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An unexpected effect of TNF-α on F508del-CFTR maturation and function.
F1000Research , 2015 | Pubmed ID: 26594334
Analysis of nasal potential in murine cystic fibrosis models.
The international journal of biochemistry & cell biology 11, 2016 | Pubmed ID: 27717840
Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons.
ERJ open research Jan, 2018 | Pubmed ID: 29497617
Might Brushed Nasal Cells Be a Surrogate for CFTR Modulator Clinical Response?
American journal of respiratory and critical care medicine 01, 2019 | Pubmed ID: 30326728
Predictive factors for lumacaftor/ivacaftor clinical response.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 05, 2019 | Pubmed ID: 30595473
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
New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation.
Scientific reports 03, 2021 | Pubmed ID: 33767236
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
Sweat Chloride Testing and Nasal Potential Difference (NPD) Are Primary Outcome Parameters in Treatment with Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators.
Journal of personalized medicine Jul, 2021 | Pubmed ID: 34442373
Author Correction: New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation.
Scientific reports Sep, 2021 | Pubmed ID: 34526640
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
Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society Dec, 2021 | Pubmed ID: 34949556
Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice.
Scientific reports Apr, 2022 | Pubmed ID: 35413967
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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