MTM1 gene

Known as: MTM1, MYOTUBULARIN, myotubularin 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2017
051019972017

Papers overview

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2006
2006
Mutations in myotubularin-related protein-2 (MTMR2) or MTMR13/set-binding factor-2 (SBF2) genes are responsible for the severe… (More)
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Highly Cited
2004
Highly Cited
2004
Myotubularin and related proteins constitute a large and highly conserved family possessing phosphoinositide 3-phosphatase… (More)
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2003
2003
Myotubularin-related proteins are a large subfamily of protein tyrosine phosphatases (PTPs) that dephosphorylate D3… (More)
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2003
2003
X-linked myotubular myopathy is a muscle disorder caused by mutations on the myotubular myopathy-1 (MTM-1) gene, coding for… (More)
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2002
2002
The myotubularin-related 1 (MTMR1) gene belongs to a highly conserved family of eucaryotic phosphatases, with at least 11 members… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in the gene encoding myotubularin-related protein 2 (MTMR2) are responsible for autosomal recessive Charcot-Marie-Tooth… (More)
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Highly Cited
2002
Highly Cited
2002
Myotubularin is a ubiquitously expressed phosphatase that acts on phosphatidylinositol 3-monophosphate [PI(3)P], a lipid… (More)
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Highly Cited
2000
Highly Cited
2000
The lipid second messenger phosphatidylinositol 3-phosphate [PI(3)P] plays a crucial role in intracellular membrane trafficking… (More)
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Highly Cited
2000
Highly Cited
2000
Myotubular myopathy (MTM1) is an X-linked disease, characterized by severe neonatal hypotonia and generalized muscle weakness… (More)
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Highly Cited
1998
Highly Cited
1998
Several proteins that contribute to epigenetic mechanisms of gene regulation contain a characteristic motif of unknown function… (More)
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