×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GermlineCausalMutation
ORPHANET
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
<b>Aim:</b> Detection of drug-induced dystrophin in patient muscle biopsy is a surrogate outcome measure for Duchenne muscular dystrophy .
31379197
2019
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
AlteredExpression
BEFREE
(+)-Negamycin, a natural dipeptide-like antibiotic, may restore some dystrophin expression in the skeletal muscles of mice with Duchenne muscular dystrophy , and this compound has been recognized as a potential therapeutic agent for diseases caused by nonsense mutations.
28951602
2018
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD ) and Becker muscular dystrophy (BMD) are X-linked neuromuscular disorders associated with alterations in the dystrophin gene.
10094565
1999
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
DMD is associated with an abnormal electroretinogram (ERG) if the mutation disrupts the translation of retinal dystrophin (Dp260 ).
10227401
1999
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne Muscular Dystrophy (DMD ) originates from deleterious mutations in the dystrophin gene, with a complete loss of the protein product.
11525743
2001
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD) is an X-linked recessive muscle wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin .
11726694
2001
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD ) is characterized by progressive muscle degeneration that results from the absence of dystrophin .
11734539
2001
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy is an X-linked disease of muscle caused by an absence of the protein dystrophin .
11929208
2002
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD ) is a fatal neuromuscular disease caused by the absence of dystrophin .
11997063
2002
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) is a severe progressive muscle-wasting disorder caused by mutations in the dystrophin gene.
12235112
2002
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
AlteredExpression
BEFREE
Duchenne muscular dystrophy (DMD ) is a fatal childhood disease caused by mutations that abolish the expression of dystrophin in muscle.
12235137
2002
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD ), caused by the absence of dystrophin , is associated with decreased muscle cell proliferation.
12732930
2003
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD ) is caused by the absence of dystrophin , which triggers complex molecular and biological events in skeletal and cardiac muscle tissues.
12875769
2003
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
AlteredExpression
BEFREE
Duchenne muscular dystrophy is a fatal childhood disease caused by mutations that abolish the expression of dystrophin in muscle.
15172107
2004
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD ) and the allelic milder form of Becker muscular dystrophy (BMD) are caused by mutations of the dystrophin gene on the short arm of the X chromosome.
1537352
1992
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) is a lethal genetic muscle disorder caused by recessive mutations in the dystrophin gene.
15454965
2004
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are common X-chromosomal recessive disorders caused by mutations in the dystrophin gene.
15655674
2005
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, making it a potential target for gene therapy.
15709034
2005
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused in the majority of cases by deletions of the DMD gene and are readily detectable in affected males by multiplex polymerase chain reaction (PCR).
15841391
2005
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) is a lethal X-linked recessive disorder with an incidence of approximately 1 in 3500 males, caused by mutation in the DMD gene.
16353285
2005
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy and Becker muscular dystrophy (DMD and BMD) are caused by mutations in the dystrophin gene (Xp21 ).
16608904
2006
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
AlteredExpression
BEFREE
DMD cultures showed significant gene expression changes, even before dystrophin is expressed.
16679024
2006
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
GeneticVariation
BEFREE
Duchenne muscular dystrophy (DMD) is a genetic disease caused by mutations in the dystrophin gene and characterized by progressive skeletal muscle degeneration.
16874448
2006
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
BEFREE
Duchenne muscular dystrophy (DMD ) is a common X-linked disease resulting from the absence of dystrophin in muscle.
17185606
2007