The Role of Specialized Pro-Resolving Mediators in Cystic Fibrosis Airways Disease

Cystic Fibrosis (CF) is a recessive genetic disease due to mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene encoding the CFTR chloride channel. The ion transport abnormalities related to CFTR mutation generate a dehydrated airway surface liquid (ASL) layer, which is r...

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Detalles Bibliográficos
Autores principales: Briottet, Maelle, Shum, Mickael, Urbach, Valerie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493015/
https://www.ncbi.nlm.nih.gov/pubmed/32982730
http://dx.doi.org/10.3389/fphar.2020.01290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493015/
https://www.ncbi.nlm.nih.gov/pubmed/32982730
http://dx.doi.org/10.3389/fphar.2020.01290

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