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Faial Sângera In speranta a mouse model for the cystic fibrosis delta f508 mutation Nu se mișcă pendulă Opt

Cystic Fibrosis Is Associated with a Defect in Apical Receptor–Mediated Endocytosis in Mouse and Human Kidney | American Society of Nephrology
Cystic Fibrosis Is Associated with a Defect in Apical Receptor–Mediated Endocytosis in Mouse and Human Kidney | American Society of Nephrology

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

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

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

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

Cystic fibrosis - The Lancet
Cystic fibrosis - The Lancet

Cystic Fibrosis Mouse Models
Cystic Fibrosis Mouse Models

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

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

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

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

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

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

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

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

Biomolecules | Free Full-Text | Decoding F508del Misfolding in Cystic Fibrosis | HTML
Biomolecules | Free Full-Text | Decoding F508del Misfolding in Cystic Fibrosis | HTML

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

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

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

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

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

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

Structure-Function Relationships of CFTR in Health and Disease: The Pancreas Story | Pancreapedia
Structure-Function Relationships of CFTR in Health and Disease: The Pancreas Story | Pancreapedia