Free Radicals in Biology and Medicine

Reactive oxygen species: Metabolism, oxidative stress, and signal transduction

Apel, K., & Hirt, H. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141701 · Cited by 11,723

Oxidants, antioxidants, and the degenerative diseases of aging.

Ames, B. N., Shigenaga, M. K., & Hagen, T. M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.7915 · Cited by 5,958

[1] Role of free radicals and catalytic metal ions in human disease: An overview

Halliwell, B., & Gutteridge, J. M. C. (1990) · Methods in Enzymology · doi:10.1016/0076-6879(90)86093-b · Cited by 4,994

Reactive Oxygen Species and the Central Nervous System

Halliwell, B. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb10990.x · Cited by 2,947

Free Radicals: Properties, Sources, Targets, and Their Implication in Various Diseases

Phaniendra, A., Jestadi, D. B., & Periyasamy, L. (2015) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-014-0446-0 · Cited by 2,886

Environmentally induced oxidative stress in aquatic animals

Lushchak, V. I. (2011) · Aquatic Toxicology · doi:10.1016/j.aquatox.2010.10.006 · Cited by 2,729

Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer

WISEMAN, H., & HALLIWELL, B. (1996) · Biochemical Journal · doi:10.1042/bj3130017 · Cited by 2,345

Antioxidants and antioxidant methods: an updated overview

Gulcin, İ. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02689-3 · Cited by 2,205

Oxidative stress and the amyloid beta peptide in Alzheimer’s disease

Cheignon, C., Tomas, M., Bonnefont-Rousselot, D., Faller, P., Hureau, C., & Collin, F. (2018) · Redox Biology · doi:10.1016/j.redox.2017.10.014 · Cited by 2,185

Strategies of antioxidant defense

SIES, H. (1993) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1993.tb18025.x · Cited by 1,976

Antioxidants in health and disease

Young, I. S., & Woodside, J. V. (2001) · Journal of Clinical Pathology · doi:10.1136/jcp.54.3.176 · Cited by 1,949

Free radicals, oxidative stress, and antioxidants in human health and disease

Aruoma, O. I. (1998) · Journal of the American Oil Chemists' Society · doi:10.1007/s11746-998-0032-9 · Cited by 1,682

Toxicity of iron and hydrogen peroxide: the Fenton reaction

Winterbourn, C. C. (1995) · Toxicology Letters · doi:10.1016/0378-4274(95)03532-x · Cited by 1,415

Superoxide activates mitochondrial uncoupling proteins

Echtay, K. S., Roussel, D., St-Pierre, J., Jekabsons, M. B., Cadenas, S., Stuart, J. A., Harper, J. A., Roebuck, S. J., Morrison, A., Pickering, S., et al. (2002) · Nature · doi:10.1038/415096a · Cited by 1,382

Blockade of Microglial Activation Is Neuroprotective in the 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine Mouse Model of Parkinson Disease

Wu, D. C., Jackson-Lewis, V., Vila, M., Tieu, K., Teismann, P., Vadseth, C., Choi, D.-K., Ischiropoulos, H., & Przedborski, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01763.2002 · Cited by 1,183

Regulation of ferritin genes and protein

Torti, F. M., & Torti, S. V. (2002) · Blood · doi:10.1182/blood.v99.10.3505 · Cited by 1,173

Radicals and oxidative stress in diabetes

West, I. C. (2000) · Diabetic Medicine · doi:10.1046/j.1464-5491.2000.00259.x · Cited by 913

Free radical theory of aging

Harman, D. (1992) · Mutation Research/DNAging · doi:10.1016/0921-8734(92)90030-s · Cited by 902

Mitochondrial damage induced by conditions of oxidative stress

Kowaltowski, A. J., & Vercesi, A. E. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00216-0 · Cited by 866

The selenoprotein GPX4 is essential for mouse development and protects from radiation and oxidative damage insults

Yant, L. J., Ran, Q., Rao, L., Van Remmen, H., Shibatani, T., Belter, J. G., Motta, L., Richardson, A., & Prolla, T. A. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01360-6 · Cited by 797

The Advanced Glycation End Product, N∊-(Carboxymethyl)lysine, Is a Product of both Lipid Peroxidation and Glycoxidation Reactions

Fu, M.-X., Requena, J. R., Jenkins, A. J., Lyons, T. J., Baynes, J. W., & Thorpe, S. R. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.17.9982 · Cited by 822

Nitric oxide and redox mechanisms in the immune response

Wink, D. A., Hines, H. B., Cheng, R. Y. S., Switzer, C. H., Flores-Santana, W., Vitek, M. P., Ridnour, L. A., & Colton, C. A. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.1010550 · Cited by 765

Review: Alzheimer's Amyloid β-Peptide-Associated Free Radical Oxidative Stress and Neurotoxicity

Varadarajan, S., Yatin, S., Aksenova, M., & Butterfield, D. A. (2000) · Journal of Structural Biology · doi:10.1006/jsbi.2000.4274 · Cited by 735

Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport

Dancis, A., Yuan, D. S., Haile, D., Askwith, C., Eide, D., Moehle, C., Kaplan, J., & Klausner, R. D. (1994) · Cell · doi:10.1016/0092-8674(94)90345-x · Cited by 659

Neuroprotection by the Metabolic Antioxidant α-Lipoic Acid

Packer, L., Tritschler, H. J., & Wessel, K. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(96)00269-9 · Cited by 639

Regulation of the hypothalamic corticotropin-releasing hormone neurosecretory system

Whitnall, M. H. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90035-q · Cited by 582

Iron Homeostasis, Oxidative Stress, and DNA Damage

Meneghini, R. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00016-6 · Cited by 578

The structure of human mitochondrial manganese superoxide dismutase reveals a novel tetrameric interface of two 4-helix bundles

Borgstahl, G. E. O., Parge, H. E., Hickey, M. J., Beyer, W. F., Hallewell, R. A., & Tainer, J. A. (1992) · Cell · doi:10.1016/0092-8674(92)90270-m · Cited by 472

Iron-induced carcinogenesis: The role of redox regulation

Toyokuni, S. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)02111-6 · Cited by 471

Mutagenicity and repair of oxidative DNA damage: insights from studies using defined lesions

Wang, D., Kreutzer, D. A., & Essigmann, J. M. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(98)00066-9 · Cited by 464

The role of free radicals in asbestos-induced diseases

Kamp, D. W., Graceffa, P., Pryor, W. A., & Weitzman, S. A. (1992) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(92)90117-y · Cited by 428

Selective iron chelation in Friedreich ataxia: biologic and clinical implications

Boddaert, N., Le Quan Sang, K. H., Rötig, A., Leroy-Willig, A., Gallet, S., Brunelle, F., Sidi, D., Thalabard, J.-C., Munnich, A., & Cabantchik, Z. I. (2007) · Blood · doi:10.1182/blood-2006-12-065433 · Cited by 409

The Biological Relevance of Direct Antioxidant Effects of Polyphenols for Cardiovascular Health in Humans Is Not Established1–4

Hollman, P. C. H., Cassidy, A., Comte, B., Heinonen, M., Richelle, M., Richling, E., Serafini, M., Scalbert, A., Sies, H., & Vidry, S. (2011) · The Journal of Nutrition · doi:10.3945/jn.110.131490 · Cited by 406

Faster superoxide dismutase mutants designed by enhancing electrostatic guidance

Getzoff, E. D., Cabelli, D. E., Fisher, C. L., Parge, H. E., Viezzoli, M. S., Banci, L., & Hallewell, R. A. (1992) · Nature · doi:10.1038/358347a0 · Cited by 399

Artifacts in Cell Culture: Rapid Generation of Hydrogen Peroxide on Addition of (−)-Epigallocatechin, (−)-Epigallocatechin Gallate, (+)-Catechin, and Quercetin to Commonly Used Cell Culture Media

Long, L. H., Clement, M. V., & Halliwell, B. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2895 · Cited by 390

Chapter 7 Protein Oxidation Processes in Aging Brain

Butterfield, D. A., & Stadtman, E. R. (1997) · Advances in cell aging and gerontology · doi:10.1016/s1566-3124(08)60057-7 · Cited by 390

Characterization of three isoforms of mammalian peroxiredoxin that reduce peroxides in the presence of thioredoxin

Chae, H. Z., Kim, H. J., Kang, S. W., & Rhee, S. G. (1999) · Diabetes Research and Clinical Practice · doi:10.1016/s0168-8227(99)00037-6 · Cited by 390

Complexes of Iron with Phenolic Compounds from Soybean Nodules and Other Legume Tissues: Prooxidant and Antioxidant Properties

Moran, J. F., Klucas, R. V., Grayer, R. J., Abian, J., & Becana, M. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(96)00426-1 · Cited by 369

Antioxidant defense mechanisms in murine epidermis and dermis and their responses to ultraviolet light

Shindo, Y., Witt, E., & Packer, L. (1993) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12469048 · Cited by 363

β-Amyloid-Associated Free Radical Oxidative Stress and Neurotoxicity: Implications for Alzheimer’s Disease

Butterfield, D. A. (1997) · Chemical Research in Toxicology · doi:10.1021/tx960130e · Cited by 364

The chemistry of nitroxyl (HNO) and implications in biology

Miranda, K. M. (2005) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2004.08.010 · Cited by 339

Molecular mechanisms of iron uptake in fungi

Kosman, D. J. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03368.x · Cited by 331

Antioxidant activity of mycosporine-like amino acids isolated from three red macroalgae and one marine lichen

de la Coba, F., Aguilera, J., Figueroa, F. L., de Gálvez, M. V., & Herrera, E. (2009) · Journal of Applied Phycology · doi:10.1007/s10811-008-9345-1 · Cited by 302

Effects of polystyrene microbeads in marine planktonic crustaceans

Gambardella, C., Morgana, S., Ferrando, S., Bramini, M., Piazza, V., Costa, E., Garaventa, F., & Faimali, M. (2017) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2017.07.036 · Cited by 296

Modulation of leukocyte–endothelial interactions by reactive metabolites of oxygen and nitrogen: relevance to ischemic heart disease

Grisham, M. B., Granger, D. N., & Lefer, D. J. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00094-x · Cited by 293

Design of iron chelators with therapeutic application

Liu, Z. D., & Hider, R. C. (2002) · Coordination Chemistry Reviews · doi:10.1016/s0010-8545(02)00050-4 · Cited by 287

A novel hypothesis of lipofuscinogenesis and cellular aging based on interactions between oxidative stress and autophagocytosis

Brunk, U. T., Jones, C. B., & Sohal, R. S. (1992) · Mutation Research/DNAging · doi:10.1016/0921-8734(92)90042-n · Cited by 274

Metabolism of Alcohol

Lieber, C. S. (2005) · Clinics in Liver Disease · doi:10.1016/j.cld.2004.10.005 · Cited by 274

Design of clinically useful iron(III)‐selective chelators

Liu, Z. D., & Hider, R. C. (2002) · Medicinal Research Reviews · doi:10.1002/med.1027 · Cited by 266

The antioxidant action of ergothioneine

Akanmu, D., Cecchini, R., Aruoma, O. I., & Halliwell, B. (1991) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(91)90158-f · Cited by 251

Effects of ultraviolet radiation on corals and other coral reef organisms

SHICK, J. M., LESSER, M. P., & JOKIEL, P. L. (1996) · Global Change Biology · doi:10.1111/j.1365-2486.1996.tb00065.x · Cited by 251

Cellular injury induced by oxidative stress is mediated through lysosomal damage

Öllinger, K., & Brunk, U. T. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)00062-3 · Cited by 243

Food consumption and the incidence of type II diabetes mellitus

Montonen, J., Järvinen, R., Heliövaara, M., Reunanen, A., Aromaa, A., & Knekt, P. (2005) · European Journal of Clinical Nutrition · doi:10.1038/sj.ejcn.1602094 · Cited by 237

Dose-response effects of acute ultraviolet irradiation on antioxidants and molecular markers of oxidation in murine epidermis and dermis

Shindo, Y., Witt, E., Han, D., & Packer, L. (1994) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12373027 · Cited by 234

Inhibition of NADH-Linked Mitochondrial Respiration by 4-Hydroxy-2-nonenal

Humphries, K. M., Yoo, Y., & Szweda, L. I. (1998) · Biochemistry · doi:10.1021/bi971958i · Cited by 231

Perhydroxyl radical (HOO.) initiated lipid peroxidation. The role of fatty acid hydroperoxides

Aikens, J., & Dix, T. A. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)98591-1 · Cited by 228

Long-lived reactive species on free-radical-damaged proteins

Simpson, J. A., Narita, S., Gieseg, S., Gebicki, S., Gebicki, J. M., & Dean, R. T. (1992) · Biochemical Journal · doi:10.1042/bj2820621 · Cited by 225

Skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease

Hussain, S., Cheol, K., & Mofarrahi, M. (2008) · International Journal of Chronic Obstructive Pulmonary Disease · doi:10.2147/copd.s4480 · Cited by 224

Free Hydroxyl Radicals are Formed on Reaction Between the Neutrophil-Derived Species Superoxide Anion and Hypochlorous Acid

Candeias, L. P., Patel, K. B., Stratford, M. R. L., & Wardman, P. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80394-a · Cited by 212

What Is Responsible for the Initiating Chemistry of Iron-Mediated Lipid Peroxidation: An Update

Cheng, Z., & Li, Y. (2007) · Chemical Reviews · doi:10.1021/cr040077w · Cited by 211

H-ferritin subunit overexpression in erythroid cells reduces the oxidative stress response and induces multidrug resistance properties

Epsztejn, S., Glickstein, H., Picard, V., Slotki, I. N., Breuer, W., Beaumont, C., & Cabantchik, Z. I. (1999) · Blood · doi:10.1182/blood.v94.10.3593.422k26_3593_3603 · Cited by 209

Micronutritional approaches to periodontal therapy

Van der Velden, U., Kuzmanova, D., & Chapple, I. L. C. (2011) · Journal of Clinical Periodontology · doi:10.1111/j.1600-051x.2010.01663.x · Cited by 199

New insights on oxidative stress in the artery wall

STOCKER, R., & KEANEY, J. F. (2005) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2005.01370.x · Cited by 188

In Vitro Methods of Assay of Antioxidants: An Overview

Singh, S., & Singh, R. P. (2008) · Food Reviews International · doi:10.1080/87559120802304269 · Cited by 182

An embryoprotective role for glucose‐6‐phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis

NICOL, C. J., ZIELENSKI, J., TSUI, L., & WELLS, P. G. (2000) · The FASEB Journal · doi:10.1096/fasebj.14.1.111 · Cited by 180

Apoptosis or Senescence-like Growth Arrest: Influence of Cell-Cycle Position, P53, P21 and Bax in H2O2 Response of Normal Human FIbroblasts

CHEN, Q. M., LIU, J., & MERRETT, J. B. (2000) · Biochemical Journal · doi:10.1042/bj3470543 · Cited by 280

Oxidative and antioxidative mechanisms in oral cancer and precancer: A review

Choudhari, S. K., Chaudhary, M., Gadbail, A. R., Sharma, A., & Tekade, S. (2014) · Oral Oncology · doi:10.1016/j.oraloncology.2013.09.011 · Cited by 177

Chromium induced lipid peroxidation in the plants of Pistia stratiotes L.: Role of antioxidants and antioxidant enzymes

Sinha, S., Saxena, R., & Singh, S. (2005) · Chemosphere · doi:10.1016/j.chemosphere.2004.08.071 · Cited by 176

Scientific Opinion on Dietary Reference Values for vitamin C

EFSA Panel on Dietetic Products, N. A. A. (. (2013) · EFSA Journal · doi:10.2903/j.efsa.2013.3418 · Cited by 173

The excessive use of antioxidant therapy: a possible cause of male infertility?

Henkel, R., Sandhu, I. S., & Agarwal, A. (2019) · Andrologia · doi:10.1111/and.13162 · Cited by 169

Antioxidant Peptidomics Reveals Novel Skin Antioxidant System

Yang, H., Wang, X., Liu, X., Wu, J., Liu, C., Gong, W., Zhao, Z., Hong, J., Lin, D., Wang, Y., et al. (2009) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800297-mcp200 · Cited by 156

Future of ToxicologyIron Chelators and Differing Modes of Action and Toxicity: The Changing Face of Iron Chelation Therapy

Kalinowski, D. S., & Richardson, D. R. (2007) · Chemical Research in Toxicology · doi:10.1021/tx700039c · Cited by 145

Oxidative and nitrosative stress pathways in the brain of socially isolated adult male rats demonstrating depressive- and anxiety-like symptoms

Filipović, D., Todorović, N., Bernardi, R. E., & Gass, P. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1218-9 · Cited by 138

UVR-induced oxidative stress in human skin in vivo: Effects of oral vitamin C supplementation

McArdle, F., Rhodes, L. E., Parslew, R., Jack, C. I. A., Friedmann, P. S., & Jackson, M. J. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01042-0 · Cited by 132

Arsenic stress in rice: Redox consequences and regulation by iron

Nath, S., Panda, P., Mishra, S., Dey, M., Choudhury, S., Sahoo, L., & Panda, S. K. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.04.013 · Cited by 131

Comparative effects of β-carotene and fucoxanthin on retinol deficiency induced oxidative stress in rats

Sangeetha, R. K., Bhaskar, N., & Baskaran, V. (2009) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-009-0145-y · Cited by 126

Activation of the Nrf2 Cell Defense Pathway by Ancient Foods: Disease Prevention by Important Molecules and Microbes Lost from the Modern Western Diet

Senger, D. R., Li, D., Jaminet, S.-C., & Cao, S. (2016) · PLOS ONE · doi:10.1371/journal.pone.0148042 · Cited by 124

Radical–radical reactions of superoxide: A potential route to toxicity

Winterbourn, C. C., & Kettle, A. J. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00810-6 · Cited by 118

A novel type of glutathione peroxidase: expression and regulation during wound repair

MUNZ, B., FRANK, S., HÜBNER, G., OLSEN, E., & WERNER, S. (1997) · Biochemical Journal · doi:10.1042/bj3260579 · Cited by 118

Selective Pick-Up of Increased Iron by Deferoxamine-Coupled Cellulose Abrogates the Iron-Driven Induction of Matrix-Degrading Metalloproteinase 1 and Lipid Peroxidation in Human Dermal Fibroblasts In Vitro: A New Dressing Concept

Wenk, J., Sabiwalsky, A., Dissemond, J., Meewes, C., Brenneisen, P., Wlaschek, M., Scharffetter-Kochanek, K., Foitzik, A., Achterberg, V., Reitz, A., et al. (2001) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2001.01345.x · Cited by 115

Requirements for superoxide-dependent tyrosine hydroperoxide formation in peptides

WINTERBOURN, C. C., PARSONS-MAIR, H. N., GEBICKI, S., GEBICKI, J. M., & DAVIES, M. J. (2004) · Biochemical Journal · doi:10.1042/bj20040259 · Cited by 112

The catecholic metal sequestering agent 1,2-dihydroxybenzene-3,5-disulfonate confers protection against oxidative cell damage

Krishna, C. M., Liebmann, J. E., Kaufman, D., DeGraff, W., Hahn, S. M., McMurry, T., Mitchell, J. B., & Russo, A. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90142-j · Cited by 110

Role of mangiferin on biochemical alterations and antioxidant status in isoproterenol-induced myocardial infarction in rats

Prabhu, S., Jainu, M., Sabitha, K. E., & Devi, C. S. S. (2006) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2006.02.014 · Cited by 103

The role of ultraviolet radiation in melanomagenesis

Von Thaler, A., Kamenisch, Y., & Berneburg, M. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.01025.x · Cited by 100

Isoleukotrienes are biologically active free radical products of lipid peroxidation

Harrison, K. A., & Murphy, R. C. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.29.17273 · Cited by 98

Physical inactivity, insulin resistance, and the oxidative-inflammatory loop

Gratas-Delamarche, A., Derbré, F., Vincent, S., & Cillard, J. (2014) · Free Radical Research · doi:10.3109/10715762.2013.847528 · Cited by 99

Real‐time measurement of nitric oxide in single mature mouse skeletal muscle fibres during contractions

Pye, D., Palomero, J., Kabayo, T., & Jackson, M. J. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.125930 · Cited by 96

Isolation of Lactic Acid Bacteria Showing Antioxidative and Probiotic Activities from Kimchi and Infant Feces

Ji, K., Jang, N. Y., & Kim, Y. T. (2015) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1501.01077 · Cited by 94

Garlic increases antioxidant levels in diabetic and hypertensive rats determined by a modified peroxidase method

Drobiova, H., Thomson, M., Al-Qattan, K., Peltonen-Shalaby, R., Al-Amin, Z., & Ali, M. (2011) · Evidence-Based Complementary and Alternative Medicine · doi:10.1093/ecam/nep011 · Cited by 91

The Ferroxidase Activity of Yeast Frataxin

Park, S., Gakh, O., Mooney, S. M., & Isaya, G. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206711200 · Cited by 88

Quantitation of Protein-Bound 3-Nitrotyrosine and 3,4-Dihydroxyphenylalanine by High-Performance Liquid Chromatography with Electrochemical Array Detection

Hensley, K., Maidt, M. L., Pye, Q. N., Stewart, C. A., Wack, M., Tabatabaie, T., & Floyd, R. A. (1997) · Analytical Biochemistry · doi:10.1006/abio.1997.2281 · Cited by 89

Induction of a wide range of C2-12 aldehydes and C7-12 acyloins in the kidney of Wistar rats after treatment with a renal carcinogen, ferric nitrilotriacetate

Toyokuni, S., Luo, X.-P., Tanaka, T., Uchida, K., Hiai, H., & Lehotay, D. C. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(96)00489-3 · Cited by 84

Developmental and physiological challenges of octopus (Octopus vulgaris) early life stages under ocean warming

Repolho, T., Baptista, M., Pimentel, M. S., Dionísio, G., Trübenbach, K., Lopes, V. M., Lopes, A. R., Calado, R., Diniz, M., & Rosa, R. (2014) · Journal of Comparative Physiology B · doi:10.1007/s00360-013-0783-y · Cited by 85

Effects of nitrite on modulating ROS generation following ischemia and reperfusion

Raat, N. J. H., Shiva, S., & Gladwin, M. T. (2009) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.02.002 · Cited by 79

Reflections of an aging free radical

Halliwell, B. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.010 · Cited by 75

Iron, oxidative stress and the example of solar ultraviolet a radiation.

Aroun, A., Zhong, J. L., Tyrrell, R. M., & Pourzand, C. (2012) · Photochemical & Photobiological Sciences · doi:10.1039/c1pp05204g · Cited by 74

Aging increases the oxidation of dichlorohydrofluorescein in single isolated skeletal muscle fibers at rest, but not during contractions

Palomero, J., Vasilaki, A., Pye, D., McArdle, A., & Jackson, M. J. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00530.2012 · Cited by 71

The role of oxidative stress in postoperative delirium

Karlidag, R., Unal, S., Sezer, O. H., Bay Karabulut, A., Battaloğlu, B., But, A., & Ozcan, C. (2006) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2006.06.002 · Cited by 72

Long-term overexpression of heme oxygenase 1 promotes tau aggregation in mouse brain by inducing tau phosphorylation

Hui, Y., Wang, D., Li, W., Zhang, L., Jin, J., Ma, N., Zhou, L., Nakajima, O., Zhao, W., & Gao, X. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-102061 · Cited by 71

8‐Oxodeoxyguanosine Formation in the DNA of Cultured Cells After Exposure to H2O2 Alone or with UVB or UVA Irradiation

Rosen, J. E., Prahalad, A. K., & Williams, G. M. (1996) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1996.tb02430.x · Cited by 68