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Adenoviral Human BCL-2 Transgene Expression Attenuates Early Donor Cell Death After Cardiomyoblast Transplantation Into Ischemic Rat Hearts
Author(s) -
Ingo Kutschka,
Theo Kofidis,
Ian Y. Chen,
Georges von Degenfeld,
Monika Zwierzchoniewska,
Grant Hoyt,
Takayasu Arai,
Darren R. Lebl,
Stephen L. Hendry,
Ahmad Y. Sheikh,
David T. Cooke,
Andrew J. Connolly,
Helen M. Blau,
Sanjiv S. Gambhir,
Robert C. Robbins
Publication year - 2006
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.001370
Subject(s) - medicine , transplantation , bioluminescence imaging , ligation , ejection fraction , apoptosis , heart transplantation , myocardial infarction , genetic enhancement , cardiology , andrology , urology , pathology , luciferase , heart failure , biology , transfection , gene , biochemistry
Cell transplantation for myocardial repair is limited by early cell death. Gene therapy with human Bcl-2 (hBcl-2) has been shown to attenuate apoptosis in the experimental setting. Therefore, we studied the potential benefit of hBcl-2 transgene expression on the survival of cardiomyoblast grafts in ischemic rat hearts.

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