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MTM1 gene

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

Related topics

Related topics

1 relation
X-linked centronuclear myopathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment.
2011
2011
Molecular Pathogenesis of Genetic and Inherited Diseases Inhibition of Activin Receptor Type IIB Increases Strength and Lifespan in Myotubularin-Deficient Mice
From the Division of Genetics and Program in Genomics,* Manton Center for Orphan Disease Research, Children’s Hospital Boston… 
2011
2011
The phosphoinositide phosphatase MTM-1 regulates apoptotic cell corpse clearance through CED-5–CED-12 in C. elegans
Multicellular organisms use programmed cell death to eliminate unwanted or potentially harmful cells. Improper cell corpse… 
Highly Cited
2003
Highly Cited
2003
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve.
Charcot-Marie-Tooth disease type 4B1, CMT4B1, is a severe, autosomal-recessive, demyelinating peripheral neuropathy, due to… 
2003
2003
PTEN and myotubularins: families of phosphoinositide phosphatases.
Highly Cited
2001
Highly Cited
2001
Regulation of Sertoli cell myotubularin (rMTM) expression by germ cells in vitro.
Recent studies have shown that rat myotubularin (rMTM), the homolog of human myotubularin, which is a putative protein tyrosine… 
Review
2001
Review
2001
PTEN and myotubularin phosphoinositide phosphatases: bringing bioinformatics to the lab bench.
2001
2001
Characterization of an adapter subunit to a phosphatidylinositol (3)P 3-phosphatase: Identification of a myotubularin-related protein lacking catalytic activity
The D3-phosphoinositides act as second messengers by recruiting, and thereby activating, diverse signaling proteins. We have… 
1998
1998
Myotubular myopathy: morphological, immunohistochemical and clinical variation
1998
1998
Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1).
MTM1 is responsible for X-linked recessive myotubular myopathy, which is a congenital muscle disorder linked to Xq28. MTM1 is… 
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