A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Channels (Austin)
Autor principal: Linsdell, Paul
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2018
Assuntos:
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!