New understanding of gating mechanism of CFTR chloride channel
Monday, April 26, 2010 - 12:01
in Health & Medicine
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 László Csanády (Semmelweis University) appear in the May issue of the Journal of General Physiology.