Cationic lipid-nanoceria hybrids, a novel nonviral vector-mediated gene delivery into mammalian cells: investigation of the cellular uptake mechanism
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep29197.pdf
Reference51 articles.
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3. Hu, W. W., Wang, Z., Hollister, S. J. & Krebsbach, P. H. Localized viral vector delivery to enhance in situ regenerative gene therapy. Gene Ther 14, 891–901 (2007).
4. Kay, M. A., Glorioso, J. C. & Naldini, L. Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics. Nat Med 7, 33–40 (2001)
5. Waehler, R., Russell, S. J. & Curiel, D. T. Engineering targeted viral vectors for gene therapy. Nat Rev Genet 8, 573–587 (2007).
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