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CFTR Inhibitors
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is a cAMP-regulated Cl(−) channel whose major function is to facilitate epithelial fluid secretion. Loss-of-function mutations in CFTR cause the genetic disease cystic fibrosis. CFTR is required for transepithelial fluid transpor...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2013
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4012685/ https://ncbi.nlm.nih.gov/pubmed/23331030 |
| Tagiau: |
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