DMD gene

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

Topic mentions per year

Topic mentions per year

1977-2018
020406019772018

Papers overview

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Highly Cited
2012
Highly Cited
2012
A major obstacle in the application of cell-based therapies for the treatment of neuromuscular disorders is obtaining the… (More)
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2006
2006
The detection of duplications in Duchenne (DMD)/Becker Muscular Dystrophy (BMD) has long been a neglected issue. However, recent… (More)
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2005
2005
We have designed a multiplex ligation-dependent probe amplification (MLPA) assay to simultaneously screen all 79 DMD gene exons… (More)
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Highly Cited
2002
Highly Cited
2002
Duplications and deletions are known to cause a number of genetic disorders, yet technical difficulties and financial… (More)
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Highly Cited
1993
Highly Cited
1993
BACKGROUND X-linked cardiomyopathy (XLCM) is a rapidly progressive primary myocardial disorder presenting in teenage males as… (More)
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Highly Cited
1991
Highly Cited
1991
Dystrophin-related protein (DRP) is an autosomal gene product with high homology to dystrophin. We have used highly specific… (More)
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Highly Cited
1989
Highly Cited
1989
We have studied 34 Becker and 160 Duchenne muscular dystrophy (DMD) patients with the dystrophin cDNA, using conventional blots… (More)
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Highly Cited
1988
Highly Cited
1988
The application of recombinant DNA technology to prenatal diagnosis of many recessively inherited X-linked diseases is… (More)
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Highly Cited
1987
Highly Cited
1987
The 14 kb human Duchenne muscular dystrophy (DMD) cDNA corresponding to a complete representation of the fetal skeletal muscle… (More)
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Highly Cited
1986
Highly Cited
1986
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-linked muscle-wasting disorders… (More)
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