The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor

The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl(−) channel that governs the quantity and composition of epithelial secretions. CFTR function is normally tightly controlled as dysregulation can lead to life-threatening diseases such as secretory diarrhoea and cystic fibrosis. C...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Pflugers Arch
Main Authors: Broadbent, Steven D., Ramjeesingh, Mohabir, Bear, Christine E., Argent, Barry E., Linsdell, Paul, Gray, Michael A.
Format: Artigo
Sprog:Inglês
Udgivet: Springer Berlin Heidelberg 2014
Fag:
Ion Channels, Receptors and Transporters
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4502298/
https://ncbi.nlm.nih.gov/pubmed/25277268
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00424-014-1618-8
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker