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Garry R Cutting

Showing results (71-80 of 158) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 8, 2022
Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variantsKaren S Raraigh, Michelle H Lewis, Joseph M Collaco, et al.
The Journal of Biological Chemistry|August 9, 2002
PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulatorAgnieszka Swiatecka-Urban, Marc Duhaime, Bonita Coutermarsh, et al.
Plos One|November 30, 2011
Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort studyJoseph M Collaco, John McGready, Deanna M Green, et al.
The Journal of Biological Chemistry|November 15, 2001
A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expressionJie Cheng, Bryan D Moyer, Michal Milewski, et al.
American Journal of Human Genetics|April 24, 2012
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2CHila Romi, Idan Cohen, Daniella Landau, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 24, 2015
Creation and characterization of an airway epithelial cell line for stable expression of CFTR variantsLaura B Gottschalk, Briana Vecchio-Pagan, Neeraj Sharma, et al.
Biorxiv : the Preprint Server for Biology|June 29, 2026
Clinical and primary cell evidence reveals complex CFTR function-phenotype relationshipsKristen A Miller, Audrey Pion, Ana Topasna, et al.
International Forum of Allergy & Rhinology|April 14, 2020
Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosisNicholas M Dalesio, Melis A Aksit, Kwangmi Ahn, et al.
Plos One|November 30, 2020
Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputationHong Dang, Deepika Polineni, Rhonda G Pace, et al.
Pediatric Research|March 23, 2021
Characterizing mucociliary clearance in young children with cystic fibrosisBeth L Laube, Kathryn A Carson, Christopher M Evans, et al.
Pageof 16

Showing results (71-80 of 158) with videos related to

Sort By:
Pageof 16
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 8, 2022
Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variantsKaren S Raraigh, Michelle H Lewis, Joseph M Collaco, et al.
The Journal of Biological Chemistry|August 9, 2002
PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulatorAgnieszka Swiatecka-Urban, Marc Duhaime, Bonita Coutermarsh, et al.
Plos One|November 30, 2011
Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort studyJoseph M Collaco, John McGready, Deanna M Green, et al.
The Journal of Biological Chemistry|November 15, 2001
A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expressionJie Cheng, Bryan D Moyer, Michal Milewski, et al.
American Journal of Human Genetics|April 24, 2012
Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2CHila Romi, Idan Cohen, Daniella Landau, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 24, 2015
Creation and characterization of an airway epithelial cell line for stable expression of CFTR variantsLaura B Gottschalk, Briana Vecchio-Pagan, Neeraj Sharma, et al.
Biorxiv : the Preprint Server for Biology|June 29, 2026
Clinical and primary cell evidence reveals complex CFTR function-phenotype relationshipsKristen A Miller, Audrey Pion, Ana Topasna, et al.
International Forum of Allergy & Rhinology|April 14, 2020
Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosisNicholas M Dalesio, Melis A Aksit, Kwangmi Ahn, et al.
Plos One|November 30, 2020
Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputationHong Dang, Deepika Polineni, Rhonda G Pace, et al.
Pediatric Research|March 23, 2021
Characterizing mucociliary clearance in young children with cystic fibrosisBeth L Laube, Kathryn A Carson, Christopher M Evans, et al.
Pageof 16