Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes

Lieu D, Fu J, Chiamvimonvat N, Chan Tung K, McNerney G, Huser T, Keller G, Kong C-W, Li R (2013)
Circulation: Arrhythmia and Electrophysiology 6(1): 191-201.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Circulation: Arrhythmia and Electrophysiology
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6
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1
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191-201
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Lieu D, Fu J, Chiamvimonvat N, et al. Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes. Circulation: Arrhythmia and Electrophysiology. 2013;6(1):191-201.
Lieu, D., Fu, J., Chiamvimonvat, N., Chan Tung, K., McNerney, G., Huser, T., Keller, G., et al. (2013). Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes. Circulation: Arrhythmia and Electrophysiology, 6(1), 191-201. doi:10.1161/circep.111.973420
Lieu, D., Fu, J., Chiamvimonvat, N., Chan Tung, K., McNerney, G., Huser, T., Keller, G., Kong, C. - W., and Li, R. (2013). Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes. Circulation: Arrhythmia and Electrophysiology 6, 191-201.
Lieu, D., et al., 2013. Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes. Circulation: Arrhythmia and Electrophysiology, 6(1), p 191-201.
D. Lieu, et al., “Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes”, Circulation: Arrhythmia and Electrophysiology, vol. 6, 2013, pp. 191-201.
Lieu, D., Fu, J., Chiamvimonvat, N., Chan Tung, K., McNerney, G., Huser, T., Keller, G., Kong, C.-W., Li, R.: Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes. Circulation: Arrhythmia and Electrophysiology. 6, 191-201 (2013).
Lieu, Deborah, Fu, J., Chiamvimonvat, N., Chan Tung, K., McNerney, Gregory, Huser, Thomas, Keller, G., Kong, C.-W., and Li, Ronald. “Mechanism-based facilitated maturation of human pluripotent stem cell-derived cardiomyocytes”. Circulation: Arrhythmia and Electrophysiology 6.1 (2013): 191-201.

78 Zitationen in Europe PMC

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Relaxin suppresses atrial fibrillation by reversing fibrosis and myocyte hypertrophy and increasing conduction velocity and sodium current in spontaneously hypertensive rat hearts.
Parikh A, Patel D, McTiernan CF, Xiang W, Haney J, Yang L, Lin B, Kaplan AD, Bett GC, Rasmusson RL, Shroff SG, Schwartzman D, Salama G., Circ Res 113(3), 2013
PMID: 23748429
Materials science and tissue engineering: repairing the heart.
Radisic M, Christman KL., Mayo Clin Proc 88(8), 2013
PMID: 23910415

43 References

Daten bereitgestellt von Europe PubMed Central.

Metabolic gene expression in fetal and failing human heart.
Razeghi P, Young ME, Alcorn JL, Moravec CS, Frazier OH, Taegtmeyer H., Circulation 104(24), 2001
PMID: 11739307
Extracellular K+ dependence of inward rectification kinetics in human left ventricular cardiomyocytes.
Bailly P, Mouchoniere M, Benitah JP, Camilleri L, Vassort G, Lorente P., Circulation 98(24), 1998
PMID: 9851963
Facilitated maturation of Ca2+ handling properties of human embryonic stem cell-derived cardiomyocytes by calsequestrin expression.
Liu J, Lieu DK, Siu CW, Fu JD, Tse HF, Li RA., Am. J. Physiol., Cell Physiol. 297(1), 2009
PMID: 19357236
Interactive effects of surface topography and pulsatile electrical field stimulation on orientation and elongation of fibroblasts and cardiomyocytes
Au HT, Cheng I, Chowdhury MF, Radisic M., 2007
Functional assembly of engineered myocardium by electrical stimulation of cardiac myocytes cultured on scaffolds.
Radisic M, Park H, Shing H, Consi T, Schoen FJ, Langer R, Freed LE, Vunjak-Novakovic G., Proc. Natl. Acad. Sci. U.S.A. 101(52), 2004
PMID: 15604141
Reduction of I(to) causes hypertrophy in neonatal rat ventricular myocytes.
Kassiri Z, Zobel C, Nguyen TT, Molkentin JD, Backx PH., Circ. Res. 90(5), 2002
PMID: 11909822
Mechanotransduction in cardiac myocytes.
Lammerding J, Kamm RD, Lee RT., Ann. N. Y. Acad. Sci. 1015(), 2004
PMID: 15201149
In vivo cardiac gene transfer of Kv4.3 abrogates the hypertrophic response in rats after aortic stenosis.
Lebeche D, Kaprielian R, del Monte F, Tomaselli G, Gwathmey JK, Schwartz A, Hajjar RJ., Circulation 110(22), 2004
PMID: 15557376
Prevention of hypertrophy by overexpression of Kv4.2 in cultured neonatal cardiomyocytes.
Zobel C, Kassiri Z, Nguyen TT, Meng Y, Backx PH., Circulation 106(18), 2002
PMID: 12403671
Stretch-induced alterations of human Kir2.1 channel currents.
He Y, Xiao J, Yang Y, Zhou Q, Zhang Z, Pan Q, Liu Y, Chen Y., Biochem. Biophys. Res. Commun. 351(2), 2006
PMID: 17067550
Embryonic stem cell-derived cardiomyocyte heterogeneity and the isolation of immature and committed cells for cardiac remodeling and regeneration.
Boheler KR, Joodi RN, Qiao H, Juhasz O, Urick AL, Chuppa SL, Gundry RL, Wersto RP, Zhou R., Stem Cells Int 2011(), 2011
PMID: 21912557
Electrophysiological maturation and integration of murine fetal cardiomyocytes after transplantation.
Halbach M, Pfannkuche K, Pillekamp F, Ziomka A, Hannes T, Reppel M, Hescheler J, Muller-Ehmsen J., Circ. Res. 101(5), 2007
PMID: 17641227
Human ISL1 heart progenitors generate diverse multipotent cardiovascular cell lineages.
Bu L, Jiang X, Martin-Puig S, Caron L, Zhu S, Shao Y, Roberts DJ, Huang PL, Domian IJ, Chien KR., Nature 460(7251), 2009
PMID: 19571884
Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversification.
Moretti A, Caron L, Nakano A, Lam JT, Bernshausen A, Chen Y, Qyang Y, Bu L, Sasaki M, Martin-Puig S, Sun Y, Evans SM, Laugwitz KL, Chien KR., Cell 127(6), 2006
PMID: 17123592

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