Sample records for kaart jaan praks
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PRAK, a novel protein kinase regulated by the p38 MAP kinase.
New, L; Jiang, Y; Zhao, M; Liu, K; Zhu, W; Flood, L J; Kato, Y; Parry, G C; Han, J
1998-01-01
We have identified and cloned a novel serine/ threonine kinase, p38-regulated/activated protein kinase (PRAK). PRAK is a 471 amino acid protein with 20-30% sequence identity to the known MAP kinase-regulated protein kinases RSK1/2/3, MNK1/2 and MAPKAP-K2/3. PRAK was found to be expressed in all human tissues and cell lines examined. In HeLa cells, PRAK was activated in response to cellular stress and proinflammatory cytokines. PRAK activity was regulated by p38alpha and p38beta both in vitro and in vivo and Thr182 was shown to be the regulatory phosphorylation site. Activated PRAK in turn phosphorylated small heat shock protein 27 (HSP27) at the physiologically relevant sites. An in-gel kinase assay demonstrated that PRAK is a major stress-activated kinase that can phosphorylate small heat shock protein, suggesting a potential role for PRAK in mediating stress-induced HSP27 phosphorylation in vivo. PMID:9628874
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2006-05-30
Cheng et al., 2006; Luning Prak and O’Sullivan, 2006; Monteil- Rivera et al., 2005; Monteil-Rivera et al., 2006), formal technical report (Walker et... Luning Prak and O’Sullivan. 2006, Monteil-Rivera et al. 2005, Monteil-Rivera, et al. 2006), formal technical report (Walker et al. 2006), and invited...by Pseudoxanthomonas sp. JA40. J. Young Investigators. (in submission) D) Luning Prak, D. J., and D. W. O’Sullivan. 2006. Solubility of 2,4
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2011-05-12
Dinitrobenzaldehyde from Solubility Values in Pure Water and Seawater at Temperatures between (280 and 313) K Dianne J. Luning Prak* and Daniel W. O’Sullivan...1998, 37, 25–31. (7) O’Sullivan, D. W.; Denzel, J. R.; Luning Prak, D. J. Photolysis of 2,4-Dinitrotoluene and 2,6-Dinitrotoluene in Seawater. Aquat...Solubility of Aromatic Compounds.Chemosphere 1984, 13, 881–888. (13) Luning Prak, D. J.; O’Sullivan, D. W. Solubility of 2,4-Dini- trotoluene and 2,4,6
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2013-06-01
SAE Int. J. Engines, vol. 1, no. 1, 2008. [12] P. A. Caton, S. A.Williams, R. A. Kamin, D. Luning -Prak, L. J. Hamilton and J. S. Cowart...Detroit, MI, Feb. 27- Mar. 2, 1984. [14] J. Cowart, M. Carr, P. Caton, L. Stoulig, D. Luning -Prak, A. Moore and L. Hamilton, “High Cetane Fuel Combustion
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Zhang, Ling; Du, Jianfeng; Yano, Naohiro; Wang, Hao; Zhao, Yu Tina; Dubielecka, Patrycja M; Zhuang, Shougang; Chin, Y Eugene; Qin, Gangjian; Zhao, Ting C
2017-08-01
Histone deacetylases are recently identified to act as key regulators for cardiac pathophysiology and metabolic disorders. However, the function of histone deacetylase (HDAC) in controlling cardiac performance in Type II diabetes and obesity remains unknown. Here, we determine whether HDAC inhibition attenuates high fat diet (HFD)-induced cardiac dysfunction and improves metabolic features. Adult mice were fed with either HFD or standard chow food for 24 weeks. Starting at 12 weeks, mice were divided into four groups randomly, in which sodium butyrate (1%), a potent HDAC inhibitor, was provided to chow and HFD-fed mice in drinking water, respectively. Glucose intolerance, metabolic parameters, cardiac function, and remodeling were assessed. Histological analysis and cellular signaling were examined at 24 weeks following euthanization of mice. HFD-fed mice demonstrated myocardial dysfunction and profound interstitial fibrosis, which were attenuated by HDAC inhibition. HFD-induced metabolic syndrome features insulin resistance, obesity, hyperinsulinemia, hyperglycemia, lipid accumulations, and cardiac hypertrophy, these effects were prevented by HDAC inhibition. Furthermore, HDAC inhibition attenuated myocyte apoptosis, reduced production of reactive oxygen species, and increased angiogenesis in the HFD-fed myocardium. Notably, HFD induced decreases in MKK3, p38, p38 regulated/activated protein kinase (PRAK), and Akt-1, but not p44/42 phosphorylation, which were prevented by HDAC inhibition. These results suggest that HDAC inhibition plays a critical role to preserve cardiac performance and mitigate metabolic disorders in obesity and diabetes, which is associated with MKK3/p38/PRAK pathway. The study holds promise in developing a new therapeutic strategy in the treatment of Type II diabetic-induced heart failure and metabolic disorders. J. Cell. Biochem. 118: 2395-2408, 2017. © 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.
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Social Contributions to the Equilibration of Action Schemes: A Longitudinal Study of Locomotion.
ERIC Educational Resources Information Center
Lightfoot, Cynthia
According to Jaan Valsiner, development takes place within culturally structured environments jointly organized by the activities of children and the people around them. When overlap between promoted activity and the child's zone of proximal development exists, the structure of action that results from the interplay of the two is internalized by…
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US National Economic Security in a Global Market
1990-01-01
13 (D) the Secretary of Commerce , 14 ( E ) the Secretary of Treasury, 15 (F) the United States Trade Representative, 16 and _ 17 (G) the Director of...OTe F!LE COPY --- National Security Program 00 N US NATIONAL ECONOMIC SECURITY IN A GLOBAL MARKET :I . DTIC ELECTE JAN14 1991 m S E D HARVARD...importantly, will become 5 I I ,,!"C is merica _ _ _ _ 44% 5AlAN leact rustwrthv __ 29% ’,’EST (E7,1RM.’y ,a ]i,- :. . 8 %FFR ANC E - 5% BRITAIN Does Jaan
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Activation and Function of the MAPKs and Their Substrates, the MAPK-Activated Protein Kinases
Cargnello, Marie; Roux, Philippe P.
2011-01-01
Summary: The mitogen-activated protein kinases (MAPKs) regulate diverse cellular programs by relaying extracellular signals to intracellular responses. In mammals, there are more than a dozen MAPK enzymes that coordinately regulate cell proliferation, differentiation, motility, and survival. The best known are the conventional MAPKs, which include the extracellular signal-regulated kinases 1 and 2 (ERK1/2), c-Jun amino-terminal kinases 1 to 3 (JNK1 to -3), p38 (α, β, γ, and δ), and ERK5 families. There are additional, atypical MAPK enzymes, including ERK3/4, ERK7/8, and Nemo-like kinase (NLK), which have distinct regulation and functions. Together, the MAPKs regulate a large number of substrates, including members of a family of protein Ser/Thr kinases termed MAPK-activated protein kinases (MAPKAPKs). The MAPKAPKs are related enzymes that respond to extracellular stimulation through direct MAPK-dependent activation loop phosphorylation and kinase activation. There are five MAPKAPK subfamilies: the p90 ribosomal S6 kinase (RSK), the mitogen- and stress-activated kinase (MSK), the MAPK-interacting kinase (MNK), the MAPK-activated protein kinase 2/3 (MK2/3), and MK5 (also known as p38-regulated/activated protein kinase [PRAK]). These enzymes have diverse biological functions, including regulation of nucleosome and gene expression, mRNA stability and translation, and cell proliferation and survival. Here we review the mechanisms of MAPKAPK activation by the different MAPKs and discuss their physiological roles based on established substrates and recent discoveries. PMID:21372320
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Paliga, Andrew J M; Natale, David R; Watson, Andrew J
2005-08-01
The MAPK (mitogen-activated protein kinase) superfamily of proteins consists of four separate signalling cascades: the c-Jun N-terminal kinase or stress-activated protein kinases (JNK/SAPK); the ERKs (extracellular-signal-regulated kinases); the ERK5 or big MAPK1; and the p38 MAPK group of protein kinases, all of which are highly conserved. To date, our studies have focused on defining the role of the p38 MAPK pathway during preimplantation development. p38 MAPK regulates actin filament formation through the downstream kinases MAPKAPK2/3 (MAPK-activated protein kinase 2/3) or MAPKAPK5 [PRAK (p38 regulated/activated kinase)] and subsequently through HSP25/27 (heat-shock protein 25/27). We recently reported that 2-cell-stage murine embryos treated with cytokine-suppressive anti-inflammatory drugs (CSAIDtrade mark; SB203580 and SB220025) display a reversible blockade of development at the 8-16-cell stage, indicating that p38 (MAPK) activity is required to complete murine preimplantation development. In the present study, we have investigated the stage-specific action and role of p38 MAPK in regulating filamentous actin during murine preimplantation development. Treatment of 8-cell-stage embryos with SB203580 and SB220025 (CSAIDtrade mark) resulted in a blockade of preimplantation development, loss of rhodamine phalloidin fluorescence, MK-p (phosphorylated MAPKAPK2/3), HSP-p (phosphorylated HSP25/27) and a redistribution of alpha-catenin immunofluorescence by 12 h of treatment. In contrast, treatment of 2- and 4-cell-stage embryos with CSAIDtrade mark drugs resulted in a loss of MK-p and HSP-p, but did not result in a loss of rhodamine phalloidin fluorescence. All these effects of p38 MAPK inhibition were reversed upon removal of the inhibitor, and development resumed in a delayed but normal manner to the blastocyst stage. Treatment of 8-cell embryos with PD098059 (ERK pathway inhibitor) did not affect development or fluorescence of MK-p, HSP-p or rhodamine phalloidin
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ERIC Educational Resources Information Center
Lee, Lung-Sheng; Chen, Ya-Yan
In Taiwan, human resource development (HRD) is defined as the systematic education, training, and development employers provide for their employees as well as organizational development for corporations. A history of HRD development indicates that in the 1960s, the government began to implement planning measures for HRD in business and industry;…
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ERIC Educational Resources Information Center
Youniss, James
1994-01-01
Briefly summarizes Vygotsky's life, the appeal and subsequent abandonment of his ideas in the 1960s, and renewal of interest in the 1970s and 1980s (often at the expense of Piaget). Praises van der Veer and Valsinger's book as a realistic picture of Vygotsky's background, life, and work, of the scientific and political context in Russia and of his…
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van Doorn, J.; Hollinger, T. C.; Oudega, B.
2001-01-01
A sensitive and specific detection method was developed for Xanthomonas hyacinthi; this method was based on amplification of a subsequence of the type IV fimbrial-subunit gene fimA from strain S148. The fimA gene was amplified by PCR with degenerate DNA primers designed by using the N-terminal and C-terminal amino acid sequences of trypsin fragments of FimA. The nucleotide sequence of fimA was determined and compared with the nucleotide sequences coding for the fimbrial subunits in other type IV fimbria-producing bacteria, such as Xanthomonas campestris pv. vesicatoria, Neisseria gonorrhoeae, and Moraxella bovis. In a PCR internal primers JAAN and JARA, designed by using the nucleotide sequences of the variable central and C-terminal region of fimA, amplified a 226-bp DNA fragment in all X. hyacinthi isolates. This PCR was shown to be pathovar specific, as assessed by testing 71 Xanthomonas pathovars and bacterial isolates belonging to other genera, such as Erwinia and Pseudomonas. Southern hybridization experiments performed with the labelled 226-bp DNA amplicon as a probe suggested that there is only one structural type IV fimbrial-gene cluster in X. hyacinthi. Only two Xanthomonas translucens pathovars cross-reacted weakly in PCR. Primers amplifying a subsequence of the fimA gene of X. campestris pv. vesicatoria (T. Ojanen-Reuhs, N. Kalkkinen, B. Westerlund-Wikström, J. van Doorn, K. Haahtela, E.-L. Nurmiaho-Lassila, K. Wengelink, U. Bonas, and T. K. Korhonen, J. Bacteriol. 179: 1280–1290, 1997) were shown to be pathovar specific, indicating that the fimbrial-subunit sequences are more generally applicable in xanthomonads for detection purposes. Under laboratory conditions, approximately 1,000 CFU of X. hyacinthi per ml could be detected. In inoculated leaves of hyacinths the threshold was 5,000 CFU/ml. The results indicated that infected hyacinths with early symptoms could be successfully screened for X. hyacinthi with PCR. PMID:11157222
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Hydraulic risk assessment of bridges using UAV photogrammetry
NASA Astrophysics Data System (ADS)
Hackl, Jürgen; Adey, Bryan T.; Woźniak, Michał; Schümperlin, Oliver
2017-04-01
investigated includes: the use of geo-referenced images, taken by an UAV, the exportation of these images into a photogrammetric software, the creation of a 3D mesh of the terrain from these images, the conversion of the 3D mesh to a computational mesh, the use of the computational mesh to build a hydrodynamic model, and the use of the hydrodynamic model to run flow simulations. The process was used to estimate the complex water flow near a single span concrete bridge in the Canton of Grisons, Switzerland. The hydraulic events (abutment scour and overflow) predicted by the developed model were compared with with historical observations from a recent flood event in the region. The hydraulic events predicted by the developed model correspond with historical observations, indicating that the topological information collected in this way is sufficiently accurate to be used to simulate complex flow situations, which can be used in bridge risk assessments. Hackl, J., Adey, B.T., Heitzler, M., and Iosifescu Enescu, I. (2015). "An Overarching Risk Assessment Process to Evaluate the Risks Associated with Infrastructure Networks due to Natural Hazards." International Journal of Performability Engineering, 11(2), 153-168. Adey, B.T., Hackl, J., Lam, J.C., van Gelder, P., Prak, P., van Erp, N., Heitzler, M., Iosifescu Enescu, I., and Hurni, L. (2016). "Ensuring acceptable levels of infrastructure related risks due to natural hazards with emphasis on conducting stress tests." 1st International Symposium on Infrastructure Asset Management (SIAM2016), K. Kobayashi, ed., Kyoto, Japan, 19-29 (Jan).
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The member of the Academy H.P. Keres and the Relativity theory in Estonia
NASA Astrophysics Data System (ADS)
Kuusk, P.; Muursepp, P. V.; Piir, Ivar
1987-10-01
The first popular lecture on the Einstein theory of relativity was given in Estonia already in 1914 by Jaan Sarv (1877-1954)[1],afterwards a professor of mathematics at the Tartu University. The first student courses on special relativity were delivered by Professor of Mathematics Juri Nuut (1892-1952): non-Euclidean geometry (1930), the mathematical theory of relativity (1932/1933),the Lorenz transformations (1937). His own research work concerned the Lobachevsky geometry [7] and its application to cosmology [6]. Harald Keres qraguated from the Tartu University in 1936. He gave the first student course on general relativity (based on books [11-14]in 1940.In 1942,he got the dr.phil.nat degree form the Tartu University for his theses "Raum und Zeit in der allgemeinen Relativitatstheorie". The degree of the doctor of mathematical and physical sciences was confirmed by VAK (the All-Union Higher Attestation Commission) in 1949.In this period, he got aquainted with the leading Soviet scientists working on General Relativity, prof.V.A.Fock,Prof.D.D.Ivanenko,Prof.A.Z.Petrov,and Prof.M.F.Shirokov. After World War two all-union university courses were introduced in Tartu State University. According to the curriculum of the course the special theory of relativity is a part of electrodynamics obligatory for all students of the department of Physics. From 1947 till 1985 this course was delivered by Prof.PaulKard(1914-1985).He also published a number of text-books on the subject [15-19]. The general theory of relativity was read by Prof.H.Keres in 1951-1960 and later by his pupils R.Lias and A.Koppel [20-23] as a special course for students specializing in theoretical Physics. The first PHD-s in general relativity were made by R.Lias [27](1954) and I.Piir [28] (1955). In 1961, Prof.H.Keres was elected a member of the Academy of Sciences of the Estonian S.S.R. He left the TArtu State University and began to work in the Institute of Physics as the head of the Department of