Functions of DNA Polymerases

Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid

WATSON, J. D., & CRICK, F. H. C. (1953) · Nature · doi:10.1038/171737a0 · Cited by 13,584

DNA Repair and Mutagenesis

Friedberg, E. C., Walker, G. C., Siede, W., Wood, R. D., Schultz, R. A., & Ellenberger, T. (2005) · doi:10.1128/9781555816704 · Cited by 5,683

DNA repair and mutagenesis

Bootsma, D., & Hoeijmakers, J. H. J. (1996) · Trends in Genetics · doi:10.1016/0168-9525(96)81408-9 · Cited by 2,285

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

Hoege, C., Pfander, B., Moldovan, G., Pyrowolakis, G., & Jentsch, S. (2002) · Nature · doi:10.1038/nature00991 · Cited by 2,202

Quality Control by DNA Repair

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

Deletion of a DNA Polymerase β Gene Segment in T Cells Using Cell Type-Specific Gene Targeting

Gu, H., Marth, J. D., Orban, P. C., Mossmann, H., & Rajewsky, K. (1994) · Science · doi:10.1126/science.8016642 · Cited by 1,397

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

Structure of large fragment of Escherichia coli DNA polymerase I complexed with dTMP

Ollis, D. L., Brick, P., Hamlin, R. C., Xuong, N., & Steitz, T. A. (1985) · Nature · doi:10.1038/313762a0 · Cited by 848

V(D)J Recombination: RAG Proteins, Repair Factors, and Regulation

Gellert, M. F. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.090501.150203 · Cited by 771

DNA Replication Fidelity

Kunkel, T. A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.r400006200 · Cited by 754

DNA polymerases in nonhomologous end joining: Are there any benefits to standing out from the crowd?

Ramsden, D. A., & Asagoshi, K. (2012) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21725 · Cited by 38

Basis of Miscoding of the DNA Adduct N2,3-Ethenoguanine by Human Y-family DNA Polymerases

Zhao, L., Pence, M. G., Christov, P. P., Wawrzak, Z., Choi, J.-Y., Rizzo, C. J., Egli, M., & Guengerich, F. P. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.403253 · Cited by 36

AP endonuclease independent repair of abasic sites in Schizosaccharomyces pombe

Nilsen, L. B., Forstrøm, R. J., Bjørås, M., & Alseth, I. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr933 · Cited by 36

Editing of misaligned 3'-termini by an intrinsic 3'-5' exonuclease activity residing in the PHP domain of a family X DNA polymerase

Baños, B., Lázaro, J. M., Villar, L., Salas, M., & de Vega, M. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn526 · Cited by 36

Revealing the role of the product metal in DNA polymerase β catalysis

Perera, L., Freudenthal, B., Beard, W. A., Pedersen, L. G., & Wilson, S. H. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkw1363 · Cited by 36

In crystallo observation of three metal ion promoted DNA polymerase misincorporation

Chang, C., Luo, C. L., & Gao, Y. (2022) · Nature Communications · doi:10.1038/s41467-022-30005-3 · Cited by 35

DNA polymerases provide a canon of strategies for translesion synthesis past oxidatively generated lesions

Zahn, K. E., Wallace, S. S., & Doublié, S. (2011) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2011.03.008 · Cited by 34

Molecular and biochemical characterisation of a novel mutation in POLGassociated with Alpers syndrome

Schaller, A., Hahn, D., Jackson, C. B., Kern, I., Chardot, C., Belli, D. C., Gallati, S., & Nuoffer, J. (2011) · BMC Neurology · doi:10.1186/1471-2377-11-4 · Cited by 34

Computational Simulations of DNA Polymerases: Detailed Insights on Structure/Function/Mechanism from Native Proteins to Cancer Variants

Walker, A. R., & Cisneros, G. A. (2017) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.7b00161 · Cited by 33

DNA Polymerase ε

Hogg, M., & Johansson, E. (2012) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-4572-8_13 · Cited by 34

Intrinsic properties of the two replicative DNA polymerases of Pyrococcus abyssi in replicating abasic sites: possible role in DNA damage tolerance?

Palud, A., Villani, G., L’Haridon, S., Quérellou, J., Raffin, J., & Henneke, G. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06446.x · Cited by 33

Epicatechin conjugated with fatty acid is a potent inhibitor of DNA polymerase and angiogenesis

Matsubara, K., Saito, A., Tanaka, A., Nakajima, N., Akagi, R., Mori, M., & Mizushina, Y. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.01.049 · Cited by 32

Characterization of SpPol4, a unique X-family DNA polymerase in Schizosaccharomyces pombe

González‐Barrera, S., Sanchez, A., Ruiz, J. F., Juárez, R., Picher, Á. J., Terrados, G., Andrade, P. B., & Blanco, L. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki780 · Cited by 32

Structural Insights Into DNA Repair by RNase T—An Exonuclease Processing 3′ End of Structured DNA in Repair Pathways

Hsiao, Y.-Y., Fang, W.-H., Lee, C.-C., Chen, Y.-P., & Yuan, H. S. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001803 · Cited by 33

Polymerase-Tailored Variations in the Water-Mediated and Substrate-Assisted Mechanism for Nucleotidyl Transfer: Insights from a Study of T7 DNA Polymerase

Wang, L., Broyde, S. B., & Zhang, Y. (2009) · Journal of Molecular Biology · doi:10.1016/j.jmb.2009.04.029 · Cited by 31

Calcium-driven DNA synthesis by a high-fidelity DNA polymerase

Ralec, C., Henry, E., Lemor, M., Killelea, T., & Henneke, G. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx927 · Cited by 33

The handbook of plant mutation screening: mining of natural and induced alleles.

Meksem, K., & Kahl, G. (2010) · Cited by 31

Microsatellite Interruptions Stabilize Primate Genomes and Exist as Population-Specific Single Nucleotide Polymorphisms within Individual Human Genomes

Ananda, G., Hile, S. E., Breski, A., Wang, Y., Kelkar, Y., Makova, K. D., & Eckert, K. A. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004498 · Cited by 29

Homology modeling of four Y-family, lesion-bypass DNA polymerases: The case that E. coli Pol IV and human Pol κ are orthologs, and E. coli Pol V and human Pol η are orthologs

Lee, C. H., Chandani, S., & Loechler, E. L. (2006) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2005.10.009 · Cited by 30

Carcinogenic adducts induce distinct DNA polymerase binding orientations

Vrtis, K. B., Markiewicz, R. P., Romano, L. J., & Rueda, D. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt554 · Cited by 28

DNA polymerase kappa microsatellite synthesis: Two distinct mechanisms of slippage‐mediated errors

Baptiste, B. A., & Eckert, K. A. (2012) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21721 · Cited by 28

The In Vitro Fidelity Of Yeast DNA Polymerase δ And Polymerase ε Holoenzymes During Dinucleotide Microsatellite DNA Synthesis

Abdulovic, A. L., Hile, S., Kunkel, T., & Eckert, K. (2011) · DNA Repair · doi:10.1016/j.dnarep.2011.02.003 · Cited by 28

Understanding the Physical and Molecular Basis of Stability of Arabidopsis DNA Pol λ under UV-B and High NaCl Stress

Roy, S., Banerjee, V., & Das, K. P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133843 · Cited by 26

Novel Terpenoids, Trichoderonic Acids A and B Isolated fromTrichoderma virens, Are Selective Inhibitors of Family X DNA Polymerases

YAMAGUCHI, Y., Manita, D., Takeuchi, T., Kuramochi, K., Kuriyama, I., Sugawara, F., Yoshida, H., & Mizushina, Y. (2010) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.90843 · Cited by 27

Principal Aspects Regarding the Maintenance of Mammalian Mitochondrial Genome Integrity

Vasileiou, P. V. S., Mourouzis, I. S., & Pantos, C. I. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081821 · Cited by 27

Anti-cancer gallotannin penta-O-galloyl-beta-d-glucose is a nanomolar inhibitor of select mammalian DNA polymerases

Mizushina, Y., Zhang, J., Pugliese, A., Kim, S., & Lü, J. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.06.031 · Cited by 26

Monogalactosyl diacylglycerol, a replicative DNA polymerase inhibitor, from spinach enhances the anti-cell proliferation effect of gemcitabine in human pancreatic cancer cells

Akasaka, H., Sasaki, R., Yoshida, K., Takayama, I., Yamaguchi, T., Yoshida, H., & Mizushina, Y. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.11.004 · Cited by 26

Inhibitory effects of vitamin K3 on DNA polymerase and angiogenesis

Matsubara (1998) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000034 · Cited by 26

Inhibitory Effects of Cholesterol Derivatives on DNA Polymerase and Topoisomerase Activities, and Human Cancer Cell Growth

Ishimaru, C., Yonezawa, Y., Kuriyama, I., Nishida, M., Yoshida, H., & Mizushina, Y. (2008) · Lipids · doi:10.1007/s11745-007-3149-y · Cited by 26

A Mg2+‐induced conformational switch rendering a competent DNA polymerase catalytic complex

Mendieta, J., Cases‐González, C. E., Matamoros, T., Ramı́rez, G., & Menéndez‐Arias, L. (2007) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.21711 · Cited by 26

Modulating the DNA polymerase β reaction equilibrium to dissect the reverse reaction

Shock, D. D., Freudenthal, B., Beard, W. A., & Wilson, S. H. (2017) · Nature Chemical Biology · doi:10.1038/nchembio.2450 · Cited by 26

Cancers from Novel Pole -Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade

Galati, M. A., Hodel, K. P., Gams, M. S., Sudhaman, S., Bridge, T., Zahurancik, W. J., Ungerleider, N., Park, V. S., Ercan, A. B., Joksimovic, L., et al. (2020) · Cancer Research · doi:10.1158/0008-5472.can-20-0624 · Cited by 25

Examination of the Long-range Effects of Aminofluorene-induced Conformational Heterogeneity and Its Relevance to the Mechanism of Translesional DNA Synthesis

Meneni, S., Liang, F., & Cho, B. P. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.12.023 · 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

Synergistic Effects of the in cis T251I and P587L Mitochondrial DNA Polymerase γ Disease Mutations

DeBalsi, K. L., Longley, M. J., Hoff, K. E., & Copeland, W. C. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.773341 · Cited by 22

Exploring the Identity of the General Base for a DNA Polymerase Catalyzed Reaction Using QM/MM: The Case Study of Human Translesion Synthesis Polymerase η

Wilson, K. A., Fernandes, P. A., Ramos, M. J., & Wetmore, S. D. (2019) · ACS Catalysis · doi:10.1021/acscatal.8b04889 · Cited by 23

PrimPol: A Breakthrough among DNA Replication Enzymes and a Potential New Target for Cancer Therapy

Díaz‐Talavera, A., Montero‐Conde, C., Leandro-Garcia, L. J., & Robledo, M. (2022) · Biomolecules · doi:10.3390/biom12020248 · Cited by 26

Multiple solutions to inefficient lesion bypass by T7 DNA polymerase

McCulloch, S. D., & Kunkel, T. A. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.06.003 · Cited by 21

Targeting DNA Polymerase ß for Therapeutic Intervention

Goellner, E. M., Svilar, D., Almeida, K. H., & Sobol, R. W. (2011) · Current Molecular Pharmacology · doi:10.2174/1874-470211205010068 · Cited by 31

Solution structures of 2 : 1 and 1 : 1 DNA polymerase–DNA complexes probed by ultracentrifugation and small-angle X-ray scattering

Tang, K., Niebuhr, M., AULABAUGH, A. E., & Tsai, M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm1101 · Cited by 22

Mechanisms of T-DNA integration

Ziemienowicz, A., Tzfira, T., & Höhn, B. (2007) · Springer eBooks · doi:10.1007/978-0-387-72290-0_11 · Cited by 21

Purification and functional characterization of human mitochondrial DNA polymerase gamma harboring disease mutations

Kasiviswanathan, R., Longley, M. J., Young, M. J., & Copeland, W. C. (2010) · Methods · doi:10.1016/j.ymeth.2010.02.015 · Cited by 20

Involvement of 29 DNA polymerase thumb subdomain in the proper coordination of synthesis and degradation during DNA replication

Pérez-Arnaiz, P. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl402 · Cited by 21

DNA Replication Fidelity: Proofreading in Trans

Albertson, T., & Preston, B. D. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.031 · Cited by 23

DNA Polymerases for Whole Genome Amplification: Considerations and Future Directions

Ordóñez, C. D., & Redrejo‐Rodríguez, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119331 · Cited by 22

Analysis of Adaptive Olaparib Resistance Effects on Cisplatin Sensitivity in Triple Negative Breast Cancer Cells

Gajan, A., Sarma, A., Kim, S., Gurdziel, K., Wu, G. S., & Shekhar, M. P. V. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.694793 · 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

Introduction to the Molecular Biology of the Cell

Marín-García, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00001-9 · Cited by 20

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

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

Molecular mechanisms of radiation resistance in doxorubicin-resistant breast adenocarcinoma cells

Luzhna, L., Golubov, A., Ilnytskyy, S., Chekhun, V. F., & Kovalchuk, O. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.1845 · Cited by 17

Findings made in gene panel to whole genome sequencing: data, knowledge, ethics – and consequences?

Winkler, E. C., & Wiemann, S. (2016) · Expert Review of Molecular Diagnostics · doi:10.1080/14737159.2016.1212662 · 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

Pyrophosphate release acts as a kinetic checkpoint during high-fidelity DNA replication by the Staphylococcus aureus replicative polymerase PolC

Fagan, S. P., Mukherjee, P., Jaremko, W. J., Nelson-Rigg, R., Wilson, R. C., Dangerfield, T. L., Johnson, K. A., Lahiri, I., & Pata, J. D. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab613 · Cited by 16

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

Translesion Synthesis in Plants: Ultraviolet Resistance and Beyond

Sakamoto, A. N. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01208 · Cited by 19

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

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

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

Mizushina, Y., Kuriyama, I., Yamazaki, A., Akashi, T., & Yoshida, H. (2013) · Food Chemistry · doi:10.1016/j.foodchem.2013.04.048 · Cited by 15

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

Anti-Tumor Effects of Novel 5-O-Acyl Plumbagins Based on the Inhibition of Mammalian DNA Replicative Polymerase Activity

Kawamura, M., Kuriyama, I., Maruo, S., Kuramochi, K., Tsubaki, K., Yoshida, H., & Mizushina, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088736 · Cited by 14

Mapping Functional Substrate–Enzyme Interactions in the pol β Active Site through Chemical Biology: Structural Responses to Acidity Modification of Incoming dNTPs

Batra, V. K., Oertell, K., Beard, W. A., Kashemirov, B. A., McKenna, C. E., Goodman, M. F., & Wilson, S. H. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00418 · Cited by 14

Diallyl sulfides: Selective inhibitors of family X DNA polymerases from garlic (Allium sativum L.)

Nishida, M., Hada, T., Kuramochi, K., Yoshida, H., Yonezawa, Y., Kuriyama, I., Sugawara, F., Yoshida, H., & Mizushina, Y. (2007) · Food Chemistry · doi:10.1016/j.foodchem.2007.11.007 · 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

Y-Family DNA polymerases may use two different dNTP shapes for insertion: A hypothesis and its implications

Chandani, S., & Loechler, E. L. (2008) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2008.11.003 · Cited by 14

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

Screening of Novel Bioactive Compounds from Food Components and Nutrients

Mizushina, Y. (2011) · Nippon Eiyo Shokuryo Gakkaishi · doi:10.4327/jsnfs.64.377 · Cited by 13

Characterisation of the circulating acellular proteome of healthy sheep using LC-MS/MS-based proteomics analysis of serum

Chemonges, S., Gupta, R., Mills, P. C., Kopp, S. R., & Sadowski, P. G. (2016) · Proteome Science · doi:10.1186/s12953-017-0119-z · Cited by 13

Evolution of Base Excision Repair in Entamoeba histolytica is shaped by gene loss, gene duplication, and lateral gene transfer

Trasviña‐Arenas, C. H., David, S. S., Delaye, L., Azuara-Liceaga, E. I., & Brieba, L. G. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.02.009 · Cited by 13

RanBP2-Mediated SUMOylation Promotes Human DNA Polymerase Lambda Nuclear Localization and DNA Repair

Moreno-Oñate, M., Herrero-Ruíz, A., García‐Domínguez, M., Cortés‐Ledesma, F., & Ruiz, J. F. (2020) · Journal of Molecular Biology · doi:10.1016/j.jmb.2020.03.020 · Cited by 13

Inhibitory effect of coenzyme Q1 on eukaryotic DNA polymerase γ and DNA topoisomerase II activities on the growth of a human cancer cell line

Yonezawa, Y., Kuriyama, I., Fukuoh, A., Muta, T., Kang, D., Takemura, M., Kato, I., Yoshida, H., & Mizushina, Y. (2006) · Cancer Science · doi:10.1111/j.1349-7006.2006.00236.x · Cited by 13

An insight into the biological functions of family X-DNA polymerase in DNA replication and repair of plant genome

Roy, S., Singh, S. K., Choudhury, S. R., & Sengupta, D. N. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.7.9077 · Cited by 12

A Nuclear Family A DNA Polymerase from Entamoeba histolytica Bypasses Thymine Glycol

Pastor-Palacios, G., Azuara-Liceaga, E. I., & Brieba, L. G. (2010) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0000786 · Cited by 12

Inhibitory effects of catechin derivatives on mammalian DNA polymerase and topoisomerase activities and mouse one-cell zygote development

Yoshida, N., Kuriyama, I., Yoshida, H., & Mizushina, Y. (2012) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2012.10.001 · Cited by 11

An archaeal family-B DNA polymerase variant able to replicate past DNA damage: occurrence of replicative and translesion synthesis polymerases within the B family

Jóźwiakowski, S. K., Keith, B. J., Gilroy, L., Doherty, A. J., & Connolly, B. A. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku683 · Cited by 13

Inhibitory effects of docosyl p-coumarate on DNA topoisomerase activity and human cancer cell growth

Mizushina (2010) · International Journal of Oncology · doi:10.3892/ijo_00000750 · Cited by 11

Structure and function of 2:1 DNA polymerase·DNA complexes

Tang, K., & Tsai, M. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21458 · Cited by 10

Polbase: a repository of biochemical, genetic and structural information about DNA polymerases

Langhorst, B. W., Jack, W. E., Reha-Krantz, L. J., & Nichols, N. M. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr847 · Cited by 10

In vivo evidence that phenylalanine 171 acts as a molecular brake for translesion DNA synthesis across benzo[a]pyrene DNA adducts by human DNA polymerase κ

Sassa, A., Suzuki, T., Kanemaru, Y., Niimi, N., Fujimoto, H., Katafuchi, A., Grúz, P., Yasui, M., Gupta, R. C., Johnson, F., et al. (2014) · DNA repair · doi:10.1016/j.dnarep.2013.12.008 · Cited by 10

Measuring the Fidelity of Translesion DNA Synthesis

McCulloch, S. D., & Kunkel, T. A. (2006) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(06)08021-9 · Cited by 10

Inhibition of repair-related DNA polymerases by vitamin Ks, their related quinone derivatives and associated inflammatory activity

Mizushina, Y., Nishiumi, S., Nishida, M., Yoshida, H., Azuma, T., & Yoshida, M. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.1771 · Cited by 10

Involvement of the TPR2 subdomain movement in the activities of 29 DNA polymerase

Rodriguez, I., Lázaro, J. M., Salas, M. A., & de Vega, M. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn928 · Cited by 10

Low intensity infrared laser affects expression of oxidative DNA repair genes in mitochondria and nucleus

da Fonseca, A. D. S., Magalhães, L. A. G., Mencalha, A. L., Geller, M., & de Paoli, F. (2014) · Laser Physics · doi:10.1088/1054-660x/24/11/115605 · Cited by 10

Detrimental effects of UV‐B radiation in a xeroderma pigmentosum‐variant cell line

Herman, K. N., Toffton, S. M., & McCulloch, S. D. (2014) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21857 · Cited by 10

Kinetic Analysis of the Unique Error Signature of Human DNA Polymerase ν

Arana, M. E., Potapova, O., Kunkel, T. A., & Joyce, C. M. (2011) · Biochemistry · doi:10.1021/bi201197p · Cited by 9

Novel ribonucleotide discrimination in the RNA polymerase-like two-barrel catalytic core of Family D DNA polymerases

Zatopek, K. M., Alpaslan, E., Evans, T. C., Sauguet, L., & Gardner, A. F. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa986 · Cited by 9

From chromosome theory to the template principle

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