New understanding of gating mechanism of CFTR chloride channel

New research advances our understanding of the gating mechanism of the CFTR, the chloride channel mutated in cystic fibrosis patients. The study by Tzyh-Chang Hwang and colleagues (University of Missouri), and accompanying Commentary by Laszlo Csanady (Semmelweis University) appear in the May issue of the Journal of General Physiology (www.jgp.org)...

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