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Cystic fibrosis transmembrane conductance regulator (CFTR): Making an ion channel out of an active transporter structure
Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is a member of the ATP-binding cassette (ABC) family of membrane transport proteins, most members of which function as ATP-dependent pumps. CFTR is unique among human ABC proteins in functi...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Taylor & Francis
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986785/ https://www.ncbi.nlm.nih.gov/pubmed/30152709 http://dx.doi.org/10.1080/19336950.2018.1502585 |