Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators
|Disease Area:||Cystic Fibrosis|
|Type:||Primary human NHBE cells|
|Application:||Identification of Biomarkers|
|Biological Endpoints:||CTFR Activity|
|Throughput:||Medium / Low (Lab scale)|
|Potential:||High Potential to become a disease model|
|Authors:||Pranke, Iwona M. - Hatton, Aurelie - Simonin, Juliette - Jais, Jean Philippe - Le Pimpec-Barthes, Francoise - Carsin, Ania - Bonnette, Pierre - Fayon, Michael - Stremler-Le Bel, Nathalie - Grenet, Dominique - Thumerel, Matthieu - Mazenq, Julie - Urbach, Valerie - Mesbahi, Myriam - Girodon-Boulandet, Emanuelle - Hinzpeter, Alexandre - Edelman, Aleksander - Sermet-Gaudelus, Isabelle|
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