NACFC 2022 | W36: Genetic and Cell-Based Approaches to Cystic Fibrosis Therapy
CF Foundation | Exploring Treatments for Nonsense and Rare Mutations
NACFC 2020: How Genetic-Based Therapies Could Restore CFTR Function
CF Foundation | Gene Editing in Cystic Fibrosis
CF Foundation | How Gene Editing Could Be Used for CF
Advances in Gene Therapy for Cystic Fibrosis – Paul McCray, MD
CF Foundation | Research Overview: Genetic Therapies in Cystic Fibrosis
Bugs, drugs and genes: seeking new treatments for cystic fibrosis
CF Foundation | RNA Therapy
CF Foundation | Emerging Genetic-Based Therapies for CF
ResearchCon 2020 | Beyond Modulators: Genetic Therapies on the Horizon
GENE THERAPY FOR CYSTIC FIBROSIS
NACFC 2023 | Genetic Therapies for All: Harnessing Cross-Disease Knowledge for Breakthroughs in CF
A New Approach to Treating Cystic Fibrosis
CF Foundation | CFTR Restoration for all People with CF
CF Foundation | Challenges & Progress in the Pursuit of Genetic Therapies for Cystic Fibrosis
ResearchCon 2020 | Therapeutic Approaches for Rare and Nonsense Mutations
A "Patient-Driven" Approach to Cystic Fibrosis Research | Webinar | Ambry Genetics
Professor Brandon Wainwright explains gene therapy for cystic fibrosis
Is gene therapy for everyone? | CF WEEK 2023