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Michael R Knowles

Showing results (161-170 of 196) with videos related to

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American Journal of Respiratory and Critical Care Medicine|August 31, 2017
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease SeverityDeepika Polineni, Hong Dang, Paul J Gallins, et al.
Plos Genetics|July 30, 2016
Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human DiseaseWesley R Lewis, Erik B Malarkey, Douglas Tritschler, et al.
Thorax|December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureMichael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
Nucleic Acids Research|December 10, 2024
Long G4-rich enhancers target promoters via a G4 DNA-based mechanismJeffrey D DeMeis, Justin T Roberts, Haley A Delcher, et al.
Nature Medicine|January 31, 2020
Author Correction: A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearanceRaghu R Chivukula, Daniel T Montoro, Hui Min Leung, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 26, 2017
Frequency of untreated hypogammaglobulinemia in bronchiectasisMelanie A Ruffner, Timothy R Aksamit, Byron Thomashow, et al.
American Journal of Human Genetics|December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaMichael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
American Journal of Human Genetics|October 9, 2012
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaAmjad Horani, Todd E Druley, Maimoona A Zariwala, et al.
HGG Advances|February 7, 2022
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patientsQuan Sun, Weifang Liu, Jonathan D Rosen, et al.
Cells|September 26, 2025
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in QuebecMarie-Hélène Bourassa, Guillaume Sillon, Shuizi Ding, et al.
Pageof 20

Showing results (161-170 of 196) with videos related to

Sort By:
Pageof 20
American Journal of Respiratory and Critical Care Medicine|August 31, 2017
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease SeverityDeepika Polineni, Hong Dang, Paul J Gallins, et al.
Plos Genetics|July 30, 2016
Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human DiseaseWesley R Lewis, Erik B Malarkey, Douglas Tritschler, et al.
Thorax|December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureMichael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
Nucleic Acids Research|December 10, 2024
Long G4-rich enhancers target promoters via a G4 DNA-based mechanismJeffrey D DeMeis, Justin T Roberts, Haley A Delcher, et al.
Nature Medicine|January 31, 2020
Author Correction: A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearanceRaghu R Chivukula, Daniel T Montoro, Hui Min Leung, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 26, 2017
Frequency of untreated hypogammaglobulinemia in bronchiectasisMelanie A Ruffner, Timothy R Aksamit, Byron Thomashow, et al.
American Journal of Human Genetics|December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaMichael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
American Journal of Human Genetics|October 9, 2012
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaAmjad Horani, Todd E Druley, Maimoona A Zariwala, et al.
HGG Advances|February 7, 2022
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patientsQuan Sun, Weifang Liu, Jonathan D Rosen, et al.
Cells|September 26, 2025
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in QuebecMarie-Hélène Bourassa, Guillaume Sillon, Shuizi Ding, et al.
Pageof 20