The DOI matches its Crossref record; 173 of the 173 references it cites were found in a registry or an index.
Repair of DNA Double-Strand Breaks by the Nonhomologous End Joining Pathway
Open accessAbstract
DNA double-strand breaks pose a serious threat to genome stability. In vertebrates, these breaks are predominantly repaired by nonhomologous end joining (NHEJ), which pairs DNA ends in a multiprotein synaptic complex to promote their direct ligation. NHEJ is a highly versatile pathway that uses an array of processing enzymes to modify damaged DNA ends and enable their ligation. The mechanisms of end synapsis and end processing have important implications for genome stability. Rapid and stable synapsis is necessary to limit chromosome translocations that result from the mispairing of DNA ends. Furthermore, end processing must be tightly regulated to minimize mutations at the break site. Here, we review our current mechanistic understanding of vertebrate NHEJ, with a particular focus on end synapsis and processing.
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
“NHEJ operates by recognizing DSBs, processing the DNA ends, and ligating them, infrequently resulting in insertions or deletions (indels) that can disrupt gene function (Stinson & Loparo, 2021; Takata et al., 1998).”
From CRISPR/Cas9 Ribonucleoprotein Nucleofection for Genome Editing in Primary Human Keratinocytes: Knockouts, Deletions, and Homology‐Directed Repair Mutagenesis (2024) · cites this paper as Stinson & Loparo, 2021
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
The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway
Lieber, M. R. (2010) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.052308.093131 · Cited by 2,882
DNA Topoisomerases: Structure, Function, and Mechanism
Champoux, J. J. (2001) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.70.1.369 · Cited by 2,804
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
Stephens, P. J., Greenman, C. D., Fu, B., Yang, F., Bignell, G. R., Mudie, L. J., Pleasance, E. D., Lau, K. W., Beare, D., Stebbings, L. A., et al. (2011) · Cell · doi:10.1016/j.cell.2010.11.055 · Cited by 2,414
Double-Strand Break End Resection and Repair Pathway Choice
Symington, L. S., & Gautier, J. (2011) · Annual Review of Genetics · doi:10.1146/annurev-genet-110410-132435 · Cited by 1,556
DNA double-strand break repair-pathway choice in somatic mammalian cells
Scully, R., Panday, A., Elango, R., & Willis, N. A. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0152-0 · Cited by 1,542
Repair Pathway Choices and Consequences at the Double-Strand Break
Ceccaldi, R., Rondinelli, B., & D’Andrea, A. D. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.07.009 · Cited by 1,499
Conserved modes of recruitment of ATM, ATR and DNA-PKcs to sites of DNA damage
Falck, J., Coates, J., & Jackson, S. P. (2005) · Nature · doi:10.1038/nature03442 · Cited by 1,304
Takata, M., Sasaki, M. S., Sonoda, E., Morrison, C., Hashimoto, M., Utsumi, H., Yamaguchi‐Iwai, Y., Shinohara, A., & Takeda, S. (1998) · The EMBO Journal · doi:10.1093/emboj/17.18.5497 · Cited by 1,229
Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair
Walker, J. R., Corpina, R. A., & Goldberg, J. D. (2001) · Nature · doi:10.1038/35088000 · Cited by 1,216
Chu, V. T., Weber, T., Wefers, B., Wurst, W., Sander, S., Rajewsky, K., & Kühn, R. (2015) · Nature Biotechnology · doi:10.1038/nbt.3198 · Cited by 1,210
Cited by
Sorted by citations
CRISPR-based genome editing through the lens of DNA repair
Nambiar, T. S., Baudrier, L., Billon, P., & Ciccia, A. (2022) · Molecular Cell · doi:10.1016/j.molcel.2021.12.026 · Cited by 227
Annual review of PROTAC degraders as anticancer agents in 2022
Wang, X., Qin, Z.-L., Li, N., Jia, M.-Q., Liu, Q.-G., Bai, Y., Song, J., Yuan, S., & Zhang, S. (2024) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2024.116166 · Cited by 107
Gene therapy for CNS disorders: modalities, delivery and translational challenges
Gao, J., Gunasekar, S., Xia, Z. J., Shalin, K., Jiang, C., Chen, H., Lee, D., Lee, S., Pisal, N. D., Luo, J. N., et al. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00829-7 · Cited by 100
Recent advances in CRISPR-Cas9-based genome insertion technologies
Chen, X., Du, J., Yun, S., Xue, C., Yao, Y., & Rao, S. (2024) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2024.102138 · Cited by 71
Combining targeted DNA repair inhibition and immune-oncology approaches for enhanced tumor control
Concannon, K., Morris, B. B., Gay, C. M., & Byers, L. A. (2023) · Molecular Cell · doi:10.1016/j.molcel.2022.12.031 · Cited by 71
Liquid-liquid phase separation in DNA double-strand breaks repair
Wang, Y., Zhao, W.-W., Shi, J., Wan, X., Zheng, J., & Fan, X. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06267-0 · Cited by 62
Pismataro, M. C., Astolfi, A., Barreca, M. L., Pacetti, M., Schenone, S., Bandiera, T., Carbone, A., & Massari, S. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c02101 · Cited by 60
Schaub, J. M., Soniat, M. M., & Finkelstein, I. J. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac119 · Cited by 58
Meiotic DNA breaks drive multifaceted mutagenesis in the human germ line
Hinch, R., Donnelly, P., & Hinch, A. G. (2023) · Science · doi:10.1126/science.adh2531 · Cited by 55
Mladenov, E., Mladenova, V., Stuschke, M., & Iliakis, G. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914956 · Cited by 53
PAXX binding to the NHEJ machinery explains functional redundancy with XLF
Dahan, M. S. E., Stavridi, A. K., Frit, P., Hardwick, S. W., Chirgadze, D. Y., de Oliveira, T. M., Andréani, J., Britton, S., Barboule, N., Bossaert, M., et al. (2023) · Science Advances · doi:10.1126/sciadv.adg2834 · Cited by 43
The dark side of homology-directed repair
Al-Zain, A., & Symington, L. S. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103181 · Cited by 43
Zhang, T., Yang, H., Zhou, Z., Bai, Y., Wang, J., & Wang, W. (2022) · Nature Communications · doi:10.1038/s41467-022-32920-x · Cited by 40
Disparate Pathways for Extrachromosomal DNA Biogenesis and Genomic DNA Repair
Rose, J. C., Belk, J. A., Wong, I. T.-L., Luebeck, J., Horn, H. T., Dániel, B., Jones, M. G., Yost, K. E., Hung, K. L., Kolahi, K. S., et al. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-1117 · Cited by 38
DNA double-strand break end synapsis by DNA loop extrusion
Yang, J. H., Brandão, H. B., & Hansen, A. S. (2023) · Nature Communications · doi:10.1038/s41467-023-37583-w · Cited by 36
Characterizing and controlling CRISPR repair outcomes in nondividing human cells
Ramadoss, G. N., Namaganda, S. J., Kumar, M. M., Hamilton, J. R., Sharma, R. K., Chow, K. G., Workley, L. A., Macklin, B. L., Sun, M., Ha, A. S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66058-3 · Cited by 35
Structure and mechanism in non-homologous end joining
Vogt, A., & He, Y. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103547 · Cited by 40
Structural analysis of the basal state of the Artemis:DNA-PKcs complex
Watanabe, G., Lieber, M. R., & Williams, D. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac564 · Cited by 33
Cryo-EM visualization of DNA-PKcs structural intermediates in NHEJ
Chen, S., Vogt, A., Lee, L., Naila, T., McKeown, R., Tomkinson, A. E., Lees‐Miller, S. P., & He, Y. (2023) · Science Advances · doi:10.1126/sciadv.adg2838 · Cited by 32
Histone and Chromatin Dynamics Facilitating DNA repair
Mohan, C., Das, C., & Tyler, J. K. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103183 · Cited by 35
DNA Double-Strand Break Repairs and Their Application in Plant DNA Integration
Shen, H., & Li, Z. (2022) · Genes · doi:10.3390/genes13020322 · Cited by 30
TRIM21-dependent target protein ubiquitination mediates cell-free Trim-Away
Mevissen, T. E. T., Prasad, A. V., & Walter, J. C. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112125 · Cited by 31
Lei, L., Pan, W., Shou, X., Shao, Y., Ye, S., Zhang, J., Kolliputi, N., & Shi, L. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02627-w · Cited by 32
Han, Y., Zhao, H., Li, G., Jin, J., Guo, H., Tan, J., Sun, X., Li, S., Ran, Q., Bai, C., et al. (2024) · British Journal of Cancer · doi:10.1038/s41416-024-02636-4 · Cited by 28
Targeting the DNA damage response in cancer
Guffanti, F., Chiappa, M., & Damia, G. L. M. (2024) · MedComm · doi:10.1002/mco2.788 · Cited by 30
Zhao, H., Gao, S., Han, Y., Xie, D., Xuan, L., Huang, X., Luo, J., Ran, Q., Li, G., Guo, H., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02210-1 · Cited by 28
Frigerio, C., Nisio, E. D., Galli, M., Colombo, C. V., Negri, R., & Clerici, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043248 · Cited by 29
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
Function and Evolution of the Loop Extrusion Machinery in Animals
Kabirova, E., Nurislamov, A. R., Shadskiy, A., Smirnov, A. V., Popov, A., Salnikov, P., Баттулин, Н. Р., & Fishman, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24055017 · Cited by 27
Structural role for DNA Ligase IV in promoting the fidelity of non-homologous end joining
Stinson, B. M., Carney, S. M., Walter, J. C., & Loparo, J. J. (2024) · Nature Communications · doi:10.1038/s41467-024-45553-z · Cited by 24
Self-citationPARP inhibitors in small cell lung cancer: The underlying mechanisms and clinical implications
Wang, X., Zeng, X., Li, D., Zhu, C., Guo, X., Feng, L., & Yu, Z. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113458 · Cited by 24
Frit, P., Amin, H., Zahid, S., Barboule, N., Hall, C., Matharu, G., Hardwick, S. W., Chauvat, J., Britton, S., Chirgadze, D. Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59133-2 · Cited by 23
Synthesis and biological evaluation of a tumor-selective degrader of PARP1
Pu, C., Wang, S., Luo, D., Liu, Y., Ma, X., Zhang, H., Yu, S., Lan, S., Huang, Q., Deng, R., et al. (2022) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2022.116908 · Cited by 24
Break‐induced RNA–DNA hybrids (BIRDHs) in homologous recombination: friend or foe?
Gómez‐González, B., & Aguilera, A. (2023) · EMBO Reports · doi:10.15252/embr.202357801 · Cited by 23
Potential therapeutic strategies for osteoarthritis via CRISPR/Cas9 mediated gene editing
Vlashi, R., Zhang, X., Li, H., & Chen, G. (2023) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-023-09860-y · Cited by 24
Single-molecule imaging reveals the kinetics of non-homologous end-joining in living cells
Mikhova, M., Goff, N. J., Janovič, T., Heyza, J. R., Meek, K., & Schmidt, J. C. (2024) · Nature Communications · doi:10.1038/s41467-024-54545-y · Cited by 24
The importance of DNAPKcs for blunt DNA end joining is magnified when XLF is weakened
Cisneros‐Aguirre, M., Lopezcolorado, F. W., Tsai, L. J., Bhargava, R., & Stark, J. M. (2022) · Nature Communications · doi:10.1038/s41467-022-31365-6 · Cited by 21
The Ku complex promotes DNA end-bridging and this function is antagonized by Tel1/ATM kinase
Rinaldi, C., Pizzul, P., Casari, E., Mangiagalli, M., Tisi, R., & Longhese, M. P. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad062 · Cited by 20
Holding it together: DNA end synapsis during non-homologous end joining
Loparo, J. J. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103553 · Cited by 25
Self-citationBhakat, K. K., & Ray, S. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103246 · Cited by 24
The tripartite motif-containing 24 is a multifunctional player in human cancer
Yao, Y., Zhou, S., Yue, Y., Fu, K., & Xiao, S. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01289-3 · Cited by 20
In vivo liver targeted genome editing as therapeutic approach: progresses and challenges
Simoni, C., Barbon, E., Muro, A. F., & Cantore, A. (2024) · Frontiers in Genome Editing · doi:10.3389/fgeed.2024.1458037 · Cited by 20
Dynamic assemblies and coordinated reactions of non-homologous end joining
Liu, L., Li, J., Cisneros‐Aguirre, M., Merkell, A., Stark, J. M., Gellert, M. F., & Yang, W. (2025) · Nature · doi:10.1038/s41586-025-09078-9 · Cited by 18
Vu, D.-D., Bonucci, A., Brenière, M., Cisneros‐Aguirre, M., Pelupessy, P., Wang, Z., Carlier, L., Bouvignies, G., Cortés, P., Aggarwal, A. K., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01339-x · Cited by 18
Frey, Y., Haj, M., Ziv, Y., Elkon, R., & Shiloh, Y. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1257 · Cited by 18
Chen, W., Mi, C., Zhang, Y., Yang, Y., Huang, W., Xu, Z., Zhao, J., Wang, R., Wang, M., Wan, S., et al. (2024) · Advanced Science · doi:10.1002/advs.202207435 · Cited by 17
Waters, K. L., & Spratt, D. E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031676 · Cited by 17
Editing of the ethylene biosynthesis gene in carnation using CRISPR-Cas9 ribonucleoprotein complex
Adedeji, O. S., Naing, A. H., Kang, H., Xu, J., Chung, M. Y., & Kim, C. K. (2024) · Plant Methods · doi:10.1186/s13007-024-01143-0 · Cited by 17
Quercetin exhibits cytotoxicity in cancer cells by inducing two-ended DNA double-strand breaks
Someya, Y., Saito, S., Takeda, S., Adachi, N., & Kurosawa, A. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.150977 · Cited by 17
APLF and long non-coding RNA NIHCOLE promote stable DNA synapsis in non-homologous end joining
de Bragança, S., Aicart-Ramos, C., Arribas-Bosacoma, R., Rivera-Calzada, Á., Unfried, J. P., Prats-Mari, L., Marín-Baquero, M., Fortes, P., Llorca, Ó., & Moreno‐Herrero, F. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111917 · Cited by 17
DNA repair pathways in breast cancer: from mechanisms to clinical applications
Tufail, M. (2023) · Breast Cancer Research and Treatment · doi:10.1007/s10549-023-06995-z · Cited by 18
Huang, Q., Jing, Y., Xiong, L., Li, L., Feng, J., & Cheng, J. G. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06640-x · Cited by 18
New insights into the DNA repair pathway choice with NuA4/TIP60
Lashgari, A., Tchara, P.-E. K., Lambert, J., & Côté, J. (2022) · DNA repair · doi:10.1016/j.dnarep.2022.103315 · Cited by 17
Recent insights into eukaryotic double-strand DNA break repair unveiled by single-molecule methods
de Bragança, S., Dillingham, M. S., & Moreno‐Herrero, F. (2023) · Trends in Genetics · doi:10.1016/j.tig.2023.09.004 · Cited by 18
The power and the promise of synthetic lethality for clinical application in cancer treatment
Liu, Q., Yang, Z., Tang, Q.-H., Wang, W.-E., Chu, D.-S., Ji, J.-F., Fan, Q.-Y., Jiang, H., Yang, Q.-X., Zhang, H., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116288 · Cited by 17
Identification of the main barriers to Ku accumulation in chromatin
Bossaert, M., Moreno, A., Peixoto, A., Pillaire, M., Chanut, P., Frit, P., Calsou, P., Loparo, J. J., & Britton, S. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114538 · Cited by 17
Self-citationCST/Polα/primase-mediated fill-in synthesis at DSBs
Mirman, Z., Cai, S. W., & de Lange, T. (2022) · Cell Cycle · doi:10.1080/15384101.2022.2123886 · Cited by 16
Sadek, M., Sheth, A., Zimmerman, G., Hays, E., & Vélez-Cruz, R. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1071786 · Cited by 18
Kaempferol inhibits non-homologous end joining repair via regulating Ku80 stability in glioma cancer
Chen, M., Zhao, E., Li, M., Xu, M., Hao, S., Gao, Y., Wu, X., Li, X., Yu, Y., Yu, Z., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154876 · Cited by 15
DNA repair deficiency and the immune microenvironment: A pathways perspective
Zhou, Y., & Mouw, K. W. (2023) · DNA repair · doi:10.1016/j.dnarep.2023.103594 · Cited by 16
Kulkarni, S., Gajjar, K. B., & Madhusudan, S. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1414112 · Cited by 15
Mechanistic Insights From Single-Molecule Studies of Repair of Double Strand Breaks
Kong, M., & Greene, E. C. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.745311 · Cited by 17
Yang, K., Liang, X., & Wen, K. (2022) · Oncology Reports · doi:10.3892/or.2022.8390 · Cited by 15
Bone Marrow Failure and Immunodeficiency Associated with Human RAD50 Variants
Takagi, M., Hoshino, A., Bousset, K., Röddecke, J., Martin, H. L., Folcut, I., Tomomasa, D., Yang, X., Kobayashi, J., Sakata, N., et al. (2023) · Journal of Clinical Immunology · doi:10.1007/s10875-023-01591-8 · Cited by 14
Zhang, M., Wang, Z., Su, Y. A., Yan, W., Ouyang, Y., Fan, Y., Yu, Y., & Yang, H. C. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.108072 · Cited by 13
Pizzul, P., Casari, E., Rinaldi, C., Gnugnoli, M., Mangiagalli, M., Tisi, R., & Longhese, M. P. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkad1246 · Cited by 13
Light‐Triggered CRISPR/Cas12a for Genomic Editing and Tumor Regression
Liu, H., Dong, J., Wu, R., Dai, J., Lou, X., Xia, F., Willner, I., & Huang, F. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202502892 · Cited by 12
Sun, H., Chen, G., Guo, B., Lv, S., & Yuan, G. (2023) · Journal of Cancer · doi:10.7150/jca.80097 · Cited by 11
DNA-PK participates in pre-rRNA biogenesis independent of DNA double-strand break repair
Li, P., Gai, X., Li, Q., Yang, Q., & Yu, X. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae316 · Cited by 11
Shining light on CRISPR/Cas9 therapeutics for inherited retinal diseases
Geiger, A., Kennedy, J. G., Staker, L. G., Wensel, T. G., Casson, R. J., & Thomas, P. Q. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2025.101376 · Cited by 11
Long-read sequencing reveals pre-meiotic gene conversion in sperm
Schweiger, R., Lee, S. Y., Zhou, C., Yang, T.-P., Li, S., Sanghvi, R., Neville, M. D. C., Smith, K., Roberts, K., Nessa, A., et al. (2026) · Nature · doi:10.1038/s41586-026-10901-0 · Cited by 14
Pustovalova, M. V., Mohammad, R., Wang, Y., Xue, W., Malakhov, P., Nekrasov, V., Kontareva, E., Nofal, Z., Saburov, V. O., Kolesov, D. V., et al. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl36415 · Cited by 10
Yan, J., Bu, L., Wang, Y., Yao, H., Li, G., Zheng, K., & Huang, J. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf543 · Cited by 10
Feng, Y.-L., Liu, S., Chen, R.-D., Sun, X., Xiao, J., Xiang, J.-F., & Xie, A. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad116 · Cited by 10
CRISPR applications in microbial World: Assessing the opportunities and challenges
Kursheed, F., Naz, E., Mateen, S., & Kulsoom, U. (2024) · Gene · doi:10.1016/j.gene.2024.149075 · Cited by 10
The Role of SWI / SNF Complex in Bladder Cancer
Lei, Z., Han, Y., Liao, J., Li, X., Su, Q., & Yang, Z. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70348 · Cited by 9
Morris, B. B., Heeke, S., Xi, Y., Diao, L., Wang, Q., Rocha, P., Arriola, E., Lee, M. C., Tyson, D. R., Concannon, K., et al. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02291-0 · Cited by 9
The mammalian Ku70 C-terminus SAP domain is required to repair DNA damage
Wang, Y., Czap, M. S., Kim, H., Masaka, P. M., Wang, H., Beg, M. A., Lu, H., Liu, J., Chang, Y., Romanienko, P. J., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf499 · Cited by 9
DNA Damage and Repair in Thyroid Physiology and Disease
Arczewska, K. D., Sys, D., Nilsen, H. L., & Piekiełko‐Witkowska, A. (2025) · Endocrine Reviews · doi:10.1210/endrev/bnaf035 · Cited by 9
Pandya, K., & Kumar, D. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102922 · Cited by 9
The emerging impact of CRISPR and gene editing on global crop improvement
Mansi, M., & Danai, P. (2026) · Transgenic Research · doi:10.1007/s11248-026-00484-x · Cited by 12
DNA polymerases in precise and predictable CRISPR/Cas9-mediated chromosomal rearrangements
Mehryar, M. M., Shi, X., Li, J., & Wu, Q. (2023) · BMC Biology · doi:10.1186/s12915-023-01784-y · Cited by 9
DNA-PK: A synopsis beyond synapsis
Goff, N. J., Mikhova, M., Schmidt, J. C., & Meek, K. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103716 · Cited by 9
A transposase-derived gene required for human brain development
Jubierre, L., Lewis, S. A., Gutierrez, R. L., Yamada, M., Rodríguez-Fos, E., Planas-Fèlix, M., Cameron, D., Demarest, P., Nabila, A., Mueller, H., et al. (2026) · Science Advances · doi:10.1126/sciadv.adv7530 · Cited by 9
Alyafeai, E., Qaed, E., Al-mashriqi, H. S., Al‐Maamari, A., Almansory, A. H., Futini, F. A., Sultan, M., & Tang, Z. (2024) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2024.111883 · Cited by 10
Borphukan, B., Khatun, M., Fartyal, D., James, D., & Reddy, M. K. (2025) · Plants · doi:10.3390/plants14030477 · Cited by 8
García‐Lepe, U. O., Torres‐Dimas, E., Espinal‐Centeno, A., Cruz‐Ramírez, A., & Bermúdez‐Cruz, R. M. (2022) · Developmental Dynamics · doi:10.1002/dvdy.455 · Cited by 9
Gene therapy strategies for RAG1 deficiency: Challenges and breakthroughs
Gilioli, G., Lankester, A. C., de Kivit, S., Staal, F. J. T., & de Bruin, L. M. O. (2024) · Immunology Letters · doi:10.1016/j.imlet.2024.106931 · Cited by 8
Wang, Y., Feng, Y.-L., Liu, Q., Xiao, J., Liu, S., Huang, Z., & Xie, A. (2023) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2023.102072 · Cited by 8
Cold snapshots of DNA repair: Cryo-EM structures of DNA-PKcs and NHEJ machinery
Amin, H., Zahid, S., Hall, C., & Chaplin, A. K. (2023) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2023.11.007 · Cited by 8
Proteins Associated with Neurodegenerative Diseases: Link to DNA Repair
Khodyreva, S. N., Dyrkheeva, N. S., & Lavrik, O. I. (2024) · Biomedicines · doi:10.3390/biomedicines12122808 · Cited by 7
Simoes‐Sousa, S., Amin, N., Lane, K. A., Harrod, A., Pedersen, M., Pardo, M., Rasetti‐Escargueil, C., Kozik, Z., Begg, K., Ribeiro, A., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116277 · Cited by 7
SUMOylation is destined for regulatory T cell-related immune dysregulation
Qian, J., Yu, L., Tian, M., Li, X., Bai, X., Yang, J., Deng, R., Liu, Q., Lü, A., Xiao, C., et al. (2026) · Cell Death Discovery · doi:10.1038/s41420-026-02946-x · Cited by 7
Kang, Y., An, S., Min, D., & Lee, J. Y. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.973314 · Cited by 7
Application and progress of CRISPR/Cas9 gene editing in B-cell lymphoma: a narrative review
Jin, Y., Wu, H., Liu, J., Cho, W. C. S., & Song, G. (2024) · Translational Cancer Research · doi:10.21037/tcr-23-1146 · Cited by 7
Giannakakis, A., Tsifintaris, M., Gouzouasis, V., Ow, G. S., Aau, M. Y., Papp, C., Ivshina, A. V., & Kuznetsov, V. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1227151 · Cited by 7
Replicative Instability Drives Cancer Progression
Morris, B. B., Smith, J. P., Zhang, Q., Jiang, Z., Hampton, O. A., Churchman, M. L., Arnold, S. M., Owen, D. H., Gray, J. E., Dillon, P. M., et al. (2022) · Biomolecules · doi:10.3390/biom12111570 · Cited by 8
The role of RNF138 in DNA end resection is regulated by ubiquitylation and CDK phosphorylation
Locke, A. J., Farraj, R. A., Tran, C., Zeinali, E., Mashayekhi, F., Ali, J. Y. H., Glover, J. N. M., & Ismail, I. H. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.105709 · Cited by 6
Lombardi, S., Zilocchi, M., Nicsanu, R., & Barabino, S. M. L. (2025) · DNA repair · doi:10.1016/j.dnarep.2025.103846 · Cited by 6
Advancing Genotoxicity Assessment by Building a Global AOP Network
Demuynck, E., Vanhaecke, T., Thienpont, A., Cappoen, D., Goethem, F. V., Winkelman, L. M. T., Beltman, J. B., Murugadoss, S., Olsen, A.-K. H., Marcon, F., et al. (2025) · Environmental and Molecular Mutagenesis · doi:10.1002/em.70022 · Cited by 6
Metadata
- Authors
- Stinson, B. M., & Loparo, J. J.
- Affiliations
- Harvard University (US)
- Corresponding author
- Loparo, Joseph J.
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2021-06-20
- Volume
- 90
- Issue
- 1
- Pages
- 137-164
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- PMC
- PMC8899865
- OpenAlex
- W3127347270
- Cited by
- 223
- References
- 173
- Citations by year
- 2026: 49 · 2025: 61 · 2024: 57 · 2023: 33 · 2022: 19 · 2021: 4
- FWCI
- 3.04
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Damon Runyon Cancer Research Foundation
- National Institutes of Health
- National Institute of General Medical Sciences (R01GM115487)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Keywords
- non-homologous end joining, DNA double-strand breaks, DNA end processing, genome stability, chromosomal translocation, DNA ligation
- MeSH terms
- Animals, Enzymes, Humans, Models, Biological, Genomic Instability, Multiprotein Complexes, DNA Breaks, Double-Stranded, DNA End-Joining Repair, V(D)J Recombination
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