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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

Related topics

Related topics

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Transcription Factor Brn-3C

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Pou4f3 gene mutation promotes autophagy and apoptosis of cochlear hair cells in cisplatin-induced deafness mice.
2017
2017
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic hereditary hearing loss… 
2016
2016
Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss
Hearing impairment, or deafness (in its most severe form), is one of the most common human sensory disorders. There have been… 
2016
2016
A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss
POU4F3 gene encodes a transcription factor which plays an essential role in the maturation and maintenance of hair cells in… 
2013
2013
SNP Linkage Analysis and Whole Exome Sequencing Identify a Novel POU4F3 Mutation in Autosomal Dominant Late-Onset Nonsyndromic Hearing Loss (DFNA15)
Autosomal dominant non-syndromic hearing loss (AD-NSHL) is one of the most common genetic diseases in human and is well-known for… 
2009
2009
Mild and Variable Audiometric and Vestibular Features in a Third DFNA15 Family with a Novel Mutation in POU4F3
Objectives: Cochleovestibular characteristics were investigated in a Dutch DFNA15 family with a novel POU4F3 mutation, L223P… 
Highly Cited
2008
Highly Cited
2008
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding
In a Dutch pedigree suffering from autosomal dominant nonsyndromic hearing impairment (ADNSHI), linkage was found to the locus… 
2008
2008
Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.
OBJECTIVE To report on the audiometric characteristics of a large Dutch family linked to DFNA15 with a novel mutation (p.L289F… 
Highly Cited
2003
Highly Cited
2003
The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity
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
Brn3b/Brn3c double knockout mice reveal an unsuspected role for Brn3c in retinal ganglion cell axon outgrowth.
In mice, Brn3 POU domain transcription factors play essential roles in the differentiation and survival of projection neurons… 
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