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PUBMED FOR HANDHELDS

Journal Abstract Search


331 related items for PubMed ID: 23684427

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  • 3. In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells.
    Fatima A, Xu G, Shao K, Papadopoulos S, Lehmann M, Arnáiz-Cot JJ, Rosa AO, Nguemo F, Matzkies M, Dittmann S, Stone SL, Linke M, Zechner U, Beyer V, Hennies HC, Rosenkranz S, Klauke B, Parwani AS, Haverkamp W, Pfitzer G, Farr M, Cleemann L, Morad M, Milting H, Hescheler J, Saric T.
    Cell Physiol Biochem; 2011; 28(4):579-92. PubMed ID: 22178870
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  • 4. Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations.
    Kujala K, Paavola J, Lahti A, Larsson K, Pekkanen-Mattila M, Viitasalo M, Lahtinen AM, Toivonen L, Kontula K, Swan H, Laine M, Silvennoinen O, Aalto-Setälä K.
    PLoS One; 2012; 7(9):e44660. PubMed ID: 22962621
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  • 10. Mutation-specific differences in arrhythmias and drug responses in CPVT patients: simultaneous patch clamp and video imaging of iPSC derived cardiomyocytes.
    Pölönen RP, Swan H, Aalto-Setälä K.
    Mol Biol Rep; 2020 Feb; 47(2):1067-1077. PubMed ID: 31786768
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  • 12. Calcium Signaling Consequences of RyR2-S4938F Mutation Expressed in Human iPSC-Derived Cardiomyocytes.
    Toth N, Zhang XH, Zamaro A, Morad M.
    Int J Mol Sci; 2023 Oct 18; 24(20):. PubMed ID: 37894987
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  • 13. Modeling of catecholaminergic polymorphic ventricular tachycardia with patient-specific human-induced pluripotent stem cells.
    Itzhaki I, Maizels L, Huber I, Gepstein A, Arbel G, Caspi O, Miller L, Belhassen B, Nof E, Glikson M, Gepstein L.
    J Am Coll Cardiol; 2012 Sep 11; 60(11):990-1000. PubMed ID: 22749309
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  • 16. Molecular characterization of the calcium release channel deficiency syndrome.
    Tester DJ, Kim CSJ, Hamrick SK, Ye D, O'Hare BJ, Bombei HM, Fitzgerald KK, Haglund-Turnquist CM, Atkins DL, Nunez LAO, Law I, Temple J, Ackerman MJ.
    JCI Insight; 2020 Aug 06; 5(15):. PubMed ID: 32663189
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  • 17. Catecholaminergic polymorphic ventricular tachycardia is caused by mutation-linked defective conformational regulation of the ryanodine receptor.
    Uchinoumi H, Yano M, Suetomi T, Ono M, Xu X, Tateishi H, Oda T, Okuda S, Doi M, Kobayashi S, Yamamoto T, Ikeda Y, Ohkusa T, Ikemoto N, Matsuzaki M.
    Circ Res; 2010 Apr 30; 106(8):1413-24. PubMed ID: 20224043
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  • 20. Slowed depolarization and irregular repolarization in catecholaminergic polymorphic ventricular tachycardia: a study from cellular Ca2+ transients and action potentials to clinical monophasic action potentials and electrocardiography.
    Paavola J, Väänänen H, Larsson K, Penttinen K, Toivonen L, Kontula K, Laine M, Aalto-Setälä K, Swan H, Viitasalo M.
    Europace; 2016 Oct 30; 18(10):1599-1607. PubMed ID: 26705554
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