DMPK gene

Known as: MT-PK, DMK, DM1PK 
 
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
Severe skeletal muscle wasting is the most debilitating symptom experienced by individuals with myotonic dystrophy type 1 (DM1… (More)
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Highly Cited
2007
Highly Cited
2007
The genetic basis of myotonic dystrophy type 1 (DM1) is a CTG expansion in the 3' untranslated region (UTR) of DMPK. The… (More)
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Highly Cited
2004
Highly Cited
2004
Myotonic dystrophy type 1 (DM1) is caused by expansion of a CTG repeat in the DMPK gene. In skeletal muscles, DM1 may involve a… (More)
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Highly Cited
2004
Highly Cited
2004
Spontaneous autoimmune diabetes development in NOD mice requires both CD8(+) and CD4(+) T cells. Three pathogenic CD8(+) T cell… (More)
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Highly Cited
2002
Highly Cited
2002
Myotonic dystrophy is a complex neuromuscular disorder associated with DNA expansion mutations in two different genes. In DM1 a… (More)
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Highly Cited
2002
Highly Cited
2002
In myotonic dystrophy (dystrophia myotonica, DM), expression of RNAs that contain expanded CUG or CCUG repeats is associated with… (More)
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Highly Cited
2001
Highly Cited
2001
Myotonic dystrophy (DM1) is the most common form of adult muscular dystrophy and is inherited as an autosomal dominant trait. The… (More)
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Highly Cited
2001
Highly Cited
2001
Myotonic dystrophy (DM), the most common form of muscular dystrophy in adults, can be caused by a mutation on either chromosome… (More)
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Highly Cited
1999
Highly Cited
1999
Myotonic dystrophy (DM) is the most common form of muscular dystrophy and is caused by expansion of a CTG trinucleotide repeat on… (More)
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Highly Cited
1997
Highly Cited
1997
Myotonic dystrophy, or dystrophia myotonica (DM), is a highly variable multisystem disease in which the classic adult-onset form… (More)
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