From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
about
Syne-1, a dystrophin- and Klarsicht-related protein associated with synaptic nuclei at the neuromuscular junctionDesmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desminSpecific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19.Sarcospan-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 dystrophyGenomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complexSarcoglycan isoforms in skeletal musclerAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophyLocalization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: triple immunogold labeling electron microscopyBiomechanics of the sarcolemma and costameres in single skeletal muscle fibers from normal and dystrophin-null miceParaffin wax embedded muscle is suitable for the diagnosis of muscular dystrophyAge-related dystrophin-glycoprotein complex structure and function in the rat extensor digitorum longus and soleus muscleMyopathic changes in murine skeletal muscle lacking syneminEarlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce.Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD.Making sense of the limb-girdle muscular dystrophies.Inherited skeletal muscle disorders.Immunocytochemical analysis of human muscular dystrophy.Dystrophin and utrophin: genetic analyses of their role in skeletal muscle.Sarcolemmal organization in skeletal muscle lacking desmin: evidence for cytokeratins associated with the membrane skeleton at costameres.Alpha vs. gamma sarcoglycanopathy: DNA tests solve a case from Argentina.Novel approaches to treat muscular dystrophies.Role of nitric oxide in the pathogenesis of muscular dystrophies: a "two hit" hypothesis of the cause of muscle necrosis.Our trails and trials in the subsarcolemmal cytoskeleton network and muscular dystrophy researches in the dystrophin era.Molecular diagnosis of myocardial disease.Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse.From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.Phenotypic and immunohistochemical characterization of sarcoglycanopathies.A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesAbnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse modelsViral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advancesSarcoglycan complex in masseter and sternocleidomastoid muscles of baboons: an immunohistochemical study.The sarcoglycan-sarcospan complex localization in mouse retina is independent from dystrophins.A delta-sarcoglycan gene polymorphism as a risk factor for hypertrophic cardiomyopathy.Progressive muscular dystrophy in alpha-sarcoglycan-deficient miceA novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor-regulated channel.Processing and assembly of the dystrophin glycoprotein complex.Emerging strategies for cell and gene therapy of the muscular dystrophiesPrimary myopathies and the heart.
P2860
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P2860
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@ast
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@en
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@nl
type
label
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@ast
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@en
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@nl
prefLabel
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@ast
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@en
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@nl
P2093
P2860
P1433
P1476
From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.
@en
P2093
P2860
P304
P356
10.1002/(SICI)1097-4598(199804)21:4<421::AID-MUS1>3.0.CO;2-B
P577
1998-04-01T00:00:00Z