Wird geladen...
The Epithelial Sodium Channel (ENaC) as a Therapeutic Target for Cystic Fibrosis
Cystic fibrosis (CF) is a monogenic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CFTR dysfunction is characterized by abnormal mucociliary transport due to a dehydrated airway surface liquid (ASL) and hyperviscous mucus, among other pathologies...
Gespeichert in:
| Veröffentlicht in: | Curr Opin Pharmacol |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2018
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6294660/ https://ncbi.nlm.nih.gov/pubmed/30340955 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coph.2018.09.007 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|