Published in Gene Therapy Weekly, May 26th, 2005
According to a report from Australia, "the potential dangers of using viruses to deliver and integrate DNA into host cells in gene therapy have been poignantly highlighted in recent clinical trials. Safer, non-viral gene delivery approaches have been largely ignored in the past because of their inefficient delivery and the resulting transient transgene expression. However, recent advances indicate that efficient, long-term gene expression can be achieved by non-viral means."
"In particular, integration of DNA can be targeted to specific genomic sites without deleterious...
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Source: Gene Therapy Weekly (2005-05-26)
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