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Human cystic fibrosis airway epithelia have reduced Cl(−) conductance but not increased Na(+) conductance
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) anion channel function causes cystic fibrosis (CF) lung disease. CFTR is expressed in airway epithelia, but how CF alters electrolyte transport across airway epithelia has remained uncertain. Recent studies of a porcine model showed...
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| Main Authors: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
2011
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3121869/ https://ncbi.nlm.nih.gov/pubmed/21646513 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1106695108 |
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