Modulator Combination Improves In Vitro the Microrheological Properties of the Airway Surface Liquid of Cystic Fibrosis Airway Epithelia

Cystic fibrosis (CF) is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) protein, a plasma membrane protein expressed on the apical surface of secretory epithelia of the airways. In the airways, defective or absent function of the CFTR protein d...

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Detalles Bibliográficos
Autores principales: Ludovico, Alessandra, Moran, Oscar, Baroni, Debora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569604/
https://www.ncbi.nlm.nih.gov/pubmed/36232697
http://dx.doi.org/10.3390/ijms231911396

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569604/
https://www.ncbi.nlm.nih.gov/pubmed/36232697
http://dx.doi.org/10.3390/ijms231911396

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