Vasoregulation by the β1 subunit of the calcium-activated potassium channel von Nelson, Mark T, Eckman, Delrae M, Bonev, Adrian D, Wiler, Steven W, Brenner, Robert, Patterson, Andrew J, Aldrich, Richard W, Kosek, Jon C, Peréz, Guillermo J

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Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss von Vallverdú-Prats, Marta, Carreras, David, Pérez, Guillermo J, Campuzano, Oscar, Brugada, Ramon, Alcalde, Mireia

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Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient von Selga, Elisabet, Sendfeld, Franziska, Martinez-Moreno, Rebecca, Medine, Claire N., Tura-Ceide, Olga, Wilmut, Sir Ian, Pérez, Guillermo J., Scornik, Fabiana S., Brugada, Ramon, Mills, Nicholas L.

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Experimental Models of Brugada syndrome von Sendfeld, Franziska, Selga, Elisabet, Scornik, Fabiana S, Pérez, Guillermo J, Mills, Nicholas L, Brugada, Ramon

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Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia von Wangüemert, Fernando, PhD, MD, Bosch Calero, Cristina, MSc, Pérez, Carmelo, BD, Campuzano, Oscar, PhD, Beltran-Alvarez, Pedro, PhD, Scornik, Fabiana S., PhD, Iglesias, Anna, MSc, Berne, Paola, MD, Allegue, Catarina, PhD, Ruiz Hernandez, Pablo M., PhD, MD, Brugada, Josep, PhD, MD, Pérez, Guillermo J., PhD, Brugada, Ramon, PhD, MD

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Loss of sodium current caused by a Brugada syndrome–associated variant is determined by patient-specific genetic background von Martínez-Moreno, Rebecca, Carreras, David, Sarquella-Brugada, Georgia, Pérez, Guillermo J., Selga, Elisabet, Scornik, Fabiana S., Brugada, Ramon

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Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient von Martínez-Moreno, Rebecca, Pérez-Serra, Alexandra, Selga, Elisabet, Carreras, David, Aran, Begoña, Kuebler, Bernd, Scornik, Fabiana S, Pérez, Guillermo J, Brugada, Ramon

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Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle von Carreras, David, Martinez-Moreno, Rebecca, Pinsach-Abuin, Mel Lina, Santafe, Manel M., Goma, Pol, Brugada, Ramon, Scornik, Fabiana S., Perez, Guillermo J., Pagans, Sara

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Generation of an induced pluripotent stem cell line from a healthy Caucasian male von Martínez-Moreno, Rebecca, Pérez-Serra, Alexandra, Carreras, David, Aran, Begoña, Kuebler, Bernd, Brugada, Ramon, Scornik, Fabiana S., Pérez, Guillermo J., Selga, Elisabet

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Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males von DI DIEGO, José M, CORDEIRO, Jonathan M, GOODROW, Robert J, FISH, Jeffrey M, ZYGMUNT, Andrew C, PEREZ, Guillermo J, SCORNIK, Fabiana S, ANTZELEVITCH, Charles

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Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A von Martínez-Moreno, Rebecca, Carreras, David, Aran, Begoña, Kuebler, Bernd, Sarquella-Brugada, Georgia, Brugada, Ramon, Pérez, Guillermo J., Scornik, Fabiana S., Selga, Elisabet

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Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A von Cuyàs, Elisabet, Gumuzio, Juan, Lozano-Sánchez, Jesús, Carreras, David, Verdura, Sara, Llorach-Parés, Laura, Sanchez-Martinez, Melchor, Selga, Elisabet, Pérez, Guillermo J, Scornik, Fabiana S, Brugada, Ramon, Bosch-Barrera, Joaquim, Segura-Carretero, Antonio, Martin, Ángel G, Encinar, José Antonio, Menendez, Javier A

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Protein arginine methyl transferases-3 and -5 increase cell surface expression of cardiac sodium channel von Beltran-Alvarez, Pedro, Espejo, Alexsandra, Schmauder, Ralf, Beltran, Carlos, Mrowka, Ralf, Linke, Thomas, Batlle, Montserrat, Pérez-Villa, Félix, Pérez, Guillermo J., Scornik, Fabiana S., Benndorf, Klaus, Pagans, Sara, Zimmer, Thomas, Brugada, Ramon

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A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome von Tarradas, Anna, Selga, Elisabet, Beltran-Alvarez, Pedro, Pérez-Serra, Alexandra, Riuró, Helena, Picó, Ferran, Iglesias, Anna, Campuzano, Oscar, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Pérez, Guillermo J, Scornik, Fabiana S, Brugada, Ramon

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A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death von Nof, Eyal, Cordeiro, Jonathan M, Pérez, Guillermo J, Scornik, Fabiana S, Calloe, Kirstine, Love, Barry, Burashnikov, Elena, Caceres, Gabriel, Gunsburg, Moshe, Antzelevitch, Charles

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Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons von Pérez, Guillermo J, Desai, Mayurika, Anderson, Seth, Scornik, Fabiana S

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A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome von Riuró, Helena, MS, Campuzano, Oscar, PhD, Arbelo, Elena, MD, PhD, Iglesias, Anna, MS, Batlle, Montserrat, PhD, Pérez-Villa, Felix, MD, PhD, Brugada, Josep, MD, PhD, Pérez, Guillermo J., PhD, Scornik, Fabiana S., PhD, Brugada, Ramon, MD, PhD

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Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation von Santori, Montserrat, Gil, Rocío, Blanco-Verea, Alejandro, Riuró, Helena, Díaz-Castro, Óscar, López-Abel, Bernardo, Brugada, Ramón, Carracedo, Ángel, Pérez, Guillermo J, Scornik, Fabiana S, Brion, María

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DiBAC₄(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²⁺-activated potassium channels independently of the β₁-subunit von Scornik, Fabiana S, Bucciero, Ronald S, Wu, Yuesheng, Selga, Elisabet, Bosch Calero, Cristina, Brugada, Ramon, Pérez, Guillermo J

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An SCN1B Variant Affects Both Cardiac-Type (Na V 1.5) and Brain-Type (Na V 1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders von Martinez-Moreno, Rebecca, Selga, Elisabet, Riuró, Helena, Carreras, David, Parnes, Mered, Srinivasan, Chandra, Wangler, Michael F, Pérez, Guillermo J, Scornik, Fabiana S, Brugada, Ramon

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