Guillermo J Pérez

发表

Electrophysiologic Properties and Antiarrhythmic Actions of a Novel Antianginal Agent

J. M. Di Diego, J. Fish, C. Antzelevitch, 2004, Journal of cardiovascular pharmacology and therapeutics.

Kir2.3 knock‐down decreases I K1 current in neonatal rat cardiomyocytes

R. Brugada, P. Brugada, Yusong He, 2008, FEBS letters.

A Missense Mutation in the Sodium Channel β2 Subunit Reveals SCN2B as a New Candidate Gene for Brugada Syndrome

J. Brugada, R. Brugada, P. Brugada, 2013, Human mutation.

The smooth muscle-type β1 subunit potentiates activation by DiBAC4(3) in recombinant BK channels

R. Brugada, E. Selga, Guillermo J Pérez, 2014, Channels.

An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders

Michael F. Wangler, R. Brugada, M. Wangler, 2020, Frontiers in Cell and Developmental Biology.

Dibac 4 (3) Hits a " Sweet Spot " for the Activation of Arterial Large-conductance Ca 2ϩ -activated Potassium Channels Independently of the ␤ 1 -subunit

R. Brugada, E. Selga, Y. Wu, 2022 .

Edinburgh Research Explorer Experimental Models of Brugada syndrome

R. Brugada, N. Mills, E. Selga, 2019 .

Final Degree Project Biomedical Engineering Degree Alternative data representations for a Deep Learning-based segmentation pipeline applied to fetal Doppler echocardiography

F. Crispi, B. Bijnens, Guillermo J Pérez, 2022 .

Flecainide Reduces Ventricular Arrhythmias in Patients With Genotype RyR2-positive Catecholaminergic Polymorphic Ventricular Tachycardia.

M. G. Groba Marco, Guillermo J Pérez, J. Brugada Terradellas, 2017, Revista espanola de cardiologia.

Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient

Claire N. Medine, R. Brugada, N. Mills, 2018, Journal of molecular and cellular cardiology.

DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit.

R. Brugada, E. Selga, Y. Wu, 2013, American journal of physiology. Heart and circulatory physiology.

Genetics and cardiac channelopathies

R. Brugada, Pedro Beltran-Alvarez, A. Iglesias, 2010, Genetics in Medicine.

Elucidating the Role of K+ Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role?

R. Brugada, M. Yeste, E. Pinart, 2019, International journal of molecular sciences.

Protein arginine methyl transferases‐3 and ‐5 increase cell surface expression of cardiac sodium channel

R. Brugada, R. Mrowka, C. Beltrán, 2013, FEBS letters.

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia.

P. Berne, J. Brugada, R. Brugada, 2015, Heart rhythm.

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

R. Brugada, I. Fernández‐Lozano, Pedro Beltran-Alvarez, 2013, PloS one.

Ionic and Cellular Basis for the Predominance of the Brugada Syndrome Phenotype in Males

Andrew C. Zygmunt, Charles Antzelevitch, Jonathan M. Cordeiro, 2002, Circulation.

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing cate-cholaminergic polymorphic ventricular tachycardia

P. Berne, J. Brugada, R. Brugada, 2015 .

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.

R. Brugada, Á. Carracedo, R. Gil, 2019, Forensic science international. Genetics.

Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss

R. Brugada, Guillermo J Pérez, M. Alcalde, 2023, International journal of molecular sciences.

Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A

J. Lozano-Sánchez, A. Segura‐Carretero, R. Brugada, 2019, Nutrients.

Functional expression of "cardiac-type" Nav1.5 sodium channel in canine intracardiac ganglia.

R. Brugada, C. Antzelevitch, G. Pollevick, 2006, Heart rhythm.

Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle

R. Brugada, M. Santafé, S. Pagans, 2021, International journal of molecular sciences.

A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death

C. Antzelevitch, J. Cordeiro, K. Calloe, 2010, Circulation. Cardiovascular genetics.

Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia

R. Brugada, E. Selga, A. Pérez-Serra, 2013, Channels.

High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation.

R. Brugada, P. Brugada, Luying Peng, 2008, Journal of applied physiology.

A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome.

J. Brugada, R. Brugada, M. Batlle, 2014, Heart rhythm.

Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.

R. Brugada, P. Brugada, S. Van Dooren, 2015, Circulation journal : official journal of the Japanese Circulation Society.

Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.

Martin Borggrefe, Ryan Pfeiffer, Charles Antzelevitch, 2010, Canadian journal of physiology and pharmacology.

Experimental Models of Brugada syndrome

N. Mills, E. Selga, F. Sendfeld, 2019, International journal of molecular sciences.

How Do We Measure Repolarization Inside the Heart

J. Fish, C. Antzelevitch, A. Zygmunt, 2003 .