Stimulation of Wild-Type, F508del- and G551D-CFTR Chloride Channels by Non-Toxic Modified pyrrolo[2,3-b]pyrazine Derivatives
Cystic fibrosis (CF) is a major inherited disorder involving abnormalities of fluid and electrolyte transport in a number of different organs due to abnormal function of cystic fibrosis transmembrane conductance regulator (CFTR) protein. We recently identified a family of CFTR activators, which cont...
Main Authors: | , , , , , |
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Format: | Online |
Language: | English |
Published: |
Frontiers Research Foundation
2011
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159890/ |