Cftr Correction

Correcting the ΔF508 mutation of the CF gene by CRISPR/Cas9

The Physiological Society

CF Foundation | 2017 VLC: New Advances in Characterizing and Correcting CFTR Mutations Round 1

Cystic Fibrosis Foundation

CF Foundation | CFTR Restoration for all People with CF

Cystic Fibrosis Foundation

CF Foundation | 2017 VLC: New Advances in Characterizing and Correcting CFTR Mutations Round 2

Cystic Fibrosis Foundation

NACFC 2022 | S13: Progress Towards Genomic Correction of Cystic Fibrosis Lung Disease

Cystic Fibrosis Foundation

NACFC 2021 | W22: Targeting CFTR DNA/RNA Repair for Rescue

Cystic Fibrosis Foundation

CF Foundation | Gene Editing in Cystic Fibrosis

Cystic Fibrosis Foundation

NACFC 2021 | W23: Processing, Trafficking, and Interactions of Misfolded CFTR Mutants

Cystic Fibrosis Foundation

NACFC 2021 | W31: Difficult to Treat CFTR Mutations, Novel Modulator, RNA Editing Tech to Fix CFTR

Cystic Fibrosis Foundation

Lentivirus-mediated Gene Transfer in Stem Cells for Correction of Cystic Fibrosis Defect in Airway

NACFC 2021 | Restoring CFTR When There is None: Emerging Strategies to Overcome Refractory Variants

Cystic Fibrosis Foundation

NACFC 2021 | W14: New Developments Correcting the Basic Defect

Cystic Fibrosis Foundation

Cystic Fibrosis Mechanism and Treatment | HHMI BioInteractive Video

NACFC 2021 | S17: Gene Editing to Target CFTR DNA Repair

Cystic Fibrosis Foundation

NACFC 2021 | S18: Modulating the CFTR Molecule

Cystic Fibrosis Foundation

Cystic Fibrosis - ∆F508 mutation of CFTR

Elliot Nicholson

NACFC 2020 | S21: CFTR: Biology Boosting CFTR Expression and Function

Cystic Fibrosis Foundation

NACFC 2023 | W05: Rescuing CFTR Premature Truncation Alleles

Cystic Fibrosis Foundation

How CFTR Modulators Work for People with One F508del Mutation

Cystic Fibrosis Foundation

NACFC 2020: How Genetic-Based Therapies Could Restore CFTR Function

Cystic Fibrosis Foundation