Cargando...

CONTROL OF THE CFTR CHANNEL’S GATES

Unique among ABC (ATP-binding cassette) protein family members, CFTR (cystic fibrosis transmembrane conductance regulator), encoded by the gene mutated in cystic fibrosis patients, functions as an ion channel. Opening and closing of its anion-selective pore are linked to ATP binding and hydrolysis a...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Vergani, Paola, Basso, Claudia, Mense, Martin, Nairn, Angus C., Gadsby, David C.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2005
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2728124/
https://ncbi.nlm.nih.gov/pubmed/16246032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20051003
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!