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 תאי אפיתל האף האנושיים העיקריים: ביובנקינג בהקשר של רפואה מדויקת 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
תאי אפיתל האף האנושיים העיקריים: ביובנקינג בהקשר של רפואה מדויקת 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
