Published in Gene Therapy Weekly, December 18th, 2008
"Previous studies have focused on the use of vector-based gene therapy for GBM by direct intratumoral injection with expression of therapeutic proteins by tumor cells themselves. However, as antitumor proteins are generally lethal to tumor cells, the therapeutic reservoir is rapidly depleted, allowing escape of residual tumor cells. Moreover, it has been...
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Source: Gene Therapy Weekly (2008-12-18)
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