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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Determination of CFTR chloride channel activity and pharmacology using radiotracer flux methodsCaroline Norez, Ghanshyam D Heda, Timothy Jensen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 25, 2026
Clinical, functional and therapeutic evaluation of CFTR variant I507delNeeraj Sharma, Katherine Starego, Hongyu Li, et al.
JCI Insight|July 27, 2018
Residual function of cystic fibrosis mutants predicts response to small molecule CFTR modulatorsSangwoo T Han, Andras Rab, Matthew J Pellicore, et al.
Respiratory Research|April 25, 2024
In vitro platform to model the function of ionocytes in the human airway epitheliumMarta Vilà-González, Laetitia Pinte, Ricardo Fradique, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
The patch-clamp and planar lipid bilayer techniques: powerful and versatile tools to investigate the CFTR Cl- channelDavid N Sheppard, Michael A Gray, Xiandi Gong, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|May 14, 2025
Managing an ageing cystic fibrosis population: challenges and prioritiesFreddy J Frost, Daniel G Peckham, Imogen C Felton, et al.
Molecular Biology of the Cell|January 30, 2016
From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutationsGudio Veit, Radu G Avramescu, Annette N Chiang, et al.
JCI Insight|March 22, 2022
CFTR bearing variant p.Phe312del exhibits function inconsistent with phenotype and negligible response to ivacaftorKaren S Raraigh, Kathleen C Paul, Jennifer L Goralski, et al.
Nature Biotechnology|April 29, 2008
CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expressionStephen C Hyde, Ian A Pringle, Syahril Abdullah, et al.
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