Impaired cell volume regulation in intestinal crypt epithelia of cystic fibrosis mice.
Cystic fibrosis is a disease characterized by abnormalities in the epithelia of the lungs, intestine, salivary and sweat glands, liver, and reproductive systems, often as a result of inadequate hydration of their secretions. The primary defect in cystic fibrosis is the altered activity of a cAMP-act...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1995
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC40919/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7568068/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.20.9038 |
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