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Journal of Visualized Experiments : Jove|October 2, 2018
Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD)George M Solomon, Inez Bronsveld, Kathryn Hayes, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 4, 2017
A multiple reader scoring system for Nasal Potential Difference parametersGeorge M Solomon, Bo Liu, Isabelle Sermet-Gaudelus, et al.The Pediatric Infectious Disease Journal|September 19, 2002
Foodborne disease outbreaks in United States schoolsNicholas A Daniels, Linda MacKinnon, Steven M Rowe, et al.Respiratory Research|September 20, 2017
Roflumilast reverses CFTR-mediated ion transport dysfunction in cigarette smoke-exposed miceS Vamsee Raju, Lawrence Rasmussen, Peter A Sloane, et al.International Forum of Allergy & Rhinology|November 26, 2018
Ivacaftor improves rhinologic, psychologic, and sleep-related quality of life in G551D cystic fibrosis patientsJustin McCormick, Do-Yeon Cho, Brooks Lampkin, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2016
Therapeutic benefit observed with the CFTR potentiator, ivacaftor, in a CF patient homozygous for the W1282X CFTR nonsense mutationVenkateshwar Mutyam, Emily Falk Libby, Ning Peng, et al.Plos One|April 17, 2015
ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartmentsLianwu Fu, Andras Rab, Li ping Tang, et al.American Journal of Rhinology & Allergy|December 22, 2011
Quercetin increases cystic fibrosis transmembrane conductance regulator-mediated chloride transport and ciliary beat frequency: therapeutic implications for chronic rhinosinusitisShaoyan Zhang, Nicholas Smith, Daniel Schuster, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|July 23, 2013
Reduced microtubule acetylation in cystic fibrosis epithelial cellsSharon M Rymut, Alyssa Harker, Deborah A Corey, et al.Journal of Magnetic Resonance Imaging : JMRI|February 20, 2018
Assessment of pulmonary structure-function relationships in young children and adolescents with cystic fibrosis by multivolume proton-MRI and CTFrancesca Pennati, David J Roach, John P Clancy, et al.Pageof 34