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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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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2010
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| Assuntos: | |
| Acesso em linha: | 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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