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Expert Opinion on Emerging Drugs|December 22, 2017
An update on new and emerging therapies for cystic fibrosisKristin M Hudock, John Paul ClancyMethods in Molecular Biology (Clifton, N.J.)|May 20, 2011
Nasal potential difference measurements to assess CFTR ion channel activitySteven M Rowe, John Paul Clancy, Michael WilschanskiThe Journal of Biological Chemistry|April 29, 2005
Activating cystic fibrosis transmembrane conductance regulator channels with pore blocker analogsWei Wang, Ge Li, John Paul Clancy, et al.Viruses|September 24, 2013
Respiratory syncytial virus infection disrupts monolayer integrity and function in cystic fibrosis airway cellsMichele Kong, Patrick Maeng, Jeong Hong, et al.Molecular Medicine (Cambridge, Mass.)|January 30, 2010
Human neutrophil elastase-mediated cleavage sites of MMP-9 and TIMP-1: implications to cystic fibrosis proteolytic dysfunctionPatricia L Jackson, Xin Xu, Landon Wilson, et al.The Journal of Biological Chemistry|October 13, 2007
Cystic fibrosis transmembrane conductance regulator trafficking is mediated by the COPI coat in epithelial cellsJessica Rennolds, Cristy Tower, Lois Musgrove, et al.American Journal of Respiratory Cell and Molecular Biology|March 4, 2008
DETANO and nitrated lipids increase chloride secretion across lung airway cellsLan Chen, Charles A Bosworth, Tristant Pico, et al.Viruses|August 13, 2015
Matrix Metalloproteinase-9 Mediates RSV Infection in Vitro and in VivoMichele Y F Kong, Richard J Whitley, Ning Peng, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 22, 2020
The impact of SARS-CoV-2 on the cystic fibrosis foundation therapeutics development networkKelsie Pearson, Nicole Mayer-Hamblett, Christopher H Goss, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 19, 2021
Long-term amikacin liposome inhalation suspension in cystic fibrosis patients with chronic P. aeruginosa infectionDiana Bilton, Isabelle Fajac, Tacjana Pressler, et al.Pageof 2