| Literature DB >> 15372435 |
Michael R Rosen1, Richard B Robinson, Peter Brink, Ira S Cohen.
Abstract
In recent years, several groups have reported a variety of strategies for developing biological pacemakers whose ultimate function would be to supplement/replace electronic pacemakers. Strategies have included gene therapy using naked plasmids or viral vectors and cell therapy for which both adult human mesenchymal stem cells (hMSCs) and human embryonic stem cells have been employed. This article reviews the various approaches and summarizes our own research in which the pacemaker gene, HCN2, is administered via viral vector or in an hMSC platform to produce pacemaker function in the intact canine heart. copyright 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 15372435 DOI: 10.1002/ar.a.20073
Source DB: PubMed Journal: Anat Rec A Discov Mol Cell Evol Biol ISSN: 1552-4884