ΔF508 - an overview | ScienceDirect Topics
Frontiers | Bone Cells Differentiation: How CFTR Mutations May Rule the Game of Stem Cells Commitment?
Frontiers | On the Corner of Models and Cure: Gene Editing in 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
PDF) Generation and characterization of a ΔF508 cystic fibrosis mouse model
Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR - Journal of Cystic Fibrosis
Animal models of cystic fibrosis - Journal of Cystic Fibrosis
Generation and characterization of a ~F508 cystic fibrosis mouse model
Generation and characterization of a ~F508 cystic fibrosis mouse model
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
Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis | Scientific Reports
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
Increased CFTR expression and function from an optimized lentiviral vector for cystic fibrosis gene therapy: Molecular Therapy - Methods & Clinical Development
Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse | Scientific Reports
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
Generation and characterization of a ~F508 cystic fibrosis mouse model
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
Generation and characterization of a ~F508 cystic fibrosis mouse model
ΔF508 in cystic fibrosis: willing but not able | Archives of Disease in Childhood
iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation: Molecular Therapy - Methods & Clinical Development
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect
Genes | Free Full-Text | Cystic Fibrosis Gene Therapy: Looking Back, Looking Forward | HTML
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - The American Journal of Pathology
In vivo correction of cystic fibrosis mediated by PNA nanoparticles | Science Advances
Generation and characterization of a ~F508 cystic fibrosis mouse model
