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Scientific Reports|December 12, 2025
Native CFTR codon bias controls translation rate to balance off-pathway aggregation and channel function by conformational imprintingJae Seok Yoon, Hongyu Li, Yonjung Kim, et al.
Organic & Biomolecular Chemistry|January 30, 2018
Anion transport by ortho-phenylene bis-ureas across cell and vesicle membranesChristopher M Dias, Hongyu Li, Hennie Valkenier, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 14, 2006
Revertant mutants G550E and 4RK rescue cystic fibrosis mutants in the first nucleotide-binding domain of CFTR by different mechanismsMónica Roxo-Rosa, Zhe Xu, André Schmidt, et al.
British Journal of Pharmacology|October 15, 2013
Loop diuretics are open-channel blockers of the cystic fibrosis transmembrane conductance regulator with distinct kineticsMin Ju, Toby S Scott-Ward, Jia Liu, et al.
The Journal of Biological Chemistry|June 17, 2010
Folding and rescue of a cystic fibrosis transmembrane conductance regulator trafficking mutant identified using human-murine chimeric proteinsAna Carina Da Paula, Marisa Sousa, Zhe Xu, et al.
Chemical Science|September 23, 2017
Targeted anion transporter delivery by coiled-coil driven membrane fusionNestor Lopez Mora, Azadeh Bahreman, Hennie Valkenier, et al.
The Journal of Physiology|March 5, 2014
Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTRZhe Xu, Luísa S Pissarra, Carlos M Farinha, et al.
Biochemical and Biophysical Research Communications|January 20, 2020
Parathyroid hormone increases CFTR expression and function in Caco-2 intestinal epithelial cellsWalailak Jantarajit, Kannikar Wongdee, Kornkamon Lertsuwan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|September 16, 2020
Carbon monoxide-releasing molecules inhibit the cystic fibrosis transmembrane conductance regulator Cl- channelMayuree Rodrat, Walailak Jantarajit, Demi R S Ng, et al.
The Journal of Biological Chemistry|January 15, 2017
Two Small Molecules Restore Stability to a Subpopulation of the Cystic Fibrosis Transmembrane Conductance Regulator with the Predominant Disease-causing MutationXin Meng, Yiting Wang, Xiaomeng Wang, et al.
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