BPK2660 Citations (11)

Originally described in: Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition.
Kleinstiver BP, Prew MS, Tsai SQ, Nguyen NT, Topkar VV, Zheng Z, Joung JK Nat Biotechnol. 2015 Nov 2. doi: 10.1038/nbt.3404. PubMed Journal

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Articles Citing BPK2660

Articles
Delete_enChIP systems using different CRISPR orthologues and epitope tags. Fujita T, Yuno M, Fujii H. BMC Res Notes. 2018 Feb 27;11(1):154. doi: 10.1186/s13104-018-3262-4. PubMed
CRISPR-SKIP: programmable gene splicing with single base editors. Gapinske M, Luu A, Winter J, Woods WS, Kostan KA, Shiva N, Song JS, Perez-Pinera P. Genome Biol. 2018 Aug 15;19(1):107. doi: 10.1186/s13059-018-1482-5. PubMed
Increasing the specificity of CRISPR systems with engineered RNA secondary structures. Kocak DD, Josephs EA, Bhandarkar V, Adkar SS, Kwon JB, Gersbach CA. Nat Biotechnol. 2019 Jun;37(6):657-666. doi: 10.1038/s41587-019-0095-1. Epub 2019 Apr 15. PubMed
Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis Pigmentosa. Li P, Kleinstiver BP, Leon MY, Prew MS, Navarro-Gomez D, Greenwald SH, Pierce EA, Joung JK, Liu Q. CRISPR J. 2018 Feb;1(1):55-64. doi: 10.1089/crispr.2017.0009. PubMed
Expanding the RNA-Guided Endonuclease Toolkit for Mouse Genome Editing. Robertson L, Pederick D, Piltz S, White M, Nieto A, Ahladas M, Adikusuma F, Thomas PQ. CRISPR J. 2018 Dec;1:431-439. doi: 10.1089/crispr.2018.0050. PubMed
Precise and broad scope genome editing based on high-specificity Cas9 nickases. Wang Q, Liu J, Janssen JM, Le Bouteiller M, Frock RL, Goncalves MAFV. Nucleic Acids Res. 2021 Jan 25;49(2):1173-1198. doi: 10.1093/nar/gkaa1236. PubMed Associated Plasmids BA31_pU.CAG.SaCas9-D10A.rBGpA AA69_pU.CAG.Cas9-eSp(1.1)-D10A.rBGpA.2NLS AP76_pU.CAG.Cas9-D10A-K848A.rBGpA AP70_pU.CAG.Cas9-D10A-K848A-R1060A.rBGpA AB65_pCAG.Cas9-D10A.rBGpA More ...
Enabling large-scale genome editing at repetitive elements by reducing DNA nicking. Smith CJ, Castanon O, Said K, Volf V, Khoshakhlagh P, Hornick A, Ferreira R, Wu CT, Guell M, Garg S, Ng AHM, Myllykallio H, Church GM. Nucleic Acids Res. 2020 May 21;48(9):5183-5195. doi: 10.1093/nar/gkaa239. PubMed Associated Plasmids dABE dCBE4-gam pSB700 HL1gR4
In vivo gene editing via homology-independent targeted integration for adrenoleukodystrophy treatment. Hong SA, Seo JH, Wi S, Jung ES, Yu J, Hwang GH, Yu JH, Baek A, Park S, Bae S, Cho SR. Mol Ther. 2022 Jan 5;30(1):119-129. doi: 10.1016/j.ymthe.2021.05.022. Epub 2021 May 29. PubMed
Efficient C*G-to-G*C base editors developed using CRISPRi screens, target-library analysis, and machine learning. Koblan LW, Arbab M, Shen MW, Hussmann JA, Anzalone AV, Doman JL, Newby GA, Yang D, Mok B, Replogle JM, Xu A, Sisley TA, Weissman JS, Adamson B, Liu DR. Nat Biotechnol. 2021 Jun 28. pii: 10.1038/s41587-021-00938-z. doi: 10.1038/s41587-021-00938-z. PubMed Associated Plasmids pCMV_Anc689-nCas9 pCMV_Anc689-NG-nCas9 pCMV_APOBEC1-UdgX-nCas9 pCMV_APOBEC1-UdgX-NG-nCas9 pCMV_eA3A-nCas9 More ...
CRISPR-mediated activation of autism gene Itgb3 restores cortical network excitability via mGluR5 signaling. Jaudon F, Thalhammer A, Zentilin L, Cingolani LA. Mol Ther Nucleic Acids. 2022 Jul 20;29:462-480. doi: 10.1016/j.omtn.2022.07.013. eCollection 2022 Sep 13. PubMed
High-capacity adenovector delivery of forced CRISPR-Cas9 heterodimers fosters precise chromosomal deletions in human cells. Tasca F, Brescia M, Liu J, Janssen JM, Mamchaoui K, Goncalves MAFV. Mol Ther Nucleic Acids. 2023 Feb 22;31:746-762. doi: 10.1016/j.omtn.2023.02.025. eCollection 2023 Mar 14. PubMed

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