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ZFHX4 gene

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

Papers overview

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2019
2019
The study sought to explore novel genetic aberration driving squamous cell lung carcinoma (LUSC). The whole exome (WES), whole… Expand
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2017
2017
Recent genome-sequencing studies have revealed dozens of genes frequently mutated in esophageal squamous cell carcinoma, but few… Expand
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Review
2016
Review
2016
Peters anomaly is a form of anterior segment dysgenesis characterized by central ocular opacity and corneo-lenticular adhesions… Expand
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Highly Cited
2014
Highly Cited
2014
Glioblastoma (GBM) harbors subpopulations of therapy-resistant tumor-initiating cells (TICs) that are self-renewing and… Expand
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Highly Cited
2013
Highly Cited
2013
Copy-number variations (CNVs) are a common cause of intellectual disability and/or multiple congenital anomalies (ID/MCA… Expand
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2011
2011
We report eight unrelated individuals with intellectual disability and overlapping submicroscopic deletions of 8q21.11 (0.66-13… Expand
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2008
2008
AbstractHereditary congenital ptosis (PTOS) is defined as drooping of the upper eyelid without any other accompanying symptoms… Expand
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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… Expand
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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… Expand
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