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The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor
The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl(−) channel that governs the quantity and composition of epithelial secretions. CFTR function is normally tightly controlled as dysregulation can lead to life-threatening diseases such as secretory diarrhoea and cystic fibrosis. C...
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| Publicado no: | Pflugers Arch |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4502298/ https://ncbi.nlm.nih.gov/pubmed/25277268 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00424-014-1618-8 |
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