Home

pastel Transporta Reprezinta a mouse model for the cystic fibrosis delta f508 mutation Inutil latra Rambursa

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

Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect | PNAS
Human–mouse cystic fibrosis transmembrane conductance regulator (CFTR) chimeras identify regions that partially rescue CFTR-ΔF508 processing and alter its gating defect | PNAS

Animal and model systems for studying cystic fibrosis - Journal of Cystic Fibrosis
Animal and model systems for studying cystic fibrosis - Journal of Cystic Fibrosis

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

Animal and Cell Culture Models for Cystic Fibrosis - The American Journal of Pathology
Animal and Cell Culture Models for Cystic Fibrosis - The American Journal of Pathology

A mouse model for the cystic fibrosis delta F508 mutation. | The EMBO Journal
A mouse model for the cystic fibrosis delta F508 mutation. | The EMBO Journal

Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse | Scientific Reports
Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse | Scientific Reports

CF mouse strains - Case Western Reserve University Cystic Fibrosis Mouse Models Core
CF mouse strains - Case Western Reserve University Cystic Fibrosis Mouse Models Core

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

PDF] A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo. | Semantic Scholar
PDF] A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo. | Semantic Scholar

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

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

A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies | PLOS ONE
A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies | PLOS ONE

Cystic fibrosis - The Lancet
Cystic fibrosis - The Lancet

JCI - A mouse model for the delta F508 allele of cystic fibrosis.
JCI - A mouse model for the delta F508 allele of cystic fibrosis.

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

Cystic Fibrosis Mouse Model
Cystic Fibrosis Mouse Model

CF mouse strains - Case Western Reserve University Cystic Fibrosis Mouse Models Core
CF mouse strains - Case Western Reserve University Cystic Fibrosis Mouse Models Core

The Primary Folding Defect and Rescue of ΔF508 CFTR Emerge during Translation of the Mutant Domain | PLOS ONE
The Primary Folding Defect and Rescue of ΔF508 CFTR Emerge during Translation of the Mutant Domain | PLOS ONE

Treating Cystic Fibrosis with mRNA and CRISPR | Human Gene Therapy
Treating Cystic Fibrosis with mRNA and CRISPR | Human Gene Therapy

Cystic Fibrosis Mouse Models
Cystic Fibrosis Mouse Models

PDF) A mouse model for the cystic fibrosis ΔF508 mutation
PDF) A mouse model for the cystic fibrosis ΔF508 mutation

A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies | PLOS ONE
A G542X cystic fibrosis mouse model for examining nonsense mutation directed therapies | PLOS ONE

Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice | Scientific Reports
Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice | Scientific Reports

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