Suchergebnisse - Hector Barajas‐Martínez

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  1. 1
    The potential anti-arrhythmic effect of SGLT2 inhibitors

    The potential anti-arrhythmic effect of SGLT2 inhibitors von Hong-Yi Duan, Hector Barajas‐Martínez, Charles Antzelevitch, Dan Hu

    Veröffentlicht 2024
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  2. 2
    Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation

    Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation von Alexander Burashnikov, Alyssa Petroski, Dan Hu, Hector Barajas‐Martínez, Charles Antzelevitch

    Veröffentlicht 2011
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  3. 3
    Brugada-Like Syndrome in Infancy Presenting With Rapid Ventricular Tachycardia and Intraventricular Conduction Delay

    Brugada-Like Syndrome in Infancy Presenting With Rapid Ventricular Tachycardia and Intraventricular Conduction Delay von Ronald J. Kanter, Ryan Pfeiffer, Dan Hu, Hector Barajas‐Martínez, Michael P. Carboni, Charles Antzelevitch

    Veröffentlicht 2011
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  4. 4
    Mechanisms of atrial-selective block of Na<sup>+</sup> channels by ranolazine: I. Experimental analysis of the use-dependent block

    Mechanisms of atrial-selective block of Na<sup>+</sup> channels by ranolazine: I. Experimental analysis of the use-dependent block von Andrew C. Zygmunt, Vladislav V. Nesterenko, Sridharan Rajamani, Dan Hu, Hector Barajas‐Martínez, Luiz Belardinelli, Charles Antzelevitch

    Veröffentlicht 2011
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  5. 5
    Host-range restriction of vaccinia virus E3L-specific deletion mutants

    Host-range restriction of vaccinia virus E3L-specific deletion mutants von Elizabeth Beattie, Elizabeth B. Kauffman, Héctor Barajas Martínez, Marion E. Perkus, Bertram L. Jacobs, Enzo Paoletti, James Tartaglia

    Veröffentlicht 1996
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  6. 6
    Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome

    Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome von István Koncz, Zsolt Gurabi, Bence Patocskai, Brian K. Panama, Tamás Szél, Dan Hu, Hector Barajas‐Martínez, Charles Antzelevitch

    Veröffentlicht 2014
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  7. 7
    Hypertension as a sequela in patients of SARS-CoV-2 infection

    Hypertension as a sequela in patients of SARS-CoV-2 infection von Ganxiao Chen, Xun Li, Zuojiong Gong, Hao Xia, Yao Wang, Xuefen Wang, Yan Huang, Hector Barajas‐Martínez, Dan Hu

    Veröffentlicht 2021
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  8. 8
    Further Insights in the Most Common <i>SCN5A</i> Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

    Further Insights in the Most Common <i>SCN5A</i> Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect von Christian Veltmann, Hector Barajas‐Martínez, Christian Wolpert, Martin Borggrefe, Rainer Schimpf, Ryan Pfeiffer, Gabriel Cáceres, Elena Burashnikov, Charles Antzelevitch, Dan Hu

    Veröffentlicht 2016
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  9. 9
    Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome

    Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome von Yoshino Minoura, Brian K. Panama, Vladislav V. Nesterenko, Matthew J. Betzenhauser, Hector Barajas‐Martínez, Dan Hu, José M. Di Diego, Charles Antzelevitch

    Veröffentlicht 2013
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  10. 10
    Ranolazine for Congenital Long-QT Syndrome Type III

    Ranolazine for Congenital Long-QT Syndrome Type III von Ehud Chorin, Dan Hu, Charles Antzelevitch, Aviram Hochstadt, Luiz Belardinelli, David Zeltser, Hector Barajas‐Martínez, Uri Rozovski, Raphaël Rosso, Arnon Adler, Jesaia Benhorin, Sami Viskin

    Veröffentlicht 2016
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  11. 11
    A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

    A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype von Dan Hu, Hector Barajas‐Martínez, Elena Burashnikov, Michael Springer, Yuesheng Wu, András Varró, Ryan Pfeiffer, Tamara T. Koopmann, Jonathan M. Cordeiro, Alejandra Guerchicoff, Guido D. Pollevick, Charles Antzelevitch

    Veröffentlicht 2009
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  12. 12
    Compound Heterozygous Mutations P336L and I1660V in the Human Cardiac Sodium Channel Associated With the Brugada Syndrome

    Compound Heterozygous Mutations P336L and I1660V in the Human Cardiac Sodium Channel Associated With the Brugada Syndrome von Jonathan M. Cordeiro, Hector Barajas‐Martínez, Kui Hong, Elena Burashnikov, Ryan Pfeiffer, Anne-Marie Orsino, Yue Wu, Dan Hu, Josép Brugada, Pedro Brugada, Charles Antzelevitch, Robert Dumaine, Ramón Brugada

    Veröffentlicht 2006
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  13. 13
    Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

    Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction von Dan Hu, Sami Viskin, Antonio Oliva, Tabitha Carrier, Jonathan M. Cordeiro, Hector Barajas‐Martínez, Yuesheng Wu, Elena Burashnikov, Serge Sicouri, Ramón Brugada, Rafael Rosso, Alejandra Guerchicoff, Guido D. Pollevick, Charles Antzelevitch

    Veröffentlicht 2007
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  14. 14
    Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on IKr

    Maximum Diastolic Potential of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Depends Critically on IKr von Michael Xavier Doss, José M. Di Diego, Robert J. Goodrow, Yuesheng Wu, Jonathan M. Cordeiro, Vladislav V. Nesterenko, Hector Barajas‐Martínez, Dan Hu, Janire Urrutia, Mayurika Desai, Jacqueline A. Treat, Agapios Sachinidis, Charles Antzelevitch

    Veröffentlicht 2012
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  15. 15
    A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis

    A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis von Jessica A. Hennessey, Nicole J. Boczek, Yong-hui Jiang, Joelle D. Miller, William L. Patrick, Ryan Pfeiffer, Brittan Sutphin, David J. Tester, Hector Barajas‐Martínez, Michael J. Ackerman, Charles Antzelevitch, Ronald J. Kanter, Geoffrey S. Pitt

    Veröffentlicht 2014
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  16. 16
    Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

    Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) von Christian Templin, Jelena R. Ghadri, Jean‐Sébastien Rougier, Alessandra Baumer, V. A. Kaplan, Maxime Albesa, Heinrich Sticht, Anita Rauch, Chris Puleo, Dan Hu, Hector Barajas‐Martínez, Charles Antzelevitch, Thomas F. Lüscher, Hugues Abriel, Fırat Duru

    Veröffentlicht 2011
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  17. 17
    Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

    Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8 von Hector Barajas‐Martínez, Dan Hu, Tania Ferrer, Carlos G. Onetti, Yuesheng Wu, Elena Burashnikov, Madalene Boyle, Tyler Surman, Janire Urrutia, Christian Veltmann, Rainer Schimpf, Martin Borggrefe, Christian Wolpert, Bassiema Ibrahim, José A. Sánchez‐Chapula, Stephen L. Winters, Michel Haı̈ssaguerre, Charles Antzelevitch

    Veröffentlicht 2011
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  18. 18
    A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents

    A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents von Dan Hu, Hector Barajas‐Martínez, Argelia Medeiros‐Domingo, Lia Crotti, Christian Veltmann, Rainer Schimpf, Janire Urrutia, Aintzane Alday, Óscar Casis, Ryan Pfeiffer, Elena Burashnikov, Gabriel Cáceres, David J. Tester, Christian Wolpert, Martin Borggrefe, Peter J. Schwartz, Michael J. Ackerman, Charles Antzelevitch

    Veröffentlicht 2011
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  19. 19
    ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene

    ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene von Dan Hu, Hector Barajas‐Martínez, André Terzic, Sungjo Park, Ryan Pfeiffer, Elena Burashnikov, Yuesheng Wu, Martin Borggrefe, Christian Veltmann, Rainer Schimpf, John Cai, Gi-Byong Nam, Pramod Deshmukh, Melvin M. Scheinman, Mark W. Preminger, Jonathan S. Steinberg, Angélica López-Izquierdo, Daniela Ponce‐Balbuena, Christian Wolpert, Michel Haı̈ssaguerre, José A. Sánchez‐Chapula, Charles Antzelevitch

    Veröffentlicht 2014
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  20. 20
    Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

    Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death von Elena Burashnikov, Ryan Pfeiffer, Hector Barajas‐Martínez, Eva Delpón, Dan Hu, Mayurika Desai, Martin Borggrefe, Michel Haı̈ssaguerre, Ronald J. Kanter, Guido D. Pollevick, Alejandra Guerchicoff, R. Laino, Mark Marieb, Koonlawee Nademanee, Gi‐Byoung Nam, Roberto Monreal‐Robles, Rainer Schimpf, Dwight Stapleton, Sami Viskin, Stephen L. Winters, Christian Wolpert, Samuel H. Zimmern, Christian Veltmann, Charles Antzelevitch

    Veröffentlicht 2010
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