Maintaining genome stability at the replication fork

Instability and decay of the primary structure of DNA

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Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints

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DNA Topoisomerases: Structure, Function, and Mechanism

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Cellular roles of DNA topoisomerases: a molecular perspective

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RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO

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Concepts in sumoylation: a decade on

Geiss‐Friedlander, R., & Melchior, F. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2293 · Cited by 1,844

DNA TOPOISOMERASES

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Trinucleotide Repeat Disorders

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Regulation of DNA repair throughout the cell cycle

Branzei, D., & Foiani, M. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2351 · Cited by 1,228

The Bloom's syndrome helicase suppresses crossing over during homologous recombination

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Genome-Protective Topoisomerase 2a-Dependent G2 Arrest Requires p53 in hTERT-Positive Cancer Cells

Lockwood, N., Martini, S., Lopez-Pardo, A., Deiss, K., Segeren, H. A., Semple, R. K., Collins, I., Repana, D., Cobbaut, M., Soliman, T. N., et al. (2022) · Cancer Research · doi:10.1158/0008-5472.can-21-1785 · Cited by 5

Quick replication fork stop by overproduction of Escherichia coli DinB produces non-proliferative cells with an aberrant chromosome

Ikeda, M., Shinozaki, Y., Uchida, K., Ohshika, Y., Furukohri, A., Maki, H., & Akiyama, M. T. (2012) · Genes & Genetic Systems · doi:10.1266/ggs.87.221 · Cited by 5

Systematic Identification of Determinants for Single-Strand Annealing-Mediated Deletion Formation inSaccharomyces cerevisiae

Segura‐Wang, M., Onishi‐Seebacher, M., Stütz, A. M., Mardin, B. R., & Korbel, J. O. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.300165 · Cited by 5

Proteolytic control of genome integrity at the replication fork

Rageul, J., Weinheimer, A. S., Park, J. J., & Kim, H. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102657 · Cited by 5

Active Replication Checkpoint Drives Genome Instability in Fission Yeast mcm4 Mutant

Kim, S. M., & Forsburg, S. L. (2020) · Molecular and Cellular Biology · doi:10.1128/mcb.00033-20 · Cited by 5

Uncovering Novel lncRNAs Linked to Melanoma Growth and Migration with CRISPR Inhibition Screening

Petroulia, S., Hockemeyer, K., Tiwari, S., Berico, P., Shamloo, S., Banijamali, S. E., de Miera, E. V., Gong, Y., Thandapani, P., Wang, E., et al. (2025) · Cancer Research Communications · doi:10.1158/2767-9764.crc-24-0416 · Cited by 4

Radiation-Induced Delayed Genome Instability and Hypermutation in Mammalian Cells

Allen, C., Fujimori, A., Okayasu, R., & Nickoloff, J. A. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6280-4_9 · Cited by 4

DNA Repair Dysregulation in Cancer: From Molecular Mechanisms to Synthetic Lethal Opportunities

Nickoloff, J. A. (2014) · Springer eBooks · doi:10.1007/978-94-017-9421-3_2 · Cited by 5

Extension, torque, and supercoiling in single, stretched, and twisted DNA molecules

Lam, P.-M., & Zhen, Y. (2015) · The Journal of Chemical Physics · doi:10.1063/1.4934988 · Cited by 4

Checkpoint phosphorylation sites on budding yeast Rif1 protect nascent DNA from degradation by Sgs1-Dna2

Gali, V. K., Monerawela, C., Laksir, Y., Hiraga, S., & Donaldson, A. D. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1011044 · Cited by 4

The DNA Damage Response: Roles in Cancer Etiology and Treatment

Butler, L. R., Gilad, O., & Brown, E. J. (2018) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-75836-7_2 · Cited by 4

Cooperation between non-essential DNA polymerases contributes to genome stability in Saccharomyces cerevisiae

Meyer, D. H., Fu, B. X. H., Chavez, M., Loeillet, S., Cerqueira, P. G., Nicolas, A. G., & Heyer, W. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.02.004 · Cited by 5

A Conserved Histone H3-H4 Interface Regulates DNA Damage Tolerance and Homologous Recombination during the Recovery from Replication Stress

Hayashi, M., Keyamura, K., Yoshida, A., Ariyoshi, M., Akanuma, G., & Hishida, T. (2021) · Molecular and Cellular Biology · doi:10.1128/mcb.00044-20 · Cited by 4

An algorithm and application to efficiently analyse DNA fibre data

Kirilov, T., Gospodinov, A. G., & Kirilov, K. (2023) · Biotechnology & Biotechnological Equipment · doi:10.1080/13102818.2023.2206488 · Cited by 4

DNA damage tolerance branches out toward sister chromatid cohesion

Branzei, D. (2015) · Molecular & Cellular Oncology · doi:10.1080/23723556.2015.1035478 · Cited by 4

Replication forks reverse at high frequency upon replication stress in Physarum polycephalum

Maric, C. A., & Bénard, M. (2014) · Chromosoma · doi:10.1007/s00412-014-0471-z · Cited by 4

Inter-telomeric recombination is present in telomerase-positive human cells

Dlaska, M., Schöffski, P., & Bechter, O. E. (2013) · Cell Cycle · doi:10.4161/cc.25136 · Cited by 5

Schizosaccharomyces pombe Assays to Study Mitotic Recombination Outcomes

Hylton, H. M., Lucas, B. E., & Petreaca, R. C. (2020) · Genes · doi:10.3390/genes11010079 · Cited by 4

A novel function for the mitotic checkpoint protein Mad2p in translation

Gay, S. (2018) · Molecular & Cellular Oncology · doi:10.1080/23723556.2018.1494949 · Cited by 4

Cytosolic DNA and intracellular Ca2+: Maintaining genome stability during replication stress

Li, S., Lu, H.-T., & You, Z. (2025) · DNA repair · doi:10.1016/j.dnarep.2025.103877 · Cited by 3

The Converging Roles of Nucleases and Helicases in Genome Maintenance and the Aging Process

Margariti, A., Daniil, P., & Rampias, T. N. (2025) · Life · doi:10.3390/life15111729 · Cited by 3

Genome instability: Does genetic diversity amplification drive tumorigenesis?

Lane, A. B., & Clarke, D. J. (2012) · BioEssays · doi:10.1002/bies.201200082 · Cited by 3

Research progress on the fanconi anemia signaling pathway in non-obstructive azoospermia

Xu, H., Zhang, Y., Wang, C., Fu, Z., Lv, J., Yang, Y., Zhang, Z., Qi, Y., Meng, K., Yuan, J., et al. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1393111 · Cited by 3

The multifaceted roles of the Ctf4 replisome hub in the maintenance of genome integrity

Branzei, D., Bene, S., Gangwani, L., & Szakál, B. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103742 · Cited by 3

Nicotine interacts with DNA lesions induced by alpha radiation which may contribute to erroneous repair in human lung epithelial cells

Boroumand, N., Baghdissar, C., Elihn, K., & Lundholm, L. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117009 · Cited by 3

Clearance of roadblocks in replication fork restart

Longerich, S., & Sung, P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110698108 · Cited by 3

LIM protein Ajuba promotes liver cell proliferation through its involvement in DNA replication and DNA damage control

Dommann, N., Gavini, J., Sánchez‐Taltavull, D., Baier, F. A., Birrer, F., Loforese, G., Candinas, D., & Stroka, D. (2022) · FEBS Letters · doi:10.1002/1873-3468.14371 · Cited by 3

Fork restart protein, PriA, binds around oriC after depletion of nucleotide precursors: Replication fork arrest near the replication origin

Tanaka, T., Nishito, Y., & Masai, H. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.01.108 · Cited by 3

Expression profile and in silico characterization of novel RTF2h gene under oxidative stress in Indian catfish, Clarias magur (Hamilton 1822)

Yadav, P., Tripathi, R. K., Singh, R. K., & Mohindra, V. (2016) · Molecular Biology Reports · doi:10.1007/s11033-016-4081-0 · Cited by 3

Double-Strand Break Repair

Gelot, C., Guen, T. L., Ragu, S., & López, B. S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00020-3 · Cited by 3

Cell-Autonomous (Cell-Intrinsic) Stress Responses

Land, W. G. (2018) · Springer eBooks · doi:10.1007/978-3-319-78655-1_18 · Cited by 4

Spontaneous DNA-RNA hybrids: differential impacts throughout the cell cycle

Gómez‐González, B., Barroso, S. I., Herrera‐Moyano, E., & Aguilera, A. (2020) · Cell Cycle · doi:10.1080/15384101.2020.1728015 · Cited by 3

Mechanisms of genome instability in Hutchinson-Gilford progeria

Zhang, H., & Cao, K. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1435-x · Cited by 2

Alterations in Synthesis and Repair of DNA during the Development of Loach Misgurnus fossilis

Gening, L. V., Лахин, А. В., Makarova, I., Nenasheva, V. V., Andreeva, L., & Tarantul, V. Z. (2016) · Journal of Developmental Biology · doi:10.3390/jdb4010006 · Cited by 2

Exploring Bioinformatics Tools to Analyze the Role of CDC6 in the Progression of Polycystic Ovary Syndrome to Endometrial Cancer by Promoting Immune Infiltration

Song, Y., Zhang, J., Li, Y., Cheng, L., Song, H., Zhang, Y., Du, G., Yu, S., Zou, Y., & Xu, Q. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312974 · Cited by 2

Determination of DNA lesion bypass using a ChIP-based assay

Wu, D., Banerjee, A. T., Cai, S., Li, N., Han, C., Bai, X., Zhang, J., & Wang, Q. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103230 · Cited by 2

Isovalerylspiramycin I inhibits proliferation, migration and invasion of osteosarcoma cells by targeting Topoisomerase 1 and suppressing the ataxia telangiectasia and Rad3‐related/checkpoint kinase 1 pathway

Liang, J., Zhang, P., He, K., Zhang, Y., Ding, X., Li, Q., Zhou, W., Hu, H., Zhang, J., & Zhou, Y. (2023) · Clinical and Translational Discovery · doi:10.1002/ctd2.203 · Cited by 2

The regulatory subunits of CK2 complex mediate DNA damage response and virulence in Candida Glabrata

Ni, Q., Wu, X., Su, T., Jiang, C., Dong, D., Wang, D., Chen, W., Cui, Y., & Peng, Y. (2023) · BMC Microbiology · doi:10.1186/s12866-023-03069-4 · Cited by 2

Ubiquitin protease Ubp1 cooperates with Ubp10 and Ubp12 to revert lysine-164 PCNA ubiquitylation at replication forks

Zamarreño, J., Rodríguez, S., Muñoz, S., Bueno, A., & Sacristán, M. P. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf076 · Cited by 3

Wnt10b signaling regulates replication stress–induced chromosomal instability in human cancer

Haas, A., Wenz, F., Hattemer, J., Wesslowski, J., Davidson, G. R., Voloshanenko, O., Boutros, M., Acebrón, S. P., & Bastians, H. (2025) · Life Science Alliance · doi:10.26508/lsa.202503295 · Cited by 2

Real-time imaging of rotation during synthesis by the replisome

Retzer, T. M., Rajappa, L., Takahashi, M., Hamdan, S. M., & Duderstadt, K. E. (2026) · Science Advances · doi:10.1126/sciadv.adx4089 · Cited by 2

Cell Cycle Regulation of DNA Replication in S. cerevisiae

Jorrit, M. (2011) · InTech eBooks · doi:10.5772/19055 · Cited by 2

Extending the Interaction Repertoire of FHA and BRCT Domains

Lindsay, A., & Guarné, A. (2013) · InTech eBooks · doi:10.5772/51670 · Cited by 2

Utilization of fluorescence in situ hybridization with cytokeratin discriminators in TOP2A assessment of chemotherapy-treated patients with breast cancer

Pierceall, W. E., Sprott, K. M., Heikkinen, T., Heikkilä, P., Alaparthi, L. P., Aittomäki, K., Al-Adhami, M., Villegas-Bergazzi, V., Meyer, J. L., Kutok, J. L., et al. (2011) · Human Pathology · doi:10.1016/j.humpath.2011.08.018 · Cited by 2

The programme of DNA replication: beyond genome duplication

Gómez‐Escoda, B., & Wu, P.-Y. J. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130209 · Cited by 2

Synchronization and Desynchronization of Cells by Interventions on the Spindle Assembly Checkpoint

Jèmaà, M., Manic, G., & Vitale, I. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6603-5_5 · Cited by 2

Rapid Detection of γ-H2Av Foci in Ex Vivo MMS-Treated Drosophila Imaginal Discs

Khodaverdian, V. Y., & McVey, M. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7187-9_19 · Cited by 2

More tasks for Dna2 in S-phase

Aparicio, T., & Gautier, J. (2012) · Cell Cycle · doi:10.4161/cc.22807 · Cited by 2

Characterization of the multifunctional XPG protein during Nucleotide-excision-repair

Schubert, S. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4515 · Cited by 2

Folate deficiency facilitates coordination of KDM6A with p53 in response to DNA damagePreprint

Gao, J., Zou, J., Li, J., Zhang, Y., Qiao, L., Wang, F., Bao, Y., Hu, J., Zhang, T., Xie, Q., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/591768 · Cited by 2

Asprosin-driven metabolic-epigenetic rewiring attenuates mesenchymal stem cell senescence with therapeutic benefits for infarcted hearts

Zhang, Z., Wang, Z., Zhu, L., Chen, T., Chen, R., Wu, Z., Chen, J., Zhang, H., Wang, M., Liu, J., et al. (2026) · Journal of Advanced Research · doi:10.1016/j.jare.2026.01.073 · Cited by 1

Cancer mutations in RAD51 and its paralogues

Valentine, A. L., Huth, I. L., Duff, N. M., Rabbani, A. Z., Donahue, K. N., Bush, W. A., Bouley, R. A., & Petreaca, R. C. (2026) · PLoS ONE · doi:10.1371/journal.pone.0349105 · Cited by 1

Eukaryote DNA Replication and Recombination: an Intimate Association

Ramsay, J., Al-Zeer, K., & Jacob, Z. (2011) · InTech eBooks · doi:10.5772/19995 · Cited by 1

Mechanisms of Recurrent Chromosomal Translocations

Frock, R. L., Hu, J., & Alt, F. W. (2015) · Springer eBooks · doi:10.1007/978-3-319-19983-2_3 · Cited by 1

Giardia duodenalis carries out canonical homologous recombination and single-strand annealing

García‐Lepe, U. O., Espinoza-Corona, S., Bazán‐Tejeda, M. L., Núñez-Jurado, F. M., & Bermúdez‐Cruz, R. M. (2022) · Research in Microbiology · doi:10.1016/j.resmic.2022.103984 · Cited by 1

The central role of Pin1 in age-related cancer signaling pathways

Xie, G., Okuda, S., Gao, J., Wu, T., Jeong, J., Lu, K. P., & Zhou, X. Z. (2025) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2025.05.011 · Cited by 3

Regulation of DNA Synthesis and Replication Checkpoint Activation During C. elegans Development

Ruijtenberg, S., van den Heuvel, S., & The, I. (2011) · InTech eBooks · doi:10.5772/19397 · Cited by 1

Methods to Study the Atypical Roles of DNA Repair and SMC Proteins in Gene Silencing

Peterson, M. R., Hamdani, O., & Kamakaka, R. T. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6545-8_10 · Cited by 1

Homologous recombination in mammalian cells: From molecular mechanisms to pathology

Ragu, S., Matos-Rodrigues, G. E., THOMAS, M. L., & López, B. S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85679-9.00020-9 · Cited by 2

Expression and functional analysis of various structural domains of tobacco topoisomerase II: To understand the mechanistic insights of plant type II topoisomerases

Singh, B. N., Achary, V. M. M., Venkatapuram, A. K., Parmar, H., Karippadakam, S., Sopory, S. K., & Reddy, M. K. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.11.019 · Cited by 1

The kinase MK2 in DNA replication upon genotoxic stress and chemotherapy

Köpper, F. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1445 · Cited by 1

New insights on human essential genes based on integrated analysisPreprint

Chen, H., Zhang, Z., Jiang, S., Li, R., Li, W., Zhao, C., Hong, H., Huang, X., Li, H., & Bo, X. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/260224 · Cited by 1

Bacterial chromosome replication: does precatenation occur in vivo?

Tolmatcheva, A. O. (2019) · Enlighten: Theses (The University of Glasgow) · doi:10.5525/gla.thesis.40938 · Cited by 1

Managing Single-Stranded DNA during Replication Stress in Fission Yeast

Sabatinos, S., & Forsburg, S. L. (2021) · doi:10.32920/14637963 · Cited by 1

DNA Replication: Mammalian

Smith, S. J., Li, C. M., Hickey, R. J., & Malkas, L. H. (2014) · Wiley eBooks · doi:10.1002/9780470015902.a0001041.pub3 · Cited by 1

Replication | DNA Polymerase α – Primase Complex: A Fundamental Element in the Maintenance of Genome Integrity

Muzi-Falconi, M., & Plevani, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00126-2 · Cited by 1

Distinctive nuclear zone for RAD51-mediated homologous recombinational DNA repairPreprint

Horikoshi, Y., Shima, H., 孫, 継., Kobayashi, W., Schmid, V. J., Ochiai, H., Shi, L., Fukuto, A., Kinugasa, Y., Kurumizaka, H., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.29.470307 · Cited by 1

The Relationship Between Replication and Recombination

Bedina, A. (2011) · InTech eBooks · doi:10.5772/18485

Promoting replication and repair in the right place at the right time (comment on DOI 10.1002/bies.201300161)

Alabert, C. (2014) · BioEssays · doi:10.1002/bies.201400037

Model Systems Facilitating an Understanding of Mechanisms for Oncogene Amplification

Watanabe, T. (2013) · InTech eBooks · doi:10.5772/55119

DNA Damage Checkpoint Signaling Pathways in Human Cancer

Abraham, R. T., & Halazonetis, T. D. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1216-8_3

Role of the RPA-Sgs1 interaction in stabilizing stalled replication forks

Hegnauer, A. M. (2011) · edoc (University of Basel) · doi:10.5451/unibas-005705705

The Mcm2-7 Replicative Helicase is Essential to Coordinate DNA replication, Checkpoint Regulation and Sister Chromatid Cohesion

Tsai, F.-L. (2012) · D-Scholarship@Pitt (University of Pittsburgh)

Estudo das funções da proteína Kin3 de Saccharomyces cerevisiae na resposta a danos no DNA

Moura, D. J. (2010) · Americanae (AECID Library)

FBH1: A new checkpoint factor

Boyer, A.-S., & Sørensen, C. S. (2015) · Oncotarget · doi:10.18632/oncotarget.5099

Biological activity of a Py-Im polyamide androgen receptor antagonist

Phillips, J. W. (2011) · Journal of Pediatric Hematology/Oncology · doi:10.7907/mph7-d492

Checkpoint tension relief

Schuldt, A. J. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3178

DNA-Protein Complexes Created by Mutant EcoRII Methyltransferase and Quinolone Antibiotics in Escherichia coli

Henderson, M. L. (2014) · DukeSpace (Duke University)

Taking the stress out of replication

Leslie, M. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.2121if

Molecular characterization of pluripotency in embryos and embryonic stem cells

Gómez, J. P. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Selective targeting of cancer cells through inhibition of Checkpoint kinase 1

Hasvold, G. (2012) · NORA - Norwegian Open Research Archives

Système de recombineering pour les bactériophages infectant Lactococcus lactis

Moisan, M. (2012) · Corpus Université Laval (Université Laval)

UNIVERSIDADE FEDERAL DO RIO GRANDE DO NORTE CENTRO DE CIÊNCIAS BIOLÓGICAS PROGRAMA DE PÓS-GRADUAÇÃO EM BIOQUÍMICA

Maíra, N., & de Medeiros, C. (2014)

UNIVERSITÁ DEGLI STUDI DI MILANO-BICOCCA Facoltà di Scienze Matematiche Fisiche e Naturali Dipartimento di Biotecnologie e Bioscienze Dottorato in Biotecnologie industriali, XXVI ciclo

Longhese, M. P. (2013)

The Involvement of 5-Hydroxymethylcytosine in Two DNA Metabolism Pathways: Transcription and double stranded DNA Breaks

Robertson, J. H. (2015) · NORA - Norwegian Open Research Archives

Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination

Mundia, M. M. (2016) · The Atrium (University of Guelph)

Characterization of RACK7 as a Novel Factor Involved in BRCA1 Mutation Mediated Breast Cancer

Verma, I. M., Zhu, Q., Preyer, M., & Kretz-Rommel, A. (2012)

Assembly of Slx4 Checkpoint Signaling Complexes Behind Stressed DNA Replication Forks

Balint, A. (2016) · TSpace (University of Toronto)

Identification of Proteins Involved in the Maintenance of Genome Stability

Cheng, Y., & Hang, E. (2015) · TSpace (University of Toronto)

DNA Polymerase Zeta-Dependent Mutagenesis: Molecular Specificity, Extent of Error-Prone Synthesis, and the Role of dNTP Pools

Kochenova, O. V. (2016) · DigitalCommons@UNMC

USP9X controls DNA replication fork stability and the replication stress checkpoint through Claspin

McGarry, E. (2016) · Arrow@dit (Dublin Institute of Technology) · doi:10.13025/17576

Aging: Fewer Obstacles to DNA Replication?

Ivessa, A. (2017) · Trends in cancer · doi:10.1016/j.trecan.2017.04.003

Characterizing the functions of Trypanosoma brucei TIF2 and TRF in regulation of antigenic variation

Jehi, S. E. (2014) · OhioLink ETD Center (Ohio Library and Information Network)

Function of the Rad53 Checkpoint Kinase Molecular Basis of the Essential S Phase

Pellicioli, A., Chabes, A., Tsai, M., Wang, S., Fazio, A., Hammet, A., Hoch, N. C., & Buckland, R. J. (2014)

Replicating Chromatin in the Eukaryotic Genome

Gordon, M. R., Bartlett, D. A., & Gilbert, D. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803480-4.00017-x

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

Drug Candidate Discovery: Targeting Bacterial Topoisomerase I Enzymes for Novel Antibiotic Leads

Sandhaus, S. (2017) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fidc004005

Oncofetal HMGA2 as a key regulator of telomere stability through control of DNA topology

Ramani, P. D. (2018) · doi:10.32657/10220/46217

Genomic Instability: DNA Repair and Cancer

Carlos, A. R. (2019) · Learning materials in biosciences · doi:10.1007/978-3-030-11812-9_5

A DNS-hibaelkerülő útvonalak szabályozásának genetikai vizsgálata

Gervai, J. Z. (2018) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2017.136

The progress in the mechanistic studies of maintaining replication fork stability in eukaryotic cells

Liu, Y. (2014) · Shengming kexue

The DNA damage response during DNA replication

Branzei, D., & Foiani, M. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.09.003 · Cited by 240

Interplay of replication checkpoints and repair proteins at stalled replication forks

Branzei, D., & Foiani, M. (2007) · DNA repair · doi:10.1016/j.dnarep.2007.02.018 · Cited by 133

Preventing replication fork collapse to maintain genome integrity

Cortez, D. (2015) · DNA Repair · doi:10.1016/j.dnarep.2015.04.026 · Cited by 223

Replication forks and replication checkpoints in repair

Branzei, D., & Foiani, M. (2007) · Topics in current genetics · doi:10.1007/978-3-540-71021-9_7