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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 fibrosis
Erin 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 disorders
Deyanira 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 cells
Anya 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 fibrosis
Erin 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 panel
Michael 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 fibrosis
Margaret 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 loci
Sylvia 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 Sites
Melissa 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 Traits
Melis 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 manifestations
Rebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
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of 16
Search research articles
Search
Showing results (111-120 of 158) with videos related to
Sort By:
Page
of 16
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Base editing and nanoparticle transfection of airway cell types essential for treatment of cystic fibrosis
Erin 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 disorders
Deyanira 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 cells
Anya 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 fibrosis
Erin 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 panel
Michael 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 fibrosis
Margaret 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 loci
Sylvia 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 Sites
Melissa 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 Traits
Melis 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 manifestations
Rebecca J Darrah, Frank J Jacono, Neha Joshi, et al.
Page
of 16