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Retargeting Adenoviral Vectors to Improve Gene Transfer into Tumors

Gene targeting to tumors using adenoviral vectors holds great potential for cancer imaging and therapy, but the limited efficacy of current methods used to improve delivery to target tissues and reduce unwanted interactions remain substantial barriers to further development. Progress in characterizi...

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Hlavní autoři: Hogg, Richard T., Thorpe, Philip, Gerard, Robert D.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2010
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3060954/
https://ncbi.nlm.nih.gov/pubmed/21183946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/cgt.2010.78
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