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Michael R Knowles

Showing results (121-130 of 196) with videos related to

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Plos Genetics|August 9, 2020
Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesiaXimena M Bustamante-Marin, Amjad Horani, Mihaela Stoyanova, et al.
American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.
OTO Open|February 24, 2025
Progression of Otologic and Nasal Symptoms in Primary Ciliary Dyskinesia Throughout ChildhoodIsabelle Dagher, Adam J Kimple, Thomas W Ferkol, et al.
Circulation|May 23, 2007
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaMarcus P Kennedy, Heymut Omran, Margaret W Leigh, 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.
Pediatric Pulmonology|May 12, 2009
IL1B polymorphisms modulate cystic fibrosis lung diseaseHara Levy, Amy Murphy, Fei Zou, 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.
The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Pageof 20

Showing results (121-130 of 196) with videos related to

Sort By:
Pageof 20
Plos Genetics|August 9, 2020
Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesiaXimena M Bustamante-Marin, Amjad Horani, Mihaela Stoyanova, et al.
American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.
OTO Open|February 24, 2025
Progression of Otologic and Nasal Symptoms in Primary Ciliary Dyskinesia Throughout ChildhoodIsabelle Dagher, Adam J Kimple, Thomas W Ferkol, et al.
Circulation|May 23, 2007
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaMarcus P Kennedy, Heymut Omran, Margaret W Leigh, 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.
Pediatric Pulmonology|May 12, 2009
IL1B polymorphisms modulate cystic fibrosis lung diseaseHara Levy, Amy Murphy, Fei Zou, 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.
The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Pageof 20