Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.
Cystic fibrosis (CF) is characterized by an abnormality in cAMP-regulated chloride transport that results from a primary defect in the protein product of the CF gene, the CF transmembrane conductance regulator (CFTR). In this report, antibodies against CFTR peptides were used to localize the CFTR pr...
保存先:
| 出版年: | J Clin Invest |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
1991
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295422/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1713921/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115358 |
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