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MTM1 gene

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

Papers overview

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Highly Cited
2010
Highly Cited
2010
Mutations in the MTM1 gene encoding myotubularin cause X-linked myotubular myopathy (XLMTM), a well-defined subtype of human… Expand
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Highly Cited
2007
Highly Cited
2007
The Protein Tyrosine Phosphatase (PTP) family comprises a large and diverse group of enzymes, regulating a range of biological… Expand
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Highly Cited
2006
Highly Cited
2006
It is increasingly recognized that the compartmental organization of signaling processes has a profound influence on cellular… Expand
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2006
2006
Myotubularins, a large family of catalytically active and inactive proteins, belong to a unique subgroup of protein tyrosine… Expand
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2005
2005
KCa3.1 is an intermediate conductance Ca2+-activated K+ channel that is expressed predominantly in hematopoietic cells, smooth… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract When Sertoli cells were cultured in vitro on Matrigel-coated bicameral units, the assembly of the inter-Sertoli tight… Expand
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Review
2001
Review
2001
Protein tyrosine phosphatases (PTPs) are a diverse group of enzymes that contain a highly conserved active site motif, Cys-x5-Arg… Expand
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Review
2000
Review
2000
X-linked myotubular myopathy (XLMTM; MIM# 310400) is a severe congenital muscle disorder caused by mutations in the MTM1 gene… Expand
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Highly Cited
2000
Highly Cited
2000
A gene mutated in Charcot-Marie-Tooth disease type 4B (CMT4B), an autosomal recessive demyelinating neuropathy with myelin… Expand
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1997
1997
X-linked recessive myotubular myopathy (XLMTM) is characterized by severe hypotonia and generalized muscle weakness, with… Expand
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