EXO1-A multi-tasking eukaryotic nuclease

Global Mapping of the Yeast Genetic Interaction Network

Tong, A. H. Y., Lesage, G., Bader, G. D., Ding, H., Xu, H., Xin, X., Young, J., Berriz, G. F., Brost, R. L., Chang, M., et al. (2004) · Science · doi:10.1126/science.1091317 · Cited by 2,089

Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family

Keeney, S., Giroux, C. N., & Kleckner, N. E. (1997) · Cell · doi:10.1016/s0092-8674(00)81876-0 · Cited by 1,824

MISMATCH REPAIR IN REPLICATION FIDELITY, GENETIC RECOMBINATION, AND CANCER BIOLOGY

Modrich, P. L., & Lahue, R. S. (1996) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.65.070196.000533 · Cited by 1,510

TELOMERE LENGTH REGULATION

Greider, C. W. (1996) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.65.070196.002005 · Cited by 1,032

Eukaryotic DNA mismatch repair

Kolodner, R. D., & Marsischky, G. (1999) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(99)80013-6 · Cited by 861

Loss of a yeast telomere: Arrest, recovery, and chromosome loss

Sandell, L. J. (1993) · Cell · doi:10.1016/0092-8674(93)90493-a · Cited by 792

Single-Stranded DNA Arising at Telomeres in cdc13 Mutants May Constitute a Specific Signal for the RAD9 Checkpoint

Garvik, B. M., Carson, M., & Hartwell, L. H. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.11.6128 · Cited by 629

Analysis of wild-type and rad50 mutants of yeast suggests an intimate relationship between meiotic chromosome synapsis and recombination

Alani, E. A., Padmore, R., & Kleckner, N. E. (1990) · Cell · doi:10.1016/0092-8674(90)90524-i · Cited by 613

Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double‐strand break repair and serves as a barrier to error‐prone DNA repair pathways.

Boulton, S. J., & Jackson, S. P. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00890.x · Cited by 502

DNA Mismatch Repair: Molecular Mechanisms and Biological Function

Schofield, M. J., & Hsieh, P. (2003) · Annual Review of Microbiology · doi:10.1146/annurev.micro.57.030502.090847 · Cited by 498

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

Mechanisms and functions of DNA mismatch repair

Li, G. (2007) · Cell Research · doi:10.1038/cr.2007.115 · Cited by 1,479

The multifaceted mismatch-repair system

Jiricny, J. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1907 · Cited by 1,375

Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break processing

Mimitou, E. P., & Symington, L. S. (2008) · Nature · doi:10.1038/nature07312 · Cited by 1,060

DNA helicases Sgs1 and BLM promote DNA double-strand break resectionPreprint

Gravel, S., Chapman, J. R., Magill, C. P., & Jackson, S. P. (2008) · Genes & Development · doi:10.1101/gad.503108 · Cited by 595

Eukaryotic Mismatch Repair in Relation to DNA Replication

Kunkel, T. A., & Erie, D. A. (2015) · Annual Review of Genetics · doi:10.1146/annurev-genet-112414-054722 · Cited by 459

Identification of Holliday junction resolvases from humans and yeast

Ip, S. C. Y., Rass, U., Blanco, M. G., Flynn, H. R., Skehel, M. J., & West, S. C. (2008) · Nature · doi:10.1038/nature07470 · Cited by 416

DNA resection in eukaryotes: deciding how to fix the break

Huertas, P. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1710 · Cited by 424

Quantitative Proteomic Atlas of Ubiquitination and Acetylation in the DNA Damage Response

Elia, A. E. H., Boardman, A. P., Wang, D. C., Huttlin, E. L., Everley, R. A., Dephoure, N., Zhou, C., Koren, I., Gygi, S. P., & Elledge, S. J. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.05.006 · Cited by 341

End Resection at Double-Strand Breaks: Mechanism and RegulationPreprint

Symington, L. S. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016436 · Cited by 307

Temporally and Biochemically Distinct Activities of Exo1 during Meiosis: Double-Strand Break Resection and Resolution of Double Holliday Junctions

Zakharyevich, K., Ma, Y., Tang, S., Hwang, P. Y.-H., Boiteux, S., & Hunter, N. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.11.032 · Cited by 256

MLH1 Deficiency-Triggered DNA Hyperexcision by Exonuclease 1 Activates the cGAS-STING Pathway

Guan, J., Lu, C., Jin, Q., Lu, H., Chen, X., Tian, L., Zhang, Y., Ortega, J., Zhang, J., Siteni, S., et al. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.11.004 · Cited by 245

Saccharomyces cerevisiae Mre11/Rad50/Xrs2 and Ku proteins regulate association of Exo1 and Dna2 with DNA breaks

Shim, E. Y., Chung, W.-H., Nicolette, M. L., Zhang, Y., Davis, M., Zhu, Z., Paull, T. T., Ira, G., & Lee, S. E. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.219 · Cited by 254

DNA Repair Mechanisms and the Bypass of DNA Damage in Saccharomyces cerevisiae

Boiteux, S., & Jinks-Robertson, S. (2013) · Genetics · doi:10.1534/genetics.112.145219 · Cited by 250

Human Mismatch Repair

Constantin, N., Dzantiev, L., Kadyrov, F. A., & Modrich, P. L. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509701200 · Cited by 225

Nucleases and helicases take center stage in homologous recombination

Mimitou, E. P., & Symington, L. S. (2009) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2009.01.010 · Cited by 238

Identification of early molecular markers for breast cancer

Kretschmer, C., Sterner‐Kock, A., Siedentopf, F., Schoenegg, W., Schlag, P. M., & Kemmner, W. (2011) · Molecular Cancer · doi:10.1186/1476-4598-10-15 · Cited by 205

DNA mismatch repair and its many roles in eukaryotic cells

Liu, D., Keijzers, G., & Rasmussen, L. J. (2017) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2017.07.001 · Cited by 209

Phosphorylation of EXO1 by CDKs 1 and 2 regulates DNA end resection and repair pathway choice

Tomimatsu, N., Mukherjee, B., Hardebeck, M. C., Ilcheva, M., Camacho, C. V., Harris, J. L., Porteus, M. H., Llorente, B., Khanna, K. K., & Burma, S. (2014) · Nature Communications · doi:10.1038/ncomms4561 · Cited by 187

Checkpoint-dependent phosphorylation of Exo1 modulates the DNA damage response

Morin, I., Ngo, H., Greenall, A., Zubko, M. K., Morrice, N., & Lydall, D. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.171 · Cited by 164

DNA polymerase proofreading: Multiple roles maintain genome stability

Reha-Krantz, L. J. (2009) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2009.06.012 · Cited by 162

Ku: A multifunctional protein involved in telomere maintenance

Fisher, T. S., & Zakian, V. A. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.04.021 · Cited by 152

Exo1 plays a major role in DNA end resection in humans and influences double-strand break repair and damage signaling decisions

Tomimatsu, N., Mukherjee, B., Deland, K., Kurimasa, A., Bolderson, E., Khanna, K. K., & Burma, S. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.01.006 · Cited by 139

Exonuclease 1-dependent and independent mismatch repair

Goellner, E. M., Putnam, C. D., & Kolodner, R. D. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.04.010 · Cited by 138

Replication and Recombination Factors Contributing to Recombination-Dependent Bypass of DNA Lesions by Template Switch

Vanoli, F., Fumasoni, M., Szakál, B., Maloisel, L., & Branzei, D. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001205 · Cited by 134

Exo1 competes with repair synthesis, converts NER intermediates to long ssDNA gaps, and promotes checkpoint activation

Giannattasio, M., Follonier, C., Tourrière, H., Puddu, F., Lazzaro, F., Pasero, P., Lopes, M., Plevani, P., & Muzi-Falconi, M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.004 · Cited by 121

DNA Repair Pathways and Mechanisms

Dexheimer, T. S. (2012) · Springer eBooks · doi:10.1007/978-94-007-4590-2_2 · Cited by 133

Microhomology-Mediated End Joining in Fission Yeast Is Repressed by Pku70 and Relies on Genes Involved in Homologous Recombination

Decottignies, A. (2007) · Genetics · doi:10.1534/genetics.107.071621 · Cited by 112

Mus81 is essential for sister chromatid recombination at broken replication forks

Roseaulin, L., Yamada, Y., Tsutsui, Y., Russell, P. R., Iwasaki, H., & Arcangioli, B. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.65 · Cited by 103

Cell cycle-dependent control of homologous recombination

Zhao, X., Wei, C., Li, J., Xing, P., Li, J., Zheng, S., & Chen, X. (2017) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmx055 · Cited by 113

Meiotic recombination

Hunter, N. (2007) · Topics in current genetics · doi:10.1007/978-3-540-71021-9_14 · Cited by 102

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 Caenorhabditis elegans Homolog of Gen1/Yen1 Resolvases Links DNA Damage Signaling to DNA Double-Strand Break Repair

Bailly, A., Freeman, A. D. J., Hall, J., Déclais, A., Alpi, A. F., Lilley, D. M. J., Ahmed, S. C., & Gartner, A. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001025 · Cited by 102

Single-molecule imaging reveals the mechanism of Exo1 regulation by single-stranded DNA binding proteins

Myler, L. R., Gallardo, I. F., Zhou, Y., Gong, F., Yang, S.-H., Wold, M. S., Miller, K. M., Paull, T. T., & Finkelstein, I. J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1516674113 · Cited by 94

DNA mismatch repair promotes APOBEC3-mediated diffuse hypermutation in human cancers

Mas-Ponte, D., & Supek, F. (2020) · Nature Genetics · doi:10.1038/s41588-020-0674-6 · Cited by 97

PCNA promotes processive DNA end resection by Exo1

Chen, X., Paudyal, S. C., Chin, R.-I., & You, Z. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt672 · Cited by 86

Functional Characterization of Pathogenic Human MSH2 Missense Mutations in Saccharomyces cerevisiae

Gammie, A. E., Erdeniz, N., Beaver, J. A., Devlin, B., Nanji, A., & Rose, M. D. (2007) · Genetics · doi:10.1534/genetics.107.071084 · Cited by 89

The SOSS1 single‐stranded DNA binding complex promotes DNA end resection in concert with Exo1

Yang, S.-H., Zhou, R., Campbell, J. L., Chen, J., Ha, T., & Paull, T. T. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.314 · Cited by 89

FOXM1 Modulates Cisplatin Sensitivity by Regulating EXO1 in Ovarian Cancer

Zhou, J., Wang, Y., Wang, Y., Yin, X., He, Y., Chen, L., Wang, W., Liu, T., & Di, W. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096989 · Cited by 86

A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine

Hansen, M. F., Johansen, J. A., Bjørnevoll, I., Sylvander, A. E., Steinsbekk, K. S., Sætrom, P., Sandvik, A. K., Drabløs, F., & Sjursen, W. (2015) · Familial Cancer · doi:10.1007/s10689-015-9803-2 · Cited by 83

ATR-dependent pathways control hEXO1 stability in response to stalled forks

El‐Shemerly, M., Heß, D., Pyakurel, A., Moselhy, S. S., & Ferrari, S. M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm1052 · Cited by 82

DNA-damage-induced degradation of EXO1 exonuclease limits DNA end resection to ensure accurate DNA repair

Tomimatsu, N., Mukherjee, B., Harris, J. L., Boffo, F. L., Hardebeck, M. C., Potts, P. R., Khanna, K. K., & Burma, S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.772475 · Cited by 85

Human exonuclease 1 connects nucleotide excision repair (NER) processing with checkpoint activation in response to UV irradiation

Sertic, S., Pizzi, S., Cloney, R., Lehmann, A. R., Marini, F., Plevani, P., & Muzi-Falconi, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108547108 · Cited by 80

The Multiple Biological Roles of the 3′→5′ Exonuclease ofSaccharomyces cerevisiaeDNA Polymerase δ Require Switching between the Polymerase and Exonuclease Domains

Jin, Y. H., Garg, P., Stith, C. M. W., Al-Refai, H., Sterling, J. F., Murray, L. J. W., Kunkel, T. A., Resnick, M. A., Burgers, P., & Gordenin, D. A. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.25.1.461-471.2005 · Cited by 80

Pathway Analysis of Single-Nucleotide Polymorphisms Potentially Associated with Glioblastoma Multiforme Susceptibility Using Random Forests

Chang, J. S.-M., Yeh, R., Wiencke, J. K., Wiemels, J. L., Smirnov, I. V., Pico, A. R., Tihan, T., Patoka, J., Miike, R., Sison, J. D., et al. (2008) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-07-2830 · Cited by 78

Efficient gene targeting by TAL effector nucleases coinjected with exonucleases in zygotes

Mashimo, T., Kaneko, T., Sakuma, T., Kobayashi, J., Kunihiro, Y., Voigt, B., Yamamoto, T., & Serikawa, T. (2013) · Scientific Reports · doi:10.1038/srep01253 · Cited by 77

DNA double-strand break repair in Caenorhabditis elegans

Lemmens, B. B. L. G., & Tijsterman, M. (2010) · Chromosoma · doi:10.1007/s00412-010-0296-3 · Cited by 76

The yeast Snm1 protein is a DNA 5′-exonuclease

Li, X., Hejna, J., & Moses, R. E. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.08.012 · Cited by 69

O 6 -methylguanine-induced cell death involves exonuclease 1 as well as DNA mismatch recognition in vivo

Klapacz, J., Meira, L. B., Luchetti, D., Calvo, J. A., Bronson, R. T., Edelmann, W., & Samson, L. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811991106 · Cited by 64

Mechanism of Action: The Unique Pattern of Bendamustine-Induced Cytotoxicity

Leoni, L. M., & Hartley, J. A. (2011) · Seminars in Hematology · doi:10.1053/j.seminhematol.2011.03.003 · Cited by 67

Identification of the Xenopus DNA2 protein as a major nuclease for the 5'->3' strand-specific processing of DNA ends

Liao, S., Toczylowski, T., & Yan, H. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn616 · Cited by 66

The PIN domain of EXO1 recognizes poly(ADP-ribose) in DNA damage response

Zhang, F., Shi, J., Chen, S.-H., Bian, C., & Yu, X. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv939 · Cited by 67

Dominant Mutations in S. cerevisiae PMS1 Identify the Mlh1-Pms1 Endonuclease Active Site and an Exonuclease 1-Independent Mismatch Repair Pathway

Smith, C. E., Mendillo, M. L., Bowen, N., Hombauer, H., Campbell, C. S., Desai, A. B., Putnam, C. D., & Kolodner, R. D. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003869 · Cited by 60

Sensing and Processing of DNA Interstrand Crosslinks by the Mismatch Repair Pathway

Kato, N., Kawasoe, Y., Williams, H., Coates, E., Roy, U., Shi, Y., Beese, L. S., Schärer, O. D., Yan, H., Gottesman, M. E., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.032 · Cited by 61

EXO1 overexpression is associated with poor prognosis of hepatocellular carcinoma patients

Dai, Y., Tang, Z., Yang, Z., Zhang, L., Deng, Q., Zhang, X., Yu, Y., Liu, X., & Zhu, J. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1534511 · Cited by 56

Gene Expression Profile and Toxic Effects in Human Bronchial Epithelial Cells Exposed to Zearalenone

So, M. Y., Tian, Z., Phoon, Y. S., Sha, S., Antoniou, M. N., Zhang, J., Wu, R. S. S., & Tan-Un, K. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096404 · Cited by 56

A mutation in EXO1 defines separable roles in DNA mismatch repair and post-replication repair

Tran, P. T., Fey, J. P., Erdeniz, N., Gellon, L., Boiteux, S., & Liskay, R. M. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.05.004 · Cited by 60

Send in the Clamps: Control of DNA Translesion Synthesis in Eukaryotes

Jansen, J. G., Fousteri, M. I., & de Wind, N. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.11.005 · Cited by 55

Human Adipose Stromal Cells (ASC) for the Regeneration of Injured Cartilage Display Genetic Stability after In Vitro Culture Expansion

Neri, S., Bourin, P., Peyrafitte, J.-A., Cattini, L., Facchini, A., & Mariani, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077895 · Cited by 53

The search for a human Holliday junction resolvase

West, S. C. (2009) · Biochemical Society Transactions · doi:10.1042/bst0370519 · Cited by 53

Mutagenic roles of DNA “repair” proteins in antibody diversity and disease-associated trinucleotide repeat instability

Slean, M. M., Panigrahi, G. B., Ranum, L. P. W., & Pearson, C. E. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.014 · Cited by 54

Mechanism of DNA damage tolerance

Bi, X. (2015) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v6.i3.48 · Cited by 59

Structural Basis of SOSS1 Complex Assembly and Recognition of ssDNA

Ren, W., Chen, H., Sun, Q., Tang, X., Lim, S. C., Huang, J., & Song, H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.020 · Cited by 48

The hSNM1 protein is a DNA 5'-exonuclease

Hejna, J., Philip, S., Ott, J., Faulkner, C., & Moses, R. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm530 · Cited by 49

Coordinated Activity of Y Family TLS Polymerases and EXO1 Protects Non-S Phase Cells from UV-Induced Cytotoxic Lesions

Sertic, S., Mollica, A., Campus, I., Roma, S., Tumini, E., Aguilera, A., & Muzi-Falconi, M. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.02.017 · Cited by 45

Human exonuclease 1 (EXO1) activity characterization and its function on flap structures

Keijzers, G., Bohr, V. A., & Rasmussen, L. J. (2015) · Bioscience Reports · doi:10.1042/bsr20150058 · Cited by 48

Vpr and Its Cellular Interaction Partners: R We There Yet?

Fábryová, H., & Strebel, K. (2019) · Cells · doi:10.3390/cells8111310 · Cited by 46

hMSH4-hMSH5 Adenosine Nucleotide Processing and Interactions with Homologous Recombination Machinery

Snowden, T., Shim, K.-S., Schmütte, C., Acharya, S., & Fishel, R. A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m704060200 · Cited by 47

The SNM1/Pso2 family of ICL repair nucleases: From yeast to man

Cattell, E., Sengerová, B., & McHugh, P. J. (2010) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20556 · Cited by 46

Mind the gap: keeping UV lesions in check

Novarina, D., Amara, F., Lazzaro, F., Plevani, P., & Muzi-Falconi, M. (2011) · DNA Repair · doi:10.1016/j.dnarep.2011.04.030 · Cited by 43

RAD50 Is Required for Efficient Initiation of Resection and Recombinational Repair at Random, γ-Induced Double-Strand Break Ends

Westmoreland, J., Ma, W., Yan, Y., Hulle, K. V., Malkova, A., & Resnick, M. A. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000656 · Cited by 44

Distinct roles of RECQ1 in the maintenance of genomic stability

Wu, Y., & Brosh, R. M. (2010) · DNA repair · doi:10.1016/j.dnarep.2009.12.010 · Cited by 41

Exonuclease 1 preferentially repairs mismatches generated by DNA polymerase α

Liberti, S. E., Larrea, A. A., & Kunkel, T. A. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.11.001 · Cited by 40

Exonuclease 1 (Exo1) Participates in Mammalian Non-Homologous End Joining and Contributes to Drug Resistance in Ovarian Cancer

He, D., Li, T., Sheng, M., & Yang, B. (2020) · Medical Science Monitor · doi:10.12659/msm.918751 · Cited by 40

Homologous Recombination Rescues Mismatch-Repair-Dependent Cytotoxicity of SN1-Type Methylating Agents in S. cerevisiae

Ćejka, P., Mojaš, N., Gillet, L. C. J., Schär, P., & Jiricny, J. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.032 · Cited by 40

DNA double-strand break processing: the beginning of the endPreprint

Raynard, S. J., Niu, H., & Sung, P. (2008) · Genes & Development · doi:10.1101/gad.1742408 · Cited by 42

Inhibition of DNA double-strand break repair by the Ku heterodimer in mrx mutants of Saccharomyces cerevisiae

Wasko, B. M., Holland, C., Resnick, M. A., & Lewis, L. K. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.09.010 · Cited by 39

Activation of Saccharomyces cerevisiae Mlh1-Pms1 Endonuclease in a Reconstituted Mismatch Repair System

Smith, C. E., Bowen, N., Graham, W. J., Goellner, E. M., Srivatsan, A., & Kolodner, R. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.662189 · Cited by 35

Comparative Analysis of Meiotic Progression in Female Mice Bearing Mutations in Genes of the DNA Mismatch Repair Pathway1

Kan, R., Sun, X., Kolas, N. K., Avdievich, E., Kneitz, B., Edelmann, W., & Cohen, P. E. (2007) · Biology of Reproduction · doi:10.1095/biolreprod.107.065771 · Cited by 38

Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates

Ehmsen, K. T., & Heyer, W. (2008) · Genome dynamics and stability · doi:10.1007/7050_2008_039 · Cited by 35

The significance of Exonuclease 1 K589E polymorphism on hepatocellular carcinoma susceptibility in the Turkish population: a case–control study

Bayram, S., Akkız, H., Bekar, A., Akgöllü, E., & Yıldırım, S. (2011) · Molecular Biology Reports · doi:10.1007/s11033-011-1406-x · Cited by 36

Homologous recombination rescues ssDNA gaps generated by nucleotide excision repair and reduced translesion DNA synthesis in yeast G2 cells

Ma, W., Westmoreland, J. W., & Resnick, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301676110 · Cited by 33

DNA repair gene polymorphisms and tobacco smoking in the risk for colorectal adenomas

Gao, Y., Hayes, R. B., Huang, W., Caporaso, N. E., Burdette, L. A., Yeager, M., Chanock, S. J., & Berndt, S. I. (2011) · Carcinogenesis · doi:10.1093/carcin/bgr071 · Cited by 34

Alterations in cellular metabolism triggered by URA7 or GLN3 inactivation cause imbalanced dNTP pools and increased mutagenesis

Schmidt, T. T., Reyes, G. X., Gries, K., Ceylan, C. Ü., Sharma, S., Meurer, M., Knop, M., Chabes, A., & Hombauer, H. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618714114 · Cited by 33

Brc1-Mediated Rescue of Smc5/6 Deficiency: Requirement for Multiple Nucleases and a Novel Rad18 Function

Lee, K. M., Nizza, S. T., Hayes, T., Bass, K. L., Irmisch, A., Murray, J. M., & O’Connell, M. J. (2007) · Genetics · doi:10.1534/genetics.106.067801 · Cited by 33

Activities of human exonuclease 1 that promote cleavage of transcribed immunoglobulin switch regions

Vallur, A. C., & Maizels, N. (2008) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0805327105 · Cited by 31

Proteomic Analysis Reveals a Novel Mutator S (MutS) Partner Involved in Mismatch Repair Pathway

Chen, Z., Tran, M. K., Tang, M., Wang, W., Gong, Z., & Chen, J. (2016) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.056093 · Cited by 33

Tumor progression in Apc1638N mice with Exo1 and Fen1 deficiencies

Kucherlapati, M. H., Nguyen, A. A., Kuraguchi, M., Yang, K., Fan, K., Bronson, R. T., Wei, K., Lipkin, M., Edelmann, W., & Kucherlapati, R. (2007) · Oncogene · doi:10.1038/sj.onc.1210453 · Cited by 33

Crystal structure of the NurA–dAMP–Mn2+ complex

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