ロード中...
The Cystic Fibrosis Transmembrane Conductance Regulator Impedes Proteolytic Stimulation of the Epithelial Na(+) Channel
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) that prevent its proper folding and trafficking to the apical membrane of epithelial cells. Absence of cAMP-mediated Cl(−) secretion in CF airways causes poorly hydrated airway surfaces in CF patients, a...
保存先:
| 主要な著者: | , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Biochemistry and Molecular Biology
2010
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2952223/ https://ncbi.nlm.nih.gov/pubmed/20709758 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.155259 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|