Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function. - Wikidata - wikimedia - TriplyDB

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

http://www.wikidata.org/entity/Q35056189

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O Mannosylation of alpha-dystroglycan is essential for lymphocytic choriomeningitis virus receptor function Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity A role of fukutin, a gene responsible for Fukuyama type congenital muscular dystrophy, in cancer cells: a possible role to suppress cell proliferation Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration Developmental and pathogenic mechanisms of basement membrane assembly Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardation Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductance POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome Traversing the basement membrane in vivo: a diversity of strategies Polarity in mammalian epithelial morphogenesis Caveolae regulation of mechanosensitive channel function in myotubes The Laminin 511/521 binding site on the Lutheran blood group glycoprotein is located at the flexible junction of Ig domains 2 and 3 Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies A Method to Produce and Purify Full-Length Recombinant Alpha Dystroglycan: Analysis of N- and O-Linked Monosaccharide Composition in CHO Cells with or without LARGE Overexpression MEGF9: a novel transmembrane protein with a strong and developmentally regulated expression in the nervous system A rostrocaudal muscular dystrophy caused by a defect in choline kinase beta, the first enzyme in phosphatidylcholine biosynthesis AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality Evidence that dystroglycan is associated with dynamin and regulates endocytosis Laminin-6 assembles into multimolecular fibrillar complexes with perlecan and participates in mechanical-signal transduction via a dystroglycan-dependent, integrin-independent mechanism Brain alpha-dystroglycan displays unique glycoepitopes and preferential binding to laminin-10/11 LARGE2 generates the same xylose- and glucuronic acid-containing glycan structures as LARGE Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan Sugar-free frosting, a homolog of SAD kinase, drives neural-specific glycan expression in the Drosophila embryo.Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study Dynamic developmental elaboration of N-linked glycan complexity in the Drosophila melanogaster embryo.Regulation of mammalian protein O-mannosylation: preferential amino acid sequence for O-mannose modification.Disruption of perlecan binding and matrix assembly by post-translational or genetic disruption of dystroglycan function.C. elegans agrin is expressed in pharynx, IL1 neurons and distal tip cells and does not genetically interact with genes involved in synaptogenesis or muscle function.Uncovering cryptic glycan markers in multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE).Dystrophin glycoprotein complex-associated Gbetagamma subunits activate phosphatidylinositol-3-kinase/Akt signaling in skeletal muscle in a laminin-dependent manner.Glial dystrophin-associated proteins, laminin and agrin, are downregulated in the brain of mdx mouse.Lentiviral vectors can be used for full-length dystrophin gene therapy Increased apoptosis of myoblasts in Drosophila model for the Walker-Warburg syndrome Computational study of the human dystrophin repeats: interaction properties and molecular dynamics.Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes.Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding.Tumor necrosis factor-alpha augments matrix metalloproteinase-9 production in skeletal muscle cells through the activation of transforming growth factor-beta-activated kinase 1 (TAK1)-dependent signaling pathway

P2860

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P2860

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

http://www.wikidata.org/entity/Q35056189

description

2003 nî lūn-bûn

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2003 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի հունվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

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name

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

@ast

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

@en

type

label

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

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Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

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Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

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Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

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Journal of Biological Chemistry

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Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function

@en

P2093

Daniel E Michele

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P2860

Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1

Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy

Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin

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15457-15460

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scholarly article

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10.1074/JBC.R200031200

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18

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278

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Kevin P Campbell

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2003-01-29T00:00:00Z

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10927860

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12556455

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