Generation and characterization of a ~F508 cystic fibrosis mouse model
Generation and characterization of a ~F508 cystic fibrosis mouse model
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect
Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR - Journal of Cystic Fibrosis
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9 - Dreano - 2019 - Animal Models and Experimental Medicine - Wiley Online Library
Frontiers | Animal Models in the Pathophysiology of Cystic Fibrosis
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9 - Dreano - 2019 - Animal Models and Experimental Medicine - Wiley Online Library
Animal models of cystic fibrosis - Journal of Cystic Fibrosis
ΔF508 - an overview | ScienceDirect Topics
Frontiers | On the Corner of Models and Cure: Gene Editing in Cystic Fibrosis
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect
The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis–Like Disease in Pigs | Science Translational Medicine
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9 - Dreano - 2019 - Animal Models and Experimental Medicine - Wiley Online Library
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9 - Dreano - 2019 - Animal Models and Experimental Medicine - Wiley Online Library
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - The American Journal of Pathology
ΔF508 in cystic fibrosis: willing but not able | Archives of Disease in Childhood
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9 - Dreano - 2019 - Animal Models and Experimental Medicine - Wiley Online Library
Frontiers | Adapting Proteostasis and Autophagy for Controlling the Pathogenesis of Cystic Fibrosis Lung Disease
Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse | Scientific Reports
Generation and characterization of a ~F508 cystic fibrosis mouse model
A mouse model for the cystic fibrosis delta F508 mutation. - Abstract - Europe PMC
Increased CFTR expression and function from an optimized lentiviral vector for cystic fibrosis gene therapy: Molecular Therapy - Methods & Clinical Development
