List of works - Fabiana S Scornik

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

scientific article

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

scientific article published in July 2014

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

scientific article published on 29 April 2013

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

scientific article

A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.

scientific article

Ca2+ role on the effect of phorbol esters on the spontaneous quantal release of neurotransmitter at the mouse neuromuscular junction.

scientific article published on August 1990

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

scientific article published in July 2015

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

scientific article

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

scientific article published on 29 March 2013

Effect of ω-conotoxin GVIA on neurotransmitter release at the mouse neuromuscular junction ⬇️

scientific article published on August 23, 1991

Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.

scientific article published in September 2004

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

scientific article published on 15 December 2019

Experimental Models of Brugada syndrome. ⬇️

scientific article published on 29 April 2019

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

scientific article

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

scientific article

Genetics and cardiac channelopathies.

scientific article published on May 2010

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

scientific article published in October 2002

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

scientific article published on 28 November 2012

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

scientific article published on 27 June 2013

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

scientific article published on 9 October 2017

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

scientific article published on 3 December 2013

List of works by Fabiana S Scornik

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

A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.

Ca2+ role on the effect of phorbol esters on the spontaneous quantal release of neurotransmitter at the mouse neuromuscular junction.

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.

Effect of ω-conotoxin GVIA on neurotransmitter release at the mouse neuromuscular junction ⬇️

Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.

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

Experimental Models of Brugada syndrome. ⬇️

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

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

Genetics and cardiac channelopathies.

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.

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.