CFTR modulates RPS27 gene expression using chloride anion as signaling effector
Abstract: In Cystic Fibrosis (CF), the impairment of the CFTR channel activity leads to a variety of alterations, including differential gene expression. However, the CFTR signaling mechanisms remain unclear. Recently, culturing IB3-1 CF cells under different intracellular Clconcentrations ([Cl-...
Guardado en:
| Autores principales: | Valdivieso, Ángel Gabriel, Mori, Consuelo, Clauzure, Mariángeles, Massip Copiz, María Macarena, Santa Coloma, Tomás Antonio |
|---|---|
| Formato: | Artículo |
| Lenguaje: | Inglés |
| Publicado: |
Elsevier
2022
|
| Materias: | |
| Acceso en línea: | https://repositorio.uca.edu.ar/handle/123456789/14560 |
| Aporte de: |
Ejemplares similares
-
c- Src and its role in cystic fibrosis
por: Massip Copiz, María Macarena, et al.
Publicado: (2022) -
Measurement of cystic fibrosis transmembrane conductance regulator activity using fluorescence spectrophotometry
por: Valdivieso, Ángel Gabriel, et al.
Publicado: (2022) -
CFTR chloride channel activity modulates the mitochondrial morphology in cultured epithelial cells
por: García Solcá, Rocío, et al.
Publicado: (2022) -
NLR family pyrin domain containing 3 (NLRP3) and caspase 1 (CASP1) modulation by intracellular Cl– concentration
por: Clauzure, Mariángeles, et al.
Publicado: (2022) -
CFTR impairment upregulates c-Src activity through IL-1β autocrine signaling
por: Massip Copiz, María Macarena, et al.
Publicado: (2019)