Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing
Author:
Funder
National Institute on Deafness and Other Communication Disorders
Publisher
Elsevier BV
Subject
Neurology
Reference38 articles.
1. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice;Ahmad;Biochem. Biophys. Res. Commun.,2003
2. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness;Ahmad;Proc. Natl. Acad. Sci. U. S. A.,2007
3. Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness;Beltramello;Nat. Cell Biol.,2005
4. Quo vadis, hair cell regeneration?;Brigande;Nat. Neurosci.,2009
5. Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice;Chang;PLoS ONE,2008
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