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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Detalles Bibliográficos
Autor principal: Linsdell, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Review
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

Internet

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

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