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|
Did you find what you were looking for?Yes, I found it! No, I did not!
Thanks for your feedback! Please note that we cannot reply to you unless you send us an email.
What are you looking for?
We value your feedback so we can improve the information on the page. Please add your email address if you would like a reply. Thank you in advance for your help.!Please contact us by email if you have any questions.