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R Knowles

Showing results (901-910 of 950) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 7, 2024
Diamond surface functionalization via visible light-driven C-H activation for nanoscale quantum sensingLila V H Rodgers, Suong T Nguyen, James H Cox, et al.
Journal of Psychosomatic Research|July 4, 2021
The impact of the coronavirus (COVID-19) pandemic on individuals with gastrointestinal disorders: A protocol of an international collaborative studyNuno Ferreira, Antonina Mikocka-Walus, Miranda A L van Tilburg, et al.
American Journal of Human Genetics|February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypesWanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
American Journal of Human Genetics|January 23, 2019
Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary ClearanceXimena M Bustamante-Marin, Wei-Ning Yin, Patrick R Sears, et al.
Annals of the American Thoracic Society|November 28, 2022
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and GenotypeBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
Pediatric Pulmonology|April 5, 2011
A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studiesChelsea Taylor, Clayton W Commander, Joseph M Collaco, et al.
The Journal of Pediatrics|February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta SyndromeAdam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
Hepatology (Baltimore, Md.)|March 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesisJaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins, et al.
Neurogastroenterology and Motility|May 11, 2026
A Clinical Practice Update for the Management of Patients With Disorders of Gut-Brain Interaction and Altered Food Intake BehaviorAyesha Shah, Nicholas J Talley, Simon R Knowles, et al.
Plos Genetics|February 27, 2019
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier lociJiafen Gong, Fan Wang, Bowei Xiao, et al.
Pageof 95

Showing results (901-910 of 950) with videos related to

Sort By:
Pageof 95
Proceedings of the National Academy of Sciences of the United States of America|March 7, 2024
Diamond surface functionalization via visible light-driven C-H activation for nanoscale quantum sensingLila V H Rodgers, Suong T Nguyen, James H Cox, et al.
Journal of Psychosomatic Research|July 4, 2021
The impact of the coronavirus (COVID-19) pandemic on individuals with gastrointestinal disorders: A protocol of an international collaborative studyNuno Ferreira, Antonina Mikocka-Walus, Miranda A L van Tilburg, et al.
American Journal of Human Genetics|February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypesWanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
American Journal of Human Genetics|January 23, 2019
Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary ClearanceXimena M Bustamante-Marin, Wei-Ning Yin, Patrick R Sears, et al.
Annals of the American Thoracic Society|November 28, 2022
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and GenotypeBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
Pediatric Pulmonology|April 5, 2011
A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studiesChelsea Taylor, Clayton W Commander, Joseph M Collaco, et al.
The Journal of Pediatrics|February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta SyndromeAdam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
Hepatology (Baltimore, Md.)|March 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesisJaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins, et al.
Neurogastroenterology and Motility|May 11, 2026
A Clinical Practice Update for the Management of Patients With Disorders of Gut-Brain Interaction and Altered Food Intake BehaviorAyesha Shah, Nicholas J Talley, Simon R Knowles, et al.
Plos Genetics|February 27, 2019
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier lociJiafen Gong, Fan Wang, Bowei Xiao, et al.
Pageof 95