Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
about
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cellsFunctional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AHILS1 is a spermatid-specific linker histone H1-like protein implicated in chromatin remodeling during mammalian spermiogenesisMutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A 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.Sarcospan-deficient mice maintain normal muscle functionExpressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy geneThe seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiencyMultiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsTelethonin, a novel sarcomeric protein of heart and skeletal muscleCaveolin regulates endocytosis of the muscle repair protein, dysferlinCharacterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophyGenetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.Plasma membrane cytoskeleton of muscle: a fine structural analysis.Sarcoglycans in muscular dystrophy.Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex.Overview of the Muscle Cytoskeleton.Dystrophin-associated proteins and the muscular dystrophies: a glossary.Dystrophin in the nervous system.Expression pattern of mRNA A and mRNA B of alpha sarcoglycan gene during mouse embryonic development and regulation of their expression by myogenic and cardiogenic transcription factors.Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum
P2860
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P2860
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
description
1994 nî lūn-bûn
@nan
1994 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@ast
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en-gb
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@nl
type
label
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@ast
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en-gb
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@nl
prefLabel
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@ast
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en-gb
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@nl
P2093
P2860
P356
P1476
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21
@en
P2093
P2860
P304
P356
10.1073/PNAS.91.21.9690
P407
P577
1994-10-11T00:00:00Z