AAV_Efs_hSpCas9_NLS_FLAG-SV40 Citations (3)

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_Efs_hSpCas9_NLS_FLAG-SV40

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
PRMT5-mediated homologous recombination repair is essential to maintain genomic integrity of neural progenitor cells. Wang YJ, Cao JB, Yang J, Liu T, Yu HL, He ZX, Bao SL, He XX, Zhu XJ. Cell Mol Life Sci. 2024 Mar 8;81(1):123. doi: 10.1007/s00018-024-05154-x. PubMed

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