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In vitro Methods for the Development and Analysis of Human Primary Airway Epithelia

Cystic fibrosis (CF) is a chronic disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, which encodes for a channel expressed at the apical surface of epithelial tissues. Defective chloride and bicarbonate secretion, arising from CFTR mutations, cause a multi-organ d...

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Detalles Bibliográficos
Autores principales: Gianotti, Ambra, Delpiano, Livia, Caci, Emanuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6212516/
https://www.ncbi.nlm.nih.gov/pubmed/30416443
http://dx.doi.org/10.3389/fphar.2018.01176