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Useful Literature:

Bajpai, R. Lentiviral Transduction. hESC Training Course Choc and Burnham, 1-9 (2004).

Bajpai, R., Terskikh, A. Genetic Manipulation of hESC: Lentivirus Vectors, 1-8 (2006).

Dull, T. et al. A third-generation lentivirus vector with a conditional packaging system. J. Virol. 72, 8463-8471 (1998).

Federico, M. edt. Lentivirus gene engineering protocols, Meth. Mol. Biol. 229, (2003).

Naldini, L. et al. Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector. Proc. Natl. Acad. Sci. USA 93, 11382-11388 (1996).

Root, D. E. et al. Genome-scale loss-of-function screening with a lentiviral RNAi library. Nat. Methods 3, 715-719 (2006).

Stewart, S. A. et al. Lentivirus-delivered stable gene silencing by RNAi in primary cells., RNA 9, 493-501 (2003).

Trono, D. edt. Lentiviral Vectors. Curr. Top. in Microbiol. Immunol. 261, (2002).

Zufferey R. et al. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo., Nat. Biotechnol. 15, 871-85 (1997).

Zufferey, R. et al. Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J Virol. 72, 9873-9880 (1998).

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