Publications by authors named "Michel Partiseti"

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The atypic antipsychotic clozapine inhibits multiple cardiac ion channels.
Marguerite Le Marois, Camille Sanson, Magali-Anne Maizières, Michel Partiseti, G Andrees Bohme

Naunyn Schmiedebergs Arch Pharmacol· January 2023

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The grapefruit polyphenol naringenin inhibits multiple cardiac ion channels.
Camille Sanson, Rachid Boukaiba, Sylvie Houtmann, Magali-Anne Maizières, Sophie Fouconnier, Michel Partiseti

Naunyn Schmiedebergs Arch Pharmacol· June 2022

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In vitro ion channel profile and ex vivo cardiac electrophysiology properties of the R(-) and S(+) enantiomers of hydroxychloroquine.
Véronique Ballet, G Andrees Bohme, Eric Brohan, Rachid Boukaiba, Jean-Marie Chambard, Michel Partiseti

Eur J Pharmacol· January 2022

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Fluorescent- and tagged-protoxin II peptides: potent markers of the Na 1.7 channel pain target.
Jérôme Montnach, Stephan De Waard, Sébastien Nicolas, Sophie Burel, Nancy Osorio, Michel Partiseti

Br J Pharmacol· July 2021

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Cannabidiol inhibits multiple cardiac ion channels and shortens ventricular action potential duration in vitro.
Marguerite Le Marois, Véronique Ballet, Camille Sanson, Magali-Anne Maizières, Thierry Carriot, Michel Partiseti

Eur J Pharmacol· November 2020

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Lysophosphatidic Acid Receptor Agonism: Discovery of Potent Nonlipid Benzofuran Ethanolamine Structures.
Etienne Guillot, Jean-Christophe Le Bail, Pascal Paul, Valérie Fourgous, Pascale Briand, Michel Partiseti

J Pharmacol Exp Ther· August 2020

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From identification to functional characterization of cyriotoxin-1a, an antinociceptive toxin from the spider Cyriopagopus schioedtei.
Tânia C Gonçalves, Evelyne Benoit, Michael Kurz, Laetitia Lucarain, Sophie Fouconnier, Michel Partiseti

Br J Pharmacol· May 2019

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Electrophysiological and Pharmacological Characterization of Human Inwardly Rectifying K2.1 Channels on an Automated Patch-Clamp Platform.
Camille Sanson, Brigitte Schombert, Bruno Filoche-Rommé, Michel Partiseti, G Andrees Bohme

Assay Drug Dev Technol· April 2019

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Corrigendum: The Na1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons.
Tânia C Gonçalves, Evelyne Benoit, Michel Partiseti, Denis Servent

Front Pharmacol· October 2018

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The Na1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons.
Tânia C Gonçalves, Evelyne Benoit, Michel Partiseti, Denis Servent

Front Pharmacol· September 2018

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Direct evidence for high affinity blockade of Na1.6 channel subtype by huwentoxin-IV spider peptide, using multiscale functional approaches.
Tânia C Gonçalves, Rachid Boukaiba, Jordi Molgó, Muriel Amar, Michel Partiseti

Neuropharmacology· May 2018

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Automated Patch-Clamp Methods for the hERG Cardiac Potassium Channel.
Sylvie Houtmann, Brigitte Schombert, Camille Sanson, Michel Partiseti, G Andrees Bohme

Methods Mol Biol· April 2018

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Functional Studies of Sodium Channels: From Target to Compound Identification.
Daniel Bertrand, Bruno Biton, Thomas Licher, Jean-Marie Chambard, Christophe Lanneau, Michel Partiseti

Curr Protoc Pharmacol· December 2016

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Design and validation of a homogeneous time-resolved fluorescence cell-based assay targeting the ligand-gated ion channel 5-HT3A.
Emilie Blanc, Patrick Wagner, Fabrice Plaisier, Martine Schmitt, Thierry Durroux, Michel Partiseti

Anal Biochem· September 2015

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Transforming TRP channel drug discovery using medium-throughput electrophysiological assays.
Jean-Marie Chambard, Eric Tagat, Philippe Boudeau, Michel Partiseti

J Biomol Screen· March 2014

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