The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD.
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Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR miceX-inactivation patch size in human female tissue confounds the assessment of tumor clonalityMental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectMuscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia.Isolation and characterization of human fetal myoblasts.Tumor necrosis factor inhibits human myogenesis in vitroIncreased chloride efflux in fibroblasts from X-linked muscular dystrophies and clones from Duchenne carriers.Giorgio Filippi, April 4, 1935-January 19, 1996.Examination of telomere lengths in muscle tissue casts doubt on replicative aging as cause of progression in Duchenne muscular dystrophy.Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophy.
P2860
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P2860
The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PD.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
The myoblast defect identified ...... o X-linked loci: DMD and G6PD.
@en
type
label
The myoblast defect identified ...... o X-linked loci: DMD and G6PD.
@en
prefLabel
The myoblast defect identified ...... o X-linked loci: DMD and G6PD.
@en
P2093
P356
P1433
P1476
The myoblast defect identified ...... o X-linked loci: DMD and G6PD.
@en
P2093
C Mastropaolo
M Siniscalco
P2888
P356
10.1007/BF00278789
P577
1986-09-01T00:00:00Z
P6179
1016619587