GJB3 protein, human

Known as: connexin-31, connexin Cx31, Gap junction beta-3 protein, human 
 
National Institutes of Health

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2012
2012
Mutations in Connexin-31 (Cx31) are associated with multiple human diseases including erythrokeratodermia variabilis (EKV). The… (More)
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2010
2010
Hearing impairment (HI) affects 1/1000 children and over 2% of the aged population. We have previously reported that mutations in… (More)
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2008
2008
A 51-year-old woman presented with well-demarcated, erythematous patches and hyperkeratotic plaques that were arranged… (More)
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2003
2003
Erythrokeratodermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like or generalized… (More)
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2002
2002
Communication and interaction between cells has been shown to be important during the embryonic development of the vertebrate… (More)
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2001
2001
The connexin31 (Cx31) gene, a member of the connexin multigene family, is expressed in a characteristic spatiotemporal pattern… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in the GJB3 gene encoding connexin31 (Cx31) can cause a dominant non-syndromic form of hearing loss (DFNA2). To… (More)
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Highly Cited
1999
Highly Cited
1999
factors1. Mutations in the connexin26 gene (GJB2), located on 13q12, are responsible for non-syndromic recessive and dominant… (More)
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1997
1997
 During segmentation of the mouse hindbrain (d8.0–8.5 pc), expression of the gap junction gene connexin31 (cx31) is precisely… (More)
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1991
1991
A new member of the connexin gene family has been identified and designated rat connexin-31 (Cx31) based on its predicted… (More)
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