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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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| Udgivet i: | Channels (Austin) |
|---|---|
| Hovedforfatter: | |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Taylor & Francis
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6986785/ https://ncbi.nlm.nih.gov/pubmed/30152709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336950.2018.1502585 |
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