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Garry R Cutting

Showing results (111-120 of 158) with videos related to

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Biorxiv : the Preprint Server for Biology|November 24, 2025
Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosisErin W Kavanagh, Anya T Joynt, Audrey R Pion, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Molecular Therapy. Nucleic Acids|August 7, 2023
Protospacer modification improves base editing of a canonical splice site variant and recovery of CFTR function in human airway epithelial cellsAnya T Joynt, Erin W Kavanagh, Gregory A Newby, et al.
JCI Insight|May 8, 2026
Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosisErin W Kavanagh, Anya T Joynt, Audrey R Pion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 17, 2004
Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panelMichael S Watson, Garry R Cutting, Robert J Desnick, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 16, 2021
Comparing encounter-based and annualized chronic pseudomonas infection definitions in cystic fibrosisMargaret Rosenfeld, Anna V Faino, Frankline Onchiri, et al.
Human Mutation|January 7, 2010
Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal lociSylvia Quemener, Jian-Min Chen, Nadia Chuzhanova, et al.
American Journal of Human Genetics|May 6, 2017
Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice SitesMelissa Lee, Patrick Roos, Neeraj Sharma, et al.
The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
Pageof 16

Showing results (111-120 of 158) with videos related to

Sort By:
Pageof 16
Biorxiv : the Preprint Server for Biology|November 24, 2025
Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosisErin W Kavanagh, Anya T Joynt, Audrey R Pion, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Molecular Therapy. Nucleic Acids|August 7, 2023
Protospacer modification improves base editing of a canonical splice site variant and recovery of CFTR function in human airway epithelial cellsAnya T Joynt, Erin W Kavanagh, Gregory A Newby, et al.
JCI Insight|May 8, 2026
Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosisErin W Kavanagh, Anya T Joynt, Audrey R Pion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 17, 2004
Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panelMichael S Watson, Garry R Cutting, Robert J Desnick, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 16, 2021
Comparing encounter-based and annualized chronic pseudomonas infection definitions in cystic fibrosisMargaret Rosenfeld, Anna V Faino, Frankline Onchiri, et al.
Human Mutation|January 7, 2010
Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal lociSylvia Quemener, Jian-Min Chen, Nadia Chuzhanova, et al.
American Journal of Human Genetics|May 6, 2017
Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice SitesMelissa Lee, Patrick Roos, Neeraj Sharma, et al.
The Journal of Clinical Endocrinology and Metabolism|November 8, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related TraitsMelis A Aksit, Rhonda G Pace, Briana Vecchio-Pagán, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2018
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestationsRebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
Pageof 16