Measurement of cystic fibrosis transmembrane conductance regulator activity using fluorescence spectrophotometry
Abstract: Cystic fibrosis (CF) is a frequent autosomal recessive disease caused by mutations that impair the CF transmembrane conductance regulator (CFTR) protein function. CFTR is a chloride channel activated by cyclic AMP (cAMP) via protein kinase A (PKA) and ATP hydrolysis. We describe here a m...
Guardado en:
| Autores principales: | Valdivieso, Ángel Gabriel, Marín, María C., Clauzure, Mariángeles, Santa Coloma, Tomás Antonio |
|---|---|
| Formato: | Artículo |
| Lenguaje: | Inglés |
| Publicado: |
Elsevier
2022
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| Materias: | |
| Acceso en línea: | https://repositorio.uca.edu.ar/handle/123456789/14595 |
| Aporte de: |
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