Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
about
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cellsSarcospan-deficient mice maintain normal muscle functionBrain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophyAnalysis of human sarcospan as a candidate gene for CFEOM1Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophyProteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathyExpression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complexInteractions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinasesSarcoglycan isoforms in skeletal muscleLimb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninLocalization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: triple immunogold labeling electron microscopyThe Dystrophin Complex: Structure, Function, and Implications for TherapyNkx2-5 and Sarcospan genetically interact in the development of the muscular ventricular septum of the heartHigh levels of sarcospan are well tolerated and act as a sarcolemmal stabilizer to address skeletal muscle and pulmonary dysfunction in DMD.Plasma membrane cytoskeleton of muscle: a fine structural analysis.Sarcoglycans in muscular dystrophy.Conservation of components of the dystrophin complex in Drosophila.Laminins and human disease.The molecular neuropathology of the muscular dystrophies: a review and update.Rescue of sarcoglycan mutations by inhibition of endoplasmic reticulum quality control is associated with minimal structural modifications.Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin.Just in time and place: NOS/NO system assembly in neuromuscular junction formation.Our trails and trials in the subsarcolemmal cytoskeleton network and muscular dystrophy researches in the dystrophin era.Dystrobrevin increases dystrophin's binding to the dystrophin-glycoprotein complex and provides protection during cardiac stressPhysiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments.Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex.From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex.Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamsterSarcoglycanopathies: molecular pathogenesis and therapeutic prospectsThe muscular dystrophies: from genes to therapies.A novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins.Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains.alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.Progressive muscular dystrophy in alpha-sarcoglycan-deficient miceDystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice.Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.
P2860
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P2860
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@ast
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en-gb
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@nl
type
label
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@ast
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en-gb
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@nl
prefLabel
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@ast
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en-gb
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@nl
P2093
P2860
P921
P356
P1476
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex
@en
P2093
D P Venzke
J Heighway
K P Campbell
R H Crosbie
P2860
P304
P356
10.1074/JBC.272.50.31221
P407
P577
1997-12-12T00:00:00Z