Fabiana Scornik, PhD

Affiliations: 
Masonic Medical Research Laboratory, Utica, Frankfort, NY, United States 
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"Fabiana Scornik"
Mean distance: 17.21 (cluster 32)
 
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Publications

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Selga E, Sendfeld F, Martinez-Moreno R, et al. (2017) Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient. Journal of Molecular and Cellular Cardiology
Peeters U, Scornik F, Riuró H, et al. (2015) Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. Circulation Journal : Official Journal of the Japanese Circulation Society. 79: 2118-29
Wangüemert F, Bosch Calero C, Pérez C, et al. (2015) Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1636-43
Riuró H, Campuzano O, Berne P, et al. (2015) Genetic analysis, in silico prediction, and family segregation in long QT syndrome. European Journal of Human Genetics : Ejhg. 23: 79-85
Riuró H, Campuzano O, Arbelo E, et al. (2014) A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1202-9
Bosch Calero C, Selga E, Brugada R, et al. (2014) The smooth muscle-type β1 subunit potentiates activation by DiBAC4(3) in recombinant BK channels. Channels (Austin, Tex.). 8: 95-102
Beltran-Alvarez P, Espejo A, Schmauder R, et al. (2013) Protein arginine methyl transferases-3 and -5 increase cell surface expression of cardiac sodium channel. Febs Letters. 587: 3159-65
Selga E, Pérez-Serra A, Moreno-Asso A, et al. (2013) Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia. Channels (Austin, Tex.). 7: 322-8
Riuró H, Beltran-Alvarez P, Tarradas A, et al. (2013) A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome. Human Mutation. 34: 961-6
Scornik FS, Bucciero RS, Wu Y, et al. (2013) DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit. American Journal of Physiology. Heart and Circulatory Physiology. 304: H1471-82
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