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Michael R Knowles

Showing results (91-100 of 196) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|March 10, 2007
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutationsJohn P Clancy, Steven M Rowe, Zsuzsa Bebok, et al.
Human Genome Variation|July 5, 2017
Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Human Genome Variation|July 14, 2016
Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Molecular Genetics & Genomic Medicine|July 5, 2019
Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patientsKozo Morimoto, Minako Hijikata, Maimoona A Zariwala, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Basic protocol for transepithelial nasal potential difference measurementsDaniel Schüler, Isabelle Sermet-Gaudelus, Michael Wilschanski, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
The Journal of Pediatrics|March 31, 2010
Primary ciliary dyskinesia in Amish communitiesHauw Lie, Maimoona A Zariwala, Cynthia Helms, et al.
ERJ Open Research|January 21, 2026
Mucociliary and cough clearance in primary ciliary dyskinesia as affected by mutations in <i>RSPH1</i> or <i>DNAH5</i>Lawrence E Ostrowski, Sara Abu-Nasser, Kirby L Zeman, et al.
Plos One|October 15, 2011
Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5ACXueliang Guo, Rhonda G Pace, Jaclyn R Stonebraker, et al.
G3 (Bethesda, Md.)|July 4, 2015
Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary DyskinesiaChristian R Marshall, Stephen W Scherer, Maimoona A Zariwala, et al.
Pageof 20

Showing results (91-100 of 196) with videos related to

Sort By:
Pageof 20
American Journal of Respiratory Cell and Molecular Biology|March 10, 2007
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutationsJohn P Clancy, Steven M Rowe, Zsuzsa Bebok, et al.
Human Genome Variation|July 5, 2017
Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Human Genome Variation|July 14, 2016
Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Molecular Genetics & Genomic Medicine|July 5, 2019
Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patientsKozo Morimoto, Minako Hijikata, Maimoona A Zariwala, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Basic protocol for transepithelial nasal potential difference measurementsDaniel Schüler, Isabelle Sermet-Gaudelus, Michael Wilschanski, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
The Journal of Pediatrics|March 31, 2010
Primary ciliary dyskinesia in Amish communitiesHauw Lie, Maimoona A Zariwala, Cynthia Helms, et al.
ERJ Open Research|January 21, 2026
Mucociliary and cough clearance in primary ciliary dyskinesia as affected by mutations in <i>RSPH1</i> or <i>DNAH5</i>Lawrence E Ostrowski, Sara Abu-Nasser, Kirby L Zeman, et al.
Plos One|October 15, 2011
Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5ACXueliang Guo, Rhonda G Pace, Jaclyn R Stonebraker, et al.
G3 (Bethesda, Md.)|July 4, 2015
Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary DyskinesiaChristian R Marshall, Stephen W Scherer, Maimoona A Zariwala, et al.
Pageof 20