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WDR62 gene
Known as:
WD REPEAT-CONTAINING PROTEIN 62
, WDR62
, WD repeat domain 62
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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.
2020
2020
A case report of microcephaly and refractory West syndrome associated with WDR62 mutation
P. Zhou
,
Xin Ding
,
Qi Zeng
,
Huafang Zou
,
J. Liao
,
Dezhi Cao
Acta Epileptologica
2020
Corpus ID: 214618393
The autosomal recessive form of primary microcephaly (MCPH) is a rare disorder characterized by microcephaly with variable degree…
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2018
2018
WDR62 mediates TNFα-dependent JNK activation via TRAF2-MLK3 axis
E. Prinz
,
Sharon Aviram
,
A. Aronheim
Molecular Biology of the Cell
2018
Corpus ID: 51939654
The mitogen-activated protein kinases (MAPKs) regulate a variety of cellular processes. The three main MAPK cascades are the…
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2017
2017
WDR62 overexpression is associated with a poor prognosis in patients with lung adenocarcinoma
K. Shinmura
,
Hisami Kato
,
+10 authors
H. Sugimura
Molecular Carcinogenesis
2017
Corpus ID: 9162107
Human WDR62, which is localized in the cytoplasm including the centrosome, is known to be responsible for primary microcephaly…
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2017
2017
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
M. Naseer
,
M. Rasool
,
+5 authors
M. Al-Qahtani
Annals of Saudi Medicine
2017
Corpus ID: 40461764
BACKGROUND Primary microcephaly (MCPH) is a rare developmental defect characterized by impaired cognitive functions, retarded…
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2017
2017
WDR62, a causative gene product for primary microcephaly, regulates astral microtubule polymerization to maintain mitotic spindle orientation
T. Miyamoto
,
Akihiro Fukumitsu
,
+4 authors
S. Matsuura
2017
Corpus ID: 90662724
2016
2016
Novel mutations c.28G>T (p.Ala10Ser) and c.189G>T (p.Glu63Asp) in WDR62 associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly type 2
S. Banerjee
,
Huishuang Chen
,
+12 authors
Xunhua Li
OncoTarget
2016
Corpus ID: 3389731
Microcephaly (MCPH) is a developmental disorder characterized by reduced brain size and intellectual disability. A proportion of…
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2015
2015
The association of the JNK scaffold protein, WDR62, with the mixed lineage kinase 3, MLK3
Miriam Hadad
,
Sharon Aviram
,
I. Darlyuk-Saadon
,
Ksenya Cohen-Katsenelson
,
A. Whitmarsh
,
A. Aronheim
2015
Corpus ID: 49330420
Mitogen-activated protein kinases (MAPKs) form a kinase tier module in which MAPK, MAP2K and MAP3K are held by scaffold proteins…
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2015
2015
WDR62 is the critical target for the Aurora-A overexpression phenotype
Anja Eskat
2015
Corpus ID: 87910106
2012
2012
Exploring microcephaly and human brain evolution
J. Murray
,
A. Jackson
Developmental Medicine & Child Neurology
2012
Corpus ID: 31037612
Microcephaly, a commonly documented finding in paediatric neurological practice, confers little diagnostic specificity. Defined…
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