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DMD gene

Known as: muscular dystrophy, Duchenne and Becker types, DXS270, APO-DYSTROPHIN 1 
This gene is involved in muscle development.
National Institutes of Health

Related topics

Related topics

10 relations
Becker Muscular DystrophyCell MovementCytokinesisDuchenne and Becker Muscular Dystrophy

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DMD wt Allele

Papers overview

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Highly Cited
2008
Highly Cited
2008
Human multipotent adipose‐derived stem cells restore dystrophin expression of Duchenne skeletal‐muscle cells in vitro
Background information. DMD (Duchenne muscular dystrophy) is a devastating X‐linked disorder characterized by progressive muscle… 
Highly Cited
2003
Highly Cited
2003
Proteomic analysis of mdx skeletal muscle: Great reduction of adenylate kinase 1 expression and enzymatic activity
To investigate the pathophysiological events of Duchenne muscular dystrophy, we analyzed alterations of protein expression in… 
Highly Cited
2000
Highly Cited
2000
Large-scale analysis of differential gene expression in the hindlimb muscles and diaphragm of mdx mouse.
Highly Cited
1999
Highly Cited
1999
Distribution of ten laminin chains in dystrophic and regenerating muscles
Highly Cited
1998
Highly Cited
1998
Genetic Structure of the Ancestral Population of Modern Humans
Abstract. Neutral DNA polymorphisms from an 8-kb segment of the dystrophin gene, previously ascertained in a worldwide sample (n… 
Highly Cited
1995
Highly Cited
1995
Successful histocompatible myoblast transplantation in dystrophin- deficient mdx mouse despite the production of antibodies against dystrophin
Myoblast transplantation has been considered a potential treatment for some muscular disorders. It has proven very successful… 
Highly Cited
1992
Highly Cited
1992
The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain
Chromosome 6-encoded dystrophin-related-protein (DRP) shows significant structural similarities to dystrophin at the carboxyl… 
Highly Cited
1991
Highly Cited
1991
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence
Highly Cited
1989
Highly Cited
1989
Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy
Highly Cited
1989
Highly Cited
1989
The Dictyostelium gelation factor shares a putative actin binding site with alpha-actinins and dystrophin and also has a rod domain containing six 100-residue motifs that appear to have a cross-beta…
The 120-kD gelation factor and alpha-actinin are among the most abundant F-actin cross-linking proteins in Dictyostelium… 
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