alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.
about
Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase IDystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy geneImmunohistochemical distribution of basement membrane proteins in the human inner ear from older subjectsMutations 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.Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparinThe dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membraneMechanistic distinctions between agrin and laminin-1 induced aggregation of acetylcholine receptorsSarcoglycan isoforms in skeletal muscleIntegrins as receptors for lamininsLaminin-10/11 and fibronectin differentially prevent apoptosis induced by serum removal via phosphatidylinositol 3-kinase/Akt- and MEK1/ERK-dependent pathwaysDystrophin-glycoprotein complex and Ras and Rho GTPase signaling are altered in muscle atrophyIdentification of new dystroglycan complexes in skeletal musclePregnancy-induced amelioration of muscular dystrophy phenotype in mdx mice via muscle membrane stabilization effect of glucocorticoidDynamic restoration of dystrophin to dystrophin-deficient myotubes.Dystroglycan and mitochondrial ribosomal protein L34 regulate differentiation in the Drosophila eye.Plasma membrane cytoskeleton of muscle: a fine structural analysis.Sarcoglycans in muscular dystrophy.LARGE expression augments the glycosylation of glycoproteins in addition to α-dystroglycan conferring laminin binding.Retinal ectopias and mechanically weakened basement membrane in a mouse model of muscle-eye-brain (MEB) disease congenital muscular dystrophyLaminins of the neuromuscular system.Differential glycosylation of α-dystroglycan and proteins other than α-dystroglycan by like-glycosyltransferasePompe disease results in a Golgi-based glycosylation deficit in human induced pluripotent stem cell-derived cardiomyocytes.Breaches of the pial basement membrane are associated with defective dentate gyrus development in mouse models of congenital muscular dystrophiesThe cytoskeleton-associated PDZ-LIM protein, ALP, acts on serum response factor activity to regulate muscle differentiation.Developmental expression of the neuron-specific N-acetylglucosaminyltransferase Vb (GnT-Vb/IX) and identification of its in vivo glycan products in comparison with those of its paralog, GnT-VLaminin-1 redistributes postsynaptic proteins and requires rapsyn, tyrosine phosphorylation, and Src and Fyn to stably cluster acetylcholine receptors.Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation.The roles of integrin-linked kinase in the regulation of myogenic differentiation.Conditional knockout of protein O-mannosyltransferase 2 reveals tissue-specific roles of O-mannosyl glycosylation in brain development.Biochemical and biophysical changes underlie the mechanisms of basement membrane disruptions in a mouse model of dystroglycanopathy.Contributions of the LG modules and furin processing to laminin-2 functions.The role of laminins in the organization and function of neuromuscular junctions.Can Human Pluripotent Stem Cell-Derived Cardiomyocytes Advance Understanding of Muscular Dystrophies?Integrin-mediated muscle cell spreading. The role of protein kinase c in outside-in and inside-out signaling and evidence of integrin cross-talk.Dystrophin mutations predict cellular susceptibility to oxidative stress.RPTPζ/phosphacan is abnormally glycosylated in a model of muscle-eye-brain disease lacking functional POMGnT1Laminin deposition in the extracellular matrix: a complex picture emerges.Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution.An extracellular pathway for dystroglycan function in acetylcholine receptor aggregation and laminin deposition in skeletal myotubes.The significance of post-translational removal of α-DG-N in early stage endometrial cancer development.
P2860
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P2860
alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@ast
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@en
type
label
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@ast
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@en
prefLabel
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@ast
alpha-Dystroglycan is a lamini ...... bes and muscle cell viability.
@en
P2860
P356
P1476
alpha-Dystroglycan is a lamini ...... ubes and muscle cell viability
@en
P2093
M Lindenbaum
S Carbonetto
P2860
P304
P356
10.1083/JCB.145.6.1325
P407
P577
1999-06-01T00:00:00Z