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POU4F3 gene

Known as: POU class 4 homeobox 3, POU DOMAIN, CLASS 4, TRANSCRIPTION FACTOR 3, BRN3.1, MOUSE, HOMOLOG OF 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Hearing impairment, or deafness (in its most severe form), is one of the most common human sensory disorders. There have been… 
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2017
2017
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic hereditary hearing loss… 
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2016
2016
POU4F3 gene encodes a transcription factor which plays an essential role in the maturation and maintenance of hair cells in… 
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2013
2013
Autosomal dominant non-syndromic hearing loss (AD-NSHL) is one of the most common genetic diseases in human and is well-known for… 
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2012
2012
Hearing loss is mainly caused by loss of sensory hair cells (HCs) in the organ of Corti or cochlea. Although embryonic stem (ES… 
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2009
2009
Objectives: Cochleovestibular characteristics were investigated in a Dutch DFNA15 family with a novel POU4F3 mutation, L223P… 
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Highly Cited
2008
Highly Cited
2008
In a Dutch pedigree suffering from autosomal dominant nonsyndromic hearing impairment (ADNSHI), linkage was found to the locus… 
2008
2008
OBJECTIVE To report on the audiometric characteristics of a large Dutch family linked to DFNA15 with a novel mutation (p.L289F… 
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Highly Cited
2003
Highly Cited
2003
ABSTRACT A mutation in the POU4F3 gene (BRN-3.1, BRN3C) is responsible for DFNA15 (MIM 602459), autosomal-dominant nonsyndromic… 
Highly Cited
2002
Highly Cited
2002
In mice, Brn3 POU domain transcription factors play essential roles in the differentiation and survival of projection neurons… 
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