Free radicals in biology and medicine

Quantitative analysis of cell death and ferritin expression in response to cortical iron: implications for hypoxia–ischemia and stroke

Bishop, G. M., & Robinson, S. R. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02303-4 · Cited by 104

Does exercise reduce brain oxidative stress? A systematic review

Camiletti‐Moirón, D., Aparicio, V. A., Aranda, P., & Radak, Z. (2013) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/sms.12065 · Cited by 104

Age-Associated Changes in Superoxide Dismutase Activity, Thiobarbituric Acid Reactivity and Reduced Glutathione Level in the Brain and Liver in Senescence Accelerated Mice (SAM): A Comparison with DdY Mice

Liu, J., & Mori, A. (1993) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(93)90032-m · Cited by 104

Fenton reaction induced cancer in wild type rats recapitulates genomic alterations observed in human cancer

Akatsuka, S., Yamashita, Y., Ohara, H., Liu, Y.-T., Izumiya, M., Abe, K., Ochiai, M., Jiang, L., Nagai, H., Okazaki, Y., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043403 · Cited by 102

Progeric Effects of Catalase Inactivation in Human Cells

Koepke, J. I., Wood, C. S., Terlecky, L. J., Walton, P. A., & Terlecky, S. R. (2008) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2008.06.004 · Cited by 101

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

Impact of Lactic Acid on Cell Proliferation and Free Radical-Induced Cell Death in Monolayer Cultures of Neural Precursor Cells

Lampe, K. J., Namba, R. M., Silverman, T. R., Bjugstad, K. B., & Mahoney, M. J. (2009) · Biotechnology and Bioengineering · doi:10.1002/bit.22352 · Cited by 98

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

Production of the Carbonate Radical Anion during Xanthine Oxidase Turnover in the Presence of Bicarbonate

Bonini, M. G., Miyamoto, S., Mascio, P. D., & Augusto, O. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406929200 · Cited by 99

Metformin induces oxidative stress in white adipocytes and raises uncoupling protein 2 levels

Anedda, A., Rial, E., & González-Barroso, M. M. (2008) · Journal of Endocrinology · doi:10.1677/joe-08-0278 · 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

Plasmalogen phospholipids protect internodal myelin from oxidative damage

Luoma, A. M., Kuo, F., Cakici, O., Crowther, M. N., Denninger, A. R., Avila, R. L., Brites, P., & Kirschner, D. A. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.03.012 · Cited by 97

Iron Accumulation during Cellular Senescence

KILLILEA, D. W., WONG, S. L., CAHAYA, H. S., ATAMNA, H., & AMES, B. N. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.063 · Cited by 97

Oxidative stress in humans training in a cold, moderate altitude environment and their response to a phytochemical antioxidant supplement

Schmidt, M. C., Askew, E. W., Roberts, D. E., Prior, R. L., Ensign Jr, W. Y., & Hesslink Jr, R. E. (2002) · Wilderness & Environmental Medicine · doi:10.1580/1080-6032(2002)013[0094:osihti]2.0.co;2 · Cited by 97

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

Free Radicals in the Guinea Pig Inner Ear following Gentamicin Exposure

Takumida, M., Popa, R., & Anniko, M. (1999) · ORL · doi:10.1159/000027643 · Cited by 91

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

Iron and genome stability: an update

Prá, D., Franke, S. I. R., Henriques, J. A. P., & Fenech, M. (2012) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2012.02.001 · Cited by 91

Carotenoids Inhibit Lipid Peroxidation and Hemoglobin Oxidation, but Not the Depletion of Glutathione Induced by ROS in Human Erythrocytes

Chisté, R. C., Freitas, M., Mercadante, A. Z., & Fernandes, E. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.01.059 · Cited by 90

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

Oxidative Parameters Differences during Non-Lethal and Lethal Sepsis Development1

Andrades, M., Ritter, C., Moreira, J. C. F., & Dal-Pizzol, F. (2005) · Journal of Surgical Research · doi:10.1016/j.jss.2004.11.008 · Cited by 86

Enhanced catabolism of mitochondrial superoxide/hydrogen peroxide and aging in transgenic Drosophila

Bayne, A.-C. V., Mockett, R. J., Orr, W. C., & Sohal, R. S. (2005) · Biochemical Journal · doi:10.1042/bj20041872 · Cited by 84

The Myeloperoxidase-Derived Oxidant HOSCN Inhibits Protein Tyrosine Phosphatases and Modulates Cell Signalling via the Mitogen-Activated Protein Kinase (MAPK) Pathway in Macrophages

Lane, A. E., Tan, J. T. M., Hawkins, C. L., Heather, A. K., & Davies, M. J. (2010) · Biochemical Journal · doi:10.1042/bj20100082 · Cited by 86

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

Antioxidants in Personalized Nutrition and Exercise

Margaritelis, N. V., Paschalis, V., Theodorou, A. A., Kyparos, A., & Nikolaidis, M. G. (2018) · Advances in Nutrition · doi:10.1093/advances/nmy052 · Cited by 84

Tinospora cordifolia (Willd.) Miers: Protection mechanisms and strategies against oxidative stress-related diseases

Arunachalam, K., Yang, X., & San, T. T. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114540 · Cited by 82

Extrahepatic synthesis of complement proteins in inflammation

Laufer, J. (2001) · Molecular Immunology · doi:10.1016/s0161-5890(01)00044-x · Cited by 81

Role of Radicals and Singlet Oxygen in Photoactivated DNA Cleavage by the Anticancer Drug Camptothecin: An Electron Paramagnetic Resonance Study

Brezova, V., Valko, M., Breza, M., Morris, H., Telser, J., Dvoranova, D., Kaiserova, K., Varecka, L., Mazur, M., & Leibfritz, D. (2003) · The Journal of Physical Chemistry B · doi:10.1021/jp027743m · Cited by 80

Heart Disease Link to Fetal Hypoxia and Oxidative Stress

Giussani, D. A., Niu, Y., Herrera, E. A., Richter, H. G., Camm, E. J., Thakor, A. S., Kane, A. D., Hansell, J. A., Brain, K. L., Skeffington, K. L., et al. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-1031-1_7 · Cited by 81

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

Human RPE Melanosomes Protect from Photosensitized and Iron-Mediated Oxidation but Become Pro-oxidant in the Presence of Iron upon Photodegradation

Rozanowski, B., Burke, J. M., Boulton, M. E., Sarna, T., & Rozanowska, M. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-1700 · Cited by 76

Overexpression of plant uncoupling mitochondrial protein in transgenic tobacco increases tolerance to oxidative stress

Brandalise, M., Maia, I. G., Borecký, J., Vercesi, A. E., & Arruda, P. (2003) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1024603530043 · Cited by 76

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

Friedreich's Ataxia, No Changes in Mitochondrial Labile Iron in Human Lymphoblasts and Fibroblasts

Sturm, B., Bistrich, U., Schranzhofer, M., Sarsero, J. P., Rauen, U., Scheiber-Mojdehkar, B., de Groot, H., Ioannou, P., & Petrat, F. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m408717200 · Cited by 73

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

Body iron store as a predictor of oxidative DNA damage in healthy men and women

Hori, A., Mizoue, T., Kasai, H., Kawai, K., Matsushita, Y., Nanri, A., Sato, M., & Ohta, M. (2010) · Cancer Science · doi:10.1111/j.1349-7006.2009.01394.x · Cited by 72

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

Celastrus paniculatus seed oil and organic extracts attenuate hydrogen peroxide- and glutamate-induced injury in embryonic rat forebrain neuronal cells

Godkar, P. B., Gordon, R. K., Ravindran, A., & Doctor, B. P. (2006) · Phytomedicine · doi:10.1016/j.phymed.2003.11.011 · Cited by 72

Fatty Acids and Homocysteine Levels in Patients with Recurrent Depression: An Explorative Pilot Study

Assies, J., Lok, A., Bockting, C. L., Weverling, G. J., Lieverse, R., Visser, I., Abeling, N. G. G. M., Duran, M., & Schene, A. H. (2004) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2003.12.009 · 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

An ultrasensitive fluorescent assay for the in vivo quantification of superoxide radical in organisms

Georgiou, C. D., Papapostolou, I., Patsoukis, N., Tsegenidis, T., & Sideris, T. (2005) · Analytical Biochemistry · doi:10.1016/j.ab.2005.09.013 · Cited by 70

Regulation of Apoptosis by Vitamin C

Vissers, M. C. M., Lee, W.-G., & Hampton, M. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107664200 · Cited by 70

Oxidative Stress and Cancer: The Role of Redox Regulation

Toyokuni, S. (1998) · Biotherapy · doi:10.1023/a:1007934229968 · Cited by 69

Oxidative stress in Rett syndrome: natural history, genotype, and variants

Leoncini, S., De Felice, C., Signorini, C., Pecorelli, A., Durand, T., Valacchi, G., Ciccoli, L., & Hayek, J. (2011) · Redox Report · doi:10.1179/1351000211y.0000000004 · Cited by 69

Peroxiredoxins in Regulation of MAPK Signalling Pathways; Sensors and Barriers to Signal Transduction

Latimer, H. R., & Veal, E. A. (2016) · Molecules and Cells · doi:10.14348/molcells.2016.2327 · Cited by 68

Oxidative stress defense in human-skin-derived mesenchymal stem cells versus human keratinocytes: Different mechanisms of protection and cell selection

Orciani, M., Gorbi, S., Benedetti, M., Di Benedetto, G., Mattioli-Belmonte, M., Regoli, F., & Di Primio, R. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.06.007 · Cited by 67

Succinate modulation of H2O2 release at NADH:ubiquinone oxidoreductase (complex I) in brain mitochondria

Zoccarato, F., Cavallini, L., Bortolami, S., & Alexandre, A. (2007) · Biochemical Journal · doi:10.1042/bj20070215 · Cited by 66

Spatio-temporal Model of Endogenous ROS and Raft-Dependent WNT/Beta-Catenin Signaling Driving Cell Fate Commitment in Human Neural Progenitor Cells

Haack, F., Lemcke, H., Ewald, R., Rharass, T., & Uhrmacher, A. M. (2015) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1004106 · Cited by 66

Mitochondrial reactive oxygen species are scavenged by Cockayne syndrome B protein in human fibroblasts without nuclear DNA damage

Cleaver, J. E., Brennan-Minnella, A. M., Swanson, R. A., Fong, K.-W., Chen, J., Chou, K.-M., Chen, Y.-W., Revet, I., & Bezrookove, V. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414135111 · Cited by 65

Oxidative stress and air pollution exposure during pregnancy: A molecular assessment

Nagiah, S., Phulukdaree, A., Naidoo, D., Ramcharan, K., Naidoo, R., Moodley, D., & Chuturgoon, A. (2015) · Human & Experimental Toxicology · doi:10.1177/0960327114559992 · Cited by 65

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

Vitamin C Deficiency Causes Muscle Atrophy and a Deterioration in Physical Performance

Takisawa, S., Funakoshi, T., Yatsu, T., Nagata, K., Aigaki, T., Machida, S., & Ishigami, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-41229-7 · Cited by 63

Hypocatalasemic Fibroblasts Accumulate Hydrogen Peroxide and Display Age-Associated Pathologies

Wood, C. S., Koepke, J. I., Teng, H., Boucher, K. K., Katz, S., Chang, P., Terlecky, L. J., Papanayotou, I., Walton, P. A., & Terlecky, S. R. (2006) · Traffic · doi:10.1111/j.1600-0854.2005.00358.x · Cited by 55

Dual fluorophore-nitronyl probe for investigation of superoxide dynamics and antioxidant status of biological systems

Medvedeva, N., Martin, V. V., Weis, A. L., & Likhtenshten, G. I. (2004) · Journal of Photochemistry and Photobiology A: Chemistry · doi:10.1016/s1010-6030(03)00430-1 · Cited by 62

Hyperresistance to photosensitized lipid peroxidation and apoptotic killing in 5-aminolevulinate-treated tumor cells overexpressing mitochondrial GPX4

Kriska, T., Korytowski, W., & Girotti, A. W. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01078-x · Cited by 59

Evaluation of the compounds commonly known as superoxide dismutase and catalase mimics in cellular models

Vincent, A., Thauvin, M., Quévrain, E., Mathieu, E., Layani, S., Seksik, P., Batinic-Haberle, I., Vriz, S., Policar, C., & Delsuc, N. (2021) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2021.111431 · Cited by 58

The dual face of endogenous α-aminoketones: Pro-oxidizing metabolic weapons

Bechara, E. J. H., Dutra, F., Cardoso, V. E. S., Sartori, A., Olympio, K. P. K., Penatti, C. A. A., Adhikari, A., & Assunção, N. A. (2007) · Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology · doi:10.1016/j.cbpc.2006.07.004 · Cited by 57

Effect of irradiance on fatty acid, carotenoid, total protein composition and growth of Microcystis aeruginosa

Walsh, K., Jones, G. J., & Hugh Dunstan, R. (1997) · Phytochemistry · doi:10.1016/s0031-9422(96)00573-0 · Cited by 57

Anxiolytic activity of Evolvulus alsinoides and Convulvulus pluricaulis in rodents

Nahata, A., Patil, U. K., & Dixit, V. K. (2009) · Pharmaceutical Biology · doi:10.1080/13880200902822596 · Cited by 57

Eurycoma longifolia : Medicinal Plant in the Prevention and Treatment of Male Osteoporosis due to Androgen Deficiency

Mohd Effendy, N., Mohamed, N., Muhammad, N., Naina Mohamad, I., & Shuid, A. N. (2012) · Evidence-Based Complementary and Alternative Medicine · doi:10.1155/2012/125761 · Cited by 55

Systemic toxicity induced by paclitaxel in vivo is associated with the solvent cremophor EL through oxidative stress-driven mechanisms

Campos, F. C., Victorino, V. J., Martins-Pinge, M. C., Cecchini, A. L., Panis, C., & Cecchini, R. (2014) · Food and Chemical Toxicology · doi:10.1016/j.fct.2014.03.013 · Cited by 53

Strenuous Acute Exercise Induces Slow and Fast Twitch-Dependent NADPH Oxidase Expression in Rat Skeletal Muscle

Osório Alves, J., Matta Pereira, L., Cabral Coutinho do Rêgo Monteiro, I., Pontes dos Santos, L. H., Soares Marreiros Ferraz, A., Carneiro Loureiro, A. C., Calado Lima, C., Leal-Cardoso, J. H., Pires Carvalho, D., Soares Fortunato, R., et al. (2020) · Antioxidants · doi:10.3390/antiox9010057 · Cited by 53

Potential protection of skin by acute UVA irradiation - from cellular to animal models

Tyrrell, R. M., & Reeve, V. E. (2006) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2006.02.002 · Cited by 53

Beneficial effect of vitamin E on the metabolic parameters of diabetic rats

Al Shamsi, M. S., Amin, A., & Adeghate, E. (2004) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000028735.79172.9b · Cited by 53

Mechanical Ventilation Antioxidant Trial

Howe, K. P., Clochesy, J. M., Goldstein, L. S., & Owen, H. (2015) · American Journal of Critical Care · doi:10.4037/ajcc2015335 · Cited by 52

Contrasting genome-wide distribution of 8-hydroxyguanine and acrolein-modified adenine during oxidative stress-induced renal carcinogenesis

Akatsuka, S., Aung, T. T., Dutta, K. K., Jiang, L., Lee, W.-H., Liu, Y.-T., Onuki, J., Shirase, T., Yamasaki, K., Ochi, H., et al. (2006) · The American Journal of Pathology · doi:10.2353/ajpath.2006.051280 · Cited by 51

Involvement of NRF2 in Breast Cancer and Possible Therapeutical Role of Polyphenols and Melatonin

Tascioglu Aliyev, A., Panieri, E., Stepanić, V., Gurer-Orhan, H., & Saso, L. (2021) · Molecules · doi:10.3390/molecules26071853 · Cited by 50

Natural antioxidants’ effects on endoplasmic reticulum stress-related diseases

Reyes-Fermín, L. M., Aparicio-Trejo, O. E., Avila-Rojas, S. H., Gómez-Sierra, T., Martínez-Klimova, E., & Pedraza-Chaverri, J. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111229 · Cited by 50

Effect of the antioxidant action of Ginkgo biloba extract (EGb 761) on aging and oxidative stress

Droy-Lefaix, M. T. (1997) · AGE · doi:10.1007/s11357-997-0013-1 · Cited by 49

A nuclear microscopy study of trace elements Ca, Fe, Zn and Cu in atherosclerosis

Watt, F., Rajendran, R., Ren, M. Q., Tan, B. K. H., & Halliwell, B. (2006) · Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms · doi:10.1016/j.nimb.2006.03.073 · Cited by 48

Role of glutathione in the oxidative stress response in the fungal pathogen Candida glabrata

Gutiérrez-Escobedo, G., Orta-Zavalza, E., Castaño, I., & De Las Peñas, A. (2013) · Current Genetics · doi:10.1007/s00294-013-0390-1 · Cited by 47

In vitro screening of essential oil from young and mature leaves of Artemisia scoparia compared to its major constituents for free radical scavenging activity

Singh, H. P., Kaur, S., Mittal, S., Batish, D. R., & Kohli, R. K. (2010) · Food and Chemical Toxicology · doi:10.1016/j.fct.2010.01.017 · Cited by 47

Magnesium supplementation diminishes peripheral blood lymphocyte DNA oxidative damage in athletes and sedentary young man

Petrović, J., Stanić, D., Dmitrašinović, G., Plećaš-Solarović, B., Ignjatović, S., Batinić, B., Popović, D., & Pešić, V. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/2019643 · Cited by 45

Inactivation of Enzymes of the Glutathione Antioxidant System by Treatment of Cultured Human Keratinocytes with Peroxides

Vessey, D. A., & Lee, K.-H. (1993) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12476735 · Cited by 45

Effect of spirulina maxima on the haloperidol induced tardive dyskinesia and oxidative stress in rats

Thaakur, S. R., & Jyothi, B. (2007) · Journal of Neural Transmission · doi:10.1007/s00702-007-0744-2 · Cited by 44

Evaluation of antioxidant activity of marine algae-extracts from Korea

Lee, J.-H., & Kim, G.-H. (2015) · Journal of Aquatic Food Product Technology · doi:10.1080/10498850.2013.770809 · Cited by 43

Antioxidative and free radical scavenging effects of ecdysteroids from Serratula strangulata

Cai, Y.-J., Dai, J.-Q., Fang, J.-G., Ma, L.-P., Hou, L.-F., Yang, L., & Liu, Z.-L. (2002) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y02-152 · Cited by 43

Water deficit‐induced oxidative stress affects artemisinin content and expression of proline metabolic genes in Artemisia annua L.

Soni, P., & Abdin, M. Z. (2017) · FEBS Open Bio · doi:10.1002/2211-5463.12184 · Cited by 41

Nitric oxide pros and cons: The role of l-arginine, a nitric oxide precursor, and idebenone, a coenzyme-Q analogue in ameliorating cerebral hypoxia in rat

Baky, N. A. A., Zaidi, Z. F., Fatani, A. J., Sayed-Ahmed, M. M., & Yaqub, H. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.07.004 · Cited by 41

Modulation of DNA single-strand breaks by intracellular glutathione in human lung cells exposed to asbestos fibers

Puhakka, A., Ollikainen, T., Soini, Y., Kahlos, K., Säily, M., Koistinen, P., Pääkkö, P., Linnainmaa, K., & Kinnula, V. L. (2002) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/s1383-5718(01)00322-9 · Cited by 40

A novel exopolysaccharide from deep-sea bacterium Zunongwangia profunda SM-A87: Low-cost fermentation, moisture retention, and antioxidant activities

Sun, M.-L., Liu, S.-B., Qiao, L.-P., Chen, X.-L., Pang, X., Shi, M., Zhang, X.-Y., Qin, Q.-L., Zhou, B.-C., Zhang, Y.-Z., et al. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5839-8 · Cited by 39

Comet assay and analysis of micronucleus formation in patients with rheumatoid arthritis.

Karaman, A., Binici, D. N., & Melikoğlu, M. A. (2011) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2010.11.014 · Cited by 39

Reaction of cysteine and glutathione (GSH) at the freshly fractured quartz surface: a possible role in silica-related diseases?

Fenoglio, I., Fonsato, S., & Fubini, B. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00398-8 · Cited by 38

Selenium supplementation and exercise: Effect on oxidant stress in overweight adults

Savory, L. A., Kerr, C. J., Whiting, P., Finer, N., McEneny, J., & Ashton, T. (2012) · Obesity · doi:10.1038/oby.2011.83 · Cited by 37

Role of Glutaredoxin-1 and Glutathionylation in Cardiovascular Diseases

Burns, M., Rizvi, S. H. M., Tsukahara, Y., Pimentel, D. R., Luptak, I., Hamburg, N. M., Matsui, R., & Bachschmid, M. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186803 · Cited by 36

N-acetyl-cysteine prevents toxic oxidative effects induced by IFN-α in human neurons

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