Publications by authors named "Vincent Portero"

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Optoelectronic control of cardiac rhythm: Toward shock-free ambulatory cardioversion of atrial fibrillation.
Vincent Portero, Shanliang Deng, Gerard J J Boink, Guo Qi Zhang, Antoine de Vries

J Intern Med· February 2024

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Light transmittance in human atrial tissue and transthoracic illumination in rats support translatability of optogenetic cardioversion of atrial fibrillation.
Emile C A Nyns, Vincent Portero, Shanliang Deng, Tianyi Jin, Niels Harlaar

J Intern Med· September 2023

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Microtubule plus-end tracking proteins: novel modulators of cardiac sodium channels and arrhythmogenesis.
Gerard A Marchal, Niels Galjart, Vincent Portero, Carol Ann Remme

Cardiovasc Res· July 2023

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Optical ventricular cardioversion by local optogenetic targeting and LED implantation in a cardiomyopathic rat model.
Emile C A Nyns, Tianyi Jin, Magda S Fontes, Titus van den Heuvel, Vincent Portero

Cardiovasc Res· July 2022

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Chronically elevated branched chain amino acid levels are pro-arrhythmic.
Vincent Portero, Thomas Nicol, Svitlana Podliesna, Gerard A Marchal, Antonius Baartscheer

Cardiovasc Res· June 2022

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Targeting the Microtubule EB1-CLASP2 Complex Modulates Na1.5 at Intercalated Discs.
Gerard A Marchal, Mariam Jouni, David Y Chiang, Marta Pérez-Hernández, Svitlana Podliesna, Vincent Portero

Circ Res· July 2021

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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation.
Arie O Verkerk, Suzan J G Knottnerus, Vincent Portero, Jeannette C Bleeker, Sacha Ferdinandusse

Front Pharmacol· January 2021

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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates.
Suzan J G Knottnerus, Isabella Mengarelli, Rob C I Wüst, Antonius Baartscheer, Jeannette C Bleeker, Vincent M Portero

Int J Mol Sci· April 2020

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Absence of Functional Na1.8 Channels in Non-diseased Atrial and Ventricular Cardiomyocytes.
Simona Casini, Gerard A Marchal, Makiri Kawasaki, Fransisca A Nariswari, Vincent Portero

Cardiovasc Drugs Ther· December 2019

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RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Nadjet Belbachir, Vincent Portero, Zeina R Al Sayed, Jean-Baptiste Gourraud, Florian Dilasser

Eur Heart J· October 2019

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Functional Consequences of the -p.Y1977N Mutation within the PY Ubiquitylation Motif: Discrepancy between HEK293 Cells and Transgenic Mice.
Simona Casini, Maxime Albesa, Zizun Wang, Vincent Portero, Daniela Ross-Kaschitza

Int J Mol Sci· October 2019

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K4.3 Expression Modulates Na1.5 Sodium Current.
Vincent Portero, Ronald Wilders, Simona Casini, Flavien Charpentier, Arie O Verkerk

Front Physiol· March 2018

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Anti-arrhythmic potential of the late sodium current inhibitor GS-458967 in murine Scn5a-1798insD+/- and human SCN5A-1795insD+/- iPSC-derived cardiomyocytes.
Vincent Portero, Simona Casini, Maaike Hoekstra, Arie O Verkerk, Isabella Mengarelli

Cardiovasc Res· June 2017

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Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, Sophie Burel, Jean-Baptiste Gourraud

J Am Heart Assoc· June 2016

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Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, Pierre Lindenbaum, Stéphanie Bonnaud, Vincent Portero

Hum Mol Genet· May 2015

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Block copolymer/DNA vaccination induces a strong allergen-specific local response in a mouse model of house dust mite asthma.
Camille Rolland-Debord, David Lair, Tiphaine Roussey-Bihouée, Dorian Hassoun, Justine Evrard, Vincent Portero

PLoS One· October 2014

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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Connie R Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean-Baptiste Gourraud, Vincent Portero

Nat Genet· September 2013

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Identification of large families in early repolarization syndrome.
Jean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, Stéphanie Chatel, Nicolas Derval, Vincent Portero

J Am Coll Cardiol· January 2013

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Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME.
Pierre Lindenbaum, Solena Le Scouarnec, Vincent Portero, Richard Redon

Bioinformatics· November 2011

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