Engineered HSV vector achieves safe long-term transgene expression in the central nervous system
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-01635-1.pdf
Reference23 articles.
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2. Miyagawa, Y. et al. Herpes simplex viral-vector design for efficient transduction of nonneuronal cells without cytotoxicity. Proc Natl Acad Sci USA 112, E1632–1641, doi: 10.1073/pnas.1423556112 (2015).
3. Ferenczy, M. W. & DeLuca, N. A. Reversal of heterochromatic silencing of quiescent herpes simplex virus type 1 by ICP0. J Virol 85, 3424–3435, doi: 10.1128/JVI.02263-10 (2011).
4. Boutell, C. & Everett, R. D. Regulation of alphaherpesvirus infections by the ICP0 family of proteins. J Gen Virol 94, 465–481, doi: 10.1099/vir.0.048900-0 (2013).
5. Uchida, H. et al. A double mutation in glycoprotein gB compensates for ineffective gD-dependent initiation of herpes simplex virus type 1 infection. J Virol 84, 12200–12209, doi: 10.1128/JVI.01633-10 (2010).
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