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WHSC1 gene

Known as: WOLF-HIRSCHHORN SYNDROME CANDIDATE 1, MMSET, MULTIPLE MYELOMA SET DOMAIN 
This gene is involved in development and the suppression of nucleotide transcription.
National Institutes of Health

Papers overview

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2018
2018
Ultraviolet (UV) irradiation triggers the recruitment of DNA repair factors to the lesion sites and the deposition of histone… 
Highly Cited
2011
Highly Cited
2011
MMSET (WHSC1/NSD2) is a SET domain-containing histone lysine methyltransferase the expression of which is deregulated in a… 
2010
2010
Interstitial Microdeletion of 4p16.3: Contribution of WHSC1 Haploinsufficiency to the Pathogenesis of Developmental Delay in Wolf… 
2007
2007
The t(4;14)(p16;q32) translocation, found in 15% of multiple myeloma (MM) cases, indicates a poor prognosis. Plasma cells (PC… 
2005
2005
Sotos syndrome is an overgrowth condition predominantly caused by truncating mutations, missense mutations restricted to… 
Highly Cited
2004
Highly Cited
2004
Purpose: Our purpose in this report was to define genes and pathways dysregulated as a consequence of the t(4;14) in myeloma, and… 
2004
Highly Cited
2003
Highly Cited
2003
The t(4;14) translocation in multiple myeloma (MM) is identified in 15% of patient samples and dysregulates both FGFR3 and… 
Review
2002
Review
2002
The t(4;14)(p16.3;q32) translocation that occurs uniquely in a subset of multiple myeloma tumors results in ectopic expression of…