Cystic fibrosis transmembrane conductance regulator (CFTR) is an ATP-gated channel that regulates anion fluxes across the plasma membrane of multiple cell types. Loss-of-function mutations of CFTR ...
Shaoyi Zhang, Gautier Stoll, José Manuel Bravo‐San Pedro, Valentina Sica, Allan Sauvat, Florine Obrist, Oliver Kepp, Yousheng Li, Luigi Maiuri, Naoufal Zamzami, Guido Guido Kroemer
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