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John P Clancy

Showing results (71-80 of 121) with videos related to

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Annals of the American Thoracic Society|August 24, 2016
Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung DiseaseDavid J Roach, Yannick Crémillieux, Robert J Fleck, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 18, 2019
Current state of the art MRI for the longitudinal assessment of cystic fibrosisJason C Woods, Jim M Wild, Mark O Wielpütz, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|May 5, 2021
Patient personalized translational tools in cystic fibrosis to transform data from bench to bed-side and backKavisha Arora, Fanmuyi Yang, John Brewington, et al.
NAR Genomics and Bioinformatics|June 6, 2020
CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regionsWilliam D Stuart, Minzhe Guo, Iris M Fink-Baldauf, et al.
Chest|February 16, 2013
Reduced sodium transport with nasal administration of the prostasin inhibitor camostat in subjects with cystic fibrosisSteven M Rowe, Ginger Reeves, Heather Hathorne, et al.
The Journal of Biological Chemistry|December 20, 2005
Up-regulation of AMP-activated kinase by dysfunctional cystic fibrosis transmembrane conductance regulator in cystic fibrosis airway epithelial cells mitigates excessive inflammationKenneth R Hallows, Adam C Fitch, Christine A Richardson, et al.
The European Respiratory Journal|December 7, 2013
Pulmonary matrix metalloproteinase-9 activity in mechanically ventilated children with respiratory syncytial virusMichele Y F Kong, John P Clancy, Ning Peng, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 7, 2021
Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulationEmrah Gecili, Weiji Su, Cole Brokamp, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2002
A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKAAnjaparavanda P Naren, Bryan Cobb, Chunying Li, et al.
American Journal of Respiratory and Critical Care Medicine|August 27, 2024
Elexacaftor/Tezacaftor/Ivacaftor Markedly Reduces <i>Aspergillus fumigatus</i> in Cystic FibrosisSarah J Morgan, David P Nichols, Windy Ni, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Annals of the American Thoracic Society|August 24, 2016
Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung DiseaseDavid J Roach, Yannick Crémillieux, Robert J Fleck, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 18, 2019
Current state of the art MRI for the longitudinal assessment of cystic fibrosisJason C Woods, Jim M Wild, Mark O Wielpütz, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|May 5, 2021
Patient personalized translational tools in cystic fibrosis to transform data from bench to bed-side and backKavisha Arora, Fanmuyi Yang, John Brewington, et al.
NAR Genomics and Bioinformatics|June 6, 2020
CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regionsWilliam D Stuart, Minzhe Guo, Iris M Fink-Baldauf, et al.
Chest|February 16, 2013
Reduced sodium transport with nasal administration of the prostasin inhibitor camostat in subjects with cystic fibrosisSteven M Rowe, Ginger Reeves, Heather Hathorne, et al.
The Journal of Biological Chemistry|December 20, 2005
Up-regulation of AMP-activated kinase by dysfunctional cystic fibrosis transmembrane conductance regulator in cystic fibrosis airway epithelial cells mitigates excessive inflammationKenneth R Hallows, Adam C Fitch, Christine A Richardson, et al.
The European Respiratory Journal|December 7, 2013
Pulmonary matrix metalloproteinase-9 activity in mechanically ventilated children with respiratory syncytial virusMichele Y F Kong, John P Clancy, Ning Peng, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 7, 2021
Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulationEmrah Gecili, Weiji Su, Cole Brokamp, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2002
A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKAAnjaparavanda P Naren, Bryan Cobb, Chunying Li, et al.
American Journal of Respiratory and Critical Care Medicine|August 27, 2024
Elexacaftor/Tezacaftor/Ivacaftor Markedly Reduces <i>Aspergillus fumigatus</i> in Cystic FibrosisSarah J Morgan, David P Nichols, Windy Ni, et al.
Pageof 13