Iwona Pranke Institut Necker Enfants Malades Biography Publications Institution JoVE Articles Iwona Pranke has not added a biography. If you are Iwona Pranke 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 Pharmacological Chaperones Improve Intra-domain Stability and Inter-domain Assembly Via Distinct Binding Sites to Rescue Misfolded CFTR Cellular and Molecular Life Sciences : CMLS. Dec, 2021 | Pubmed ID: 34714360 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 New Insights into Structure and Function of Bis-phosphinic Acid Derivatives and Implications for CFTR Modulation Scientific Reports. 03, 2021 | Pubmed ID: 33767236 Modulators of CFTR. Updates on Clinical Development and Future Directions European Journal of Medicinal Chemistry. Mar, 2021 | Pubmed ID: 33524685 Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal Disease International Journal of Molecular Sciences. Sep, 2020 | Pubmed ID: 32927759 Author Correction: Airway Surface Liquid Acidification Initiates Host Defense Abnormalities in Cystic Fibrosis Scientific Reports. Nov, 2019 | Pubmed ID: 31754179 Cystic Fibrosis Diagnosis in Newborns, Children, and Adults Seminars in Respiratory and Critical Care Medicine. 12, 2019 | Pubmed ID: 31679154 Airway Surface Liquid Acidification Initiates Host Defense Abnormalities in Cystic Fibrosis Scientific Reports. 04, 2019 | Pubmed ID: 31019198 Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine Frontiers in Pharmacology. 2019 | Pubmed ID: 30873022 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 Cis Variants Identified in F508del Complex Alleles Modulate CFTR Channel Rescue by Small Molecules Human Mutation. 04, 2018 | Pubmed ID: 29271547 The Suppression of Premature Termination Codons and the Repair of Splicing Mutations in CFTR Current Opinion in Pharmacology. 06, 2017 | Pubmed ID: 29128743 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