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MicroRNA-9 downregulates the ANO1 chloride channel and contributes to cystic fibrosis lung pathology
Cystic fibrosis results from reduced cystic fibrosis transmembrane conductance regulator protein activity leading to defective epithelial ion transport. Ca(2+)-activated Cl(−) channels mediate physiological functions independently of cystic fibrosis transmembrane conductance regulator. Anoctamin 1 (...
Guardat en:
| Publicat a: | Nat Commun |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5617894/ https://ncbi.nlm.nih.gov/pubmed/28955034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-017-00813-z |
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