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SBF2 gene

Known as: SBF2, MTMR13, KIAA1766 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Abstract IA09: Impact of genetically determined race on outcomes in E5103
Background: African Americans (AAs) have inferior breast cancer outcomes. AAs have a higher percentage of the poor prognosis… 
2016
2016
RETRACTED: siRNA-Mediated SBF2 Silencing May Inhibit Pancreatic Cancer Cells via Attenuation of the TGF-β Signaling Pathway
OBJECTIVE To investigate the effects of small-interfering RNA (siRNA)-mediated silencing of SET binding factor 2 (SBF2) on… 
2008
2008
Multiple disease‐linked myotubularin mutations cause NFL assembly defects in cultured cells and disrupt myotubularin dimerization
J. Neurochem.(2008) 104, 1536–1552. 
2007
2007
Myotubularines et maladie de Charcot-Marie-Tooth
La maladie de Charcot Marie Tooth (CMT) est la neuropathie peripherique hereditaire la plus commune chez l'homme ; elle affecte… 
2006
2006
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2.
2005
2005
- 1THE PHOSPHOINOSITIDE 3-PHOSPHATASE MTMR 2 ASSOCIATES WITH MTMR 13 , A NOVEL MEMBRANE-ASSOCIATED PSEUDOPHOSPHATASE ALSO MUTATED IN TYPE 4 B CHARCOT-MARIE-TOOTH DISEASE
THE PHOSPHOINOSITIDE 3-PHOSPHATASE MTMR2 ASSOCIATES WITH MTMR13, A NOVEL MEMBRANE-ASSOCIATED PSEUDOPHOSPHATASE ALSO MUTATED IN… 
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