טוען...
Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect
Due to genetic defects in apical membrane chloride channels, the cystic fibrosis (CF) intestine does not secrete chloride normally. Depressed chloride secretion leaves CF intestinal absorptive processes unopposed, which results in net fluid hyperabsorption, dehydration of intestinal contents, and a...
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| Main Authors: | , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Clinical Investigation
2003
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC162286/ https://ncbi.nlm.nih.gov/pubmed/12840066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200317667 |
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