Muscular dystrophies and the dystrophin-glycoprotein complex.
about
Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscleA gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.Sarcospan-deficient mice maintain normal muscle functionBiglycan binds to alpha- and gamma-sarcoglycan and regulates their expression during developmentThe small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscleAn epidermal plakin that integrates actin and microtubule networks at cellular junctionsThe dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteinsThe dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actinChanges in mechanosensitive channel gating following mechanical stimulation in skeletal muscle myotubes from the mdx mouseZac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines.Characterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation.Guanine analogues enhance antisense oligonucleotide-induced exon skipping in dystrophin gene in vitro and in vivo.Gene and cell-mediated therapies for muscular dystrophy.Sarcolemmal organization in skeletal muscle lacking desmin: evidence for cytokeratins associated with the membrane skeleton at costameres.Association of the DTNBP1 locus with schizophrenia in a U.S. populationRole of dystrophin in airway smooth muscle phenotype, contraction and lung function.Skeletal muscle homeostasis in duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy.Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx miceStructure and dynamics of coxsackievirus B4 2A proteinase, an enyzme involved in the etiology of heart diseaseChanges in muscle T2 and tissue damage after downhill running in mdx mice.Transgenic expression of {alpha}7{beta}1 integrin maintains muscle integrity, increases regenerative capacity, promotes hypertrophy, and reduces cardiomyopathy in dystrophic mice.Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, Largemyd and mdx/Largemyd.From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.Intricacies of cardiac damage in coxsackievirus B3 infection: implications for therapy.Muscle degeneration without mechanical injury in sarcoglycan deficiencyElevated subsarcolemmal Ca2+ in mdx mouse skeletal muscle fibers detected with Ca2+-activated K+ channels.Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamsterViral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advancesSarcoglycan complex in masseter and sternocleidomastoid muscles of baboons: an immunohistochemical study.Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatmentDystrophin-compromised sarcoglycan-δ-knockout diaphragm requires full wild-type embryonic stem cell reconstitution for correction.Acetylcholinesterase mobility and stability at the neuromuscular junction of living miceA novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.Computational Analysis of Muscular Dystrophy Sub-types Using A Novel Integrative SchemeNicotinic acetylcholine receptor stability at the NMJ deficient in α-syntrophin in vivo.A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells.Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.Progressive muscular dystrophy in alpha-sarcoglycan-deficient miceMembrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle
P2860
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P2860
Muscular dystrophies and the dystrophin-glycoprotein complex.
description
1997 nî lūn-bûn
@nan
1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի ապրիլին 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
Muscular dystrophies and the dystrophin-glycoprotein complex.
@ast
Muscular dystrophies and the dystrophin-glycoprotein complex.
@en
Muscular dystrophies and the dystrophin-glycoprotein complex.
@nl
type
label
Muscular dystrophies and the dystrophin-glycoprotein complex.
@ast
Muscular dystrophies and the dystrophin-glycoprotein complex.
@en
Muscular dystrophies and the dystrophin-glycoprotein complex.
@nl
prefLabel
Muscular dystrophies and the dystrophin-glycoprotein complex.
@ast
Muscular dystrophies and the dystrophin-glycoprotein complex.
@en
Muscular dystrophies and the dystrophin-glycoprotein complex.
@nl
P1476
Muscular dystrophies and the dystrophin-glycoprotein complex.
@en
P2093
P304
P577
1997-04-01T00:00:00Z