Investigating CFTR and KCa3.1 Protein/Protein Interactions.

In epithelia, Cl- channels play a prominent role in fluid and electrolyte transport. Of particular importance is the cAMP-dependent cystic fibrosis transmembrane conductance regulator Cl- channel (CFTR) with mutations of the CFTR encoding gene causing cystic fibrosis. The bulk transepithelial transp...

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Bibliographic Details
Main Authors: Hélène Klein, Asmahan Abu-Arish, Nguyen Thu Ngan Trinh, Yishan Luo, Paul W Wiseman, John W Hanrahan, Emmanuelle Brochiero, Rémy Sauvé
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4836752?pdf=render