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TSPAN12 gene

Known as: NET2, NET-2, TETRASPANIN 12 
 
National Institutes of Health

Papers overview

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2017
2017
Purpose Familial exudative vitreoretinopathy (FEVR) is a severe hereditary retinal disorder characterized by defects in retinal… Expand
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2017
2017
Accessory proteins in Frizzled (FZD) receptor complexes are thought to determine ligand selectivity and signaling amplitude… Expand
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2015
2015
PURPOSE Familial exudative vitreoretinopathy (FEVR) is a rare hereditary disorder characterized by the failure of peripheral… Expand
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2014
2014
Communication between cancer cells and their microenvironment controls cancer progression. Although the tumor suppressor p53… Expand
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2013
2013
Ablation of tetraspanin protein TSPAN12 from human MDA-MB-231 cells significantly decreased primary tumor xenograft growth, while… Expand
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2012
2012
PURPOSE Familial exudative vitreoretinopathy (FEVR) is an inherited disorder that disrupts the development of the retinal… Expand
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2011
2011
PURPOSE Mutations in tetraspanin 12 (TSPAN12) have recently been identified as a cause of autosomal dominant familial exudative… Expand
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Highly Cited
2010
Highly Cited
2010
Familial exudative vitreoretinopathy (FEVR) is an inherited blinding disorder of the retinal vascular system. Although mutations… Expand
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Highly Cited
2009
Highly Cited
2009
Mutations in the genes encoding the Wnt receptor Frizzled-4 (FZD4), coreceptor LRP5, or the ligand Norrin disrupt retinal… Expand
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Highly Cited
2009
Highly Cited
2009
Using mass spectrometry, we identified ADAM10 (a membrane-associated metalloproteinase) as a partner for TSPAN12, a tetraspanin… Expand
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