Free radicals in biology and medicine

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

Redox regulation of cell migration and adhesion

Hurd, T. R., DeGennaro, M., & Lehmann, R. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.11.002 · Cited by 263

Mitochondrial NADPH, transhydrogenase and disease

Rydström, J. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.03.010 · Cited by 256

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

Reduction in mitochondrial superoxide dismutase modulates Alzheimer’s disease-like pathology and accelerates the onset of behavioral changes in human amyloid precursor protein transgenic mice

Esposito, L., Raber, J., Kekonius, L., Yan, F., Yu, G.-Q., Bien-Ly, N., Puoliväli, J., Scearce-Levie, K., Masliah, E., & Mucke, L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0482-06.2006 · Cited by 254

Lifestyle and nutritional imbalances associated with Western diseases: causes and consequences of chronic systemic low-grade inflammation in an evolutionary context

Ruiz-Núñez, B., Pruimboom, L., Dijck-Brouwer, D. A. J., & Muskiet, F. A. J. (2013) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2013.02.009 · Cited by 246

Antioxidant supplementation prevents exercise-induced lipid peroxidation, but not inflammation, in ultramarathon runners

Mastaloudis, A., Morrow, J. D., Hopkins, D. W., Devaraj, S., & Traber, M. G. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.02.069 · Cited by 244

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

Urinary biomarkers of oxidative status

Il'yasova, D., Scarbrough, P., & Spasojevic, I. (2012) · Clinica Chimica Acta · doi:10.1016/j.cca.2012.06.012 · Cited by 235

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

Amelioration of cognitive deficits and neurodegeneration by curcumin in rat model of sporadic dementia of Alzheimer’s type (SDAT)

Ishrat, T., Hoda, M. N., Khan, M. B., Yousuf, S., Ahmad, M., Khan, M. M., Ahmad, A., & Islam, F. (2009) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2009.02.002 · Cited by 230

4-Hydroxy-2-nonenal, a reactive product of lipid peroxidation, and neurodegenerative diseases: a toxic combination illuminated by redox proteomics studies

Perluigi, M., Coccia, R., & Butterfield, D. A. (2012) · Antioxidants & Redox Signaling · doi:10.1089/ars.2011.4406 · Cited by 229

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

Photoprotection

Jansen, R., Osterwalder, U., Wang, S. Q., Burnett, M., & Lim, H. W. (2013) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2013.08.022 · Cited by 224

Role of iron in postischemic renal injury in the rat

Paller, M. S., Hedlund, B. E., Sikora, J. J., Faassen, A., & Waterfield, R. (1988) · Kidney International · doi:10.1038/ki.1988.205 · Cited by 222

The Aspergillus fumigatus Transcriptional Regulator AfYap1 Represents the Major Regulator for Defense against Reactive Oxygen Intermediates but Is Dispensable for Pathogenicity in an Intranasal Mouse Infection Model

Lessing, F., Kniemeyer, O., Wozniok, I., Loeffler, J., Kurzai, O., Haertl, A., & Brakhage, A. A. (2007) · Eukaryotic Cell · doi:10.1128/ec.00267-07 · Cited by 221

Peroxisome-generated hydrogen peroxide as important mediator of lipotoxicity in insulin-producing cells

Elsner, M., Gehrmann, W., & Lenzen, S. (2011) · Diabetes · doi:10.2337/db09-1401 · Cited by 221

After Cellular Internalization, Quercetin Causes Nrf2 Nuclear Translocation, Increases Glutathione Levels, and Prevents Neuronal Death against an Oxidative Insult

Arredondo, F., Echeverry, C., Abin-Carriquiry, J. A., Blasina, F., Antúnez, K., Jones, D. P., Go, Y.-M., Liang, Y.-L., & Dajas, F. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.05.020 · Cited by 220

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

Proton‐translocating transhydrogenase and NAD‐ and NADP‐linked isocitrate dehydrogenases operate in a substrate cycle which contributes to fine regulation of the tricarboxylic acid cycle activity in mitochondria

Sazanov, L. A., & Jackson, J. B. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00370-x · Cited by 205

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

Oxidative stress and antioxidants: Distress or eustress?

Niki, E. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.11.017 · Cited by 209

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

Exercise prevents sleep deprivation-associated anxiety-like behavior in rats: Potential role of oxidative stress mechanisms

Vollert, C., Zagaar, M., Hovatta, I., Taneja, M., Vu, A., Dao, A., Levine, A., Alkadhi, K., & Salim, S. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.05.010 · Cited by 207

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

Metabolomics of Human Brain Aging and Age-Related Neurodegenerative Diseases

Jové, M., Portero-Otín, M., Naudí, A., Ferrer, I., & Pamplona, R. (2014) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000091 · Cited by 195

A novel transferrin/TfR2-mediated mitochondrial iron transport system is disrupted in Parkinson's disease

Mastroberardino, P. G., Hoffman, E. K., Horowitz, M. P., Betarbet, R., Taylor, G., Cheng, D., Na, H. M., Gutekunst, C.-A., Gearing, M., Trojanowski, J. Q., et al. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.02.009 · Cited by 195

Antioxidant defense responses to sleep loss and sleep recovery

Everson, C. A., Laatsch, C. D., & Hogg, N. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00565.2004 · Cited by 192

Mitochondrial iron metabolism and its role in neurodegeneration

Horowitz, M. P., & Greenamyre, J. T. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100354 · Cited by 195

Cellular pathways for transport and efflux of ascorbate and dehydroascorbate

Corti, A., Casini, A. F., & Pompella, A. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.05.014 · Cited by 193

Mechanisms of DNA Oxidation

Aust, A. E., & Eveleigh, J. F. (1999) · Proceedings of the Society for Experimental Biology and Medicine · doi:10.1046/j.1525-1373.1999.d01-141.x · Cited by 191

Sleep and Nutrition Interactions: Implications for Athletes

Doherty, R., Madigan, S., Warrington, G., & Ellis, J. (2019) · Nutrients · doi:10.3390/nu11040822 · Cited by 186

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

Air pollution and circulating biomarkers of oxidative stress

Delfino, R. J., Staimer, N., & Vaziri, N. D. (2011) · Air Quality, Atmosphere & Health · doi:10.1007/s11869-010-0095-2 · Cited by 181

Do polyphenols enter the brain and does it matter? Some theoretical and practical considerations

Schaffer, S., & Halliwell, B. (2012) · Genes & Nutrition · doi:10.1007/s12263-011-0255-5 · Cited by 178

Amyloid-β is an antioxidant for lipoproteins in cerebrospinal fluid and plasma

Kontush, A., Berndt, C., Weber, W., Akopyan, V., Arlt, S., Schippling, S., & Beisiegel, U. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00458-5 · Cited by 180

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

Oxidative Stress Gated by Fenton and Haber Weiss Reactions and Its Association With Alzheimer’s Disease

Kanti Das, T., Wati, M. R., & Fatima-Shad, K. (2014) · Archives of Neuroscience · doi:10.5812/archneurosci.20078 · Cited by 177

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

The neglected significance of “antioxidative stress”

Poljsak, B., & Milisav, I. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/480895 · 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

Effect of Wild-type or Mutant Parkin on Oxidative Damage, Nitric Oxide, Antioxidant Defenses, and the Proteasome

Hyun, D.-H., Lee, M., Hattori, N., Kubo, S.-I., Mizuno, Y., Halliwell, B., & Jenner, P. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200666200 · Cited by 172

Chemistry and analysis of HNE and other prominent carbonyl-containing lipid oxidation compounds

Sousa, B. C., Pitt, A. R., & Spickett, C. M. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.02.003 · Cited by 172

A Bax-Induced Pro-Oxidant State Is Critical for Cytochrome c Release during Programmed Neuronal Death

Kirkland, R. A., Windelborn, J. A., Kasprzak, J. M., & Franklin, J. L. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06480.2002 · Cited by 165

ROS-induced ROS release in vascular biology: redox-redox signaling

Zinkevich, N. S., & Gutterman, D. D. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01271.2010 · Cited by 163

Fate of micelles and quantum dots in cells

Maysinger, D., Lovrić, J., Eisenberg, A., & Savić, R. (2007) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2006.08.011 · Cited by 160

Structure and function of the respiratory muscles in patients with COPD: impairment or adaptation?: Fig. 1.—

Orozco-Levi, M. (2003) · European Respiratory Journal · doi:10.1183/09031936.03.00004607 · Cited by 158

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

Morphological and Chemical Mechanisms of Elongated Mineral Particle Toxicities

Aust, A. E., Cook, P. M., & Dodson, R. F. (2011) · Journal of Toxicology and Environmental Health, Part B · doi:10.1080/10937404.2011.556046 · Cited by 155

Temporal relationship of peroxynitrite-induced oxidative damage, calpain-mediated cytoskeletal degradation and neurodegeneration after traumatic brain injury

DENG, Y., THOMPSON, B., GAO, X., & HALL, E. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.01.023 · Cited by 153

Relations of glycemic index and glycemic load with plasma oxidative stress markers

Hu, Y., Block, G., Norkus, E. P., Morrow, J. D., Dietrich, M., & Hudes, M. (2006) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/84.1.70 · Cited by 154

Antioxidant properties of -carboline alkaloids are related to their antimutagenic and antigenotoxic activities

Moura, D. J., Richter, M. F., Boeira, J. M., Pegas Henriques, J. A., & Saffi, J. (2007) · Mutagenesis · doi:10.1093/mutage/gem016 · Cited by 152

High rates of superoxide production in skeletal-muscle mitochondria respiring on both complex I- and complex II-linked substrates

Muller, F. L., Liu, Y., Abdul-Ghani, M. A., Lustgarten, M. S., Bhattacharya, A., Jang, Y. C., & Van Remmen, H. (2008) · Biochemical Journal · doi:10.1042/bj20071162 · Cited by 150

Signaling and stress: The redox landscape in NOS2 biology

Thomas, D. D., Heinecke, J. L., Ridnour, L. A., Cheng, R. Y., Kesarwala, A. H., Switzer, C. H., McVicar, D. W., Roberts, D. D., Glynn, S., Fukuto, J. M., et al. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.06.002 · Cited by 150

Noninvasive detection of hydroxyl radical generation in lung by diesel exhaust particles

Han, J.-Y., Takeshita, K., & Utsumi, H. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00501-3 · Cited by 148

Heavy Metal Induced Oxidative Damage in Terrestrial Plants

Shaw, B. P., Sahu, S. K., & Mishra, R. K. (2004) · Heavy Metal Stress in Plants · doi:10.1007/978-3-662-07743-6_4 · Cited by 153

Protein Expression Regulation under Oxidative Stress

Vogel, C., Silva, G. M., & Marcotte, E. M. (2011) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.009217 · Cited by 144

Diets enriched in foods with high antioxidant activity reverse age-induced decreases in cerebellar β-adrenergic function and increases in proinflammatory cytokines

Gemma, C., Mesches, M. H., Sepesi, B., Choo, K., Holmes, D. B., & Bickford, P. C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-14-06114.2002 · Cited by 143

The reaction of superoxide radical with N-acetylcysteine

Benrahmoune, M., Thérond, P., & Abedinzadeh, Z. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00380-4 · Cited by 143

Formation of Hydroxyl Radicals on Reaction of Hypochlorous Acid With Ferrocyanide, a Model Iron(II) Complex

Candeias, L. P., Stratford, M. R. L., & Wardman, P. (1994) · Free Radical Research · doi:10.3109/10715769409147520 · Cited by 139

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

Differential oxidative status and immune characterization of the early and advanced stages of human breast cancer

Panis, C., Victorino, V. J., Herrera, A. C. S. A., Freitas, L. F., De Rossi, T., Campos, F. C., Simão, A. N. C., Barbosa, D. S., Pinge-Filho, P., Cecchini, R., et al. (2012) · Breast Cancer Research and Treatment · doi:10.1007/s10549-011-1851-1 · Cited by 138

Modulatory effects of an algal extract containing astaxanthin on UVA-irradiated cells in culture

Lyons, N. M., & O'Brien, N. M. (2002) · Journal of Dermatological Science · doi:10.1016/s0923-1811(02)00063-4 · Cited by 134

Dual effect of oxidative stress on leukemia cancer induction and treatment

Udensi, U. K., & Tchounwou, P. B. (2014) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-014-0106-5 · Cited by 135

Yeast lacking superoxide dismutase (s) show elevated levels of “free iron” as measured by whole cell electron paramagnetic resonance

Srinivasan, C., Liba, A., Imlay, J. A., Valentine, J. S., & Gralla, E. B. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004239200 · Cited by 134

Antioxidants, Food Processing and Health

Poljsak, B., Kovač, V., & Milisav, I. (2021) · Antioxidants · doi:10.3390/antiox10030433 · Cited by 133

Determination of metal-based hydroxyl radical generating capacity of ambient and diesel exhaust particles

DiStefano, E., Eiguren-Fernandez, A., Delfino, R. J., Sioutas, C., Froines, J. R., & Cho, A. K. (2009) · Inhalation Toxicology · doi:10.1080/08958370802491433 · Cited by 133

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

Abnormal iron parameters in the pregnancy syndrome preeclampsia

Rayman, M. P., Barlis, J., Evans, R. W., Redman, C. W. G., & King, L. J. (2002) · American Journal of Obstetrics and Gynecology · doi:10.1067/mob.2002.123895 · Cited by 126

The 2013 SFRBM Discovery Award: Selected discoveries from the Butterfield laboratory of oxidative stress and its sequela in brain in cognitive disorders exemplified by Alzheimer disease and chemotherapy induced cognitive impairment

Butterfield, D. A. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.06.006 · Cited by 126

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

Antioxidant α‐tocopherol ameliorates glycemic control of GK rats, a model of type 2 diabetes

Ihara, Y., Yamada, Y., Toyokuni, S., Miyawaki, K., Ban, N., Adachi, T., Kuroe, A., Iwakura, T., Kubota, A., Hiai, H., et al. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01489-7 · Cited by 124

Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome

De Felice, C., Della Ragione, F., Signorini, C., Leoncini, S., Pecorelli, A., Ciccoli, L., Scalabrì, F., Marracino, F., Madonna, M., Belmonte, G., et al. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.04.006 · Cited by 126

In vitro toxicity of Tetrabromobisphenol-A on cerebellar granule cells: cell death, free radical formation, calcium influx and extracellular glutamate

Reistad, T., Mariussen, E., Ring, A., & Fonnum, F. (2006) · Toxicological Sciences · doi:10.1093/toxsci/kfl198 · Cited by 125

Oxygen free radical generating mechanisms in the colon: do the semiquinones of vitamin K play a role in the aetiology of colon cancer?

Valko, M., Morris, H., Mazúr, M., Rapta, P., & Bilton, R. F. (2001) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(01)00163-5 · Cited by 124

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

Correlation of oxidant status with oxidative tissue damage in patients with rheumatoid arthritis

Datta, S., Kundu, S., Ghosh, P., De, S., Ghosh, A., & Chatterjee, M. (2014) · Clinical Rheumatology · doi:10.1007/s10067-014-2597-z · Cited by 123

Assessment of Chelatable Mitochondrial Iron by Using Mitochondrion‐Selective Fluorescent Iron Indicators with Different Iron‐Binding Affinities

Rauen, U., Springer, A., Weisheit, D., Petrat, F., Korth, H., de Groot, H., & Sustmann, R. (2007) · ChemBioChem · doi:10.1002/cbic.200600311 · Cited by 121

Interplay Among Oxidants, Antioxidants, and Cytokines in Skin Disorders: Present Status and Future Considerations

Portugal, M., Barak, V., Ginsburg, I., & Kohen, R. (2007) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2007.05.010 · Cited by 121

The mitochondria-targeted antioxidant MitoQ inhibits memory loss, neuropathology, and extends lifespan in aged 3xTg-AD mice

Young, M. L., & Franklin, J. L. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.103409 · Cited by 120

Essential oil composition and antioxidant and antimicrobial properties of the aerial parts of Salvia eremophila Boiss. from Iran

Ebrahimabadi, A. H., Mazoochi, A., Kashi, F. J., Djafari-Bidgoli, Z., & Batooli, H. (2010) · Food and Chemical Toxicology · doi:10.1016/j.fct.2010.03.003 · Cited by 120

Does Vitamin C and E Supplementation Impair the Favorable Adaptations of Regular Exercise?

Nikolaidis, M. G., Kerksick, C. M., Lamprecht, M., & McAnulty, S. R. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/707941 · Cited by 116

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 neuro-immune model of myalgic encephalomyelitis/chronic fatigue syndrome

Morris, G., & Maes, M. (2013) · Metabolic Brain Disease · doi:10.1007/s11011-012-9324-8 · Cited by 117

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

Magnetic resonance imaging of brain iron

Schenck, J. F. (2003) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(02)00431-8 · Cited by 116

Oxidative Stress, Glucose Metabolism, and the Prevention of Type 2 Diabetes: Pathophysiological Insights

Shah, S., Iqbal, M., Karam, J., Salifu, M., & McFarlane, S. I. (2007) · Antioxidants & Redox Signaling · doi:10.1089/ars.2007.1629 · Cited by 115

Mechanisms for the induction of HNE- MDA- and AGE-adducts, RAGE and VEGF in retinal pigment epithelial cells.

Zhou, J., Cai, B., Jang, Y. P., Pachydaki, S., Schmidt, A. M., & Sparrow, J. R. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2004.11.009 · Cited by 113

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 origin and future of oxidative stress pathology: From the recognition of carcinogenesis as an iron addiction with ferroptosis‐resistance to non‐thermal plasma therapy

Toyokuni, S. (2016) · Pathology International · doi:10.1111/pin.12396 · Cited by 111

Photoaging and chronological aging profile: Understanding oxidation of the skin

Peres, P. S., Terra, V. A., Guarnier, F. A., Cecchini, R., & Cecchini, A. L. (2011) · Journal of Photochemistry and Photobiology B: Biology · doi:10.1016/j.jphotobiol.2011.01.019 · 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

Lifespan and mitochondrial control of neurodegeneration

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