Viral vectors for gene therapy : the art of turning infectious agents into vehicles of therapeutics.
In summary, non-invasive imaging technology will help to design and improve gene therapy applications.
It is essential for the success of gene therapy vectors that an appropriate promoter is linked to the gene of interest.
Transcriptional targeting modalities in breast cancer gene therapy using adenovirus vectors controlled by alpha-lactalbumin promoter.
Deciphering the molecular mechanisms of integration site selection might have practical applications in improving the safety of retroviral vectors for use in human gene therapy.
Table 3 summarises several published studies that have utilised plasmid- and viral-mediated gene therapy to treat peripheral neuropathies.
The above definition of gene therapy formed the basis for including or excluding protocols.
This case prompted a thorough revision of the safety standards for gene therapy trials.