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Alexandre Hinzpeter

Showing results (41-50 of 60) with videos related to

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Frontiers in Pharmacology|December 27, 2023
Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epitheliumMiroslaw Zajac, Agathe Lepissier, Elise Dréano, et al.
Human Mutation|December 23, 2017
Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small moleculesNesrine Baatallah, Sara Bitam, Natacha Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 1, 2019
Predictive factors for lumacaftor/ivacaftor clinical responseAlexandra Masson, Elena K Schneider-Futschik, Nesrine Baatallah, et al.
ERJ Open Research|March 3, 2018
Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codonsIwona Pranke, Laure Bidou, Natacha Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 24, 2021
Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forwardAurelie Hatton, Anne Bergougnoux, Katarzyna Zybert, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Immunohistochemistry of CFTR in native tissues and primary epithelial cell culturesFilipa Mendes, Laurent Doucet, Alexandre Hinzpeter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 26, 2011
A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practiceCatherine Costa, Virginie Pruliere-Escabasse, Alix de Becdelievre, et al.
European Journal of Medicinal Chemistry|February 21, 2020
Targeting different binding sites in the CFTR structures allows to synergistically potentiate channel activityLionel Froux, Ahmad Elbahnsi, Benjamin Boucherle, et al.
Scientific Reports|August 9, 2017
Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulatorsIwona M Pranke, Aurélie Hatton, Juliette Simonin, et al.
Cellular and Molecular Life Sciences : CMLS|August 31, 2022
Keratin 8 is a scaffolding and regulatory protein of ERAD complexesIwona Maria Pranke, Benoit Chevalier, Aiswarya Premchandar, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Frontiers in Pharmacology|December 27, 2023
Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epitheliumMiroslaw Zajac, Agathe Lepissier, Elise Dréano, et al.
Human Mutation|December 23, 2017
Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small moleculesNesrine Baatallah, Sara Bitam, Natacha Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 1, 2019
Predictive factors for lumacaftor/ivacaftor clinical responseAlexandra Masson, Elena K Schneider-Futschik, Nesrine Baatallah, et al.
ERJ Open Research|March 3, 2018
Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codonsIwona Pranke, Laure Bidou, Natacha Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 24, 2021
Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forwardAurelie Hatton, Anne Bergougnoux, Katarzyna Zybert, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Immunohistochemistry of CFTR in native tissues and primary epithelial cell culturesFilipa Mendes, Laurent Doucet, Alexandre Hinzpeter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 26, 2011
A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practiceCatherine Costa, Virginie Pruliere-Escabasse, Alix de Becdelievre, et al.
European Journal of Medicinal Chemistry|February 21, 2020
Targeting different binding sites in the CFTR structures allows to synergistically potentiate channel activityLionel Froux, Ahmad Elbahnsi, Benjamin Boucherle, et al.
Scientific Reports|August 9, 2017
Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulatorsIwona M Pranke, Aurélie Hatton, Juliette Simonin, et al.
Cellular and Molecular Life Sciences : CMLS|August 31, 2022
Keratin 8 is a scaffolding and regulatory protein of ERAD complexesIwona Maria Pranke, Benoit Chevalier, Aiswarya Premchandar, et al.
Pageof 6