Investigación
Educación
Iniciar sesión
ES
EN - English
CN - 中文
DE - Deutsch
ES - Español
KR - 한국어
IT - Italiano
FR - Français
PT - Português
Iwona Pranke has not added Biography.
If you are Iwona Pranke and would like to personalize this page please email our Author Liaison for assistance.
An unexpected effect of TNF-α on F508del-CFTR maturation and function.
F1000Research , 2015 | Pubmed ID: 26594334
The suppression of premature termination codons and the repair of splicing mutations in CFTR.
Current opinion in pharmacology 06, 2017 | Pubmed ID: 29128743
Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules.
Human mutation 04, 2018 | Pubmed ID: 29271547
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
Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine.
Frontiers in pharmacology , 2019 | Pubmed ID: 30873022
Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Scientific reports 04, 2019 | Pubmed ID: 31019198
Cystic Fibrosis Diagnosis in Newborns, Children, and Adults.
Seminars in respiratory and critical care medicine 12, 2019 | Pubmed ID: 31679154
Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Scientific reports Nov, 2019 | Pubmed ID: 31754179
Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal Disease.
International journal of molecular sciences Sep, 2020 | Pubmed ID: 32927759
Modulators of CFTR. Updates on clinical development and future directions.
European journal of medicinal chemistry Mar, 2021 | Pubmed ID: 33524685
New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation.
Scientific reports 03, 2021 | Pubmed ID: 33767236
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
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
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
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
Assistance Publique Hôpitaux 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
Privacidad
Condiciones de uso
Políticas
Contáctenos
RECOMIENDE A LA BIBLIOTECA
BOLETINES de JoVE
JoVE Journal
Colecciones de métodos
JoVE Encyclopedia of Experiments
Archivo
JoVE Core
JoVE Business
JoVE Science Education
JoVE Lab Manual
Centro de recursos académicos
Autores
Bibliotecarios
Acceso
ACERCA DE JoVE
Copyright © 2024 MyJoVE Corporation. Todos los derechos reservados