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 Cellule epiteliali nasali umane primarie: biobanking nel contesto della medicina di precisione 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
Cellule epiteliali nasali umane primarie: biobanking nel contesto della medicina di precisione 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