CFTR Protein: Not Just a Chloride Channel?
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). The CFTR protein is known to acts as a chloride (Cl<sup>−</sup>) channel expressed in the exocrine glands of several bod...
Guardado en:
Autores principales: | Laurence S. Hanssens, Jean Duchateau, Georges J. Casimir |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/d265e9e8330342e58ed891de8c5be39f |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Comprehensive Analysis of Combinatorial Pharmacological Treatments to Correct Nonsense Mutations in the CFTR Gene
por: Arianna Venturini, et al.
Publicado: (2021) -
Búsqueda de la mutación delta F508 y análisis de dos polimorfismos de nucleótido único en el gen CFTR, en una muestra de población general de Valparaíso, Chile
por: Vera L,Alejandra, et al.
Publicado: (2005) -
Impact of Airway Inflammation on the Efficacy of CFTR Modulators
por: Carla M. P. Ribeiro, et al.
Publicado: (2021) -
TMEM16A/ANO1: Current Strategies and Novel Drug Approaches for Cystic Fibrosis
por: Christie Mitri, et al.
Publicado: (2021) -
XV-2c and KM: 19 haplotype analysis in Chilean patients with cystic fibrosis and unknown CFTR gene mutations
por: REPETTO,GABRIELA M, et al.
Publicado: (2007)