Lista de obras - Fabiana S Scornik - 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

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

artículo científico publicado en 2007

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

artículo científico publicado en 1990

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

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

artículo científico publicado el 23 de agosto de 1991

Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.

artículo científico publicado en 2004

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

artículo científico

Experimental Models of Brugada syndrome. ⬇️

artículo científico publicado en 2019

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

artículo científico publicado en 2006

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

artículo científico publicado en 2014

Genetics and cardiac channelopathies.

artículo científico publicado en 2010

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

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 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.