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

A multistep genomic screen identifies new genes required for repair of DNA double-strand breaks in Saccharomyces cerevisiae

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

End-processing during non-homologous end-joining: a role for exonuclease 1

Bahmed, K., Seth, A., Nitiss, K. C., & Nitiss, J. L. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq886 · Cited by 29

Exo1 independent DNA mismatch repair involves multiple compensatory nucleases

Desai, A. B., & Gerson, S. L. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.06.005 · Cited by 28

Poly(ADP-ribose)-binding promotes Exo1 damage recruitment and suppresses its nuclease activities

Cheruiyot, A., Paudyal, S. C., Kim, I.-K., Sparks, M. A., Ellenberger, T., Piwnica-Worms, H. M., & You, Z. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.09.021 · Cited by 27

FANCD2-Associated Nuclease 1 Partially Compensates for the Lack of Exonuclease 1 in Mismatch Repair

Kratz, K., Borán, M. S., Kobayashi-Era, S., Koh, C. C., Oliveira, G. P., Kobayashi, S., Oliveira, A. M., Zou, X., Richter, J., Tsuda, M., et al. (2021) · Molecular and Cellular Biology · doi:10.1128/mcb.00303-21 · Cited by 27

TREX1 DNA exonuclease deficiency, accumulation of single stranded DNA and complex human genetic disorders

O’Driscoll, M. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.02.010 · Cited by 27

Mutant huntingtin protein induces MLH1 degradation, DNA hyperexcision, and cGAS–STING-dependent apoptosis

Sun, X., Liu, L., Wu, C., Li, X., Guo, J., Zhang, J., Guan, J., Wang, N., Gu, L., Yang, X., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2313652121 · Cited by 28

Engineering a robust Cas12i3 variant‐mediated wheat genome editing system

Wang, W., Yan, L., Li, J., Zhang, C., He, Y., Li, S., & Xia, L. (2024) · Plant Biotechnology Journal · doi:10.1111/pbi.14544 · Cited by 25

SMYD3 Promotes Homologous Recombination via Regulation of H3K4-mediated Gene Expression

Chen, Y., Tsai, C.-H., Wang, P.-Y., & Teng, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-03385-6 · Cited by 31

Nucleases in homologous recombination as targets for cancer therapy

Bartošová, Z., & Krejčí, L. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.06.010 · Cited by 25

The nature of meiotic chromosome dynamics and recombination in budding yeast

Hong, S., Joo, J. H., Yun, H., & Kim, K. (2019) · The Journal of Microbiology · doi:10.1007/s12275-019-8541-9 · Cited by 25

Exonuclease 1 (EXO1) gene variation and melanoma risk

Song, F., Qureshi, A. A., Zhan, J., Amos, C. I., Lee, J. E., Wei, Q., & Han, J. (2012) · DNA repair · doi:10.1016/j.dnarep.2011.12.005 · Cited by 24

Bacterial DNA repair genes and their eukaryotic homologues: 2. Role of bacterial mutator gene homologues in human disease. Overview of nucleotide pool sanitization and mismatch repair systems.

Arczewska, K. D., & Kuśmierek, J. T. (2007) · Acta Biochimica Polonica · doi:10.18388/abp.2007_3220 · Cited by 23

Hydrolytic function of Exo1 in mammalian mismatch repair

Shao, H., Baitinger, C., Soderblom, E. J., Burdett, V., & Modrich, P. L. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku420 · Cited by 23

Genetic polymorphisms in CDH1 and Exo1 genes elevate the prostate cancer risk in Bangladeshi population

Imtiaz, H., Afroz, S., Hossain, M. A., Bellah, S. F., Rahman, M. M., Kadir, M. S., Sultana, R., Mazid, M. A., & Rahman, M. M. (2019) · Tumor Biology · doi:10.1177/1010428319830837 · Cited by 23

EXO1 is critical for embryogenesis and the DNA damage response in mice with a hypomorphicNbs1allele

Rein, K., Yanez, D. A., Terré, B., Palenzuela, L., Aivio, S., Wei, K., Edelmann, W., Stark, J. M., & Stracker, T. H. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv691 · Cited by 21

Mechanistic Analysis of a DNA End Processing Pathway Mediated by the Xenopus Werner Syndrome Protein

Toczylowski, T., & Yan, H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605044200 · Cited by 22

Wot the ‘L—Does MutL do?

Polosina, Y. Y., & Cupples, C. G. (2010) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2010.07.002 · Cited by 21

Yeast Exonuclease 5 Is Essential for Mitochondrial Genome Maintenance

Burgers, P., Stith, C. M. W., Yoder, B. L., & Sparks, J. L. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01321-09 · Cited by 21

Emerging role of protein phosphatases changes the landscape of phospho-signaling in DNA damage response

Zheng, X.-F., Kalev, P., & Chowdhury, D. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.04.014 · Cited by 24

Exo1 and Mre11 execute meiotic DSB end resection in the protist Tetrahymena

Lukaszewicz, A., Shodhan, A., & Loidl, J. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.08.005 · Cited by 19

Ovarian Cysts in MRL/MpJ Mice Originate from Rete Ovarii

Kon, Y., Konno, A., Hashimoto, Y., & Endoh, D. (2006) · Anatomia Histologia Embryologia · doi:10.1111/j.1439-0264.2006.00728.x · Cited by 19

Biochemical characterization of a cancer-associated E109K missense variant of human exonuclease 1

Bregenhorn, S., & Jiricny, J. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku419 · Cited by 17

Significant association of the EXO1 rs851797 polymorphism with clinical outcome of ovarian cancer

Shi, T., Jiang, R., Wang, P., Xu, Y., Yin, S., Cheng, X., & Zang, R. (2017) · OncoTargets and Therapy · doi:10.2147/ott.s141668 · Cited by 18

EXO1 suppresses double-strand break induced homologous recombination between diverged sequences in mammalian cells

Chen, C.-C., Avdievich, E., Zhang, Y., Zhang, Y., Wei, K., Lee, K., Edelmann, W., Jasin, M., & LaRocque, J. R. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.07.003 · Cited by 18

Exo1 protects DNA nicks from ligation to promote crossover formation during meiosis

Gioia, M., Payero, L., Salim, S., Valamparamban, G. F., Farnaz, A. F., Pannafino, G., Chen, J. J., Ajith, V. P., Momoh, S., Scotland, M. K., et al. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002085 · Cited by 17

Crossover recombination between homologous chromosomes in meiosis: recent progress and remaining mysteries

Payero, L., & Alani, E. (2024) · Trends in Genetics · doi:10.1016/j.tig.2024.09.009 · Cited by 17

DNA Repair in Haploid Context

Mourrain, L., & Boissonneault, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212418 · Cited by 17

The OsGEN-L protein from Oryza sativa possesses Holliday junction resolvase activity as well as 5'-flap endonuclease activity

Yang, Y., Ishino, S., Yamagami, T., Kumamaru, T., Satoh, H., & Ishino, Y. (2012) · The Journal of Biochemistry · doi:10.1093/jb/mvr145 · Cited by 18

Cdc73 suppresses genome instability by mediating telomere homeostasis

Nene, R. V., Putnam, C. D., Li, B.-Z., Nguyen, K. G., Srivatsan, A., Campbell, C. S., Desai, A. B., & Kolodner, R. D. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007170 · Cited by 16

Local nucleosome dynamics and eviction following a double-strand break are reversible by NHEJ-mediated repair in the absence of DNA replicationPreprint

Tripuraneni, V., Memişoğlu, G., MacAlpine, H. K., Tran, T. Q., Zhu, W., Hartemink, A. J., Haber, J. E., & MacAlpine, D. M. (2021) · Genome Research · doi:10.1101/gr.271155.120 · Cited by 16

The Role of Exo1p Exonuclease in DNA End Resection to Generate Gene Conversion Tracts in Saccharomyces cerevisiae

Yin, Y. A., & Petes, T. D. (2014) · Genetics · doi:10.1534/genetics.114.164517 · Cited by 15

Exo1 phosphorylation inhibits exonuclease activity and prevents fork collapse in rad53 mutants independently of the 14-3-3 proteins

Morafraile, E. C., Bugallo, A., Carreira, R., Fernández-García, M., Martı́n-Castellanos, C., Blanco, M. G., & Segurado, M. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa054 · Cited by 13

Biochemical Mechanisms of Genetic Recombination and DNA Repair

Raina, V. B., Jessop, A. M., & Greene, E. C. (2025) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-083024-113931 · Cited by 14

Exonuclease 1 (Exo1) is required for activating response to SN1 DNA methylating agents

Izumchenko, E., Saydi, J., & Brown, K. D. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.09.004 · Cited by 13

The Mre11-Rad50-Xrs2 Complex Is Required for Yeast DNA Postreplication Repair

Ball, L. G., Hanna, M. D., Lambrecht, A. D., Mitchell, B. A., Ziola, B. R., Cobb, J. A., & Xiao, W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109292 · Cited by 15

The Role of Oncogenic Tyrosine Kinase NPM-ALK in Genomic Instability

Lobello, C., Bikos, V., Janíková, A., & Pospı́šilová, Š. (2018) · Cancers · doi:10.3390/cancers10030064 · Cited by 13

Potentially Functional SNPs (pfSNPs) as Novel Genomic Predictors of 5-FU Response in Metastatic Colorectal Cancer Patients

Wang, J., Wang, X., Zhao, M., Choo, S. P., Ong, S. J., Ong, S. Y. K., Chong, S. S., Teo, Y. Y., & Lee, C. G. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111694 · Cited by 12

Differential genetic interactions between Sgs1, DNA-damage checkpoint components and DNA repair factors in the maintenance of chromosome stability

Doerfler, L., Harris, L., Viebranz, E., & Schmidt, K. H. (2011) · Genome Integrity · doi:10.1186/2041-9414-2-8 · Cited by 10

Sgs1 helicase is required for efficient PCNA monoubiquitination and translesion DNA synthesis in Saccharomyces cerevisiae

Li, F., Ball, L. G., Fan, L., Hanna, M. D., & Xiao, W. (2017) · Current Genetics · doi:10.1007/s00294-017-0753-0 · Cited by 11

To trim or not to trim: Progression and control of DSB end resection

Granata, M., Panigada, D., Galati, E., Lazzaro, F., Pellicioli, A., Plevani, P., & Muzi-Falconi, M. (2013) · Cell Cycle · doi:10.4161/cc.25042 · Cited by 12

Sharpening the ends for repair: mechanisms and regulation of DNA resection

Paudyal, S. C., & You, Z. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw043 · Cited by 14

Integrative genomic and network analysis identified novel genes associated with the development of advanced cervical squamous cell carcinoma

Roychowdhury, A., Samadder, S., Das, P. K., Mandloi, S., Addya, S., Chakraborty, C., Basu, P. S., Mondal, R. K., Roy, A. K., Chakrabarti, S., et al. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.09.014 · Cited by 11

Telomere Shortening Mechanisms

Grach, A. (2013) · InTech eBooks · doi:10.5772/55244 · Cited by 11

Altered gene expression profiles and higher frequency of spontaneous DNA strand breaks in APEX2-null thymus

Dan, Y., Ohta, Y., Tsuchimoto, D., Ohno, M., Ide, Y., Sami, M., Kanda, T., Sakumi, K., & Nakabeppu, Y. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.05.003 · Cited by 11

The Significance of Exo1 K589E Polymorphism on Cancer Susceptibility: Evidence Based on a Meta-Analysis

Duan, F., Song, C., Dai, L., Cui, S., Zhang, X., & Zhao, X. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096764 · Cited by 11

Forkhead box proteins as the critical regulators of cisplatin response in tumor cells

Maharati, A., & Moghbeli, M. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175937 · Cited by 9

Evidence that YycJ is a novel 5′–3′ double-stranded DNA exonuclease acting in Bacillus anthracis mismatch repair

Yang, H., Yung, M., Li, L., Hoch, J. A., Ryan, C. M., Kar, U. K., Souda, P., Whitelegge, J. P., & Miller, J. H. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.02.002 · Cited by 11

Inverted repeat-stimulated sister-chromatid exchange events are RAD1-independent but reduced in a msh2 mutant

Nag, D. K. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki835 · Cited by 9

Drug-Sensitive DNA Polymerase δ Reveals a Role for Mismatch Repair in Checkpoint Activation in Yeast

Reha-Krantz, L. J., Siddique, M. S. P., Murphy, K. M., Tam, A. J. C., O’Carroll, M., Lou, S., Schultz, A., & Boone, C. M. (2011) · Genetics · doi:10.1534/genetics.111.131938 · Cited by 8

Inferring cell cycle feedback regulation from gene expression data

Ferrazzi, F., Engel, F. B., Wu, E., Moseman, A. P., Kohane, I. S., Bellazzi, R., & Ramoni, M. F. (2011) · Journal of Biomedical Informatics · doi:10.1016/j.jbi.2011.02.002 · Cited by 8

DNA duplex recognition activates Exo1 nuclease activity

Li, Y., Shen, J., & Niu, H. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.008549 · Cited by 8

Post-replicative lesion processing limits DNA damage-induced mutagenesis

Masłowska, K. H., Wong, R. P. C., Ulrich, H. D., & Pagès, V. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf198 · Cited by 9

Effects of mutations in SGS1 and in genes functionally related to SGS1 on inverted repeat-stimulated spontaneous unequal sister-chromatid exchange in yeast

Nag, D. K., & Cavallo, S. J. (2007) · BMC Molecular Biology · doi:10.1186/1471-2199-8-120 · Cited by 7

XPG-related nucleases are hierarchically recruited for double-stranded rDNA break resection

Barnum, K. J., Nguyen, Y. T., & O’Connell, M. J. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005415 · Cited by 7

EXO1 promotes the meiotic MLH1-MLH3 endonuclease through conserved interactions with MLH1, MSH4 and DNA

Roy, M., Sanchez, A., Guérois, R., Senoussi, I., Cerana, A., Sgrignani, J., Cavalli, A., Rinaldi, A., & Ćejka, P. (2025) · Nature Communications · doi:10.1038/s41467-025-59470-2 · Cited by 5

Identification and fine mapping of qPBR10-1, a novel locus controlling panicle blast resistance in Pigm-containing P/TGMS line

Wu, Y., Xiao, N., Li, Y., Gao, Q., Ning, Y., Yu, L. M., Cai, Y., Pan, C., Zhang, X., Huang, N., et al. (2021) · Molecular Breeding · doi:10.1007/s11032-021-01268-3 · Cited by 6

Mre11 nuclease and C-terminal tail-mediated DDR functions are required for initiating yeast telomere healing

Bhattacharyya, M. K., Matthews, K. M., & Lustig, A. J. (2008) · Chromosoma · doi:10.1007/s00412-008-0153-9 · Cited by 6

Construction and validation of a hypoxia-related risk signature identified EXO1 as a prognostic biomarker based on 12 genes in lung adenocarcinoma

Chen, Q., Chen, S., Wang, J., Zhao, Y., Ye, X., Fu, Y., & Liu, Y. (2023) · Aging · doi:10.18632/aging.204613 · Cited by 5

No association of the exonuclease 1 T439M polymorphism and risk of hepatocellular carcinoma development in the Turkish population: a case-control study.

Bayram, S., Akkız, H., Bekar, A., Akgöllü, E., & Yıldırım, S. (2011) · PubMed · Cited by 5

Breast cancer-associated SNP rs72755295 is a cis-regulatory variation for human EXO1

Shi, Q., Yao, X.-Y., Wang, H., Li, Y.-J., Zhang, X., & Sun, C. (2022) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2021-0420 · Cited by 5

Inhibition of the 5′ to 3′ exonuclease activity of hEXO1 by 8‐oxoguanine

McDowell, H. D., Carney, J. P., & Wilson, T. (2008) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20398 · Cited by 5

Mating-type switching in S. pombe

Arcangioli, B., Roseaulin, L., & Holmes, A. M. (2007) · Topics in current genetics · doi:10.1007/978-3-540-71021-9_9 · Cited by 5

Morphogenetic investigation of metaphase-specific cell death in meiotic spermatocytes in mice

Kon, Y. (2005) · Anatomical Science International · doi:10.1111/j.1447-073x.2005.00117.x · Cited by 5

Discovery of ART5537: A Potent and Selective Small-Molecule Probe for EXO1

Mann, S. E., Davis, O. A., Bomke, J., Cornaciu, I., Elinati, E., Follows, B., Galbiati, A., Geo, L., Grande, D., Jorand‐Lebrun, C., et al. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c02593 · Cited by 4

Association of DNA repair gene polymorphisms with response to cisplatin-based concurrent chemoradiotherapy in patients with cervical carcinoma

Liu, J., Xi, P., Chai, Y., Wang, J., Wang, T., Liu, Z., & Dai, P. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.03.015 · Cited by 4

Analysis of E-cadherin (CDH1) Gene Polymorphism and Its Association with Cervical Cancer Risk in Bangladeshi Women

Rahman, M. A., Hasan, M. M., Hossain, A., Alam, K. M., Razia, S., Mazid, M. A., & Rahman, M. M. (2023) · Asian Pacific Journal of Cancer Prevention · doi:10.31557/apjcp.2023.24.7.2361 · Cited by 4

The roles of fission yeast exonuclease 5 in nuclear and mitochondrial genome stability

Sparks, J. L., Gerik, K. J., Stith, C. M. W., Yoder, B. L., & Burgers, P. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102720 · Cited by 4

Association between three exonuclease 1 polymorphisms and cancer risks: a meta-analysis

Zhou, J., Chen, Z., Zheng, S.-R., Zhuang, X., & Zhong, J. H. (2016) · OncoTargets and Therapy · doi:10.2147/ott.s95258 · Cited by 4

Novel Sensitive Fluorometric Determination of Exonuclease I Using Polydopamine Nanospheres

Li, L., Zhao, Y., Yu, R., Chen, T., & Chu, X. (2017) · Analytical Letters · doi:10.1080/00032719.2017.1368530 · Cited by 3

DNA mismatch repair mediated by Mlh1–Pms1 endonuclease-catalyzed mispair excision

Palacio, T., Calil, F. A., Bowen, N., Griffith, J. D., Putnam, C. D., & Kolodner, R. D. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2528670122 · Cited by 3

Role of Repair Enzymes - Damage Control of DNA From Ageing pans

Singh, S., & Purohit, M. (2016) · Pharmaceutical and Biosciences Journal · doi:10.20510/ukjpb/4/i3/107832 · Cited by 2

Exo1-protected DNA nicks direct crossover formation in meiosisPreprint

Gioia, M., Payero, L., Pannafino, G., Chen, J. J., Salim, S., Fajith, G., Farnaz, A. F., Momoh, S., Scotland, M. K., Raghavan, V., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.29.458102 · Cited by 2

A sequence-dependent exonuclease activity from Tetrahymena thermophila

Tom, H.-I., & Greider, C. W. (2010) · BMC Biochemistry · doi:10.1186/1471-2091-11-45 · Cited by 1

Identification of key enzalutamide-resistance-related genes in castration-resistant prostate cancer and verification of RAD51 functions

Xu, W., Liu, L., Cui, Z., Li, M., Ni, J., Huang, N. J., Zhang, Y., Luo, J., Sun, L., & Sun, F. (2023) · Open Medicine · doi:10.1515/med-2023-0715 · Cited by 1

Exo1 cooperates with Tel1/ATM in promoting recombination events at DNA replication forks

Galli, M., Frigerio, C., Colombo, C. V., Casari, E., Longhese, M. P., & Clerici, M. (2024) · iScience · doi:10.1016/j.isci.2024.110410 · Cited by 1

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

Bohr, V. A., & Rasmussen, L. J. (2015) · Cited by 1

Allosteric inhibition of human exonuclease1 (hExo1) through a novel extended β-sheet conformation

Umar, A. A., Liddell, S., Hussain, R., Siligardi, G., Harris, G., Carr, S. B., Asiani, K., Gowers, D. M., Odell, M., & Scott, D. J. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129730 · Cited by 1

Mating-Type Switching in S. Pombe

Arcangioli, B., Roseaulin, L., & Holmes, A. M. (2006) · Springer eBooks · doi:10.1007/4735_2006_0204 · Cited by 1

Nuclease

Zhang, L., & Reha-Krantz, L. J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-374984-0.01069-x · Cited by 1

Functional Characterization of MutS Homologue Mismatch Repair Proteins and their Variants

Kantelinen, J. (2012) · Työväentutkimus Vuosikirja

The mechanism of DNA double-strand break (DSB) resection in human cells

Yang, S.-H. (2013) · Texas ScholarWorks (Texas Digital Library)

Single Nucleotide Polymorphism (K589E) of the EXO1 Gene: Association with Colorectal Cancer Susceptibility and Clinicopathological Features

Aghdaei, H. A. (2014) · Gastroenterology & Hepatology Open Access · doi:10.15406/ghoa.2014.01.00018

THE MULTIFACETED ROLE OF EXONUCLEASE 1 IN DNA REPAIR AND ADULT STEM CELL POPULATIONS

Desai, A. B. (2014) · OhioLink ETD Center (Ohio Library and Information Network)

The Role of Nej1-Lif1 in Double Strand Break Repair Pathway Choice and Non-Homologous End-Joining

Sorenson, K. (2017) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28337

NEW MARKERS FOR BREAST CANCER

Kolab, W. A. E.-M. (2012) · Biochemistry Letters · doi:10.21608/blj.2012.64253

EXPLORING GENOME INTEGRITY PATHWAYS IN SACCHAROMYCES CEREVISIAE

Shanmugan, M. K. (2014) · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) · doi:10.13130/shanmugam-muthukumar_phd2014-01-24

Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation

Mills, C. A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/6jgr-c775

Biochemical characterization of human exonuclease1 (hExo1)

Umar, A. A., Abdulhamid, A., Bagudo, A. I., & Magami, I. M. (2020) · Journal of King Saud University - Science · doi:10.1016/j.jksus.2019.12.025

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