AAV_Actb HMEJ donor_U6_sgRNA_EF1a_GFP_polyA Citations (2)

Originally described in: Homology-mediated end joining-based targeted integration using CRISPR/Cas9.
Yao X, Wang X, Hu X, Liu Z, Liu J, Zhou H, Shen X, Wei Y, Huang Z, Ying W, Wang Y, Nie YH, Zhang CC, Li S, Cheng L, Wang Q, Wu Y, Huang P, Sun Q, Shi L, Yang H Cell Res. 2017 May 19. doi: 10.1038/cr.2017.76. PubMed Journal

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Articles Citing AAV_Actb HMEJ donor_U6_sgRNA_EF1a_GFP_polyA

Articles
CRISPR/Cas9-mediated Targeted Integration In Vivo Using a Homology-mediated End Joining-based Strategy. Yao X, Wang X, Liu J, Shi L, Huang P, Yang H. J Vis Exp. 2018 Mar 12;(133). doi: 10.3791/56844. PubMed
Tild-CRISPR Allows for Efficient and Precise Gene Knockin in Mouse and Human Cells. Yao X, Zhang M, Wang X, Ying W, Hu X, Dai P, Meng F, Shi L, Sun Y, Yao N, Zhong W, Li Y, Wu K, Li W, Chen ZJ, Yang H. Dev Cell. 2018 May 21;45(4):526-536.e5. doi: 10.1016/j.devcel.2018.04.021. PubMed

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