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The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels.
García IE, Villanelo F, Contreras GF, Pupo A, Pinto BI, Contreras JE, Pérez-Acle T, Alvarez O, Latorre R, Martínez AD, González C. García IE, et al. Among authors: villanelo f. J Gen Physiol. 2018 May 7;150(5):697-711. doi: 10.1085/jgp.201711782. Epub 2018 Apr 11. J Gen Physiol. 2018. PMID: 29643172 Free PMC article.
Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti.
Abbott AC, García IE, Villanelo F, Flores-Muñoz C, Ceriani R, Maripillán J, Novoa-Molina J, Figueroa-Cares C, Pérez-Acle T, Sáez JC, Sánchez HA, Martínez AD. Abbott AC, et al. Among authors: villanelo f. Front Cell Dev Biol. 2023 Jan 9;10:1071202. doi: 10.3389/fcell.2022.1071202. eCollection 2022. Front Cell Dev Biol. 2023. PMID: 36699003 Free PMC article.
13 results