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Michael R Knowles

Showing results (31-40 of 196) with videos related to

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Proteomics|December 13, 2005
Detection of gender differences in rat lens proteins using 2-D-DIGEPaul C Guest, Heather A Skynner, Kamran Salim, et al.
American Journal of Respiratory and Critical Care Medicine|November 2, 2002
Increasing concentration of inhaled saline with or without amiloride: effect on mucociliary clearance in normal subjectsNamita Sood, William D Bennett, Kirby Zeman, et al.
The New England Journal of Medicine|January 20, 2006
Mucus clearance and lung function in cystic fibrosis with hypertonic salineScott H Donaldson, William D Bennett, Kirby L Zeman, et al.
American Journal of Respiratory Cell and Molecular Biology|November 25, 2003
Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesiaMaimoona Zariwala, Wanda K O'Neal, Peadar G Noone, et al.
The Journal of General Physiology|January 5, 2002
In vivo airway surface liquid Cl- analysis with solid-state electrodesRay A Caldwell, Barbara R Grubb, Robert Tarran, et al.
Chest|March 15, 2002
Mutations in DNAI1 (IC78) cause primary ciliary dyskinesiaPeadar G Noone, Maimoona Zariwala, Aruna Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|August 22, 2019
High-Speed Videomicroscopy Analysis Presents Limitations in Diagnosis of Primary Ciliary DyskinesiaAdam J Shapiro, Thomas W Ferkol, Michele Manion, et al.
BMC Pulmonary Medicine|July 27, 2019
Primary ciliary dyskinesia in Japan: systematic review and meta-analysisAtsushi Inaba, Masanori Furuhata, Kozo Morimoto, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 11, 2021
Immunoglobulin GM and KM allotypes are associated with antibody responses to Pseudomonas aeruginosa antigens in chronically infected cystic fibrosis patientsJanardan P Pandey, Aryan M Namboodiri, Paul J Nietert, et al.
Pediatric Pulmonology|February 22, 2011
Plasma TGF-β₁ in pediatric cystic fibrosis: potential biomarker of lung disease and response to therapyWilliam T Harris, Marianne S Muhlebach, Robert A Oster, et al.
Pageof 20

Showing results (31-40 of 196) with videos related to

Sort By:
Pageof 20
Proteomics|December 13, 2005
Detection of gender differences in rat lens proteins using 2-D-DIGEPaul C Guest, Heather A Skynner, Kamran Salim, et al.
American Journal of Respiratory and Critical Care Medicine|November 2, 2002
Increasing concentration of inhaled saline with or without amiloride: effect on mucociliary clearance in normal subjectsNamita Sood, William D Bennett, Kirby Zeman, et al.
The New England Journal of Medicine|January 20, 2006
Mucus clearance and lung function in cystic fibrosis with hypertonic salineScott H Donaldson, William D Bennett, Kirby L Zeman, et al.
American Journal of Respiratory Cell and Molecular Biology|November 25, 2003
Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesiaMaimoona Zariwala, Wanda K O'Neal, Peadar G Noone, et al.
The Journal of General Physiology|January 5, 2002
In vivo airway surface liquid Cl- analysis with solid-state electrodesRay A Caldwell, Barbara R Grubb, Robert Tarran, et al.
Chest|March 15, 2002
Mutations in DNAI1 (IC78) cause primary ciliary dyskinesiaPeadar G Noone, Maimoona Zariwala, Aruna Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|August 22, 2019
High-Speed Videomicroscopy Analysis Presents Limitations in Diagnosis of Primary Ciliary DyskinesiaAdam J Shapiro, Thomas W Ferkol, Michele Manion, et al.
BMC Pulmonary Medicine|July 27, 2019
Primary ciliary dyskinesia in Japan: systematic review and meta-analysisAtsushi Inaba, Masanori Furuhata, Kozo Morimoto, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 11, 2021
Immunoglobulin GM and KM allotypes are associated with antibody responses to Pseudomonas aeruginosa antigens in chronically infected cystic fibrosis patientsJanardan P Pandey, Aryan M Namboodiri, Paul J Nietert, et al.
Pediatric Pulmonology|February 22, 2011
Plasma TGF-β₁ in pediatric cystic fibrosis: potential biomarker of lung disease and response to therapyWilliam T Harris, Marianne S Muhlebach, Robert A Oster, et al.
Pageof 20