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Nesrine Baatallah

Showing results (1-10 of 14) with videos related to

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International Journal of Molecular Sciences|December 23, 2022
Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded MutantsNesrine Baatallah, Ahmad Elbahnsi, Benoit Chevalier, et al.
Cellular and Molecular Life Sciences : CMLS|October 7, 2024
Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activationSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
Cellular and Molecular Life Sciences : CMLS|October 29, 2021
Pharmacological chaperones improve intra-domain stability and inter-domain assembly via distinct binding sites to rescue misfolded CFTRNesrine Baatallah, Ahmad Elbahnsi, Jean-Paul Mornon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 20, 2020
Exon identity influences splicing induced by exonic variants and in silico prediction efficacyNatacha Martin, Anne Bergougnoux, Nesrine Baatallah, et al.
Cellular and Molecular Life Sciences : CMLS|September 27, 2022
Pharmacological chaperone-rescued cystic fibrosis CFTR-F508del mutant overcomes PRAF2-gated access to endoplasmic reticulum exit sitesKusumika Saha, Benoit Chevalier, Stéphane Doly, et al.
International Journal of Molecular Sciences|August 26, 2022
Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC TransportersBenoît Chevalier, Nesrine Baatallah, Matthieu Najm, et al.
Frontiers in Pharmacology|January 9, 2019
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated MechanismEmanuela Pesce, Elvira Sondo, Loretta Ferrera, et al.
Journal of Molecular Biology|December 25, 2022
Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance RegulatorMarc Ravatin, Norbert Odolczyk, Nathalie Servel, 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.
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.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
International Journal of Molecular Sciences|December 23, 2022
Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded MutantsNesrine Baatallah, Ahmad Elbahnsi, Benoit Chevalier, et al.
Cellular and Molecular Life Sciences : CMLS|October 7, 2024
Novel gain-of-function mutants identify a critical region within CFTR membrane-spanning domain 2 controlling cAMP-dependent and ATP-independent channel activationSolène Castanier, Ahmad Elbahnsi, Benoit Chevalier, et al.
Cellular and Molecular Life Sciences : CMLS|October 29, 2021
Pharmacological chaperones improve intra-domain stability and inter-domain assembly via distinct binding sites to rescue misfolded CFTRNesrine Baatallah, Ahmad Elbahnsi, Jean-Paul Mornon, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 20, 2020
Exon identity influences splicing induced by exonic variants and in silico prediction efficacyNatacha Martin, Anne Bergougnoux, Nesrine Baatallah, et al.
Cellular and Molecular Life Sciences : CMLS|September 27, 2022
Pharmacological chaperone-rescued cystic fibrosis CFTR-F508del mutant overcomes PRAF2-gated access to endoplasmic reticulum exit sitesKusumika Saha, Benoit Chevalier, Stéphane Doly, et al.
International Journal of Molecular Sciences|August 26, 2022
Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC TransportersBenoît Chevalier, Nesrine Baatallah, Matthieu Najm, et al.
Frontiers in Pharmacology|January 9, 2019
The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated MechanismEmanuela Pesce, Elvira Sondo, Loretta Ferrera, et al.
Journal of Molecular Biology|December 25, 2022
Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance RegulatorMarc Ravatin, Norbert Odolczyk, Nathalie Servel, 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.
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.
Pageof 2