Laddar...

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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Front Pharmacol
Huvudupphovsmän: Gianotti, Ambra, Delpiano, Livia, Caci, Emanuela
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2018
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6212516/
https://ncbi.nlm.nih.gov/pubmed/30416443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2018.01176
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!