Aurelie Hatton Institut Necker Enfants Malades Biography Publications Institution JoVE Articles Aurelie Hatton has not added a biography. If you are Aurelie Hatton and would like to personalize this page please email our Author Liaison for assistance. Publications Systemic Bis-phosphinic Acid Derivative Restores Chloride Transport in Cystic Fibrosis Mice Scientific Reports. Apr, 2022 | Pubmed ID: 35413967 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 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 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 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 New Insights into Structure and Function of Bis-phosphinic Acid Derivatives and Implications for CFTR Modulation Scientific Reports. 03, 2021 | Pubmed ID: 33767236 Author Correction: Airway Surface Liquid Acidification Initiates Host Defense Abnormalities in Cystic Fibrosis Scientific Reports. Nov, 2019 | Pubmed ID: 31754179 Airway Surface Liquid Acidification Initiates Host Defense Abnormalities in Cystic Fibrosis Scientific Reports. 04, 2019 | Pubmed ID: 31019198 Predictive Factors for Lumacaftor/ivacaftor Clinical Response Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 05, 2019 | Pubmed ID: 30595473 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 Factors Influencing Readthrough Therapy for Frequent Cystic Fibrosis Premature Termination Codons ERJ Open Research. Jan, 2018 | Pubmed ID: 29497617 Analysis of Nasal Potential in Murine Cystic Fibrosis Models The International Journal of Biochemistry & Cell Biology. 11, 2016 | Pubmed ID: 27717840 An Unexpected Effect of TNF-α on F508del-CFTR Maturation and Function F1000Research. 2015 | Pubmed ID: 26594334 Primaire menselijke neusepitheelcellen: biobanking in de context van precisiegeneeskunde Mairead Kelly1,2, Elise Dreano1,2, Aurelie Hatton1,2, Agathe Lepissier1,2, Anita Golec1,2, Isabelle Sermet-Gaudelus1,2,3, Iwona Pranke1,2,3 1Institut Necker Enfants Malades, 2Université de Paris, 3Centre de Référence Maladies Rares Mucoviscidose et Maladies apparentées, Assistance Publique Hôpitaux de Paris JoVE 63409 Biology
Primaire menselijke neusepitheelcellen: biobanking in de context van precisiegeneeskunde Mairead Kelly1,2, Elise Dreano1,2, Aurelie Hatton1,2, Agathe Lepissier1,2, Anita Golec1,2, Isabelle Sermet-Gaudelus1,2,3, Iwona Pranke1,2,3 1Institut Necker Enfants Malades, 2Université de Paris, 3Centre de Référence Maladies Rares Mucoviscidose et Maladies apparentées, Assistance Publique Hôpitaux de Paris JoVE 63409 Biology