Biological Therapies for Cardiac Arrhythmias Can Genes and Cells Replace Drugs and Devices?HEE CHEOL CHO; MARBAN, Eduardo.Circulation research. 2010, Vol 106, Num 4, pp 674-685, issn 0009-7330, 12 p.Article

Gene transfer of a synthetic pacemaker channel into the heart : A novel strategy for biological pacingKASHIWAKURA, Yuji; HEE CHEOL CHO; BARTH, Andreas S et al.Circulation (New York, N.Y.). 2006, Vol 114, Num 16, pp 1682-1686, issn 0009-7322, 5 p.Article

Engineered Electrical Conduction Tract Restores Conduction in Complete Heart Block: From In Vitro to In Vivo Proof of ConceptCINGOLANI, Eugenio; IONTA, Vittoria; KE CHENG et al.Journal of the American College of Cardiology. 2014, Vol 64, Num 24, pp 2575-2585, issn 0735-1097, 11 p.Article

Gene therapy to inhibit the calcium channel β subunit : Physiological consequences and pathophysiological effects in models of cardiac hypertrophyCINGOLANI, Eugenio; RAMIREZ CORREA, Genaro A; KIZANA, Eddy et al.Circulation research. 2007, Vol 101, Num 2, pp 166-175, issn 0009-7330, 10 p.Article

Selective inhibition of inward rectifier K⁺ channels (Kir2.1 or Kir2.2) abolishes protection by ischemic preconditioning in rabbit ventricular cardiomyocytesDIAZ, Roberto J; ZOBEL, Carsten; HEE CHEOL CHO et al.Circulation research. 2004, Vol 95, Num 3, pp 325-332, issn 0009-7330, 8 p.Article

Functional integration of electrically active cardiac derivatives from genetically engineered human embryonic stem cells with quiescent recipient ventricular cardiomyocytes insights into the development of cell-based pacemakersTIAN XUE; HEE CHEOL CHO; AKAR, Fadi G et al.Circulation (New York, N.Y.). 2005, Vol 111, Num 1, pp 11-20, issn 0009-7322, 10 p.Article