DNA Base Damage by Reactive Oxygen Species, Oxidizing Agents, and UV Radiation

Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1

Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836 · see citing works

Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine

Ito, S., Shen, L., Dai, Q., Wu, S. C., Collins, L. B., Swenberg, J. A., He, C., & Zhang, Y. (2011) · Science · doi:10.1126/science.1210597 · Cited by 3,451 · see citing works

The Nuclear DNA Base 5-Hydroxymethylcytosine Is Present in Purkinje Neurons and the Brain

Kriaucionis, S., & Heintz, N. (2009) · Science · doi:10.1126/science.1169786 · Cited by 2,700 · see citing works

Reconciling the chemistry and biology of reactive oxygen species

Winterbourn, C. C. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.85 · Cited by 2,504 · see citing works

Hollow Capsule Processing through Colloidal Templating and Self-Assembly

Caruso, F. (2000) · Chemistry - A European Journal · doi:10.1002/(sici)1521-3765(20000204)6:3 · Cited by 883 · see citing works

Free-Radical-Induced DNA Damage and Its Repair

von Sonntag, C. (2006) · Springer eBooks · doi:10.1007/3-540-30592-0 · Cited by 811 · see citing works

Mutations induced by ultraviolet light

Pfeifer, G. P., You, Y., & Nia, A. B. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2004.06.057 · Cited by 770 · see citing works

Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine

Iqbal, K., Jin, S., Pfeifer, G. P., & Szabó, P. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014033108 · Cited by 693 · see citing works

Cyclobutane pyrimidine dimers are predominant DNA lesions in whole human skin exposed to UVA radiation

Mouret, S., Baudouin, C., Charveron, M., Favier, A., Cadet, J., & Douki, T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604213103 · Cited by 684 · see citing works

Mechanisms and functions of Tet protein-mediated 5-methylcytosine oxidationPreprint

Wu, H., & Zhang, Y. (2011) · Genes & Development · doi:10.17615/800j-yk16 · Cited by 665 · see citing works

Wavelength dependence of oxidative DNA damage induced by UV and visible light

Kielbassa, C. (1997) · Carcinogenesis · doi:10.1093/carcin/18.4.811 · Cited by 616 · see citing works

Oxidatively Generated Damage to the Guanine Moiety of DNA: Mechanistic Aspects and Formation in Cells

Cadet, J., Douki, T., & Ravanat, J.-L. (2008) · Accounts of Chemical Research · doi:10.1021/ar700245e · Cited by 555 · see citing works

Oxidatively generated base damage to cellular DNA

Cadet, J., Douki, T., & Ravanat, J. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.03.025 · Cited by 543 · see citing works

Mechanisms of formation, genotoxicity, and mutation of guanine oxidation products

Neeley, W. L., & Essigmann, J. M. (2006) · Chemical Research in Toxicology · doi:10.1021/tx0600043 · Cited by 510 · see citing works

The Discovery of 5‐Formylcytosine in Embryonic Stem Cell DNA

Pfaffeneder, T., Hackner, B., Truß, M., Münzel, M., Müller, M., Deiml, C. A., Hagemeier, C., & Carell, T. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201103899 · Cited by 483 · see citing works

Bipyrimidine Photoproducts Rather than Oxidative Lesions Are the Main Type of DNA Damage Involved in the Genotoxic Effect of Solar UVA Radiation

Douki, T., Reynaud-Angelin, A., Cadet, J., & Sage, E. (2003) · Biochemistry · doi:10.1021/bi034593c · Cited by 452 · see citing works

5-Hydroxymethylcytosine Is Strongly Depleted in Human Cancers but Its Levels Do Not Correlate with IDH1 Mutations

Jin, S., Jiang, Y., Qiu, R., Rauch, T. A., Wang, Y., Schackert, G., Krex, D., Lü, Q., & Pfeifer, G. P. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-2023 · Cited by 441 · see citing works

Myeloperoxidase: a target for new drug development?

Malle, E., Furtmüller, P. G., Sattler, W., & Obinger, C. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707358 · Cited by 411 · see citing works

Quantification of the Sixth DNA Base Hydroxymethylcytosine in the Brain

Münzel, M., Globisch, D., Brückl, T., Wagner, M., Welzmiller, V., Michalakis, S., Müller, M., Biel, M., & Carell, T. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201002033 · Cited by 390 · see citing works

Individual Determination of the Yield of the Main UV-Induced Dimeric Pyrimidine Photoproducts in DNA Suggests a High Mutagenicity of CC Photolesions

Douki, T., & Cadet, J. (2001) · Biochemistry · doi:10.1021/bi0022543 · Cited by 337 · see citing works

2,2-Diamino-4-[(3,5-di-O-acetyl-2-deoxy-.beta.-D-erythro- pentofuranosyl)amino]-5-(2H)-oxazolone: a Novel and Predominant Radical Oxidation Product of 3',5'-Di-O-acetyl-2'-deoxyguanosine

Cadet, J., Berger, M., Buchko, G. W., Joshi, P. C., Raoul, S., & Ravanat, J. (1994) · Journal of the American Chemical Society · doi:10.1021/ja00095a052 · Cited by 333 · see citing works

Singlet Oxygen Induces Oxidation of Cellular DNA

Ravanat, J., Mascio, P. D., Martinez, G. R., de Medeiros, M. H. G., & Cadet, J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006681200 · Cited by 327 · see citing works

Photoinduced Damage to Cellular DNA: Direct and Photosensitized Reactions^†

Cadet, J., Mouret, S., Ravanat, J., & Douki, T. (2012) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2012.01200.x · Cited by 300 · see citing works

Thymine DNA glycosylase specifically recognizes 5-carboxylcytosine-modified DNA

Zhang, L., Lu, X., Lu, J., Liang, H., Dai, Q., Xu, G., Luo, C., Jiang, H., & He, C. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.914 · Cited by 299 · see citing works

NMR structural studies of the ionizing radiation adduct 7-hydro-8-oxodeoxyguanosine (8-oxo-7H-dG) opposite deoxyadenosine in a DNA duplex. 8-Oxo-7H-dG(syn).cntdot.dA(anti) alignment at lesion site

Kouchakdjian, M., Bodepudi, V., Shibutani, S., Eisenberg, M., Johnson, F., Grollman, A. P., & Patel, D. J. (1991) · Biochemistry · doi:10.1021/bi00219a034 · Cited by 298 · see citing works

New functions of XPC in the protection of human skin cells from oxidative damage

D'Errico, M., Parlanti, E., Teson, M., de Jesus, B. M. B., Degan, P., Calcagnile, A., Jaruga, P., Bjørås, M., Crescenzi, M., Pedrini, A. M., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601277 · Cited by 271 · see citing works

High-performance liquid chromatography--tandem mass spectrometry measurement of radiation-induced base damage to isolated and cellular DNA

Frelon, S., Douki, T., Ravanat, J.-L., Pouget, J.-P., Tornabene, C., & Cadet, J. (2000) · Chemical Research in Toxicology · doi:10.1021/tx000085h · Cited by 271 · see citing works

Endogenous oxidative damage of deoxycytidine in DNA.

Wagner, J. R., Hu, C. A., & Ames, B. N. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.8.3380 · Cited by 271 · see citing works

5‐Hydroxymethylcytosine, the Sixth Base of the Genome

Münzel, M., Globisch, D., & Carell, T. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101547 · Cited by 252 · see citing works

Formation of the Main UV-induced Thymine Dimeric Lesions within Isolated and Cellular DNA as Measured by High Performance Liquid Chromatography-Tandem Mass Spectrometry

Douki, T., Court, M., Sauvaigo, S., Odin, F., & Cadet, J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.11678 · Cited by 239 · see citing works

Oxidatively generated complex DNA damage: Tandem and clustered lesions

Cadet, J., Ravanat, J.-L., TavernaPorro, M., Menoni, H., & Angelov, D. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.04.005 · Cited by 233 · see citing works

Measurement and Meaning of Oxidatively Modified DNA Lesions in Urine

Cooke, M. S., Oliński, R., & Loft, S. H. (2008) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-07-0751 · Cited by 222 · see citing works

Oxidative DNA Damage Associated with Combination of Guanine and Superoxide Radicals and Repair Mechanisms via Radical Trapping

Misiaszek, R., Crean, C. W., Joffe, A., Geacintov, N. E., & Shafirovich, V. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313904200 · Cited by 221 · see citing works

Formation of Modified DNA Bases in Cells Exposed either to Gamma Radiation or to High-LET Particles1

Pouget, J., Frelon, S., Ravanat, J., Testard, I., Odin, F., & Cadet, J. (2002) · Radiation Research · doi:10.1667/0033-7587(2002)157[0589:fomdbi]2.0.co;2 · Cited by 219 · see citing works

NMR studies of a DNA containing 8-hydroxydeoxyguanosine

Oda, Y., Uesugi, S., Ikehara, M., Nishimura, S., Kawase, Y., Ishikawa, H. T., Inoue, H., & Ohtsuka, E. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.7.1407 · Cited by 217 · see citing works

The Chemical Toxicology of 2-Deoxyribose Oxidation in DNA

Dedon, P. C. (2007) · Chemical Research in Toxicology · doi:10.1021/tx700283c · Cited by 213 · see citing works

Sensitized formation of oxidatively generated damage to cellular DNA by UVA radiation

Cadet, J., Douki, T., Ravanat, J.-L., & Di Mascio, P. (2009) · Photochemical & Photobiological Sciences · doi:10.1039/b905343n · Cited by 213 · see citing works

Hypochlorite-Induced Damage to DNA, RNA, and Polynucleotides: Formation of Chloramines and Nitrogen-Centered Radicals

Hawkins, C. L., & Davies, M. J. (2002) · Chemical Research in Toxicology · doi:10.1021/tx015548d · Cited by 208 · see citing works

The carbonate radical and related oxidants derived from bicarbonate buffer

Medinas, D. B., Cerchiaro, G., Trindade, D. F., & Augusto, O. (2007) · IUBMB Life · doi:10.1080/15216540701230511 · Cited by 198 · see citing works

DNA oxidation: Investigating its key role in environmental mutagenesis with the comet assay

Azqueta, A., Shaposhnikov, S. A., & Collins, A. R. (2008) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2008.10.013 · Cited by 191 · see citing works

Oxidation Reactions of Cytosine DNA Components by Hydroxyl Radical and One-Electron Oxidants in Aerated Aqueous Solutions

Wagner, J. R., & Cadet, J. (2010) · Accounts of Chemical Research · doi:10.1021/ar9002637 · Cited by 167 · see citing works

Guanine Oxidation: One‐ and Two‐Electron Reactions

Pratviel, G., & Meunier, B. (2006) · Chemistry - A European Journal · doi:10.1002/chem.200600539 · Cited by 159 · see citing works

Oxidation of the sugar moiety of DNA by ionizing radiation or bleomycin could induce the formation of a cluster DNA lesion

Regulus, P., Duroux, B., Bayle, A., Favier, A. E., Cadet, J., & Ravanat, J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706044104 · Cited by 157 · see citing works

Repair of the three main types of bipyrimidine DNA photoproducts in human keratinocytes exposed to UVB and UVA radiations

Courdavault, S., Baudouin, C., Charveron, M., Canguilhem, B., Favier, A., Cadet, J., & Douki, T. (2005) · DNA Repair · doi:10.1016/j.dnarep.2005.05.001 · Cited by 156 · see citing works

Structural and conformational analyses of 8-hydroxy-2'-deoxyguanosine

Culp, S. J., Cho, B. P., Kadlubar, F. F., & Evans, F. E. (1989) · Chemical Research in Toxicology · doi:10.1021/tx00012a010 · Cited by 153 · see citing works

UVA-induced cyclobutane pyrimidine dimers in DNA: a direct photochemical mechanism?

Mouret, S., Philippe, C., Gracia-Chantegrel, J., Banyasz, A., Karpati, S., Markovitsi, D., & Douki, T. (2010) · Organic & Biomolecular Chemistry · doi:10.1039/b924712b · Cited by 149 · see citing works

Low values of 5‐hydroxymethylcytosine (5hmC), the “sixth base,” are associated with anaplasia in human brain tumors

Kraus, T. F. J., Globisch, D., Wagner, M., Eigenbrod, S., Widmann, D., Münzel, M., Müller, M., Pfaffeneder, T., Hackner, B., Feiden, W., et al. (2012) · International Journal of Cancer · doi:10.1002/ijc.27429 · Cited by 146 · see citing works

Tet Proteins Can Convert 5-Methylcytosine to 5-Formylcytosine and 5-Carboxylcytosine

Wu, S. C., Zhang, Y., Collins, L. B., et al. (2020) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/w7hh-zy88 · Cited by 145 · see citing works

Chlorination of Guanosine and Other Nucleosides by Hypochlorous Acid and Myeloperoxidase of Activated Human Neutrophils

Masuda, M., Suzuki, T., Friesen, M. D., Ravanat, J.-L., Cadet, J., Pignatelli, B., Nishino, H., & Ohshima, H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102700200 · Cited by 144 · see citing works

Biologically relevant oxidants and terminology, classification and nomenclature of oxidatively generated damage to nucleobases and 2-deoxyribose in nucleic acids

Cadet, J., Loft, S. H., Oliński, R., Evans, M. D., Białkowski, K., Wagner, J. R., Dedon, P. C., Möller, P., Greenberg, M. M., & Cooke, M. S. (2012) · Free Radical Research · doi:10.3109/10715762.2012.659248 · Cited by 143 · see citing works

The oxidative DNA lesions 8,5′-cyclopurines accumulate with aging in a tissue-specific manner

Wang, J., Clauson, C. L., Robbins, P. D., Niedernhofer, L. J., & Wang, Y. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00828.x · Cited by 142 · see citing works

Characterization of Lysine−Guanine Cross-Links upon One-Electron Oxidation of a Guanine-Containing Oligonucleotide in the Presence of a Trilysine Peptide

Perrier, S., Hau, J., Gasparutto, D., Cadet, J., Favier, A., & Ravanat, J.-L. (2006) · Journal of the American Chemical Society · doi:10.1021/ja057656i · Cited by 141 · see citing works

UVA1 induces cyclobutane pyrimidine dimers but not 6-4 photoproducts in human skin in vivo

Tewari, A., Sarkany, R. P., & Young, A. R. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.283 · Cited by 141 · see citing works

Pattern of hydroxy radical reaction with adenine and its nucleosides and nucleotides. Characterization of two types of isomeric hydroxy adduct and their unimolecular transformation reactions

Vieira, A. J. S. C., & Steenken, S. (1990) · Journal of the American Chemical Society · doi:10.1021/ja00175a036 · Cited by 141 · see citing works

Purine 5′,8-cyclonucleoside lesions: chemistry and biology

Chatgilialoglu, C., Ferreri, C., & Terzidis, M. A. (2011) · Chemical Society Reviews · doi:10.1039/c0cs00061b · Cited by 137 · see citing works

HO • radicals induce an unexpected high proportion of tandem base lesions refractory to repair by DNA glycosylases

Bergeron, F., Auvré, F., Radicella, J. P., & Ravanat, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000193107 · Cited by 137 · see citing works

The role of CSA in the response to oxidative DNA damage in human cells

D'Errico, M., Parlanti, E., Teson, M., Degan, P., Lemma, T., Calcagnile, A., Iavarone, I., Jaruga, P., Ropolo, M., Pedrini, A. M., et al. (2007) · Oncogene · doi:10.1038/sj.onc.1210232 · Cited by 137 · see citing works

Measurement of oxidatively generated base damage in cellular DNA

Cadet, J., Douki, T., & Ravanat, J.-L. (2011) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2011.02.004 · Cited by 136 · see citing works

Oxidation of Guanine in Cellular DNA by Solar UV Radiation: Biological Role†

Douki, T., Perdiz, D., Grof, P., Kuluncsics, Z., Moustacchi, E., Cadet, J., & Sage, E. (1999) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1999.tb07988.x · Cited by 133 · see citing works

Oxidatively generated damage to DNA by UVA radiation in cells and human skin

Cadet, J., & Douki, T. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.51 · Cited by 116 · see citing works

Endoperoxide formation in a guanosine derivative

Sheu, C., & Foote, C. S. (1993) · Journal of the American Chemical Society · doi:10.1021/ja00075a105 · Cited by 111 · see citing works

Quantification of Oxidative DNA Lesions in Tissues of Long-Evans Cinnamon Rats by Capillary High-Performance Liquid Chromatography−Tandem Mass Spectrometry Coupled with Stable Isotope-Dilution Method

Wang, J., Yuan, B., Guerrero, C. R., Bahde, R., Gupta, S. K., & Wang, Y. (2011) · Analytical Chemistry · doi:10.1021/ac103099s · Cited by 110 · see citing works

Tandem Base Lesions Are Generated by Hydroxyl Radical within Isolated DNA in Aerated Aqueous Solution

Bourdat, A.-G., Douki, T., Frelon, S., Gasparutto, D., & Cadet, J. (2000) · Journal of the American Chemical Society · doi:10.1021/ja994282i · Cited by 109 · see citing works

Characterization and Chemical Stability of Photooxidized Oligonucleotides that Contain 2,2-Diamino-4-[(2-deoxy-β- d -erythro-pentofuranosyl)amino]-5(2H)-oxazolone

Gasparutto, D., Ravanat, J., Gérot, O., & Cadet, J. (1998) · Journal of the American Chemical Society · doi:10.1021/ja980674y · Cited by 108 · see citing works

Base Pairing Enhances Fluorescence and Favors Cyclobutane Dimer Formation Induced upon Absorption of UVA Radiation by DNA

Banyasz, A., Vayá, I., Changenet-Barret, P., Gustavsson, T., Douki, T., & Markovitsi, D. (2011) · Journal of the American Chemical Society · doi:10.1021/ja110879m · Cited by 106 · see citing works

Minor contribution of direct ionization to DNA base damage inducedby heavy ions

Douki, T., Ravanat, J.-L., Pouget, J.-P., Testard, I., & Cadet, J. (2006) · International Journal of Radiation Biology · doi:10.1080/09553000600573788 · Cited by 106 · see citing works

Glutathione and ascorbate are negatively correlated with oxidative DNA damage in human lymphocytes

Lenton, K. J., Therriault, H., Fülöp, T., Payette, H., & Wagner, J. R. (1999) · Carcinogenesis · doi:10.1093/carcin/20.4.607 · Cited by 102 · see citing works

Thymidine Hydroperoxides: Structural Assignment, Conformational Features, and Thermal Decomposition in Water

Wagner, J. R., van Lier, J. E., Berger, M., & Cadet, J. (1994) · Journal of the American Chemical Society · doi:10.1021/ja00085a001 · Cited by 101 · see citing works

UV Laser Photolysis of DNA:  Effect of Duplex Stability on Charge-Transfer Efficiency

Douki, T., Angelov, D., & Cadet, J. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016426a · Cited by 100 · see citing works

Quantitative analysis of the oxidative DNA lesion, 2,2-diamino-4-(2-deoxy-β-d-erythro-pentofuranosyl)amino]-5(2H)-oxazolone (oxazolone), in vitro and in vivo by isotope dilution-capillary HPLC-ESI-MS/MS

Matter, B. A., Malejka‐Giganti, D., Csallany, A. S., & Tretyakova, N. Y. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl596 · Cited by 99 · see citing works

Radiation-induced formation of purine 5′,8-cyclonucleosides in isolated and cellular DNA: high stereospecificity and modulating effect of oxygen

Belmadoui, N., Boussicault, F., Guerra, M., Ravanat, J., Chatgilialoglu, C., & Cadet, J. (2010) · Organic & Biomolecular Chemistry · doi:10.1039/c004531d · Cited by 97 · see citing works

Mechanism of DNA damage induced by bromate differs from general types of oxidative stress

Kawanishi, S., & Murata, M. (2006) · Toxicology · doi:10.1016/j.tox.2006.01.002 · Cited by 95 · see citing works

The specificity of UVA-induced DNA damage in human melanocytes

Mouret, S., Forestier, A., & Douki, T. (2012) · Photochemical & Photobiological Sciences · doi:10.1039/c1pp05185g · Cited by 94 · see citing works

Hypochlorite-Induced Damage to Nucleosides: Formation of Chloramines and Nitrogen-Centered Radicals

Hawkins, C. L., & Davies, M. J. (2001) · Chemical Research in Toxicology · doi:10.1021/tx010071r · Cited by 94 · see citing works

Differential repair of UVB-induced cyclobutane pyrimidine dimers in cultured human skin cells and whole human skin

Mouret, S., Charveron, M., Favier, A., Cadet, J., & Douki, T. (2008) · DNA Repair · doi:10.1016/j.dnarep.2008.01.005 · Cited by 92 · see citing works

DNA Tandem Lesions Containing 8-Oxo-7,8-dihydroguanine and Formamido Residues Arise from Intramolecular Addition of Thymine Peroxyl Radical to Guanine

Douki, T., Rivière, J., & Cadet, J. (2002) · Chemical Research in Toxicology · doi:10.1021/tx0155909 · Cited by 90 · see citing works

The Discovery of 5‐Formylcytosine in Embryonic Stem Cell DNA

Pfaffeneder, T., Hackner, B., Truß, M., Münzel, M., Müller, M., Deiml, C. A., Hagemeier, C., & Carell, T. (2011) · Angewandte Chemie · doi:10.1002/ange.201103899 · Cited by 90 · see citing works

Photosensitized Oxidation of 5-Methyl-2‘-deoxycytidine by 2-Methyl-1,4-naphthoquinone: Characterization of 5-(Hydroperoxymethyl)-2‘-deoxycytidine and Stable Methyl Group Oxidation Products

Bienvenu, C., Wagner, J. R., & Cadet, J. (1996) · Journal of the American Chemical Society · doi:10.1021/ja962073h · Cited by 89 · see citing works

Singlet oxygen-mediated damage to cellular DNA determined by the comet assay associated with DNA repair enzymes

Ravanat, J., Sauvaigo, S., Caillat, S., Martinez, G. R., de Medeiros, M. H. G., Mascio, P. D., Favier, A. E., & Cadet, J. (2004) · Biological Chemistry · doi:10.1515/bc.2004.003 · Cited by 84 · see citing works

Characterization and Mechanism of Formation of Tandem Lesions in DNA by a Nucleobase Peroxyl Radical

Hong, I. S., Carter, K. N., Sato, K., & Greenberg, M. M. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0692276 · Cited by 81 · see citing works

An ab initio molecular orbital study on the characteristics of 8-hydroxyguanine

Aida, M., & Nishimura, S. (1987) · Mutation Research Letters · doi:10.1016/0165-7992(87)90101-1 · Cited by 79 · see citing works

The Insulated SolarFenton Hybrid Process: Fundamental Investigations

Sagawe, G., Lehnard, A., Lübber, M., & Bahnemann, D. W. (2001) · Helvetica Chimica Acta · doi:10.1002/1522-2675(20011219)84:12 · Cited by 78 · see citing works

Mechanism of UV‐Induced Formation of Dewar Lesions in DNA

Haiser, K., Fingerhut, B. P., Heil, K., Glas, A. F., Herzog, T. T., Pilles, B. M., Schreier, W. J., Zinth, W., de Vivie‐Riedle, R., & Carell, T. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201106231 · Cited by 78 · see citing works

Multiple forms of DNA Damage Caused by UVA Photoactivation of DNA 6‐Thioguanine

Brem, R., & Karran, P. (2012) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2011.01043.x · Cited by 76 · see citing works

Hydroxyl-Radical-Induced Decomposition of 2‘-Deoxycytidine in Aerated Aqueous Solutions

Wagner, J. R., Decarroz, C., Berger, M., & Cadet, J. (1999) · Journal of the American Chemical Society · doi:10.1021/ja982461e · Cited by 75 · see citing works

New Insights into the Reaction Paths of Hydroxyl Radicals with 2′-Deoxyguanosine

Chatgilialoglu, C., D’Angelantonio, M., Kciuk, G., & Bobrowski, K. (2011) · Chemical Research in Toxicology · doi:10.1021/tx2003245 · Cited by 74 · see citing works

Detection of chlorinated DNA and RNA nucleosides by HPLC coupled to tandem mass spectrometry as potential biomarkers of inflammation

Badouard, C., Masuda, M., Nishino, H., Cadet, J., Favier, A. E., & Ravanat, J. (2005) · Journal of Chromatography B · doi:10.1016/j.jchromb.2005.03.025 · Cited by 73 · see citing works

Nitrogen-15 nuclear magnetic resonance studies on the tautomerism of 8-hydroxy-2'-deoxyguanosine, 8-hydroxyguanosine, and other C8-substituted guanine nucleosides

Cho, B. P., Kadlubar, F. F., Culp, S. J., & Evans, F. E. (1990) · Chemical Research in Toxicology · doi:10.1021/tx00017a010 · Cited by 71 · see citing works

Isolation, Characterization, and Independent Synthesis of Guanine Oxidation Products

Gimisis, T., & Cismaş, C. (2006) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200500581 · Cited by 71 · see citing works

Scope and Mechanism of Interstrand Cross-Link Formation by the C4′-Oxidized Abasic Site

Sczepanski, J. T., Jacobs, A. C., Majumdar, A. K., & Greenberg, M. M. (2009) · Journal of the American Chemical Society · doi:10.1021/ja903404v · Cited by 69 · see citing works

In Vivo Formation and in Vitro Replication of a Guanine−Thymine Intrastrand Cross-Link Lesion

Jiang, Y., Hong, H., Cao, H., & Wang, Y. (2007) · Biochemistry · doi:10.1021/bi7012195 · Cited by 66 · see citing works

Mechanisms of Oxidation of Guanine in DNA by Carbonate Radical Anion, a Decomposition Product of Nitrosoperoxycarbonate

Lee, Y. A., Yun, B. H., Kim, S. K., Margolin, Y., Dedon, P. C., Geacintov, N. E., & Shafirovich, V. (2007) · Chemistry - A European Journal · doi:10.1002/chem.200601434 · Cited by 62 · see citing works

Chemical and Immunochemical Detection of 8-Halogenated Deoxyguanosines at Early Stage Inflammation

Asahi, T., KONDO, H., Masuda, M., Nishino, H., Aratani, Y., Naito, Y., Yoshikawa, T., Hisaka, S., Kato, Y., & Osawa, T. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.054213 · Cited by 62 · see citing works

2′-Deoxycytidine Glycols, a Missing Link in the Free Radical-mediated Oxidation of DNA

Tremblay, S., Douki, T., Cadet, J., & Wagner, J. R. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.30.20833 · Cited by 60 · see citing works

Recommendations for Standardized Description of and Nomenclature Concerning Oxidatively Damaged Nucleobases in DNA

Cooke, M. S., Loft, S. H., Oliński, R., Evans, M. D., Białkowski, K., Wagner, J. R., Dedon, P. C., Möller, P., Greenberg, M. M., & Cadet, J. (2010) · Chemical Research in Toxicology · doi:10.1021/tx1000706 · Cited by 58 · see citing works

Effects of Duplex Stability on Charge-Transfer Efficiency within DNA

Douki, T., Ravanat, J., Angelov, D., Wagner, J. R., & Cadet, J. (2012) · Topics in current chemistry · doi:10.1007/b94409 · Cited by 57 · see citing works

Profiling Cytosine Oxidation in DNA by LC-MS/MS

Samson-Thibault, F., Madugundu, G. S., Gao, S., Cadet, J., & Wagner, J. R. (2012) · Chemical Research in Toxicology · doi:10.1021/tx300195f · Cited by 53 · see citing works

No formation of DNA double-strand breaks and no activation of recombination repair with UVA

Rizzo, J. L., Dunn, J., Rees, A., & Rünger, T. M. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.365 · Cited by 50 · see citing works

Deficiency of the Cockayne syndrome B (CSB) gene aggravates the genomic instability caused by endogenous oxidative DNA base damage in mice

Trapp, C., Reite, K., Klungland, A., & Epe, B. (2007) · Oncogene · doi:10.1038/sj.onc.1210167 · Cited by 49 · see citing works

Efficient DNA interstrand crosslinking by 6-thioguanine and UVA radiation

Brem, R., Daehn, I., & Karran, P. (2011) · DNA Repair · doi:10.1016/j.dnarep.2011.05.010 · Cited by 48 · see citing works

Crosslinking of DNA repair and replication proteins to DNA in cells treated with 6-thioguanine and UVA

Gueranger, Q., Kia, A., Frith, D., & Karran, P. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr112 · Cited by 47 · see citing works

Ionizing Radiation Causes Greater DNA Base Damage in Radiation-Sensitive Mutant M10 Cells Than in Parent Mouse Lymphoma L5178Y Cells

Mori, T., & Dizdaroğlu, M. (1994) · Radiation Research · doi:10.2307/3578572 · Cited by 47 · see citing works

Radical Oxidation of the Adenine Moiety of Nucleoside and DNA: 2-Hydroxy-2′-deoxyadenosine is a Minor Decomposition Product

Frelon, S., Douki, T., & Cadet, J. (2002) · Free Radical Research · doi:10.1080/10715760290025889 · Cited by 45 · see citing works

Generation of Guanine–Thymidine Cross-Links in DNA by Peroxynitrite/Carbon Dioxide

Yun, B. H., Geacintov, N. E., & Shafirovich, V. (2011) · Chemical Research in Toxicology · doi:10.1021/tx200139c · Cited by 44 · see citing works

Individual Photosensitivity of Human Skin and UVA-Induced Pyrimidine Dimers in DNA

Mouret, S., Leccia, M. ‐., Bourrain, J. ‐., Douki, T., & Béani, J. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.47 · Cited by 43 · see citing works

Ascorbate and H2O2 induced oxidative DNA damage in Jurkat cells

Rivière, J., Ravanat, J., & Wagner, J. R. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.02.003 · Cited by 43 · see citing works

Guanine–thymine intrastrand cross-linked lesion containing oligonucleotides: from chemical synthesis to in vitro enzymatic replication

Bellon, S., Gasparutto, D., Saint‐Pierre, C., & Cadet, J. (2006) · Organic & Biomolecular Chemistry · doi:10.1039/b609460k · Cited by 43 · see citing works

Hydroxylation of the C-8 position of deoxyguanosine by reducing agents in the presence of oxygen.

Kasai, H., & Nishimura, S. (1983) · PubMed · Cited by 43 · see citing works

Singlet oxygen induces oxidation of cellular DNA.

Ravanat, J.-L., Di Mascio, P., Martinez, G. R., Medeiros, M. G., & Cadet, J. (2001) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)46360-6 · Cited by 42 · see citing works

Detection of new radiation‐induced DNA lesions by liquid chromatography coupled to tandem mass spectrometry

Regulus, P., Spessotto, S., Gateau, M., Cadet, J., Favier, A. E., & Ravanat, J. (2004) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.1612 · Cited by 42 · see citing works

Tautomeric equilibria in 8-oxopurines: Implications for mutagenicity

Venkateswarlu, D., & Leszczyński, J. (1998) · Journal of Computer-Aided Molecular Design · doi:10.1023/a:1008067110965 · Cited by 41 · see citing works

Vicinal Lesions in X-irradiated DNA?

Box, H. C., Budzinski, E. E., Freund, H. G., Evans, M. S., Patrzyc, H. B., Wallace, J. C., & Maccubbin, A. E. (1993) · International Journal of Radiation Biology · doi:10.1080/09553009314551411 · Cited by 41 · see citing works

Site-specific radical formation in DNA induced by Cu(II)–H2O2 oxidizing system, using ESR, immuno-spin trapping, LC-MS, and MS/MS

Bhattacharjee, S., Deterding, L. J., Chatterjee, S., Jiang, J., Ehrenshaft, M., Lardinois, O. M., Ramírez, D. C., Tomer, K. B., & Mason, R. P. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.02.034 · Cited by 40 · see citing works

Measurement of oxidatively generated base damage to nucleic acids in cells: facts and artifacts

Cadet, J., Douki, T., Ravanat, J.-L., & Wagner, J. R. (2012) · Bioanalytical Reviews · doi:10.1007/s12566-012-0029-6 · Cited by 38 · see citing works

Measurement of (5′R)- and (5′S)-8,5′-cyclo-2′-deoxyadenosines in DNA in vivo by liquid chromatography/isotope-dilution tandem mass spectrometry

Jaruga, P., Xiao, Y., Nelson, B. C., & Dizdaroğlu, M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.06.107 · Cited by 38 · see citing works

Invited Review A Compilation of Physical, Spectroscopic and Photophysical Properties of Polycyclic Aromatic Hydrocarbons

Dabestani, R., & Ivanov, I. N. (1999) · Photochemistry and Photobiology · doi:10.1562/0031-8655(1999)070 · Cited by 38 · see citing works

It’s All about Position: The Basal Layer of Human Epidermis Is Particularly Susceptible to Different Types of Sunlight-Induced DNA Damage

Halliday, G. M., & Cadet, J. (2012) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.281 · Cited by 35 · see citing works

Dehydration, deamination and enzymatic repair of cytosine glycols from oxidized poly(dG-dC) and poly(dI-dC)

Tremblay, S., & Wagner, J. R. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm1013 · Cited by 35 · see citing works

Oxidation of 5-Hydroxy-2‘-deoxyuridine into Isodialuric Acid, Dialuric Acid, and Hydantoin Products

Rivière, J., Bergeron, F., Tremblay, S., Gasparutto, D., Cadet, J., & Wagner, J. R. (2004) · Journal of the American Chemical Society · doi:10.1021/ja049438f · Cited by 33 · see citing works

Generation of 2′-Deoxyadenosine N6-Aminyl Radicals from the Photolysis of Phenylhydrazone Derivatives

Kuttappan-Nair, V., Samson-Thibault, F., & Wagner, J. R. (2009) · Chemical Research in Toxicology · doi:10.1021/tx900268r · Cited by 31 · see citing works

Structural, energetic and dynamic properties of guanine(C8)–thymine(N3) cross-links in DNA provide insights on susceptibility to nucleotide excision repair

Ding, S., Kropachev, K. Y., Cai, Y., Kolbanovskiy, M., Durandina, S. A., Liu, Z., Shafirovich, V., Broyde, S. B., & Geacintov, N. E. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1087 · Cited by 28 · see citing works

High-resolution crystal structure of the intramolecular d(TpA) thymine-adenine photoadduct and its mechanistic implications

Davies, R. J. H., Malone, J. F., Gan, Y., Cardin, C. J., Lee, M. P., & Neidle, S. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl1101 · Cited by 27 · see citing works

A New Photoproduct of 5-Methylcytosine and Adenine Characterized by High-Performance Liquid Chromatography and Mass Spectrometry

Su, D. G. T., Taylor, J.-S. A., & Gross, M. L. (2010) · Chemical Research in Toxicology · doi:10.1021/tx9003962 · Cited by 26 · see citing works

Isolation and Mass Spectrometric Characterization of Dimeric Adenine Photoproducts in Oligodeoxynucleotides

Wang, Y., Taylor, J., & Gross, M. L. (2001) · Chemical Research in Toxicology · doi:10.1021/tx010009u · Cited by 26 · see citing works

Kinetics of deamination and Cu(II)/H 2 O 2 /Ascorbate-induced formation of 5-methylcytosine glycol at CpG sites in duplex DNA

Cao, H., Jiang, Y., & Wang, Y. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp615 · Cited by 26 · see citing works

Surviving an Oxygen Atmosphere: DNA Damage and Repair

Burrows, C. J. (2009) · ACS symposium series · doi:10.1021/bk-2009-1025.ch008 · Cited by 25 · see citing works

Detection and imaging of the free radical DNA in cells--Site-specific radical formation induced by Fenton chemistry and its repair in cellular DNA as seen by electron spin resonance, immuno-spin trapping and confocal microscopy

Bhattacharjee, S., Chatterjee, S., Jiang, J., Sinha, B. K., & Mason, R. P. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks180 · Cited by 24 · see citing works

Formation of 2′-deoxyuridine hydrates upon exposure of nucleosides to gamma radiation and UVC-irradiation of isolated and cellular DNA

Douki, T., Vadesne-Bauer, G., & Cadet, J. (2002) · Photochemical & Photobiological Sciences · doi:10.1039/b201612e · Cited by 22 · see citing works

Oxidation of 5-Hydroxypyrimidine Nucleosides to 5-Hydroxyhydantoin and Its α-Hydroxy-ketone Isomer

Rivière, J., Klarskov, K., & Wagner, J. R. (2005) · Chemical Research in Toxicology · doi:10.1021/tx050121i · Cited by 22 · see citing works

UV-Induced TA Photoproducts: Formation and Hydrolysis in Double-Stranded DNA

Asgatay, S., Martinez, A., Coantic-Castex, S., Harakat, D., Philippe, C., Douki, T., & Clivio, P. (2010) · Journal of the American Chemical Society · doi:10.1021/ja1023173 · Cited by 21 · see citing works

8-Hydroxyguanine: A base for discovery

Nishimura, S. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.04.006 · Cited by 20 · see citing works

Probing DNA interstrand cross-link formation by an oxidized abasic site using nonnative nucleotides

Sczepanski, J. T., Hiemstra, C. N., & Greenberg, M. M. (2011) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.08.024 · Cited by 20 · see citing works

Oxidation of 2‘-Deoxycytidine to Four Interconverting Diastereomers of N1-Carbamoyl-4,5-dihydroxy-2-oxoimidazolidine Nucleosides

Tremblay, S., Gantchev, T. G., Tremblay, L., Lavigne, P., Cadet, J., & Wagner, J. R. (2007) · The Journal of Organic Chemistry · doi:10.1021/jo062386n · Cited by 14 · see citing works

Unrepaired Cyclobutane Pyrimidine Dimers Do Not Prevent Proliferation of UV‐B‐irradiated Cultured Human Fibroblasts^¶

Courdavault, S., Baudouin, C., Sauvaigo, S., Mouret, S., Candéias, S., Charveron, M., Favier, A., Cadet, J., & Douki, T. (2004) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2004.tb00004.x · Cited by 12 · see citing works

Oxidatively Generated Nucleobase Modifications in Isolated and Cellular DNA

Cadet, J., Douki, T., Gasparutto, D., Ravanat, J., & Wagner, J. R. (2012) · Wiley eBooks · doi:10.1002/9781119953678.rad038 · Cited by 7 · see citing works

Chlorination of guanosine and other nucleosides by hypochlorous acid and myeloperoxidase of activated human neutrophils : Catalysis by nicotine and trimethylamine

増田, 光. (2002) · Medical Entomology and Zoology · Cited by 6 · see citing works

Measurement of oxidatively generated base damage to nucleic acids in cells: facts and artifacts

Cadet, J., Douki, T., Ravanat, J., & Wagner, J. R. (2013) · Springer eBooks · doi:10.1007/978-3-642-36303-0_13 · Cited by 3 · see citing works

Unrepaired Cyclobutane Pyrimidine Dimers Do Not Prevent Proliferation of UV-B–irradiated Cultured Human Fibroblasts

Courdavault, S., Baudouin, C., Sauvaigo, S., et al. (2004) · BioOne Complete (BioOne) · doi:10.1562/0031-8655(2004)079<0145:ucpddn>2.0.co;2 · Cited by 3 · see citing works

Guanine Oxidation: One‐ and Two‐Electron Reactions

Pratviel, G., & Meunier, B. (2006) · ChemInform · doi:10.1002/chin.200647248 · Cited by 2 · see citing works

Isolation, Characterization, and Independent Synthesis of Guanine Oxidation Products

Gimisis, T., & Cismaş, C. (2006) · ChemInform · doi:10.1002/chin.200624238 · Cited by 1 · see citing works

Lifestyle, oxidative stress, and antioxidants: Back and forth in the pathophysiology of chronic diseases

Sharifi-Rad, M., Anil Kumar, N. V., Zucca, P., Varoni, E. M., Dini, L., Panzarini, E., Rajkovic, J., Tsouh Fokou, P. V., Azzini, E., Peluso, I., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00694 · Cited by 1,971 · see citing works

Arsenic Uptake, Toxicity, Detoxification, and Speciation in Plants: Physiological, Biochemical, and Molecular Aspects

Abbas, G., Murtaza, B., Bibi, I., Shahid, M. A. R., Niazi, N. K., Khan, M. I., Amjad, M., Hussain, M., & Natasha, N. (2018) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph15010059 · Cited by 896 · see citing works

Restoration of TET2 Function Blocks Aberrant Self-Renewal and Leukemia Progression

Cimmino, L., Dolgalev, I., Wang, Y., Yoshimi, A., Martin, G. H., Wang, J., Ng, V., Xia, B., Witkowski, M. T., Mitchell-Flack, M., et al. (2017) · Cell · doi:10.1016/j.cell.2017.07.032 · Cited by 707 · see citing works

Modulating ROS to overcome multidrug resistance in cancer

Cui, Q., Wang, J., Assaraf, Y. G., Ren, L., Gupta, P., Wei, L., Ashby, C. R., Yang, D., & Chen, Z. (2018) · Drug Resistance Updates · doi:10.1016/j.drup.2018.11.001 · Cited by 664 · see citing works

Singlet Molecular Oxygen Reactions with Nucleic Acids, Lipids, and Proteins

Mascio, P. D., Martinez, G. R., Miyamoto, S., Ronsein, G. E., de Medeiros, M. H. G., & Cadet, J. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00554 · Cited by 665 · see citing works

Functions of ROS in Macrophages and Antimicrobial Immunity

Herb, M., & Schramm, M. (2021) · Antioxidants · doi:10.3390/antiox10020313 · Cited by 633 · see citing works

The emerging role of RNA modifications in the regulation of mRNA stability

Boo, S. H., & Kim, Y. K. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0407-z · Cited by 588 · see citing works

Sleep Loss Can Cause Death through Accumulation of Reactive Oxygen Species in the Gut

Vaccaro, A., Kaplan Dor, Y., Nambara, K., Pollina, E. A., Lin, C., Greenberg, M. E., & Rogulja, D. (2020) · Cell · doi:10.1016/j.cell.2020.04.049 · Cited by 541 · see citing works

The impact of oxidative DNA damage and stress on telomere homeostasis

Barnes, R. P., Fouquerel, E., & Opresko, P. L. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.03.013 · Cited by 558 · see citing works

Bactericidal Antibiotics Induce Toxic Metabolic Perturbations that Lead to Cellular Damage

Belenky, P. A., Ye, J. D., Porter, C. B. M., Cohen, N. R., Lobritz, M. A., Ferrante, T. C., Jain, S. R., Korry, B. J., Schwarz, E. G., Walker, G. C., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.059 · Cited by 512 · see citing works

DNA origami nanostructures can exhibit preferential renal uptake and alleviate acute kidney injury

Jiang, D., Ge, Z., Im, H., England, C. G., Ni, D., Hou, J., Zhang, L., Kutyreff, C. J., Yan, Y., Liu, Y., et al. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0317-8 · Cited by 449 · see citing works

Formation of UV-induced DNA damage contributing to skin cancer development

Cadet, J., & Douki, T. (2018) · Photochemical & Photobiological Sciences · doi:10.1039/c7pp00395a · Cited by 435 · see citing works

Photodynamic Therapy: Current Status and Future Directions

Benov, L. (2014) · Medical Principles and Practice · doi:10.1159/000362416 · Cited by 428 · see citing works

Hypermutation in human cancer genomes: footprints and mechanisms

Roberts, S. A., & Gordenin, D. A. (2014) · Nature reviews. Cancer · doi:10.1038/nrc3816 · Cited by 397 · see citing works

Flavonoids and their role in oxidative stress, inflammation, and human diseases

Jomová, K., Alomar, S. Y., Valko, R., Líška, J., Nepovimová, E., Kuča, K., & Valko, M. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111489 · Cited by 413 · see citing works

Oxidatively Generated Damage to Cellular <scp>DNA</scp> by <scp>UVB</scp> and <scp>UVA</scp>  Radiation ^,

Cadet, J., Douki, T., & Ravanat, J. (2015) · Photochemistry and Photobiology · doi:10.1111/php.12368 · Cited by 355 · see citing works

Formation and repair of oxidatively generated damage in cellular DNA

Cadet, J., Davies, K. J. A., de Medeiros, M. H. G., Mascio, P. D., & Wagner, J. R. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.049 · Cited by 356 · see citing works

Biocompatibility characteristics of the metal organic framework ZIF-8 for therapeutical applications

Hoop, M., Walde, C. F., Riccò, R., Mushtaq, F., Terzopoulou, A., Chen, X., deMello, A. J., Doonan, C. J., Falcaro, P., Nelson, B. J., et al. (2018) · Applied Materials Today · doi:10.1016/j.apmt.2017.12.014 · Cited by 350 · see citing works

Reactive Oxygen Species and Antioxidants in Postharvest Vegetables and Fruits

Meitha, K., Pramesti, Y., & Suhandono, S. (2020) · International Journal of Food Science · doi:10.1155/2020/8817778 · Cited by 342 · see citing works

Tumor-Associated Neutrophils in Cancer: Going Pro

Wu, L., Saxena, S., Awaji, M. I., & Singh, R. K. (2019) · Cancers · doi:10.3390/cancers11040564 · Cited by 338 · see citing works

E-waste management: A review of recycling process, environmental and occupational health hazards, and potential solutions

Ahirwar, R., & Tripathi, A. K. (2020) · Environmental Nanotechnology Monitoring & Management · doi:10.1016/j.enmm.2020.100409 · Cited by 317 · see citing works

Update on Keratinocyte Carcinomas

Nehal, K. S., & Bichakjian, C. K. (2018) · New England Journal of Medicine · doi:10.1056/nejmra1708701 · Cited by 315 · see citing works

Silver nanoparticles in aquatic environments: Physiochemical behavior and antimicrobial mechanisms

Zhang, C., Hu, Z., & Deng, B. (2015) · Water Research · doi:10.1016/j.watres.2015.10.025 · Cited by 315 · see citing works

Oxidative damage in neurodegeneration: roles in the pathogenesis and progression of Alzheimer disease

Marzia Perluigi, A., Domenico, F. D., & Butterfield, D. A. (2023) · Physiological Reviews · doi:10.1152/physrev.00030.2022 · Cited by 306 · see citing works

Reactive oxygen species: a volatile driver of field cancerization and metastasis

Liao, Z., Chua, D., & Tan, N. S. (2019) · Molecular Cancer · doi:10.1186/s12943-019-0961-y · Cited by 284 · see citing works

Oxidatively induced DNA damage and its repair in cancer

Dizdaroğlu, M. (2014) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2014.11.002 · Cited by 254 · see citing works

DNA Damage: From Threat to Treatment

Carusillo, A., & Mussolino, C. (2020) · Cells · doi:10.3390/cells9071665 · Cited by 246 · see citing works

Role of reactive oxygen species in ultraviolet-induced photodamage of the skin

Wei, M., He, X., Liu, N., & Deng, H. (2024) · Cell Division · doi:10.1186/s13008-024-00107-z · Cited by 244 · see citing works

Achieving Controlled Biomolecule–Biomaterial Conjugation

Spicer, C. D., Pashuck, E. T., & Stevens, M. M. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00253 · Cited by 239 · see citing works

Base excision repair of oxidative DNA damage from mechanism to disease

Freudenthal, B. (2017) · Frontiers in bioscience · doi:10.2741/4555 · Cited by 230 · see citing works

Exploiting innate immunity for cancer immunotherapy

Yi, M., Li, T., Niu, M., Mei, Q., Zhao, B., Chu, Q., Dai, Z., & Wu, K. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01885-w · Cited by 236 · see citing works

Neutrophil-induced genomic instability impedes resolution of inflammation and wound healing

Butin‐Israeli, V., Bui, T. M., Wiesolek, H. L., Mascarenhas, L., Lee, J. J., Mehl, L. C., Knutson, K. R., Adam, S. A., Goldman, R. D., Beyder, A., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci122085 · Cited by 221 · see citing works

The current state of eukaryotic DNA base damage and repair

Bauer, N. C., Corbett, A. H., & Doetsch, P. W. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1136 · Cited by 216 · see citing works

HDAC1 modulates OGG1-initiated oxidative DNA damage repair in the aging brain and Alzheimer’s disease

Pao, P.-C., Patnaik, D., Watson, L. A., Gao, F., Pan, L., Wang, J., Adaikkan, C., Penney, J., Cam, H. P., Huang, W.-C., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16361-y · Cited by 216 · see citing works

Impaired ribosome biogenesis: mechanisms and relevance to cancer and aging

Turi, Z., Lacey, M., Mistrík, M., & Moudrý, P. (2019) · Aging · doi:10.18632/aging.101922 · Cited by 209 · see citing works

Dual Role of Reactive Oxygen Species and their Application in Cancer Therapy

Huang, R., Chen, H., Liang, J., Li, Y., Yang, J., Luo, C., Tang, Y., Ding, Y., Liu, X., Yuan, Q., et al. (2021) · Journal of Cancer · doi:10.7150/jca.54699 · Cited by 218 · see citing works

Recent Developments in Antimicrobial Polymers: A Review

Santos, M. R. E., Fonseca, A. C., Mendonça, P. V., Branco, R., Serra, A. C., Morais, P. V., & Coelho, J. F. J. (2016) · Materials · doi:10.3390/ma9070599 · Cited by 212 · see citing works

Photosensitization Reactions of Biomolecules: Definition, Targets and Mechanisms

Baptista, M. S., Cadet, J., Greer, A., & Thomas, A. H. (2021) · Photochemistry and Photobiology · doi:10.1111/php.13470 · Cited by 205 · see citing works

Integrated block copolymer prodrug nanoparticles for combination of tumor oxidative stress amplification and ROS-responsive drug release

Yin, W., Ke, W., Chen, W., Xi, L., Zhou, Q., Mukerabigwi, J. F., & Ge, Z. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.12.032 · Cited by 203 · see citing works

Antioxidant Activity, Metabolism, and Bioavailability of Polyphenols in the Diet of Animals

Bešlo, D., Golubić, N., Rastija, V., Agić, D., Karnaš, M., Šubarić, D., & Lučić, B. (2023) · Antioxidants · doi:10.3390/antiox12061141 · Cited by 215 · see citing works

Snake extract–laden hemostatic bioadhesive gel cross-linked by visible light

Guo, Y., Wang, Y., Zhao, X., Li, X., Wang, Q., Zhong, W., Mequanint, K., Zhan, R., Xing, M. M. Q., & Luo, G. (2021) · Science Advances · doi:10.1126/sciadv.abf9635 · Cited by 187 · see citing works

How do cells cope with RNA damage and its consequences?

Yan, L. L., & Zaher, H. S. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.rev119.006513 · Cited by 185 · see citing works

Neutrophils in the Tumor Microenvironment

Wu, L., Saxena, S., & Singh, R. K. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-35723-8_1 · Cited by 186 · see citing works

RNA-binding Proteins in Regulating mRNA Stability and Translation: Roles and Mechanisms in Cancer

Li, W., Deng, X., & Chen, J.-J. (2022) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2022.03.025 · Cited by 168 · see citing works

Bactericidal effect of 266 to 279 nm wavelength UVC-LEDs for inactivation of Gram positive and Gram negative foodborne pathogenic bacteria and yeasts

Kim, D.-K., Kim, S.-J., & Kang, D. (2017) · Food Research International · doi:10.1016/j.foodres.2017.04.009 · Cited by 176 · see citing works

Focus on UV-Induced DNA Damage and Repair—Disease Relevance and Protective Strategies

Kciuk, M., Marciniak, B., Mojzych, M., & Kontek, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197264 · Cited by 168 · see citing works

The Many Facets of Therapy Resistance and Tumor Recurrence in Glioblastoma

Goenka, A., Tiek, D., Song, X., Huang, T., Hu, B., & Cheng, S.-Y. (2021) · Cells · doi:10.3390/cells10030484 · Cited by 169 · see citing works

Oxidatively generated base damage to cellular DNA by hydroxyl radical and one-electron oxidants: similarities and differences

Cadet, J., & Wagner, J. R. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.05.001 · Cited by 169 · see citing works

New insights into abasic site repair and tolerance

Thompson, P. S., & Cortez, D. (2020) · DNA repair · doi:10.1016/j.dnarep.2020.102866 · Cited by 170 · see citing works

Transport and accumulation of plasma generated species in aqueous solution

Verlackt, C. C. W., Boxem, W. V., & Bogaerts, A. (2018) · Physical Chemistry Chemical Physics · doi:10.1039/c7cp07593f · Cited by 166 · see citing works

Detection and interpretation of 8-oxodG and 8-oxoGua in urine, plasma and cerebrospinal fluid

Poulsen, H. E., Llovera, L., Broedbaek, K., Nielsen, P. E., & Weimann, A. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.06.009 · Cited by 162 · see citing works

Proanthocyanidins against Oxidative Stress: From Molecular Mechanisms to Clinical Applications

Yang, L., Xian, D., Xiong, X., Lai, R., Song, J., & Zhong, J. (2018) · BioMed Research International · doi:10.1155/2018/8584136 · Cited by 160 · see citing works

Cellular Stresses and Stress Responses in the Pathogenesis of Insulin Resistance

Onyango, A. N. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/4321714 · Cited by 160 · see citing works

DNA adducts: Formation, biological effects, and new biospecimens for mass spectrometric measurements in humans

Yun, B. H., Guo, J., Bellamri, M., & Turesky, R. J. (2018) · Mass Spectrometry Reviews · doi:10.1002/mas.21570 · Cited by 157 · see citing works

One-electron oxidation reactions of purine and pyrimidine bases in cellular DNA

Cadet, J., Wagner, J. R., Shafirovich, V., & Geacintov, N. E. (2013) · International Journal of Radiation Biology · doi:10.3109/09553002.2013.877176 · Cited by 152 · see citing works

Simulation of early DNA damage after the irradiation of a fibroblast cell nucleus using Geant4-DNA

Meylan, S., Incerti, S., Karamitros, M., Tang, N., Bueno, M. T., Clairand, I., & Villagrasa, C. (2017) · Scientific Reports · doi:10.1038/s41598-017-11851-4 · Cited by 154 · see citing works

DNA damage related crosstalk between the nucleus and mitochondria

Saki, M. R., & Prakash, A. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.050 · Cited by 151 · see citing works

Photochemical and Photodynamical Properties of Sulfur‐Substituted Nucleic Acid Bases,

Ashwood, B., Pollum, M., & Crespo‐Hernández, C. E. (2018) · Photochemistry and Photobiology · doi:10.1111/php.12975 · Cited by 149 · see citing works

Immune System Modulation and Viral Persistence in Bats: Understanding Viral Spillover

Subudhi, S., Rapin, N., & Misra, V. (2019) · Viruses · doi:10.3390/v11020192 · Cited by 146 · see citing works

The immunomodulatory role of matrix metalloproteinases in colitis-associated cancer

He, L., Kang, Q., Chan, K. I., Zhang, Y., Zhong, Z., & Tan, W. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1093990 · Cited by 144 · see citing works

Oxidation and alkylation stresses activate ribosome-quality control

Yan, L. L., Simms, C. L., McLoughlin, F., Vierstra, R. D., & Zaher, H. S. (2019) · Nature Communications · doi:10.1038/s41467-019-13579-3 · Cited by 123 · see citing works

Solar UV Radiation-Induced DNA Bipyrimidine Photoproducts: Formation and Mechanistic Insights

Cadet, J., Grand, A., & Douki, T. (2014) · Topics in current chemistry · doi:10.1007/128_2014_553 · Cited by 130 · see citing works

Nucleotide-Resolution Genome-Wide Mapping of Oxidative DNA Damage by Click-Code-Seq

Wu, J., McKeague, M., & Sturla, S. J. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b03715 · Cited by 123 · see citing works

Poly(ADP-ribose) polymerases covalently modify strand break termini in DNA fragmentsin vitro

Talhaoui, I., Lebedeva, N. A., Zarkovic, G., Saint‐Pierre, C., Kutuzov, M. M., Sukhanova, M. V., Matkarimov, B. T., Gasparutto, D., Saparbaev, M. K., Lavrik, O. I., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw675 · Cited by 128 · see citing works

Telomeric 8-oxo-guanine drives rapid premature senescence in the absence of telomere shortening

Barnes, R. P., Rosa, M. D., Thosar, S. A., Detwiler, A. C., Roginskaya, V. Y., Houten, B. V., Bruchez, M. P., Stewart-Ornstein, J., & Opresko, P. L. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00790-y · Cited by 136 · see citing works

The Similarities between Human Mitochondria and Bacteria in the Context of Structure, Genome, and Base Excision Repair System

Boguszewska, K., Szewczuk, M., Kaźmierczak-Barańska, J., & Karwowski, B. T. (2020) · Molecules · doi:10.3390/molecules25122857 · Cited by 144 · see citing works

Antioxidant response mechanism of freshwater microalgae species to reactive oxygen species production: a mini review

Ugya, A. Y., Imam, T. S., Li, A., Ma, J., & Hua, X. (2019) · Chemistry and Ecology · doi:10.1080/02757540.2019.1688308 · Cited by 121 · see citing works

Activation of the DNA damage response in vivo in synucleinopathy models of Parkinson’s disease

Milanese, C., Cerri, S., Ulusoy, A., Gornati, S. V., Plat, A., Gabriels, S., Blandini, F., Di Monte, D. A., Hoeijmakers, J. H., & Mastroberardino, P. G. (2018) · Cell Death &amp; Disease · doi:10.1038/s41419-018-0848-7 · Cited by 118 · see citing works

Oxidative Stress in Cancer Therapy: Friend or Enemy?

Azmanova, M., & Pitto‐Barry, A. (2022) · ChemBioChem · doi:10.1002/cbic.202100641 · Cited by 119 · see citing works

Antibacterial activity of metal oxide nanoparticles

Stanić, V. D., & Tanasković, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819943-5.00011-7 · Cited by 116 · see citing works

The biology of tardigrade disordered proteins in extreme stress tolerance

Hesgrove, C., & Boothby, T. C. (2020) · Cell Communication and Signaling · doi:10.1186/s12964-020-00670-2 · Cited by 109 · see citing works

Research progress on skin photoaging and oxidative stress

Chen, X., Yang, C., & Jiang, G. (2021) · Advances in Dermatology and Allergology · doi:10.5114/ada.2021.112275 · Cited by 120 · see citing works

Oxidative Stress, Mitochondrial Dysfunction and the Mitochondria Theory of Aging

Kong, Y., Trabucco, S. E., & Zhang, H. (2014) · Interdisciplinary topics in gerontology and geriatrics · doi:10.1159/000358901 · Cited by 112 · see citing works

Strategies for the evaluation of DNA damage and repair mechanisms in cancer

Figueroa‐González, G., & Pérez‐Plasencia, C. (2017) · Oncology Letters · doi:10.3892/ol.2017.6002 · Cited by 110 · see citing works

Estrogen-related receptors are targetable ROS sensorsPreprint

Vernier, M., Dufour, C. R., McGuirk, S., Scholtes, C., Li, X., Bourmeau, G., Kuasne, H., Park, M., St‐Pierre, J., Audet‐Walsh, É., et al. (2020) · Genes & Development · doi:10.1101/gad.330746.119 · Cited by 110 · see citing works

An injectable magnesium-loaded hydrogel releases hydrogen to promote osteoporotic bone repair via ROS scavenging and immunomodulation

Zhou, H., He, Z., Cao, Y., Chu, L., Liang, B., Yu, K., & Deng, Z. (2024) · Theranostics · doi:10.7150/thno.97412 · Cited by 115 · see citing works

Main nitric oxide (NO) hallmarks to relieve arsenic stress in higher plants

Bhat, J. A., Ahmad, P., & Corpas, F. J. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.124289 · Cited by 107 · see citing works

ATM: Expanding roles as a chief guardian of genome stability

Shiloh, Y. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.09.002 · Cited by 107 · see citing works

Protecting DNA from errors and damage: an overview of DNA repair mechanisms in plants compared to mammals

Spampinato, C. P. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2436-2 · Cited by 110 · see citing works

A Guanosine‐Quadruplex Hydrogel as Cascade Reaction Container Consuming Endogenous Glucose for Infected Wound Treatment—A Study in Diabetic Mice

Li, Y., Su, L., Zhang, Y., Liu, Y., Huang, F., Ren, Y., An, Y., Shi, L., van der Mei, H. C., & Busscher, H. J. (2022) · Advanced Science · doi:10.1002/advs.202103485 · Cited by 105 · see citing works

Radiotherapy Using High-Intensity Pulsed Radiation Beams (FLASH): A Radiation-Chemical Perspective

Wardman, P. (2020) · Radiation Research · doi:10.1667/rade-19-00016 · Cited by 104 · see citing works

Model studies of the role of oxygen in the FLASH effect

Favaudon, V., Labarbe, R., & Limoli, C. L. (2021) · Medical Physics · doi:10.1002/mp.15129 · Cited by 101 · see citing works

Targeting Photoinduced DNA Destruction by Ru(II) Tetraazaphenanthrene in Live Cells by Signal Peptide

Burke, C. S., Byrne, A., & Keyes, T. E. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b02711 · Cited by 100 · see citing works

A Summary of In Vitro and In Vivo Studies Evaluating the Impact of E-Cigarette Exposure on Living Organisms and the Environment

Merecz-Sadowska, A., Sitarek, P., Zielińska‐Bliźniewska, H., Malinowska, K., Zajdel, K., Zakonnik, Ł., & Zajdel, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020652 · Cited by 96 · see citing works

Oxidative Stress and Marine Carotenoids: Application by Using Nanoformulations

Genç, Y., Bardakçı, H., Yücel, Ç., Karatoprak, G. Ş., Akkol, E. K., Barak, T. H., & Sobarzo‐Sánchez, E. (2020) · Marine Drugs · doi:10.3390/md18080423 · Cited by 94 · see citing works

DNA damage as a biological sensor for environmental sunlight

Schuch, A. P., Machado Garcia, C. C., Makita, K., & Menck, C. F. M. (2013) · Photochemical &amp; Photobiological Sciences · doi:10.1039/c3pp00004d · Cited by 90 · see citing works

Untitled work

Zhang (2017) · doi:10.3390/molecules23020228 · Cited by 93 · see citing works

Next-generation DNA damage sequencing

Mingard, C., Wu, J., McKeague, M., & Sturla, S. J. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00647e · Cited by 92 · see citing works

Excessive Reactive Oxygen Species and Exotic DNA Lesions as an Exploitable Liability

AbdulSalam, S. F., Thowfeik, F. S., & Merino, E. J. (2016) · Biochemistry · doi:10.1021/acs.biochem.6b00703 · Cited by 91 · see citing works

Ultrafast Barrierless Photoisomerization and Strong Ultraviolet Absorption of Photoproducts in Plant Sunscreens

Luo, J. X., Liu, Y., Yang, S., Flourat, A. L., Allais, F., & Han, K. (2017) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.7b00083 · Cited by 90 · see citing works

Gold Nanoshell-Linear Tetrapyrrole Conjugates for Near Infrared-Activated Dual Photodynamic and Photothermal Therapies

Wang, J., Potocny, A. M., Rosenthal, J., & Day, E. S. (2019) · ACS Omega · doi:10.1021/acsomega.9b04150 · Cited by 89 · see citing works

Physical exercise and catecholamines response: benefits and health risk: possible mechanisms

Kruk, J., Kotarska, K., & Aboul-Enein, B. H. (2020) · Free Radical Research · doi:10.1080/10715762.2020.1726343 · Cited by 89 · see citing works

Measurement of oxidatively induced DNA damage and its repair, by mass spectrometric techniques

Dizdaroğlu, M., Coşkun, E., & Jaruga, P. (2015) · Free Radical Research · doi:10.3109/10715762.2015.1014814 · Cited by 86 · see citing works

Mitochondrial reactive oxygen species cause major oxidative mitochondrial DNA damages and repair pathways

Huang, Z., Chen, Y., & Zhang, Y. (2020) · Journal of Biosciences · doi:10.1007/s12038-020-00055-0 · Cited by 91 · see citing works

Reactive Oxygen Species: Do They Play a Role in Adaptive Immunity?

Bassoy, E. Y., Walch, M., & Martinvalet, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.755856 · Cited by 90 · see citing works

The Clinical Significance of Iron Overload and Iron Metabolism in Myelodysplastic Syndrome and Acute Myeloid Leukemia

Weber, S., Parmon, A., Kurrle, N., Schnütgen, F., & Serve, H. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.627662 · Cited by 86 · see citing works

The thymoquinone-induced production of reactive oxygen species promotes dedifferentiation through the ERK pathway and inflammation through the p38 and PI3K pathways in rabbit articular chondrocytes

Yu, S., & Kim, S. J. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.2014 · Cited by 85 · see citing works

The Effects of Ionising and Non-Ionising Electromagnetic Radiation on Extracellular Matrix Proteins

Tuieng, R. J., Cartmell, S. H., Kirwan, C., & Sherratt, M. J. (2021) · Cells · doi:10.3390/cells10113041 · Cited by 85 · see citing works

Oxidative Stress in Poultry: Lessons from the Viral Infections

Rehman, Z. U., Meng, C., Sun, Y., Safdar, A., Pasha, R. H., Munir, M., & Ding, C. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/5123147 · Cited by 84 · see citing works

Quercetin inhibits DNA damage responses to induce apoptosis via SIRT5/PI3K/AKT pathway in non-small cell lung cancer

Zhou, B., Yang, Y., Pang, X., Shi, J., Jiang, T., & Zheng, X. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115071 · Cited by 81 · see citing works

Oxidatively generated base damage to cellular DNA

Cadet, J., Douki, T., & Ravanat, J. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.03.025 · Cited by 543 · see citing works

Oxidative degradation pathways of cellular DNA: product formation and mechanistic insights

Cadet, J. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.10.598 · Cited by 17 · see citing works

Oxidatively Generated Nucleobase Modifications in Isolated and Cellular DNA

Cadet, J., Douki, T., Gasparutto, D., Ravanat, J., & Wagner, J. R. (2012) · Wiley eBooks · doi:10.1002/9781119953678.rad038 · Cited by 7 · see citing works

Oxidatively generated base damage to cellular DNA by hydroxyl radical and one-electron oxidants: similarities and differences

Cadet, J., & Wagner, J. R. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.05.001 · Cited by 169 · see citing works

Oxidatively Generated Damage to the Guanine Moiety of DNA: Mechanistic Aspects and Formation in Cells

Cadet, J., Douki, T., & Ravanat, J.-L. (2008) · Accounts of Chemical Research · doi:10.1021/ar700245e · Cited by 555 · see citing works