Editing base in mouse model

References

[1] BogdanoveAJ, VoytasDF (2011) TAL effectors: customizable proteins for DNA targeting.Science333:1843–1846.

[2] DelkerRK, Fugmann SD, PapavasiliouFN (2009) A coming-of-age story: activation-induced cytidine deaminase turns 10.Nat Immunol10:1147–1153.

[3] DoudnaJA, Charpentier E (2014) Genome editing. The new frontier of genome engineering with CRISPR-Cas9.Science346:1258096.

[4] KimK (2017) Highly efficient RNA-guided base editing in mouse embryos.Nat Biotechnol35:435–437.

[5] KleinstiverBP (2016) High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects.Nature529:490–495.

[6] KomorAC, KimYB, PackerMS, Zuris JA, LiuDR (2016) Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.Nature533:420–424.

[7] MaY (2016) Targeted AID-mediated mutagenesis (TAM) enables efficient genomic diversification in mammalian cells.Nat Methods13:1029–1035.

[8] NishidaK (2016) Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems.Science.

[9] QinW (2015) Efficient CRISPR/Cas9-mediated genome editing in mice by zygote electroporation of nuclease.Genetics200:423–430.

[10] SilvaG (2011) Meganucleases and other tools for targeted genome engineering: perspectives and challenges for gene therapy.Curr Gene Ther11:11–27

[11] UrnovFD, RebarEJ, HolmesMC, Zhang HS, GregoryPD (2010) Genome editing with engineered zinc finger nucleases.Nat Rev Genet11:636–646.

[12] WangW (2016) Delivery of Cas9 protein into mouse zygotes through a series of electroporation dramatically increases the efficiency of model creation.J Genet Genom43:319–327.

[13] WilesMV, QinW, ChengAW, Wang H (2015) CRISPR-Cas9-mediated genome editing and guide RNA design.Mamm Genome26:501–510.

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2017 The Author(s) 2017. This article is an open access publication