Intracellular chloride concentration changes modulate IL-1β expression and secretion in human bronchial epithelial cultured cells
Abstract: Cystic fibrosis (CF) is caused by mutations in the CFTR gene, which encodes a cAMP-regulated chloride channel. Several cellular functions are altered in CF cells. However, it is not clear how the CFTR failure induces those alterations. We have found previously several genes differentially...
Guardado en:
| Autores principales: | Clauzure, Mariángeles, Valdivieso, Ángel Gabriel, Massip Copiz, María Macarena, Mori, Consuelo, Dugour, Andrea V., Figueroa, Juan M., Santa Coloma, Tomás Antonio |
|---|---|
| Formato: | Artículo |
| Lenguaje: | Inglés |
| Publicado: |
Wiley
2019
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| Materias: | |
| Acceso en línea: | https://repositorio.uca.edu.ar/handle/123456789/8778 |
| Aporte de: |
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