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CRISPR-Cas9 gene editing of hepatitis B virus in chronically infected humanized mice.
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In vitro Inactivation of Latent HSV by Targeted Mutagenesis Using an HSV-specific Homing Endonuclease.
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megaTALs: a rare-cleaving nuclease architecture for therapeutic genome engineering.
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Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases.
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Rationally designed capsid and transgene cassette of AAV6 vectors for dendritic cell-based cancer immunotherapy.
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A novel DNA vaccine technology conveying protection against a lethal herpes simplex viral challenge in mice.
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Highly significant antiviral activity of HIV-1 LTR-specific tre-recombinase in humanized mice.
PLoS Pathog. 2013;9(9):e1003587. doi: 10.1371/journal.ppat.1003587. Epub 2013 Sep 26.
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Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.
Cell. 2013 Sep 12;154(6):1380-9. doi: 10.1016/j.cell.2013.08.021. Epub 2013 Aug 29.
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Harnessing the CRISPR/Cas9 system to disrupt latent HIV-1 provirus.
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CRISPR/Cas9 systems targeting β-globin and CCR5 genes have substantial off-target activity.
Nucleic Acids Res. 2013 Nov;41(20):9584-92. doi: 10.1093/nar/gkt714. Epub 2013 Aug 11.

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