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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 sensing
Lila 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 study
Nuno 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 phenotypes
Wanda 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 Clearance
Ximena 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 Genotype
BreAnna 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 studies
Chelsea 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 Syndrome
Adam 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 pathogenesis
Jaclyn 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 Behavior
Ayesha 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 loci
Jiafen Gong, Fan Wang, Bowei Xiao, et al.
Page
of 95
Search research articles
Search
Showing results (901-910 of 950) with videos related to
Sort By:
Page
of 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 sensing
Lila 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 study
Nuno 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 phenotypes
Wanda 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 Clearance
Ximena 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 Genotype
BreAnna 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 studies
Chelsea 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 Syndrome
Adam 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 pathogenesis
Jaclyn 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 Behavior
Ayesha 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 loci
Jiafen Gong, Fan Wang, Bowei Xiao, et al.
Page
of 95