Synergy of cAMP and calcium signaling pathways in CFTR regulation
Cystic fibrosis results from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel, leading to defective apical chloride transport. Patients also experience overactivation of inflammatory processes, including increased calcium signaling. Many investigations hav...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 114; no. 11; pp. E2086 - E2095 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
14.03.2017
|
Series | PNAS Plus |
Subjects | |
Online Access | Get full text |
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