The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
Open accessAbstract
Methods to introduce targeted double-strand breaks (DSBs) into DNA enable precise genome editing by increasing the rate at which externally supplied DNA fragments are incorporated into the genome through homologous recombination. The efficiency of these methods is limited by nonhomologous end joining (NHEJ), an alternative DNA repair pathway that competes with homology-directed repair (HDR). To promote HDR at the expense of NHEJ, we targeted DNA ligase IV, a key enzyme in the NHEJ pathway, using the inhibitor Scr7. Scr7 treatment increased the efficiency of HDR-mediated genome editing, using Cas9 in mammalian cell lines and in mice for all four genes examined, up to 19-fold. This approach should be applicable to other customizable endonucleases, such as zinc finger nucleases and transcription activator-like effector nucleases, and to nonmammalian cells with sufficiently conserved mechanisms of NHEJ and HDR.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Even in the presence of donor template DNA, NHEJ is the more frequent repair mechanism observed from CRISPR/Cas9 editing (Maruyama et al., 2015).”
From Delivering CRISPR: a review of the challenges and approaches (2018) · cites this paper as Maruyama et al., 2015
The cited source says what the claim attributes to it.
In the citing paper
“or inhibiting the NHEJ pathway [113] have shown to be useful as means of increasing the efficiency of HDR after Cas9 cleavage.”
From CRISPR-Cas: Converting A Bacterial Defence Mechanism into A State-of-the-Art Genetic Manipulation Tool (2019) · cites this paper as [113]
In the citing paper
“Although inhibiting the NHEJ pathway with gene silencing or chemical inhibitors can partially increase the efficiency of HDR pathway, the gene repair efficacy still needs to be further improved for disease therapy [82, 85].”
From Non-viral delivery systems for CRISPR/Cas9-based genome editing: challenges and opportunities (2018) · cites this paper as [85]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Robinson, J. T., Thorvaldsdóttir, H., Winckler, W., Guttman, M., Lander, E. S., Getz, G., & Mesirov, J. P. (2011) · Nature Biotechnology · doi:10.1038/nbt.1754 · Cited by 15,390
RNA-Guided Human Genome Engineering via Cas9
Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210
Wang, H., Yang, H., Shivalila, C. S., Dawlaty, M. M., Cheng, A. W., Zhang, F., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.04.025 · Cited by 3,495
CRISPR-Cas systems for editing, regulating and targeting genomes
Sander, J. D., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2842 · Cited by 3,153
Genetic screens in human cells using the CRISPR-Cas9 system
Wang, T., Wei, J. J., Sabatini, D. M., & Lander, E. S. (2014) · Science · doi:10.1126/science.1246981 · Cited by 2,856
RNA-guided editing of bacterial genomes using CRISPR-Cas systems
Jiang, W., Bikard, D., Cox, D., Zhang, F., & Marraffini, L. A. (2013) · Nature Biotechnology · doi:10.1038/nbt.2508 · Cited by 2,429
RNA-guided genetic silencing systems in bacteria and archaea
Wiedenheft, B., Sternberg, S. H., & Doudna, J. A. (2012) · Nature · doi:10.1038/nature10886 · Cited by 1,851
Yang, H., Wang, H., Shivalila, C. S., Cheng, A. W., Shi, L., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.08.022 · Cited by 1,596
Double-strand break repair: 53BP1 comes into focus
Panier, S., & Boulton, S. J. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3719 · Cited by 1,168
Kamentsky, L. D., Jones, T. R., Fraser, A. N., Bray, M., Logan, D. J., Madden, K. L., Ljosa, V., Rueden, C., Eliceiri, K. W., & Carpenter, A. E. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr095 · Cited by 1,002
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 1,000
A possible aid in targeted insertion of large DNA elements by CRISPR/Cas in mouse zygotes
Nakao, H., Harada, T., Nakao, K., Kiyonari, H., Inoue, K., Furuta, Y., & Aiba, A. (2015) · genesis · doi:10.1002/dvg.22914 · Cited by 36
The expanding footprint of CRISPR/Cas9 in the plant sciences
Schaeffer, S. M., & Nakata, P. A. (2016) · Plant Cell Reports · doi:10.1007/s00299-016-1987-x · Cited by 37
CRISPR-Cas immunity, DNA repair and genome stability
Cubbon, A., Ivančić-Baće, I., & Bolt, E. L. (2018) · Bioscience Reports · doi:10.1042/bsr20180457 · Cited by 39
Rath, A., Mishra, A., Ferreira, V. D., Hu, C., Omerza, G., Kelly, K., Hesse, A., Reddi, H. V., Grady, J. P., & Heinen, C. D. (2019) · Human Mutation · doi:10.1002/humu.23848 · Cited by 36
Enhancing site-specific DNA integration by a Cas9 nuclease fused with a DNA donor-binding domain
Ma, S., Wang, X., Hu, Y., Lv, J., Liu, C., Liao, K., Guo, X., Wang, D., Lin, Y., & Rong, Z. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa779 · Cited by 36
Wang, C., Cheng, J. K. W., Zhang, Q., Hughes, N. W., Xia, Q., Winslow, M. M., & Cong, L. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa1264 · Cited by 36
Systematically attenuating DNA targeting enables CRISPR-driven editing in bacteria
Collias, D., Vialetto, E., Yu, J., Co, K., Almási, É. D. H., Rüttiger, A.-S., Achmedov, T., Strowig, T., & Beisel, C. L. (2023) · Nature Communications · doi:10.1038/s41467-023-36283-9 · Cited by 37
HAP1, a new revolutionary cell model for gene editing using CRISPR-Cas9
Llargués‐Sistac, G., Bonjoch, L., & Castellvı́-Bel, S. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1111488 · Cited by 40
Arras, S. D. M., & Fraser, J. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163049 · Cited by 36
Nick-initiated homologous recombination: Protecting the genome, one strand at a time
Vriend, L. E. M., & Krawczyk, P. M. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.12.005 · Cited by 37
DNA repair protein RAD51 enhances the CRISPR/Cas9-mediated knock-in efficiency in brain neurons
Kurihara, T., Kouyama-Suzuki, E., Satoga, M., Li, X., Badawi, M., Thiha, Baig, D. N., Yanagawa, T., Uemura, T., Mori, T., et al. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.01.132 · Cited by 36
Optimizing cancer treatment: the synergistic potential of CAR-T cell therapy and CRISPR/Cas9
Amiri, M., Moaveni, A. K., Zolbin, M. M., Shademan, B., & Nourazarian, A. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1462697 · Cited by 37
Use of genome-editing tools to treat sickle cell disease
Tasan, I., Jain, S., & Zhao, H. (2016) · Human Genetics · doi:10.1007/s00439-016-1688-0 · Cited by 36
CRISPR Genome Engineering for Human Pluripotent Stem Cell Research
Chaterji, S., Ahn, E. H., & Kim, D. (2017) · Theranostics · doi:10.7150/thno.18456 · Cited by 35
Liu, S., Wang, Q., Yu, X., Li, Y., Guo, Y., Liu, Z., Sun, F., Hou, W., Li, C., Wu, L. J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-26894-4 · Cited by 35
Strategies for the Enrichment and Selection of Genetically Modified Cells
Ren, C., Xu, K., Segal, D. J., & Zhang, Z. (2018) · Trends in biotechnology · doi:10.1016/j.tibtech.2018.07.017 · Cited by 35
One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation
Samlali, K., Ahmadi, F., Quach, A. B. V., Soffer, G., & Shih, S. C. C. (2020) · Small · doi:10.1002/smll.202002400 · Cited by 36
Applications of Alternative Nucleases in the Age of CRISPR/Cas9
Guha, T. K., & Edgell, D. R. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18122565 · Cited by 37
Nakagawa, Y., Sakuma, T., Nishimichi, N., Yokosaki, Y., Yanaka, N., Takeo, T., Nakagata, N., & Yamamoto, T. (2016) · Biology Open · doi:10.1242/bio.019349 · Cited by 34
Strategies for precise gene edits in mammalian cells
Fichter, K. M., Setayesh, T., & Malik, P. (2023) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2023.04.012 · Cited by 34
Functional interrogation of non-coding DNA through CRISPR genome editing
Canver, M. C., Bauer, D. E., & Orkin, S. H. (2017) · Methods · doi:10.1016/j.ymeth.2017.03.008 · Cited by 36
CRISPR RNA-guided FokI nucleases repair a PAH variant in a phenylketonuria model
Pan, Y., Shen, N., Jung‐Klawitter, S., Betzen, C., Hoffmann, G. F., Hoheisel, J. D., & Blau, N. (2016) · Scientific Reports · doi:10.1038/srep35794 · Cited by 34
Multiplex CRISPR/Cas9-based genome engineering enhanced by Drosha-mediated sgRNA-shRNA structure
Yan, Q., Xu, K., Xing, J., Zhang, T., Wang, X., Wei, Z., Ren, C., Liu, Z., Shao, S., & Zhang, Z. (2016) · Scientific Reports · doi:10.1038/srep38970 · Cited by 33
Highly Efficient and Versatile Plasmid-Based Gene Editing in Primary T Cells
Kornete, M., Marone, R., & Jeker, L. T. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701121 · Cited by 33
Parola, C., Neumeier, D., Friedensohn, S., Csepregi, L., Tacchio, M. D., Mason, D. M., & Reddy, S. T. (2019) · mAbs · doi:10.1080/19420862.2019.1662691 · Cited by 33
DNA repair-dependent immunogenic liabilities in colorectal cancer: opportunities from errors
Amodio, V., Vitiello, P. P., Bardelli, A., & Germano, G. (2024) · British Journal of Cancer · doi:10.1038/s41416-024-02848-8 · Cited by 33
A non-inheritable maternal Cas9-based multiple-gene editing system in mice
Sakurai, T., Kamiyoshi, A., Kawate, H., Mori, C., Watanabe, S., Tanaka, M., Uetake, R., Sato, M., & Shindo, T. (2016) · Scientific Reports · doi:10.1038/srep20011 · Cited by 32
Application of the genome editing tool CRISPR/Cas9 in non-human primates.
Luo, X., Li, M., & Su, B. (2016) · Europe PMC (PubMed Central) · doi:10.13918/j.issn.2095-8137.2016.4.214 · Cited by 32
Jung, C., Ménoret, S., Brusselle, L., Tesson, L., Usal, C., Chenouard, V., Remy, S., Ouisse, L., Poirier, N., Vanhove, B., et al. (2016) · Scientific Reports · doi:10.1038/srep31455 · Cited by 34
Luo, Z., Gao, M., Huang, N., Wang, X., Yang, Z., Yang, H., Huang, Z., & Feng, W. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-019-1229-5 · Cited by 33
CRISPR and Target-Specific DNA Endonucleases for Efficient DNA Knock-in in Eukaryotic Genomes.
Lee, S. H., Kim, S., & Hur, J. K. (2018) · Europe PMC (PubMed Central) · doi:10.14348/molcells.2018.0408 · Cited by 32
CRISPR-Cas systems: Challenges and future prospects
Gohil, N., Bhattacharjee, G., Lam, N. L., Perli, S. D., & Singh, V. (2021) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2021.01.008 · Cited by 33
Strategies for Enhancing the Homology-Directed Repair Efficiency of CRISPR-Cas Systems
Sun, W., Liu, H., Yin, W., Qiao, J., Zhao, X., & Liu, Y. (2022) · The CRISPR Journal · doi:10.1089/crispr.2021.0039 · Cited by 33
Superior Fidelity and Distinct Editing Outcomes of SaCas9 Compared with SpCas9 in Genome Editing
Yang, Z.-X., Fu, Y.-W., Zhao, J.-J., Zhang, F., Li, S.-A., Zhao, M., Wen, W., Zhang, L., Cheng, T., Zhang, J., et al. (2022) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2022.12.003 · Cited by 32
Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies
Nguyen, Q., Lim, K. R. Q., & Yokota, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030733 · Cited by 33
CRISPR/Cas9 ribonucleoprotein-mediated knockin generation in hTERT-RPE1 cells
Ghetti, S., Burigotto, M., Mattivi, A., Magnani, G., Casini, A., Bianchi, A., Cereseto, A., & Fava, L. L. (2021) · STAR Protocols · doi:10.1016/j.xpro.2021.100407 · Cited by 31
Duan, Y., Ma, G., Huang, X., D'Amore, P. A., Zhang, F., & Lei, H. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.729467 · Cited by 31
In Vivo Applications of CRISPR-Based Genome Editing in the Retina
Yu, W., & Wu, Z. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00053 · Cited by 32
Ways of improving precise knock-in by genome-editing technologies
Smirnikhina, S., Anuchina, A. A., & Лавров, А. В. (2018) · Human Genetics · doi:10.1007/s00439-018-1953-5 · Cited by 32
Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development
Wang, P., Yan, F., Li, Z., Yu, Y., Parnell, S. E., & Xiong, Y. (2019) · Journal of Clinical Investigation · doi:10.1172/jci129107 · Cited by 31
Genome Editing in Large Animals
West, J. D., & Gill, W. (2016) · Journal of Equine Veterinary Science · doi:10.1016/j.jevs.2016.03.008 · Cited by 31
Xie, S., Bian, W.-P., Wang, C., Junaid, M., Zou, J., & Pei, D. (2016) · Scientific Reports · doi:10.1038/srep34555 · Cited by 31
Reuven, N. B., Adler, J., Broennimann, K., Myers, N., & Shaul, Y. (2019) · Biomolecules · doi:10.3390/biom9100584 · Cited by 31
Gene Therapy for Inherited Retinal Degeneration
Arbabi, A., Liu, A., & Ameri, H. (2019) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2018.0087 · Cited by 30
The Interface of Gene Editing with Regenerative Medicine
Farag, V., Devey, E. A., & Leong, K. W. (2024) · Engineering · doi:10.1016/j.eng.2024.10.019 · Cited by 30
Shen, Y., Xu, K., Yuan, Z., Guo, J., Zhao, H., Zhang, X., Zhao, L., Qing, Y., Li, H., Pan, W., et al. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-017-1327-0 · Cited by 30
Development of a multi-locus CRISPR gene drive system in budding yeast
Yan, Y., & Finnigan, G. C. (2018) · Scientific Reports · doi:10.1038/s41598-018-34909-3 · Cited by 33
Genetic Transformation of Filamentous Fungi: Achievements and Challenges
Lichius, A., Moreno-Ruiz, D., & Zeilinger, S. (2020) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-030-29541-7_5 · Cited by 30
Gene Editing for the Treatment of Primary Immunodeficiency Diseases
Rai, R., Thrasher, A. J., & Cavazza, A. (2020) · Human Gene Therapy · doi:10.1089/hum.2020.185 · Cited by 30
Modulating CRISPR/Cas9 genome-editing activity by small molecules
Chen, S., Chen, D., Liu, B., & Haisma, H. J. (2021) · Drug Discovery Today · doi:10.1016/j.drudis.2021.11.018 · Cited by 32
Recent Advances in the Production of Genome-Edited Rats
Sato, M., Nakamura, S., Inada, E., & Takabayashi, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052548 · Cited by 31
CRISPR/Cas9—A Promising Therapeutic Tool to Cure Blindness: Current Scenario and Future Prospects
Ahmad, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911482 · Cited by 30
Hough, S. H., Kancleris, K., Brody, L., Humphryes-Kirilov, N., Wolanski, J., Dunaway, K. W., Ajetunmobi, A., & Dillard, V. (2017) · BMC Bioinformatics · doi:10.1186/s12859-017-1581-4 · Cited by 30
Generation of genetically-engineered animals using engineered endonucleases
Lee, J. G., Sung, Y. H., & Baek, I. (2018) · Archives of Pharmacal Research · doi:10.1007/s12272-018-1037-z · Cited by 31
Ray, U., Raul, S. K., Gopinatha, V. K., Ghosh, D., Rangappa, K. S., Mantelingu, K., & Raghavan, S. C. (2020) · Molecular Carcinogenesis · doi:10.1002/mc.23186 · Cited by 30
Li, Z., Theile, C. S., Chen, G., Bilate, A. M. B., Duarte, J. N., Avalos, A. M., Fang, T., Barberena, R., Sato, S., & Ploegh, H. L. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201505277 · Cited by 29
Self-citationFeehan, J. M., Chiu, C. N., Stanar, P., Tam, B. M., Ahmed, S. N., & Moritz, O. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-07153-4 · Cited by 31
Shin, S. W., & Lee, J. S. (2020) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-020-0093-7 · Cited by 29
CRISPR-Mediated Modification of DNA Methylation Pattern in the New Era of cancer therapy
Maroufi, F., Maali, A., Abdollahpour‐Alitappeh, M., Ahmadi, M. H., & Azad, M. (2020) · Epigenomics · doi:10.2217/epi-2020-0110 · Cited by 29
Small-molecule inhibitors of histone deacetylase improve CRISPR-based adenine base editing
Shin, H. R., See, J.-E., Kweon, J., Kim, H. S., Sung, G., Park, S., Jang, A.-H., Jang, G., Choi, K., Kim, I., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab052 · Cited by 29
Bhattacharjee, R., Jana, A., Nandi, A., Sinha, A., Bhattacharjee, A., Mitra, S., Kar, S., Dey, A., Singh, S. K., Varma, R. S., et al. (2022) · Materials & Design · doi:10.1016/j.matdes.2022.111415 · Cited by 29
CRISPR/Cas9 Technology as an Emerging Tool for Targeting Amyotrophic Lateral Sclerosis (ALS)
Kruminis-Kaszkiel, E., Juranek, J. K., Maksymowicz, W., & Wojtkiewicz, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19030906 · Cited by 29
Generation of mouse conditional knockout alleles in one step using thei-GONAD methodPreprint
Shang, R., Zhang, H., & Bi, P. (2020) · Genome Research · doi:10.1101/gr.265439.120 · Cited by 30
New Therapeutics for Extracellular Vesicles: Delivering CRISPR for Cancer Treatment
Yan, B., & Liang, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415758 · Cited by 28
Gene Therapies in Clinical Development to Treat Retinal Disorders
McClements, M. E., Elsayed, M. E. A. A., Major, L., de la Cámara, C. M.-F., & MacLaren, R. E. (2024) · Molecular Diagnosis & Therapy · doi:10.1007/s40291-024-00722-0 · Cited by 28
Exploring CRISPR-Cas: The transformative impact of gene editing in molecular biology
Pandey, V. P., Sharma, S., & Pokharel, Y. R. (2025) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2025.102717 · Cited by 29
Sheridan, R. M., & Bentley, D. L. (2016) · BioTechniques · doi:10.2144/000114378 · Cited by 28
CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy
Zhang, X., Wang, L., Liu, M., & Li, D. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9057-2 · Cited by 28
Production of knock-in mice in a single generation from embryonic stem cells
Ukai, H., Kiyonari, H., & Ueda, H. R. (2017) · Nature Protocols · doi:10.1038/nprot.2017.110 · Cited by 28
Acosta, S., Fiore, L., Carota, I. A., & Oliver, G. C. (2018) · genesis · doi:10.1002/dvg.23212 · Cited by 28
CRISPR Craze to Transform Cardiac Biology
van Kampen, S. J., & van Rooij, E. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.06.008 · Cited by 30
Dicks, N., Gutierrez, K., Currin, L., de Macedo, M. P., Glanzner, W. G., Michalak, M., Agellon, L. B., & Bordignon, V. (2019) · Molecular Reproduction and Development · doi:10.1002/mrd.23305 · Cited by 28
Genome editing using CRISPR/Cas9 to treat hereditary hematological disorders
Chen, Y., Wen, R., Yang, Z., & Chen, Z. (2021) · Gene Therapy · doi:10.1038/s41434-021-00247-9 · Cited by 29
Improvement of the LbCas12a-crRNA System for Efficient Gene Targeting in Tomato
Vu, T. V., Doan, D., Tran, M. T., Sung, Y. W., Song, Y. J., & Kim, J. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.722552 · Cited by 28
Chen, Y., Wang, C., Xiao, D., He, B., Li, M., Yi, X., Zhang, W., Yin, J., & Liu, Z. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105934 · Cited by 28
Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression
Zhou, M., Tang, S., Duan, N., Xie, M., Li, Z., Feng, M., Wu, L., Hu, Z., & Liang, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147941 · Cited by 28
Lee, B., Gin, A. L., Wu, C., Singh, K., Grice, M. Z., Mortlock, R. D., Abraham, D. M., Fan, X., Zhou, Y., Aljanahi, A. A., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.02.010 · Cited by 30
Programmable Single and Multiplex Base-Editing in Bombyx mori Using RNA-Guided Cytidine Deaminases
Li, Y., Ma, S., Sun, L., Zhang, T., Chang, J., Lü, W., Chen, X., Liu, Y., Wang, X., Shi, R., et al. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200134 · Cited by 28
Genome editing in macroalgae: advances and challenges
Saeger, J. D., Vandelannoote, E. C., Lee, H., Park, J., & Blomme, J. (2024) · Frontiers in Genome Editing · doi:10.3389/fgeed.2024.1380682 · Cited by 27
CRISPR activation: identifying and using novel genes for plant disease resistance breeding
McLaughlin, J. E., Foka, I. C. K., Lawton, M. A., & Di, R. (2025) · Frontiers in Genome Editing · doi:10.3389/fgeed.2025.1596600 · Cited by 28
Germline Modification and Engineering in Avian Species
Lee, H. J., Lee, H. C., & Han, J. Y. (2015) · Molecules and Cells · doi:10.14348/molcells.2015.0225 · Cited by 27
The Yin and Yang of nucleic acid-based therapy in the brain
Gustincich, S., Zucchelli, S., & Mallamaci, A. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.11.001 · Cited by 27
A comparison of CRISPR/Cas9 and siRNA-mediated ALDH2 gene silencing in human cell lines
Wang, F., Guo, T., Jiang, H., Li, R., Wang, T., Zeng, N., Dong, G., Zeng, X., Li, D., Xiao, Y., et al. (2018) · Molecular Genetics and Genomics · doi:10.1007/s00438-018-1420-y · Cited by 27
Evolution of CRISPR towards accurate and efficient mammal genome engineering
Ryu, S.-M., Hur, J. W., & Kim, K. (2019) · BMB Reports · doi:10.5483/bmbrep.2019.52.8.149 · Cited by 28
Yan, N., Sun, Y., Fang, Y., Deng, J., Mu, L., Xu, K., Mymryk, J. S., & Zhang, Z. (2019) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2019.12.021 · Cited by 29
Köcher, T., Bischof, J., Haas, S. A., March, O. P., Liemberger, B., Hainzl, S., Illmer, J., Hoog, A., Muigg, K., Binder, H., et al. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.05.015 · Cited by 27
Movahedi, A., Wei, H., Zhou, X., Fountain, J. C., Chen, Z., Mu, Z., Sun, W., Zhang, J., Li, D., Guo, B. Z., et al. (2022) · Horticulture Research · doi:10.1093/hr/uhac154 · Cited by 27
Li, C., Steighner, J. R., Sweatt, G., Thiele, T. R., & Juntti, S. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-94577-8 · Cited by 27
Merkert, S., & Martin, U. (2016) · Stem Cell Research · doi:10.1016/j.scr.2016.02.027 · Cited by 27
Efficient Knock-in of a Point Mutation in Porcine Fibroblasts Using the CRISPR/Cas9-GMNN Fusion Gene
Gerlach, M., Kraft, T., Brenner, B., Petersen, B., Niemann, H., & Montag, J. (2018) · Genes · doi:10.3390/genes9060296 · Cited by 27
Wang, Y., Wang, Y., Chang, T., Huang, H., & Yee, J.-K. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkw1057 · Cited by 26
Taher, M., Aminondin, S. '., Nasir, N. A., Jasmadi, N. A., Nizam, N. I. N., Shahrul, I. S., Susanti, D., Khotib, J., Faiyazuddin, M., Widodo, R. T., et al. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1630994 · Cited by 28
Rapid CLIP dissociation from MHC II promotes an unusual antigen presentation pathway in autoimmunity
Ito, Y., Ashenberg, O., Pyrdol, J. W., Luoma, A., Rozenblatt–Rosen, O., Hofree, M., Christian, E., de Andrade, L. F., Tay, R. E., Teyton, L., et al. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20180300 · Cited by 26
Self-citationDevelopment of CRISPR/Cas9-mediated gene disruption systems in Giardia lamblia
Lin, Z., Gan, S. W., Tung, S.-Y., Ho, C.-C., Su, L., & Sun, C. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213594 · Cited by 26
Kelm, J. M., Samarbakhsh, A., Pillai, A., VanderVere-Carozza, P. S., Aruri, H., Pandey, D. S., Pawelczak, K. S., Turchi, J. J., & Gavande, N. S. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.850883 · Cited by 27
The evolution of CRISPR/Cas9 and their cousins: hope or hype?
Bhushan, K., Chattopadhyay, A., & Pratap, D. (2018) · Biotechnology Letters · doi:10.1007/s10529-018-2506-7 · Cited by 27
Slijkerman, R. W. N., Goloborodko, A., Broekman, S., de Vrieze, E., Hetterschijt, L., Peters, T. A., Gerits, M., Kremer, H., & van Wijk, E. (2018) · Zebrafish · doi:10.1089/zeb.2018.1613 · Cited by 26
RS‐1 enhances CRISPR‐mediated targeted knock‐in in bovine embryos
Lamas‐Toranzo, I., Martínez‐Moro, Á., Callaghan, E., de la Blanca, M. G. M., Sánchez, J. M., Lonergan, P., & Bermejo‐Álvarez, P. (2020) · Molecular Reproduction and Development · doi:10.1002/mrd.23341 · Cited by 29
Alberti, F., Kaleem, S., & Weaver, J. A. (2020) · Biology Open · doi:10.1242/bio.056010 · Cited by 26
Kondo, K., Tanaka, A., & Kunieda, T. (2024) · PLoS Genetics · doi:10.1371/journal.pgen.1011298 · Cited by 26
Metadata
- Authors
- Maruyama, T., Dougan, S. K., Truttmann, M. C., Bilate, A. M., Ingram, J. R., & Ploegh, H. L.
- Affiliations
- Whitehead Institute for Biomedical Research (US)
- Corresponding author
- Ploegh, Hidde L
- ORCID
- Venue
- Nature Biotechnology
- Published
- 2015-03-23
- Volume
- 33
- Issue
- 5
- Pages
- 538-542
- ISSN
- 0733-222X (ISSN-L)
- 1087-0156
- 1546-1696
- PMC
- PMC4618510
- OpenAlex
- W2008147758
- Cited by
- 1,137
- References
- 32
- Citations by year
- 2026: 39 · 2025: 58 · 2024: 62 · 2023: 67 · 2022: 108 · 2021: 101 · 2020: 117 · 2019: 122 · 2018: 125 · 2017: 139 · 2016: 143 · 2015: 55
- FWCI
- 66.47
- Type
- journal article
- Language
- en
- Update notices
- erratum (2016-02-05)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-sa)
- PMC
- Funders
- National Institute of Allergy and Infectious Diseases (R01AI087879)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- CRISPR/Cas9, genome editing efficiency, non-homologous end joining, homology-directed repair, DNA ligase IV, DNA double-strand break repair, zinc finger nucleases, TALEN
- MeSH terms
- DNA Ligase ATP, Animals, Cell Line, DNA Repair, Genetic Engineering, DNA Ligases, Pyrimidines, Schiff Bases, Zinc Fingers, Genome, Mice, DNA Breaks, Double-Stranded, Homologous Recombination, DNA End-Joining Repair, CRISPR-Cas Systems
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review