Triplet CFTR modulators: future prospects for treatment of cystic fibrosis

Cystic fibrosis (CF) is an autosomal recessive genetic disease characterized by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR). CFTR is a chloride channel responsible for ion flow across epithelial surfaces of lung, sinuses, pancreas, intestine, and liver. Researchers ha...

Descripción completa

Detalles Bibliográficos
Autor principal: Chaudary, Nauman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287538/
https://www.ncbi.nlm.nih.gov/pubmed/30584312
http://dx.doi.org/10.2147/TCRM.S147164

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287538/
https://www.ncbi.nlm.nih.gov/pubmed/30584312
http://dx.doi.org/10.2147/TCRM.S147164

Ejemplares similares