Cftr and ENaC ion channels mediate NaCl absorption in the mouse submandibular gland

Cystic fibrosis is caused by mutations in CFTR, the cystic fibrosis transmembrane conductance regulator gene. Disruption of CFTR-mediated anion conductance results in defective fluid and electrolyte movement in the epithelial cells of organs such as the pancreas, airways and sweat glands, but the fu...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Catalán, Marcelo A, Nakamoto, Tetsuji, Gonzalez-Begne, Mireya, Camden, Jean M, Wall, Susan M, Clarke, Lane L, Melvin, James E
Format: Artigo
Langue:Inglês
Publié: Blackwell Science Inc 2010
Sujets:
Alimentary
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2828142/
https://ncbi.nlm.nih.gov/pubmed/20026617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2009.183541
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires