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Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine.
Frontiers in pharmacology , 2019 | Pubmed ID: 30873022
Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Scientific reports 04, 2019 | Pubmed ID: 31019198
Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Scientific reports Nov, 2019 | Pubmed ID: 31754179
Modulators of CFTR. Updates on clinical development and future directions.
European journal of medicinal chemistry Mar, 2021 | Pubmed ID: 33524685
Antisense oligonucleotide-based drug development for Cystic Fibrosis patients carrying the 3849+10 kb C-to-T splicing mutation.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 09, 2021 | Pubmed ID: 34226157
Correlating genotype with phenotype using CFTR-mediated whole-cell Cl currents in human nasal epithelial cells.
The Journal of physiology Mar, 2022 | Pubmed ID: 34761808
Institut Necker Enfants Malades
Université de paris
Université de Paris
Mairead Kelly1,2,
Elise Dreano1,2,
Aurelie Hatton1,2,
Agathe Lepissier1,2,
Anita Golec1,2,
Isabelle Sermet-Gaudelus1,2,3,
Iwona Pranke1,2,3
1, Institut Necker Enfants Malades,
2, Université de Paris,
3Centre de Référence Maladies Rares Mucoviscidose et Maladies apparentées, Assistance Publique Hôpitaux de Paris
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