Lista de obras - Guillermo J Pérez - Dominio Público Uruguay

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

artículo científico publicado en 2010

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

artículo científico publicado en 2014

A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.

artículo científico publicado en 2013

A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome

artículo científico publicado en 2013

Characterization of large-conductance, calcium-activated potassium channels from human myometrium

scientific article published on 01 February 1993

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Dual effect of tamoxifen on arterial KCa channels does not depend on the presence of the beta1 subunit.

artículo científico publicado en 2005

Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.

artículo científico publicado en 2004

Experimental Models of Brugada syndrome. ⬇️

artículo científico publicado en 2019

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

scientific article published on 19 July 2019

Functional coupling of ryanodine receptors to KCa channels in smooth muscle cells from rat cerebral arteries.

artículo científico publicado en 1999

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

artículo científico publicado en 2006

Genetics and cardiac channelopathies.

artículo científico publicado en 2010

High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation

artículo científico publicado en 2008

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

artículo científico publicado en 2002

Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons.

artículo científico publicado en 2012

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

artículo científico publicado en 2013

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

artículo científico publicado en 2010

Reconstitution of expressed KCa channels from Xenopus oocytes to lipid bilayers.

artículo científico publicado en 1994

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Lista de obras de Guillermo J Pérez

A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.

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

A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.

A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome

Characterization of large-conductance, calcium-activated potassium channels from human myometrium

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

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

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

Dual effect of tamoxifen on arterial KCa channels does not depend on the presence of the beta1 subunit.

Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.

Experimental Models of Brugada syndrome. ⬇️

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

Functional coupling of ryanodine receptors to KCa channels in smooth muscle cells from rat cerebral arteries.

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

Genetics and cardiac channelopathies.

High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation

Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males

Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons.

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

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

Reconstitution of expressed KCa channels from Xenopus oocytes to lipid bilayers.

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

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