xCas9(3.7)-ABE(7.10) Citations (11)

Originally described in: Evolved Cas9 variants with broad PAM compatibility and high DNA specificity.
Hu JH, Miller SM, Geurts MH, Tang W, Chen L, Sun N, Zeina CM, Gao X, Rees HA, Lin Z, Liu DR Nature. 2018 Feb 28. pii: nature26155. doi: 10.1038/nature26155. PubMed Journal

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Articles Citing xCas9(3.7)-ABE(7.10)

Articles
Boosting activity of high-fidelity CRISPR/Cas9 variants using a tRNA(Gln)-processing system in human cells. He X, Wang Y, Yang F, Wang B, Xie H, Gu L, Zhao T, Liu X, Zhang D, Ren Q, Liu X, Liu Y, Gao C, Gu F. J Biol Chem. 2019 Jun 7;294(23):9308-9315. doi: 10.1074/jbc.RA119.007791. Epub 2019 Apr 22. PubMed
CRISPR-Pass: Gene Rescue of Nonsense Mutations Using Adenine Base Editors. Lee C, Hyun Jo D, Hwang GH, Yu J, Kim JH, Park SE, Kim JS, Kim JH, Bae S. Mol Ther. 2019 May 24. pii: S1525-0016(19)30227-8. doi: 10.1016/j.ymthe.2019.05.013. PubMed
Development of a Simple and Quick Method to Assess Base Editing in Human Cells. Lv X, Qiu K, Tu T, He X, Peng Y, Ye J, Fu J, Deng R, Wang Y, Wu J, Liu C, Zhao J, Gu F. Mol Ther Nucleic Acids. 2020 Jun 5;20:580-588. doi: 10.1016/j.omtn.2020.03.004. Epub 2020 Mar 17. PubMed
BEON: A Functional Fluorescence Reporter for Quantification and Enrichment of Adenine Base-Editing Activity. Wang P, Xu L, Gao Y, Han R. Mol Ther. 2020 Jul 8;28(7):1696-1705. doi: 10.1016/j.ymthe.2020.04.009. Epub 2020 Apr 16. PubMed
Restoration of visual function in adult mice with an inherited retinal disease via adenine base editing. Suh S, Choi EH, Leinonen H, Foik AT, Newby GA, Yeh WH, Dong Z, Kiser PD, Lyon DC, Liu DR, Palczewski K. Nat Biomed Eng. 2021 Feb;5(2):169-178. doi: 10.1038/s41551-020-00632-6. Epub 2020 Oct 19. PubMed
Aglycosylated antibody-producing mice for aglycosylated antibody-lectin coupled immunoassay for the quantification of tumor markers (ALIQUAT). Lee NE, Kim SH, Yu DY, Woo EJ, Kim MI, Seong GS, Lee SM, Ko JH, Kim YS. Commun Biol. 2020 Oct 30;3(1):636. doi: 10.1038/s42003-020-01363-9. PubMed
One-step genotyping method in CRISPR based on short inner primer-assisted, tetra primer-paired amplifications. Lee NE, Ha DI, Ko JH, Kim YS. Mol Cell Probes. 2021 Feb;55:101675. doi: 10.1016/j.mcp.2020.101675. Epub 2020 Nov 25. PubMed
Analysis of conventional and alternative CRISPR/Cas9 genome editing to enhance a single-base pair knock-in mutation. Edmondson C, Zhou Q, Liu X. BMC Biotechnol. 2021 Jul 27;21(1):45. doi: 10.1186/s12896-021-00707-5. PubMed
Combined CRISPRi and proteomics screening reveal a cohesin-CTCF-bound allele contributing to increased expression of RUVBL1 and prostate cancer progression. Tian Y, Dong D, Wang Z, Wu L, Park JY, Wei GH, Wang L. Am J Hum Genet. 2023 Aug 3;110(8):1289-1303. doi: 10.1016/j.ajhg.2023.07.003. PubMed
Isogenic induced pluripotent stem cell line ICGi036-A-1 from a patient with familial hypercholesterolaemia, derived by correcting a pathogenic variant of the gene LDLR c.530C>T. Zueva AS, Shevchenko AI, Medvedev SP, Elisaphenko EA, Sleptcov AA, Nazarenko MS, Tmoyan NA, Zakian SM, Zakharova IS. Vavilovskii Zhurnal Genet Selektsii. 2025 Apr;29(2):189-199. doi: 10.18699/vjgb-25-22. PubMed
Base editing in the AUTS2 gene and high-throughput NGS genotyping of clones: a strategy for generating a cellular model. Yan AP, Salnikov PA, Buzdin capital A, Cyrilliccapital A, Cyrillic, capital KA, Cyrillicovalskaia Vcapital A, Cyrillic, Musatova EV, Orlov PS, Ryzhkova capital O, CyrillicP, Subbotovskaia AI, Suntsova capital EM, CyrillicV, Khristichenko capital A, CyrillicU, Khabarova capital A, Cyrilliccapital A, Cyrillic. Vavilovskii Zhurnal Genet Selektsii. 2026 Mar;30(1):72-84. doi: 10.18699/vjgb-26-04. PubMed

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