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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 7, 2020
Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTRSamuel J Bose, Georg Krainer, Demi R S Ng, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
Mouse models of cystic fibrosis: phenotypic analysis and research applicationsMartina Wilke, Ruvalic M Buijs-Offerman, Jamil Aarbiou, et al.
The Journal of Physiology|November 11, 2021
Correlating genotype with phenotype using CFTR-mediated whole-cell Cl- currents in human nasal epithelial cellsSabrina Noel, Nathalie Servel, Aurélie Hatton, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 14, 2009
Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTRKate J Treharne, Zhe Xu, Jeng-Haur Chen, et al.
Nature Chemical Biology|August 3, 2021
A topological switch in CFTR modulates channel activity and sensitivity to unfoldingDaniel Scholl, Maud Sigoillot, Marie Overtus, et al.
The Journal of Biological Chemistry|February 10, 2007
Protein kinase CK2, cystic fibrosis transmembrane conductance regulator, and the deltaF508 mutation: F508 deletion disrupts a kinase-binding siteKate J Treharne, Russell M Crawford, Zhe Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 5, 2007
Chimeric constructs endow the human CFTR Cl- channel with the gating behavior of murine CFTRToby S Scott-Ward, Zhiwei Cai, Elizabeth S Dawson, et al.
Chemical Science|March 19, 2019
Fluorinated synthetic anion carriers: experimental and computational insights into transmembrane chloride transportMichael J Spooner, Hongyu Li, Igor Marques, et al.
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