How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution

Reduction potentials of one-electron couples involving free radicals in aqueous solution

Wardman, P. (1989) · Journal of Physical and Chemical Reference Data · doi:10.1063/1.555843 · Cited by 2,123 · see citing works

Purine bases, nucleosides, and nucleotides: aqueous solution redox chemistry and transformation reactions of their radical cations and e- and OH adducts

Steenken, S. (1989) · Chemical Reviews · doi:10.1021/cr00093a003 · Cited by 1,232 · see citing works

Nucleobase-Specific Quenching of Fluorescent Dyes. 1. Nucleobase One-Electron Redox Potentials and Their Correlation with Static and Dynamic Quenching Efficiencies

Seidel, C. A. M., Schulz, A., & Sauer, M. (1996) · The Journal of Physical Chemistry · doi:10.1021/jp951507c · Cited by 1,006 · see citing works

Oxidation-Reduction Potentials of Organic Systems.

SHINER, V. J. J. (1960) · Journal of the American Chemical Society · doi:10.1021/ja01505a062 · Cited by 479 · see citing works

New trends in photobiology

Tuite, E., & Kelly, J. M. (1993) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(93)80173-7 · Cited by 328 · see citing works

Formation of 8-hydroxy(deoxy)guanosine and generation of strand breaks at guanine residues in DNA by singlet oxygen

Devasagayam, T. P. A., Steenken, S., Obendorf, M. S. W., Schulz, W. A., & Sies, H. (1991) · Biochemistry · doi:10.1021/bi00239a029 · Cited by 304 · see citing works

Formation of radical cations of methoxylated benzenes by reaction with hydroxyl radicals, thallium(2+), silver(2+), and peroxysulfate (SO4.-) in aqueous solution. Optical and conductometric pulse radiolysis and in situ radiolysis electron spin resonance study

O’Neill, P., Steenken, S., & Schulte‐Frohlinde, D. (1975) · The Journal of Physical Chemistry · doi:10.1021/j100592a013 · Cited by 270 · see citing works

Ionization of purine nucleosides and nucleotides and their components by 193-nm laser photolysis in aqueous solution: model studies for oxidative damage of DNA

Candeias, L. P., & Steenken, S. (1992) · Journal of the American Chemical Society · doi:10.1021/ja00028a043 · Cited by 216 · see citing works

Pulse radiolytic measurement of redox potentials: the tyrosine and tryptophan radicals

DeFelippis, M. R., Murthy, C. P., Faraggi, M., & Klapper, M. H. (1989) · Biochemistry · doi:10.1021/bi00437a049 · Cited by 192 · see citing works

One-electron redox potentials of purines and pyrimidines

Jovanović, S. V., & Simic, M. G. (1986) · The Journal of Physical Chemistry · doi:10.1021/j100277a053 · Cited by 187 · see citing works

Reduction potentials and exchange reactions of thiyl radicals and disulfide anion radicals

Surdhar, P. S., & Armstrong, D. A. (1987) · The Journal of Physical Chemistry · doi:10.1021/j100310a022 · Cited by 159 · see citing works

One-electron reduction of nitrobenzenes by .alpha.-hydroxyalkyl radicals via addition/elimination. An example of an organic inner-sphere electron-transfer reaction

Jagannadham, V., & Steenken, S. (1984) · Journal of the American Chemical Society · doi:10.1021/ja00334a015 · Cited by 112 · see citing works

Electron transfer from indoles, phenol, and sulfite (SO32-) to chlorine dioxide (ClO2.)

Merényi, G., Lind, J. U., & Shen, X. (1988) · The Journal of Physical Chemistry · doi:10.1021/j100312a029 · Cited by 109 · see citing works

Electron-transfer reactions of alkylperoxy radicals

Jovanović, S. V., Janković, I. A., & Josimovic, L. (1992) · Journal of the American Chemical Society · doi:10.1021/ja00049a037 · Cited by 105 · see citing works

Specific formation of electron gain and loss centres in X-irradiated oriented fibres of DNA at low temperatures

Hüttermann, J., Voit, K., Oloff, H., et al. (1984) · Faraday Discussions of the Chemical Society · doi:10.1039/dc9847800135 · Cited by 85 · see citing works

The DNA guanyl radical: kinetics and mechanisms of generation and repair

Jovanović, S. V., & Simic, M. G. (1989) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(89)90167-x · Cited by 84 · see citing works

193 NM LIGHT INDUCES SINGLE STRAND BREAKAGE OF DNA PREDOMINANTLY AT GUANINE

Melvin, T., Plumb, M., Botchway, S. W., et al. (1995) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1995.tb09873.x · Cited by 82 · see citing works

Redox chemistry of substituted benzenes: the one-electron reduction potentials of methoxy-substituted benzene radical cations

Jonsson, M., Lind, J. U., Reitberger, T., et al. (1993) · The Journal of Physical Chemistry · doi:10.1021/j100145a027 · Cited by 81 · see citing works

Ionization of Polynucleotides and DNA in Aqueous Solution by 193nm Pulsed Laser Light: Identification of Base-derived Radicals

Candeias, L. P., O'Neill, P., Jones, G. D. D., & Steenken, S. (1992) · International Journal of Radiation Biology · doi:10.1080/09553009214550571 · Cited by 72 · see citing works

The Influence of Hydration on the Absolute Yields of Primary Ionic Free Radicals in γ-Irradiated DNA at 77 K: I. Total Radical Yields

Wang, W., Becker, D. A., & Sevilla, M. D. (1993) · Radiation Research · doi:10.2307/3578289 · Cited by 63 · see citing works

Photoaddition of ruthenium(II)-tris-1,4,5,8-tetraazaphenanthrene to DNA and mononucleotides

Feeney, M. M., Kelly, J. M., Tossi, A., et al. (1994) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(93)06985-c · Cited by 62 · see citing works

Kinetics and energetics of one-electron-transfer reactions involving tryptophan neutral and cation radicals

Jovanović, S. V., Steenken, S., & Simic, M. G. (1991) · The Journal of Physical Chemistry · doi:10.1021/j100155a035 · Cited by 55 · see citing works

Hydration Effects on Free Radical Yields in DNA X-Irradiated at 4 K

Mroczka, N., & Bernhard, W. A. (1993) · Radiation Research · doi:10.2307/3578290 · Cited by 41 · see citing works

Redox properties of 4-substituted aryl methyl chalcogenides in water

Jönsson, M., Lind, J., Merényi, G., & Eriksen, T. E. (1995) · Journal of the Chemical Society Perkin Transactions 2 · doi:10.1039/p29950000067 · Cited by 33 · see citing works

Radiation damage in DNA

Atherton, N. M., DAVIES, M. J., Gilbert, B. C., Sevilla, M. D., & Becker, D. A. (1994) · Royal Society of Chemistry eBooks · doi:10.1039/9781847553515-00130 · Cited by 24 · see citing works

1 H NMR Studies of g-Irradiated Polynucleotides and DNA in N 2 O-Saturated Aqueous Solutions: Release of Undamaged and Modified Bases

Hildenbrand, K., Mirtsch, S., & Schulte‐Frohlinde, D. (1993) · Radiation Research · doi:10.2307/3578187 · Cited by 9 · see citing works

Oxidative Nucleobase Modifications Leading to Strand Scission

Burrows, C. J., & Muller, J. G. (1998) · Chemical Reviews · doi:10.1021/cr960421s · Cited by 1,736 · see citing works

Proton-coupled electron transfer

Huynh, M. H. V., & Meyer, T. J. (2007) · Chemical Reviews · doi:10.1021/cr0500030 · Cited by 1,659 · see citing works

Free radical-induced damage to DNA: mechanisms and measurement

Dizdaroglu, M., Jaruga, P., Birincioglu, M., & Rodriguez, H. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00826-2 · Cited by 953 · see citing works

Mechanisms for DNA Charge Transport

Genereux, J. C., & Barton, J. K. (2010) · Chemical Reviews · doi:10.1021/cr900228f · Cited by 787 · see citing works

Long-Range Charge Transfer in DNA:  Transient Structural Distortions Control the Distance Dependence

Schuster, G. B. (2000) · Accounts of Chemical Research · doi:10.1021/ar980059z · Cited by 778 · 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

Tea chemistry

Harbowy, M. E., Balentine, D. A., Davies, A. P., & Cai, Y. (1997) · Critical Reviews in Plant Sciences · doi:10.1080/07352689709701956 · Cited by 459 · 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

DNA damage by singlet oxygen and cellular protective mechanisms

Agnez-Lima, L. F., Melo, J. T. A., Silva, A. E., Oliveira, A. H. S., Timoteo, A. R. S., Lima-Bessa, K. M., Martinez, G. R., Medeiros, M. H. G., Di Mascio, P., Galhardo, R. S., et al. (2012) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2011.12.005 · Cited by 205 · 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

Comparison of DNA Damage Photoinduced by Ketoprofen, Fenofibric Acid and Benzophenone via Electron and Energy Transfer¶

Lhiaubet, V., Paillous, N., & Chouini-Lalanne, N. (2007) · Photochemistry and Photobiology · doi:10.1562/0031-8655(2001)0740670coddpb2.0.co2 · Cited by 72 · see citing works

DNA−Protein Cross-Linking from Oxidation of Guanine via the Flash−Quench Technique

Nguyen, K. L., Steryo, M., Kurbanyan, K., Nowitzki, K. M., Butterfield, S. M., Ward, S. R., & Stemp, E. D. A. (2000) · Journal of the American Chemical Society · doi:10.1021/ja993502p · Cited by 59 · see citing works

DNA−Protein Cross-Linking via Guanine Oxidation:  Dependence upon Protein and Photosensitizer

Kurbanyan, K., Nguyen, K. L., To, P., Rivas, E. V., Lueras, A. M. K., Kosinski, C., Steryo, M., González, A., Mah, D. A., & Stemp, E. D. A. (2003) · Biochemistry · doi:10.1021/bi020713p · Cited by 53 · see citing works

Rag1 immunodeficiency-induced early aging and senescence in zebrafish are dependent on chronic inflammation and oxidative stress

Novoa, B., Pereiro, P., López‐Muñoz, A., Varela, M., Forn‐Cuní, G., Anchelin, M., Dios, S., Romero, A., Martinez‐López, A., Medina‐Gali, R. M., et al. (2019) · Aging Cell · doi:10.1111/acel.13020 · Cited by 41 · see citing works

The other side of the superoxide radical anion: Its ability to chemically repair DNA oxidized sites

Muñoz-Rugeles, L., Galano, A., & Alvarez-Idaboy, J. R. (2018) · Chemical Communications · doi:10.1039/c8cc07834c · Cited by 18 · see citing works

Dependence of DNA–Protein Cross-Linking via Guanine Oxidation upon Local DNA Sequence As Studied by Restriction Endonuclease Inhibition

Madison, A. L., Perez, Z. A., To, P., Maisonet, T., Rios, E. V., Trejo, Y., Ochoa-Paniagua, C., Reno, A., & Stemp, E. D. A. (2012) · Biochemistry · doi:10.1021/bi201087q · Cited by 18 · see citing works

Optical Voltammetry of Polymer-Encapsulated Single-Walled Carbon Nanotubes

Horoszko, C. P., Jena, P. V., Roxbury, D., Rotkin, S. V., & Heller, D. A. (2019) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.9b07626 · Cited by 9 · see citing works

Marie Curie Palliative Care Institute

Arthur, M. (2014) · Nursing Standard · doi:10.7748/ns.29.3.32.s36 · Cited by 17 · see citing works

Marie Curie Cancer Care

(2013) · Trends in Urology & Men s Health · doi:10.1002/tre.315 · Cited by 1 · see citing works

The electron spin resonance spectra of radicals obtained by the addition of amino- and hydroxyl radicals to alkenes

Griffiths, W. E., Longster, G. F., Myatt, J., et al. (1967) · Journal of the Chemical Society B Physical Organic · doi:10.1039/j29670000530 · Cited by 22 · see citing works

Trapping Sites of Polypropylene Mechano-Radicals

Kurokawa, N., Sakaguchi, M., & Sohma, J. (1978) · Polymer Journal · doi:10.1295/polymj.10.93 · Cited by 24 · see citing works

The Curie's Lab and its Women (1906–1934) Le laboratoire Curie et ses Femmes (1906–1934)

Micault, N. P. (2012) · Annals of Science · doi:10.1080/00033790.2011.644194 · Cited by 7 · see citing works