A Cell Junctional Protein Network Associated with Connexin-26

GJB2 mutations are the leading cause of non-syndromic inherited hearing loss. GJB2 encodes connexin-26 (CX26), which is a connexin (CX) family protein expressed in cochlea, skin, liver, and brain, displaying short cytoplasmic N-termini and C-termini. We searched for CX26 C-terminus binding partners...

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Dettagli Bibliografici
Pubblicato in:Int J Mol Sci
Autori principali: Batissoco, Ana C., Salazar-Silva, Rodrigo, Oiticica, Jeanne, Bento, Ricardo F., Mingroni-Netto, Regina C., Haddad, Luciana A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2018
Soggetti:
Communication
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6163694/
https://ncbi.nlm.nih.gov/pubmed/30150563
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19092535
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