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A common mechanism for CFTR potentiators
Cystic fibrosis (CF) is a channelopathy caused by loss-of-function mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which encodes a phosphorylation-activated and adenosine triphosphate (ATP)–gated chloride channel. In the past few years, high-throughput drug screenin...
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| Yayımlandı: | J Gen Physiol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Rockefeller University Press
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5715911/ https://ncbi.nlm.nih.gov/pubmed/29079713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.201711886 |
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