Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.
The transepithelial chloride permeability of airway and sweat ductal epithelium has been reported to be decreased in patients with cystic fibrosis (CF). In the present study, we investigated whether the airway epithelial defect was in the cell path by characterizing the relative ion permeabilities o...
שמור ב:
| הוצא לאור ב: | J Clin Invest |
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| Principais autores: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
1987
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423991/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3793933/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112812 |
| תגים: |
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