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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...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Physiological Society
2011
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| Materias: | |
| Acceso en línea: | 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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