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Journal of Cell Science|January 21, 2022
Lipid-driven CFTR clustering is impaired in cystic fibrosis and restored by corrector drugsAsmahan Abu-Arish, Elvis Pandžić, Yishan Luo, et al.
American Journal of Respiratory and Critical Care Medicine|February 25, 2006
Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokersAndré M Cantin, John W Hanrahan, Ginette Bilodeau, et al.
Chembiochem : a European Journal of Chemical Biology|May 15, 2007
Correctors of protein trafficking defects identified by a novel high-throughput screening assayGraeme W Carlile, Renaud Robert, Donglei Zhang, et al.
Cell|June 17, 2008
BAP31 interacts with Sec61 translocons and promotes retrotranslocation of CFTRDeltaF508 via the derlin-1 complexBing Wang, Hannah Heath-Engel, Donglei Zhang, et al.
Lab on a Chip|July 24, 2019
Magnetic microboats for floating, stiffness tunable, air-liquid interface epithelial culturesArvind Chandrasekaran, Sonya Kouthouridis, Wontae Lee, et al.
American Journal of Respiratory Cell and Molecular Biology|March 23, 2023
Ionocyte-Specific Regulation of Cystic Fibrosis Transmembrane Conductance RegulatorYukiko Sato, Dusik Kim, Mark J Turner, et al.
Molecular Biology of the Cell|September 14, 2012
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epitheliaGuido Veit, Florian Bossard, Julie Goepp, et al.
Channels (Austin, Tex.)|December 10, 2015
Potential sites of CFTR activation by tyrosine kinasesArnaud Billet, Yanlin Jia, Timothy J Jensen, et al.
ACS Nano|January 18, 2025
Nanoscale Viscometry Reveals an Inherent Mucus Defect in Cystic FibrosisOlga Ponomarchuk, Francis Boudreault, Ignacy Gryczynski, et al.
The Journal of Physiology|July 11, 2012
Bicarbonate-dependent chloride transport drives fluid secretion by the human airway epithelial cell line Calu-3Jiajie Shan, Jie Liao, Junwei Huang, et al.
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