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...

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Библиографические подробности
Главные авторы: Catalán, Marcelo A, Nakamoto, Tetsuji, Gonzalez-Begne, Mireya, Camden, Jean M, Wall, Susan M, Clarke, Lane L, Melvin, James E
Формат: Artigo
Язык:Inglês
Опубликовано: Blackwell Science Inc 2010
Предметы:
Alimentary
Online-ссылка: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
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