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Richard B Moss

Showing results (31-40 of 61) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 22, 2012
Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosisRichard B Moss, Sunil J Mistry, Michael W Konstan, et al.
American Journal of Respiratory and Critical Care Medicine|December 21, 2010
Denufosol tetrasodium in patients with cystic fibrosis and normal to mildly impaired lung functionFrank J Accurso, Richard B Moss, Robert W Wilmott, et al.
Scientific Reports|November 4, 2018
Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adultsJeeyeon Kim, Miesha Farahmand, Colleen Dunn, et al.
The Lancet. Respiratory Medicine|June 14, 2015
Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trialRichard B Moss, Patrick A Flume, J Stuart Elborn, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung functionOsric A Forrest, Daniel M Chopyk, Yael Gernez, et al.
Pediatric Pulmonology|September 25, 2004
Quantitative air-trapping analysis in children with mild cystic fibrosis lung diseaseAnne-Sophie Bonnel, Samuel Moon-Ho Song, Krishnaveni Kesavarju, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 22, 2012
Blood basophils from cystic fibrosis patients with allergic bronchopulmonary aspergillosis are primed and hyper-responsive to stimulation by aspergillus allergensYael Gernez, Colleen E Dunn, Cassie Everson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 13, 2008
Profound functional and signaling changes in viable inflammatory neutrophils homing to cystic fibrosis airwaysRabindra Tirouvanziam, Yael Gernez, Carol K Conrad, et al.
American Journal of Respiratory and Critical Care Medicine|May 15, 2003
Composite spirometric-computed tomography outcome measure in early cystic fibrosis lung diseaseTerry E Robinson, Ann N Leung, William H Northway, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2005
Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrumIris Schrijver, Sudha Ramalingam, Ramalingam Sankaran, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 22, 2012
Safety and early treatment effects of the CXCR2 antagonist SB-656933 in patients with cystic fibrosisRichard B Moss, Sunil J Mistry, Michael W Konstan, et al.
American Journal of Respiratory and Critical Care Medicine|December 21, 2010
Denufosol tetrasodium in patients with cystic fibrosis and normal to mildly impaired lung functionFrank J Accurso, Richard B Moss, Robert W Wilmott, et al.
Scientific Reports|November 4, 2018
Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adultsJeeyeon Kim, Miesha Farahmand, Colleen Dunn, et al.
The Lancet. Respiratory Medicine|June 14, 2015
Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trialRichard B Moss, Patrick A Flume, J Stuart Elborn, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung functionOsric A Forrest, Daniel M Chopyk, Yael Gernez, et al.
Pediatric Pulmonology|September 25, 2004
Quantitative air-trapping analysis in children with mild cystic fibrosis lung diseaseAnne-Sophie Bonnel, Samuel Moon-Ho Song, Krishnaveni Kesavarju, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 22, 2012
Blood basophils from cystic fibrosis patients with allergic bronchopulmonary aspergillosis are primed and hyper-responsive to stimulation by aspergillus allergensYael Gernez, Colleen E Dunn, Cassie Everson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 13, 2008
Profound functional and signaling changes in viable inflammatory neutrophils homing to cystic fibrosis airwaysRabindra Tirouvanziam, Yael Gernez, Carol K Conrad, et al.
American Journal of Respiratory and Critical Care Medicine|May 15, 2003
Composite spirometric-computed tomography outcome measure in early cystic fibrosis lung diseaseTerry E Robinson, Ann N Leung, William H Northway, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2005
Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrumIris Schrijver, Sudha Ramalingam, Ramalingam Sankaran, et al.
Pageof 7