Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
about
Mutations in the integrin alpha7 gene cause congenital myopathyEmerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophyClinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD geneIdentification of Dp71e, a new dystrophin with a novel carboxy-terminal endIntegrated 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.A comprehensive database of Duchenne and Becker muscular dystrophy patients (0-18 years old) in East ChinaCorrelation of Utrophin Levels with the Dystrophin Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.Dystrophin in frameshift deletion patients with Becker muscular dystrophyExploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.Diagnostic immunohistology of muscle diseases.Use of epitope libraries to identify exon-specific monoclonal antibodies for characterization of altered dystrophins in muscular dystrophy.An alternative dystrophin transcript specific to peripheral nerve.Cell-matrix interactions in muscle disease.Monoclonal antibodies against the muscle-specific N-terminus of dystrophin: characterization of dystrophin in a muscular dystrophy patient with a frameshift deletion of exons 3-7.Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.Mild 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.An intact cysteine-rich domain is required for dystrophin function.Localization of dystrophin COOH-terminal domain by the fracture-label technique.Functional significance of dystrophin positive fibres in Duchenne muscular dystrophyEvolutionary conservation of the dystrophin central rod domainDose-dependent restoration of dystrophin expression in cardiac muscle of dystrophic mice by systemically delivered morpholino.
P2860
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P2860
Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
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
Preservation of the C-terminus ...... rom Becker muscular dystrophy.
@en
type
label
Preservation of the C-terminus ...... rom Becker muscular dystrophy.
@en
prefLabel
Preservation of the C-terminus ...... rom Becker muscular dystrophy.
@en
P2093
P1476
Preservation of the C-terminus ...... rom Becker muscular dystrophy.
@en
P2093
Ishiguro T
Tsukahara T
P304
P356
10.1016/0022-510X(91)90039-A
P577
1991-02-01T00:00:00Z