ZFHX4 gene

Known as: ZFHX4, ZFH4, FLJ20980 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2017
01220052017

Papers overview

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2018
2018
Genetic investigations of people with impaired development of spoken language provide windows into key aspects of human biology… (More)
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2017
2017
Recent genome-sequencing studies have revealed dozens of genes frequently mutated in esophageal squamous cell carcinoma, but few… (More)
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2016
2016
Discovery and validation of genetic variants that influence disease severity in children with sickle cell anemia (SCA) could lead… (More)
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2014
2014
Glioblastoma (GBM) harbors subpopulations of therapy-resistant tumor-initiating cells (TICs) that are self-renewing and… (More)
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2014
2014
Congenital heart defects (CHDs) are common malformations, affecting four to eight per 1,000 total births. Conotruncal defects are… (More)
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2011
2011
We report eight unrelated individuals with intellectual disability and overlapping submicroscopic deletions of 8q21.11 (0.66-13… (More)
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2009
2009
BACKGROUND Interferon beta is 1 of 2 first-line treatments for relapsing-remitting multiple sclerosis (MS). However, not all… (More)
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2008
2008
AbstractHereditary congenital ptosis (PTOS) is defined as drooping of the upper eyelid without any other accompanying symptoms… (More)
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2006
2006
Human ZFHX4 has recently been shown to be a candidate gene for congenital bilateral isolated ptosis. Here, we report molecular… (More)
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2005
2005
The zinc finger-homeodomain (ZFH) transcription factors contain a zinc finger motif and a homeodomain that might regulate neural… (More)
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