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Increased folding and channel activity of a rare cystic fibrosis mutant with CFTR modulators
Cystic fibrosis (CF) is a lethal recessive genetic disease caused by mutations in the CFTR gene. The gene product is a PKA-regulated anion channel that is important for fluid and electrolyte transport in the epithelia of lung, gut, and ducts of the pancreas and sweat glands. The most common CFTR mut...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Physiological Society
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3174745/ https://ncbi.nlm.nih.gov/pubmed/21642448 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00044.2011 |
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