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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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

Displacement of Slow-Turnover DNA Glycosylases by Molecular Traffic on DNA

Yudkina, A. V., Endutkin, A. V., Diatlova, E. A., Moor, N. A., Vokhtantsev, I. P., Грин, И. Р., & Zharkov, D. O. (2020) · Genes · doi:10.3390/genes11080866 · 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

Replication, Repair, and Translesion Polymerase Bypass of N6-Oxopropenyl-2′-deoxyadenosine

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Engineering Nucleobases and Polymerases for an Expanded Genetic Alphabet

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Increase in error threshold for quasispecies by heterogeneous replication accuracy

Aoki, K., & Furusawa, M. (2003) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.68.031904 · 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

Xeroderma Pigmentosum Variant, XP-V: Its Product and Biological Roles

Masutani, C., Hanaoka, F., & Ahmad, S. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-09599-8_10 · Cited by 10

SV40 DNA Replication Inhibition by the Monofunctional DNA Alkylator Et743

Dziegielewska, B., Kowalski, D., & Beerman, T. A. (2004) · Biochemistry · doi:10.1021/bi049407x · Cited by 10

The bypass of DNA lesions by DNA and RNA polymerases

Holmquist, G. P., & Maher, V. M. (2002) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(02)00247-6 · Cited by 10

HMGB3 and SUB1 Bind to and Facilitate the Repair of N 2 -Alkylguanine Lesions in DNA

Zhao, T. S., He, X., Liang, X., Kellum, A. H., Tang, F., Yin, J., Guo, S., Wang, Y., Gao, Z., & Wang, Y. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.4c06680 · Cited by 9

Strand Annealing and Terminal Transferase Activities of a B-family DNA Polymerase

Zuo, Z., Lin, H.-K., & Trakselis, M. A. (2011) · Biochemistry · doi:10.1021/bi200421g · Cited by 9

Involvement of specialized DNA polymerases Pol II, Pol IV and DnaE2 in DNA replication in the absence of Pol I in Pseudomonas putida

Sidorenko, J., Jatsenko, T., Saumaa, S., Teras, R., Tark‐Dame, M., Hõrak, R., & Kivisaar, M. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.06.013 · Cited by 9

Germinal Center B-Cell-Associated Nuclear Protein (GANP) Involved in RNA Metabolism for B Cell Maturation

Sakaguchi, N., & Maeda, K. (2016) · Advances in immunology · doi:10.1016/bs.ai.2016.02.003 · Cited by 9

The control of the discrimination between dNTP and rNTP in DNA and RNA polymerase

Yoon, H., & Warshel, A. (2016) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.25104 · Cited by 9

Replisome Dynamics during Chromosome Duplication

Kurth, I., & O’Donnell, M. E. (2009) · EcoSal Plus · doi:10.1128/ecosalplus.4.4.2 · Cited by 11

DNA polymerases β and λ as potential participants of TLS during genomic DNA replication on the lagging strand

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Broad-Spectrum Antibacterial Peptide Kills Extracellular and Intracellular Bacteria Without Affecting Epithelialization

Nepal, A., Ræder, S. B., Søgaard, C. K., Haugan, M. S., & Otterlei, M. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.764451 · Cited by 9

A Nucleotide-Analogue-Induced Gain of Function Corrects the Error-Prone Nature of Human DNA Polymerase iota

Ketkar, A. D., Zafar, M. K., Banerjee, S., Márquez, V. E., Egli, M., & Eoff, R. L. (2012) · Journal of the American Chemical Society · doi:10.1021/ja304176q · Cited by 9

DNA ADDUCTS OF BENZO[ A ]PYRENE- AND DIBENZO[ A,L ]PYRENE-DIOL EPOXIDES IN HUMAN LUNG EPITHELIAL CELLS: KINETICS OF ADDUCT REMOVAL, EFFECTS ON CELL CYCLE CHECKPOINTS, AND GENE EXPRESSION

Dreij, K., Bajak, E., Sundberg, K., Cotgreave, I. A., Jernström, B., Seidel, A., & Gusnanto, A. (2004) · Polycyclic aromatic compounds · doi:10.1080/10406630490471645 · Cited by 9

Impact of Chemical Adducts on Translesion Synthesis in Replicative and Bypass DNA Polymerases: From Structure to Function

Eoff, R. L., Egli, M., & Guengerich, F. P. (2010) · Wiley eBooks · doi:10.1002/9783527630110.ch13 · Cited by 9

Sequence Context Effect on Strand Slippage in Natural DNA Primer–Templates

Chi, L. M., & Lam, S. L. (2012) · The Journal of Physical Chemistry B · doi:10.1021/jp211666k · Cited by 8

RNA Primer Extension Hinders DNA Synthesis by Escherichia coli Mutagenic DNA Polymerase IV

Tashjian, T. F., Lin, I., Belt, V., Cafarelli, T. M., & Godoy, V. G. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00288 · Cited by 8

Genomic diversity of Taylorella equigenitalis introduced into the United States from 1978 to 2012

Hicks, J. A., Stuber, T. P., Lantz, K., Erdman, M. M., Robbe‐Austerman, S., & Huang, X. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194253 · Cited by 9

Investigating the Conformational Dynamics of a Y-Family DNA Polymerase during Its Folding and Binding to DNA and a Nucleotide

Chu, X., Suo, Z., & Wang, J. (2021) · JACS Au · doi:10.1021/jacsau.1c00368 · Cited by 8

Role of damage-specific DNA polymerases in M13 phage mutagenesis induced by a major lipid peroxidation product trans-4-hydroxy-2-nonenal

Janowska, B., Kurpios-Piec, D., Prorok, P., Szparecki, G., Komisarski, M., Kowalczyk, P., Janion, C., & Tudek, B. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.09.006 · Cited by 8

The role of the DNA damage checkpoint in regulation of translesion DNA synthesis

Koren, A. (2007) · Mutagenesis · doi:10.1093/mutage/gem003 · Cited by 8

Targeting DNA Repair Systems in Antitubercular Drug Development

Minias, A. E., Brzostek, A. M., & Dziadek, J. (2018) · Current Medicinal Chemistry · doi:10.2174/0929867325666180129093546 · Cited by 8

Chronological Switch from Translesion Synthesis to Homology-Dependent Gap RepairIn Vivo

藤井, 慎., Isogawa, A., & Fuchs, R. P. (2018) · Toxicological Research · doi:10.5487/tr.2018.34.4.297 · Cited by 8

Integration Host Factor IHF facilitates homologous recombination and mutagenic processes in Pseudomonas putida

Mikkel, K., Tagel, M., Ukkivi, K., Ilves, H., & Kivisaar, M. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102745 · Cited by 8

Effects of Spatial Structure and Reduced Growth Rates on Evolution in Bacterial Populations

France, M., Ridenhour, B. J., & Forney, L. J. (2018) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-319-69078-0_8 · Cited by 9

Spontaneous transformation of an immortalized hepatocyte cell line: potential role of a nuclear protease

Drubin, D. A., & Clawson, G. A. (2004) · Cancer Letters · doi:10.1016/j.canlet.2004.03.045 · 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

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

Somatic Hypermutation Patterns in Germinal Center B Cell Malignancies

Σταματόπουλος, Κ., Belessi, C., Papadaki, T., Stavroyianni, N., Hadzidimitriou, A., Kosmas, C., Laoutaris, N. P., Fassas, Α., & Anagnostopoulos, Α. (2003) · Hematology · doi:10.1080/10245330310001612143 · Cited by 8

The antioxidant drug N-acetylcysteine abolishes SOS-mediated mutagenesis produced by fluoroquinolones in bacteriaPreprint

Rodríguez-Rosado, A. I., Morante, E. Y. V., Rodríguez-Rojas, A., Costas, C., Galhardo, R. S., Blázquez, J., & Rodríguez-Beltrán, J. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/428961 · 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

Bulky Lesion Bypass Requires Dpo4 Binding in Distinct Conformations

Liyanage, P. S., Walker, A. R., Brenlla, A., Cisneros, G. A., Romano, L. J., & Rueda, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-17643-0 · Cited by 7

The RecX protein interacts with the RecA protein and modulates its activity in Herbaspirillum seropedicae

Galvão, C. W., de Souza, E. M., Etto, R. M., Pedrosa, F. O., Chubatsu, L. S., Yates, M. G., Schumacher, J., Buck, M., & Steffens, M. B. R. (2012) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2012007500160 · Cited by 7

Identification of mammary epithelial cells subject to chronic oxidative stress in mammary epithelium of young women and teenagers living in USA

Weisz, J., Shearer, D. A., Murata, E., Patrick, S. D., Han, B., Berg, A. S., & Clawson, G. A. (2012) · Cancer Biology & Therapy · doi:10.4161/cbt.13.2.18873 · Cited by 8

Effect of Mn(II) on error-prone DNA polymerase iota activity in extracts from human normal and tumor cells

Лахин, А. В., Efremova, A. S., Makarova, I. V., Гришина, Е. Е., Shram, S. I., Tarantul, V. Z., & Gening, L. V. (2013) · Molecular Genetics Microbiology and Virology · doi:10.3103/s0891416813010035 · Cited by 7

RAD18 and associated proteins are immobilized in nuclear foci in human cells entering S-phase with ultraviolet light-induced damage

Watson, N. B., Nelson, E., Digman, M. A., Thornburg, J. M., Alphenaar, B., & McGregor, W. G. (2008) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2008.09.006 · Cited by 8

Preferential occurrence of 1-2 microindels

Hill, K. A., Hagman, K. D. F., Scaringe, W. A., Wang, J., & Sommer, S. S. (2005) · Human Mutation · doi:10.1002/humu.20260 · Cited by 7

TB or Not TB

Friedberg, E. C., & Fischhaber, P. L. (2003) · Cell · doi:10.1016/s0092-8674(03)00275-7 · Cited by 7

Altered translesion synthesis in E. coli Pol V mutants selected for increased recombination inhibition

Sommer, S., Bécherel, O. J., Coste, G., Bailone, A., & Fuchs, R. P. (2003) · DNA repair · doi:10.1016/j.dnarep.2003.08.008 · Cited by 7

The boundaries of the distribution of somatic hypermutation of rearranged immunoglobulin variable genes

Blanden, R. V., Franklin, A., & Steele, E. J. (2004) · Immunology and Cell Biology · doi:10.1046/j.0818-9641.2004.01226.x · 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

EXPOSURE OF MAMMALIAN CELLS TO DIOL EPOXIDES FROM BENZO[A]PYRENE AND DIBENZO[A,L]PYRENE AND EFFECTS ON Mdm2 AND P53

Pääjärvi, G., Jernström, B., Stenius, U., & Seidel, A. (2004) · Polycyclic aromatic compounds · doi:10.1080/10406630490471636 · Cited by 9

Genetics just got SEXY

Sleator, R. D. (2014) · Bioengineered · doi:10.4161/bioe.29306 · Cited by 7

Hallmarks of DNA replication stress responses in Escherichia coli and Bacillus subtilis

Torres, R., Carrasco, B., Ayora, S., & Alonso, J. C. (2025) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf041 · Cited by 8

Complete nucleotide sequence of pGS18, a 62.8-kb plasmid from Geobacillus stearothermophilus strain 18

Stuknytė, M., Guglielmetti, S., Mora, D., Kuisienė, N., Parini, C., & Čitavičius, D. J. (2008) · Extremophiles · doi:10.1007/s00792-008-0145-y · Cited by 6

60 years of SOS repair

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

Recent Patents of Gene Sequences Relative to DNA Polymerases

Reha-Krantz, L. J. (2008) · Recent Patents on DNA & Gene Sequences · doi:10.2174/187221508786241729 · Cited by 6

Kinetic Approaches to Understanding the Mechanisms of Fidelity of the Herpes Simplex Virus Type 1 DNA Polymerase

Zhu, Y., Stroud, J., Song, L., & Parris, D. S. (2010) · Journal of Nucleic Acids · doi:10.4061/2010/631595 · Cited by 6

A nucleotide binding rectification Brownian ratchet model for translocation of Y-family DNA polymerases

Xie, P. (2011) · Theoretical Biology and Medical Modelling · doi:10.1186/1742-4682-8-22 · Cited by 6

Increased Processivity, Misincorporation, and Nucleotide Incorporation Efficiency in Sulfolobus solfataricus Dpo4 Thumb Domain Mutants

Wang, L., Liang, C., Wu, J., Liu, L., & Tyo, K. E. J. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01013-17 · Cited by 6

Response of Sulfolobus solfataricus Dpo4 polymerase in vitro to a DNA G-quadruplex

Berroyer, A., Alvarado, G., & Larson, E. D. (2019) · Mutagenesis · doi:10.1093/mutage/gez010 · Cited by 6

Photo-activatable Ub-PCNA probes reveal new structural features of the Saccharomyces cerevisiae Polη/PCNA complex

Shen, S., Davidson, G. A., Yang, K., & Zhuang, Z. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab646 · Cited by 6

The impact of genomics on discovering drugs against infectious diseases

Boshoff, H. I., & Manjunatha, U. H. (2006) · Microbes and Infection · doi:10.1016/j.micinf.2005.11.018 · Cited by 6

Translesion Synthesis And Errorprone Polymerases

Green, C., & Lehmann, A. R. (2006) · Springer eBooks · doi:10.1007/1-4020-3764-3_7 · Cited by 6

Constraints on Variation from Genotype through Phenotype to Fitness

Ancel, L. W. (2005) · Elsevier eBooks · doi:10.1016/b978-012088777-4/50008-9 · Cited by 6

Molecular evolution steered structural adaptations in the DNA polymerase III α subunit of halophilic bacterium Salinibacter ruber

Sengupta, A., Das, K., Jha, N., Akhter, Y., & Kumar, A. (2023) · Extremophiles · doi:10.1007/s00792-023-01306-2 · Cited by 5

Bypass DNA Polymerases

Choi, J., Eoff, R. L., & Guengerich, F. P. (2010) · Humana Press eBooks · doi:10.1007/978-1-61737-995-6_16 · Cited by 5

Purification and Characterization of Escherichia coli DNA Polymerase V

Schlacher, K., Jiang, Q., Woodgate, R., & Goodman, M. F. (2006) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(06)08023-2 · Cited by 5

Establishment of a Method for Analyzing Translesion DNA Synthesis across a Single Bulky Adduct in Human Cells

Sawai, T., Kawanishi, M., Takamura‐Enya, T., & Yagi, T. (2009) · Genes and Environment · doi:10.3123/jemsge.31.24 · Cited by 5

Chlamydial DNA polymerase I can bypass lesions in vitro

Liu, X., Hou, J., & Liu, J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.05.021 · Cited by 5

Global Genome Nucleotide Excision Repair Proteins Rhp7p and Rhp41p Are Involved in Abasic Site Repair of Schizosaccharomyces pombe

Sakurai, E., Susuki, M., Kanamitsu, K., Kawano, S., & Ikeda, S. (2015) · Advances in Bioscience and Biotechnology · doi:10.4236/abb.2015.64026 · Cited by 5

DNA polymerase ι of mammals as a participant in translesion synthesis of DNA

Gening, L. V. (2011) · Biochemistry (Moscow) · doi:10.1134/s0006297911010081 · Cited by 5

Molecular mechanisms of microbial resistance to disinfectants

Kovalchuk, S. N., Fedorova, L. P., & Ilina, E. N. (2023) · Antibiot Khimioter = Antibiotics and Chemotherapy · doi:10.37489/0235-2990-2023-68-1-2-45-56 · Cited by 5

DNA repair in Chromobacterium violaceum.

Duarte, F. T., de Carvalho, F. M., da Silva, U. B., Scortecci, K. C., Blaha, C. A. G., Agnez‐Lima, L. F., & de Medeiros, S. R. B. (2004) · PubMed · Cited by 5

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

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

Alternative splicing of two translesion synthesis DNA polymerases from Arabidopsis thaliana

Santiago, M. J., Alejandre-Durán, E., & Ruiz‐Rubio, M. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.01.018 · Cited by 5

Ubiquitous expression of two translesion synthesis DNA polymerase genes in Arabidopsis

Santiago, M. J., Ruiz‐Rubio, M., Dio, L. D., González-Reyes, J. A., & Alejandre-Durán, E. (2008) · Planta · doi:10.1007/s00425-008-0698-0 · Cited by 5

Lighting torches in the DNA repair field: development of key concepts

Walker, G. C. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.03.010 · Cited by 5

DNA Polymerases and Diseases

Ramadan, K., Maga, G., & Hübscher, U. (2006) · Springer eBooks · doi:10.1007/7050_005 · Cited by 5

Molecular modeling of the major benzo[a]pyrene N2-dG adduct in cases where mutagenesis results are known in double stranded DNA

Lee, C. H., & Loechler, E. L. (2003) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(03)00107-6 · Cited by 5

Low-fidelity DNA polymerases

Lehmann, A. R. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00518-9 · Cited by 5

Steric Constraints Dependent on Nucleobase Pair Orientation Vary in Different DNA Polymerase Active Sites

Streckenbach, F., Gopinath, R., Möller, H. M., & Marx, A. (2009) · ChemBioChem · doi:10.1002/cbic.200900123 · Cited by 5

Changes in the genomes and methylomes of three Salmonella enterica serovars after long-term storage in ground black pepper

Davies, C. P., Jurkiw, T., Haendiges, J., Reed, E. A., Anderson, N. M., Grasso‐Kelley, E. M., Hoffmann, M., & Zheng, J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.970135 · Cited by 4

The PAD region in the mycobacterial DinB homologue MsPolIV exhibits positional heterogeneity

Sharma, A. S., Subramanian, V., & Nair, D. T. (2012) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444912017623 · Cited by 4

Enhancement of silencing DNA polymerase β on the radiotherapeutic sensitivity of human esophageal carcinoma cell lines

Wang, Y., Chen, X., Hu, X., Ren, Z., Du, Y., Zang, W., Dong, Z., & Zhao, G. (2014) · Tumor Biology · doi:10.1007/s13277-014-2308-z · Cited by 4

Replication fidelity in E. coli: Differential leading and lagging strand effects for dnaE antimutator alleles

Makiela‐Dzbenska, K., Masłowska, K. H., Kuban, W., Gaweł, D., Jonczyk, P., Schaaper, R. M., & Fijałkowska, I. J. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102643 · Cited by 4

Identification of a signature of evolutionarily conserved stress-induced mutagenesis in cancer

Cisneros, L. H., Vaske, C. J., & Bussey, K. J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.932763 · Cited by 4

Analysis of DNA replication damage bypass and its role in immunoglobulin repertoire development

Sale, J. E., Ross, A.-L., & Simpson, L. J. (2006) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-1-4020-4896-8_16 · Cited by 4

Molecular Mechanism of Hypermutation

Maizels, N., & Scharff, M. D. (2004) · Elsevier eBooks · doi:10.1016/b978-012053641-2/50022-8 · Cited by 4

Application of XeCl308 nmexcimer laser radiation to mutagenesis of industrial microorganisms

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Roadworks of DNA Damage Bypass during and after Replication

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