[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
about
Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes.Proteomic profiling of the dystrophin complex and membrane fraction from dystrophic mdx muscle reveals decreases in the cytolinker desmoglein and increases in the extracellular matrix stabilizers biglycan and fibronectin.Proteomic profiling of liver tissue from the - mouse model of Duchenne muscular dystrophy
P2860
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh-hant
name
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@en
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@nl
type
label
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@en
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@nl
prefLabel
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@en
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@nl
P2860
P1433
P1476
[Molecular pathogenesis of Duchenne muscular dystrophy-related fibrosis].
@en
P2093
D Swandulla
P2860
P2888
P356
10.1007/S00292-017-0265-1
P407
P577
2017-01-17T00:00:00Z