamic, functioning ecosystem. But despite the significance of these properties, managers have little awareness of the biotic world beneath their feet. Much of our working knowledge of soil <span class="hlt">biology</span> seems anchored in myth and misunderstanding. To...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_20 --> <div id="page_21" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="401"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012PhDT........27W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012PhDT........27W"><span>A theoretical lens <span class="hlt">on</span> a <span class="hlt">biology</span> intensive orientation program: A study of self-efficacy and self-regulation of freshman <span class="hlt">biology</span> majors</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wheeler, Erin R.</p> <p></p> <p>There is a national effort to increase the number of undergraduate students graduating in science, math, engineering, and technology (STEM) (National Science Foundation, 2007). The majority of students initially populating these STEM majors ultimately switch to and graduate from non-STEM majors (Seymour & Hewitt, 2000; Seymour, 2002). The source of attrition from STEM fields lies within the difficulty of concepts presented in freshman STEM introductory courses (Jensen & Moore, 2007, 2008, 2009; Seymour & Hewitt, 2000). These gateway courses are considered high-risk because nearly half of students enrolled in these courses receive either a "D" or "F" or completely withdraw from the course (Labov, 2004). Research shows that students who have uncalibrated self-efficacy and an attenuated self-regulated learning are unsuccessful in high-risk courses (Kitsantas et al., 2008; Ross, Green, Salisbury-Glennon, & Tollefson, 2006; Zimmerman, 2002). Traditional academic assistance, such as tutoring, learning to learn courses, and supplemental instruction, does not explicitly develop an undergraduate's self-efficacy and self-regulated learning as it specifically relates to the STEM domains (Cao & Nietfeld, 2007; Dembo & Seli, 2006; Ross et al., 2006; Simpson, Hind, Nist, Burrell, 1997). Some STEM departments have <span class="hlt">created</span> academic interventions, such as one-credit seminars, orientation programs, and bridge programs, to directly address the needs of STEM majors (Belzer, 2003; Bonner, 2009; Chevalier, Chrisman, & Kelsey, 2001; Hutchison-Green, Follman, & Bodner, 2008; D. J. Minchella, Yazvac, C. W., Fodrea, R. A., Ball G., 2007; Reyes, Anderson-Rowland, & McCartney, 1998). This study focused <span class="hlt">on</span> the effect of a <span class="hlt">biology</span>-intensive orientation program <span class="hlt">on</span> <span class="hlt">biology</span> majors' self-efficacy and self-regulated learning. The study utilized approximately 300 undergraduate <span class="hlt">biology</span> majors participating in a <span class="hlt">biology</span>-intensive orientation that occurred <span class="hlt">on</span> August 7-12, 2011, at a public state</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29727189','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29727189"><span>Moving Contact <span class="hlt">Lines</span>: Linking Molecular Dynamics and Continuum-Scale Modeling.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Smith, Edward R; Theodorakis, Panagiotis E; Craster, Richard V; Matar, Omar K</p> <p>2018-05-17</p> <p>Despite decades of research, the modeling of moving contact <span class="hlt">lines</span> has remained a formidable challenge in fluid dynamics whose resolution will impact numerous industrial, <span class="hlt">biological</span>, and daily life applications. <span class="hlt">On</span> the one hand, molecular dynamics (MD) simulation has the ability to provide unique insight into the microscopic details that determine the dynamic behavior of the contact <span class="hlt">line</span>, which is not possible with either continuum-scale simulations or experiments. <span class="hlt">On</span> the other hand, continuum-based models provide a link to the macroscopic description of the system. In this Feature Article, we explore the complex range of physical factors, including the presence of surfactants, which governs the contact <span class="hlt">line</span> motion through MD simulations. We also discuss links between continuum- and molecular-scale modeling and highlight the opportunities for future developments in this area.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29758614','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29758614"><span>General method to find the attractors of discrete dynamic models of <span class="hlt">biological</span> systems.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gan, Xiao; Albert, Réka</p> <p>2018-04-01</p> <p>Analyzing the long-term behaviors (attractors) of dynamic models of <span class="hlt">biological</span> networks can provide valuable insight. We propose a general method that can find the attractors of multilevel discrete dynamical systems by extending a method that finds the attractors of a Boolean network model. The previous method is based <span class="hlt">on</span> finding stable motifs, subgraphs whose nodes' states can stabilize <span class="hlt">on</span> their own. We extend the framework from binary states to any finite discrete levels by <span class="hlt">creating</span> a virtual node for each level of a multilevel node, and describing each virtual node with a quasi-Boolean function. We then <span class="hlt">create</span> an expanded representation of the multilevel network, find multilevel stable motifs and oscillating motifs, and identify attractors by successive network reduction. In this way, we find both fixed point attractors and complex attractors. We implemented an algorithm, which we test and validate <span class="hlt">on</span> representative synthetic networks and <span class="hlt">on</span> published multilevel models of <span class="hlt">biological</span> networks. Despite its primary motivation to analyze <span class="hlt">biological</span> networks, our motif-based method is general and can be applied to any finite discrete dynamical system.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018PhRvE..97d2308G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018PhRvE..97d2308G"><span>General method to find the attractors of discrete dynamic models of <span class="hlt">biological</span> systems</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gan, Xiao; Albert, Réka</p> <p>2018-04-01</p> <p>Analyzing the long-term behaviors (attractors) of dynamic models of <span class="hlt">biological</span> networks can provide valuable insight. We propose a general method that can find the attractors of multilevel discrete dynamical systems by extending a method that finds the attractors of a Boolean network model. The previous method is based <span class="hlt">on</span> finding stable motifs, subgraphs whose nodes' states can stabilize <span class="hlt">on</span> their own. We extend the framework from binary states to any finite discrete levels by <span class="hlt">creating</span> a virtual node for each level of a multilevel node, and describing each virtual node with a quasi-Boolean function. We then <span class="hlt">create</span> an expanded representation of the multilevel network, find multilevel stable motifs and oscillating motifs, and identify attractors by successive network reduction. In this way, we find both fixed point attractors and complex attractors. We implemented an algorithm, which we test and validate <span class="hlt">on</span> representative synthetic networks and <span class="hlt">on</span> published multilevel models of <span class="hlt">biological</span> networks. Despite its primary motivation to analyze <span class="hlt">biological</span> networks, our motif-based method is general and can be applied to any finite discrete dynamical system.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22985679','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22985679"><span>Engineering plant metabolism into microbes: from systems <span class="hlt">biology</span> to synthetic <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Xu, Peng; Bhan, Namita; Koffas, Mattheos A G</p> <p>2013-04-01</p> <p>Plant metabolism represents an enormous repository of compounds that are of pharmaceutical and biotechnological importance. Engineering plant metabolism into microbes will provide sustainable solutions to produce pharmaceutical and fuel molecules that could one day replace substantial portions of the current fossil-fuel based economy. Metabolic engineering entails targeted manipulation of biosynthetic pathways to maximize yields of desired products. Recent advances in Systems <span class="hlt">Biology</span> and the emergence of Synthetic <span class="hlt">Biology</span> have accelerated our ability to design, construct and optimize cell factories for metabolic engineering applications. Progress in predicting and modeling genome-scale metabolic networks, versatile gene assembly platforms and delicate synthetic pathway optimization strategies has provided us exciting opportunities to exploit the full potential of cell metabolism. In this review, we will discuss how systems and synthetic <span class="hlt">biology</span> tools can be integrated to <span class="hlt">create</span> tailor-made cell factories for efficient production of natural products and fuel molecules in microorganisms. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28796421','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28796421"><span>Novel technologies in doubled haploid <span class="hlt">line</span> development.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ren, Jiaojiao; Wu, Penghao; Trampe, Benjamin; Tian, Xiaolong; Lübberstedt, Thomas; Chen, Shaojiang</p> <p>2017-11-01</p> <p>haploid inducer <span class="hlt">line</span> can be transferred (DH) technology can not only shorten the breeding process but also increase genetic gain. Haploid induction and subsequent genome doubling are the two main steps required for DH technology. Haploids have been generated through the culture of immature male and female gametophytes, and through inter- and intraspecific via chromosome elimination. Here, we focus <span class="hlt">on</span> haploidization via chromosome elimination, especially the recent advances in centromere-mediated haploidization. Once haploids have been induced, genome doubling is needed to produce DH <span class="hlt">lines</span>. This study has proposed a new strategy to improve haploid genome doubling by combing haploids and minichromosome technology. With the progress in haploid induction and genome doubling methods, DH technology can facilitate reverse breeding, cytoplasmic male sterile (CMS) <span class="hlt">line</span> production, gene stacking and a variety of other genetic analysis. © 2017 The Authors. Plant Biotechnology Journal published by Society for Experimental <span class="hlt">Biology</span> and The Association of Applied Biologists and John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/2512415','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/2512415"><span>[<span class="hlt">Biological</span> experiments <span class="hlt">on</span> "Kosmos-1887"].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Alpatov, A M; I'lin, E A; Antipov, V V; Tairbekov, M G</p> <p>1989-01-01</p> <p>In the 13-ray space flight <span class="hlt">on</span> Kosmos-1887 various experiments in the field of cell <span class="hlt">biology</span>, genetics, biorhythm, developmental <span class="hlt">biology</span> and regeneration were performed using bacteria, protozoa, plants, worms, insects, fish and amphibia. Paramecia showed enhanced cell proliferation, spheroidization and diminished protein content. Experiments <span class="hlt">on</span> fruit-flies, newt oocytes and primate lymphocytes confirmed involvement of the cell genetic apparatus in responses to microgravity. Beetles exhibited a reduction of the length of the spontaneous period of freely running circadian rhythms. Carausius morosus developed latent changes in early embryogenesis which manifested at later stages of ontogenesis. Exposure to microgravity did not prevent recovery of injured tissues; moreover their regeneration may be accelerated after recovery. <span class="hlt">Biology</span> research programs in future biosatellite flights are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23486277','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23486277"><span>Generation of stable human cell <span class="hlt">lines</span> with Tetracycline-inducible (Tet-<span class="hlt">on</span>) shRNA or cDNA expression.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gomez-Martinez, Marta; Schmitz, Debora; Hergovich, Alexander</p> <p>2013-03-05</p> <p>A major approach in the field of mammalian cell <span class="hlt">biology</span> is the manipulation of the expression of genes of interest in selected cell <span class="hlt">lines</span>, with the aim to reveal one or several of the gene's function(s) using transient/stable overexpression or knockdown of the gene of interest. Unfortunately, for various cell <span class="hlt">biological</span> investigations this approach is unsuitable when manipulations of gene expression result in cell growth/proliferation defects or unwanted cell differentiation. Therefore, researchers have adapted the Tetracycline repressor protein (TetR), taken from the E. coli tetracycline resistance operon(1), to generate very efficient and tight regulatory systems to express cDNAs in mammalian cells(2,3). In short, TetR has been modified to either (1) block initiation of transcription by binding to the Tet-operator (TO) in the promoter region upon addition of tetracycline (termed Tet-off system) or (2) bind to the TO in the absence of tetracycline (termed Tet-<span class="hlt">on</span> system) (Figure 1). Given the inconvenience that the Tet-off system requires the continuous presence of tetracycline (which has a half-life of about 24 hr in tissue cell culture medium) the Tet-<span class="hlt">on</span> system has been more extensively optimized, resulting in the development of very tight and efficient vector systems for cDNA expression as used here. Shortly after establishment of RNA interference (RNAi) for gene knockdown in mammalian cells(4), vectors expressing short-hairpin RNAs (shRNAs) were described that function very similar to siRNAs(5-11). However, these shRNA-mediated knockdown approaches have the same limitation as conventional knockout strategies, since stable depletion is not feasible when gene targets are essential for cellular survival. To overcome this limitation, van de Wetering et al.(12) modified the shRNA expression vector pSUPER(5) by inserting a TO in the promoter region, which enabled them to generate stable cell <span class="hlt">lines</span> with tetracycline-inducible depletion of their target genes of</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22225766','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22225766"><span><span class="hlt">Biological</span> indicators, tools to verify the effect of sterilisation processes - position paper prepared <span class="hlt">on</span> behalf of group 1 (<span class="hlt">biological</span> methods and statistical analysis).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Haberer, K; van Doorne, H</p> <p>2011-11-01</p> <p><span class="hlt">Biological</span> indicators (BIs) are test systems containing viable microorganisms (usually spores of bacteria) providing a defined challenge to a specified sterilisation process. General chapter 5.1.2 of the European Pharmacopoeia [1] (Ph. Eur.) sets specifications for BIs and gives some guidance for their use. As shown in this text, the approach followed by Ph. Eur. as well as by ISO standards is outdated and could <span class="hlt">create</span> nowadays some confusion among the users of the pharmacopoeia. It is the objective of this paper to provide the theoretical background of BIs as tools for the design and qualification of reliable moist heat sterilisation processes. The principles laid down in this article will form the basis of a future draft <span class="hlt">on</span> a revised chapter <span class="hlt">on</span> BIs in Pharmeuropa.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25448512','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25448512"><span><span class="hlt">Creating</span> and selling embryos for "donation": ethical challenges.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Klitzman, Robert; Sauer, Mark V</p> <p>2015-02-01</p> <p>The commercial creation and sale of embryos has begun, which poses a series of ethical questions that have received little scholarly attention. Some of the concerns that arise are similar to those posed by the sale of gametes, while other issues differ markedly. Questions emerge, first, regarding the rights of the unborn children and their ability to know their <span class="hlt">biological</span> parents. Companies that <span class="hlt">create</span> human embryos de novo may wish to keep gamete providers anonymous. Many of these offspring thus will never learn that their parents are not their <span class="hlt">biologic</span> parents. Yet, such disclosures, regarding not only one but both of these <span class="hlt">biologic</span> parents, may be important for these individuals; and a lack of this knowledge may impede their physical and psychological health. Second, questions surface regarding the fees that providers should charge for embryos and whether these amounts should vary based <span class="hlt">on</span> the traits of 1 or both of the gamete donors. Some prospective parents may seek specific traits in a baby (eg, height or eye/hair coloring), which prompts the creation of embryos from 2 gamete donors who possess these characteristics. Third, ownership of embryos <span class="hlt">created</span> without an advanced directive by patients poses dilemmas (eg, disposition of any remaining embryos). Fourth, guidelines do not yet exist to limit the number of embryos sold from each pair of gamete donors. Hence, unbeknownst to each other, full siblings could potentially meet, get married, and procreate. This discussion has several critical implications for future practice and professional education and policy. Patients with diseases associated with genetic tests may well ask obstetricians, gynecologists, and other physicians about these techniques and practices. Clinicians can refer such patients to assisted reproductive technology specialists; however, familiarity with the basic aspects of the issues and complexities involved could aid these providers and their patients Several of these issues can be</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22740447','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22740447"><span>A new <span class="hlt">biologic</span> prognostic model based <span class="hlt">on</span> immunohistochemistry predicts survival in patients with diffuse large B-cell lymphoma.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Perry, Anamarija M; Cardesa-Salzmann, Teresa M; Meyer, Paul N; Colomo, Luis; Smith, Lynette M; Fu, Kai; Greiner, Timothy C; Delabie, Jan; Gascoyne, Randy D; Rimsza, Lisa; Jaffe, Elaine S; Ott, German; Rosenwald, Andreas; Braziel, Rita M; Tubbs, Raymond; Cook, James R; Staudt, Louis M; Connors, Joseph M; Sehn, Laurie H; Vose, Julie M; López-Guillermo, Armando; Campo, Elias; Chan, Wing C; Weisenburger, Dennis D</p> <p>2012-09-13</p> <p><span class="hlt">Biologic</span> factors that predict the survival of patients with a diffuse large B-cell lymphoma, such as cell of origin and stromal signatures, have been discovered by gene expression profiling. We attempted to simulate these gene expression profiling findings and <span class="hlt">create</span> a new <span class="hlt">biologic</span> prognostic model based <span class="hlt">on</span> immunohistochemistry. We studied 199 patients (125 in the training set, 74 in the validation set) with de novo diffuse large B-cell lymphoma treated with rituximab and CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) or CHOP-like therapies, and immunohistochemical stains were performed <span class="hlt">on</span> paraffin-embedded tissue microarrays. In the model, 1 point was awarded for each adverse prognostic factor: nongerminal center B cell-like subtype, SPARC (secreted protein, acidic, and rich in cysteine) < 5%, and microvascular density quartile 4. The model using these 3 <span class="hlt">biologic</span> markers was highly predictive of overall survival and event-free survival in multivariate analysis after adjusting for the International Prognostic Index in both the training and validation sets. This new model delineates 2 groups of patients, 1 with a low <span class="hlt">biologic</span> score (0-1) and good survival and the other with a high score (2-3) and poor survival. This new <span class="hlt">biologic</span> prognostic model could be used with the International Prognostic Index to stratify patients for novel or risk-adapted therapies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22167707-microlensing-quasar-broad-emission-lines-constraints-broad-line-region-size','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22167707-microlensing-quasar-broad-emission-lines-constraints-broad-line-region-size"><span>MICROLENSING OF QUASAR BROAD EMISSION <span class="hlt">LINES</span>: CONSTRAINTS <span class="hlt">ON</span> BROAD <span class="hlt">LINE</span> REGION SIZE</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Guerras, E.; Mediavilla, E.; Jimenez-Vicente, J.</p> <p>2013-02-20</p> <p>We measure the differential microlensing of the broad emission <span class="hlt">lines</span> between 18 quasar image pairs in 16 gravitational lenses. We find that the broad emission <span class="hlt">lines</span> are in general weakly microlensed. The results show, at a modest level of confidence (1.8{sigma}), that high ionization <span class="hlt">lines</span> such as C IV are more strongly microlensed than low ionization <span class="hlt">lines</span> such as H{beta}, indicating that the high ionization <span class="hlt">line</span> emission regions are more compact. If we statistically model the distribution of microlensing magnifications, we obtain estimates for the broad <span class="hlt">line</span> region size of r{sub s} = 24{sup +22} {sub -15} and r{sub s}more » = 55{sup +150} {sub -35} lt-day (90% confidence) for the high and low ionization <span class="hlt">lines</span>, respectively. When the samples are divided into higher and lower luminosity quasars, we find that the <span class="hlt">line</span> emission regions of more luminous quasars are larger, with a slope consistent with the expected scaling from photoionization models. Our estimates also agree well with the results from local reveberation mapping studies.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=Sex+AND+gender&id=EJ1044292','ERIC'); return false;" href="https://eric.ed.gov/?q=Sex+AND+gender&id=EJ1044292"><span>Exploring Contemporary Issues in Genetics & Society: Karyotyping, <span class="hlt">Biological</span> Sex, & Gender</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Brown, Julie C.</p> <p>2013-01-01</p> <p>In this two-part activity, high school <span class="hlt">biology</span> students examine human karyotyping, sex-chromosome-linked disorders, and the relationship between <span class="hlt">biological</span> sex and gender. Through interactive simulations and a structured discussion lab, students <span class="hlt">create</span> a human karyotype and diagnose chromosomal disorders in hypothetical patients, as well as…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2998071','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2998071"><span>Microfluidic tools for cell <span class="hlt">biological</span> research</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Velve-Casquillas, Guilhem; Le Berre, Maël; Piel, Matthieu; Tran, Phong T.</p> <p>2010-01-01</p> <p>Summary Microfluidic technology is <span class="hlt">creating</span> powerful tools for cell biologists to control the complete cellular microenvironment, leading to new questions and new discoveries. We review here the basic concepts and methodologies in designing microfluidic devices, and their diverse cell <span class="hlt">biological</span> applications. PMID:21152269</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16192813','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16192813"><span>Surgeon contribution to hospital bottom <span class="hlt">line</span>: not all are <span class="hlt">created</span> equal.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Resnick, Andrew S; Corrigan, Diane; Mullen, James L; Kaiser, Larry R</p> <p>2005-10-01</p> <p>We hypothesized that surgeon productivity is directly related to hospital operating margin, but significant variation in margin contribution exists between specialties. As the independent practitioner becomes an endangered species, it is critical to better understand the surgeon's importance to a hospital's bottom <span class="hlt">line</span>. An appreciation of surgeon contribution to hospital profitability may prove useful in negotiations relating to full-time employment or other models. Surgeon total relative value units (RVUs), a measure of productivity, were collected from operating room (OR) logs. Annual hospital margin per specialty was provided by hospital finance. Hospital margin data were normalized by dividing by a constant such that the highest relative hospital margin (RHM) in fiscal year 2004 expressed as margin units (mu) was 1 million mu. For each specialty, data analyzed included RHM/OR HR, RHM/case, and RHM/RVU. Thoracic (34.55 mu/RVU) and transplant (25.13 mu/RVU) were the biggest contributors to hospital margin. Plastics (-0.57 mu/RVU), maxillofacial (1.41 mu/RVU), and gynecology (1.66 mu/RVU) contributed least to hospital margin. Relative hospital margin per OR HR for transplant slightly exceeded thoracic (275.74 mu vs 233.94 mu) at the top and plastics and maxillofacial contributed the least (-3.83 mu/OR HR vs 9.36 mu/OR HR). Surgeons contribute significantly to hospital margin with certain specialties being more profitable than others. Payer mix, the penetration of managed care, and negotiated contracts as well as a number of other factors all have an impact <span class="hlt">on</span> an individual hospital's margin. Surgeons should be fully cognizant of their significant influence in the marketplace.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25496918','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25496918"><span>Enabling plant synthetic <span class="hlt">biology</span> through genome engineering.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Baltes, Nicholas J; Voytas, Daniel F</p> <p>2015-02-01</p> <p>Synthetic <span class="hlt">biology</span> seeks to <span class="hlt">create</span> new <span class="hlt">biological</span> systems, including user-designed plants and plant cells. These systems can be employed for a variety of purposes, ranging from producing compounds of industrial or therapeutic value, to reducing crop losses by altering cellular responses to pathogens or climate change. To realize the full potential of plant synthetic <span class="hlt">biology</span>, techniques are required that provide control over the genetic code - enabling targeted modifications to DNA sequences within living plant cells. Such control is now within reach owing to recent advances in the use of sequence-specific nucleases to precisely engineer genomes. We discuss here the enormous potential provided by genome engineering for plant synthetic <span class="hlt">biology</span>. Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=salton&id=ED057824','ERIC'); return false;" href="https://eric.ed.gov/?q=salton&id=ED057824"><span><span class="hlt">On-Line</span> Retrieval II.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Kurtz, Peter; And Others</p> <p></p> <p>This report is concerned with the implementation of two interrelated computer systems: an automatic document analysis and classification package, and an <span class="hlt">on-line</span> interactive information retrieval system which utilizes the information gathered during the automatic classification phase. Well-known techniques developed by Salton and Dennis have been…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=bioethics&pg=3&id=EJ904922','ERIC'); return false;" href="https://eric.ed.gov/?q=bioethics&pg=3&id=EJ904922"><span>Professional Development for <span class="hlt">Biology</span> Teachers in the Knowledge Economy</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Eiser, Simone; Knight, Bruce Allen</p> <p>2008-01-01</p> <p>Increasingly, the general media cover new advancements and research in the field of <span class="hlt">biology</span>. Stem cell research, emerging diseases and bioethics are some of the issues gaining public attention. The rate of increase of these new developments <span class="hlt">creates</span> additional challenges to teachers of <span class="hlt">biology</span> as they try to remain abreast of new information and…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3277621','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3277621"><span>Simbios: an NIH national center for physics-based simulation of <span class="hlt">biological</span> structures</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Delp, Scott L; Ku, Joy P; Pande, Vijay S; Sherman, Michael A</p> <p>2011-01-01</p> <p>Physics-based simulation provides a powerful framework for understanding <span class="hlt">biological</span> form and function. Simulations can be used by biologists to study macromolecular assemblies and by clinicians to design treatments for diseases. Simulations help biomedical researchers understand the physical constraints <span class="hlt">on</span> <span class="hlt">biological</span> systems as they engineer novel drugs, synthetic tissues, medical devices, and surgical interventions. Although individual biomedical investigators make outstanding contributions to physics-based simulation, the field has been fragmented. Applications are typically limited to a single physical scale, and individual investigators usually must <span class="hlt">create</span> their own software. These conditions <span class="hlt">created</span> a major barrier to advancing simulation capabilities. In 2004, we established a National Center for Physics-Based Simulation of <span class="hlt">Biological</span> Structures (Simbios) to help integrate the field and accelerate biomedical research. In 6 years, Simbios has become a vibrant national center, with collaborators in 16 states and eight countries. Simbios focuses <span class="hlt">on</span> problems at both the molecular scale and the organismal level, with a long-term goal of uniting these in accurate multiscale simulations. PMID:22081222</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27481531','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27481531"><span>Phage Therapy in the Era of Synthetic <span class="hlt">Biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Barbu, E Magda; Cady, Kyle C; Hubby, Bolyn</p> <p>2016-10-03</p> <p>For more than a century, bacteriophage (or phage) research has enabled some of the most important discoveries in <span class="hlt">biological</span> sciences and has equipped scientists with many of the molecular <span class="hlt">biology</span> tools that have advanced our understanding of replication, maintenance, and expression of genetic material. Phages have also been recognized and exploited as natural antimicrobial agents and nanovectors for gene therapy, but their potential as therapeutics has not been fully exploited in Western medicine because of challenges such as narrow host range, bacterial resistance, and unique pharmacokinetics. However, increasing concern related to the emergence of bacteria resistant to multiple antibiotics has heightened interest in phage therapy and the development of strategies to overcome hurdles associated with bacteriophage therapeutics. Recent progress in sequencing technologies, DNA manipulation, and synthetic <span class="hlt">biology</span> allowed scientists to refactor the entire bacterial genome of Mycoplasma mycoides, thereby <span class="hlt">creating</span> the first synthetic cell. These new strategies for engineering genomes may have the potential to accelerate the construction of designer phage genomes with superior therapeutic potential. Here, we discuss the use of phage as therapeutics, as well as how synthetic <span class="hlt">biology</span> can <span class="hlt">create</span> bacteriophage with desirable attributes. Copyright © 2016 Cold Spring Harbor Laboratory Press; all rights reserved.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_21 --> <div id="page_22" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="421"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4260604','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4260604"><span>Evolutionary cell <span class="hlt">biology</span>: Two origins, one objective</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Lynch, Michael; Field, Mark C.; Goodson, Holly V.; Malik, Harmit S.; Pereira-Leal, José B.; Roos, David S.; Turkewitz, Aaron P.; Sazer, Shelley</p> <p>2014-01-01</p> <p>All aspects of <span class="hlt">biological</span> diversification ultimately trace to evolutionary modifications at the cellular level. This central role of cells frames the basic questions as to how cells work and how cells come to be the way they are. Although these two <span class="hlt">lines</span> of inquiry lie respectively within the traditional provenance of cell <span class="hlt">biology</span> and evolutionary <span class="hlt">biology</span>, a comprehensive synthesis of evolutionary and cell-<span class="hlt">biological</span> thinking is lacking. We define evolutionary cell <span class="hlt">biology</span> as the fusion of these two eponymous fields with the theoretical and quantitative branches of biochemistry, biophysics, and population genetics. The key goals are to develop a mechanistic understanding of general evolutionary processes, while specifically infusing cell <span class="hlt">biology</span> with an evolutionary perspective. The full development of this interdisciplinary field has the potential to solve numerous problems in diverse areas of <span class="hlt">biology</span>, including the degree to which selection, effectively neutral processes, historical contingencies, and/or constraints at the chemical and biophysical levels dictate patterns of variation for intracellular features. These problems can now be examined at both the within- and among-species levels, with single-cell methodologies even allowing quantification of variation within genotypes. Some results from this emerging field have already had a substantial impact <span class="hlt">on</span> cell <span class="hlt">biology</span>, and future findings will significantly influence applications in agriculture, medicine, environmental science, and synthetic <span class="hlt">biology</span>. PMID:25404324</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20396881','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20396881"><span>Synthetic <span class="hlt">biology</span> approaches in drug discovery and pharmaceutical biotechnology.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Neumann, Heinz; Neumann-Staubitz, Petra</p> <p>2010-06-01</p> <p>Synthetic <span class="hlt">biology</span> is the attempt to apply the concepts of engineering to <span class="hlt">biological</span> systems with the aim to <span class="hlt">create</span> organisms with new emergent properties. These organisms might have desirable novel biosynthetic capabilities, act as biosensors or help us to understand the intricacies of living systems. This approach has the potential to assist the discovery and production of pharmaceutical compounds at various stages. New sources of bioactive compounds can be <span class="hlt">created</span> in the form of genetically encoded small molecule libraries. The recombination of individual parts has been employed to design proteins that act as biosensors, which could be used to identify and quantify molecules of interest. New biosynthetic pathways may be designed by stitching together enzymes with desired activities, and genetic code expansion can be used to introduce new functionalities into peptides and proteins to increase their chemical scope and <span class="hlt">biological</span> stability. This review aims to give an insight into recently developed individual components and modules that might serve as parts in a synthetic <span class="hlt">biology</span> approach to pharmaceutical biotechnology.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4651430','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4651430"><span>The effect of family therapy <span class="hlt">on</span> the changes in the severity of <span class="hlt">on-line</span> game play and brain activity in adolescents with <span class="hlt">on-line</span> game addiction</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Han, Doug Hyun; Kim, Sun Mi; Lee, Young Sik; Renshaw, Perry F.</p> <p>2015-01-01</p> <p>We evaluated whether a brief 3-week family therapy intervention would change patterns of brain activation in response to affection and gaming cues in adolescents from dysfunctional families who met criteria for <span class="hlt">on-line</span> game addiction. Fifteen adolescents with <span class="hlt">on-line</span> game addiction and fifteen adolescents without problematic <span class="hlt">on-line</span> game play and an intact family structure were recruited. Over 3 weeks, families were asked to carry out homework assignments focused <span class="hlt">on</span> increasing family cohesion for more than 1 hour/day and 4 days/week. Before therapy, adolescents with <span class="hlt">on-line</span> game addiction demonstrated decreased activity as measured by functional magnetic resonance imaging (fMRI) within the caudate, middle temporal gyrus, and occipital lobe in response to images depicting parental affection and increased activity of the middle frontal and inferior parietal in response scenes from <span class="hlt">on-line</span> games, relative to healthy comparison subjects. Improvement in perceived family cohesion following 3 weeks of treatment was associated with an increase in the activity of the caudate nucleus in response to affection stimuli and was inversely correlated with changes in <span class="hlt">on-line</span> game playing time. With evidence of brain activation changes in response to <span class="hlt">on-line</span> game playing cues and images depicting parental love, the present findings suggest that family cohesion may be an important factor in the treatment of problematic <span class="hlt">on-line</span> game playing. PMID:22698763</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28370171','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28370171"><span>A review <span class="hlt">on</span> acridinylthioureas and its derivatives: <span class="hlt">biological</span> and cytotoxic activity.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kožurková, Mária; Sabolová, Danica; Kristian, Pavol</p> <p>2017-10-01</p> <p>Acridines possess two characteristics that have led many researchers to consider the agents interesting targets for future development as potential farmacophores: the planar acridine skeleton, which is able to intercalate into DNA, and the intense fluorescence of the agents. This review offers a study of the multifunctional character of acridines and the synthesis of novel acridine derivatives, with particular focus being placed <span class="hlt">on</span> isothiocyanates and their congeners, e.g. thioureas, isothioureas, quaternary ammonium salts and platinum/gold conjugates. The review provides an overview of the structure, spectral properties, DNA binding and <span class="hlt">biological</span> activity of acridinylthiourea congeners. These acridinylthiourea derivatives display significant cytotoxic activities against different types of cancer cell <span class="hlt">lines</span> at micromolar concentrations. Copyright © 2017 John Wiley & Sons, Ltd. Copyright © 2017 John Wiley & Sons, Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.nsrl.ttu.edu/publications/specpubs','USGSPUBS'); return false;" href="http://www.nsrl.ttu.edu/publications/specpubs"><span>United States <span class="hlt">Biological</span> Survey: A compendium of its history, personalities, impacts, and conflicts</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Schmidly, David J.; Tydeman, W. E.; Gardner, Alfred L.</p> <p>2016-01-01</p> <p>In 1885, a small three-person unit was <span class="hlt">created</span> in the U.S. Department of Agriculture to gather and analyze information <span class="hlt">on</span> bird migrations. Originally called the Section of Economic Ornithology, over the next 55 years this unit underwent three name changes and accumulated ever-increasing responsibilities for the nation’s faunal resources. Transferred to the Department of the Interior in 1939, this agency was merged with the Bureau of Fisheries in 1940 to <span class="hlt">create</span> the U.S. Fish and Wildlife Service (FWS). The following account details the chronology, directorship, and growth of the U.S. Bureau of <span class="hlt">Biological</span> Survey up to its renovation as the FWS. This account also profiles some employees of the <span class="hlt">Biological</span> Survey.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1169062','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/1169062"><span>Methods for isolation and viability assessment of <span class="hlt">biological</span> organisms</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Letant, Sonia Edith; Baker, Sarah Elyse; Bond, Tiziana; Chang, Allan Shih-Ping</p> <p>2015-02-03</p> <p>Isolation of <span class="hlt">biological</span> or chemical organisms can be accomplished using a surface enhanced Raman scattering (SERS) system. The SERS system can be a single or a stacked plurality of photonic crystal membranes with noble-metal <span class="hlt">lined</span> through pores for flowing analyte potentially containing the <span class="hlt">biological</span> or chemical organisms. The through pores can be adapted to trap individual <span class="hlt">biological</span> or chemical organisms and emit SERS spectra, which can then be detected by a detector and further analyzed for viability of the <span class="hlt">biological</span> or chemical organism.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EurSS..49..831R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EurSS..49..831R"><span>The informativeness of coefficients a and b of the soil <span class="hlt">line</span> for the analysis of remote sensing materials</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rukhovich, D. I.; Rukhovich, A. D.; Rukhovich, D. D.; Simakova, M. S.; Kulyanitsa, A. L.; Bryzzhev, A. V.; Koroleva, P. V.</p> <p>2016-08-01</p> <p>The coefficients of the soil <span class="hlt">line</span> are often taken into account in calculations of vegetation indices. These coefficients are usually calculated for the entire satellite image, or are taken as constants without any calculations. In both cases, the informativeness of these coefficients is low and insufficient for the needs of soil mapping. In our study, we calculated soil <span class="hlt">line</span> coefficients at 8000 lattice points for the territory of Plavsk, Arsen'evsk, and Chern districts of Tula oblast <span class="hlt">on</span> the basis of 34 Landsat 5, 7, and 8 images obtained in 1985-2014. In order to distinguish between the soil <span class="hlt">line</span> calculated for a given image and the soil <span class="hlt">line</span> calculated for lattice points <span class="hlt">on</span> the basis of dozens of multitemporal images, we suggest that the latter can be referred to as the temporal soil <span class="hlt">line</span>. The temporal soil <span class="hlt">line</span> is described by a classical equation: NIR = RED a + b, where a is its slope relative to the horizontal axis (RED), and b is the Y-axis (NIR) intercept. Both coefficients were used to <span class="hlt">create</span> soil maps. The verification of the maps was performed with the use of data <span class="hlt">on</span> 1985 soil pits. The informativeness of these coefficients appeared to be sufficient for delineation of eight groups of soils of different taxonomic levels: soddy moderately podzolic soils, soddy slightly podzolic soils, soddy-podzolic soils, light gray forest soils, gray forest soils, dark gray forest soils, podzolized chernozems, and leached chernozems. The b coefficient proved to be more informative, as it allowed us to <span class="hlt">create</span> the soil map precisely <span class="hlt">on</span> its basis. In order to <span class="hlt">create</span> the soil map <span class="hlt">on</span> the basis of the a coefficient, we had to apply some threshold values of the b coefficient. The bare soil <span class="hlt">on</span> each of Landsat scenes was separated with the help of the mask of agricultural fields and the notion of the spectral neighborhood of soil <span class="hlt">line</span> (SNSL).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28483428','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28483428"><span>Toxicity of silver nanoparticles in <span class="hlt">biological</span> systems: Does the complexity of <span class="hlt">biological</span> systems matter?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Vazquez-Muñoz, Roberto; Borrego, Belen; Juárez-Moreno, Karla; García-García, Maritza; Mota Morales, Josué D; Bogdanchikova, Nina; Huerta-Saquero, Alejandro</p> <p>2017-07-05</p> <p>Currently, nanomaterials are more frequently in our daily life, specifically in biomedicine, electronics, food, textiles and catalysis just to name a few. Although nanomaterials provide many benefits, recently their toxicity profiles have begun to be explored. In this work, the toxic effects of silver nanoparticles (35nm-average diameter and Polyvinyl-Pyrrolidone-coated) <span class="hlt">on</span> <span class="hlt">biological</span> systems of different levels of complexity was assessed in a comprehensive and comparatively way, through a variety of viability and toxicological assays. The studied organisms included viruses, bacteria, microalgae, fungi, animal and human cells (including cancer cell <span class="hlt">lines</span>). It was found that <span class="hlt">biological</span> systems of different taxonomical groups are inhibited at concentrations of silver nanoparticles within the same order of magnitude. Thus, the toxicity of nanomaterials <span class="hlt">on</span> <span class="hlt">biological</span>/living systems, constrained by their complexity, e.g. taxonomic groups, resulted contrary to the expected. The fact that cells and virus are inhibited with a concentration of silver nanoparticles within the same order of magnitude could be explained considering that silver nanoparticles affects very primitive cellular mechanisms by interacting with fundamental structures for cells and virus alike. Copyright © 2017 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=Egan&pg=4&id=EJ496855','ERIC'); return false;" href="https://eric.ed.gov/?q=Egan&pg=4&id=EJ496855"><span><span class="hlt">On</span> <span class="hlt">Line</span> in New York.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Egan, David</p> <p>1994-01-01</p> <p>The International Education and Resource Network (I*EARN) <span class="hlt">creates</span> an international classroom in which students work together <span class="hlt">on</span> global education projects and literary and current events publications. Teacher David Egan describes some of the many activities available to students <span class="hlt">on</span> the network. (LZ/Author)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/12833272','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/12833272"><span><span class="hlt">Creating</span> a histology-embryology free digital image database using high-end microscopy and computer techniques for <span class="hlt">on-line</span> biomedical education.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Silva-Lopes, Victor W; Monteiro-Leal, Luiz H</p> <p>2003-07-01</p> <p>The development of new technology and the possibility of fast information delivery by either Internet or Intranet connections are changing education. Microanatomy education depends basically <span class="hlt">on</span> the correct interpretation of microscopy images by students. Modern microscopes coupled to computers enable the presentation of these images in a digital form by <span class="hlt">creating</span> image databases. However, the access to this new technology is restricted entirely to those living in cities and towns with an Information Technology (IT) infrastructure. This study describes the creation of a free Internet histology database composed by high-quality images and also presents an inexpensive way to supply it to a greater number of students through Internet/Intranet connections. By using state-of-the-art scientific instruments, we developed a Web page (http://www2.uerj.br/~micron/atlas/atlasenglish/index.htm) that, in association with a multimedia microscopy laboratory, intends to help in the reduction of the IT educational gap between developed and underdeveloped regions. Copyright 2003 Wiley-Liss, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23012581','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23012581"><span>Perspectives <span class="hlt">on</span> an education in computational <span class="hlt">biology</span> and medicine.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rubinstein, Jill C</p> <p>2012-09-01</p> <p>The mainstream application of massively parallel, high-throughput assays in biomedical research has <span class="hlt">created</span> a demand for scientists educated in Computational <span class="hlt">Biology</span> and Bioinformatics (CBB). In response, formalized graduate programs have rapidly evolved over the past decade. Concurrently, there is increasing need for clinicians trained to oversee the responsible translation of CBB research into clinical tools. Physician-scientists with dedicated CBB training can facilitate such translation, positioning themselves at the intersection between computational biomedical research and medicine. This perspective explores key elements of the educational path to such a position, specifically addressing: 1) evolving perceptions of the role of the computational biologist and the impact <span class="hlt">on</span> training and career opportunities; 2) challenges in and strategies for obtaining the core skill set required of a biomedical researcher in a computational world; and 3) how the combination of CBB with medical training provides a logical foundation for a career in academic medicine and/or biomedical research.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017E%26ES...82a2085C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017E%26ES...82a2085C"><span>Feasibility analysis of marine ecological <span class="hlt">on-line</span> integrated monitoring system</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chu, D. Z.; Cao, X.; Zhang, S. W.; Wu, N.; Ma, R.; Zhang, L.; Cao, L.</p> <p>2017-08-01</p> <p>The in-situ water quality sensors were susceptible to <span class="hlt">biological</span> attachment. Moreover, sea water corrosion and wave impact damage, and many sensors scattered distribution would cause maintenance inconvenience. The paper proposed a highly integrated marine ecological <span class="hlt">on-line</span> integrated monitoring system, which can be used inside monitoring station. All sensors were reasonably classified, the similar in series, the overall in parallel. The system composition and workflow were described. In addition, the paper proposed attention issues of the system design and corresponding solutions. Water quality multi-parameters and 5 nutrient salts as the verification index, in-situ and systematic data comparison experiment were carried out. The results showed that the data consistency of nutrient salt, PH and salinity was better. Temperature and dissolved oxygen data trend was consistent, but the data had deviation. Turbidity fluctuated greatly; the chlorophyll trend was similar with it. Aiming at the above phenomena, three points system optimization direction were proposed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23998575','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23998575"><span>[Effect of DOT1L gene silence <span class="hlt">on</span> proliferation of acute monocytic leukemia cell <span class="hlt">line</span> THP-1].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Yu-Juan; Li, Hua-Wen; Chang, Guo-Qiang; Zhang, Hong-Ju; Wang, Jian; Lin, Ya-Ni; Zhou, Jia-Xi; Li, Qing-Hua; Pang, Tian-Xiang</p> <p>2013-08-01</p> <p>This study was aimed to investigate the influence of short hairpin RNA (shRNA) <span class="hlt">on</span> proliferation of human leukemia cell <span class="hlt">line</span> THP-1. The shRNA targeting the site 732-752 of DOT1L mRNA was designed and chemically synthesized, then a single-vector lentiviral, tet-inducible shRNA-DOT1L system (Plko-Tet-<span class="hlt">On</span>) was generated. Thereafter, the THP-1 cells with lentivirus were infected to <span class="hlt">create</span> stable cell <span class="hlt">line</span> with regulatable shRNA expression. The expression of DOT1L in the THP-1 cell <span class="hlt">line</span> was assayed by RT-PCR. Effect of shRNA-DOT1L <span class="hlt">on</span> the proliferation of THP-1 cells was detected with MTT method,and the change of colony forming potential of THP-1 cells was analyzed by colony forming unit test. Cell cycle distribution was tested by flow cytometry. The results indicated that the expression of DOT1L was statistically lower than that in the control groups. The proliferation and colony forming capacity of THP-1 cells were significantly inhibited. The percentage of cells at G0/G1 phase increased in THP-1/shRNA cells treated with Dox while the percentage of cells at S phase significantly decreased as compared with that in the control group. It is concluded that the shRNA targeting DOT1L can effectively inhibit the proliferation of acute monocytic leukemia cell <span class="hlt">line</span> THP-1.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26896791','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26896791"><span>Effects of imputation <span class="hlt">on</span> correlation: implications for analysis of mass spectrometry data from multiple <span class="hlt">biological</span> matrices.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Taylor, Sandra L; Ruhaak, L Renee; Kelly, Karen; Weiss, Robert H; Kim, Kyoungmi</p> <p>2017-03-01</p> <p>With expanded access to, and decreased costs of, mass spectrometry, investigators are collecting and analyzing multiple <span class="hlt">biological</span> matrices from the same subject such as serum, plasma, tissue and urine to enhance biomarker discoveries, understanding of disease processes and identification of therapeutic targets. Commonly, each <span class="hlt">biological</span> matrix is analyzed separately, but multivariate methods such as MANOVAs that combine information from multiple <span class="hlt">biological</span> matrices are potentially more powerful. However, mass spectrometric data typically contain large amounts of missing values, and imputation is often used to <span class="hlt">create</span> complete data sets for analysis. The effects of imputation <span class="hlt">on</span> multiple <span class="hlt">biological</span> matrix analyses have not been studied. We investigated the effects of seven imputation methods (half minimum substitution, mean substitution, k-nearest neighbors, local least squares regression, Bayesian principal components analysis, singular value decomposition and random forest), <span class="hlt">on</span> the within-subject correlation of compounds between <span class="hlt">biological</span> matrices and its consequences <span class="hlt">on</span> MANOVA results. Through analysis of three real omics data sets and simulation studies, we found the amount of missing data and imputation method to substantially change the between-matrix correlation structure. The magnitude of the correlations was generally reduced in imputed data sets, and this effect increased with the amount of missing data. Significant results from MANOVA testing also were substantially affected. In particular, the number of false positives increased with the level of missing data for all imputation methods. No one imputation method was universally the best, but the simple substitution methods (Half Minimum and Mean) consistently performed poorly. © The Author 2016. Published by Oxford University Press. For Permissions, please email: journals.permissions@oup.com.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005SPIE.5954...48A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005SPIE.5954...48A"><span>Testing <span class="hlt">biological</span> liquid samples using modified m-<span class="hlt">line</span> spectroscopy method</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Augusciuk, Elzbieta; Rybiński, Grzegorz</p> <p>2005-09-01</p> <p>Non-chemical method of detection of sugar concentration in <span class="hlt">biological</span> (animal and plant source) liquids has been investigated. Simplified set was build to show the easy way of carrying out the survey and to make easy to gather multiple measurements for error detecting and statistics. Method is suggested as easy and cheap alternative for chemical methods of measuring sugar concentration, but needing a lot effort to be made precise.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009OptLE..47..320R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009OptLE..47..320R"><span><span class="hlt">On-line</span> dimensional measurement of small components <span class="hlt">on</span> the eyeglasses assembly <span class="hlt">line</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rosati, G.; Boschetti, G.; Biondi, A.; Rossi, A.</p> <p>2009-03-01</p> <p>Dimensional measurement of the subassemblies at the beginning of the assembly <span class="hlt">line</span> is a very crucial process for the eyeglasses industry, since even small manufacturing errors of the components can lead to very visible defects <span class="hlt">on</span> the final product. For this reason, all subcomponents of the eyeglass are verified before beginning the assembly process either with a 100% inspection or <span class="hlt">on</span> a statistical basis. Inspection is usually performed by human operators, with high costs and a degree of repeatability which is not always satisfactory. This paper presents a novel <span class="hlt">on-line</span> measuring system for dimensional verification of small metallic subassemblies for the eyeglasses industry. The machine vision system proposed, which was designed to be used at the beginning of the assembly <span class="hlt">line</span>, could also be employed in the Statistical Process Control (SPC) by the manufacturer of the subassemblies. The automated system proposed is based <span class="hlt">on</span> artificial vision, and exploits two CCD cameras and an anthropomorphic robot to inspect and manipulate the subcomponents of the eyeglass. Each component is recognized by the first camera in a quite large workspace, picked up by the robot and placed in the small vision field of the second camera which performs the measurement process. Finally, the part is palletized by the robot. The system can be easily taught by the operator by simply placing the template object in the vision field of the measurement camera (for dimensional data acquisition) and hence by instructing the robot via the Teaching Control Pendant within the vision field of the first camera (for pick-up transformation acquisition). The major problem we dealt with is that the shape and dimensions of the subassemblies can vary in a quite wide range, but different positioning of the same component can look very similar one to another. For this reason, a specific shape recognition procedure was developed. In the paper, the whole system is presented together with first experimental lab</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17179744','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17179744"><span>RNA interference: from <span class="hlt">biology</span> to drugs and therapeutics.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Appasani, Krishnarao</p> <p>2004-07-01</p> <p>RNA interference (RNAi) is a newly discovered and popular technology platform among researchers not only in the fields of RNA <span class="hlt">biology</span> and molecular cell <span class="hlt">biology</span>. It has <span class="hlt">created</span> excitement in clinical sciences such as oncology, neurology, endocrinology, infectious diseases and drug discovery. There is an urgent need to educate and connect academic and industry researchers for the purpose of knowledge transfer. Thus, GeneExpression Systems of Waltham organized its Second International Conference in Waltham City (May 2-4, 2004, MA, USA) <span class="hlt">on</span> the theme of 'RNA interference: From <span class="hlt">Biology</span> to Drugs & Therapeutics.' About 200 participants and 32 speakers attended this two and half-day event which was arranged in six scientific and three technology sessions and ended with a panel discussion. This report covers a few representative talks from academia, biotech and the drug industry.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1989SPIE.1008..215L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1989SPIE.1008..215L"><span><span class="hlt">On-Line</span> Allocation Of Robot Resources To Task Plans</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lyons, Damian M.</p> <p>1989-02-01</p> <p>In this paper, I present an approach to representing plans that make <span class="hlt">on-line</span> decisions about resource allocation. An <span class="hlt">on-line</span> decision is the evaluation of a conditional expression involving sensory information as the plan is being executed. I use a plan representation called 7ZS10'1 1,12that has been especially designed for the domain of robot programming, and in particular, for the problem of <span class="hlt">on-line</span> decisions. The resource allocation example is based <span class="hlt">on</span> the robot assembly cell architecture outlined by Venkataraman and Lyons16. I begin by setting forth a definition of <span class="hlt">on-line</span> decision making and some arguments as to why this form of decision making is important and useful. To set the context for the resource allocation example, I take some care in categorizing the types of <span class="hlt">on-line</span> decision making and the approaches adopted by other workers so far. In particular, I justify a plan-based approach to the study of <span class="hlt">on-line</span> decision making. From that, the focus shifts to one type of decision making: <span class="hlt">on-line</span> allocation of robot resources to task plans. Robot resources are the physical manipulators (grippers, wrists, arms, feeders, etc) that are available to carry out the task. I formulate the assembly cell architecture of Venkataraman and Lyons16 as an R.S plan schema, and show how the <span class="hlt">on-line</span> allocation specified in that architecture can be implemented. Finally, I show how considering the <span class="hlt">on-line</span> allocation of logical resources, that is a physical resource plus some model information, can be used as a non-traditional approach to some problems in robot task planning.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21290362','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21290362"><span><span class="hlt">On-line</span> capacity-building program <span class="hlt">on</span> "analysis of data" for medical educators in the South Asia region: a qualitative exploration of our experience.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Dongre, A R; Chacko, T V; Banu, S; Bhandary, S; Sahasrabudhe, R A; Philip, S; Deshmukh, P R</p> <p>2010-11-01</p> <p>In medical education, using the World Wide Web is a new approach for building the capacity of faculty. However, there is little information available <span class="hlt">on</span> medical education researchers' needs and their collective learning outcomes in such <span class="hlt">on-line</span> environments. Hence, the present study attempted: 1)to identify needs for capacity-building of fellows in a faculty development program <span class="hlt">on</span> the topic of data analysis; and 2) to describe, analyze and understand the collective learning outcomes of the fellows during this need-based <span class="hlt">on-line</span> session. The present research is based <span class="hlt">on</span> quantitative (<span class="hlt">on-line</span> survey for needs assessment) and qualitative (contents of e-mails exchanged in listserv discussion) data which were generated during the October 2009 Mentoring and Learning (M-L) Web discussion <span class="hlt">on</span> the topic of data analysis. The data sources were shared e-mail responses during the process of planning and executing the M-L Web discussion. Content analysis was undertaken and the categories of discussion were presented as a simple non-hierarchical typology which represents the collective learning of the project fellows. We identified the types of learning needs <span class="hlt">on</span> the topic 'Analysis of Data' to be addressed for faculty development in the field of education research. This need-based M-L Web discussion could then facilitate collective learning <span class="hlt">on</span> such topics as 'basic concepts in statistics', tests of significance, Likert scale analysis, bivariate correlation, and simple regression analysis and content analysis of qualitative data. Steps like identifying the learning needs for an <span class="hlt">on-line</span> M-L Web discussion, addressing the immediate needs of learners and <span class="hlt">creating</span> a flexible reflective learning environment <span class="hlt">on</span> the M-L Web facilitated the collective learning of the fellows <span class="hlt">on</span> the topic of data analysis. Our outcomes can be useful in the design of <span class="hlt">on-line</span> pedagogical strategies for supporting research in medical education.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20050157095&hterms=ALS&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3DALS','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20050157095&hterms=ALS&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3DALS"><span>Development Status of the Advanced Life Support <span class="hlt">On-Line</span> Project Information System</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Levri, Julie A.; Hogan, John A.; Cavazzoni, Jim; Brodbeck, Christina; Morrow, Rich; Ho, Michael; Kaehms, Bob; Whitaker, Dawn R.</p> <p>2005-01-01</p> <p>The Advanced Life Support Program has recently accelerated an effort to develop an <span class="hlt">On-line</span> Project Information System (OPIS) for research project and technology development data centralization and sharing. The core functionality of OPIS will launch in October of 2005. This paper presents the current OPIS development status. OPIS core functionality involves a Web-based annual solicitation of project and technology data directly from ALS Principal Investigators (PIS) through customized data collection forms. Data provided by PIs will be reviewed by a Technical Task Monitor (TTM) before posting the information to OPIS for ALS Community viewing via the Web. The data will be stored in an object-oriented relational database (<span class="hlt">created</span> in MySQL(R)) located <span class="hlt">on</span> a secure server at NASA ARC. Upon launch, OPIS can be utilized by Managers to identify research and technology development gaps and to assess task performance. Analysts can employ OPIS to obtain.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_22 --> <div id="page_23" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="441"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26524089','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26524089"><span>Industrial systems <span class="hlt">biology</span> and its impact <span class="hlt">on</span> synthetic <span class="hlt">biology</span> of yeast cell factories.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fletcher, Eugene; Krivoruchko, Anastasia; Nielsen, Jens</p> <p>2016-06-01</p> <p>Engineering industrial cell factories to effectively yield a desired product while dealing with industrially relevant stresses is usually the most challenging step in the development of industrial production of chemicals using microbial fermentation processes. Using synthetic <span class="hlt">biology</span> tools, microbial cell factories such as Saccharomyces cerevisiae can be engineered to express synthetic pathways for the production of fuels, biopharmaceuticals, fragrances, and food flavors. However, directing fluxes through these synthetic pathways towards the desired product can be demanding due to complex regulation or poor gene expression. Systems <span class="hlt">biology</span>, which applies computational tools and mathematical modeling to understand complex <span class="hlt">biological</span> networks, can be used to guide synthetic <span class="hlt">biology</span> design. Here, we present our perspective <span class="hlt">on</span> how systems <span class="hlt">biology</span> can impact synthetic <span class="hlt">biology</span> towards the goal of developing improved yeast cell factories. Biotechnol. Bioeng. 2016;113: 1164-1170. © 2015 Wiley Periodicals, Inc. © 2015 Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22698763','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22698763"><span>The effect of family therapy <span class="hlt">on</span> the changes in the severity of <span class="hlt">on-line</span> game play and brain activity in adolescents with <span class="hlt">on-line</span> game addiction.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Han, Doug Hyun; Kim, Sun Mi; Lee, Young Sik; Renshaw, Perry F</p> <p>2012-05-31</p> <p>We evaluated whether a brief 3-week family therapy intervention would change patterns of brain activation in response to affection and gaming cues in adolescents from dysfunctional families who met criteria for <span class="hlt">on-line</span> game addiction. Fifteen adolescents with <span class="hlt">on-line</span> game addiction and fifteen adolescents without problematic <span class="hlt">on-line</span> game play and an intact family structure were recruited. Over 3 weeks, families were asked to carry out homework assignments focused <span class="hlt">on</span> increasing family cohesion for more than 1 hour/day and 4 days/week. Before therapy, adolescents with <span class="hlt">on-line</span> game addiction demonstrated decreased activity as measured by functional magnetic resonance imaging (fMRI) within the caudate, middle temporal gyrus, and occipital lobe in response to images depicting parental affection and increased activity of the middle frontal and inferior parietal in response scenes from <span class="hlt">on-line</span> games, relative to healthy comparison subjects. Improvement in perceived family cohesion following 3 weeks of treatment was associated with an increase in the activity of the caudate nucleus in response to affection stimuli and was inversely correlated with changes in <span class="hlt">on-line</span> game playing time. With evidence of brain activation changes in response to <span class="hlt">on-line</span> game playing cues and images depicting parental love, the present findings suggest that family cohesion may be an important factor in the treatment of problematic <span class="hlt">on-line</span> game playing. Crown Copyright © 2012. Published by Elsevier Ireland Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NIMPB.411...17G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NIMPB.411...17G"><span>Review of Canadian Light Source facilities for <span class="hlt">biological</span> applications</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Grochulski, Pawel; Fodje, Michel; Labiuk, Shaun; Wysokinski, Tomasz W.; Belev, George; Korbas, Malgorzata; Rosendahl, Scott M.</p> <p>2017-11-01</p> <p>The newly-<span class="hlt">created</span> <span class="hlt">Biological</span> and Life Sciences Department at the Canadian Light Source (CLS) encompasses four sets of beamlines devoted to <span class="hlt">biological</span> studies ranging in scope from the atomic scale to cells, tissues and whole organisms. The Canadian Macromolecular Crystallography Facility (CMCF) consists of two beamlines devoted primarily to crystallographic studies of proteins and other macromolecules. The Mid-Infrared Spectromicroscopy (Mid-IR) beamline focusses <span class="hlt">on</span> using infrared energy to obtain biochemical, structural and dynamical information about <span class="hlt">biological</span> systems. The Bio-Medical Imaging and Therapy (BMIT) facility consists of two beamlines devoted to advanced imaging and X-ray therapy techniques. The <span class="hlt">Biological</span> X-ray Absorption Spectroscopy (BioXAS) facility is being commissioned and houses three beamlines devoted to X-ray absorption spectroscopy and multi-mode X-ray fluorescence imaging. Together, these beamlines provide CLS Users with a powerful array of techniques to study today's most pressing <span class="hlt">biological</span> questions. We describe these beamlines along with their current powerful features and envisioned future capabilities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19820005251','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19820005251"><span>Issues related to <span class="hlt">line</span>-oriented flight training</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Lauber, J. K.</p> <p>1981-01-01</p> <p>The use of a training simulator along with carefully structured, detailed, <span class="hlt">line</span> trip scenarios was envisioned by NASA as a means of providing a controllable, repeatable way to observe <span class="hlt">line</span> crews in a highly realistic simulation of their working environment and obtain better understanding operationally significant human factors problems and issues. Relevant research done by the agency and the results of full-mission simulation scenarios revealed potential implications for flight training. Aspects to be considered in <span class="hlt">creating</span> training programs closely related to the actual <span class="hlt">line</span> environment with a total crew application in real world incident experiences include: (1) operational, environmental, equipment, and crew problems in scenario design; (2) real time <span class="hlt">line</span> oriented flight training operation; (3) performance assessment and debriefing; (4) instructor qualification and training; and (5) other issues such as ub un initial, transition, and upgrade training; procedures developent and evaluation, and equipment evaluation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4413675','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4413675"><span>A reconfigurable <span class="hlt">on-line</span> learning spiking neuromorphic processor comprising 256 neurons and 128K synapses</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Qiao, Ning; Mostafa, Hesham; Corradi, Federico; Osswald, Marc; Stefanini, Fabio; Sumislawska, Dora; Indiveri, Giacomo</p> <p>2015-01-01</p> <p>Implementing compact, low-power artificial neural processing systems with real-time <span class="hlt">on-line</span> learning abilities is still an open challenge. In this paper we present a full-custom mixed-signal VLSI device with neuromorphic learning circuits that emulate the biophysics of real spiking neurons and dynamic synapses for exploring the properties of computational neuroscience models and for building brain-inspired computing systems. The proposed architecture allows the <span class="hlt">on</span>-chip configuration of a wide range of network connectivities, including recurrent and deep networks, with short-term and long-term plasticity. The device comprises 128 K analog synapse and 256 neuron circuits with <span class="hlt">biologically</span> plausible dynamics and bi-stable spike-based plasticity mechanisms that endow it with <span class="hlt">on-line</span> learning abilities. In addition to the analog circuits, the device comprises also asynchronous digital logic circuits for setting different synapse and neuron properties as well as different network configurations. This prototype device, fabricated using a 180 nm 1P6M CMOS process, occupies an area of 51.4 mm2, and consumes approximately 4 mW for typical experiments, for example involving attractor networks. Here we describe the details of the overall architecture and of the individual circuits and present experimental results that showcase its potential. By supporting a wide range of cortical-like computational modules comprising plasticity mechanisms, this device will enable the realization of intelligent autonomous systems with <span class="hlt">on-line</span> learning capabilities. PMID:25972778</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25972778','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25972778"><span>A reconfigurable <span class="hlt">on-line</span> learning spiking neuromorphic processor comprising 256 neurons and 128K synapses.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Qiao, Ning; Mostafa, Hesham; Corradi, Federico; Osswald, Marc; Stefanini, Fabio; Sumislawska, Dora; Indiveri, Giacomo</p> <p>2015-01-01</p> <p>Implementing compact, low-power artificial neural processing systems with real-time <span class="hlt">on-line</span> learning abilities is still an open challenge. In this paper we present a full-custom mixed-signal VLSI device with neuromorphic learning circuits that emulate the biophysics of real spiking neurons and dynamic synapses for exploring the properties of computational neuroscience models and for building brain-inspired computing systems. The proposed architecture allows the <span class="hlt">on</span>-chip configuration of a wide range of network connectivities, including recurrent and deep networks, with short-term and long-term plasticity. The device comprises 128 K analog synapse and 256 neuron circuits with <span class="hlt">biologically</span> plausible dynamics and bi-stable spike-based plasticity mechanisms that endow it with <span class="hlt">on-line</span> learning abilities. In addition to the analog circuits, the device comprises also asynchronous digital logic circuits for setting different synapse and neuron properties as well as different network configurations. This prototype device, fabricated using a 180 nm 1P6M CMOS process, occupies an area of 51.4 mm(2), and consumes approximately 4 mW for typical experiments, for example involving attractor networks. Here we describe the details of the overall architecture and of the individual circuits and present experimental results that showcase its potential. By supporting a wide range of cortical-like computational modules comprising plasticity mechanisms, this device will enable the realization of intelligent autonomous systems with <span class="hlt">on-line</span> learning capabilities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2014-title9-vol1/pdf/CFR-2014-title9-vol1-sec113-53.pdf','CFR2014'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2014-title9-vol1/pdf/CFR-2014-title9-vol1-sec113-53.pdf"><span>9 CFR 113.53 - Requirements for ingredients of animal origin used for production of <span class="hlt">biologics</span>.</span></a></p> <p><a target="_blank" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2014&page.go=Go">Code of Federal Regulations, 2014 CFR</a></p> <p></p> <p>2014-01-01</p> <p>... (African green monkey kidney) cell <span class="hlt">line</span> and of primary cells or a cell <span class="hlt">line</span> of the same species of origin... origin used for production of <span class="hlt">biologics</span>. 113.53 Section 113.53 Animals and Animal Products ANIMAL AND... ingredients of animal origin used for production of <span class="hlt">biologics</span>. Each lot of ingredient of animal origin which...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2013-title9-vol1/pdf/CFR-2013-title9-vol1-sec113-53.pdf','CFR2013'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2013-title9-vol1/pdf/CFR-2013-title9-vol1-sec113-53.pdf"><span>9 CFR 113.53 - Requirements for ingredients of animal origin used for production of <span class="hlt">biologics</span>.</span></a></p> <p><a target="_blank" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2013&page.go=Go">Code of Federal Regulations, 2013 CFR</a></p> <p></p> <p>2013-01-01</p> <p>... (African green monkey kidney) cell <span class="hlt">line</span> and of primary cells or a cell <span class="hlt">line</span> of the same species of origin... origin used for production of <span class="hlt">biologics</span>. 113.53 Section 113.53 Animals and Animal Products ANIMAL AND... ingredients of animal origin used for production of <span class="hlt">biologics</span>. Each lot of ingredient of animal origin which...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.gpo.gov/fdsys/pkg/CFR-2012-title9-vol1/pdf/CFR-2012-title9-vol1-sec113-53.pdf','CFR2012'); return false;" href="https://www.gpo.gov/fdsys/pkg/CFR-2012-title9-vol1/pdf/CFR-2012-title9-vol1-sec113-53.pdf"><span>9 CFR 113.53 - Requirements for ingredients of animal origin used for production of <span class="hlt">biologics</span>.</span></a></p> <p><a target="_blank" href="http://www.gpo.gov/fdsys/browse/collectionCfr.action?selectedYearFrom=2012&page.go=Go">Code of Federal Regulations, 2012 CFR</a></p> <p></p> <p>2012-01-01</p> <p>... (African green monkey kidney) cell <span class="hlt">line</span> and of primary cells or a cell <span class="hlt">line</span> of the same species of origin... origin used for production of <span class="hlt">biologics</span>. 113.53 Section 113.53 Animals and Animal Products ANIMAL AND... ingredients of animal origin used for production of <span class="hlt">biologics</span>. Each lot of ingredient of animal origin which...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/ED050754.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/ED050754.pdf"><span>An Evaluation of <span class="hlt">On-Line</span> Information Retrieval System Techniques.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Wolfe, Theodore</p> <p></p> <p>This report presents a review and evaluation of three remote access <span class="hlt">on-line</span> information retrieval systems and some ideas <span class="hlt">on</span> what the capabilities of an ideal <span class="hlt">on-line</span> information retrieval system should be. The three systems reviewed are the DDC Remote <span class="hlt">On-Line</span> Retrieval System, the National Aeronautics and Space Administration RECON System, and the…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19880008790','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19880008790"><span>NASA Workshop <span class="hlt">on</span> <span class="hlt">Biological</span> Adaptation</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Morey-Holton, Emily (Editor); Tischler, Marc (Editor)</p> <p>1988-01-01</p> <p>A workshop was convened to review the current program in Space <span class="hlt">Biology</span> <span class="hlt">Biological</span> Adaptation Research and its objectives and to identify future research directions. Two research areas emerged from these deliberations: gravitational effects <span class="hlt">on</span> structures and biomineralization and gravity affected regulatory mechanisms. The participants also recommended that research concentrate <span class="hlt">on</span> rapidly growing animals, since gravity effects may be more pronounced during growth and development. Both research areas were defined and future research directions were identified. The recommendations of the workshop will assist the Life Sciences Division of NASA in it assessment and long-range planning of these areas of space <span class="hlt">biology</span>. Equally important, the workshop was intended to stimulate thought and research among those attending so that they would, in turn, interest, excite, and involve other members of the academic community in research efforts relevant to these programs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29575978','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29575978"><span>Decreasing dialysis catheter rates by <span class="hlt">creating</span> a multidisciplinary dialysis access program.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rosenberry, Patricia M; Niederhaus, Silke V; Schweitzer, Eugene J; Leeser, David B</p> <p>2018-03-01</p> <p>Centers for Medicare and Medicaid Services have determined that chronic dialysis units should have <12% of their patients utilizing central venous catheters for hemodialysis treatments. <span class="hlt">On</span> the Eastern Shore of Maryland, the central venous catheter rates in the dialysis units averaged >45%. A multidisciplinary program was established with goals of decreasing catheter rates in order to decrease central <span class="hlt">line</span>-associated bloodstream infections, decrease mortality associated with central <span class="hlt">line</span>-associated bloodstream infection, decrease hospital days, and provide savings to the healthcare system. We collected the catheter rates within three dialysis centers served over a 5-year period. Using published data surrounding the incidence and related costs of central <span class="hlt">line</span>-associated bloodstream infection and mortality per catheter day, the number of central <span class="hlt">line</span>-associated bloodstream infection events, the costs, and the related mortality could be determined prior to and after the initiation of the dialysis access program. An organized dialysis access program resulted in a 82% decrease in the number of central venous catheter days which lead to a concurrent reduction in central <span class="hlt">line</span>-associated bloodstream infection and deaths. As a result of <span class="hlt">creating</span> an access program, central venous catheter rates decreased from an average rate of 45% to 8%. The cost savings related to the program was calculated to be over US$5 million. The decrease in the number of mortalities is estimated to be between 13 and 27 patients. We conclude that a formalized access program decreases catheter rates, central <span class="hlt">line</span>-associated bloodstream infection, and the resultant hospitalizations, mortality, and costs. Areas with high hemodialysis catheter rates should develop access programs to better serve their patient population.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27689785','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27689785"><span>Methionine sulfoximine supplementation enhances productivity in GS-CHOK1SV cell <span class="hlt">lines</span> through glutathione biosynthesis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Feary, Marc; Racher, Andrew J; Young, Robert J; Smales, C Mark</p> <p>2017-01-01</p> <p>In Lonza <span class="hlt">Biologics</span>' GS Gene Expression System™, recombinant protein-producing GS-CHOK1SV cell <span class="hlt">lines</span> are generated by transfection with an expression vector encoding both GS and the protein product genes followed by selection in MSX and glutamine-free medium. MSX is required to inhibit endogenous CHOK1SV GS, and in effect <span class="hlt">create</span> a glutamine auxotrophy in the host that can be complemented by the expression vector encoded GS in selected cell <span class="hlt">lines</span>. However, MSX is not a specific inhibitor of GS as it also inhibits the activity of GCL (a key enzyme in the glutathione biosynthesis pathway) to a similar extent. Glutathione species (GSH and GSSG) have been shown to provide both oxidizing and reducing equivalents to ER-resident oxidoreductases, raising the possibility that selection for transfectants with increased GCL expression could result in the isolation of GS-CHOKISV cell <span class="hlt">lines</span> with improved capacity for recombinant protein production. In this study we have begun to address the relationship between MSX supplementation, the amount of intracellular GCL subunit and mAb production from a panel of GS-CHOK1SV cell <span class="hlt">lines</span>. We then evaluated the influence of reduced GCL activity <span class="hlt">on</span> batch culture of an industrially relevant mAb-producing GS-CHOK1SV cell <span class="hlt">line</span>. To the best of our knowledge, this paper describes for the first time the change in expression of GCL subunits and recombinant mAb production in these cell <span class="hlt">lines</span> with the degree of MSX supplementation in routine subculture. Our data also shows that partial inhibition of GCL activity in medium containing 75 µM MSX increases mAb productivity, and its more specific inhibitor BSO used at a concentration of 80 µM in medium increases the specific rate of mAb production eight-fold and the concentration in harvest medium by two-fold. These findings support a link between the inhibition of glutathione biosynthesis and recombinant protein production in industrially relevant systems and provide a process-driven method for</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5969439','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5969439"><span>Investigating Undergraduates’ Perceptions of Science in Courses Taught Using the <span class="hlt">CREATE</span> Strategy †</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Hoskins, Sally G.; Gottesman, Alan J.</p> <p>2018-01-01</p> <p>Many science educators agree that 21st century students need to develop mature scientific thinking skills. Unsurprisingly, students’ and experts’ perceptions about the nature of scientific knowledge differ. Moreover, students’ naïve and entrenched epistemologies can preclude their development toward “thinking like scientists.” Novel teaching approaches that guide students toward more mature perceptions may be needed to support their development of scientific thinking skills. To address such issues, physics educators developed the Colorado Learning Attitudes About Science Survey (CLASS), subsequently adapted for chemistry and <span class="hlt">biology</span>. These surveys are “designed to compare novice and expert perceptions about the content and structure of a specific discipline; the source of knowledge about that discipline, including connection of the discipline to the real world; and problem-solving approaches” (Semsar et al., CBE Life Sci. Educ. 10:268–278; p 269). We used CLASS-Bio to track students’ perceptions of science in separate first-year and upper-level <span class="hlt">CREATE</span> (Consider, Read, Elucidate hypotheses, Analyze and interpret the data, Think of the next Experiment) electives, hypothesizing that perceptions would become significantly more expert-like across a semester. Both first-year and upper-level cohorts made significant expert-like shifts. Students also made significant critical thinking gains in <span class="hlt">CREATE</span> courses. Our findings of more mature, expert-like perceptions of science post-course contrast with those of previous studies, where students’ thinking became significantly less expert-like across a term of introductory instruction and changed little in upper-level <span class="hlt">biology</span> electives. Augmenting traditional <span class="hlt">biology</span> curricula with <span class="hlt">CREATE</span> courses could be an economical way to help undergraduates develop more mature views of science. PMID:29904553</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22767882','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22767882"><span>Effects of radio frequency identification-related radiation <span class="hlt">on</span> in vitro <span class="hlt">biologics</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Uysal, Ismail; Hohberger, Clive; Rasmussen, R Scott; Ulrich, David A; Emond, Jean-Pierre; Gutierrez, Alfonso</p> <p>2012-01-01</p> <p>The recent developments <span class="hlt">on</span> the use of e-pedigree to identify the chain of custody of drugs suggests the use of advanced track and trace technologies such as two-dimensional barcodes and radio frequency identification (RFID) tags. RFID technology is used mainly for valuable commodities such as pharmaceutical products while incorporating additional functionalities like monitoring environmental variables to ensure product safety and quality. In its guidance for the use of RFID technologies for drugs (Compliance Policy Guide Section 400.210), the Food and Drug Administration outlined multiple parameters that would apply to any study or application using RFID. However, drugs approved under a <span class="hlt">Biologics</span> License Application or protein drugs covered by a New Drug Application were excluded mainly due to concerns about the effects of radio frequency radiation (thermal and/or non-thermal) <span class="hlt">on</span> <span class="hlt">biologics</span>. Even though the thermal effects of radio frequency <span class="hlt">on</span> <span class="hlt">biologics</span> are relatively well understood, there are few studies in the literature about the non-thermal effects of radio frequency with regards to the protein structure integrity. In this paper, we analyze the non-thermal effects of radio frequency radiation by exposing a wide variety of <span class="hlt">biologics</span> including biopharmaceuticals with vaccines, hormones, and immunoglobulins, as well as cellular blood products such as red blood cells and whole blood-derived platelets as well as fresh frozen plasma. In order to represent the majority of the frequency spectrum used in RFID applications, five different frequencies (13.56 MHz, 433 MHz, 868 MHz, 915 MHz, and 2.4 GHz) are used to account for the most commonly used international frequency bands for RFID. With the help of specialized radio frequency signal-generating hardware, magnetic and electromagnetic fields are <span class="hlt">created</span> around the exposed products with power levels greater than Federal Communications Commission-regulated limits. The in vitro test results <span class="hlt">on</span> more than 100</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4028064','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4028064"><span><span class="hlt">Creating</span> Transgenic shRNA Mice by Recombinase-Mediated Cassette Exchange</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Premsrirut, Prem K.; Dow, Lukas E.; Park, Youngkyu; Hannon, Gregory J.; Lowe, Scott W.</p> <p>2014-01-01</p> <p>RNA interference (RNAi) enables sequence-specific, experimentally induced silencing of virtually any gene by tapping into innate regulatory mechanisms that are conserved among most eukaryotes. The principles that enable transgenic RNAi in cell <span class="hlt">lines</span> can also be used to <span class="hlt">create</span> transgenic animals, which express short-hairpin RNAs (shRNAs) in a regulated or tissue-specific fashion. However, RNAi in transgenic animals is somewhat more challenging than RNAi in cultured cells. The activities of promoters that are commonly used for shRNA expression in cell culture can vary enormously in different tissues, and founder <span class="hlt">lines</span> also typically vary in transgene expression due to the effects of their single integration sites. There are many ways to produce mice carrying shRNA transgenes and the method described here uses recombinase-mediated cassette exchange (RMCE). RMCE permits insertion of the shRNA transgene into a well-characterized locus that gives reproducible and predictable expression in each founder and enhances the probability of potent expression in many cell types. This procedure is more involved and complex than simple pronuclear injection, but if even a few shRNA mice are envisioned, for example, to probe the functions of several genes, the effort of setting up the processes outlined below are well worthwhile. Note that when <span class="hlt">creating</span> a transgenic mouse, one should take care to use the most potent shRNA possible. As a rule of thumb, the sequence chosen should provide >90% knockdown when introduced into cultured cells at single copy (e.g., <span class="hlt">on</span> retroviral infection at a multiplicity of ≤0.3). PMID:24003198</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=personal+AND+files&pg=2&id=EJ341410','ERIC'); return false;" href="https://eric.ed.gov/?q=personal+AND+files&pg=2&id=EJ341410"><span>Keep Your Volunteers <span class="hlt">On-Line</span>.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Lineback, Donald J.</p> <p>1986-01-01</p> <p>Good computer files can help colleges find, manage, and solicit alumni volunteers. In 1978 Rhodes College began <span class="hlt">creating</span> detailed records <span class="hlt">on</span> alumni and friends, entering gift and biographical data, mostly in coded form, into computerized personal files. (MLW)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25273755','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25273755"><span>Analysis of folded pulse forming <span class="hlt">line</span> operation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Domonkos, M T; Watrous, J; Parker, J V; Cavazos, T; Slenes, K; Heidger, S; Brown, D; Wilson, D</p> <p>2014-09-01</p> <p>A compact pulse forming <span class="hlt">line</span> (CPFL) concept based <span class="hlt">on</span> a folded transmission <span class="hlt">line</span> and high-breakdown strength dielectric was explored through an effort combining proof-of-principle experiments with electromagnetic modeling. A small-scale folded CPFL was fabricated using surface-mount ceramic multilayer capacitors. The <span class="hlt">line</span> consisted of 150 capacitors close-packed in parallel and delivered a 300 ns flat-top pulse. The concept was carried to a 10 kV class device using a polymer-ceramic nanocomposite dielectric with a permittivity of 37.6. The <span class="hlt">line</span> was designed for a 161 ns FWHM length pulse into a matched load. The <span class="hlt">line</span> delivered a 110 ns FWHM pulse, and the pulse peak amplitude exceeded the matched load ideal. Transient electromagnetic analysis using the particle-in-cell code ICEPIC was conducted to examine the nature of the unexpected pulse shortening and distortion. Two-dimensional analysis failed to capture the anomalous behavior. Three-dimensional analysis replicated the pulse shape and revealed that the bends were largely responsible for the pulse shortening. The bends not only <span class="hlt">create</span> the expected reflection of the incident TEM wave but also produce a non-zero component of the Poynting vector perpendicular to the propagation direction of the dominant electromagnetic wave, resulting in power flow largely external to the PFL. This analysis explains both the pulse shortening and the amplitude of the pulse.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014RScI...85i4708D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014RScI...85i4708D"><span>Analysis of folded pulse forming <span class="hlt">line</span> operation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Domonkos, M. T.; Watrous, J.; Parker, J. V.; Cavazos, T.; Slenes, K.; Heidger, S.; Brown, D.; Wilson, D.</p> <p>2014-09-01</p> <p>A compact pulse forming <span class="hlt">line</span> (CPFL) concept based <span class="hlt">on</span> a folded transmission <span class="hlt">line</span> and high-breakdown strength dielectric was explored through an effort combining proof-of-principle experiments with electromagnetic modeling. A small-scale folded CPFL was fabricated using surface-mount ceramic multilayer capacitors. The <span class="hlt">line</span> consisted of 150 capacitors close-packed in parallel and delivered a 300 ns flat-top pulse. The concept was carried to a 10 kV class device using a polymer-ceramic nanocomposite dielectric with a permittivity of 37.6. The <span class="hlt">line</span> was designed for a 161 ns FWHM length pulse into a matched load. The <span class="hlt">line</span> delivered a 110 ns FWHM pulse, and the pulse peak amplitude exceeded the matched load ideal. Transient electromagnetic analysis using the particle-in-cell code ICEPIC was conducted to examine the nature of the unexpected pulse shortening and distortion. Two-dimensional analysis failed to capture the anomalous behavior. Three-dimensional analysis replicated the pulse shape and revealed that the bends were largely responsible for the pulse shortening. The bends not only <span class="hlt">create</span> the expected reflection of the incident TEM wave but also produce a non-zero component of the Poynting vector perpendicular to the propagation direction of the dominant electromagnetic wave, resulting in power flow largely external to the PFL. This analysis explains both the pulse shortening and the amplitude of the pulse.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1411361-cusps-enable-line-attractors-neural-computation','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1411361-cusps-enable-line-attractors-neural-computation"><span>Cusps enable <span class="hlt">line</span> attractors for neural computation</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Xiao, Zhuocheng; Zhang, Jiwei; Sornborger, Andrew T.</p> <p></p> <p>Here, <span class="hlt">line</span> attractors in neuronal networks have been suggested to be the basis of many brain functions, such as working memory, oculomotor control, head movement, locomotion, and sensory processing. In this paper, we make the connection between <span class="hlt">line</span> attractors and pulse gating in feed-forward neuronal networks. In this context, because of their neutral stability along a one-dimensional manifold, <span class="hlt">line</span> attractors are associated with a time-translational invariance that allows graded information to be propagated from one neuronal population to the next. To understand how pulse-gating manifests itself in a high-dimensional, nonlinear, feedforward integrate-and-fire network, we use a Fokker-Planck approach to analyzemore » system dynamics. We make a connection between pulse-gated propagation in the Fokker-Planck and population-averaged mean-field (firing rate) models, and then identify an approximate <span class="hlt">line</span> attractor in state space as the essential structure underlying graded information propagation. An analysis of the <span class="hlt">line</span> attractor shows that it consists of three fixed points: a central saddle with an unstable manifold along the <span class="hlt">line</span> and stable manifolds orthogonal to the <span class="hlt">line</span>, which is surrounded <span class="hlt">on</span> either side by stable fixed points. Along the manifold defined by the fixed points, slow dynamics give rise to a ghost. We show that this <span class="hlt">line</span> attractor arises at a cusp catastrophe, where a fold bifurcation develops as a function of synaptic noise; and that the ghost dynamics near the fold of the cusp underly the robustness of the <span class="hlt">line</span> attractor. Understanding the dynamical aspects of this cusp catastrophe allows us to show how <span class="hlt">line</span> attractors can persist in <span class="hlt">biologically</span> realistic neuronal networks and how the interplay of pulse gating, synaptic coupling, and neuronal stochasticity can be used to enable attracting one-dimensional manifolds and, thus, dynamically control the processing of graded information.« less</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017PhRvE..96e2308X','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017PhRvE..96e2308X"><span>Cusps enable <span class="hlt">line</span> attractors for neural computation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Xiao, Zhuocheng; Zhang, Jiwei; Sornborger, Andrew T.; Tao, Louis</p> <p>2017-11-01</p> <p><span class="hlt">Line</span> attractors in neuronal networks have been suggested to be the basis of many brain functions, such as working memory, oculomotor control, head movement, locomotion, and sensory processing. In this paper, we make the connection between <span class="hlt">line</span> attractors and pulse gating in feed-forward neuronal networks. In this context, because of their neutral stability along a one-dimensional manifold, <span class="hlt">line</span> attractors are associated with a time-translational invariance that allows graded information to be propagated from one neuronal population to the next. To understand how pulse-gating manifests itself in a high-dimensional, nonlinear, feedforward integrate-and-fire network, we use a Fokker-Planck approach to analyze system dynamics. We make a connection between pulse-gated propagation in the Fokker-Planck and population-averaged mean-field (firing rate) models, and then identify an approximate <span class="hlt">line</span> attractor in state space as the essential structure underlying graded information propagation. An analysis of the <span class="hlt">line</span> attractor shows that it consists of three fixed points: a central saddle with an unstable manifold along the <span class="hlt">line</span> and stable manifolds orthogonal to the <span class="hlt">line</span>, which is surrounded <span class="hlt">on</span> either side by stable fixed points. Along the manifold defined by the fixed points, slow dynamics give rise to a ghost. We show that this <span class="hlt">line</span> attractor arises at a cusp catastrophe, where a fold bifurcation develops as a function of synaptic noise; and that the ghost dynamics near the fold of the cusp underly the robustness of the <span class="hlt">line</span> attractor. Understanding the dynamical aspects of this cusp catastrophe allows us to show how <span class="hlt">line</span> attractors can persist in <span class="hlt">biologically</span> realistic neuronal networks and how the interplay of pulse gating, synaptic coupling, and neuronal stochasticity can be used to enable attracting one-dimensional manifolds and, thus, dynamically control the processing of graded information.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1411361-cusps-enable-line-attractors-neural-computation','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1411361-cusps-enable-line-attractors-neural-computation"><span>Cusps enable <span class="hlt">line</span> attractors for neural computation</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Xiao, Zhuocheng; Zhang, Jiwei; Sornborger, Andrew T.; ...</p> <p>2017-11-07</p> <p>Here, <span class="hlt">line</span> attractors in neuronal networks have been suggested to be the basis of many brain functions, such as working memory, oculomotor control, head movement, locomotion, and sensory processing. In this paper, we make the connection between <span class="hlt">line</span> attractors and pulse gating in feed-forward neuronal networks. In this context, because of their neutral stability along a one-dimensional manifold, <span class="hlt">line</span> attractors are associated with a time-translational invariance that allows graded information to be propagated from one neuronal population to the next. To understand how pulse-gating manifests itself in a high-dimensional, nonlinear, feedforward integrate-and-fire network, we use a Fokker-Planck approach to analyzemore » system dynamics. We make a connection between pulse-gated propagation in the Fokker-Planck and population-averaged mean-field (firing rate) models, and then identify an approximate <span class="hlt">line</span> attractor in state space as the essential structure underlying graded information propagation. An analysis of the <span class="hlt">line</span> attractor shows that it consists of three fixed points: a central saddle with an unstable manifold along the <span class="hlt">line</span> and stable manifolds orthogonal to the <span class="hlt">line</span>, which is surrounded <span class="hlt">on</span> either side by stable fixed points. Along the manifold defined by the fixed points, slow dynamics give rise to a ghost. We show that this <span class="hlt">line</span> attractor arises at a cusp catastrophe, where a fold bifurcation develops as a function of synaptic noise; and that the ghost dynamics near the fold of the cusp underly the robustness of the <span class="hlt">line</span> attractor. Understanding the dynamical aspects of this cusp catastrophe allows us to show how <span class="hlt">line</span> attractors can persist in <span class="hlt">biologically</span> realistic neuronal networks and how the interplay of pulse gating, synaptic coupling, and neuronal stochasticity can be used to enable attracting one-dimensional manifolds and, thus, dynamically control the processing of graded information.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20040088359&hterms=breast+cancer&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dbreast%2Bcancer','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20040088359&hterms=breast+cancer&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Dbreast%2Bcancer"><span><span class="hlt">Biological</span> and genetic properties of the p53 null preneoplastic mammary epithelium</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Medina, Daniel; Kittrell, Frances S.; Shepard, Anne; Stephens, L. Clifton; Jiang, Cheng; Lu, Junxuan; Allred, D. Craig; McCarthy, Maureen; Ullrich, Robert L.</p> <p>2002-01-01</p> <p>The absence of the tumor suppressor gene p53 confers an increased tumorigenic risk for mammary epithelial cells. In this report, we describe the <span class="hlt">biological</span> and genetic properties of the p53 null preneoplastic mouse mammary epithelium in a p53 wild-type environment. Mammary epithelium from p53 null mice was transplanted serially into the cleared mammary fat pads of p53 wild-type BALB/c female to develop stable outgrowth <span class="hlt">lines</span>. The outgrowth <span class="hlt">lines</span> were transplanted for 10 generations. The outgrowths were ductal in morphology and progressed through ductal hyperplasia and ductal carcinoma in situ before invasive cancer. The preneoplastic outgrowth <span class="hlt">lines</span> were immortal and exhibited activated telomerase activity. They are estrogen and progesterone receptor-positive, and aneuploid, and had various levels of tumorigenic potential. The <span class="hlt">biological</span> and genetic properties of these <span class="hlt">lines</span> are distinct from those found in most hyperplastic alveolar outgrowth <span class="hlt">lines</span>, the form of mammary preneoplasia occurring in most traditional models of murine mammary tumorigenesis. These results indicate that the preneoplastic cell populations found in this genetically engineered model are similar in <span class="hlt">biological</span> properties to a subset of precurser lesions found in human breast cancer and provide a unique model to identify secondary events critical for tumorigenicity and invasiveness.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19940026025','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19940026025"><span><span class="hlt">Biologically</span>-inspired hexapod robot design and simulation</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Espenschied, Kenneth S.; Quinn, Roger D.</p> <p>1994-01-01</p> <p>The design and construction of a <span class="hlt">biologically</span>-inspired hexapod robot is presented. A previously developed simulation is modified to include models of the DC drive motors, the motor driver circuits and their transmissions. The application of this simulation to the design and development of the robot is discussed. The mechanisms thought to be responsible for the leg coordination of the walking stick insect were previously applied to control the straight-<span class="hlt">line</span> locomotion of a robot. We generalized these rules for a robot walking <span class="hlt">on</span> a plane. This <span class="hlt">biologically</span>-inspired control strategy is used to control the robot in simulation. Numerical results show that the general body motion and performance of the simulated robot is similar to that of the robot based <span class="hlt">on</span> our preliminary experimental results.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19256964','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19256964"><span>Packings of a charged <span class="hlt">line</span> <span class="hlt">on</span> a sphere.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Alben, Silas</p> <p>2008-12-01</p> <p>We find equilibrium configurations of open and closed <span class="hlt">lines</span> of charge <span class="hlt">on</span> a sphere, and track them with respect to varying sphere radius. Closed <span class="hlt">lines</span> transition from a circle to a spiral-like shape through two low-wave-number bifurcations-"baseball seam" and "twist"-which minimize Coulomb energy. The spiral shape is the unique stable equilibrium of the closed <span class="hlt">line</span>. Other unstable equilibria arise through tip-splitting events. An open <span class="hlt">line</span> transitions smoothly from an arc of a great circle to a spiral as the sphere radius decreases. Under repulsive potentials with faster-than-Coulomb power-law decay, the spiral is tighter in initial stages of sphere shrinkage, but at later stages of shrinkage the equilibria for all repulsive potentials converge <span class="hlt">on</span> a spiral with uniform spacing between turns. Multiple stable equilibria of the open <span class="hlt">line</span> are observed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23484675','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23484675"><span>Applying laws of <span class="hlt">biology</span> to diabetes with emphasis <span class="hlt">on</span> metabolic syndrome.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Houck, Philip D; de Oliveira, Jose Mario F</p> <p>2013-05-01</p> <p>The listed laws of <span class="hlt">biology</span> will be applied to diabetes mellitus and metabolic syndrome. (1) <span class="hlt">Biology</span> must be consistent with the fundamental laws of physics and chemistry. (2) Life, as opposed to non-living, exhibits negative entropy (known as syntropy), capable of <span class="hlt">creating</span> order out of chaos. (The energy to support negative entropy is yet to be defined.) (3) The cell is the fundamental unit of <span class="hlt">biology</span>. (4) The cell must be in homeostasis with its environment. (This property enables the process of evolution. In other words, the environment changes life.) (5) There must be a distinction between self and the environment. (Immunity and inflammation are the defenses against invaders from the environment and responsible for repair of damaged and senile cells.) (6) Electromagnetic information transfer is necessary for development and regeneration. (Life and, more specifically, regeneration of tissue will not exist in a non-electromagnetic environment, denervation results in atrophy.) A new model of disease derived from these laws is that health exists when degeneration and regeneration are in balance. Inflammation is the fulcrum between the two, being both beneficial in repair and detrimental by promoting degeneration. This model leads to a number of hypotheses. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19880035422&hterms=ionized+atoms&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dionized%2Batoms','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19880035422&hterms=ionized+atoms&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dionized%2Batoms"><span>Observations of absorption <span class="hlt">lines</span> from highly ionized atoms. [of interstellar medium</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Jenkins, Edward B.</p> <p>1987-01-01</p> <p>In the ultraviolet spectra of hot stars, absorption <span class="hlt">lines</span> can be seen from highly ionized species in the interstellar medium. Observations of these features which have been very influential in revising the perception of the medium's various physical states, are discussed. The pervasiveness of O 6 absorption <span class="hlt">lines</span>, coupled with complementary observations of a diffuse background in soft X-rays and EUV radiation, shows that there is an extensive network of low density gas (n approx. few x 0.001/cu cm) existing at coronal temperatures log T = 5.3 or 6.3. Shocks <span class="hlt">created</span> by supernova explosions or mass loss from early-type stars can propagate freely through space and eventually transfer a large amount of energy to the medium. To <span class="hlt">create</span> the coronal temperatures, the shocks must have velocities in excess of 150 km/sec; shocks at somewhat lower velocity (v = 100 km/sec) can be directly observed in the <span class="hlt">lines</span> of Si3. Observations of other <span class="hlt">lines</span> in the ultraviolet, such as Si 4V and C 5, may highlight the widespread presence of energetic UV radiation from very hot, dwarf stars. More advanced techniques in visible and X-ray astronomical spectroscopy may open up for inspection selected <span class="hlt">lines</span> from atoms in much higher stages of ionization.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007JAP...102g4911S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007JAP...102g4911S"><span><span class="hlt">On</span> the dispersion characteristics of metamaterial transmission <span class="hlt">lines</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sisó, G.; Gil, M.; Bonache, J.; Martín, F.</p> <p>2007-10-01</p> <p>In this paper, a detailed analysis of the dispersion characteristics of metamaterial transmission <span class="hlt">lines</span>, based <span class="hlt">on</span> the lumped element T-circuit model is carried out. One of the main relevant characteristics of these artificial <span class="hlt">lines</span> is the possibility to tailor the phase response. This leads to unique properties which are of interest for microwave circuit design, such as bandwidth enhancement or multiband (dual-band) operation, among others. However, it is shown in this paper that, in spite of the larger number of circuit parameters (as compared to conventional <span class="hlt">lines</span>), there exist intrinsic limitations that may limit the performance of such metamaterial transmission <span class="hlt">lines</span> under certain conditions. In this paper these limitations are pointed out from an accurate analysis of the phase response and the Foster's reactance theorem [Bell Syst. Tech. 3, 259 (1924)]. From the results of this paper, important guidelines for the design of microwave components based <span class="hlt">on</span> metamaterial transmission <span class="hlt">lines</span> are inferred. The fabrication and characterization of different metamaterial transmission <span class="hlt">lines</span> will corroborate the theoretical results.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28620041','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28620041"><span>A standard-enabled workflow for synthetic <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Myers, Chris J; Beal, Jacob; Gorochowski, Thomas E; Kuwahara, Hiroyuki; Madsen, Curtis; McLaughlin, James Alastair; Mısırlı, Göksel; Nguyen, Tramy; Oberortner, Ernst; Samineni, Meher; Wipat, Anil; Zhang, Michael; Zundel, Zach</p> <p>2017-06-15</p> <p>A synthetic <span class="hlt">biology</span> workflow is composed of data repositories that provide information about genetic parts, sequence-level design tools to compose these parts into circuits, visualization tools to depict these designs, genetic design tools to select parts to <span class="hlt">create</span> systems, and modeling and simulation tools to evaluate alternative design choices. Data standards enable the ready exchange of information within such a workflow, allowing repositories and tools to be connected from a diversity of sources. The present paper describes one such workflow that utilizes, among others, the Synthetic <span class="hlt">Biology</span> Open Language (SBOL) to describe genetic designs, the Systems <span class="hlt">Biology</span> Markup Language to model these designs, and SBOL Visual to visualize these designs. We describe how a standard-enabled workflow can be used to produce types of design information, including multiple repositories and software tools exchanging information using a variety of data standards. Recently, the ACS Synthetic <span class="hlt">Biology</span> journal has recommended the use of SBOL in their publications. © 2017 The Author(s); published by Portland Press Limited <span class="hlt">on</span> behalf of the Biochemical Society.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005AIPC..772.1583L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005AIPC..772.1583L"><span>Electric and Magnetic Manipulation of <span class="hlt">Biological</span> Systems</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lee, H.; Hunt, T. P.; Liu, Y.; Ham, D.; Westervelt, R. M.</p> <p>2005-06-01</p> <p>New types of <span class="hlt">biological</span> cell manipulation systems, a micropost matrix, a microelectromagnet matrix, and a microcoil array, were developed. The micropost matrix consists of post-shaped electrodes embedded in an insulating layer. With a separate ac voltage applied to each electrode, the micropost matrix generates dielectrophoretic force to trap and move individual <span class="hlt">biological</span> cells. The microelectromagnet matrix consists of two arrays of straight wires aligned perpendicular to each other, that are covered with insulating layers. By independently controlling the current in each wire, the microelectromagnet matrix <span class="hlt">creates</span> versatile magnetic fields to manipulate individual <span class="hlt">biological</span> cells attached to magnetic beads. The microcoil array is a set of coils implemented in a foundry using a standard silicon fabrication technology. Current sources to the coils, and control circuits are integrated <span class="hlt">on</span> a single chip, making the device self-contained. Versatile manipulation of <span class="hlt">biological</span> cells was demonstrated using these devices by generating optimized electric or magnetic field patterns. A single yeast cell was trapped and positioned with microscopic resolution, and multiple yeast cells were trapped and independently moved along the separate paths for cell-sorting.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.ars.usda.gov/research/publications/publication/?seqNo115=336411','TEKTRAN'); return false;" href="http://www.ars.usda.gov/research/publications/publication/?seqNo115=336411"><span>Cell <span class="hlt">lines</span> derived from the squash bug, anasa tristis (coreidae: hemiptera)</span></a></p> <p><a target="_blank" href="https://www.ars.usda.gov/research/publications/find-a-publication/">USDA-ARS?s Scientific Manuscript database</a></p> <p></p> <p></p> <p>The squash bug, Anasa tristis, is a pest of cucurbits that exerts direct damage <span class="hlt">on</span> crops and is a vector of plant pathogens. We established cell <span class="hlt">lines</span> from this insect to serve as tools for basic <span class="hlt">biology</span>, such as virology and immunology, as well as applied studies, such as insecticide development pr...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3084710','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3084710"><span>Eugene – A Domain Specific Language for Specifying and Constraining Synthetic <span class="hlt">Biological</span> Parts, Devices, and Systems</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Bilitchenko, Lesia; Liu, Adam; Cheung, Sherine; Weeding, Emma; Xia, Bing; Leguia, Mariana; Anderson, J. Christopher; Densmore, Douglas</p> <p>2011-01-01</p> <p>Background Synthetic <span class="hlt">biological</span> systems are currently <span class="hlt">created</span> by an ad-hoc, iterative process of specification, design, and assembly. These systems would greatly benefit from a more formalized and rigorous specification of the desired system components as well as constraints <span class="hlt">on</span> their composition. Therefore, the creation of robust and efficient design flows and tools is imperative. We present a human readable language (Eugene) that allows for the specification of synthetic <span class="hlt">biological</span> designs based <span class="hlt">on</span> <span class="hlt">biological</span> parts, as well as provides a very expressive constraint system to drive the automatic creation of composite Parts (Devices) from a collection of individual Parts. Results We illustrate Eugene's capabilities in three different areas: Device specification, design space exploration, and assembly and simulation integration. These results highlight Eugene's ability to <span class="hlt">create</span> combinatorial design spaces and prune these spaces for simulation or physical assembly. Eugene <span class="hlt">creates</span> functional designs quickly and cost-effectively. Conclusions Eugene is intended for forward engineering of DNA-based devices, and through its data types and execution semantics, reflects the desired abstraction hierarchy in synthetic <span class="hlt">biology</span>. Eugene provides a powerful constraint system which can be used to drive the creation of new devices at runtime. It accomplishes all of this while being part of a larger tool chain which includes support for design, simulation, and physical device assembly. PMID:21559524</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29236393','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29236393"><span>Validation of <span class="hlt">biological</span> activity testing procedure of recombinant human interleukin-7.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lutsenko, T N; Kovalenko, M V; Galkin, O Yu</p> <p>2017-01-01</p> <p>Validation procedure for method of monitoring the <span class="hlt">biological</span> activity of reсombinant human interleukin-7 has been developed and conducted according to the requirements of national and international recommendations. This method is based <span class="hlt">on</span> the ability of recombinant human interleukin-7 to induce proliferation of T lymphocytes. It has been shown that to control the <span class="hlt">biological</span> activity of recombinant human interleukin-7 peripheral blood mononuclear cells (PBMCs) derived from blood or cell <span class="hlt">lines</span> can be used. Validation charac­teristics that should be determined depend <span class="hlt">on</span> the method, type of product or object test/measurement and <span class="hlt">biological</span> test systems used in research. The validation procedure for the method of control of <span class="hlt">biological</span> activity of recombinant human interleukin-7 in peripheral blood mononuclear cells showed satisfactory results <span class="hlt">on</span> all parameters tested such as specificity, accuracy, precision and linearity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JASMS..25.1472S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JASMS..25.1472S"><span>Identification and Affinity-Quantification of ß-Amyloid and α-Synuclein Polypeptides Using <span class="hlt">On-Line</span> SAW-Biosensor-Mass Spectrometry</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Slamnoiu, Stefan; Vlad, Camelia; Stumbaum, Mihaela; Moise, Adrian; Lindner, Kathrin; Engel, Nicole; Vilanova, Mar; Diaz, Mireia; Karreman, Christiaan; Leist, Marcel; Ciossek, Thomas; Hengerer, Bastian; Vilaseca, Marta; Przybylski, Michael</p> <p>2014-08-01</p> <p>Bioaffinity analysis using a variety of biosensors has become an established tool for detection and quantification of biomolecular interactions. Biosensors, however, are generally limited by the lack of chemical structure information of affinity-bound ligands. <span class="hlt">On-line</span> bioaffinity-mass spectrometry using a surface-acoustic wave biosensor (SAW-MS) is a new combination providing the simultaneous affinity detection, quantification, and mass spectrometric structural characterization of ligands. We describe here an <span class="hlt">on-line</span> SAW-MS combination for direct identification and affinity determination, using a new interface for MS of the affinity-isolated ligand eluate. Key element of the SAW-MS combination is a microfluidic interface that integrates affinity-isolation <span class="hlt">on</span> a gold chip, in-situ sample concentration, and desalting with a microcolumn for MS of the ligand eluate from the biosensor. Suitable MS- acquisition software has been developed that provides coupling of the SAW-MS interface to a Bruker Daltonics ion trap-MS, FTICR-MS, and Waters Synapt-QTOF- MS systems. Applications are presented for mass spectrometric identifications and affinity (KD) determinations of the neurodegenerative polypeptides, ß-amyloid (Aß), and pathophysiological and physiological synucleins (α- and ß-synucleins), two key polypeptide systems for Alzheimer's disease and Parkinson's disease, respectively. Moreover, first in vivo applications of αSyn polypeptides from brain homogenate show the feasibility of <span class="hlt">on-line</span> affinity-MS to the direct analysis of <span class="hlt">biological</span> material. These results demonstrate <span class="hlt">on-line</span> SAW-bioaffinity-MS as a powerful tool for structural and quantitative analysis of biopolymer interactions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22188690','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22188690"><span>Facing regulatory challenges of <span class="hlt">on-line</span> hemodiafiltration.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kümmerle, Wolfgang</p> <p>2011-01-01</p> <p><span class="hlt">On-line</span> hemodiafiltration (<span class="hlt">on-line</span> HDF) is the result of a vision that triggered multifarious changes in very different areas. Driven by the idea to offer better medical treatment for renal patients, technological innovations were developed and established that also constituted new challenges in the field of regulatory affairs. The existing regulations predominantly addressed the quality and safety of those products needed to perform dialysis treatment which were supplied by industrial manufacturers. However, the complexity of treatment system required for the provision of <span class="hlt">on-line</span> fluids demanded a holistic approach encompassing all components involved. Hence, focus was placed not only <span class="hlt">on</span> single products, but much more <span class="hlt">on</span> their interfacing, and the clinical infrastructure, in particular, had to undergo substantial changes. The overall understanding of the interaction between such factors, quite different in their nature, was crucial to overcome the arising regulatory obstacles. This essay describes the evolution of the <span class="hlt">on-line</span> HDF procedure from the regulatory point of view. A simplified diagram demonstrates the path taken from the former regulatory understanding to the realization of necessary changes. That achievement was only possible through 'management of preview' and consequent promotion of technical and medical innovations as well as regulatory re-evaluations. Copyright © 2011 S. Karger AG, Basel.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29872613','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29872613"><span>Synthesis of Novel Aza-aromatic Curcuminoids with Improved <span class="hlt">Biological</span> Activities towards Various Cancer Cell <span class="hlt">Lines</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Theppawong, Atiruj; Van de Walle, Tim; Grootaert, Charlotte; Bultinck, Margot; Desmet, Tom; Van Camp, John; D'hooghe, Matthias</p> <p>2018-05-01</p> <p>Curcumin, a natural compound extracted from the rhizomes of Curcuma longa , displays pronounced anticancer properties but lacks good bioavailability and stability. In a previous study, we initiated structure modification of the curcumin scaffold by imination of the labile β-diketone moiety to produce novel β-enaminone derivatives. These compounds showed promising properties for elaborate follow-up studies. In this work, we focused <span class="hlt">on</span> another class of nitrogen-containing curcuminoids with a similar objective: to address the bioavailability and stability issues and to improve the <span class="hlt">biological</span> activity of curcumin. This paper thus reports <span class="hlt">on</span> the synthesis of new pyridine-, indole-, and pyrrole-based curcumin analogues (aza-aromatic curcuminoids) and discusses their water solubility, antioxidant activity, and antiproliferative properties. In addition, multivariate statistics, including hierarchical clustering analysis and principal component analysis, were performed <span class="hlt">on</span> a broad set of nitrogen-containing curcuminoids. Compared to their respective mother structures, that is, curcumin and bisdemethoxycurcumin, all compounds, and especially the pyridin-3-yl β-enaminone analogues, showed better water solubility profiles. Interestingly, the pyridine-, indole-, and pyrrole-based curcumin derivatives demonstrated improved <span class="hlt">biological</span> effects in terms of mitochondrial activity impairment and protein content, in addition to comparable or decreased antioxidant properties. Overall, the <span class="hlt">biologically</span> active N -alkyl β-enaminone aza-aromatic curcuminoids were shown to offer a desirable balance between good solubility and significant bioactivity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/5766103','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/5766103"><span>Potential environmental effects of 765-kV transmission <span class="hlt">lines</span>: views before the New York State Public Service Commission, Cases 26529 and 26559, 1976-1978</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Scott-Walton, B.; Clark, K. M.; Holt, B. R.</p> <p>1979-11-01</p> <p>Testimony given before the New York Public Service Commission in two recent cases <span class="hlt">on</span> the potential environmental effects of 765-kV overhead ac transmission <span class="hlt">lines</span> is reviewed. The testimony focused <span class="hlt">on</span> the potential effects of audible noise, <span class="hlt">on</span> the potential <span class="hlt">biological</span> effects of the electromagnetic fields, <span class="hlt">on</span> the potential for electric shocks to people who touch vehicles parked under the proposed <span class="hlt">lines</span>, <span class="hlt">on</span> the potential effects of the electromagnetic fields <span class="hlt">on</span> electronic cardiac pacemakers, and <span class="hlt">on</span> potential effects of ozone produced by corona discharge from the <span class="hlt">lines</span>. The testimony fully explored these questions; however, it did not resolve all of them.more » The testimony indicates potential impacts from the audible noise and from the electrostatic shocks that people can receive when they touch a large vehicle parked under the <span class="hlt">lines</span>. The testimony also indicates that certain cardiac pacemaker and lead combinations may, under certain circumstances, undergo reversion to a fixed rate of pacing in the presence of the fields under the <span class="hlt">lines</span>, but that little risk to cardiac patients results except possibly for those patients for whom competition between the heart's own rate and the pacemaker rate presents a health risk. The testimony fails to demonstrate <span class="hlt">biological</span> hazards from the field; further research is necessary to understand better the effects of the fields <span class="hlt">on</span> <span class="hlt">biological</span> systems. The testimony indicates that ozone produced by the <span class="hlt">lines</span> will not significantly affect the environment.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19003431','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19003431"><span>Diffusion of synthetic <span class="hlt">biology</span>: a challenge to biosafety.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Schmidt, Markus</p> <p>2008-06-01</p> <p>One of the main aims of synthetic <span class="hlt">biology</span> is to make <span class="hlt">biology</span> easier to engineer. Major efforts in synthetic <span class="hlt">biology</span> are made to develop a toolbox to design <span class="hlt">biological</span> systems without having to go through a massive research and technology process. With this "de-skilling" agenda, synthetic <span class="hlt">biology</span> might finally unleash the full potential of biotechnology and spark a wave of innovation, as more and more people have the necessary skills to engineer <span class="hlt">biology</span>. But this ultimate domestication of <span class="hlt">biology</span> could easily lead to unprecedented safety challenges that need to be addressed: more and more people outside the traditional biotechnology community will <span class="hlt">create</span> self-replicating machines (life) for civil and defence applications, "biohackers" will engineer new life forms at their kitchen table; and illicit substances will be produced synthetically and much cheaper. Such a scenario is a messy and dangerous one, and we need to think about appropriate safety standards now.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28399656','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28399656"><span>Teaching Old Dyes New Tricks: <span class="hlt">Biological</span> Probes Built from Fluoresceins and Rhodamines.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lavis, Luke D</p> <p>2017-06-20</p> <p>Small-molecule fluorophores, such as fluorescein and rhodamine derivatives, are critical tools in modern biochemical and <span class="hlt">biological</span> research. The field of chemical dyes is old; colored molecules were first discovered in the 1800s, and the fluorescein and rhodamine scaffolds have been known for over a century. Nevertheless, there has been a renaissance in using these dyes to <span class="hlt">create</span> tools for biochemistry and <span class="hlt">biology</span>. The application of modern chemistry, biochemistry, molecular genetics, and optical physics to these old structures enables and drives the development of novel, sophisticated fluorescent dyes. This critical review focuses <span class="hlt">on</span> an important example of chemical <span class="hlt">biology</span>-the melding of old and new chemical knowledge-leading to useful molecules for advanced biochemical and <span class="hlt">biological</span> experiments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AIPC.1829b0035Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AIPC.1829b0035Z"><span>Effect of splitting a mixed-model <span class="hlt">line</span> <span class="hlt">on</span> shortening the <span class="hlt">line</span> length under open- and closed-boundary working area settings</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Donghao; Matsuura, Haruki; Asada, Akiko</p> <p>2017-04-01</p> <p>Some automobile factories have segmented mixed-model production <span class="hlt">lines</span> into shorter sub-<span class="hlt">lines</span> according to part group, such as engine, trim, and powertrain. The effects of splitting a <span class="hlt">line</span> into sub-<span class="hlt">lines</span> have been reported from the standpoints of worker motivation, productivity improvement, and autonomy based <span class="hlt">on</span> risk spreading. There has been no mention of the possibility of shortening the <span class="hlt">line</span> length by altering the product sequence using sub-<span class="hlt">lines</span>. The purpose of the present paper is to determine the conditions under which sub-<span class="hlt">lines</span> reduce the <span class="hlt">line</span> length and the degree to which the <span class="hlt">line</span> length may be shortened. The <span class="hlt">line</span> lengths for a non-split <span class="hlt">line</span> and a <span class="hlt">line</span> that has been split into sub-<span class="hlt">lines</span> are compared using three methods for determining the working area, the standard closed boundary, the optimized open boundary, and real-life constant-length stations. The results are discussed by analyzing the upper and lower bounds of the <span class="hlt">line</span> length. Based <span class="hlt">on</span> these results, a procedure for deciding whether or not to split a production <span class="hlt">line</span> is proposed.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=exercise+AND+positive+AND+reinforce&pg=2&id=EJ822680','ERIC'); return false;" href="https://eric.ed.gov/?q=exercise+AND+positive+AND+reinforce&pg=2&id=EJ822680"><span>Just-in-Time Teaching in <span class="hlt">Biology</span>: <span class="hlt">Creating</span> an Active Learner Classroom Using the Internet</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Marrs, Kathleen A.; Novak, Gregor</p> <p>2004-01-01</p> <p>Just-in-Time Teaching (ITT) is a teaching and learning approach that combines the best features of traditional in-class instruction with the communication and resource potential available via the Web. We describe here how ITT can be used to teach <span class="hlt">biology</span> to undergraduate and graduate level students, both science majors as well as non science…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19740054688&hterms=organic+chemistry&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D40%26Ntt%3Dorganic%2Bchemistry','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19740054688&hterms=organic+chemistry&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D40%26Ntt%3Dorganic%2Bchemistry"><span>Organic chemistry and <span class="hlt">biology</span> of the interstellar medium</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Sagan, C.</p> <p>1973-01-01</p> <p>Interstellar organic chemistry is discussed as the field of study emerging from the discovery of microwave <span class="hlt">lines</span> of formaldehyde and of hydrogen cyanide in the interstellar medium. The reliability of molecular identifications and comparisons of interstellar and cometary compounds are considered, along with the degradational origin of simple organics. It is pointed out that the contribution of interstellar organic chemistry to problems in <span class="hlt">biology</span> is not substantive but analogical. The interstellar medium reveals the operation of chemical processes which, <span class="hlt">on</span> earth and perhaps <span class="hlt">on</span> vast numbers of planets throughout the universe, led to the origin of life, but the actual molecules of the interstellar medium are unlikely to play any significant <span class="hlt">biological</span> role.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28205141','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28205141"><span>Cell <span class="hlt">lines</span> derived from the squash bug, Anasa tristis (Coreidae: Hemiptera).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Goodman, Cynthia L; Ringbauer, Joseph A; Li, Yao-Fa; Lincoln, Tamra Reall; Stanley, David</p> <p>2017-05-01</p> <p>The squash bug, Anasa tristis, is a pest of cucurbits that exerts direct damage <span class="hlt">on</span> crops and is a vector of plant pathogens. We established cell <span class="hlt">lines</span> from this insect to serve as tools for basic <span class="hlt">biology</span>, including virology and immunology, as well as applied studies, such as insecticide development programs. We initiated 15 cell cultures, using nine media or combinations of media. The media yielding the best results were a modification of Kimura's medium and a combination of two commercially available cell culture media (EX-CELL 420 and L15). We designated the two cell <span class="hlt">lines</span> as BCIRL-AtE-CLG11 and BCIRL-AtE-CLG15. From the AtE-CLG15 <span class="hlt">line</span>, we isolated two sub-<span class="hlt">lines</span>, A and B. Of these, the most consistently replicating <span class="hlt">line</span> was AtE-CLG15A. We determined the doubling time of this <span class="hlt">line</span> (190 h) and its mean cell diameter (14.5 ± 0.7 μm). We characterized the AtE-CLG15A <span class="hlt">line</span> using DAF-PCR. The BCIRL-AtE-CLG15A cell <span class="hlt">line</span> is now available for researchers world-wide.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20480412','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20480412"><span>Long-term adaptation of breast tumor cell <span class="hlt">lines</span> to high concentrations of nitric oxide.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Vesper, Benjamin J; Elseth, Kim M; Tarjan, Gabor; Haines, G Kenneth; Radosevich, James A</p> <p>2010-08-01</p> <p>Nitric oxide (NO), a free radical, has been implicated in the <span class="hlt">biology</span> of human cancers, including breast cancer, yet it is still unclear how NO affects tumor development and propagation. We herein gradually adapted four human breast adenocarcinoma cell <span class="hlt">lines</span> (BT-20, Hs578T, T-47D, and MCF-7) to increasing concentrations of the NO donor DETA-NONOate up to 600 muM. The resulting model system consisted of a set of fully adapted high nitric oxide ("HNO") cell <span class="hlt">lines</span> that are <span class="hlt">biologically</span> different from the "parent" cell <span class="hlt">lines</span> from which they originated. Although each of the four parent and HNO cell <span class="hlt">lines</span> had identical morphologic appearance, the HNO cells grew faster than their corresponding parent cells and were resistant to both nitrogen- and oxygen-based free radicals. These cell <span class="hlt">lines</span> serve as a novel tool to study the role of NO in breast cancer progression and potentially can be used to predict the therapeutic response leading to more efficient therapeutic regimens.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=operating+AND+system+AND+security&pg=5&id=ED130744','ERIC'); return false;" href="https://eric.ed.gov/?q=operating+AND+system+AND+security&pg=5&id=ED130744"><span>Student System, <span class="hlt">On-Line</span> Admissions.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>White, Stephen R.</p> <p></p> <p>This report provides technical information <span class="hlt">on</span> an <span class="hlt">on-line</span> admissions system developed by Montgomery College. Part I, Systems Development, describes the background, objectives and responsibilities, system design, and reports generated by the system. Part II, Operating Instructions, describes input forms and controls, admission system functions, file…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1986SPIE..665...75H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1986SPIE..665...75H"><span>Thermographic Sensing For <span class="hlt">On-Line</span> Industrial Control</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Holmsten, Dag</p> <p>1986-10-01</p> <p>It is today's emergence of thermoelectrically cooled, highly accurate infrared linescanners and imaging systems that has definitely made <span class="hlt">on-line</span> Infraread Thermography (IRT) possible. Specifically designed for continuous use, these scanners are equipped with dedicated software capable of monitoring and controlling highly complex thermodynamic situations. This paper will outline some possible implications of using IRT <span class="hlt">on-line</span> by describing some uses of this technology in the steel-making (hot rolling) and automotive industries (machine-vision). A warning is also expressed that IRT technology not originally designed for automated applications e.g. high resolution, imaging systems, should not be directly applied to an <span class="hlt">on-line</span> measurement situation without having its measurement resolution, accuracy and especially its repeatability, reliably proven. Some suitable testing procedures are briefly outlined at the end of the paper.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://files.eric.ed.gov/fulltext/ED322266.pdf','ERIC'); return false;" href="http://files.eric.ed.gov/fulltext/ED322266.pdf"><span>Real Life Poverty in America: Where the American Public Would Set the Poverty <span class="hlt">Line</span>.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>O'Hare, William; And Others</p> <p></p> <p>This report discusses the results of a 1989 poll conducted by the Gallup Organization in which a representative sample of Americans were asked where they would set the poverty <span class="hlt">line</span>. The poverty <span class="hlt">line</span> in current use by the Federal Government was <span class="hlt">created</span> in the mid-1960s, using data from the 1950s. Setting the poverty <span class="hlt">line</span> involves a basic decision…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11639657','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11639657"><span>Beyond nature and culture: a note <span class="hlt">on</span> medicine in the age of molecular <span class="hlt">biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rheinberger, H J</p> <p>1995-01-01</p> <p>This paper is divided into two parts. In the first, I examine the relations among molecular <span class="hlt">biology</span>, gene technology, and medicine, as well as some aspects of the consequences of these relations with respect to the human genome project. I argue that the prevailing momentum of early molecular <span class="hlt">biology</span> resided in <span class="hlt">creating</span> the technical means for an extracellular representation of intracellular configurations. As such, its medical impact was rather limited. With the advent of recombinant DNA technologies, a radical change of perspective ensued. The momentum of gene technology is based <span class="hlt">on</span> the prospects of an intracellular representation of extracellular projects--the "rewriting" of life. Its medical impact is potentially unlimited. In the second part, I question the very opposition between nature and culture that implicitly underlies the notion of medicine as a "cultural system." I argue that both <span class="hlt">on</span> a macroscopic level (global ecological changes) and <span class="hlt">on</span> a microscopic level (genetic engineering), the "natural" and the "social" are no longer to be seen as ontologically different. In its uncanny oscillation between retrospection and foresight, between description and proclamation, and between assertion and hesitatiion, this essay translates an uneasiness that I have not been able to overcome while writing it. The essay conveys the tangled views of a hybrid author who himself cannot but oscillate between the perspectives of an actor in the field of molecular <span class="hlt">biology</span>, a participant in the field of science studies, and a citizen.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29797047','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29797047"><span>Physcomitrella patens, a versatile synthetic <span class="hlt">biology</span> chassis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Reski, Ralf; Bae, Hansol; Simonsen, Henrik Toft</p> <p>2018-05-24</p> <p>During three decades the moss Physcomitrella patens has been developed to a superb green cell factory with the first commercial products <span class="hlt">on</span> the market. In the past three decades the moss P. patens has been developed from an obscure bryophyte to a model organism in basic <span class="hlt">biology</span>, biotechnology, and synthetic <span class="hlt">biology</span>. Some of the key features of this system include a wide range of Omics technologies, precise genome-engineering via homologous recombination with yeast-like efficiency, a certified good-manufacturing-practice production in bioreactors, successful upscaling to 500 L wave reactors, excellent homogeneity of protein products, superb product stability from batch-to-batch, and a reliable procedure for cryopreservation of cell <span class="hlt">lines</span> in a master cell bank. About a dozen human proteins are being produced in P. patens as potential biopharmaceuticals, some of them are not only similar to their animal-produced counterparts, but are real biobetters with superior performance. A moss-made pharmaceutical successfully passed phase 1 clinical trials, a fragrant moss, and a cosmetic moss-product is already <span class="hlt">on</span> the market, highlighting the economic potential of this synthetic <span class="hlt">biology</span> chassis. Here, we focus <span class="hlt">on</span> the features of mosses as versatile cell factories for synthetic <span class="hlt">biology</span> and their impact <span class="hlt">on</span> metabolic engineering.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006PhRvL..97a7004G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006PhRvL..97a7004G"><span>Flux Cloning in Josephson Transmission <span class="hlt">Lines</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gulevich, D. R.; Kusmartsev, F. V.</p> <p>2006-07-01</p> <p>We describe a novel effect related to the controlled birth of a single Josephson vortex. In this phenomenon, the vortex is <span class="hlt">created</span> in a Josephson transmission <span class="hlt">line</span> at a T-shaped junction. The “baby” vortex arises at the moment when a “mother” vortex propagating in the adjacent transmission <span class="hlt">line</span> passes the T-shaped junction. In order to give birth to a new vortex, the mother vortex must have enough kinetic energy. Its motion can also be supported by an externally applied driving current. We determine the critical velocity and the critical driving current for the creation of the baby vortices and briefly discuss the potential applications of the found effect.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25845210','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25845210"><span>[How to be prudent with synthetic <span class="hlt">biology</span>. Synthetic <span class="hlt">Biology</span> and the precautionary principle].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rodríguez López, Blanca</p> <p>2014-01-01</p> <p>Synthetic <span class="hlt">biology</span> is a new discipline that is twofold: firstly it offers the promise to pay benefits that can alleviate some of the ills that plague mankind; <span class="hlt">On</span> the other hand, like all technologies, holds risks. Given these, the most critical and concerned about the risks, invoke the application of the precautionary principle, common in cases where an activity or new technology <span class="hlt">creates</span> risks to the environment and/or human health, but far from universally accepted happens to be currently one of the most controversial principles. In this paper the question of the risks and benefits of synthetic <span class="hlt">biology</span> and the relevance of applying the precautionary principle are analyzed. To do this we proceed as follows. The first part focuses <span class="hlt">on</span> synthetic <span class="hlt">biology</span>. At first, this discipline is characterized, with special attention to what is novel compared to the known as "genetic engineering". In the second stage both the benefits and the risks associated with it are discussed. The first part concludes with a review of the efforts currently being made to control or minimize the risks. The second part aims to analyze the precautionary principle and its possible relevance to the case of Synthetic <span class="hlt">Biology</span>. At first, the different versions and interpretations of the principle and the various criticisms of which has been the subject are reviewed. Finally, after discarding the Precautionary Principle as an useful tool, it is seen as more appropriate some recent proposals to treat technologies that take into account not only risks but also their benefits.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1995JAP....78.1614M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1995JAP....78.1614M"><span>High-resolution determination of the stress in individual interconnect <span class="hlt">lines</span> and the variation due to electromigration</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ma, Qing; Chiras, S.; Clarke, D. R.; Suo, Z.</p> <p>1995-08-01</p> <p>Large tensile stresses usually exist in metallic interconnect <span class="hlt">lines</span> <span class="hlt">on</span> silicon substrates as a result of thermal mismatch. When a current is subsequently passed any divergence of atomic flux can <span class="hlt">create</span> superimposed stress variations along the <span class="hlt">line</span>. Together, these stresses can significantly influence the growth of voids and therefore affect interconnect reliability. In this work, a high-resolution (˜2 μm) optical spectroscopy method has been used to measure the localized stresses around passivated aluminum <span class="hlt">lines</span> <span class="hlt">on</span> a silicon wafer, both as-fabricated and after electromigration testing. The method is based <span class="hlt">on</span> the piezospectroscopic properties of silicon, specifically the frequency shift of the Raman <span class="hlt">line</span> at 520 R cm-1. By focusing a laser beam at points adjacent to the aluminum <span class="hlt">lines</span>, the Raman signal was excited and collected. The stresses in the aluminum <span class="hlt">lines</span> can then be derived from the stresses in the silicon using finite element methods. Large variations of stress along an electromigration-tested <span class="hlt">line</span> were observed and compared to a theoretical model based <span class="hlt">on</span> differences in effective diffusivities from grain to grain in a polycrystalline interconnect <span class="hlt">line</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3130834','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3130834"><span>Event-based Plausibility Immediately Influences <span class="hlt">On-line</span> Language Comprehension</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Matsuki, Kazunaga; Chow, Tracy; Hare, Mary; Elman, Jeffrey L.; Scheepers, Christoph; McRae, Ken</p> <p>2011-01-01</p> <p>In some theories of sentence comprehension, linguistically-relevant lexical knowledge such as selectional restrictions is privileged in terms of the time-course of its access and influence. We examined whether event knowledge computed by combining multiple concepts can rapidly influence language understanding even in the absence of selectional restriction violations. Specifically, we investigated whether instruments can combine with actions to influence comprehension of ensuing patients. Instrument-verb-patient triplets were <span class="hlt">created</span> in a norming study designed to tap directly into event knowledge. In self-paced reading (Experiment 1), participants were faster to read patient nouns such as hair when they were typical of the instrument-action pair (Donna used the shampoo to wash vs. the hose to wash). Experiment 2 showed that these results were not due to direct instrument-patient relations. Experiment 3 replicated Experiment 1 using eyetracking, with effects of event typicality observed in first fixation and gaze durations <span class="hlt">on</span> the patient noun. This research demonstrates that conceptual event-based expectations are computed and used rapidly and dynamically during <span class="hlt">on-line</span> language comprehension. We discuss relationships among plausibility and predictability, as well as their implications. We conclude that selectional restrictions may be best considered as event-based conceptual knowledge, rather than lexical-grammatical knowledge. PMID:21517222</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28067431','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28067431"><span>Analysis of undergraduate cell <span class="hlt">biology</span> contents in Brazilian public universities.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mermelstein, Claudia; Costa, Manoel Luis</p> <p>2017-04-01</p> <p>The enormous amount of information available in cell <span class="hlt">biology</span> has <span class="hlt">created</span> a challenge in selecting the core concepts we should be teaching our undergraduates. One way to define a set of essential core ideas in cell <span class="hlt">biology</span> is to analyze what a specific cell <span class="hlt">biology</span> community is teaching their students. Our main objective was to analyze the cell <span class="hlt">biology</span> content currently being taught in Brazilian universities. We collected the syllabi of cell <span class="hlt">biology</span> courses from public universities in Brazil and analyzed the frequency of cell <span class="hlt">biology</span> topics in each course. We also compared the Brazilian data with the contents of a major cell <span class="hlt">biology</span> textbook. Our analysis showed that while some cell <span class="hlt">biology</span> topics such as plasma membrane and cytoskeleton was present in ∼100% of the Brazilian curricula analyzed others such as cell signaling and cell differentiation were present in only ∼35%. The average cell <span class="hlt">biology</span> content taught in the Brazilian universities is quite different from what is presented in the textbook. We discuss several possible explanations for these observations. We also suggest a list with essential cell <span class="hlt">biology</span> topics for any <span class="hlt">biological</span> or biomedical undergraduate course. The comparative discussion of cell <span class="hlt">biology</span> topics presented here could be valuable in other educational contexts. © 2017 The Authors. Cell <span class="hlt">Biology</span> International Published by John Wiley & Sons Ltd <span class="hlt">on</span> behalf of International Federation of Cell <span class="hlt">Biology</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4344840','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4344840"><span><span class="hlt">Creating</span> and Selling Embryos for “Donation”: Ethical Challenges</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Klitzman, Robert; Sauer, Mark V.</p> <p>2015-01-01</p> <p>The commercial creation and sale of embryos has begun, posing a series of ethical questions that have received little scholarly attention. Some of the concerns that arise are similar to those posed by the sale of gametes, while other issues differ markedly. Questions emerge, firstly, regarding the rights of the unborn children – their ability to know their <span class="hlt">biological</span> parents. Companies that <span class="hlt">create</span> human embryos de novo may wish to keep gamete providers anonymous. Many of these offspring will thus never learn that their parents are not their <span class="hlt">biological</span> parents. Yet, such disclosures – regarding not only one, but both of these <span class="hlt">biological</span> parents – may be important for these individuals; and lack of this knowledge may impede their physical and psychological health. Secondly, questions surface regarding the fees that providers should charge for embryos, and whether these amounts should vary based <span class="hlt">on</span> the traits of one or both of the gamete donors. Some prospective parents may seek specific traits in a baby (e.g., height or eye/hair coloring), prompting creation of embryos from two gamete donors who possess these characteristics. Thirdly, ownership of embryos <span class="hlt">created</span> without an advanced directive by patients poses dilemmas – e.g., disposition of any remaining embryos. Fourthly, guidelines do not yet exist to limit the number of embryos sold from each pair of gamete donors. Hence, unbeknownst to each other, full siblings could potentially meet, get married and procreate. This discussion has several critical implications for future practice, and professional education and policy. Patients with diseases associated with genetic tests may well ask obstetricians, gynecologists and other physicians about these techniques and practices. Clinicians can refer such patients to Assisted Reproductive Technology specialists, but familiarity with the basic aspects of the issues and complexities involved could aid themselves and their patients Several of these issues can be</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23134816','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23134816"><span>Boolean network inference from time series data incorporating prior <span class="hlt">biological</span> knowledge.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Haider, Saad; Pal, Ranadip</p> <p>2012-01-01</p> <p>Numerous approaches exist for modeling of genetic regulatory networks (GRNs) but the low sampling rates often employed in <span class="hlt">biological</span> studies prevents the inference of detailed models from experimental data. In this paper, we analyze the issues involved in estimating a model of a GRN from single cell <span class="hlt">line</span> time series data with limited time points. We present an inference approach for a Boolean Network (BN) model of a GRN from limited transcriptomic or proteomic time series data based <span class="hlt">on</span> prior <span class="hlt">biological</span> knowledge of connectivity, constraints <span class="hlt">on</span> attractor structure and robust design. We applied our inference approach to 6 time point transcriptomic data <span class="hlt">on</span> Human Mammary Epithelial Cell <span class="hlt">line</span> (HMEC) after application of Epidermal Growth Factor (EGF) and generated a BN with a plausible <span class="hlt">biological</span> structure satisfying the data. We further defined and applied a similarity measure to compare synthetic BNs and BNs generated through the proposed approach constructed from transitions of various paths of the synthetic BNs. We have also compared the performance of our algorithm with two existing BN inference algorithms. Through theoretical analysis and simulations, we showed the rarity of arriving at a BN from limited time series data with plausible <span class="hlt">biological</span> structure using random connectivity and absence of structure in data. The framework when applied to experimental data and data generated from synthetic BNs were able to estimate BNs with high similarity scores. Comparison with existing BN inference algorithms showed the better performance of our proposed algorithm for limited time series data. The proposed framework can also be applied to optimize the connectivity of a GRN from experimental data when the prior <span class="hlt">biological</span> knowledge <span class="hlt">on</span> regulators is limited or not unique.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70039518','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70039518"><span>Elevated CO2 did not mitigate the effect of a short-term drought <span class="hlt">on</span> <span class="hlt">biological</span> soil crusts</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Wertin, Timothy M.; Phillips, Susan L.; Reed, Sasha C.; Belnap, Jayne</p> <p>2012-01-01</p> <p><span class="hlt">Biological</span> soil crusts (biocrusts) are critical components of arid and semi-arid ecosystems that contribute significantly to carbon (C) and nitrogen (N) fixation, water retention, soil stability, and seedling recruitment. While dry-land ecosystems face a number of environmental changes, our understanding of how biocrusts may respond to such perturbation remains notably poor. To determine the effect that elevated CO2 may have <span class="hlt">on</span> biocrust composition, cover, and function, we measured percent soil surface cover, effective quantum yield, and pigment concentrations of naturally occurring biocrusts growing in ambient and elevated CO2 at the desert study site in Nevada, USA, from spring 2005 through spring 2007. During the experiment, a year-long drought allowed us to explore the interacting effects that elevated CO2 and water availability may have <span class="hlt">on</span> biocrust cover and function. We found that, regardless of CO2 treatment, precipitation was the major regulator of biocrust cover. Drought reduced moss and lichen cover to near-zero in both ambient and elevated CO2 plots, suggesting that elevated CO2 did not alleviate water stress or increase C fixation to levels sufficient to mitigate drought-induced reduction in cover. In <span class="hlt">line</span> with this result, lichen quantum yield and soil cyanobacteria pigment concentrations appeared more strongly dependent upon recent precipitation than CO2 treatment, although we did find evidence that, when hydrated, elevated CO2 increased lichen C fixation potential. Thus, an increase in atmospheric CO2 may only benefit biocrusts if overall climate patterns shift to <span class="hlt">create</span> a wetter soil environment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26693938','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26693938"><span>Second-<span class="hlt">line</span> chemotherapy in advanced biliary cancer progressed to first-<span class="hlt">line</span> platinum-gemcitabine combination: a multicenter survey and pooled analysis with published data.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fornaro, Lorenzo; Vivaldi, Caterina; Cereda, Stefano; Leone, Francesco; Aprile, Giuseppe; Lonardi, Sara; Silvestris, Nicola; Santini, Daniele; Milella, Michele; Caparello, Chiara; Musettini, Gianna; Pasquini, Giulia; Falcone, Alfredo; Brandi, Giovanni; Sperduti, Isabella; Vasile, Enrico</p> <p>2015-12-23</p> <p>After progression to a standard first-<span class="hlt">line</span> platinum and gemcitabine combination (GP), there is no established second-<span class="hlt">line</span> therapy for patients with advanced biliary tract cancers (aBTC). Indeed, literature data suggest limited activity of most second-<span class="hlt">line</span> agents evaluated so far. We collected a large retrospective series of aBTC patients treated with second-<span class="hlt">line</span> chemotherapy after progression to a first-<span class="hlt">line</span> GP regimen at different Italian institutions. We then pooled the data with those reported in previous studies, which were identified with a Medline search and the <span class="hlt">on-line</span> abstract datasets of major international oncology meetings. A total of 174 patients were included in the multicenter survey: response rate (RR) with second-<span class="hlt">line</span> chemotherapy was low (3.4 %), with median PFS and OS of 3.0 months and 6.6 months, respectively. At multivariate analysis, preserved performance status, low CA19.9 levels and absence of distant metastases were favorable prognostic factors. Data from other five presented or published series were identified, for a total of 499 patients included in the pooled analysis. The results confirmed marginal activity of second-<span class="hlt">line</span> chemotherapy (RR: 10.2 %), with limited efficacy in unselected patient populations (median PFS: 3.1 months; median OS: 6.3 months). The current analysis highlights the limited value of second-<span class="hlt">line</span> chemotherapy after a first-<span class="hlt">line</span> GP combination in aBTC. While waiting for effective <span class="hlt">biologic</span> agents in this setting, ongoing randomized trials will identify the optimal second-<span class="hlt">line</span> chemotherapy regimen and validate prognostic factors for individual patient management.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27602719','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27602719"><span>The Dark Matter of <span class="hlt">Biology</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ross, Jennifer L</p> <p>2016-09-06</p> <p>The inside of the cell is full of important, yet invisible species of molecules and proteins that interact weakly but couple together to have huge and important effects in many <span class="hlt">biological</span> processes. Such "dark matter" inside cells remains mostly hidden, because our tools were developed to investigate strongly interacting species and folded proteins. Example dark-matter species include intrinsically disordered proteins, posttranslational states, ion species, and rare, transient, and weak interactions undetectable by biochemical assays. The dark matter of <span class="hlt">biology</span> is likely to have multiple, vital roles to regulate signaling, rates of reactions, water structure and viscosity, crowding, and other cellular activities. We need to <span class="hlt">create</span> new tools to image, detect, and understand these dark-matter species if we are to truly understand fundamental physical principles of <span class="hlt">biology</span>. Copyright © 2016 Biophysical Society. Published by Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018R%26QE...60..779G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018R%26QE...60..779G"><span><span class="hlt">On</span> the Possibility of <span class="hlt">Creating</span> a Point-Like Neutron Source</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Golubev, S. V.; Skalyga, V. A.; Izotov, I. V.; Sidorov, A. V.; Razin, S. V.; Shaposhnikov, R. A.; Lapin, R. L.; Bokhanov, A. F.; Kazakov, M. Yu.</p> <p>2018-03-01</p> <p>We consider the possibility of <span class="hlt">creating</span> a compact high-power neutron generator with a small emitting area (of the order of 100 μm) and a neutron yield of 1010s-1 <span class="hlt">on</span> the basis of a deuterium-deuterium fusion reaction (or 1012 s-1 <span class="hlt">on</span> the basis of a deuterium-tritium fusion reaction). The fusion takes place under bombardment of a deuterium- (or tritium-) saturated target by a high-current (about 100 mA) focused deuterium ion beam with an energy of 100 keV. The ion beam with total current at a level of hundreds of milliamperes and small emittance (less than 0.1 π·mm·mrad), which is crucial for sharp focusing, can be generated by a quasi-gas-dynamic ion source of a new generation <span class="hlt">created</span> <span class="hlt">on</span> the basis of a discharge in an open magnetic trap sustained by high-power electromagnetic radiation of the millimeter wavelength range under electron cyclotron resonance conditions. Simulations of the focusing system for the experimentally obtained ion beam show the possibility to <span class="hlt">create</span> a deuterium ion beam with a transverse size of 200 μm <span class="hlt">on</span> the neutron-forming target. Prospects for using such a neutron source for neutron tomography are discussed.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_25 --> <div class="footer-extlink text-muted" style="margin-bottom:1rem; text-align:center;">Some links on this page may take you to non-federal websites. 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