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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Detalles Bibliográficos
Autores principales: Batissoco, Ana C., Salazar-Silva, Rodrigo, Oiticica, Jeanne, Bento, Ricardo F., Mingroni-Netto, Regina C., Haddad, Luciana A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163694/
https://www.ncbi.nlm.nih.gov/pubmed/30150563
http://dx.doi.org/10.3390/ijms19092535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163694/
https://www.ncbi.nlm.nih.gov/pubmed/30150563
http://dx.doi.org/10.3390/ijms19092535

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