The DOI matches its Crossref record; 399 of the 399 references it cites were found in a registry or an index.
Eukaryotic DNA damage checkpoint activation in response to double-strand breaks
Open accessAbstract
Double-strand breaks (DSBs) are the most detrimental form of DNA damage. Failure to repair these cytotoxic lesions can result in genome rearrangements conducive to the development of many diseases, including cancer. The DNA damage response (DDR) ensures the rapid detection and repair of DSBs in order to maintain genome integrity. Central to the DDR are the DNA damage checkpoints. When activated by DNA damage, these sophisticated surveillance mechanisms induce transient cell cycle arrests, allowing sufficient time for DNA repair. Since the term "checkpoint" was coined over 20 years ago, our understanding of the molecular mechanisms governing the DNA damage checkpoint has advanced significantly. These pathways are highly conserved from yeast to humans. Thus, significant findings in yeast may be extrapolated to vertebrates, greatly facilitating the molecular dissection of these complex regulatory networks. This review focuses on the cellular response to DSBs in Saccharomyces cerevisiae, providing a comprehensive overview of how these signalling pathways function to orchestrate the cellular response to DNA damage and preserve genome stability in eukaryotic cells.
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?
In the citing paper
“ATM-Chk2 dependent DDR is activated primarily in response to DSBs (Fig. 7) [44].”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [44]
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
Hallmarks of Cancer: The Next Generation
Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590
Crystal structure of the nucleosome core particle at 2.8 Å resolution
Luger, K., Mäder, A. W., Richmond, R. K., Sargent, D. F., & Richmond, T. J. (1997) · Nature · doi:10.1038/38444 · Cited by 9,466
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
CDK inhibitors: positive and negative regulators of G1-phase progression
Sherr, C. J., & Roberts, J. M. (1999) · Genes & Development · doi:10.1101/gad.13.12.1501 · Cited by 6,115
The DNA-damage response in human biology and disease
Jackson, S. P., & Bartek, J. (2009) · Nature · doi:10.1038/nature08467 · Cited by 6,092
Instability and decay of the primary structure of DNA
Lindahl, T. (1993) · Nature · doi:10.1038/362709a0 · Cited by 5,679
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
Rogakou, E. P., Pilch, D. R., Orr, A. H., Ivanova, V. S., & Bonner, W. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.10.5858 · Cited by 5,438
A comprehensive analysis of protein–protein interactions in Saccharomyces cerevisiae
Uetz, P., Giot, L., Cagney, G., Mansfield, T. A., Judson, R. S., Knight, J. R., Lockshon, D., Narayan, V., Srinivasan, M., Pochart, P., et al. (2000) · Nature · doi:10.1038/35001009 · Cited by 4,706
Mdm2 promotes the rapid degradation of p53
Haupt, Y., Maya, R., Kazaz, A., & Oren, M. (1997) · Nature · doi:10.1038/387296a0 · Cited by 4,506
The DNA Damage Response: Making It Safe to Play with Knives
Ciccia, A., & Elledge, S. J. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.019 · Cited by 4,368
Cited by
Sorted by citations
The ATM protein kinase: regulating the cellular response to genotoxic stress, and more
Shiloh, Y., & Ziv, Y. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3546 · Cited by 1,649
Oxidative Stress and Programmed Cell Death in Yeast
Farrugia, G., & Balzan, R. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00064 · Cited by 323
Yan, S., Sorrell, M., & Berman, Z. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1666-4 · Cited by 247
FOXM1 (Forkhead box M1) in Tumorigenesis
Wierstra, I. (2013) · Advances in cancer research · doi:10.1016/b978-0-12-407190-2.00016-2 · Cited by 190
The Transcription Factor FOXM1 (Forkhead box M1)
Wierstra, I. (2013) · Advances in cancer research · doi:10.1016/b978-0-12-407173-5.00004-2 · Cited by 180
Human single-stranded DNA binding proteins are essential for maintaining genomic stability
Ashton, N. W., Bolderson, E., Cubeddu, L., O'Byrne, K. J., & Richard, D. J. (2013) · BMC Molecular Biology · doi:10.1186/1471-2199-14-9 · Cited by 118
Pharmacological Ascorbate Radiosensitizes Pancreatic Cancer
Du, J., Cieslak, J. A., Welsh, J. L., Sibenaller, Z. A., Allen, B. G., Wagner, B. A., Kalen, A. L., Doskey, C. M., Strother, R. K., Button, A. M., et al. (2015) · Cancer Research · doi:10.1158/0008-5472.can-14-1707 · Cited by 112
Brown, A. J. P., Cowen, L. E., Pietro, A. D., & Quinn, J. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0048-2016 · Cited by 111
Cohesin and the nucleolus constrain the mobility of spontaneous repair foci
Dion, V., Kalck, V., Seeber, A., Schleker, T., & Gasser, S. M. (2013) · EMBO Reports · doi:10.1038/embor.2013.142 · Cited by 103
Controlling DNA-end resection: a new task for CDKs
Ferretti, L. P., Lafranchi, L., & Sartori, A. A. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00099 · Cited by 112
The MRE11 complex: A versatile toolkit for the repair of broken DNA
Reginato, G., & Ćejka, P. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.102869 · Cited by 102
Role of the Mre11 Complex in Preserving Genome Integrity
Oh, J., & Symington, L. S. (2018) · Genes · doi:10.3390/genes9120589 · Cited by 90
Length-dependent processing of telomeres in the absence of telomerase
Fallet, E., Jolivet, P., Soudet, J., Lisby, M., Gilson, É., & Teixeira, M. T. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1328 · Cited by 86
Giannattasio, M., & Branzei, D. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2474-4 · Cited by 67
DNA Damage Responses during the Cell Cycle: Insights from Model Organisms and Beyond
Clay, D. E., & Fox, D. T. (2021) · Genes · doi:10.3390/genes12121882 · Cited by 77
DNA in motion during double-strand break repair
Miné-Hattab, J., & Rothstein, R. J. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.05.006 · Cited by 72
Bacal, J., Moriel‐Carretero, M., Pardo, B., Barthe, A., Sharma, S., Chabes, A., Lengronne, A., & Pasero, P. (2018) · The EMBO Journal · doi:10.15252/embj.201899319 · Cited by 70
O-GlcNAc: A Sweetheart of the Cell Cycle and DNA Damage Response
Liu, C., & Li, J. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00415 · Cited by 62
Yang, C., Zang, W., Ji, Y., Li, T., Yang, Y., & Zheng, X. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.007009 · Cited by 64
Rashi‐Elkeles, S., Warnatz, H.-J., Elkon, R., Kupershtein, A., Chobod, Y., Paz, A., Amstislavskiy, V. S., Sultan, M., Safer, H. M., Nietfeld, W., et al. (2014) · Science Signaling · doi:10.1126/scisignal.2005032 · Cited by 57
Role of protein phosphatases PP1, PP2A, PP4 and Cdc14 in the DNA damage response
Ramos, F., Villoria, M. T., Alonso‐Rodríguez, E., & Clemente‐Blanco, A. (2019) · Cell Stress · doi:10.15698/cst2019.03.178 · Cited by 61
Targeting WEE1 to enhance conventional therapies for acute lymphoblastic leukemia
di Rorà, A. G. L., Beeharry, N., Imbrogno, E., Ferrari, A., Robustelli, V., Righi, S., Sabattini, E., Falzacappa, M. V. V., Ronchini, C., Testoni, N., et al. (2018) · Journal of Hematology & Oncology · doi:10.1186/s13045-018-0641-1 · Cited by 52
Quantitative sensing and signalling of single-stranded DNA during the DNA damage response
Bantele, S. C. S., Lisby, M., & Pfander, B. (2019) · Nature Communications · doi:10.1038/s41467-019-08889-5 · Cited by 55
The 9-1-1 checkpoint clamp coordinates resection at DNA double strand breaks
Ngo, H.-P., & Lydall, D. A. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv409 · Cited by 62
Glutathione is essential to preserve nuclear function and cell survival under oxidative stress
Hatem, E., Berthonaud, V., Dardalhon, M., Lagniel, G., Baudouin‐Cornu, P., Huang, M., Labarre, J., & Chdin, S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.10.746 · Cited by 49
Yu, T.-Y., Kimble, M. T., & Symington, L. S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1816539115 · Cited by 47
Saccharomyces cerevisiae as a Model to Study Replicative Senescence Triggered by Telomere Shortening
Teixeira, M. T. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00101 · Cited by 54
Glutathione is essential to preserve nuclear function and cell survival under oxidative stress
Hatem, E., Berthonaud, V., Dardalhon, M., Lagniel, G., Baudouin‐Cornu, P., Huang, M., Labarre, J., & Chédin, S. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.10.807 · Cited by 48
di Rorà, A. G. L., Iacobucci, I., Imbrogno, E., Papayannidis, C., Derenzini, E., Ferrari, A., Guadagnuolo, V., Robustelli, V., Parisi, S., Sartor, C., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.10535 · Cited by 41
Domenico, E. G. D., Romano, E., Porto, P. D., & Ascenzioni, F. (2014) · BioMed Research International · doi:10.1155/2014/787404 · Cited by 39
Litwin, I., Bocer, T., Dziadkowiec, D., & Wysocki, R. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003640 · Cited by 39
Jung, K., Lee, Y., Huh, E. Y., Lee, S. C., Lim, S., & Bahn, Y. (2019) · mBio · doi:10.1128/mbio.01726-18 · Cited by 36
Chromatin mobility upon DNA damage: state of the art and remaining questions
Zimmer, C., & Fabre, E. (2018) · Current Genetics · doi:10.1007/s00294-018-0852-6 · Cited by 35
The Dynamic Behavior of Chromatin in Response to DNA Double-Strand Breaks
Fernández, F. G., & Fabre, E. (2022) · Genes · doi:10.3390/genes13020215 · Cited by 38
Yao, S., Feng, Y., Zhang, Y., & Feng, J. (2021) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2021.11.033 · Cited by 29
Cell cycle involvement in cancer therapy; WEE1 kinase, a potential target as therapeutic strategy
Vakili‐Samiani, S., Khanghah, O. J., Gholipour, E., Najafi, F., Zeinalzadeh, E., Samadi, P., Sarvarian, P., Pourvahdani, S., Kelaye, S. K., Hamblin, M. R., et al. (2022) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2022.111776 · Cited by 30
McKinney, J. S., Sethi, S., Tripp, J. D., Nguyen, T. N., Sanderson, B. A., Westmoreland, J. W., Resnick, M. A., & Lewis, L. K. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-251 · Cited by 29
Abreu, C. M. C., Kumar, R., Hamilton, D. S., Dawdy, A., Creavin, K., Eivers, S. B., Finn, K., Balsbaugh, J. L., O’Connor, R., Kiely, P. A., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003310 · Cited by 30
Self-citationKang, M. Y., Kim, W., Jo, H.-R., Shin, Y.-J., Kim, M., & Jeong, J. (2018) · International Journal of Oncology · doi:10.3892/ijo.2018.4424 · Cited by 27
Protein kinase C controls activation of the DNA integrity checkpoint
Soriano-Carot, M., Quilis, I., Bañó, M. C., & Igual, J. C. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku373 · Cited by 29
DNA double-strand breaks in telophase lead to coalescence between segregated sister chromatid loci
Ayra‐Plasencia, J., & Machín, F. (2019) · Nature Communications · doi:10.1038/s41467-019-10742-8 · Cited by 25
Kopp, B., Dario, M., Zalko, D., & Audebert, M. (2018) · Environmental and Molecular Mutagenesis · doi:10.1002/em.22197 · Cited by 23
Chen, Z., Liu, C., Lu, Y., Yang, L., Li, M., He, M., Chen, C., Zhang, L., Yu, Z., & Zhou, Z. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000447804 · Cited by 24
Persistent DNA damage signaling and DNA polymerase theta promote broken chromosome segregation
Clay, D. E., Bretscher, H. S., Jezuit, E. A., Bush, K. B., & Fox, D. T. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202106116 · Cited by 26
Ohsawa, R., Seol, J.-H., & Tyler, J. K. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00136 · Cited by 23
CDK and Mec1/Tel1-catalyzed phosphorylation of Sae2 regulate different responses to DNA damage
Yu, T.-Y., Garcia, V., & Symington, L. S. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz814 · Cited by 22
Krishnaraj, J., Yamamoto, T., & Ohki, R. (2023) · Cancers · doi:10.3390/cancers15133399 · Cited by 22
Paths from DNA damage and signaling to genome rearrangements via homologous recombination
Nickoloff, J. A. (2017) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2017.07.008 · Cited by 23
Tumor Suppressor FBXW7 and Its Regulation of DNA Damage Response and Repair
Lan, H., & Sun, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.751574 · Cited by 24
Structural basis of Rad53 kinase activation by dimerization and activation segment exchange
Wybenga-Groot, L. E., Ho, C. S. W., Sweeney, F. D., Ceccarelli, D. F. J., McGlade, C. J., Durocher, D., & Sicheri, F. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.05.004 · Cited by 20
A history of genome editing in Saccharomyces cerevisiae
Alexander, W. G. (2017) · Yeast · doi:10.1002/yea.3300 · Cited by 20
Homologous Recombination: A GRAS Yeast Genome Editing Tool
Bernardi, B., & Wendland, J. (2020) · Fermentation · doi:10.3390/fermentation6020057 · Cited by 20
Hassel, J. C., Zimmer, L., Sickmann, T., Eigentler, T., Meier, F. E., Mohr, P., Pukrop, T., Roesch, A., Vordermark, D., Wendl, C. M., et al. (2023) · Cancers · doi:10.3390/cancers15133448 · Cited by 21
Khurana, N., Laskar, S., Bhattacharyya, M. K., & Bhattacharyya, S. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-12-0867 · Cited by 19
Processing of DNA Double-Strand Breaks in Yeast
Gnügge, R., Oh, J., & Symington, L. S. (2018) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2017.11.007 · Cited by 22
A cell cycle-independent mode of the Rad9-Dpb11 interaction is induced by DNA damage
di Cicco, G., Bantele, S. C. S., Reußwig, K.-U., & Pfander, B. (2017) · Scientific Reports · doi:10.1038/s41598-017-11937-z · Cited by 18
Quantitative Profiling of DNA Damage and Apoptotic Pathways in UV Damaged Cells Using PTMScan Direct
Stokes, M. P., Silva, J. C., Jia, X., Lee, K., Polakiewicz, R. D., & Comb, M. J. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms14010286 · Cited by 18
Maintenance of Genome Integrity by Mi2 Homologs CHD-3 and LET-418 in Caenorhabditis elegans
Turcotte, C. A., Sloat, S. A., Rigothi, J. A., Rosenkranse, E., Northrup, A. L., Andrews, N. P., & Checchi, P. M. (2018) · Genetics · doi:10.1534/genetics.118.300686 · Cited by 17
Tipin Functions in the Protection against Topoisomerase I Inhibitor
Hosono, Y., Abe, T., Higuchi, M., Kajii, K., Sakuraba, S., Tada, S., Enomoto, T., & Seki, M. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.531707 · Cited by 17
Diao, L., Chen, C., Dennehey, B. K., Pal, S., Wang, P., Shen, Z.-J., Deem, A. K., & Tyler, J. K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180556 · Cited by 19
Choi, J. E., & Chung, W. (2019) · The Journal of Microbiology · doi:10.1007/s12275-020-9520-x · Cited by 17
Tsai, F.-L., Vijayraghavan, S., Prinz, J. A., MacAlpine, H. K., MacAlpine, D. M., & Schwacha, A. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.01357-14 · Cited by 16
Adrenergic DNA damage of embryonic pluripotent cells via β2 receptor signalling
Sun, F., Ding, X., An, S.-M., Tang, Y., Yang, X., Teng, L., Zhang, C., Shen, Y. H., Chen, H., & Zhu, L. (2015) · Scientific Reports · doi:10.1038/srep15950 · Cited by 16
Litwin, I., Mucha, S., Pilarczyk, E., Wysocki, R., & Maciaszczyk-Dziubińska, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094510 · Cited by 16
Adaptation in replicative senescence: a risky business
Coutelier, H., & Xu, Z. (2019) · Current Genetics · doi:10.1007/s00294-019-00933-7 · Cited by 15
Repeated H2O2 exposure drives cell cycle progression in an in vitro model of ulcerative colitis
Poehlmann, A., Reißig, K., Schönfeld, P., Walluscheck, D., Schinlauer, A., Hartig, R., Lessel, W., Guenther, T., Silver, A. R., & Roessner, A. (2013) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12150 · Cited by 15
CTLA-4 Facilitates DNA Damage–Induced Apoptosis by Interacting With PP2A
Yan, Q., Zhang, B., Ling, X., Zhu, B., Mei, S., Yang, H., Zhang, D., Huo, J., & Zhao, Z. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.728771 · Cited by 14
PARP Inhibitors in Advanced Prostate Cancer in Tumors with DNA Damage Signatures
McNevin, C. S., Cadoo, K. A., Baird, A., Finn, S. P., & McDermott, R. (2022) · Cancers · doi:10.3390/cancers14194751 · Cited by 14
Kimble, M. T., Johnson, M. J., Nester, M. R., & Symington, L. S. (2023) · eLife · doi:10.7554/elife.84322 · Cited by 16
Uzcanga, G. L., Lara-Barba, E., Gutiérrez, F., Beaty, D., Beske, T., Terán, R., Navarro, J. C., Pasero, P., Benítez, W., & Poveda, A. (2016) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2016.1188758 · Cited by 14
DNA resection proteins Sgs1 and Exo1 are required for G1 checkpoint activation in budding yeast
Balogun, F. O., Truman, A. W., & Kron, S. J. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.06.003 · Cited by 14
Princz, L. N., Gritenaite, D., & Pfander, B. (2014) · Cell Cycle · doi:10.4161/15384101.2014.989126 · Cited by 16
Rtt107 BRCT domains act as a targeting module in the DNA damage response
Leung, G. P., Brown, J. A. R., Glover, J. N. M., & Kobor, M. S. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.10.007 · Cited by 14
Fernández, F. G., Lemos, B. R., Khalil, Y., Batrin, R., Haber, J. E., & Fabre, E. (2021) · Journal of Cell Science · doi:10.1242/jcs.258500 · Cited by 15
Yam, C., Chia, D. B., Shi, I. Y., Lim, H. H., & Surana, U. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa355 · Cited by 16
Wang, Z., Yin, H., Lv, L., Feng, Y., Chen, S., Liang, J., Huang, Y., Jiang, X., Jiang, H., Bukhari, I., et al. (2014) · Cell Cycle · doi:10.4161/cc.28296 · Cited by 14
Chromothripsis: an emerging crossroad from aberrant mitosis to therapeutic opportunities
Ejaz, U., Dou, Z., Yao, P. Y., Wang, Z., Liu, X., & Yao, X. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae016 · Cited by 13
Leung, G. P., Aristizabal, M. J., Krogan, N. J., & Kobor, M. S. (2014) · G3 Genes Genomes Genetics · doi:10.1534/g3.114.011205 · Cited by 12
Siler, J., Xia, B., Wong, C., Kath, M., & Bi, X. (2017) · DNA repair · doi:10.1016/j.dnarep.2016.12.009 · Cited by 12
Yao, G., Wan, J., Liu, Q., Mu, C., Wang, Y., & Sang, J. (2017) · Biochemical Journal · doi:10.1042/bcj20160889 · Cited by 11
Brown, A. J. P., Cowen, L. E., Pietro, A. D., & Quinn, J. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch21 · Cited by 11
Bierle, L. A., Reich, K. L., Taylor, B. E., Blatt, E. B., Middleton, S. M., Burke, S. D., Stultz, L. K., Hanson, P. K., Partridge, J. F., & Miller, M. E. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138085 · Cited by 10
Right time, right place—DNA damage and DNA replication checkpoints collectively safeguard S phase
Galanti, L., & Pfander, B. (2018) · The EMBO Journal · doi:10.15252/embj.2018100681 · Cited by 9
Akemi, N., Masuda, K., Hiromoto, T., Takahashi, K., Matsumoto, Y., Habib, A. G. K., Darwish, A. G., Yukawa, M., Tsuchiya, E., & Ueno, M. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01704-13 · Cited by 9
Su, L., Zhu, T., Liu, H., Zhu, Y., Peng, Y., Tang, T., Zhou, S., Hu, C., Chen, H., Guo, A., et al. (2023) · Cells · doi:10.3390/cells12030476 · Cited by 8
Replisome components—Post-translational modifications and their effects
Zech, J., & Dalgaard, J. Z. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.03.026 · Cited by 8
Pharmacological Ascorbate Enhances Chemotherapies in Pancreatic Ductal Adenocarcinoma
O’Leary, B. R., Ruppenkamp, E. K., Steers, G. J., Du, J., Carroll, R. S., Wagner, B. A., Buettner, G. R., & Cullen, J. J. (2022) · Pancreas · doi:10.1097/mpa.0000000000002086 · Cited by 8
Holland, C. L., Weis, M., England, C. J., Berry, A. M., Hall, P. D., & Lewis, L. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113701 · Cited by 7
Rgf1p (Rho1p GEF) is required for double-strand break repair in fission yeast
Manjón, E., Edreira, T., Muñoz, S., & Sánchez, Y. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx176 · Cited by 7
Genotoxic effect of caffeine in Yarrowia lipolytica cells deficient in DNA repair mechanisms
Quiñones-González, C. A., Arredondo-Mendoza, G. I., Jiménez‐Salas, Z., Larriba-Calle, G., Ruíz-Herrera, J., & Campos‐Góngora, E. (2019) · Archives of Microbiology · doi:10.1007/s00203-019-01658-4 · Cited by 6
Guan, M., Zhu, Z., Jiang, Y., Tian, M., Lü, Y., Xu, X., Li, S., Chen, D., & Zhang, X. (2021) · Toxicology in Vitro · doi:10.1016/j.tiv.2021.105278 · Cited by 6
Nucleolar asymmetry and the importance of septin integrity upon cell cycle arrest
Rai, U., Najm, F. J., & Tartakoff, A. M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174306 · Cited by 6
Brown, J. A. R., & Kobor, M. S. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.01.001 · Cited by 4
Gkouskou, K. K., Fragiadakis, G. S., Voutsina, A., & Alexandraki, D. (2019) · Current Genetics · doi:10.1007/s00294-019-01047-w · Cited by 4
Preserving Yeast Genetic Heritage through DNA Damage Checkpoint Regulation and Telomere Maintenance
Baldo, V., Liang, J., Wang, G., & Zhou, H. (2012) · Biomolecules · doi:10.3390/biom2040505 · Cited by 4
DNA damage checkpoint dynamics drive cell cycle phase transitionsPreprint
Chao, H. X., Poovey, C. E., Privette, A. A., Grant, G. D., Chao, H. Y., Cook, J. G., & Purvis, J. E. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/137307 · Cited by 4
Transgenerational chromosome repair in the asexual bdelloid rotifer Adineta vagaPreprint
Houtain, A., Derzelle, A., Llirós, M., Hespeels, B., Nicolas, É., Simion, P., Virgo, J., Lenormand, T., Hallet, B., & Doninck, K. V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.25.577190 · Cited by 4
Yang, J., Yue, G., Fan, Z., Zhang, N., Nie, S., Li, J., & Ji, Y. (2025) · Drug Development Research · doi:10.1002/ddr.70087 · Cited by 3
Ilioaia, O., Dudragne, L., Brocas, C., Meneu, L., Koszul, R., Dubrana, K., & Xu, Z. (2025) · Cell Genomics · doi:10.1016/j.xgen.2025.100947 · Cited by 2
Wang, Y., Wang, N., Liu, J., Zhang, Y., Li, X., & Han, Q. (2021) · FEMS Yeast Research · doi:10.1093/femsyr/foab010 · Cited by 2
Metadata
- Authors
- Finn, K., Lowndes, N. F., & Grenon, M.
- Affiliations
- Ollscoil na Gaillimhe – University of Galway (IE)
- Corresponding author
- Lowndes, Noel Francis
- Grenon, Muriel
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2011-11-15
- Volume
- 69
- Issue
- 9
- Pages
- 1447-1473
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11115150
- OpenAlex
- W1991917259
- Cited by
- 127
- References
- 399
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 2 · 2023: 6 · 2022: 6 · 2021: 8 · 2020: 5 · 2019: 14 · 2018: 12 · 2017: 15 · 2016: 7 · 2015: 9 · 2014: 15 · 2013: 16 · 2012: 3
- FWCI
- 0.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- DNA damage checkpoint, DNA double-strand breaks, DNA damage response, genome stability, cell cycle arrest, DNA repair, Saccharomyces cerevisiae, genome rearrangement, cancer
- MeSH terms
- Checkpoint Kinase 1, Cell Cycle, DNA Damage, Humans, Models, Biological, Models, Genetic, Protein Kinases, Saccharomyces cerevisiae, Signal Transduction, Protein Serine-Threonine Kinases, Cell Cycle Proteins, Saccharomyces cerevisiae Proteins, Genomic Instability, DNA Breaks, Double-Stranded, Eukaryota, Cell Cycle Checkpoints, Checkpoint Kinase 2
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