检索结果 - Martin Tristani‐Firouzi

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  1. 1
    Voltage‐dependent inactivation of the human K<sup>+</sup> channel KvLQT1 is eliminated by association with minimal K<sup>+</sup> channel (minK) subunits

    Voltage‐dependent inactivation of the human K<sup>+</sup> channel KvLQT1 is eliminated by association with minimal K<sup>+</sup> channel (minK) subunits 由 Martin Tristani‐Firouzi, Michael C. Sanguinetti

    出版 1998
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  2. 2
    Interactions between S4-S5 Linker and S6 Transmembrane Domain Modulate Gating of HERG K+ Channels

    Interactions between S4-S5 Linker and S6 Transmembrane Domain Modulate Gating of HERG K+ Channels 由 Martin Tristani‐Firouzi, Jun Chen, Michael C. Sanguinetti

    出版 2002
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  3. 3
    Blebbistatin Effectively Uncouples the Excitation-Contraction Process in Zebrafish Embryonic Heart

    Blebbistatin Effectively Uncouples the Excitation-Contraction Process in Zebrafish Embryonic Heart 由 Chuanchau J. Jou, Kenneth W. Spitzer, Martin Tristani‐Firouzi

    出版 2010
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  4. 4
    Molecular biology of K+ channels and their role in cardiac arrhythmias11Am J Med. 2001;110-50-59.

    Molecular biology of K+ channels and their role in cardiac arrhythmias11Am J Med. 2001;110-50-59. 由 Martin Tristani‐Firouzi, Jun Chen, John S. Mitcheson, Michael C. Sanguinetti

    出版 2001
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  5. 5
    The S4-S5 Linker Directly Couples Voltage Sensor Movement to the Activation Gate in the Human Ether-á-go-go-related Gene (hERG) K+ Channel

    The S4-S5 Linker Directly Couples Voltage Sensor Movement to the Activation Gate in the Human Ether-á-go-go-related Gene (hERG) K+ Channel 由 Tania Ferrer, Jason Rupp, David R. Piper, Martin Tristani‐Firouzi

    出版 2006
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  6. 6
    Gating currents associated with intramembrane charge displacement in HERG potassium channels

    Gating currents associated with intramembrane charge displacement in HERG potassium channels 由 David R. Piper, Anthony Varghese, Michael C. Sanguinetti, Martin Tristani‐Firouzi

    出版 2003
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  7. 7
    A new oral therapy for long QT syndrome

    A new oral therapy for long QT syndrome 由 Susan P. Etheridge, Steven J. Compton, Martin Tristani‐Firouzi, Jay W. Mason

    出版 2003
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  8. 8
    The S4–S5 linker couples voltage sensing and activation of pacemaker channels

    The S4–S5 linker couples voltage sensing and activation of pacemaker channels 由 Jun Chen, John S. Mitcheson, Martin Tristani‐Firouzi, Monica Lin, Michael C. Sanguinetti

    出版 2001
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  9. 9
    De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

    De novo variants in exomes of congenital heart disease patients identify risk genes and pathways 由 Çiğdem Sevim Bayrak, Peng Zhang, Martin Tristani‐Firouzi, Bruce D. Gelb, Yuval Itan

    出版 2020
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  10. 10
    Explainable Artificial Intelligence for Stroke Risk Stratification in Atrial Fibrillation

    Explainable Artificial Intelligence for Stroke Risk Stratification in Atrial Fibrillation 由 Raquel Reisinger, Edgar J. Hernández, Martin Tristani‐Firouzi, Mark Yandell, Benjamin A. Steinberg

    出版 2025
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  11. 11
    Oxygen-induced constriction of rabbit ductus arteriosus occurs via inhibition of a 4-aminopyridine-, voltage-sensitive potassium channel.

    Oxygen-induced constriction of rabbit ductus arteriosus occurs via inhibition of a 4-aminopyridine-, voltage-sensitive potassium channel. 由 Martin Tristani‐Firouzi, Helen L. Reeve, Simona Tolarová, Ε. Kenneth Weir, Stephen L. Archer

    出版 1996
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  12. 12
    Functional Effects of Mutations in KvLQT1 that Cause Long QT Syndrome

    Functional Effects of Mutations in KvLQT1 that Cause Long QT Syndrome 由 Z. WANG, Martin Tristani‐Firouzi, Q. P. Xu, M. Lin, Mark T. Keating, Michael C. Sanguinetti

    出版 1999
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  13. 13
    Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome

    Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome 由 Saı̈d Bendahhou, Matthew R. Donaldson, Nikki Plaster, Martin Tristani‐Firouzi, Ying‐Hui Fu, Louis J. Ptáček

    出版 2003
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  14. 14
    Zebrafish model for human long QT syndrome

    Zebrafish model for human long QT syndrome 由 Rima Arnaout, Tania Ferrer, Jan Huisken, Kenneth W. Spitzer, Didier Y. R. Stainier, Martin Tristani‐Firouzi, C. Neil

    出版 2007
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  15. 15
    An<i>Fgf8</i>mouse mutant phenocopies human 22q11 deletion syndrome

    An<i>Fgf8</i>mouse mutant phenocopies human 22q11 deletion syndrome 由 Deborah U. Frank, Lori Fotheringham, Judson A. Brewer, Louis J. Muglia, Martin Tristani‐Firouzi, Mario R. Capecchi, Anne Moon

    出版 2002
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  16. 16
    Conformational changes in the M2 muscarinic receptor induced by membrane voltage and agonist binding

    Conformational changes in the M2 muscarinic receptor induced by membrane voltage and agonist binding 由 Ricardo A. Navarro‐Polanco, Eloy G. Moreno Galindo, Tania Ferrer‐Villada, Marcelo Arias, John R. Rigby, José A. Sánchez‐Chapula, Martin Tristani‐Firouzi

    出版 2011
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  17. 17
    The molecular basis of chloroquine block of the inward rectifier Kir2.1 channel

    The molecular basis of chloroquine block of the inward rectifier Kir2.1 channel 由 Aldo A. Rodríguez‐Menchaca, Ricardo A. Navarro‐Polanco, Tania Ferrer‐Villada, Jason Rupp, Frank B. Sachse, Martin Tristani‐Firouzi, José A. Sánchez‐Chapula

    出版 2008
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  18. 18
    DNA methylation reprograms cardiac metabolic gene expression in end-stage human heart failure

    DNA methylation reprograms cardiac metabolic gene expression in end-stage human heart failure 由 Mark E. Pepin, Stavros G. Drakos, Chae‐Myeong Ha, Martin Tristani‐Firouzi, Craig H. Selzman, James C. Fang, Adam R. Wende, Omar Wever‐Pinzon

    出版 2019
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  19. 19
    The pharmacokinetics of methadone and its metabolites in neonates, infants, and children

    The pharmacokinetics of methadone and its metabolites in neonates, infants, and children 由 Robert M. Ward, David R. Drover, Gregory B. Hammer, Christopher Stemland, Steven E. Kern, Martin Tristani‐Firouzi, Ralph A. Lugo, Kristin Satterfield, Brian J. Anderson

    出版 2014
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  20. 20
    Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association

    Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association 由 Andrew P. Landstrom, Jeffrey J. Kim, Bruce D. Gelb, Benjamin M. Helm, Prince J. Kannankeril, Christopher Semsarian, Amy C. Sturm, Martin Tristani‐Firouzi, Stephanie M. Ware

    出版 2021
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