| Literature DB >> 11382194 |
S Di Donna1, V Renault, C Forestier, G Piron-Hamelin, D Thiesson, R N Cooper, E Ponsot, S Decary, R Amouri, F Hentati, G S Butler-Browne, V Mouly.
Abstract
In this communication, we will review the problems caused by cell-mediated gene therapy, taking skeletal muscle as a physiological model. In particular we have utilised vectors transferring telomerase under the control of retroviral promoters into human satellite cells. The set of results presented here has several implications regarding gene therapy trials. Nevertheless, more experiments will be required to fully validate this cellular model and to use telomerase to safely extend the lifespan of putative gene therapy vectors.Entities:
Mesh:
Year: 2000 PMID: 11382194 DOI: 10.1007/s100720070008
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307