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

Emerging models for DNA repair: Dictyostelium discoideum as a model for nonhomologous end-joining

Pears, C. J., & Lakin, N. D. (2014) · DNA repair · doi:10.1016/j.dnarep.2014.01.008 · 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

Screening of mammalian DNA polymerase and topoisomerase inhibitors from Garcinia mangostana L. and analysis of human cancer cell proliferation and apoptosis

Onodera, T., Takenaka, Y., Kozaki, S., Tanahashi, T., & Mizushina, Y. (2016) · International Journal of Oncology · doi:10.3892/ijo.2016.3321 · Cited by 13

Expression of a maize δ‐type DNA polymerase during seed germination

García, E., Quiroz, F., Uchiyama, Y., Sakaguchi, K., & Vázquez-Ramos, J. M. (2006) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2006.00659.x · Cited by 13

Effective form of sulfoquinovosyldiacyglycerol (SQDG) vesicles for DNA polymerase inhibition

Matsumoto, K., Sakai, H., Takeuchi, R., Tsuchiya, K., Ohta, K., Sugawara, F., Abe, M., & Sakaguchi, K. (2005) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2005.11.002 · Cited by 13

The Xenopus Cell Cycle: An Overview

Philpott, A., & Yew, P. R. (2004) · Humana Press eBooks · doi:10.1385/1-59259-857-9:095 · Cited by 14

Human DNA Polymerase β Mutations Allowing Efficient Abasic Site Bypass

Gieseking, S., Bergen, K., Pasquale, F. D., Diederichs, K., Welte, W., & Marx, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.176826 · Cited by 12

Proteome-wide analysis reveals molecular pathways affected by AgNP in a ROS-dependent manner

Miranda, R. R., Oliveira, A. C. S., Skytte, L., Rasmussen, K. L., & Kjeldsen, F. (2022) · Nanotoxicology · doi:10.1080/17435390.2022.2036844 · Cited by 12

Differential requirement for the N-terminal catalytic domain of the DNA polymerase ε p255 subunit in the mitotic cell cycle and the endocycle

Suyari, O., Kawai, M., Ida, H., Yoshida, H., Sakaguchi, K., & Yamaguchi, M. (2012) · Gene · doi:10.1016/j.gene.2011.12.056 · Cited by 12

Purified Canola Lutein Selectively Inhibits Specific Isoforms of Mammalian DNA Polymerases and Reduces Inflammatory Response

Horie, S., Okuda, C., Yamashita, T., Watanabe, K., Kuramochi, K., Hosokawa, M., Takeuchi, T., Kakuda, M., Miyashita, K., Sugawara, F., et al. (2010) · Lipids · doi:10.1007/s11745-010-3449-5 · Cited by 12

Transcriptional upregulation of DNA polymerase β by TEIF

Zhao, Y., Zheng, J., Ling, Y., Hou, L., & Zhang, B. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.05.172 · Cited by 12

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

Probing Conformational Changes of Human DNA Polymerase λ using Mass Spectrometry-Based Protein Footprinting

Fowler, J. D., Brown, J. A., Kvaratskhelia, M., & Suo, Z. (2009) · Journal of Molecular Biology · doi:10.1016/j.jmb.2009.05.037 · Cited by 12

Selective Inhibition of Mammalian DNA Polymerase α by Vitamin D2 and D3

Mizushina, Y., Xu, X., Murakami, C., Okano, T., Takemura, M., Yoshida, H., & Sakaguchi, K. (2003) · Journal of Pharmacological Sciences · doi:10.1254/jphs.92.283 · 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

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

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

The Glycine-Rich Motif of Pyrococcus abyssi DNA Polymerase D Is Critical for Protein Stability

Castrec, B., Laurent, S., Henneke, G., Flament, D., & Raffin, J. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.01.006 · Cited by 11

Human PrimPol Discrimination against Dideoxynucleotides during Primer Synthesis

Carvalho, G., Díaz‐Talavera, A., Calvo, P. A., Blanco, L., & Martínez-Jiménez, M. I. (2021) · Genes · doi:10.3390/genes12101487 · Cited by 11

Antimutagenic Role of Autonomous 3′ → 5′-Exonucleases

Krutyakov, V. M. (2004) · Molecular Biology · doi:10.1023/b:mbil.0000043939.69124.de · Cited by 11

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

On the molecular mechanism of somatic hypermutation of rearranged immunoglobulin genes

Franklin, A., & Blanden, R. V. (2004) · Immunology and Cell Biology · doi:10.1111/j.1440-1711.2004.01289.x · Cited by 11

Discovery and Mutagenicity of a Guanidinoformimine Lesion as a new Intermediate of the Oxidative Deoxyguanosine Degradation Pathway

Stathis, D., Lischke, U., Koch, S. C., Deiml, C. A., & Carell, T. (2012) · Journal of the American Chemical Society · doi:10.1021/ja211435d · Cited by 11

Telomerase activity is required for the telomere G-overhang structure in Trypanosoma brucei

Sandhu, R. S., & Li, B. (2017) · Scientific Reports · doi:10.1038/s41598-017-16182-y · Cited by 12

Free-Energy Perturbation Methods to Study Structure and Energetics of DNA Adducts: Results for the Major N2-dG Adduct of Benzo[a]pyrene in Two Conformations and Different Sequence Contexts

Chandani, S., Lee, C. H., & Loechler, E. L. (2005) · Chemical Research in Toxicology · doi:10.1021/tx049646l · Cited by 11

Comparison of Bacterial and Eukaryotic Replisome Components

Yao, N. Y., & O’Donnell, M. E. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.10038-0 · Cited by 12

The role of human replicative DNA polymerases in DNA repair and replication

Rytkönen, A. K. (2006) · Cited by 11

Following DNA Chain Extension and Protein Conformational Changes in Crystals of a Y-Family DNA Polymerase via Raman Crystallography

Espinoza, S., Gaur, V., Suo, Z., & CAREY, P. R. (2013) · Biochemistry · doi:10.1021/bi400524h · Cited by 10

DNA polymerases β and λ and their roles in DNA replication and repair

Belousova, E. A., & Lavrik, O. I. (2010) · Molecular Biology · doi:10.1134/s0026893310060014 · Cited by 10

Enhancement of human cancer cell radiosensitivity by conjugated eicosapentaenoic acid - a mammalian DNA polymerase inhibitor

Mizushina (2010) · International Journal of Oncology · doi:10.3892/ijo_00000532 · Cited by 10

Modulating the pKa of a Tyrosine in KlenTaq DNA Polymerase that Is Crucial for Abasic Site Bypass by in Vivo Incorporation of a Non‐canonical Amino Acid

Blatter, N., Prokup, A., Deiters, A., & Marx, A. (2014) · ChemBioChem · doi:10.1002/cbic.201400051 · 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

Sensitivity of human cells expressing low-fidelity or weak-catalytic-activity variants of DNA polymerase ζ to genotoxic stresses

Suzuki, T., Grúz, P., Honma, M., Adachi, N., & Nohmi, T. (2016) · DNA repair · doi:10.1016/j.dnarep.2016.06.002 · Cited by 10

Proliferating cell nuclear antigen (PCNA) interacts with a meiosis-specific RecA homologues, Lim15/Dmc1, but does not stimulate its strand transfer activity

Hamada, F. N., Koshiyama, A., Namekawa, S. H., Ishii, S., Iwabata, K., Sugawara, H., Nara, T., Sakaguchi, K., & Sawado, T. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.11.094 · Cited by 10

Multiple PolK (POLK) transcripts in mammalian testis

Guo, C., Gao, T., Confer, N., Velasco-Miguel, S., & Friedberg, E. C. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.10.006 · Cited by 10

Tuning the reaction site for enzyme-free primer-extension reactions through small molecule substituents

Rojas Stütz, J. A., & Richert, C. (2006) · Chemistry – A European Journal · doi:10.1002/chem.200501008 · Cited by 9

Thermodynamic Insights by Microscale Thermophoresis into Translesion DNA Synthesis Catalyzed by DNA Polymerases Across a Lesion of Antitumor Platinum–Acridine Complex

Hreusová, M., Nováková, O., & Brabec, V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207806 · Cited by 7

Human DNA Polymerase ν Catalyzes Correct and Incorrect DNA Synthesis with High Catalytic Efficiency

Gowda, A. S. P., Moldovan, G., & Spratt, T. E. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.653287 · Cited by 9

Activation-induced cytidine deaminase acts on double-strand breaks in vitro

SHEN, H. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.03.015 · Cited by 9

Human DNA polymerase α interacts with mismatch repair proteins MSH 2 and MSH 6

Itkonen, H. M., Kantelinen, J., Vaara, M., Parkkinen, S., Schlott, B., Große, F., Nyström, M., Syväoja, J. E., & Pospiech, H. (2016) · FEBS Letters · doi:10.1002/1873-3468.12475 · Cited by 9

Family A and B DNA Polymerases in Cancer: Opportunities for Therapeutic Interventions

Shanbhag, V., Sachdev, S., Flores, J., Modak, M. J., & Singh, K. (2018) · Biology · doi:10.3390/biology7010005 · Cited by 9

Regulatory Pathways Coordinating Cell Cycle Progression in Early Xenopus Development

Gotoh, T., Villa, L. M., Capelluto, D. G. S., & Finkielstein, C. V. (2011) · Results and problems in cell differentiation · doi:10.1007/978-3-642-19065-0_9 · Cited by 9

Role of swi7H4 Mutant Allele of DNA Polymerase α in the DNA Damage Checkpoint Response

Khan, S., & Ahmed, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124063 · Cited by 9

Mouse models of DNA polymerases

Menezes, M. R., & Sweasy, J. B. (2012) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21731 · Cited by 9

The active site of TthPolX is adapted to prevent 8-oxo-dGTP misincorporation

Garrido, P. I., Mejía, E., García–Díaz, M., Blanco, L., & Picher, Á. J. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt870 · Cited by 9

Chemical properties of fatty acid derivatives as inhibitors of DNA polymerases

Nakamura, R., Takeuchi, R., Kuramochi, K., Mizushina, Y., Ishimaru, C., Takakusagi, Y., Takemura, M., Kobayashi, S. S., Yoshida, H., Sugawara, F., et al. (2007) · Organic & Biomolecular Chemistry · doi:10.1039/b710944j · Cited by 9

On the role of proofreading exonuclease in bypass of a 1,2 d(GpG) cisplatin adduct by the herpes simplex virus-1 DNA polymerase

Arana, M. E., Song, L., Gac, N. T. L., Parris, D. S., Villani, G., & Boehmer, P. E. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.02.006 · Cited by 9

DNA stabilization at the Bacillus subtilis PolX core —a binding model to coordinate polymerase, AP-endonuclease and 3′-5′ exonuclease activities

Baños, B., Villar, L., Salas, M., & de Vega, M. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks702 · Cited by 8

Biochemical and functional characterization of Plasmodium falciparum DNA polymerase δ

Vasuvat, J., Montree, A., Moonsom, S., Leartsakulpanich, U., Petmitr, S., Focher, F., Wright, G. E., & Chavalitshewinkoon-Petmitr, P. (2016) · Malaria Journal · doi:10.1186/s12936-016-1166-0 · Cited by 8

HSV-1 DNA polymerase 3′-5′ exonuclease-deficient mutant D368A exhibits severely reduced viral DNA synthesis and polymerase expression

Lawler, J. L., & Coen, D. M. (2018) · Journal of General Virology · doi:10.1099/jgv.0.001138 · Cited by 8

Error-prone bypass patch by a low-fidelity variant of DNA polymerase zeta in human cells

Suzuki, T., Sassa, A., Grúz, P., Gupta, R. C., Johnson, F., Adachi, N., & Nohmi, T. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103052 · Cited by 8

From cue to meaning: The involvement of POLD1 gene in DNA replication, repair and aging

Murdocca, M., Spitalieri, P., D’Apice, M. R., Novelli, G., & Sangiuolo, F. C. (2023) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2023.111790 · Cited by 8

DNA Polymerases and Mutagenesis in Human Cancers

Crespan, E., Amoroso, A., & Maga, G. (2009) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-90-481-3471-7_9 · Cited by 8

Role of the second-largest subunit of DNA polymerase α in the interaction between the catalytic subunit and hyperphosphorylated retinoblastoma protein in late S phase

Takemura, M., Yoshida, S., Akiyama, T., Kitagawa, M., & Yamada, Y. (2006) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2006.06.015 · Cited by 8

Inhibitory Effect of Monogalactosyldiacylglycerol, Extracted from Spinach Using Supercritical CO2, on Mammalian DNA Polymerase Activity

Iijima, H., Musumi, K., Hada, T., Maeda, N., Yonezawa, Y., Yoshida, H., & Mizushina, Y. (2006) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf051950c · Cited by 8

.BETA.-Sitosteryl (6'-O-linoleoyl)-glucoside of Soybean (Glycine max L.) Crude Extract Inhibits Y-Family DNA Polymerases

Horie, S., Okuda, C., Yamashita, T., Watanabe, K., Satō, Y., Yamaguchi, Y., Takeuchi, T., Sugawara, F., Yoshida, H., & Mizushina, Y. (2010) · Journal of Oleo Science · doi:10.5650/jos.59.621 · Cited by 8

Dehydroaltenusin is a specific inhibitor of mammalian DNA polymerase α

Mizushina, Y., Maeda, N., Kuriyama, I., & Yoshida, H. (2011) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2011.619977 · Cited by 8

Catalytic Mechanism of DNA Polymerases

Roettger, M. P., Bakhtina, M., Kumar, S., & Tsai, M. (2010) · Elsevier eBooks · doi:10.1016/b978-008045382-8.00669-9 · Cited by 8

High frequency of nucleotide misincorporations upon the processing of double-strand breaks

Kovalchuk, I., Pelczar, P., & Kovalchuk, O. (2003) · DNA repair · doi:10.1016/j.dnarep.2003.09.011 · Cited by 8

Varied Active‐Site Constraints in the Klenow Fragment of E. coli DNA Polymerase I and the Lesion‐Bypass Dbh DNA Polymerase

Cramer, J., Gopinath, R., Marx, A., & Restle, T. (2008) · ChemBioChem · doi:10.1002/cbic.200700634 · Cited by 8

The screening of expression and purification conditions for replicative DNA polymerase associated B-subunits, assignment of the exonuclease activity to the C-terminus of archaeal pol D DP1 subunit

Jokela, M., Raki, M., Heikkinen, K., Sepponen, K., Eskelinen, A., & Syväoja, J. E. (2005) · Protein Expression and Purification · doi:10.1016/j.pep.2005.05.002 · Cited by 8

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. (2004) · Biochemistry (Moscow) · doi:10.1023/b:biry.0000026201.71587.a2 · Cited by 8

Roles of DNA polymerase epsilon and TopBP1 in DNA replication and damage response

Hillukkala, T. (2006) · Cited by 8

Eukaryotic DNA Polymerases

Cotterill, S., & Kearsey, S. E. (2002) · Wiley eBooks · doi:10.1038/npg.els.0001045 · Cited by 8

Strukturen von DNA‐Polymerasen mit 4′‐alkylierten Nucleotiden im aktiven Zentrum

Betz, K., Streckenbach, F., Schnur, A., Exner, T. E., Welte, W., Diederichs, K., & Marx, A. (2010) · Angewandte Chemie · doi:10.1002/ange.200905724 · Cited by 7

The Cell

Lalan, M. S., Bagchi, T., & Misra, A. R. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-384964-9.00001-3 · Cited by 7

Formation of dAMP-glycerol and dAMP-Tris Derivatives by Thermococcus kodakaraensis DNA Primase

Galal, W. C., Pan, M., Giulian, G. G., Yuan, W., Li, S., Edwards, J. L., Marino, J. P., Kelman, Z., & Hurwitz, J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.338160 · Cited by 7

The Establishment of an Assay to Measure DNA Polymerase-Catalyzed Repair of UVB-Induced DNA Damage in Skin Cells and Screening of DNA Polymerase Enhancers from Medicinal Plants

Ikeoka, S., Nakahara, T., Iwahashi, H., & Mizushina, Y. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17050667 · Cited by 7

Human DNA Polymerase β, but Not λ, Can Bypass a 2-Deoxyribonolactone Lesion Together with Proliferating Cell Nuclear Antigen

Crespan, E., Pasi, E., Imoto, S., Hübscher, U., Greenberg, M. M., & Maga, G. (2012) · ACS Chemical Biology · doi:10.1021/cb300542k · Cited by 7

DNA Replication and Cell Cycle

Lao-Sirieix, S.-H., Marsh, V. L., & Bell, S. D. (2014) · ASM Press eBooks · doi:10.1128/9781555815516.ch3 · Cited by 7

5-O-Acyl plumbagins inhibit DNA polymerase activity and suppress the inflammatory response

Onodera, T., Kuriyama, I., Sakamoto, Y., Kawamura, M., Kuramochi, K., Tsubaki, K., Tabata, A., Naganune, H., & Mizushina, Y. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.02.032 · Cited by 7

Accumulation of FFA-1, the Xenopus Homolog of Werner Helicase, and DNA Polymerase δ on Chromatin in Response to Replication Fork Arrest

Sasakawa, N., Fukui, T., & Waga, S. (2006) · The Journal of Biochemistry · doi:10.1093/jb/mvj130 · Cited by 7

Mutations/polymorphisms in the 55 kDa subunit of DNA polymerase epsilon in human colorectal cancer.

Zhou, Q., Talvinen, K., Sundström, J. T. T., Elzagheid, A., Pospiech, H., Syväoja, J. E., & Collan, Y. U. (2009) · PubMed · Cited by 7

The Substrate Activity of (S)-9-[3-Hydroxy-(2-phosphonomethoxy)Propyl]Adenine Diphosphate toward DNA Polymerases α, δ and ε

Birkuš, G., Rejman, D., Otmar, M., Votruba, I., Rosenberg, I., & Holý, A. (2004) · Antiviral chemistry & chemotherapy · doi:10.1177/095632020401500103 · Cited by 7

Chemotherapeutic intervention by inhibiting DNA polymerases

Dasari, A., Choi, J.-S., & Berdis, A. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803582-5.00007-3 · Cited by 7

Eukaryotic DNA Polymerase α

Lee, C.-T., & Tye, B. (2013) · Encyclopedia of Biological Chemistry · doi:10.1016/b978-0-12-378630-2.00408-4 · Cited by 7

Duplication of DNA in eukaryotic cells

Kelly, T. J., & Stillman, B. (2006) · Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) · doi:10.1101/087969766.47.1 · Cited by 7

Role of the LEXE Motif of Protein-primed DNA Polymerases in the Interaction with the Incoming Nucleotide

Santos, E., Lázaro, J. M., Pérez-Arnaiz, P., Salas, M., & de Vega, M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.530980 · Cited by 6

60 years of SOS repair

Zavilgelsky, G. B. (2013) · Molecular Biology · doi:10.1134/s0026893313050221 · Cited by 6

Biochemical, cellular and molecular identification of DNA polymerase α in yeast mitochondria

Lasserre, J.-P., Plissonneau, J., Velours, C., Bonneu, M., Litvak, S., Laquel, P., & Castroviejo, M. (2012) · Biochimie · doi:10.1016/j.biochi.2012.11.003 · Cited by 6

Validating the disruption of proliferating cell nuclear antigen interactions in the development of targeted cancer therapeutics

Smith, S. J., Hickey, R. J., & Malkas, L. H. (2016) · Cancer Biology & Therapy · doi:10.1080/15384047.2016.1139247 · Cited by 6

Interactions of Transposons with the Cellular DNA Repair Machinery

Izsvák, Z., Wang, Y., & Ivics, Z. (2009) · Genome dynamics and stability · doi:10.1007/7050_2008_043 · Cited by 6

Cholesterol hemisuccinate: A selective inhibitor of family X DNA polymerases

Ishimaru, C., Kuriyama, I., Shimazaki, N., Koiwai, O., Sakaguchi, K., Kato, I., Yoshida, H., & Mizushina, Y. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.01.034 · Cited by 6

Characterization of marine X-family DNA polymerases and comparative analysis of base excision repair proteins

Kodera, H., Takeuchi, R., Uchiyama, Y., Takakusagi, Y., Iwabata, K., Miwa, H., Hanzawa, N., Sugawara, F., & Sakaguchi, K. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.10.058 · Cited by 6

Aberrant DNA Polymerase α Is Excluded from the Nucleus by Defective Import and Degradation in the Nucleus

Eichinger, C. S., Mizuno, T., Mizuno, K., Miyake, Y., Yanagi, K., Imamoto, N., & Hanaoka, F. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.024760 · Cited by 6

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

An array of basic residues is essential for the nucleolytic activity of the PHP domain of bacterial/archaeal PolX DNA polymerases

Rodríguez, G., Martín, M. T., & de Vega, M. (2019) · Scientific Reports · doi:10.1038/s41598-019-46349-8 · Cited by 8

Analysis of DNA Polymerases Reveals Specific Genes Expansion in Leishmania and Trypanosoma spp.

Poveda, A., Méndez, M., & Armijos‐Jaramillo, V. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.570493 · Cited by 5

A Multifunctional Protein PolDIP2 in DNA Translesion Synthesis

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