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GJB6 gene

Known as: EDH, CX30, gap junction protein beta 6 
National Institutes of Health

Related topics

Related topics

3 relations
GJB6 protein, humanGJB7 geneHidrotic Ectodermal Dysplasia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Modulation of gap junction channels and hemichannels by growth factors.
Gap junction hemichannels and cell-cell channels have roles in coordinating numerous cellular processes, due to their… 
2012
2012
Extradural haematoma in children: surgical experiences and prospective analysis of 170 cases.
AIM We present our experiences in the management of extradural haematoma in children which involved an aggressive diagnostic… 
2007
2007
Astrocytic connexin distributions and rapid, extensive dye transfer via gap junctions in the inferior colliculus: Implications for [14C]glucose metabolite trafficking
The inferior colliculus has the highest rates of blood flow and metabolism in brain, and functional metabolic activity increases… 
2007
2007
GJB2 and GJB6 Mutations in Children with Congenital Cytomegalovirus Infection
Congenital cytomegalovirus (CMV) infection is a leading cause of sensorineural hearing loss (SNHL) in children. Whether connexin… 
2006
2006
Connexin-associated deafness and speech perception outcome of cochlear implantation.
OBJECTIVE To compare performance after cochlear implantation in children with mutations in connexin (Cx) 26 (GJB2) or Cx30 (GJB6… 
2006
2006
High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.
Mutations in the GJB2 (Connexin 26) gene are responsible for more than half of all cases of prelingual, recessive, inherited… 
2004
2004
Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both c.35delG of GJB2 and the 342-kb deletion involving GJB6
2003
2003
Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness
Hearing loss is a common congenital disorder that is frequently associated with mutations in the Cx26 gene (GJB2). Three recent… 
2000
2000
Expression of connexin 30 in Xenopus embryos and its involvement in hatching gland function
Connexins are a family of proteins that assemble to form gap junction channels. Cell‐cell communication through gap junctions… 
2000
2000
Growth Hormone Increases Connexin-43 Expression in the Cerebral Cortex and Hypothalamus.
Several studies indicate that systemic GH influences various brain functions. Connexin-43 forms gap junctions that mediate… 
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