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ZNF423 gene
Known as:
Ebfaz
, ZNF423
, ZINC FINGER PROTEIN 423, MOUSE, HOMOLOG OF
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This gene is involved in olfactory neurogenesis.
National Institutes of Health
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Related topics
Related topics
7 relations
Homo sapiens
JOUBERT SYNDROME 19
NEPHRONOPHTHISIS 14
Transcriptional Regulation
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Narrower (1)
ZNF423 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Evidence for Brainstem Motor Nondecussation as a Neurologic Substrate for Periodic Alternating Gaze Deviation.
M. Brodsky
,
S. Kotagal
,
P. Pichurin
,
Mai‐Lan Ho
Ophthalmology (Rochester, Minn.)
2017
Corpus ID: 42413419
2016
2016
Prognostic impact of a single-nucleotide polymorphism near the CTSO gene in hormone receptor-positive breast cancer patients
Y. Hato
,
N. Kondo
,
+8 authors
T. Toyama
International Journal of Clinical Oncology
2016
Corpus ID: 33723989
BackgroundTamoxifen can reduce the occurrence of breast cancer by a half in high-risk women. Recently, a genome-wide association…
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2015
2015
Enhanced mitogenesis in stromal vascular cells derived from subcutaneous adipose tissue of Wagyu compared with those of Angus cattle.
Shengjuan Wei
,
Xing Fu
,
+6 authors
M. Du
Journal of Animal Science
2015
Corpus ID: 30688760
Japanese Wagyu cattle are well known for their extremely high marbling and lower subcutaneous adipose tissue compared with Angus…
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2014
2014
Transcriptional dysregulation of the multifunctional zinc finger factor 423 in acute lymphoblastic leukemia of childhood
L. Harder
,
B. Otto
,
M. Horstmann
Genomics Data
2014
Corpus ID: 3253971
2013
2013
Aberrant ZNF 423 impedes B cell differentiation and is linked to adverse outcome of ETV 6-RUNX 1 negative B precursor acute lymphoblastic leukemia
L. Harder
,
Georg Eschenburg
,
+12 authors
M. Horstmann
2013
Corpus ID: 2316222
The Rockefeller University Press $30.00 J. Exp. Med. 2013 www.jem.org/cgi/doi/10.1084/jem.20130497 Cite by DOI: 10.1084/jem…
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2012
2012
A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect
M. Shoukier
,
J. Wickert
,
+8 authors
P. Burfeind
American Journal of Medical Genetics. Part A
2012
Corpus ID: 1547869
Interstitial deletions of the proximal chromosome 16q are rare. To date, only six cases with molecularly well‐characterized…
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2011
2011
Mosaic marker chromosome 16 resulting in 16q11.2–q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasia
A. Zerem
,
C. Vinkler
,
M. Michelson
,
E. Leshinsky‐Silver
,
T. Lerman-Sagie
,
D. Lev
American Journal of Medical Genetics. Part A
2011
Corpus ID: 7836299
Proximal duplications of the long arm of chromosome 16 are rare and only a few patients have been reported. Clinically, the…
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2010
2010
Antizyme Restrains Centrosome Amplification by Regulating the Accumulation of Mps1 at Centrosomes
Christopher Kasbek
,
Ching-Hui Yang
,
H. Fisk
Molecular Biology of the Cell
2010
Corpus ID: 19349106
The failure to degrade Mps1 at centrosomes causes centrosome overproduction, but the factors that target Mps1 for degradation are…
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2009
2009
[Gene expression of OAZ pathway in the patients of systemic lupus erythematosus].
Rong-liang Li
,
Jing Huang
,
Lingyun Sun
,
Xuebing Feng
Zhonghua yi xue za zhi
2009
Corpus ID: 37397419
OBJECTIVE To explore the role of Olf/EBF associated zinc finger protein (OAZ) pathway in the RNA expression level in patients…
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2008
2008
The regulation and function of Sox21 in primary neurogenesis
D. Cunningham
,
E. Casey
International Journal of Developmental…
2008
Corpus ID: 53176233
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