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
Articles Citing BPK2660
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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 |
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 |
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 |
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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