Error-Prone Repair DNA Polymerases in Prokaryotes and Eukaryotes

Class Switch Recombination and Hypermutation Require Activation-Induced Cytidine Deaminase (AID), a Potential RNA Editing Enzyme

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Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli

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Activation-Induced Cytidine Deaminase (AID) Deficiency Causes the Autosomal Recessive Form of the Hyper-IgM Syndrome (HIGM2)

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The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η

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Biochemistry of homologous recombination in Escherichia coli

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The importance of repairing stalled replication forks

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Hypermutation of multiple proto-oncogenes in B-cell diffuse large-cell lymphomas

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DNA Replication Fidelity

Kunkel, T. A., & Bebenek, K. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.497 · Cited by 1,003

Recombinational Repair of DNA Damage in Escherichia coli and Bacteriophage λ

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The Y-Family of DNA Polymerases

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Influence of grape consumption on the human microbiome

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Enhancement of Human DNA Polymerase η Activity and Fidelity Is Dependent Upon a Bipartite Interaction with the Werner Syndrome Protein

Maddukuri, L., Ketkar, A. D., Eddy, S., Zafar, M. K., Griffin, W. C., & Eoff, R. L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.410332 · Cited by 19

A Single Residue Unique to DinB-Like Proteins Limits Formation of the Polymerase IV Multiprotein Complex in Escherichia coli

Cafarelli, T. M., Rands, T. J., Benson, R. W., Rudnicki, P. A., Lin, I., & Godoy, V. G. (2013) · Journal of Bacteriology · doi:10.1128/jb.01349-12 · Cited by 19

Single Nucleotide Variant Detection Using Next Generation Sequencing

Spencer, D. H., Zhang, B., & Pfeifer, J. D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404748-8.00008-3 · Cited by 21

Genetic Requirement for Mutagenesis of the G[8,5-Me]T Cross-Link in Escherichia coli : DNA Polymerases IV and V Compete for Error-Prone Bypass

Raychaudhury, P., & Basu, A. K. (2011) · Biochemistry · doi:10.1021/bi102064z · Cited by 19

Purification and Characterization of the RecA Protein from Neisseria gonorrhoeae

Stohl, E. A., Gruenig, M. C., Cox, M. M., & Seifert, H. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017101 · Cited by 19

Inactivation of the 3′-5′ Exonuclease of the Replicative T4 DNA Polymerase Allows Translesion DNA Synthesis at an Abasic Site

Gac, N. T. L., Delagoutte, E., Germain, M., & Villani, G. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.01.005 · Cited by 19

Escherichia coli DNA polymerase II can efficiently bypass 3,N4-ethenocytosine lesions in vitro and in vivo

Mamun, A. A. M. A., & Humayun, M. Z. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.07.016 · Cited by 19

UBE2V2 (MMS2) is not required for effective immunoglobulin gene conversion or DNA damage tolerance in DT40

Simpson, L. J., & Sale, J. E. (2005) · DNA repair · doi:10.1016/j.dnarep.2004.12.002 · Cited by 19

Transcription increases methylmethane sulfonate-induced mutations in alkB strains of Escherichia coli

Fix, D. F., Canugovi, C., & Bhagwat, A. S. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.04.008 · Cited by 18

Lesion Bypass Activity of DNA Polymerase A from the Extremely Radioresistant Organism Deinococcus radiodurans

Heinz, K., & Marx, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611404200 · Cited by 18

Translesion Synthesis across 1,N6-(2-Hydroxy-3-hydroxymethylpropan-1,3-diyl)-2′-deoxyadenosine (1,N6-γ-HMHP-dA) Adducts by Human and Archebacterial DNA Polymerases

Kotapati, S., Maddukuri, L., Wickramaratne, S., Seneviratne, U. I., Goggin, M. M., Pence, M. G., Villalta, P. W., Guengerich, F. P., Marnett, L. J., & Tretyakova, N. Y. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.396788 · Cited by 19

Mechanisms of mutagenesis induced by DNA lesions: multiple factors affect mutations in translesion DNA synthesis

Zhang, H. (2020) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2020.1768205 · Cited by 18

A genomic island integrated into recA of V ibrio cholerae contains a divergent recA and provides multi‐pathway protection from DNA damage

Rapa, R. A., Islam, A., Monahan, L. G., Mutreja, A., Thomson, N. R., Charles, I. G., Stokes, H. W., & Labbate, M. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12512 · Cited by 18

Critical Analysis of Strand-Biased Somatic Mutation Signatures in TP53versusIg Genes, in Genome-Wide Data and the Etiology of Cancer

Lindley, R. A., & Steele, E. J. (2013) · ISRN Genomics · doi:10.1155/2013/921418 · Cited by 18

Error-free RAD52 pathway and error-prone REV3 pathway determines spontaneous mutagenesis in Saccharomyces cerevisiae

Endo, K., Tago, Y.-I., Daigaku, Y., & Yamamoto, K. (2007) · Genes & Genetic Systems · doi:10.1266/ggs.82.35 · Cited by 18

Comparative Mutagenesis of the C8-Guanine Adducts of 1-Nitropyrene and 1,6- and 1,8-Dinitropyrene in a CpG Repeat Sequence

Hilario, P., Yan, S. F., Hingerty, B. E., Broyde, S. B., & Basu, A. K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m208103200 · Cited by 18

Role of Base Sequence Context in Conformational Equilibria and Nucleotide Excision Repair of Benzo[a]pyrene Diol Epoxide−Adenine Adducts

Yan, S. F., Wu, M., Buterin, T., Naegeli, H., Geacintov, N. E., & Broyde, S. B. (2003) · Biochemistry · doi:10.1021/bi0270081 · Cited by 18

Opposed Steric Constraints in Human DNA Polymerase β and E. coli DNA Polymerase I

Pasquale, F. D., Fischer, D., Grohmann, D., Restle, T., Geyer, A., & Marx, A. (2008) · Journal of the American Chemical Society · doi:10.1021/ja8028284 · Cited by 18

The eternal molecule

Dennis, C., & Campbell, P. (2003) · Nature · doi:10.1038/nature01396 · Cited by 18

Accommodation of a 1S-(−)-Benzo[c]phenanthrenyl-N6-dA Adduct in the Y-Family Dpo4 DNA Polymerase Active Site: Structural Insights through Molecular Dynamics Simulations

Wang, L., Wu, M., Yan, S. F., Patel, D. J., Geacintov, N. E., & Broyde, S. B. (2005) · Chemical Research in Toxicology · doi:10.1021/tx049786v · Cited by 17

Spontaneous mutagenesis is elevated in protease‐defective cells

Mamun, A. A. M. A., & Humayun, M. Z. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06551.x · Cited by 17

Better living with hyper‐mutation

Goodman, M. F. (2016) · Environmental and Molecular Mutagenesis · doi:10.1002/em.22023 · Cited by 17

Yeast Pol η Holds a Cis−Syn Thymine Dimer Loosely in the Active Site during Elongation Opposite the 3‘-T of the Dimer, but Tightly Opposite the 5‘-T

Sun, L., Zhang, K., Zhou, L., Hohler, P. M., Kool, E. T., Yuan, F., Wang, Z., & Taylor, J. (2003) · Biochemistry · doi:10.1021/bi0345687 · Cited by 17

Thermostable DNA polymerases can perform translesion synthesis using 8-oxoguanine and tetrahydrofuran-containing DNA templates

Belousova, E. A., Rechkunova, N. I., & Lavrik, O. I. (2005) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2005.11.001 · Cited by 17

Molecular modeling benzo[a]pyrene N2-dG adducts in the two overlapping active sites of the Y-family DNA polymerase Dpo4

Chandani, S., & Loechler, E. L. (2006) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2006.05.003 · Cited by 17

Computational analysis of mutation spectra

Rogozin, I. B. (2003) · Briefings in Bioinformatics · doi:10.1093/bib/4.3.210 · Cited by 17

A false note of DNA polymerase iota in the choir of genome caretakers in mammals

Gening, L. V., Makarova, А. V., Малашенко, А. М., & Tarantul, V. Z. (2006) · Biochemistry (Moscow) · doi:10.1134/s0006297906020064 · Cited by 17

Aberrant somatic hypermutations in thyroid lymphomas

Takakuwa, T., Miyauchi, A., & Aozasa, K. (2008) · Leukemia Research · doi:10.1016/j.leukres.2008.10.007 · Cited by 17

Escherichia coli Rep DNA helicase and error‐prone DNA polymerase IV interact physically and functionally

Sladewski, T. E., Hetrick, K. M., & Foster, P. L. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07590.x · Cited by 16

Residues in the fingers domain of the translesion DNA polymerase DinB enable its unique participation in error-prone double-strand break repair

Tashjian, T. F., Danilowicz, C., Molza, A.-E., Nguyen, B. H., Prévost, C., Prentiss, M. G., & Godoy, V. G. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006233 · Cited by 16

Mutators and hypermutability in bacteria: the Escherichia coli paradigm

Jayaraman, R. (2009) · Journal of Genetics · doi:10.1007/s12041-009-0058-2 · Cited by 16

Genomic analysis of cancer tissue reveals that somatic mutations commonly occur in a specific motif

Makridakis, N. M., Ferraz, L. F. C., & Reichardt, J. K. V. (2008) · Human Mutation · doi:10.1002/humu.20810 · Cited by 16

Bacterial Stationary-State Mutagenesis and Mammalian Tumorigenesis as Stress-Induced Cellular Adaptations and the Role of Epigenetics

Karpinets, T. V., Greenwood, D., Pogribny, I. P., & Samatova, N. F. (2006) · Current Genomics · doi:10.2174/138920206779315764 · Cited by 16

Architecture of Y‐Family DNA Polymerases Relevant to Translesion DNA Synthesis as Revealed in Structural and Molecular Modeling Studies

Chandani, S., Jacobs, C. L., & Loechler, E. L. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/784081 · Cited by 16

Trans-Lesion DNA Polymerases May Be Involved in Yeast Meiosis

Arbel‐Eden, A., Joseph-Strauss, D., Masika, H., Printzental, O., Rachi, E., & Simchen, G. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.005603 · Cited by 16

Polynucleotide phosphorylase is implicated in homologous recombination and DNA repair in Escherichia coli

Carzaniga, T., Sbarufatti, G., Briani, F., & Dehò, G. (2017) · BMC Microbiology · doi:10.1186/s12866-017-0980-z · Cited by 16

Gerichtete Evolution einer thermostabilen DNA‐Polymerase zur Amplifikation ausgehend von stark geschädigten Templaten

Gloeckner, C., Sauter, K. B. M., & Marx, A. (2007) · Angewandte Chemie · doi:10.1002/ange.200603987 · Cited by 16

Use of genome sequencing to assess nucleotide structure variation of Staphylococcus aureus strains cultured in spaceflight on Shenzhou-X, under simulated microgravity and on the ground

Guo, J., Han, N., Zhang, Y., Wang, H., Zhang, X., Su, L., Liu, C., Li, J., Chen, C., & Liu, C. (2014) · Microbiological Research · doi:10.1016/j.micres.2014.09.001 · Cited by 16

Mutagenesis Induced by Oxidized DNA Precursors: Roles of Y Family DNA Polymerases in Escherichia coli

Satou, K., Yamada, M., Nohmi, T., Harashima, H., & Kamiya, H. (2005) · Chemical Research in Toxicology · doi:10.1021/tx050046b · Cited by 16

Translesion DNA replication proteins as molecular targets for cancer prevention

Watson, N. B., Mukhopadhyay, S., & McGregor, W. G. (2005) · Cancer Letters · doi:10.1016/j.canlet.2005.10.013 · Cited by 16

Kinetics of Nucleotide Incorporation Opposite Polycyclic Aromatic Hydrocarbon−DNA Adducts by Processive Bacteriophage T7 DNA Polymerase

Zang, H., Harris, T. M., & Guengerich, F. P. (2005) · Chemical Research in Toxicology · doi:10.1021/tx049683c · Cited by 16

MiR‐149 sensitizes esophageal cancer cell lines to cisplatin by targeting DNA polymerase β

Wang, Y., Chen, J., Zhang, M., Zhang, W., Li, M., Zang, W., Ziming, D., & Zhao, G. (2018) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13659 · Cited by 15

Nuclear Magnetic Resonance Investigation of Primer−Template Models: Formation of a Pyrimidine Bulge upon Misincorporation

Chi, L. M., & Lam, S. L. (2008) · Biochemistry · doi:10.1021/bi8001456 · Cited by 15

Model of the developing tumorigenic phenotype in mammalian cells and the roles of sustained stress and replicative senescence

Karpinets, T. V., & Foy, B. D. (2004) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2003.11.005 · Cited by 15

NMR investigation of DNA primer–template models: Structural insights into dislocation mutagenesis in DNA replication

Chi, L. M., & Lam, S. L. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.11.001 · Cited by 15

Conformational regulation of Escherichia coli DNA polymerase V by RecA and ATP

Jaszczur, M. M., Vo, D. D., Stanciauskas, R., Bertram, J. G., Sikand, A., Cox, M. M., Woodgate, R., Mak, C. H., Pinaud, F. F., & Goodman, M. F. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007956 · Cited by 15

Hypothesis: transcript‐templated repair of DNA double‐strand breaks

Trott, D. A., & Porter, A. C. G. (2005) · BioEssays · doi:10.1002/bies.20339 · Cited by 15

First AID (Activation-induced Cytidine Deaminase) Is Needed to Produce High Affinity Isotype-switched Antibodies

Bransteitter, R., Sneeden, J. L., Allen, S. J., Pham, P., & Goodman, M. F. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.r600006200 · Cited by 15

Targeting proliferating cell nuclear antigen (PCNA) for cancer therapy

Søgaard, C. K., & Otterlei, M. (2024) · Advances in pharmacology · doi:10.1016/bs.apha.2024.04.002 · Cited by 14

Insights into antibiotic resistance promoted by quinolone exposure

Bush, N. G., Díez-Santos, I., Krishna, P. S., Clavijo, B., & Maxwell, A. (2024) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00997-24 · Cited by 14

Amino Acid Architecture That Influences dNTP Insertion Efficiency in Y-Family DNA Polymerase V of E. coli

Seo, K. Y., Yin, J., Donthamsetti, P., Chandani, S., Lee, C. H., & Loechler, E. L. (2009) · Journal of Molecular Biology · doi:10.1016/j.jmb.2009.07.016 · Cited by 14

The mismatch repair pathway functions normally at a non-AID target in germinal center B cells

Green, B., Belcheva, A., Nepal, R. M., Boulianne, B., & Martín, A. (2011) · Blood · doi:10.1182/blood-2011-03-345991 · Cited by 15

Selective disruption of the DNA polymerase III - complex by the umuD gene products

Silva, M. C., Nevin, P., Ronayne, E. A., & Beuning, P. J. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks229 · Cited by 14

Yeast POL5 Is an Evolutionarily Conserved Regulator of rDNA Transcription Unrelated to Any Known DNA Polymerases

Yang, W., Rogozin, I. B., & Koonin, E. V. (2003) · Cell Cycle · doi:10.4161/cc.2.2.329 · Cited by 14

Herpes Simplex Virus-1 Primase: A Polymerase with Extraordinarily Low Fidelity

Ramirez‐Aguilar, K. A., & Kuchta, R. D. (2004) · Biochemistry · doi:10.1021/bi049335+ · Cited by 14

Effect of A and B Metal Ion Site Occupancy on Conformational Changes in an RB69 DNA Polymerase Ternary Complex

Wang, M., Lee, H. R., & Konigsberg, W. H. (2009) · Biochemistry · doi:10.1021/bi801627h · Cited by 14

The role of the Fanconi anemia network in the response to DNA replication stress

Gari, K., & Constantinou, A. (2009) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230903154150 · Cited by 14

Telomere Dysfunction Drives Increased Mutation by Error-Prone Polymerases Rev1 and ζ in Saccharomyces cerevisiae

Meyer, D. H., & Bailis, A. M. (2006) · Genetics · doi:10.1534/genetics.106.068130 · Cited by 14

Steric and Electrostatic Effects in DNA Synthesis by the SOS-Induced DNA Polymerases II and IV of Escherichia coli

Silverman, A. P., Jiang, Q., Goodman, M. F., & Kool, E. T. (2007) · Biochemistry · doi:10.1021/bi700851z · Cited by 14

Multiple interlinked mechanisms to circumvent DNA replication roadblocks

Eppink, B., Wyman, C., & Kanaar, R. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.06.011 · Cited by 14

Error-Prone DNA Repair System in EnteroaggregativeEscherichia coliIdentified by Subtractive Hybridization

Joo, L. M., Macfarlane-Smith, L. R., & Okeke, I. N. (2007) · Journal of Bacteriology · doi:10.1128/jb.01764-06 · Cited by 14

The role of DNA mismatch repair and oxidative DNA damage defense systems in avoidance of stationary phase mutations in Pseudomonas putida

Saumaa, S. (2007) · DSpace repository (University of Tartu) · Cited by 14

Cryo-EM reveals conformational flexibility in apo DNA polymerase ζ

Truong, C. D., Craig, T. A., Cui, G., Botuyan, M. V., Serkasevich, R. A., Chan, K.-Y., Mer, G., Chiu, P., & Kumar, R. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100912 · Cited by 13

Electrical Current Signatures of DNA Base Modifications in Single Molecules Immobilized in the α‐Hemolysin Ion Channel

Wolna, A. H., Fleming, A. M., An, N., He, L., White, H. S., & Burrows, C. J. (2013) · Israel Journal of Chemistry · doi:10.1002/ijch.201300022 · Cited by 13

The role of DNA polymerase ζ in translesion synthesis across bulky DNA adducts and cross-links in human cells

Suzuki, T., Grúz, P., Honma, M., Adachi, N., & Nohmi, T. (2016) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2016.08.004 · Cited by 13

Quantitative analysis of the mutagenic potential of 1-aminopyrene-DNA adduct bypass catalyzed by Y-family DNA polymerases

Sherrer, S. M., Taggart, D. J., Pack, L. R., Malik, C. K., Basu, A. K., & Suo, Z. (2012) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2012.08.002 · Cited by 13

Wobble dC·dA Pairing 5‘ to the Cationic Guanine N7 8,9-Dihydro-8-(N7-guanyl)-9-hydroxyaflatoxin B1 Adduct: Implications for Nontargeted AFB1 Mutagenesis

Giri, I., & Stone, M. P. (2003) · Biochemistry · doi:10.1021/bi020688n · Cited by 13

Remarkable Sensitivity to DNA Base Shape in the DNA Polymerase Active Site

Sintim, H. O., & Kool, E. T. (2006) · Angewandte Chemie · doi:10.1002/ange.200504296 · Cited by 13

Stalling of Eukaryotic Translesion DNA Polymerases at DNA-Protein Cross-Links

Yudkina, A. V., Shilkin, E. S., Makarova, А. V., & Zharkov, D. O. (2022) · Genes · doi:10.3390/genes13020166 · Cited by 12

NMR Investigation of Primer-Template Models: Structural Effect of Sequence Downstream of a Thymine Template on Mutagenesis in DNA Replication

Chi, L. M., & Lam, S. L. (2007) · Biochemistry · doi:10.1021/bi700865e · Cited by 12

Upregulation of Genes Involved in Gluconeogenesis and the Glyoxylate Cycle Suppressed the Drug Sensitivity of anN-Glycan-DeficientSaccharomyces cerevisiaeMutant

Abe, H., Fujita, Y., Chiba, Y., Jigami, Y., & Nakayama, K.-I. (2009) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.90069 · Cited by 12

Updated Understanding of Cancer as a Metabolic and Telomere-Driven Disease, and Proposal for Complex Personalized Treatment, a Hypothesis

Muresanu, C., Somasundaram, S. G., Vissarionov, S. V., Solis, L. F. T., Herrera, A. S., Kirkland, C. E., & Aliev, G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186521 · Cited by 12

Pseudouridines of tRNA Anticodon Stem-Loop Have Unexpected Role in Mutagenesis in Pseudomonas sp.

Tagel, M., Ilves, H., Leppik, M., Jürgenstein, K., Rèmme, J., & Kivisaar, M. (2020) · Microorganisms · doi:10.3390/microorganisms9010025 · Cited by 15

Physiology of the read–write genome

Shapiro, J. A. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.271130 · Cited by 12

Ability of Polymerase η and T7 DNA Polymerase to Bypass Bulge Structures

Cannistraro, V. J., & Taylor, J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608478200 · Cited by 12

In Vitro Effects of a C4‘-Oxidized Abasic Site on DNA Polymerases

Greenberg, M. M., Weledji, Y. N., Kroeger, K. M., Kim, J. C., & Goodman, M. F. (2004) · Biochemistry · doi:10.1021/bi036028f · Cited by 12

Origin of mutations in genes associated with human glioblastoma multiform cancer: random polymerase errors versus deamination

Zhang, M., Yang, D., & Gold, B. I. (2019) · Heliyon · doi:10.1016/j.heliyon.2019.e01265 · Cited by 12

Expression, purification, and DNA-binding activity of the Herbaspirillum seropedicae RecX protein

Galvão, C. W., Pedrosa, F. O., de Souza, E. M., Yates, M. G., Chubatsu, L. S., & Steffens, M. B. R. (2004) · Protein Expression and Purification · doi:10.1016/j.pep.2004.01.014 · Cited by 12

Mutagenesis of the HMGB (high-mobility group B) protein Cmb1 (cytosine-mismatch binding 1) of Schizosaccharomyces pombe: effects on recognition of DNA mismatches and damage

Kunz, C., Zurbriggen, K., & Fleck, O. (2003) · Biochemical Journal · doi:10.1042/bj20021506 · Cited by 12

DNA polymerase iota-like activity in crude cell extracts of different mouse organs

Gening, L. V., Petrochenkov, A. N., Reshetnyak, A. B., Андреева, Л. Е., & Tarantul, V. Z. (2009) · Biochemistry (Moscow) · doi:10.1134/s0006297909010192 · Cited by 12

Lyase activities intrinsic to Escherichia coli polymerases IV and V

Shen, X., Woodgate, R., & Goodman, M. F. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.08.005 · Cited by 12

Molecular Mechanisms of Carcinogenesis

Malejka‐Giganti, D., & Tretyakova, N. Y. (2005) · Chemical and functional properties of food components series · doi:10.1201/9781420039269.ch2 · Cited by 12

Modeling nucleotide excision repair and its impact on UV-induced mutagenesis during SOS-response in bacterial cells

Bugay, A. N., Krasavin, E. A., Parkhomenko, A. Y., & Vasilyeva, M. A. (2014) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2014.08.041 · Cited by 11

Translesion DNA synthesis across non-DNA segments in cultured human cells

Adar, S., & Livneh, Z. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.01.001 · Cited by 11

NGS-based analysis of base-substitution signatures created by yeast DNA polymerase eta and zeta on undamaged and abasic DNA templates in vitro

Chen, Y., & Sugiyama, T. (2017) · DNA repair · doi:10.1016/j.dnarep.2017.08.011 · Cited by 11

Elevated expression of DNA polymerase II increases spontaneous mutagenesis in Escherichia coli

Mamun, A. A. M. A. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2007.05.002 · Cited by 11

Reverse Transcriptase Mechanism of Somatic Hypermutation: 60 Years of Clonal Selection Theory

Steele, E. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01611 · Cited by 11

Unlocking the Molecular Mechanisms of DNA Repair and Platinum Drug Resistance in Cancer Chemotherapy

Yu, J. (2009) · Current Drug Therapy · doi:10.2174/157488509787081895 · Cited by 11

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Rev1 plays central roles in mammalian DNA‐damage tolerance in response to UV irradiation

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Long-Term Effects of Inducible Mutagenic DNA Repair on Relative Fitness and Phenotypic Diversification in Pseudomonas cichorii 302959

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Implications of Translesion DNA Synthesis Polymerases on Genomic Stability and Human Health

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NMR Investigation of DNA Primer-Template Models: Guanine Templates Are Less Prone to Strand Slippage upon Misincorporation

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Portraits of a Y‐family DNA polymerase

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Structural diversity of the Y-family DNA polymerases

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