Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin.
about
Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyA model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame.Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.Deletions in the 5' region of dystrophin and resulting phenotypes.Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophyHuman and murine dystrophin mRNA transcripts are differentially expressed during skeletal muscle, heart, and brain developmentSomatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.Dystrophin in frameshift deletion patients with Becker muscular dystrophyAre cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.A marginal level of dystrophin partially ameliorates hindlimb muscle passive mechanical properties in dystrophin-null mice.Preservation of muscle force in Mdx3cv mice correlates with low-level expression of a near full-length dystrophin proteinMild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophinA truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane.Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.Evolutionary conservation of the dystrophin central rod domain
P2860
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P2860
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Differentiation of Duchenne an ...... isera specific for dystrophin.
@en
type
label
Differentiation of Duchenne an ...... isera specific for dystrophin.
@en
prefLabel
Differentiation of Duchenne an ...... isera specific for dystrophin.
@en
P2093
P2860
P1476
Differentiation of Duchenne an ...... isera specific for dystrophin.
@en
P2093
Zubrzycka-Gaarn EE
P2860
P304
P407
P577
1991-02-01T00:00:00Z