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Cystic fibrosis drug ivacaftor stimulates CFTR channels at picomolar concentrations
The devastating inherited disease cystic fibrosis (CF) is caused by mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) anion channel. The recent approval of the CFTR potentiator drug ivacaftor (Vx-770) for the treatment of CF patients has marked the advent of causative CF th...
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| Pubblicato in: | eLife |
|---|---|
| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
eLife Sciences Publications, Ltd
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6594753/ https://ncbi.nlm.nih.gov/pubmed/31205003 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.46450 |
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