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DMWD gene

Known as: dystrophia myotonica, WD repeat containing, DMWD, gene59 
National Institutes of Health

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1 relation
DMWD protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
[Effects of Manure Application Rates on the Soil Carbon Fractions and Aggregate Stability].
An incubated study was conducted to explore the effect of different manure application dosages (0%, 1%, 2%, and 4%, referred to… 
2004
2004
Real-time RT-PCR for CTG repeat-containing genes.
  • M. Eriksson
  • Methods in molecular biology
  • 2004
  • Corpus ID: 1564279
Myotonic dystrophy (DM1) is a neuromuscular disorder caused by a CTGn expansion in the 3'-untranslated region (UTR) of myotonic… 
2003
2003
The DMWD protein from the myotonic dystrophy (DM1) gene region is developmentally regulated and is present most prominently in synapse-dense brain areas
2003
2003
Characterization of DMWD and its role in Myotonic Dystrophy (DM1)
The study on 'Characterization of DMWD and its role in Myotonic Dystrophy (DM1)' has provided us with improved insight into the… 
2001
2001
Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers.
Myotonic dystrophy 1 is caused by the expansion of a CTG trinucleotide repeat on chromosome 19q13.3. The repeat lies in the 3… 
1958
1958
Pregnancy in myotonica dystrophia; a case report.
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