Eukaryotic DNA Polymerases

DNA Replication in Eukaryotic Cells

Bell, S. P., & Dutta, A. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135425 · Cited by 2,065

Quality Control by DNA Repair

Lindahl, T. L., & Wood, R. D. (1999) · Science · doi:10.1126/science.286.5446.1897 · Cited by 1,521

The Cell as a Collection of Protein Machines: Preparing the Next Generation of Molecular Biologists

Alberts, B. (1998) · Cell · doi:10.1016/s0092-8674(00)80922-8 · Cited by 1,411

Telomere states and cell fates

Blackburn, E. H. (2000) · Nature · doi:10.1038/35040500 · Cited by 1,395

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

Masutani, C., Kusumoto, R., Yamada, A., Dohmae, N., Yokoi, M., Yuasa, M., Araki, M., Iwai, S., Takio, K., & Hanaoka, F. (1999) · Nature · doi:10.1038/21447 · Cited by 1,292

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

Crystal structure of the eukaryotic DNA polymerase processivity factor PCNA

Krishna, T. S. R., Kong, X., Gary, S. L., Burgers, P., & Kuriyan, J. (1994) · Cell · doi:10.1016/0092-8674(94)90014-0 · Cited by 902

The Y-Family of DNA Polymerases

Ohmori, H., Friedberg, E. C., Fuchs, R. P., Goodman, M. F., Hanaoka, F., Hinkle, D. C., Kunkel, T. A., Lawrence, C. W., Livneh, Z., Nohmi, T., et al. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00278-7 · Cited by 882

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

DNA Polymerases: Structural Diversity and Common Mechanisms

Steitz, T. A. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.25.17395 · Cited by 848

An in vivo analysis of the localisation and interactions of human p66 DNA polymerase δ subunit

Pöhler, J. R. G., Otterlei, M., & Warbrick, E. (2005) · BMC Molecular Biology · doi:10.1186/1471-2199-6-17 · Cited by 26

Translesion DNA Synthesis: Little Fingers Teach Tolerance

Fleck, O., & Schär, P. (2004) · Current Biology · doi:10.1016/j.cub.2004.05.014 · Cited by 26

DNA Mismatch Repair and Colon Cancer

Marra, G., & Jiricny, J. (2006) · Springer eBooks · doi:10.1007/1-4020-3764-3_4 · Cited by 25

Suppression of cell division-associated genes by Helicobacter pylori attenuates proliferation of RAW264.7 monocytic macrophage cells

Tan, G. M. Y., Looi, C. Y., Fernandez, K. C., Vadivelu, J., Loke, M. F., & Wong, W. F. (2015) · Scientific Reports · doi:10.1038/srep11046 · Cited by 25

Epigenetic control of DNA replication dynamics in mammals

Casas-Delucchi, C. S., & Cardoso, M. C. (2011) · Nucleus · doi:10.4161/nucl.2.5.17861 · Cited by 23

How a Low-Fidelity DNA Polymerase Chooses Non-Watson–Crick from Watson–Crick Incorporation

Wu, W., Su, M., Wu, J., Kumar, S., Lim, L.-H., Wang, C., Nelissen, F. H. T., Chen, M.-C. C., Doreleijers, J. F., Wijmenga, S. S., et al. (2014) · Journal of the American Chemical Society · doi:10.1021/ja4102375 · Cited by 25

A comprehensive mechanistic model of iron metabolism in Saccharomyces cerevisiae

Lindahl, P. A. (2019) · Metallomics · doi:10.1039/c9mt00199a · Cited by 28

Proofreading Activity of DNA Polymerase Pol2 Mediates 3′-End Processing during Nonhomologous End Joining in Yeast

Tseng, S., Gabriel, A., & Teng, S. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000060 · Cited by 25

Mutagenesis studies with four stereoisomeric N2-dG benzo[a]pyrene adducts in the identical 5′-CGC sequence used in NMR studies: G→T mutations dominate in each case

Seo, K., Nagalingam, A., Tiffany, M. R., & Loechler, E. L. (2005) · Mutagenesis · doi:10.1093/mutage/gei061 · Cited by 25

Base Selectivity Is Impaired by Mutants that Perturb Hydrogen Bonding Networks in the RB69 DNA Polymerase Active Site

Yang, G., Wang, J., & Konigsberg, W. H. (2005) · Biochemistry · doi:10.1021/bi047921x · Cited by 25

Identification and characterization of a heterotrimeric archaeal DNA polymerase holoenzyme

Yan, J., Beattie, T. R., Rojas, A. L., Schermerhorn, K. M., Gristwood, T., Trinidad, J. C., Albers, S., Roversi, P., Gardner, A. F., Abrescia, N. G. A., et al. (2017) · Nature Communications · doi:10.1038/ncomms15075 · Cited by 24

Mutagenesis of human DNA polymerase : essential roles of Tyr505 and Phe506 for both DNA polymerase and terminal transferase activities

Shevelev, I. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg896 · Cited by 24

Kinetics and Fidelity of Polymerization by DNA Polymerase III from Sulfolobus solfataricus

Bauer, R. J., Begley, M. T., & Trakselis, M. A. (2012) · Biochemistry · doi:10.1021/bi201799a · Cited by 23

RecJ-like protein from Pyrococcus furiosus has 3′–5′ exonuclease activity on RNA: implications for proofreading of 3′-mismatched RNA primers in DNA replication

Yuan, H., Liu, X., Han, Z., Allers, T., Hou, J., & Liu, J. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt275 · Cited by 23

Structures of DNA Polymerases Caught Processing Size‐Augmented Nucleotide Probes

Betz, K., Streckenbach, F., Schnur, A., Exner, T. E., Welte, W., Diederichs, K., & Marx, A. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905724 · Cited by 23

Diversity of the DNA Replication System in the Archaea Domain

Sarmiento, F., Long, F., Cann, I., & Whitman, W. B. (2014) · Archaea · doi:10.1155/2014/675946 · Cited by 24

Contribution of Partial Charge Interactions and Base Stacking to the Efficiency of Primer Extension at and beyond Abasic Sites in DNA

Xia, S., Vashishtha, A. K., Bulkley, D. P., Eom, S. H., Wang, J., & Konigsberg, W. H. (2012) · Biochemistry · doi:10.1021/bi300296q · Cited by 23

Learning from Directed Evolution: Thermus aquaticus DNA Polymerase Mutants with Translesion Synthesis Activity

Obeid, S., Schnur, A., Gloeckner, C., Blatter, N., Welte, W., Diederichs, K., & Marx, A. (2011) · ChemBioChem · doi:10.1002/cbic.201000783 · Cited by 23

The Mechanical Properties of PCNA: Implications for the Loading and Function of a DNA Sliding Clamp

Adelman, J. L., Chodera, J. D., Kuo, I.-F. W., Miller, T. F., & Barsky, D. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.03.056 · Cited by 23

The human DNA polymerase λ interacts with PCNA through a domain important for DNA primer binding and the interaction is inhibited by p21 /WAF1/CIP1

Maga, G., Blanca, G., Shevelev, I., Frouin, I., Ramadan, K., Spadari, S., Villani, G., & Hübscher, U. (2004) · The FASEB Journal · doi:10.1096/fj.04-2268fje · Cited by 23

Pre-steady state kinetic studies show that an abasic site is a cognate lesion for the yeast Rev1 protein

Pryor, J. M., & Washington, M. T. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.08.011 · Cited by 24

Inhibitory effect of novel 5-O-acyl juglones on mammalian DNA polymerase activity, cancer cell growth and inflammatory response

Maruo, S., Kuriyama, I., Kuramochi, K., Tsubaki, K., Yoshida, H., & Mizushina, Y. (2011) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.08.023 · Cited by 21

Biological and Therapeutic Relevance of Nonreplicative DNA Polymerases to Cancer

Parsons, J. L., Nicolay, N. H., & Sharma, R. A. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4203 · Cited by 24

Importance of Polη for Damage-Induced Cohesion Reveals Differential Regulation of Cohesion Establishment at the Break Site and Genome-Wide

Enervald, E., Lindgren, E. B., Katou, Y., Shirahige, K., & Ström, L. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003158 · Cited by 24

Multimachine Communication Network That Mimics the Adaptive Immune Response

Ma, P., Huang, Q., Li, H., Yin, B., & Ye, B. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.9b11545 · Cited by 22

Replitase: Complete machinery for DNA synthesis

Murthy, S., & Reddy, G. P. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20842 · Cited by 22

Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype

Grosch, M., Grüner, B., Spranger, S., Stütz, A. M., Rausch, T., Korbel, J. O., Seelow, D., Nürnberg, P., Sticht, H., Lausch, E. U., et al. (2013) · Matrix Biology · doi:10.1016/j.matbio.2013.05.001 · Cited by 22

The problem of the eukaryotic genome size

Patrushev, L. I., & Minkevich, I. G. (2008) · Biochemistry (Moscow) · doi:10.1134/s0006297908130117 · Cited by 25

Expanding the repertoire of DNA polymerase substrates: template-instructed incorporation of non-nucleoside triphosphate analogues by DNA polymerases and

Crespan, E., Alexandrova, L., Khandazhinskaya, A. L., Jasko, M. V., Kukhanova, M. K., Villani, G., Hübscher, U., Spadari, S., & Maga, G. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl1016 · Cited by 22

The effects of dehydroaltenusin, a novel mammalian DNA polymerase α inhibitor, on cell proliferation and cell cycle progression

Murakami-Nakai, C., Maeda, N., Yonezawa, Y., Kuriyama, I., Kamisuki, S., Takahashi, S., Sugawara, F., Yoshida, H., Sakaguchi, K., & Mizushina, Y. (2004) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2004.06.016 · Cited by 22

The p12 subunit of human polymerase δ uses an atypical PIP box for molecular recognition of proliferating cell nuclear antigen (PCNA)

Magaña, A. G., de Opakua, A. I., Romano‐Moreno, M., Murciano‐Calles, J., Merino, N., Luque, I., Rojas, A. L., Onesti, S., Blanco, F. J., & Biasio, A. D. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006391 · Cited by 21

SV40 T antigen interactions with ssDNA and replication protein A: a regulatory role of T antigen monomers in lagging strand DNA replication

Onwubiko, N. O., Borst, A., Diaz, S. A., Passkowski, K., Scheffel, F., Teßmer, I., & Nasheuer, H. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa138 · Cited by 21

Human DNA polymerase λ catalyzes lesion bypass across benzo[a]pyrene-derived DNA adduct during base excision repair

Skosareva, L. V., Lebedeva, N. A., Rechkunova, N. I., Kolbanovskiy, A., Geacintov, N. E., & Lavrik, O. I. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.01.002 · Cited by 23

Significance of DNA Polymerase Delta Catalytic Subunit p125 Induced by Mutant p53 in the Invasive Potential of Human Hepatocellular Carcinoma

Sanefuji, K., Taketomi, A., Iguchi, T., Sugimachi, K., Ikegami, T., Yamashita, Y., Gion, T., Soejima, Y., Shirabe, K., & Maehara, Y. (2010) · Oncology · doi:10.1159/000322374 · Cited by 21

The Pre-NH 2 -Terminal Domain of the Herpes Simplex Virus 1 DNA Polymerase Catalytic Subunit Is Required for Efficient Viral Replication

Terrell, S. L., & Coen, D. M. (2012) · Journal of Virology · doi:10.1128/jvi.01034-12 · Cited by 21

Mechanisms of HTLV-1 transformation

Kehn‐Hall, K. (2004) · Frontiers in bioscience · doi:10.2741/1401 · Cited by 21

Starting DNA Synthesis: Initiation Processes during the Replication of Chromosomal DNA in Humans

Nasheuer, H., & Meaney, A. M. (2024) · Genes · doi:10.3390/genes15030360 · Cited by 21

Analysis of DNA polymerase ν function in meiotic recombination, immunoglobulin class-switching, and DNA damage tolerance

Takata, K., Reh, S., Yousefzadeh, M. J., Żelazowski, M. J., Bhetawal, S., Trono, D., Lowery, M. G., Sandoval, M., Takata, Y., Lu, Y., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006818 · Cited by 20

Mechanistic Studies with DNA Polymerases Reveal Complex Outcomes following Bypass of DNA Damage

Eoff, R. L., Choi, J., & Guengerich, F. P. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/830473 · Cited by 20

Rose myrtle (Rhodomyrtus tomentosa) extract and its component, piceatannol, enhance the activity of DNA polymeraseand suppress the inflammatory response elicitedby UVB-induced DNA damage in skin cells

Shiratake, S., NAKAHARA, T., Iwahashi, H., Onodera, T., & Mizushina, Y. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4156 · Cited by 20

Terminal deoxynucleotidyl transferases from elasmobranchs reveal structural conservation within vertebrates

Bartl, S., Miracle, A. L., Rumfelt, L. L., Kepler, T. B., Mochon, E., Litman, G. W., & Flajnik, M. F. (2003) · Immunogenetics · doi:10.1007/s00251-003-0608-3 · Cited by 21

Integrating S-phase checkpoint signaling with trans-lesion synthesis of bulky DNA adducts

Barkley, L. R., Ohmori, H., & Vaziri, C. (2007) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-007-0032-7 · Cited by 20

DNA Damage Signalling and Repair in Dictyostelium discoideum

Hsu, D., Gaudet, P., Hudson, J. J. R., Pears, C. J., & Lakin, N. D. (2006) · Cell Cycle · doi:10.4161/cc.5.7.2626 · Cited by 20

Monoacetylcurcumin: A new inhibitor of eukaryotic DNA polymerase λ and a new ligand for inhibitor-affinity chromatography

Mizushina, Y., Ishidoh, T., Takeuchi, T., Shimazaki, N., Koiwai, O., Kuramochi, K., Kobayashi, S. S., Sugawara, F., Sakaguchi, K., & Yoshida, H. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.10.005 · Cited by 20

Translesion DNA Synthesis and Carcinogenesis

Shilkin, E. S., Boldinova, E. O., Stolyarenko, A. D., Гончарова, Р. И., Chuprov‐Netochin, R. N., Khairullin, R. F., Smal, M. P., & Makarova, А. V. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920040033 · Cited by 23

Characterization of a Natural Mutator Variant of Human DNA Polymerase λ which Promotes Chromosomal Instability by Compromising NHEJ

Terrados, G., Capp, J., Canitrot, Y., García–Díaz, M., Bębenek, K., Kirchhoff, T., Villanueva, A., Boudsocq, F., Bergoglio, V., Cazaux, C., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007290 · Cited by 19

Self-Assembled Nanocomposite Film with Tunable Enhanced Fluorescence for the Detection of DNA

Zhu, X., Wang, X., He, F., Tang, F., & Li, L. (2014) · ACS Applied Materials & Interfaces · doi:10.1021/am507772e · Cited by 19

Multiplex Single-Molecule Kinetics of Nanopore-Coupled Polymerases

Palla, M., Punthambaker, S., Stranges, B., Vigneault, F., Nivala, J., Wiegand, D. J., Ayer, A., Craig, T. K., Gremyachinskiy, D. E., Franklin, H., et al. (2020) · ACS Nano · doi:10.1021/acsnano.0c05226 · 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

Vitamin B6

Dakshinamurti, K., & Dakshinamurti, S. (2007) · CRC Press eBooks · doi:10.1201/9781420005806.ch10 · Cited by 19

Spinach and Health

Maeda, N., Yoshida, H., & Mizushina, Y. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374628-3.00026-8 · Cited by 19

Exogenous 8-oxo-dG is not utilized for nucleotide synthesis but enhances the accumulation of 8-oxo-Gua in DNA through error-prone DNA synthesis

Kim, J., Hyun, J. W., Hayakawa, H., Choi, S., Choi, J., & Chung, M. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.12.004 · Cited by 19

Aphidicolin-resistant and -sensitive base excision repair in wild-type and DNA polymerase β-defective mouse cells

Parlanti, E., Pascucci, B., Terrados, G., Blanco, L., & Eugenia Dogliotti, Y. (2004) · DNA repair · doi:10.1016/j.dnarep.2003.12.009 · Cited by 19

Base Excision Repair

Meira, L. B., Burgis, N. E., & Samson, L. D. (2006) · Springer eBooks · doi:10.1007/1-4020-3764-3_5 · Cited by 17

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

Simian Virus 40 DNA Replication Is Dependent on an Interaction between Topoisomerase I and the C-Terminal End of T Antigen

Khopde, S. M., & Simmons, D. T. (2007) · Journal of Virology · doi:10.1128/jvi.01314-07 · Cited by 18

In vivo antitumor effect of liposomes with sialyl Lewis X including monogalactosyl diacylglycerol, a replicative DNA polymerase inhibitor, from spinach

Mizushina, Y., Hada, T., & Yoshida, H. (2012) · Oncology Reports · doi:10.3892/or.2012.1893 · Cited by 18

Eukaryotic error-prone DNA polymerases: The presumed roles in replication, repair, and mutagenesis

Krutyakov, V. M. (2006) · Molecular Biology · doi:10.1134/s0026893306010018 · Cited by 18

Coordination of DNA synthesis and replicative unwinding by the S-phase checkpoint pathways

Nedelcheva‐Veleva, M., Krastev, D. B., & Stoynov, S. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl528 · 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

Characterization of Human Antigenic Proteins SchS21 and SchS34 from Stachybotrys chartarum

Shi, C., Smith, M. L., & Miller, J. D. (2010) · International Archives of Allergy and Immunology · doi:10.1159/000317243 · Cited by 17

Diketo Hexenoic Acid Derivatives Are Novel Selective Non-Nucleoside Inhibitors of Mammalian Terminal Deoxynucleotidyl Transferases, with Potent Cytotoxic Effect against Leukemic Cells

Locatelli, G. A., Santo, R. D., Crespan, E., Costi, R., Roux, A., Hübscher, U., Shevelev, I., Blanca, G., Villani, G., Spadari, S., et al. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.013326 · Cited by 17

Plant sterols as selective DNA polymerase β lyase inhibitors and potentiators of bleomycin cytotoxicity

Li, S.-S., Gao, Z., Feng, X., Jones, S. H., & Hecht, S. M. (2004) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2004.05.016 · Cited by 17

Exploiting the Nucleotide Substrate Specificity of Repair DNA Polymerases To Develop Novel Anticancer Agents

Crespan, E., Garbelli, A., Amoroso, A., & Maga, G. (2011) · Molecules · doi:10.3390/molecules16097994 · 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

A new DNA polymerase I from Geobacillus caldoxylosilyticus TK4: cloning, characterization, and mutational analysis of two aromatic residues

Sandallı, C., Singh, K., Modak, M. J., Ketkar, A. D., Çanakçı, S., Demir, İ., & Beldüz, A. O. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-1962-3 · Cited by 17

Evolution of the archaeal and mammalian information processing systems: towards an archaeal model for human disease

Lyu, Z., & Whitman, W. B. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2286-y · Cited by 17

Effects of Intermediates between Vitamins K2 and K3 on Mammalian DNA Polymerase Inhibition and Anti-Inflammatory Activity

Mizushina, Y., Maeda, J., Irino, Y., Nishida, M., Nishiumi, S., Kondo, Y., Nishio, K., Kuramochi, K., Tsubaki, K., Kuriyama, I., et al. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12021115 · Cited by 17

Formosusin A, a novel specific inhibitor of mammalian DNA polymerase β from the fungus Paecilomyces formosus

Mizushina, Y., Suzuki-Fukudome, H., Takeuchi, T., Takemoto, K., Kuriyama, I., Yoshida, H., Kamisuki, S., & Sugawara, F. (2013) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2013.12.038 · Cited by 16

Inhibitory effects of vitamin K3 derivatives on DNA polymerase and inflammatory activity

Mizushina, Y. (2011) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2011.773 · Cited by 15

The Inhibitory Action of Kohamaic Acid A Derivatives on Mammalian DNA Polymerase β

Mizushina, Y., Manita, D., Takeuchi, T., Sugawara, F., Kumamoto‐Yonezawa, Y., Matsui, Y., Takemura, M., Sasaki, M., Yoshida, H., & Takikawa, H. (2008) · Molecules · doi:10.3390/molecules14010102 · 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

Genomic changes of the 55 kDa subunit of DNA polymerase epsilon in human breast cancer.

Zhou, Q., Effati, R., Talvinen, K., Pospiech, H., Syväoja, J. E., & Collan, Y. U. (2008) · PubMed · Cited by 16

Inhibition of MCP-1 and MIP-2 transcription and translation by mimosine in muscle tissue infected with the parasite Trichinella spiralis

Conti, P., Frydas, S., Reale, M., Barbacane, R. C., Gioacchino, M. D., Felaco, M., & Trakatellis, A. C. (2002) · Molecular and Cellular Biochemistry · doi:10.1023/a:1017989014906 · Cited by 16

Precise structural elucidation of dehydroaltenusin, a specific inhibitor of mammalian DNA polymerase α

Kamisuki, S., Takahashi, S., Mizushina, Y., Sakaguchi, K., Nakata, T., & Sugawara, F. (2004) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2004.07.047 · Cited by 16

Progress Towards the Anatomy of the Eukaryotic DNA Replication Fork

Nasheuer, H., Pospiech, H., & Syväoja, J. E. (2006) · Springer eBooks · doi:10.1007/7050_016 · Cited by 16

Tertiary Conformation of the Template-Primer and Gapped DNA Substrates in Complexes with Rat Polymerase β. Fluorescence Energy Transfer Studies Using the Multiple Donor−Acceptor Approach

Jezewska, M. J., Galletto, R., & Bujalowski, W. (2003) · Biochemistry · doi:10.1021/bi030111l · Cited by 16

Dipeptide alcohol-based inhibitors of eukaryotic DNA polymerase α

Kuriyama, I., Asano, N., Kato, I., Ikeda, K., Takemura, M., Yoshida, H., Sakaguchi, K., & Mizushina, Y. (2005) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2004.12.052 · Cited by 16

Ubiquitylation of DNA polymerase λ

Markkanen, E., van Loon, B., Ferrari, E. S., & Hübscher, U. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.069 · Cited by 15

Modeling DNA Polymerase μ Motions: Subtle Transitions before Chemistry

Li, Y., & Tamar Schlick, A. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.09.056 · Cited by 15

Division of labor of Y-family polymerases in translesion-DNA synthesis for distinct types of DNA damage

Inomata, Y., Abe, T., Tsuda, M., Takeda, S., & Hirota, K. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252587 · Cited by 14

Inhibitory action of C22-fatty acids on DNA polymerases and DNA topoisomerases

Yonezawa, Y., Hada, T., Uryu, K., Iijima, H., Yoshida, H., & Mizushina, Y. (2006) · International Journal of Molecular Medicine · doi:10.3892/ijmm.18.4.583 · Cited by 15

The SV40 Large T-Antigen Origin Binding Domain Directly Participates in DNA Unwinding

Foster, E. C., & Simmons, D. T. (2010) · Biochemistry · doi:10.1021/bi901827k · Cited by 15

Identification of Critical Residues for the Tight Binding of Both Correct and Incorrect Nucleotides to Human DNA Polymerase λ

Brown, J. A., Pack, L. R., Sherrer, S. M., Kshetry, A. K., Newmister, S. A., Fowler, J. D., Taylor, J., & Suo, Z. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.09.014 · Cited by 15

A Substitution in the Fingers Domain of DNA Polymerase δ Reduces Fidelity by Altering Nucleotide Discrimination in the Catalytic Site*

Prindle, M. J., Schmitt, M. W., Parmeggiani, F., & Loeb, L. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.436410 · Cited by 15

Cycloartenyl trans-ferulate, a component of the bran byproduct of sake-brewing rice, inhibits mammalian DNA polymerase and suppresses inflammation

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