Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti

por Abbott, Ana C., García, Isaac E., Villanelo, Felipe, Flores-Muñoz, Carolina, Ceriani, Ricardo, Maripillán, Jaime, Novoa-Molina, Joel, Figueroa-Cares, Cindel, Pérez-Acle, Tomas, Sáez, Juan C., Sánchez, Helmuth A., Martínez, Agustín D.
Publicado 2023

Restraint of Human Skin Fibroblast Motility, Migration, and Cell Surface Actin Dynamics, by Pannexin 1 and P2X7 Receptor Signaling

por Flores-Muñoz, Carolina, Maripillán, Jaime, Vásquez-Navarrete, Jacqueline, Novoa-Molina, Joel, Ceriani, Ricardo, Sánchez, Helmuth A., Abbott, Ana C., Weinstein-Oppenheimer, Caroline, Brown, Donald I., Cárdenas, Ana María, García, Isaac E., Martínez, Agustín D.
Publicado 2021