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Frontiers | Animal Models in the Pathophysiology of Cystic Fibrosis
Frontiers | Animal Models in the Pathophysiology of Cystic Fibrosis

Frontiers | Adapting Proteostasis and Autophagy for Controlling the Pathogenesis of Cystic Fibrosis Lung Disease
Frontiers | Adapting Proteostasis and Autophagy for Controlling the Pathogenesis of Cystic Fibrosis Lung Disease

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 - The American Journal of Pathology
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - The American Journal of Pathology

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

Frontiers | Bone Cells Differentiation: How CFTR Mutations May Rule the Game of Stem Cells Commitment?
Frontiers | Bone Cells Differentiation: How CFTR Mutations May Rule the Game of Stem Cells Commitment?

ΔF508 - an overview | ScienceDirect Topics
ΔF508 - an overview | ScienceDirect Topics

Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR - Journal of Cystic Fibrosis
Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR - Journal of Cystic Fibrosis

Rescue of ΔF508-CFTR Trafficking via a GRASP-Dependent Unconventional Secretion Pathway: Cell
Rescue of ΔF508-CFTR Trafficking via a GRASP-Dependent Unconventional Secretion Pathway: Cell

ΔF508 in cystic fibrosis: willing but not able | Archives of Disease in Childhood
ΔF508 in cystic fibrosis: willing but not able | Archives of Disease in Childhood

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
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 - ScienceDirect
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
The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis–Like Disease in Pigs | Science Translational Medicine

Genes | Free Full-Text | Cystic Fibrosis Gene Therapy: Looking Back, Looking Forward | HTML
Genes | Free Full-Text | Cystic Fibrosis Gene Therapy: Looking Back, Looking Forward | HTML

In vivo correction of cystic fibrosis mediated by PNA nanoparticles | Science Advances
In vivo correction of cystic fibrosis mediated by PNA nanoparticles | Science Advances

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 - ScienceDirect
Phenotypic Characterization and Comparison of Cystic Fibrosis Rat Models Generated Using CRISPR/Cas9 Gene Editing - ScienceDirect

A mouse model for the cystic fibrosis delta F508 mutation. - Abstract - Europe PMC
A mouse model for the cystic fibrosis delta F508 mutation. - Abstract - Europe PMC

Animal models of cystic fibrosis - Journal of Cystic Fibrosis
Animal models of cystic fibrosis - Journal of Cystic Fibrosis

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

Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis | Scientific Reports
Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis | Scientific Reports

Generation and characterization of a ~F508 cystic fibrosis mouse model
Generation and characterization of a ~F508 cystic fibrosis mouse model

Generation and characterization of a ~F508 cystic fibrosis mouse model
Generation and characterization of a ~F508 cystic fibrosis mouse model

Cystic Fibrosis Mouse Models
Cystic Fibrosis Mouse Models