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Michael R Knowles

Showing results (101-110 of 196) with videos related to

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Chest|June 5, 2026
Accuracy of clinical phenotype for diagnosing adults with primary ciliary dyskinesiaAmanda Marino, Zofia N Zysman-Colman, Joy Agbonze, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 18, 2011
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cellsValentino Bezzerri, Pio d'Adamo, Alessandro Rimessi, et al.
American Journal of Respiratory and Critical Care Medicine|June 4, 2016
Sources of Variation in Sweat Chloride Measurements in Cystic FibrosisJoseph M Collaco, Scott M Blackman, Karen S Raraigh, et al.
Pediatric Pulmonology|April 24, 2023
First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian InuitJulia Hunter-Schouela, Michael T Geraghty, Robert A Hegele, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 16, 2021
Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatmentKaren S Raraigh, Melis A Aksit, Kurt Hetrick, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
American Journal of Human Genetics|September 11, 2024
Genetic modifiers of body mass index in individuals with cystic fibrosisHua Ling, Karen S Raraigh, Elizabeth W Pugh, et al.
Plos Genetics|August 19, 2015
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic FibrosisMary J Emond, Tin Louie, Julia Emerson, et al.
The Lancet. Respiratory Medicine|September 3, 2023
Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trialFelix C Ringshausen, Adam J Shapiro, Kim G Nielsen, et al.
Pageof 20

Showing results (101-110 of 196) with videos related to

Sort By:
Pageof 20
Chest|June 5, 2026
Accuracy of clinical phenotype for diagnosing adults with primary ciliary dyskinesiaAmanda Marino, Zofia N Zysman-Colman, Joy Agbonze, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 18, 2011
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cellsValentino Bezzerri, Pio d'Adamo, Alessandro Rimessi, et al.
American Journal of Respiratory and Critical Care Medicine|June 4, 2016
Sources of Variation in Sweat Chloride Measurements in Cystic FibrosisJoseph M Collaco, Scott M Blackman, Karen S Raraigh, et al.
Pediatric Pulmonology|April 24, 2023
First reports of primary ciliary dyskinesia caused by a shared DNAH11 allele in Canadian InuitJulia Hunter-Schouela, Michael T Geraghty, Robert A Hegele, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 16, 2021
Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatmentKaren S Raraigh, Melis A Aksit, Kurt Hetrick, et al.
The Journal of Pediatrics|March 13, 2013
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communitiesThomas W Ferkol, Erik G Puffenberger, Hauw Lie, et al.
American Journal of Human Genetics|September 11, 2024
Genetic modifiers of body mass index in individuals with cystic fibrosisHua Ling, Karen S Raraigh, Elizabeth W Pugh, et al.
Plos Genetics|August 19, 2015
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic FibrosisMary J Emond, Tin Louie, Julia Emerson, et al.
The Lancet. Respiratory Medicine|September 3, 2023
Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trialFelix C Ringshausen, Adam J Shapiro, Kim G Nielsen, et al.
Pageof 20