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British Journal of Pharmacology|October 13, 2021
A small molecule CFTR potentiator restores ATP-dependent channel gating to the cystic fibrosis mutant G551D-CFTRJia Liu, Allison P Berg, Yiting Wang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Murine epithelial cells: isolation and cultureDonald J Davidson, Michael A Gray, Fiona M Kilanowski, et al.
The Journal of Physiology|January 8, 2024
Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftorHongyu Li, Mayuree Rodrat, Majid K Al-Salmani, et al.
Plos Biology|May 17, 2017
Alteration of protein function by a silent polymorphism linked to tRNA abundanceSebastian Kirchner, Zhiwei Cai, Robert Rauscher, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 11, 2019
Differential thermostability and response to cystic fibrosis transmembrane conductance regulator potentiators of human and mouse F508del-CFTRSamuel J Bose, Marcel J C Bijvelds, Yiting Wang, et al.
The Journal of Physiology|March 13, 2015
Impact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gatingZhiwei Cai, Timea Palmai-Pallag, Pissared Khuituan, et al.
Nature Chemistry|December 18, 2015
Efficient, non-toxic anion transport by synthetic carriers in cells and epitheliaHongyu Li, Hennie Valkenier, Luke W Judd, et al.
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