The DOI matches its Crossref record; 27 of the 29 references it cites were found in a registry or an index, and 2 are not checked yet.
Homology-directed repair is a major double-strand break repair pathway in mammalian cells
Open accessAbstract
Mammalian cells have been presumed to repair potentially lethal chromosomal double-strand breaks (DSBs) in large part by processes that do not require homology to the break site. This contrasts with Saccharomyces cerevisiae where the major DSB repair pathway is homologous recombination. Recently, it has been determined that DSBs in genomic DNA in mammalian cells can stimulate homologous recombination as much as 3 or 4 orders of magnitude, suggesting that homology-directed repair may play an important role in the repair of chromosomal breaks. To determine whether mammalian cells use recombinational repair at a significant level, we have analyzed the spectrum of repair events at a defined chromosomal break by using direct physical analysis of repair products. When an endonuclease-generated DSB is introduced into one of two direct repeats, homologous repair is found to account for 30–50% of observed repair events. Both noncrossover and deletional homologous repair products are detected, at approximately a 1:3 ratio. These results demonstrate the importance of homologous recombination in the repair of DSBs in mammalian cells. In the remaining observed repair events, DSBs are repaired by nonhomologous processes. The nonhomologous repair events generally result in small deletions or insertions at the break site, although a small fraction of events result in larger chromosomal rearrangements. Interestingly, in two insertions, GT repeats were integrated at one of the broken chromosome ends, suggesting that DSB repair can contribute to the spread of microsatellite sequences in mammalian genomes.
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Alternatively, the HDR pathway is capable of repairing DSBs using a sister chromatid as a repair template, and for this reason, it is considered an error‐free system.”
From CRISPR/Cas9 Ribonucleoprotein Nucleofection for Genome Editing in Primary Human Keratinocytes: Knockouts, Deletions, and Homology‐Directed Repair Mutagenesis (2024) · cites this paper as Liang et al., 1998
Experimental — accuracy not yet measured
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
Molecular Cloning. A Laboratory Manual
Wood, E. (1983) · Biochemical Education · doi:10.1016/0307-4412(83)90068-7 · Cited by 29,534
The double-strand-break repair model for recombination
Szostak, J. W., Orr-Weaver, T. L., Rothstein, R. J., & Stahl, F. W. (1983) · Cell · doi:10.1016/0092-8674(83)90331-8 · Cited by 2,437
Hamada, H., Petrino, M. G., & Kakunaga, T. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.21.6465 · Cited by 743
Rouet, P., Smih, F., & Jasin, M. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.12.8096 · Cited by 739
Self-citationExpression of a site-specific endonuclease stimulates homologous recombination in mammalian cells.
Rouet, P., Smih, F., & Jasin, M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.13.6064 · Cited by 571
Self-citationChoulika, A., Perrin, A., Dujon, B., & Nicolas, J.-F. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.4.1968 · Cited by 459
Genetic manipulation of genomes with rare-cutting endonucleases
Jasin, M. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)10019-6 · Cited by 391
Self-citationEvolution and distribution of (GT)n repetitive sequences in mammalian genomes
Stallings, R. L., Ford, A., Nelson, D., Torney, D. C., Hildebrand, C. E., & Moyzis, R. K. (1991) · Genomics · doi:10.1016/0888-7543(91)90467-s · Cited by 379
Rouet, P., Smih, F., & Jasin, M. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.12.8096-8106.1994 · Cited by 363
Self-citationDNA double-strand break repair and V(D)J recombination: involvement of DNA-PK
Jackson, S. P., & Jeggo, P. A. (1995) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)89090-8 · Cited by 345
Flagged first, then by citations
Research works printed but not linked: 3
- T D Petes, R E Malone, L S Symington Recombination in Yeast (Cold Spring Harbor Lab. Press, Plainview, NY, 1991).
- 10.1128/mcb.10.1.103-112.1990 · DOI
- S A Schichman, M A Caligiuri, M P Strout, S L Carter, Y Gu, E Canaani, C D Bloomfield, C M Croce Cancer Res 54, 4277–4280 (1994).
Cited by
Sorted by citations
Items 301–400 of 648
Majumdar, A., Muniandy, P. A., Liu, J., Liu, J.-L., Liu, S.-T., Cuenoud, B. M., & Seidman, M. M. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800607200 · Cited by 42
Induction and Repair of DNA Double-Strand Breaks under Irradiation and Microgravity
Pross, H. D., Casares, A., & Kiefer, J. (2000) · Radiation Research · doi:10.1667/0033-7587(2000)153[0521:iarodd]2.0.co;2 · Cited by 40
Novel evidences for a tumor suppressor role of Rev3, the catalytic subunit of Pol ζ
Brondello, J., Pillaire, M., Rodriguez, C., Gourraud, P., Sèlves, J., Cazaux, C., & Piette, J. (2008) · Oncogene · doi:10.1038/onc.2008.212 · Cited by 42
XRCC4 in G1 suppresses homologous recombination in S/G2, in G1 checkpoint-defective cells
Saintigny, Y., Delacôte, F., Boucher, D., Averbeck, D., & López, B. S. (2006) · Oncogene · doi:10.1038/sj.onc.1210075 · Cited by 38
The role of DNA polymerase activity in human non-homologous end joining
Pospiech, H. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.15.3277 · Cited by 39
Slebos, R. J. C., & Taylor, J. A. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4335 · Cited by 39
A multi-scale map of protein assemblies in the DNA damage response
Kratz, A., Kim, M., Kelly, M. R., Zheng, F., Koczor, C. A., Li, J., Ono, K., Qin, Y., Churas, C., Chen, J., et al. (2023) · Cell Systems · doi:10.1016/j.cels.2023.04.007 · Cited by 36
Chailleux, C., Aymard, F., Caron, P., Daburon, V., Courilleau, C., Canitrot, Y., Legube, G., & Trouche, D. (2014) · Nature Protocols · doi:10.1038/nprot.2014.031 · Cited by 37
Homologous recombination in plants is organ specific
Boyko, A., Filkowski, J. N., Hudson, D., & Kovalchuk, I. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.11.009 · Cited by 38
Luciferase-based transgenic recombination assay is more sensitive than β-glucoronidase-based
Ilnytskyy, Y., Boyko, A., & Kovalchuk, I. (2004) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2004.02.001 · Cited by 38
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
Capture of Extranuclear DNA at Fission Yeast Double-Strand Breaks
Decottignies, A. (2005) · Genetics · doi:10.1534/genetics.105.046144 · Cited by 36
Bhattacharyya, M. K., & Kumar, N. (2003) · International Journal for Parasitology · doi:10.1016/s0020-7519(03)00212-1 · Cited by 38
Rebuzzini, P., Khoriauli, L., Azzalin, C. M., Magnani, E., Mondello, C., & Giulotto, E. (2005) · DNA repair · doi:10.1016/j.dnarep.2004.12.011 · Cited by 38
Wiese, C., Pierce, A. J., Gauny, S. S., Jasin, M., & Kronenberg, A. (2002) · PubMed · Cited by 37
Self-citationFunctions and Regulation of Artemis: A Goddess in the Maintenance of Genome Integrity
Kurosawa, A., & Adachi, N. (2010) · Journal of Radiation Research · doi:10.1269/jrr.10017 · Cited by 37
CHECKING THE FOUNDATION: RECENT RADIOBIOLOGY AND THE LINEAR NO-THRESHOLD THEORY
Ulsh, B. A. (2010) · Health Physics · doi:10.1097/hp.0b013e3181e32477 · Cited by 39
Ionizing Radiation Triggers Chromatin-bound kin17 Complex Formation in Human Cells
Biard, D. S. F., Miccoli, L., Despras, E., Frobert, Y., Créminon, C., & Angulo, J. F. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200321200 · Cited by 37
Guirouilh‐Barbat, J., Huck, S., & López, B. S. (2007) · Oncogene · doi:10.1038/sj.onc.1210807 · Cited by 37
Many P-Element Insertions Affect Wing Shape in Drosophila melanogaster
Weber, K. E., Johnson, N., Champlin, D. T., & Patty, A. (2004) · Genetics · doi:10.1534/genetics.104.027748 · Cited by 39
Francis, R. J. B., & Richardson, C. A. (2007) · Genes & Development · doi:10.1101/gad.1522807 · Cited by 37
CRISPR/Cas9 gene editing therapies for cystic fibrosis
Graham, C., & Hart, S. L. (2021) · Expert Opinion on Biological Therapy · doi:10.1080/14712598.2021.1869208 · Cited by 39
van der Wijngaart, H., Hoes, L. R., Henegouwen, J. M. V. B., van der Velden, D. L., Zeverijn, L. J., Roepman, P., van Werkhoven, E., de Leng, W. W. J., Jansen, A. M. L., Mehra, N., et al. (2021) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-21-1104 · Cited by 38
Croglio, M. P., Haake, J. M., Ryan, C. P., Wang, V. S., Lapier, J., Schlarbaum, J. P., Dayani, Y., Artuso, E., Prandi, C., Koltai, H., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.7414 · Cited by 35
So, A., Dardillac, E., Muhammad, A. A., Chailleux, C., Sesma-Sanz, L., Ragu, S., Cam, É. L., Canitrot, Y., Masson, J., Dupaigne, P., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac073 · Cited by 44
Vriend, L. E. M., Jasin, M., & Krawczyk, P. M. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-801185-0.00009-x · Cited by 35
Self-citationBannister, L., Waldman, B. C., & Waldman, A. S. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.01.001 · Cited by 36
Lin, Y., Waldman, B. C., & Waldman, A. S. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00183-0 · Cited by 35
Villemure, J.-F., Abaji, C., Cousineau, I., & Belmaaza, A. (2003) · PubMed · Cited by 35
Singha, D. L., Das, D., Sarki, Y. N., Chowdhury, N., Sharma, M., Maharana, J., & Chikkaputtaiah, C. (2021) · Planta · doi:10.1007/s00425-021-03811-0 · Cited by 35
Deleterious Mutations and Selection for Sex in Finite Diploid Populations
Roze, D., & Michod, R. E. (2010) · Genetics · doi:10.1534/genetics.109.108258 · Cited by 34
Barroso, E., Pita, G., Arias, J. I., Menéndez, P. R., Zamora, P. M., Blanco, M., Benitez, J. J., & Ribas, G. (2009) · Breast Cancer Research and Treatment · doi:10.1007/s10549-009-0439-5 · Cited by 33
Meiosis and the Evolution of Recombination at Low Mutation Rates
Gessler, D. D. G., & Xu, S. (2000) · Genetics · doi:10.1093/genetics/156.1.449 · Cited by 34
Efficient Rejoining of Radiation-induced DNA Double-strand Breaks in Centromeric DNA of Human Cells
Rief, N., & Löbrich, M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200265200 · Cited by 34
Palindromic DNA and Genome Stability: Further Studiesa
Lewis, S. M., Akgün, E., & Jasin, M. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb08864.x · Cited by 34
Self-citationOvando-Roche, P., Georgiadis, A., Smith, A. J., Pearson, R. A., & Ali, R. R. (2017) · Current Stem Cell Reports · doi:10.1007/s40778-017-0078-4 · Cited by 35
Factors Affecting Double-Strand Break-Induced Homologous Recombination in Mammalian Cells
Perez, C., Guyot, V., Cabaniols, J., Gouble, A., Micheaux, B., Smith, J., Leduc, S., Pâques, F., & Duchateau, P. N. (2005) · BioTechniques · doi:10.2144/05391gt01 · Cited by 33
Inactivation of the RAD51 recombination pathway stimulates UV-induced mutagenesis in mammalian cells
Lambert, S., & López, B. S. (2002) · Oncogene · doi:10.1038/sj.onc.1205535 · Cited by 33
Homologous recombination in extrachromosomal plasmid substrates is not suppressed by p53
俊輔, 鈴., 範久, 藤., 通良, 阿., Dahm-Daphi, J., & Powell, S. N. (2001) · Carcinogenesis · doi:10.1093/carcin/22.11.1757 · Cited by 33
Szatkowska, M., & Krupa, R. (2020) · Cancers · doi:10.3390/cancers12071838 · Cited by 33
Challenges of CRISPR-Based Gene Editing in Primary T Cells
Rezalotfi, A., Fritz, L. V., Förster, R., & Bošnjak, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031689 · Cited by 33
Della-Maria, J., Motycka, T. A., Han, M., Jasin, M., & Tomkinson, A. E. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.02.004 · Cited by 32
Self-citationThe Suppressor‐mutator element and the evolutionary riddle of transposons
Fedoroff, N. V. (1999) · Genes to Cells · doi:10.1046/j.1365-2443.1999.00233.x · Cited by 32
Qin, J., Richardson, L. L., Jasin, M., Handel, M. A., & Arnheim, N. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.4.1655-1666.2004 · Cited by 31
Self-citationElsharkasy, O. M., Hegeman, C. V., Driedonks, T. A. P., Liang, X., Lansweers, I., Cotugno, O. L., de Groot, I. Y., de Wit, Z. E. M. N. J., Garcia-Guerra, A., Moorman, N. J. A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65995-3 · Cited by 37
Olsen, P. A., Gelazauskaite, M., Randøl, M., & Krauss, S. J. K. (2010) · BMC Molecular Biology · doi:10.1186/1471-2199-11-35 · Cited by 32
Symeonidi, E., Regalado, J., Schwab, R., & Weigel, D. (2021) · Quantitative Plant Biology · doi:10.1017/qpb.2020.6 · Cited by 30
Evans, M. J. (2007) · The biomedical & life sciences collection. · doi:10.69645/cgxu7557 · Cited by 33
Smith, J. A., Waldman, B. C., & Waldman, A. S. (2005) · Genetics · doi:10.1534/genetics.104.039362 · Cited by 32
Brustel, J., Kozik, Z., Gromak, N., Savic, V., & Sweet, S. M. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-21806-y · Cited by 33
Pluth, J. M., Fried, L. M., & Kirchgessner, C. U. (2001) · PubMed · Cited by 30
Meng, Y., Liu, C., Shen, L., Zhou, M., Liu, W., Kowolik, C. M., Campbell, J. L., Zheng, L., & Shen, B. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz537 · Cited by 29
Delayed activation of DNA damage checkpoint and radiation-induced genomic instability
Suzuki, K., Ojima, M., Kodama, S., & Watanabe, M. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.04.024 · Cited by 29
van den Bosch, M. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.6.1316 · Cited by 29
Targeted disruption of the sheep MSTN gene by engineered zinc-finger nucleases
Zhang, C., Wang, L., Ren, G., Li, Z., Ren, C., Zhang, T., Xu, K., & Zhang, Z. (2013) · Molecular Biology Reports · doi:10.1007/s11033-013-2853-3 · Cited by 28
Secretan, B., Scuric, Z., Oshima, J., Bishop, A. J. R., Howlett, N. G., Yau, D., & Schiestl, R. H. (2004) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2004.05.016 · Cited by 28
Plo, I., & López, B. S. (2009) · Oncogene · doi:10.1038/onc.2009.85 · Cited by 28
Krutilina, R. I., Sl, O., Buchlow, G., Yau, P. M., Zalensky, A. O., Zalenskaya, I. A., Bradbury, E. M., & Tomilin, N. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.4143 · Cited by 28
Djuzenova, C. S., Mühl, B., Schakowski, R., Oppitz, U., & Flentje, M. P. (2004) · British Journal of Cancer · doi:10.1038/sj.bjc.6601878 · Cited by 28
Capture of linear fragments at a double-strand break in yeast
Haviv‐Chesner, A., Kobayashi, Y., Gabriel, A., & Kupiec, M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm521 · Cited by 27
Katz, S. S., Gimble, F. S., & Storici, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088840 · 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
Boubakour-Azzouz, I., Bertrand, P., Claës, A., López, B. S., & Rougeon, F. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks585 · Cited by 27
Progress in the application of CRISPR: From gene to base editing
Wu, W., Yang, Y., & Lei, H. (2018) · Medicinal Research Reviews · doi:10.1002/med.21537 · Cited by 28
Chromosomal Double-Strand Breaks Introduced in Mammalian Cells by Expression of I-Sce I Endonuclease
Richardson, C. A., Elliott, B., & Jasin, M. (2003) · Humana Press eBooks · doi:10.1385/1-59259-675-4:453 · Cited by 27
Self-citationTeo, A. K. K., Gupta, M. K., Doria, A., & Kulkarni, R. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2015.06.006 · Cited by 26
The cryo‐EM structure of full‐length RAD52 protein contains an undecameric ring
Kinoshita, C., Takizawa, Y., Saotome, M., Ogino, S., Kurumizaka, H., & Kagawa, W. (2023) · FEBS Open Bio · doi:10.1002/2211-5463.13565 · Cited by 26
Allen, C. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00139-3 · Cited by 25
Analysis of the Xenopus Werner syndrome protein in DNA double-strand break repair
Yan, H., McCane, J. E., Toczylowski, T., & Chen, C. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200502077 · Cited by 26
Canitrot, Y. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh848 · Cited by 26
de Rezende, A. A. A., Munari, C. C., de Oliveira, P. F., Ferreira, N. H., Tavares, D. C., Silva, M. L. A. E., Rezende, K. C. S., & Spanó, M. A. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.01.050 · Cited by 25
Mladenova, V., Mladenov, E., & Iliakis, G. E. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00163 · Cited by 28
CRISPR/Cas therapeutic strategies for autosomal dominant disorders
Caruso, S. M., Quinn, P. M. J., da Costa, B. L., & Tsang, S. H. (2022) · Journal of Clinical Investigation · doi:10.1172/jci158287 · Cited by 26
Outwin, E. A., Carpenter, G., Bi, W., Withers, M. A., Lupski, J. R., & O’Driscoll, M. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002247 · Cited by 25
RAD51C (RAD51L2) is involved in maintaining centrosome number in mitosis
Lindh, A. R., Schultz, N. D., Saleh-Gohari, N., & Helleday, T. (2007) · Cytogenetic and Genome Research · doi:10.1159/000097416 · Cited by 25
Induction of Chromosomal Translocations in Mouse and Human Cells Using Site-Specific Endonucleases
Weinstock, D. M., Brunet, E., & Jasin, M. (2008) · JNCI Monographs · doi:10.1093/jncimonographs/lgn009 · Cited by 25
Self-citationMegabase-scale loss of heterozygosity provoked by CRISPR-Cas9 DNA double-strand breaks
Regan, S. B., Medhi, D., Xu, Y., White, T., Jiang, Y.-Z., Kim, J. E., Wang, S.-C., Deng, Q., Su, J., Baasan, D., et al. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.10.015 · Cited by 27
Self-citationReplication stress: Driver and therapeutic target in genomically instable cancers
Schoonen, P. M., Llobet, S. G., & van Vugt, M. A. T. M. (2018) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2018.10.006 · Cited by 26
CRISPR-Cas9: A multifaceted therapeutic strategy for cancer treatment
Kaushik, I., Ramachandran, S., & Srivastava, S. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.04.018 · Cited by 25
The relevance of BRCA genetics to prostate cancer pathogenesis and treatment.
Sundararajan, S., Ahmed, A. K., & Goodman, O. B. (2011) · PubMed · Cited by 25
Kulkarni, R. M., Thomas, R. A., & Tucker, J. D. (2010) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20605 · Cited by 24
Repair of Topoisomerase-Mediated DNA Damage in Bacteriophage T4
Stohr, B. A., & Kreuzer, K. N. (2001) · Genetics · doi:10.1093/genetics/158.1.19 · Cited by 24
White, R. R., Sung, P., Vestal, C. G., Benedetto, G., Cornelio, N., & Richardson, C. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084379 · Cited by 22
Srivastava, N., & Raman, M. J. (2006) · Cell Biochemistry and Function · doi:10.1002/cbf.1375 · Cited by 23
Shibata, A., Maeda, D., Ogino, H., Tsutsumi, M., Nohmi, T., Nakagama, H., Sügimura, T., Teraoka, H., & Masutani, M. (2009) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2009.02.001 · Cited by 23
Oligo/Polynucleotide-Based Gene Modification: Strategies and Therapeutic Potential
Sargent, R. G., Kim, S., & Gruenert, D. C. (2011) · Oligonucleotides · doi:10.1089/oli.2010.0273 · Cited by 23
Clikeman, J. A., Wheeler, S. L., & Nickoloff, J. A. (2001) · Genetics · doi:10.1093/genetics/157.4.1481 · Cited by 23
Mitotic recombination is an important mutational event following oxidative damage
Turner, D. R., Dreimanis, M., Holt, D., Firgaira, F. A., & Morley, A. A. (2003) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00194-x · Cited by 22
Frankenberg-Schwager, M., Becker, M., Garg, I., Pralle, E., Wolf, H., & Frankenberg, D. (2008) · Radiation Research · doi:10.1667/rr1375.1 · Cited by 22
Bertwistle, D., & Ashworth, A. (1999) · Breast Cancer Research · doi:10.1186/bcr12 · Cited by 22
Venkitaraman, A. R. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0558 · Cited by 22
Recombination during Early Herpes Simplex Virus Type 1 Infection Is Mediated by Cellular Proteins
Yao, X.-D., & Elias, P. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m005627200 · Cited by 22
Zdzienicka, M. Z. (1999) · Biochimie · doi:10.1016/s0300-9084(99)80043-1 · Cited by 22
Zhao, Y., Dominska, M., Petrova, A., Bagshaw, H., Kokoska, R. J., & Petes, T. D. (2017) · Genetics · doi:10.1534/genetics.117.201285 · Cited by 22
Significance of HER2 and C‐MYC oncogene amplifications in breast cancer in atomic bomb survivors
Miura, S., Nakashima, M., Ito, M., Kondo, H., Meirmanov, S. K., Hayashi, T., Soda, M., Matsuo, T., & Sekine, I. (2008) · Cancer · doi:10.1002/cncr.23414 · Cited by 21
Two different forms of palindrome resolution in the human genome: deletion or translocation
Kato, T., Inagaki, H., Kogo, H., Ohye, T., Yamada, K., Emanuel, B. S., & Kurahashi, H. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn008 · Cited by 21
Browning, C. L., Wise, C. F., & Wise, J. P. (2017) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2017.04.006 · Cited by 21
Read, L. R. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh280 · Cited by 21
Versatile modification of the CRISPR/Cas9 ribonucleoprotein system to facilitate in vivo application
Sun, B., Chen, H., & Gao, X. (2021) · Journal of Controlled Release · doi:10.1016/j.jconrel.2021.08.007 · Cited by 20
Metadata
- Authors
- Liang, F., Han, M., Romanienko, P. J., & Jasin, M.
- Affiliations
- Cornell University (US)
- Corresponding author
- Jasin, Maria
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1998-04-28
- Volume
- 95
- Issue
- 9
- Pages
- 5172-5177
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC20233
- OpenAlex
- W2168809955
- Cited by
- 649
- References
- 27
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 18 · 2023: 12 · 2022: 21 · 2021: 25 · 2020: 19 · 2019: 17 · 2018: 13 · 2017: 16 · 2016: 13 · 2015: 13 · 2014: 12 · 2013: 11 · 2012: 13
- FWCI
- 15.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Cancer Society
- National Institutes of Health
- National Institute of General Medical Sciences (GM54688)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Keywords
- homology-directed repair, DNA double-strand break repair, homologous recombination, non-homologous end joining, mammalian cells, chromosomal breaks, chromosomal rearrangements
- MeSH terms
- Animals, Cells, Cultured, DNA Damage, DNA Repair, Gene Conversion, Cricetinae, Recombination, Genetic, Sequence Homology, Nucleic Acid, Restriction Mapping, CHO Cells, Sequence Deletion
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