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WHSC1 gene
Known as:
WOLF-HIRSCHHORN SYNDROME CANDIDATE 1
, MMSET
, MULTIPLE MYELOMA SET DOMAIN
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This gene is involved in development and the suppression of nucleotide transcription.
National Institutes of Health
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Related topics
Related topics
4 relations
Methylation
Protein methylation
WHSC1 protein, human
Wolf-Hirschhorn Syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
DICER- and MMSET-catalyzed H4K20me2 recruits the nucleotide excision repair factor XPA to DNA damage sites
Shalaka Chitale
,
H. Richly
Journal of Cell Biology
2018
Corpus ID: 3209331
Ultraviolet (UV) irradiation triggers the recruitment of DNA repair factors to the lesion sites and the deposition of histone…
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2017
2017
Wolf–Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation
Chuan-jiang Yu
,
Xiaomin Yao
,
+5 authors
Yuquan Wei
Neoplasia
2017
Corpus ID: 4641259
Highly Cited
2011
Highly Cited
2011
MMSET is highly expressed and associated with aggressiveness in neuroblastoma.
H. Hudlebusch
,
Julie Skotte
,
+14 authors
K. Helin
Cancer Research
2011
Corpus ID: 6898167
MMSET (WHSC1/NSD2) is a SET domain-containing histone lysine methyltransferase the expression of which is deregulated in a…
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2010
2010
Interstitial microdeletion of 4p16.3: Contribution of WHSC1 haploinsufficiency to the pathogenesis of developmental delay in Wolf–Hirschhorn syndrome
K. Izumi
,
Hironobu Okuno
,
+6 authors
K. Kosaki
American Journal of Medical Genetics. Part A
2010
Corpus ID: 28777498
Interstitial Microdeletion of 4p16.3: Contribution of WHSC1 Haploinsufficiency to the Pathogenesis of Developmental Delay in Wolf…
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2007
2007
Detection and follow‐up of fibroblast growth factor receptor 3 expression on bone marrow and circulating plasma cells by flow cytometry in patients with t(4;14) multiple myeloma
M. Chandesris
,
J. Soulier
,
+10 authors
B. Arnulf
British Journal of Haematology
2007
Corpus ID: 27076849
The t(4;14)(p16;q32) translocation, found in 15% of multiple myeloma (MM) cases, indicates a poor prognosis. Plasma cells (PC…
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2005
2005
Evaluation of NSD2 and NSD3 in overgrowth syndromes
J. Douglas
,
K. Coleman
,
+5 authors
The Childhood Overgrowth Collaboration
European Journal of Human Genetics
2005
Corpus ID: 25704442
Sotos syndrome is an overgrowth condition predominantly caused by truncating mutations, missense mutations restricted to…
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Highly Cited
2004
Highly Cited
2004
A Global Expression-based Analysis of the Consequences of the t(4;14) Translocation in Myeloma
A. Dring
,
F. Davies
,
+10 authors
G. Morgan
Clinical Cancer Research
2004
Corpus ID: 1383699
Purpose: Our purpose in this report was to define genes and pathways dysregulated as a consequence of the t(4;14) in myeloma, and…
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2004
2004
Propofol offers no advantage over isoflurane anesthesia for cerebral protection during cardiopulmonary bypass: a preliminary study of S-100ß protein levels
M. Kanbak
,
F. Sarıcaoğlu
,
Alev Avci
,
T. Ocal
,
Z. Koray
,
U. Aypar
Canadian Journal of Anaesthesia-journal Canadien…
2004
Corpus ID: 36242412
PurposeDespite advances in anesthesia, cardiopulmonary bypass (CPB) and surgical techniques, cerebral injury remains a major…
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Highly Cited
2003
Highly Cited
2003
Mutation, SNP, and isoform analysis of fibroblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients.
Obiageli N Onwuazor
,
X. Wen
,
+6 authors
A. Stewart
Blood
2003
Corpus ID: 32099128
The t(4;14) translocation in multiple myeloma (MM) is identified in 15% of patient samples and dysregulates both FGFR3 and…
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Review
2002
Review
2002
The enigma of ectopic expression of FGFR3 in multiple myeloma: a critical initiating event or just a target for mutational activation during tumor progression.
M. Chesi
,
P. Bergsagel
,
W. Kuehl
Current opinion in hematology
2002
Corpus ID: 34430768
The t(4;14)(p16.3;q32) translocation that occurs uniquely in a subset of multiple myeloma tumors results in ectopic expression of…
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