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SBF1 gene
Known as:
SBF1
, SET binding factor 1
, MYOTUBULARIN-RELATED PROTEIN 5
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Discovery of SBF1 as an allosteric inhibitor targeting the PIF-pocket of 3-phosphoinositide-dependent protein kinase-1
Wei Liu
,
Pengfei Li
,
Ye Mei
Journal of Molecular Modeling
2019
Abstract3-phosphoinositide-dependent protein kinase-1 (PDK1) plays a crucial role in the signal transduction of massive growth…
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2018
2018
Novel SBF1 splice-site null mutation broadens the clinical spectrum of Charcot-Marie-Tooth type 4B3 disease.
Hagit Flusser
,
Daniel Halperin
,
Rotem Kadir
,
Zamir Shorer
,
Ilan Shelef
,
Ohad S. Birk
Clinical genetics
2018
Four siblings of consanguineous Bedouin kindred presented at infancy with an autosomal recessive syndrome of congenital…
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2016
2016
SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement
Andreea Manole
,
Alejandro Horga
,
+7 authors
Henry Houlden
neurogenetics
2016
Biallelic mutations in the SBF1 gene have been identified in one family with demyelinating Charcot-Marie-Tooth disease (CMT4B3…
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2014
2014
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-tooth disease type 4B3.
Anas M. Alazami
,
Fatema Alzahrani
,
Saeed Bohlega
,
Fowzan S. Alkuraya
Neurology
2014
Editors' Note: In reference to “SET binding factor 1 ( SBF1 ) mutation causes Charcot-Marie-Tooth disease type 4B3,” Dr. Alkuraya…
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2014
2014
DNA microarray reveals ZNF195 and SBF1 are potential biomarkers for gemcitabine sensitivity in head and neck squamous cell carcinoma cell lines.
Min-hui Zhu
,
Shun-Long Ji
,
Cai-yun Zhang
,
Long Cui
,
Lei Xiong
,
Hongliang Zheng
International journal of clinical and…
2014
Gemcitabine is a potential chemotherapy drug for treatment of head and neck squamous cell carcinoma (HNSCC), however, the poor or…
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2013
2013
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.
Khriezhanuo Nakhro
,
Jin-Mo Park
,
+11 authors
Ki Wha Chung
Neurology
2013
OBJECTIVE To identify the genetic cause of an autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4B (CMT4B…
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Review
2011
Review
2011
The myotubularin family of lipid phosphatases in disease and in spermatogenesis.
Dolores D. Mruk
,
C Yan Cheng
The Biochemical journal
2011
The MTM (myotubularin)/MTMR (myotubularin-related) protein family is comprised of 15 lipid phosphatases, of which nine members…
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Highly Cited
2003
Highly Cited
2003
Regulation of myotubularin-related (MTMR)2 phosphatidylinositol phosphatase by MTMR5, a catalytically inactive phosphatase.
Soo-A Kim
,
Panayiotis O. Vacratsis
,
Ron Firestein
,
Michael L. Cleary
,
Jack E Dixon
Proceedings of the National Academy of Sciences…
2003
The myotubularin (MTM) family constitutes one of the most highly conserved protein-tyrosine phosphatase subfamilies in eukaryotes…
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2001
2001
Pseudo-phosphatase Sbf1 contains an N-terminal GEF homology domain that modulates its growth regulatory properties.
Ron Firestein
,
Michael L. Cleary
Journal of cell science
2001
Sbf1 (SET binding factor 1) is a pseudo-phosphatase related to the myotubularin family of dual specificity phosphatases, some of…
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1998
1998
Growth stimulation of primary B cell precursors by the anti-phosphatase Sbf1.
Immaculata De Vivo
,
Xianju Cui
,
John K. Domen
,
Michael L. Cleary
Proceedings of the National Academy of Sciences…
1998
SET binding factor 1 (Sbf1) was originally discovered by virtue of its interaction with a highly conserved motif (the SET domain…
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