Cochlear connexin 30 homomeric and heteromeric channels exhibit distinct assembly mechanisms
Author:
Funder
Fonds de la Recherche Scientifique - FNRS
Publisher
Elsevier BV
Subject
Developmental Biology,Embryology
Reference38 articles.
1. Post-translational integration and oligomerization of connexin 26 in plasma membranes and evidence of formation of membrane pores: implications for the assembly of gap junctions;Ahmad;Biochem. J.,2002
2. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice;Ahmad;Biochem. Biophys. Res. Commun.,2003
3. Mutations in Cx30 that are linked to skin disease and non-syndromic hearing loss exhibit several distinct cellular pathologies;Berger;J. Cell Sci.,2014
4. Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice;Chang;PLoS One,2008
5. Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin;Dahl;J. Biol. Chem.,1996
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