Free radicals and antioxidants – quo vadis?

Free radicals in biology and medicine

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Oxidative stress and neurodegeneration: where are we now?

Halliwell, B. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03907.x · Cited by 2,614 · see citing works

Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life

Halliwell, B. B. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.077073 · Cited by 2,402 · see citing works

Nrf2:INrf2 (Keap1) signaling in oxidative stress

Kaspar, J. W., Niture, S. K., & Jaiswal, A. K. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.07.035 · Cited by 1,646 · see citing works

Antioxidants prevent health-promoting effects of physical exercise in humans

Ristow, M., Zarse, K., Oberbach, A., Klöting, N., Birringer, M., Kiehntopf, M., Stumvoll, M., Kahn, C. R., & Blüher, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903485106 · Cited by 1,582 · see citing works

Cellular Defenses against Superoxide and Hydrogen Peroxide

Imlay, J. A. (2008) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.77.061606.161055 · Cited by 1,563 · see citing works

Role of Free Radicals in the Neurodegenerative Diseases: Therapeutic Implications for Antioxidant Treatment

Halliwell, B. (2001) · Drugs & Aging · doi:10.2165/00002512-200118090-00004 · Cited by 1,502 · see citing works

Oxidative stress and cancer: Have we moved forward?

Halliwell, B. (2007) · Biochemical Journal · doi:10.1042/bj20061131 · Cited by 1,302 · see citing works

Redox-based regulation of signal transduction: principles, pitfalls, and promises

Janssen-Heininger, Y. M. W., Mossman, B. T., Heintz, N. H., Forman, H. J., Kalyanaraman, B., Finkel, T., Stamler, J. S., Rhee, S. G., & van der Vliet, A. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.03.011 · Cited by 784 · see citing works

Are polyphenols antioxidants or pro-oxidants? What do we learn from cell culture and in vivo studies?

Halliwell, B. B. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.01.028 · Cited by 767 · see citing works

Health promotion by flavonoids, tocopherols, tocotrienols, and other phenols: direct or indirect effects? Antioxidant or not?

Halliwell, B., Rafter, J., & Jenner, A. (2005) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/81.1.268s · Cited by 711 · see citing works

Nox enzymes, ROS, and chronic disease: An example of antagonistic pleiotropy

Lambeth, J. D. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.03.027 · Cited by 677 · see citing works

Inactivation of Peroxiredoxin I by Phosphorylation Allows Localized H2O2 Accumulation for Cell Signaling

Woo, H. A., Yim, S. H., Shin, D. H., Kang, D., Yu, D., & Rhee, S. G. (2010) · Cell · doi:10.1016/j.cell.2010.01.009 · Cited by 613 · see citing works

Is the oxidative stress theory of aging dead?

Pérez, V. I., Bokov, A., Remmen, H. V., Mele, J., Ran, Q., Ikeno, Y., & Richardson, A. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.06.003 · Cited by 604 · see citing works

Superoxide Dismutase Mimics: Chemistry, Pharmacology, and Therapeutic Potential

Batinic̈‐Haberle, I., Reboucas, J. S., & Spasojević, I. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2876 · Cited by 531 · see citing works

The gastrointestinal tract: A major site of antioxidant action?

Halliwell, B. B., Zhao, K., & Whiteman, M. (2000) · Free Radical Research · doi:10.1080/10715760000301341 · Cited by 514 · see citing works

Overexpression of Catalase Targeted to Mitochondria Attenuates Murine Cardiac Aging

Dai, D., Santana, L. F., Vermulst, M., Tomazela, D. M., Emond, M. J., MacCoss, M. J., Gollahon, K. A., Martin, G. M., Loeb, L. A., Ladiges, W., et al. (2009) · Circulation · doi:10.1161/circulationaha.108.822403 · Cited by 497 · see citing works

Oxidative stress and aberrant signaling in aging and cognitive decline

Dröge, W., & Schipper, H. M. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00294.x · Cited by 479 · see citing works

Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function

Stowe, D. F., & Camara, A. K. S. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2331 · Cited by 471 · see citing works

The wanderings of a free radical

Halliwell, B. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.11.008 · Cited by 467 · see citing works

Pure dietary flavonoids quercetin and (−)-epicatechin augment nitric oxide products and reduce endothelin-1 acutely in healthy men

Loke, W. M., Hodgson, J. M., Proudfoot, J. M., McKinley, A. J., Puddey, I. B., & Croft, K. D. (2008) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/88.4.1018 · Cited by 372 · see citing works

Absence of Respiratory Burst in X-linked Chronic Granulomatous Disease Mice Leads to Abnormalities in Both Host Defense and Inflammatory Response to <i>Aspergillus fumigatus</i>

Morgenstern, D. E., Gifford, M. A. C., Li, L. L., Doerschuk, C. M., & Dinauer, M. C. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.2.207 · Cited by 370 · see citing works

Oxidative Stress and Neurodegeneration

Moreira, P. I., Smith, M. A., Zhu, X., Nunomura, A., Castellani, R. J., & Perry, G. L. (2005) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1333.062 · Cited by 366 · see citing works

Increased superoxide in vivo accelerates age‐associated muscle atrophy through mitochondrial dysfunction and neuromuscular junction degeneration

Jang, Y. C., Lustgarten, M. S., Liu, Y., Müller, F. L., Bhattacharya, A., Liang, H., Salmon, A. B., Brooks, S. V., Larkin, L. M., Hayworth, C. R., et al. (2009) · The FASEB Journal · doi:10.1096/fj.09-146308 · Cited by 290 · see citing works

AKT1 and AKT2 maintain hematopoietic stem cell function by regulating reactive oxygen species

Juntilla, M. M., Patil, V. D., Calamito, M., Joshi, R. P., Birnbaum, M. J., & Koretzky, G. A. (2010) · Blood · doi:10.1182/blood-2009-09-241000 · Cited by 284 · see citing works

Specific Dietary Polyphenols Attenuate Atherosclerosis in Apolipoprotein E–Knockout Mice by Alleviating Inflammation and Endothelial Dysfunction

Loke, W. M., Proudfoot, J. M., Hodgson, J. M., McKinley, A. J., Hime, N. J., Magat, M., Stocker, R., & Croft, K. D. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.199687 · Cited by 284 · see citing works

Effects of Vitamin E on Lipid Peroxidation in Healthy Persons

Meagher, E. A. (2001) · JAMA · doi:10.1001/jama.285.9.1178 · Cited by 269 · see citing works

Catalase and glutathione peroxidase mimics

Day, B. J. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.09.029 · Cited by 269 · see citing works

Cell line misidentification: the beginning of the end

American Type Culture Collection Standards Development Organization Workgroup ASN-0002 (2010) · Nature Reviews Cancer · doi:10.1038/nrc2852 · Cited by 266 · see citing works

Antioxidant defense and aging in C. elegans : Is the oxidative damage theory of aging wrong?

Gems, D., & Doonan, R. (2009) · Cell Cycle · doi:10.4161/cc.8.11.8595 · Cited by 264 · see citing works

The oligomeric conformation of peroxiredoxins links redox state to function

Barranco-Medina, S., Lázaro, J.-J., & Dietz, K. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.05.029 · Cited by 225 · see citing works

The protective role of ROS in autoimmune disease

Hultqvist, M. H., Olsson, L. M., Gelderman, K. A., & Holmdahl, R. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.03.004 · Cited by 224 · see citing works

The Biology of Human Longevity: Inflammation, Nutrition, and Aging in the Evolution of Lifespans

Finch, C. E. (2007) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 194 · see citing works

Phagocyte-derived reactive species: salvation or suicide?

Halliwell, B. B. (2006) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2006.07.005 · Cited by 192 · see citing works

About “Origin and evolution of the free radical theory of aging: a brief personal history, 1954–2009”

Harman, D. (2009) · Biogerontology · doi:10.1007/s10522-009-9253-z · Cited by 187 · see citing works

The mitochondrial theory of aging: Insight from transgenic and knockout mouse models

Jang, Y. C., & Remmen, H. V. (2009) · Experimental Gerontology · doi:10.1016/j.exger.2008.12.006 · Cited by 183 · see citing works

Mitochondrial Redox Cycling of Mitoquinone Leads to Superoxide Production and Cellular Apoptosis

Doughan, A. K., & Dikalov, S. I. (2007) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2007.1693 · Cited by 172 · see citing works

The mitochondrial free radical theory of ageing - Where do we stand?

Gruber, J. (2008) · Frontiers in bioscience · doi:10.2741/3174 · Cited by 168 · see citing works

An international trial of antioxidants in the prevention of preeclampsia (INTAPP)

Xu, H., Pérez‐Cuevas, R., Xiong, X., Reyes, H., Roy, C., Julien, P., Smith, G. N., von Dadelszen, P., Leduc, L., Audibert, F., et al. (2010) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2010.01.050 · Cited by 162 · see citing works

The Stomach as a “Bioreactor”: When Red Meat Meets Red Wine

Gorelik, S., Ligumsky, M., Kohen, R., & Kanner, J. (2008) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf703700d · Cited by 143 · see citing works

Instability of, and generation of hydrogen peroxide by, phenolic compounds in cell culture media

Long, L. H., Hoi, A., & Halliwell, B. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.06.012 · Cited by 140 · 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

Nrf2 Signaling, a Mechanism for Cellular Stress Resistance in Long-Lived Mice

Leiser, S. F., & Miller, R. A. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01145-09 · Cited by 137 · see citing works

Oxidative DNA damage in human white blood cells in dietary antioxidant intervention studies

Möller, P., & Loft, S. H. (2002) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/76.2.303 · Cited by 125 · see citing works

Cardioprotective Pathways During Reperfusion: Focus on Redox Signaling and Other Modalities of Cell Signaling

Pagliaro, P., Moro, F., Tullio, F., Perrelli, M.-G., & Penna, C. R. R. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3245 · Cited by 120 · see citing works

Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice

Huang, T., Carlson, E. J., Kozy, H. M., Mantha, S., Goodman, S. I., Ursell, P. C., & Epstein, C. J. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00694-3 · Cited by 114 · see citing works

Mitochondria-targeted plastoquinone derivatives as tools to interrupt execution of the aging program. 5. SkQ1 prolongs lifespan and prevents development of traits of senescence

Anisimov, V. N., Bakeeva, L. E., Egormin, P. A., Филенко, О. Ф., Филипповна, И. Е., Манских, В. Н., Mikhelson, V. M., Panteleeva, A. A., PASYUKOVA, E. G., Pilipenko, D. I., et al. (2008) · Biochemistry (Moscow) · doi:10.1134/s0006297908120055 · Cited by 113 · see citing works

An ECVAG trial on assessment of oxidative damage to DNA measured by the comet assay

Johansson, C., Möller, P., Forchhammer, L., Loft, S. H., Godschalk, R., Langie, S. A. S., Lumeij, S., Jones, G. D. D., Kwok, R. W. L., Azqueta, A., et al. (2009) · Mutagenesis · doi:10.1093/mutage/gep055 · Cited by 113 · see citing works

Systematic review: primary and secondary prevention of gastrointestinal cancers with antioxidant supplements

Bjelaković, G., Nikolova, D., Simonetti, R. G., & Gluud, C. N. (2008) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2008.03785.x · Cited by 103 · see citing works

The omega-3 fatty acids EPA and DHA decrease plasma F2-isoprostanes: Results from two placebo-controlled interventions

Mas, E., Woodman, R. J., Burke, V., Puddey, I. B., Beilin, L. J., Durand, T., & Mori, T. A. (2010) · Free Radical Research · doi:10.3109/10715762.2010.492830 · Cited by 95 · see citing works

Ageing in nematodes: do antioxidants extend lifespan in Caenorhabditis elegans?

Pun, P. B. L., Gruber, J., Tang, S. Y., Schaffer, S., Ong, R. L. S., Fong, S., Ng, L. F., Cheah, I. K.-M., & Halliwell, B. B. (2009) · Biogerontology · doi:10.1007/s10522-009-9223-5 · Cited by 94 · see citing works

Reversal of the Mitochondrial Phenotype and Slow Development of Oxidative Biomarkers of Aging in Long-lived Mclk1+/− Mice

Lapointe, J., Stepanyan, Z., Bigras, E., & Hekimi, S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.006569 · Cited by 91 · see citing works

Moderate Antioxidant Supplementation Has No Effect on Biomarkers of Oxidant Damage in Healthy Men with Low Fruit and Vegetable Intakes

Jacob, R. A., Aiello, G. M., Stephensen, C. B., Blumberg, J. B., Milbury, P. E., Wallock, L. M., & Ames, B. N. (2003) · Journal of Nutrition · doi:10.1093/jn/133.3.740 · Cited by 89 · see citing works

Oxidant species trigger late preconditioning against myocardial stunning in conscious rabbits

Tang, X., Takano, H., Rizvi, A., Turrens, J. F., Qiu, Y., Wu, W., Zhang, Q., & Bolli, R. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2002.282.1.h281 · Cited by 68 · see citing works

Hormesis can and Does Work in Humans

Rattan, S. I. S., & Demirovic, D. (2009) · Dose-Response · doi:10.2203/dose-response.09-041.rattan · Cited by 66 · see citing works

Introducing a true internal standard for the Comet assay to minimize intra- and inter-experiment variability in measures of DNA damage and repair

Zainol, M., Stoute, J., Almeida, G. M., Rapp, A. W., Bowman, K. J., Jones, G. D. D., & ECVAG (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp826 · Cited by 55 · see citing works

Mitochondrial oxidative stress and mammalian healthspan

Wanagat, J., Dai, D., & Rabinovitch, P. S. (2010) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2010.06.002 · Cited by 52 · see citing works

Can antioxidants be effective therapeutics?

Cochemé, H. M., & Murphy, M. P. (2010) · PubMed · Cited by 48 · see citing works

Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin

Kim, A., Joseph, S., Khan, A., Epstein, C. J., Sobel, R. A., & Huang, T. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.02.028 · Cited by 44 · see citing works

Redox regulation in skeletal muscle during contractile activity and aging 1

Palomero, J., & Jackson, M. J. (2009) · Journal of Animal Science · doi:10.2527/jas.2009-2436 · Cited by 33 · see citing works

Markers of Oxidative Damage Are Not Elevated in Otherwise Healthy Individuals With the Metabolic Syndrome

Seet, R. C. S., Lee, J. C., Lim, E. C. H., et al. (2010) · Diabetes Care · doi:10.2337/dc09-2124 · Cited by 31 · see citing works

Do vitamin E supplements in diets for laboratory animals jeopardize findings in animal models of disease?

Lehr, H.-A., Vajkoczy, P., Menger, M. D., et al. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00219-6 · Cited by 23 · see citing works

Oxidative Stress in Alzheimer Disease: Synergy Between the Butterfield and Markesbery Laboratories

Butterfield, D. A. (2010) · NeuroMolecular Medicine · doi:10.1007/s12017-010-8123-9 · Cited by 22 · see citing works

Biomarkers of oxidative stress in overweight men are not influenced by a combination of antioxidants

Rytter, E., Johansson, C., Vessby, B. O., Sjödin, A. M., Möller, L., Åkesson, B., & Basu, S. (2010) · Free Radical Research · doi:10.3109/10715761003647101 · Cited by 8 · see citing works

Activation of apoptosis signalling pathways by reactive oxygen species

Redza-Dutordoir, M., & Averill-Bates, D. A. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.09.012 · Cited by 3,731 · see citing works

Recent Strategies to Develop Innovative Photosensitizers for Enhanced Photodynamic Therapy

Pham, T. C., Nguyen, V.-N., Choi, Y., Lee, S., & Yoon, J. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00381 · Cited by 1,813 · see citing works

A review on antioxidants, prooxidants and related controversy: Natural and synthetic compounds, screening and analysis methodologies and future perspectives

Carocho, M., & Ferreira, I. C. F. R. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.09.021 · Cited by 1,661 · see citing works

Determination of Antioxidants by DPPH Radical Scavenging Activity and Quantitative Phytochemical Analysis of Ficus religiosa

Baliyan, S., Mukherjee, R., Priyadarshini, A., Vibhuti, A., Gupta, A., Pandey, R. P., & Chang, C.-M. (2022) · Molecules · doi:10.3390/molecules27041326 · Cited by 1,485 · see citing works

Targeting Free Radicals in Oxidative Stress-Related Human Diseases

Poprac, P., Jomova, K., Simunkova, M., Kollar, V., Rhodes, C. J., & Valko, M. (2017) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2017.04.005 · Cited by 1,107 · see citing works

ROS production in phagocytes: Why, when, and where?

Dupré-Crochet, S., Erard, M., & Nüβe, O. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1012544 · Cited by 467 · see citing works

The complex interplay of iron metabolism, reactive oxygen species, and reactive nitrogen species: insights into the potential of various iron therapies to induce oxidative and nitrosative stress

Koskenkorva-Frank, T. S., Weiss, G., Koppenol, W. H., & Burckhardt, S. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.001 · Cited by 406 · see citing works

Markers of Oxidative Stress and Neuroprogression in Depression Disorder

Vaváková, M., Ďuračková, Z., & Trebatická, J. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/898393 · Cited by 324 · see citing works

The antioxidant paradox: less paradoxical now?

Halliwell, B. (2013) · British Journal of Clinical Pharmacology · doi:10.1111/j.1365-2125.2012.04272.x · Cited by 318 · see citing works

Role of Age-Related Mitochondrial Dysfunction in Sarcopenia

Ferri, E., Marzetti, E., Calvani, R., Picca, A., Cesari, M., & Arosio, B. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155236 · Cited by 224 · see citing works

Preclinical and Clinical Evidence of Antioxidant Effects of Antidepressant Agents: Implications for the Pathophysiology of Major Depressive Disorder

Behr, G. A., Moreira, J. C. F., & Frey, B. N. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/609421 · Cited by 205 · see citing works

Potential of garlic (Allium sativum) in lowering high blood pressure: Mechanisms of action and clinical relevance

Ried, K., & Fakler, P. (2014) · Integrated Blood Pressure Control · doi:10.2147/ibpc.s51434 · Cited by 198 · see citing works

Oxidative stress markers in affective disorders

Siwek, M., Sowa-Kućma, M., Dudek, D., Styczeń, K., Szewczyk, B., Kotarska, K., Misztak, P., Pilc, A., Wolak, M., & Nowak, G. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)71517-2 · Cited by 142 · see citing works

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 · see citing works

Oxidative Stress Implications in the Affective Disorders: Main Biomarkers, Animal Models Relevance, Genetic Perspectives, and Antioxidant Approaches

Balmus, I. M., Ciobica, A., Antioch, I., Dobrin, R., & Timofte, D. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/3975101 · Cited by 103 · see citing works

Reactive oxygen species (ROS), oxygen radicals and antioxidants: Where are we now, where is the field going and where should we go?

Halliwell, B. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.08.098 · Cited by 87 · see citing works

The stress of aging

Cesari, M., Vellas, B., & Gambassi, G. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2012.10.004 · Cited by 83 · see citing works

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 · see citing works

Neurotrophins, inflammation and oxidative stress as illness activity biomarkers in bipolar disorder

Pfaffenseller, B., Fries, G. R., Wollenhaupt-Aguiar, B., Colpo, G. D., Stertz, L., Panizzutti, B., Magalhães, P. V., & Kapczinski, F. (2013) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2013.811981 · Cited by 68 · see citing works

Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndrome

Signorini, C., Leoncini, S., De Felice, C., Pecorelli, A., Meloni, I., Ariani, F., Mari, F., Amabile, S., Paccagnini, E., Gentile, M., et al. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/195935 · Cited by 61 · see citing works

The role of carbonate as a catalyst of Fenton-like reactions in AOP processes: CO ₃ ˙ ⁻ as the active intermediate

Burg, A., Shamir, D., Shusterman, I., Kornweitz, H., & Meyerstein, D. (2014) · Chem. Commun. · doi:10.1039/c4cc05852f · Cited by 40 · see citing works

Combined use of Multiple Methodologies for the Measurement of Total Antioxidant Capacity in UK Commercially Available Vegetable Juices

Wootton-Beard, P. C., & Ryan, L. (2012) · Plant Foods for Human Nutrition · doi:10.1007/s11130-012-0287-z · Cited by 25 · see citing works

Inhibition of transient receptor potential vanilloid 4: A promising novel strategy for myocardial ischemia/reperfusion injury treatment

Dong, Q., Wang, Z., Wu, Q., & Du, Y. (2025) · Biomedicine &amp; Pharmacotherapy · doi:10.1016/j.biopha.2025.118765 · Cited by 4 · see citing works

Redox reactions: inconsistencies in their description

Šíma, J. (2011) · Foundations of Chemistry · doi:10.1007/s10698-011-9143-8 · Cited by 11 · see citing works

Oxidation/Reduction Concept

Schmiermund, T. (2022) · Springer eBooks · doi:10.1007/978-3-662-64423-2_16

The oxidative carbonyl protein and carnosine protection

Zou, C. (2003) · Zhongguo laonianxue zazhi · Cited by 3 · see citing works

Redox Reactions and Electrolysis

Burgess, D. A. (1987) · doi:10.1007/978-1-349-24067-8_9

Oxidation and Reduction

Mott, H. V. (2013) · doi:10.1002/9781118747575.ch12