Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
about
Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family membersSarcoglycan subcomplex expression in normal human smooth muscleSpecific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19.Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AA novel dystrophin/utrophin-associated protein is an enzymatically inactive member of the phosphoglucomutase superfamilySarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complexEpiblast integrity requires CLASP and Dystroglycan-mediated microtubule anchoring to the basal cortex.An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophyAgrin binds to the nerve-muscle basal lamina via lamininA first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.Structure and physiological function of calpainsMutations 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.Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.Sarcospan-deficient mice maintain normal muscle functionDefective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophyFilamin 2 (FLN2): A muscle-specific sarcoglycan interacting proteinThe seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12beta-dystrobrevin, a member of the dystrophin-related protein familyMolecular organization of sarcoglycan complex in mouse myotubes in cultureBrain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophyDeficiency in Cardiac Dystrophin Affects the Abundance of the $\alpha$ -/ $\beta$ -Dystroglycan ComplexCritical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and DiseaseGalectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular DystrophyInhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expressionCloning and expression of full length mouse utrophin: the differential association of utrophin and dystrophin with AChR clustersPrivate beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalySarcoglycan isoforms in skeletal muscleAdhesion of cultured bovine aortic endothelial cells to laminin-1 mediated by dystroglycanThe dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actinThe basic helix-loop-helix transcription factors myogenin and Id2 mediate specific induction of caveolin-3 gene expression during embryonic developmentInteraction of gamma 1-syntrophin with diacylglycerol kinase-zeta. Regulation of nuclear localization by PDZ interactionsIdentification and characterization of a novel Golgi protein, GCP60, that interacts with the integral membrane protein giantinDystrophin-glycoprotein complex and Ras and Rho GTPase signaling are altered in muscle atrophyA role of dystroglycan in schwannoma cell adhesion to lamininMild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainTissue-specific expression of the human laminin alpha5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutationIntegrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophyAlpha1-syntrophin has distinct binding sites for actin and calmodulinCostameric proteins in human skeletal muscle during muscular inactivityReduced glycosaminoglycan sulfation diminishes the agrin signal transduction pathway
P2860
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P2860
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
@en
type
label
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
@en
prefLabel
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
@en
P1433
P1476
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage
@en
P2093
Campbell KP
P304
P356
10.1016/0092-8674(95)90344-5
P407
P577
1995-03-01T00:00:00Z