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Journal Abstract Search

117 related items for PubMed ID: 37660555

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  • 3. Generation of three heterozygous KCNH2 mutation-carrying human induced pluripotent stem cell lines for modeling LQT2 syndrome.
    Mondéjar-Parreño G, Jahng JWS, Belbachir N, Wu BC, Zhang X, Perez MV, Badhwar N, Wu JC.
    Stem Cell Res; 2021 Jul; 54():102402. PubMed ID: 34051449
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  • 5. The KCNH2-IVS9-28A/G mutation causes aberrant isoform expression and hERG trafficking defect in cardiomyocytes derived from patients affected by Long QT Syndrome type 2.
    Mura M, Mehta A, Ramachandra CJ, Zappatore R, Pisano F, Ciuffreda MC, Barbaccia V, Crotti L, Schwartz PJ, Shim W, Gnecchi M.
    Int J Cardiol; 2017 Aug 01; 240():367-371. PubMed ID: 28433559
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  • 7. Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered Cardiomyocytes.
    O'Hare BJ, John Kim CS, Hamrick SK, Ye D, Tester DJ, Ackerman MJ.
    Circ Genom Precis Med; 2020 Oct 01; 13(5):466-475. PubMed ID: 32940533
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  • 8. Human induced pluripotent stem cell line ZZUNEUi027-A generated from a long QT syndrome patient with a heterozygous KCNH2 (c. 128 A > G) mutant.
    Zhao J, Wang L, Zhu K, Chen X, Qin F, Li X, Dong J, Tao H.
    Stem Cell Res; 2022 Aug 01; 63():102836. PubMed ID: 35700634
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  • 11. Tbx20 controls the expression of the KCNH2 gene and of hERG channels.
    Caballero R, Utrilla RG, Amorós I, Matamoros M, Pérez-Hernández M, Tinaquero D, Alfayate S, Nieto-Marín P, Guerrero-Serna G, Liu QH, Ramos-Mondragón R, Ponce-Balbuena D, Herron T, Campbell KF, Filgueiras-Rama D, Peinado R, López-Sendón JL, Jalife J, Delpón E, Tamargo J.
    Proc Natl Acad Sci U S A; 2017 Jan 17; 114(3):E416-E425. PubMed ID: 28049825
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  • 12. Derivation and characterization of two human induced pluripotent stem cell lines (NUIGi004-A) and (NUIGi012-A) from two patients with LQT2 disease.
    Liu M, Ge N, Zhang J, Yang M, Yang F, Krawczyk J, Ward D, McInerney V, O'Brien T, Shen S, Prendiville T.
    Stem Cell Res; 2021 Oct 17; 56():102555. PubMed ID: 34628246
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  • 13. Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture.
    Lahti AL, Kujala VJ, Chapman H, Koivisto AP, Pekkanen-Mattila M, Kerkelä E, Hyttinen J, Kontula K, Swan H, Conklin BR, Yamanaka S, Silvennoinen O, Aalto-Setälä K.
    Dis Model Mech; 2012 Mar 17; 5(2):220-30. PubMed ID: 22052944
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  • 15. Genome Editing of Induced Pluripotent Stem Cells to Decipher Cardiac Channelopathy Variant.
    Garg P, Oikonomopoulos A, Chen H, Li Y, Lam CK, Sallam K, Perez M, Lux RL, Sanguinetti MC, Wu JC.
    J Am Coll Cardiol; 2018 Jul 03; 72(1):62-75. PubMed ID: 29957233
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  • 19. The Advantages, Challenges, and Future of Human-Induced Pluripotent Stem Cell Lines in Type 2 Long QT Syndrome.
    Cai D, Zheng Z, Jin X, Fu Y, Cen L, Ye J, Song Y, Lian J.
    J Cardiovasc Transl Res; 2023 Feb 03; 16(1):209-220. PubMed ID: 35976484
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