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Showing results (871-880 of 950) with videos related to

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Pediatric Pulmonology|May 12, 2009
IL1B polymorphisms modulate cystic fibrosis lung diseaseHara Levy, Amy Murphy, Fei Zou, et al.
Pediatric Pulmonology|February 2, 2011
Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experienceJ Tod Olin, Kim Burns, Johnny L Carson, et al.
American Journal of Respiratory Cell and Molecular Biology|September 10, 2013
Genome reference and sequence variation in the large repetitive central exon of human MUC5ACXueliang Guo, Shuo Zheng, Hong Dang, et al.
Chest|March 1, 2014
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxyAdam J Shapiro, Stephanie D Davis, Thomas Ferkol, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 16, 2021
Comparing encounter-based and annualized chronic pseudomonas infection definitions in cystic fibrosisMargaret Rosenfeld, Anna V Faino, Frankline Onchiri, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|May 12, 2017
Responsiveness to oral prednisolone in severe asthma is related to the degree of eosinophilic airway inflammationA R Sousa, R P Marshall, L C Warnock, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
American Journal of Respiratory and Critical Care Medicine|August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and GenotypeStephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Diabetes|May 15, 2013
Genetic modifiers of cystic fibrosis-related diabetesScott M Blackman, Clayton W Commander, Christopher Watson, et al.
Clinical Genetics|August 5, 2010
Understanding the population structure of North American patients with cystic fibrosisW Li, L Sun, M Corey, et al.
Pageof 95

Showing results (871-880 of 950) with videos related to

Sort By:
Pageof 95
Pediatric Pulmonology|May 12, 2009
IL1B polymorphisms modulate cystic fibrosis lung diseaseHara Levy, Amy Murphy, Fei Zou, et al.
Pediatric Pulmonology|February 2, 2011
Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experienceJ Tod Olin, Kim Burns, Johnny L Carson, et al.
American Journal of Respiratory Cell and Molecular Biology|September 10, 2013
Genome reference and sequence variation in the large repetitive central exon of human MUC5ACXueliang Guo, Shuo Zheng, Hong Dang, et al.
Chest|March 1, 2014
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxyAdam J Shapiro, Stephanie D Davis, Thomas Ferkol, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 16, 2021
Comparing encounter-based and annualized chronic pseudomonas infection definitions in cystic fibrosisMargaret Rosenfeld, Anna V Faino, Frankline Onchiri, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|May 12, 2017
Responsiveness to oral prednisolone in severe asthma is related to the degree of eosinophilic airway inflammationA R Sousa, R P Marshall, L C Warnock, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
American Journal of Respiratory and Critical Care Medicine|August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and GenotypeStephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Diabetes|May 15, 2013
Genetic modifiers of cystic fibrosis-related diabetesScott M Blackman, Clayton W Commander, Christopher Watson, et al.
Clinical Genetics|August 5, 2010
Understanding the population structure of North American patients with cystic fibrosisW Li, L Sun, M Corey, et al.
Pageof 95