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1
Mechanism of Abnormal Cell-Extracellular Matrix Interactions ...
1997-10-01

... Descriptors : *CELL STRUCTURE, *BREAST CANCER, MEMBRANES( BIOLOGY), CELLS, PROTEINS, NEOPLASMS, CHAINS, MOLECULAR ...

DTIC Science & Technology

2
Effects of inherited membrane abnormalities on the viscoelastic properties of erythrocyte membrane.
1987-03-01

Several workers have identified molecular abnormalities associated with inherited blood disorders. The present work examines how these alterations in molecular structure affect the viscoelastic properties of the red blood cell membrane. Changes in the membrane shear modulus, the membrane viscosity, and the apparent ...

PubMed Central

3
Effects of production of abnormal proteins on the rate of killing of Escherichia coli by streptomycin.
1990-04-01

The role of abnormal membrane proteins in modulating the rate of killing by streptomycin was investigated. Davis et al. (B.D. Davis, L. Chen, and P.T. Tai, Proc. Natl. Acad. Sci. USA 83:6164-6168, 1986) have proposed that misread membrane proteins created by the action of streptomycin on ...

PubMed Central

4
SecY alterations that impair membrane protein folding and generate a membrane stress.
2007-01-22

We report on a class of Escherichia coli SecY mutants that impair membrane protein folding. The mutants also up-regulate the Cpx/sigma(E) stress response pathways. Similar stress induction was also observed in response to a YidC defect in membrane protein biogenesis but not in response to the signal recognition ...

PubMed

5
Hereditary spherocytosis
1975-10-01

Studies of the clinical features of hereditary spherocytosis since 1871 and laboratory investigation of the cellular abnormalities since 1940 have led to the characterization of hereditary spherocytosis as a prime example of a Mendelian dominant, genetically determined disorder of the erythrocyte membrane. This review of hereditary spherocytosis emphasizes ...

Energy Citations Database

6
Biomembrane and receptor mechanisms
1987-01-01

This book cover the reviews on biomembrane dynamics; recent spectroscopic studies. Topics covered are freeze fracture: Seeing and thinking biological membranes, membrane proteins and receptors: structure and organisation; techniques to determine the transbilayer distribution and mobility of phospholipids in biological ...

Energy Citations Database

7
Prion-Induced Amyloid Heart Disease with High Blood Infectivity in Transgenic Mice

... lacking the glycophosphatydylinositol membrane anchor. In the brain, blood, and heart, both abnormal protease-resistant prion protein ( ... nontransgenic recipients. The titer of infectious scrapie in bloo...

NBII National Biological Information Infrastructure

8
Determining nuclear shape

Changes in nuclear morphology are observed in diverse developmental processes as well as in pathological conditions. Modification of nuclear membrane and nuclear lamina protein levels results in altered nuclear shapes, as it has been demonstrated in experimental systems ranging from yeast to human cells. The important role of nuclear ...

PubMed Central

9
Lipid requirements for endocytosis in yeast.
2006-08-15

Endocytosis is, besides secretion, the most prominent membrane transport pathway in eukaryotic cells. In membrane transport, defined areas of the donor membranes engulf solutes of the compartment they are bordering and bud off with the aid of coat proteins to form vesicles. These transport vehicles are guided along ...

PubMed

10
Lysosomal fusion and SNARE function are impaired by cholesterol accumulation in lysosomal storage disorders.
2010-09-24

The function of lysosomes relies on the ability of the lysosomal membrane to fuse with several target membranes in the cell. It is known that in lysosomal storage disorders (LSDs), lysosomal accumulation of several types of substrates is associated with lysosomal dysfunction and impairment of endocytic membrane traffic. By analysing ...

PubMed

11
CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.
2010-09-01

Mutations in human CEP290 cause cilia-related disorders that range in severity from isolated blindness to perinatal lethality. Here, we describe a Chlamydomonas reinhardtii mutant in which most of the CEP290 gene is deleted. Immunoelectron microscopy indicated that CEP290 is located in the flagellar transition zone in close association with the prominent microtubule-membrane ...

PubMed

12
CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content
2010-09-06

Mutations in human CEP290 cause cilia-related disorders that range in severity from isolated blindness to perinatal lethality. Here, we describe a Chlamydomonas reinhardtii mutant in which most of the CEP290 gene is deleted. Immunoelectron microscopy indicated that CEP290 is located in the flagellar transition zone in close association with the prominent microtubule�membrane ...

PubMed Central

13
Studies on the synthesis of plasma membrane proteins of fibroblasts from patients with cystic fibrosis.
1975-08-01

The characteristic increased salinity of sweat and other abnormalities of exocrine secretions in patients with cystic fibrosis (CF) suggest the possibility of a disturbed functioning of the plasma membrane in this disease. Several lines of evidence indicate that fibroblasts express the presence of the CF genotype. Therefore these cells were used in an in ...

PubMed Central

14
Clinicopathologic abnormalities associated with snake envenomation in domestic animals.
2011-08-09

Envenomation of domestic animals by snakes occurs frequently in certain geographic areas. However, reports describing clinical signs, clinicopathologic abnormalities, therapeutic approaches, and outcomes are sparse. This review summarizes various snake families, venom types associated with harmful snakes, and the significant hematologic, hemostatic, and biochemical ...

PubMed

15
Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
1982-02-01

Human erythrocytes possess a lattice work of extrinsic proteins on the inner face of the membrane (;cytoskeleton') that maintains the shape and deformability of the cell. The major proteins of the cytoskeleton are spectrin and actin, which are attached to the membrane by protein bands 2.1 ...

PubMed

16
Leaf Senescence in a Nonyellowing Mutant of Festuca pratensis: Metabolism of Cytochrome f.
1990-06-01

In a mutant genotype of Festuca pratensis Huds., net degradation of a number of thylakoid membrane proteins during senescence is impaired. Previous studies have suggested that the highly hydrophobic intrinsic chlorophyll-binding proteins were the definitive subjects of the metabolic lesion. In the present study we find that cytochrome ...

PubMed

17
Leaf Senescence in a Nonyellowing Mutant of Festuca pratensis1
1990-06-01

In a mutant genotype of Festuca pratensis Huds., net degradation of a number of thylakoid membrane proteins during senescence is impaired. Previous studies have suggested that the highly hydrophobic intrinsic chlorophyll-binding proteins were the definitive subjects of the metabolic lesion. In the present study we find that cytochrome ...

PubMed Central

18
Dysfunction of the Fusion of Pre-Synaptic Plasma Membranes and Synaptic Vesicles Caused by Oxidative Stress, and its Prevention by Vitamin E.
2011-02-14

To define whether hyperoxia induces the dysfunction of membrane fusion between synaptic vesicles with pre-synaptic plasma membranes in the nerve terminals, and whether vitamin E prevents this abnormal event, we investigated the influence of hyperoxia on the fusion ability of isolated synaptic vesicles and the inside-out type ...

PubMed

19
The mutant axolotl Short toes exhibits impaired limb regeneration and abnormal basement membrane formation.
1992-06-15

The mutant axolotl Short toes develops with abnormal kidneys, Mullerian ducts, and limbs and provides one of the few experimental systems for developmental studies in amphibia. The present paper describes another deviation from this animal's normal physiology, which is very characteristic of the wild type: amputated limbs of Short toes fail to regenerate. A blastema is formed ...

PubMed Central

20
The Mitochondrial Inner Membrane Protein Mitofilin Controls Cristae MorphologyD?
2005-03-01

Mitochondria are complex organelles with a highly dynamic distribution and internal organization. Here, we demonstrate that mitofilin, a previously identified mitochondrial protein of unknown function, controls mitochondrial cristae morphology. Mitofilin is enriched in the narrow space between the inner boundary and the outer membranes, where it forms a ...

PubMed Central

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21
Gene Structure and Functional Analysis of the Mouse Nidogen-2 Gene: Nidogen-2 Is Not Essential for Basement Membrane Formation in Mice
2002-01-01

Nidogens are highly conserved proteins in vertebrates and invertebrates and are found in almost all basement membranes. According to the classical hypothesis of basement membrane organization, nidogens connect the laminin and collagen IV networks, so stabilizing the basement membrane, and integrate other ...

E-print Network

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