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Garry R Cutting

Showing results (61-70 of 158) with videos related to

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JAMA Internal Medicine|June 16, 2025
Diseases Common in Persons With Cystic Fibrosis Among CFTR HeterozygotesChenjie Zeng, Sangwoo T Han, Thomas A Cassini, et al.
The European Respiratory Journal|January 8, 2022
<i>C</i> <i>FTR</i> variants are associated with chronic bronchitis in smokersAabida Saferali, Dandi Qiao, Wonji Kim, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 5, 2024
Establishment of a conditionally reprogrammed primary eccrine sweat gland culture for evaluation of tissue-specific CFTR functionAlice C Eastman, Gedge Rosson, Noori Kim, et al.
Journal of Medical Genetics|November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTRMolly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
JAMA|January 31, 2008
Interactions between secondhand smoke and genes that affect cystic fibrosis lung diseaseJ Michael Collaco, Lori Vanscoy, Lindsay Bremer, et al.
Human Molecular Genetics|April 22, 2008
Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosisLindsay A Bremer, Scott M Blackman, Lori L Vanscoy, et al.
The Journal of Physiology|January 8, 2024
Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftorHongyu Li, Mayuree Rodrat, Majid K Al-Salmani, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2007
Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiencyStephanie C Hsu, Joshua D Groman, Christian A Merlo, et al.
Microbiome|July 30, 2014
The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of interventionThomas H Hampton, Deanna M Green, Garry R Cutting, et al.
Respiratory Research|October 12, 2010
Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patientsDeanna M Green, Kathryn E McDougal, Scott M Blackman, et al.
Pageof 16

Showing results (61-70 of 158) with videos related to

Sort By:
Pageof 16
JAMA Internal Medicine|June 16, 2025
Diseases Common in Persons With Cystic Fibrosis Among CFTR HeterozygotesChenjie Zeng, Sangwoo T Han, Thomas A Cassini, et al.
The European Respiratory Journal|January 8, 2022
<i>C</i> <i>FTR</i> variants are associated with chronic bronchitis in smokersAabida Saferali, Dandi Qiao, Wonji Kim, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 5, 2024
Establishment of a conditionally reprogrammed primary eccrine sweat gland culture for evaluation of tissue-specific CFTR functionAlice C Eastman, Gedge Rosson, Noori Kim, et al.
Journal of Medical Genetics|November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTRMolly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
JAMA|January 31, 2008
Interactions between secondhand smoke and genes that affect cystic fibrosis lung diseaseJ Michael Collaco, Lori Vanscoy, Lindsay Bremer, et al.
Human Molecular Genetics|April 22, 2008
Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosisLindsay A Bremer, Scott M Blackman, Lori L Vanscoy, et al.
The Journal of Physiology|January 8, 2024
Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftorHongyu Li, Mayuree Rodrat, Majid K Al-Salmani, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2007
Patients with mutations in Gsalpha have reduced activation of a downstream target in epithelial tissues due to haploinsufficiencyStephanie C Hsu, Joshua D Groman, Christian A Merlo, et al.
Microbiome|July 30, 2014
The microbiome in pediatric cystic fibrosis patients: the role of shared environment suggests a window of interventionThomas H Hampton, Deanna M Green, Garry R Cutting, et al.
Respiratory Research|October 12, 2010
Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patientsDeanna M Green, Kathryn E McDougal, Scott M Blackman, et al.
Pageof 16