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MARCEL VERGÉS AIGUAVIVA

Cardiovascular Genetics
Firma
MARCEL VERGÉS-AIGUAVIVA
Position
Investigador/a Consolidat - R3
Established Researchers - R3
Projectes
Publicacions

Projectes

Cardiovascular Genetics

Ajuts per donar suport a les activitats dels grups de recerca de Catalunya (SGR-Cat 2021) - Genètica Cardiovascular (Gencardio)

Codi oficial: SGR-Cat 2021 - Genètica Cardiovascular (Gencardio) Start date:01/01/2022 Data fi: 30/06/2025 Investigador/a principal: RAMON BRUGADA TERRADELLAS Organisme finançador: AGENCIA DE GESTIO D'AJUTS UNIV. I RECER.

Publicacions

Cortada E, Serradesanferm R, Brugada R, Verges M

The voltage-gated sodium channel beta 2 subunit associates with lipid rafts by S-palmitoylation

JOURNAL OF CELL SCIENCE, 2021, 134 dx.doi.org/10.1242/jcs.252189
Cortada E, Verges M

Na(V)1.5 in embryonic heart development

ACTA PHYSIOLOGICA, 2020, 230 dx.doi.org/10.1111/apha.13542
Cortada E, Verges M

Alterations in ubiquitin-mediated degradation of Na(V)1.5 can cause arrhythmia

ACTA PHYSIOLOGICA, 2020, 229 dx.doi.org/10.1111/apha.13459
Cortada E, Brugada R, Verges M

N-Glycosylation of the voltage-gated sodium channel?2 subunit is required for efficient trafficking of Na(V)1.5/?2 to the plasma membrane

JOURNAL OF BIOLOGICAL CHEMISTRY, 2019, 294, 16123-16140 dx.doi.org/10.1074/jbc.RA119.007903
Cortada E, Brugada R, Verges M

Trafficking and Function of the Voltage-Gated Sodium Channel beta 2 Subunit

Biomolecules, 2019, 9 dx.doi.org/10.3390/biom9100604
Dulsat G, Palomeras S, Cortada E, Riuró H, Brugada R, Vergés M

Trafficking and localisation to the plasma membrane of Na v 1.5 promoted by the ß2 subunit is defective due to a ß2 mutation associated with Brugada syndrome.

BIOLOGY OF THE CELL, 2017, 109, 273-291 dx.doi.org/10.1111/boc.201600085
Pagans S, Vergés M

A mechanism for Na V 1.5 downregulation and sodium current decrease in heart failure.

ACTA PHYSIOLOGICA, 2017, 221, 11-13 dx.doi.org/10.1111/apha.12901
Riuró H, Beltran-Alvarez P, Tarradas A, Selga E, Campuzano O, Vergés M, Pagans S, Iglesias A, Brugada J, Brugada P, Vázquez FM, Pérez GJ, Scornik FS, Brugada R

A Missense Mutation in the Sodium Channel ß2 Subunit Reveals SCN2B as a New Candidate Gene for Brugada Syndrome.

HUMAN MUTATION, 2013, 34, 961-966 dx.doi.org/10.1002/humu.22328

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