Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.
Cystic fibrosis is caused by mutations in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR). To further our understanding of CFTR's function and regulation, we used confocal immunofluorescence microscopy to localize CFTR in cells stained with monoclonal antibodies ag...
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| 發表在: | J Clin Invest |
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| Principais autores: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
American Society for Clinical Investigation
1992
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC442854/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1370301/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115582 |
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