Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels

DISC ELECTROPHORESIS – II METHOD AND APPLICATION TO HUMAN SERUM PROTEINS *

Davis, B. J. (1964) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1964.tb14213.x · Cited by 16,129

Superoxide Dismutase

McCord, J. M., & Fridovich, I. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)63504-5 · Cited by 12,952

The Reduction of Cytochrome c by Milk Xanthine Oxidase

McCord, J. M., & Fridovich, I. (1968) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)91929-0 · Cited by 1,196

A Mechanism for the Production of Ethylene from Methional

Beauchamp, C., & Fridovich, I. (1970) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)62842-x · Cited by 667

Superoxide Dismutase from Escherichia coli B

Keele, B. B., McCord, J. M., & Fridovich, I. (1970) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)62675-4 · Cited by 559

The Utility of Superoxide Dismutase in Studying Free Radical Reactions

McCord, J. M., & Fridovich, I. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)63505-7 · Cited by 559

The production of superoxide anion radicals in the reaction of reduced flavins and flavoproteins with molecular oxygen

Massey, V., Strickland, S., Mayhew, S. G., Howell, L. G., Engel, P. C., Matthews, R. G., Schuman, M., & Sullivan, P. A. (1969) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(69)90287-3 · Cited by 426

The Utility of Superoxide Dismutase in Studying Free Radical Reactions

McCord, J. M., & Fridovich, I. (1970) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)63246-6 · Cited by 387

Direct demonstration of superoxide anion production during the oxidation of reduced flavin and of its catalytic decomposition by erythrocuprein

Ballou, D. P., Palmer, G., & Massey, V. (1969) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(69)90288-5 · Cited by 223

Further Characterization of Bovine Superoxide Dismutase and Its Isolation from Bovine Heart

Keele, B. B., McCord, J. M., & Fridovich, I. (1971) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)62263-x · Cited by 203

Salt stress-induced responses in cucumber plants

Lechno, S., Zamski, E., & Tel‐Or, E. (1997) · Journal of Plant Physiology · doi:10.1016/s0176-1617(97)80204-0 · Cited by 130

CHANGES IN ANTIOXIDANT ENZYME ACTIVITIES IN SOYBEAN UNDER CADMIUM STRESS

Ferreira, R. R., Fornazier, R. F., Vitória, Â. P., Lea, P. J., & Azevedo, R. A. (2002) · Journal of Plant Nutrition · doi:10.1081/pln-100108839 · Cited by 130

Mitochondrial or cytosolic catalase reverses the MnSOD-dependent inhibition of proliferation by enhancing respiratory chain activity, net ATP production, and decreasing the steady state levels of H2O2

Rodrı́guez, A. M., Carrico, P. M., Mazurkiewicz, J. E., & Melendez, J. A. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00362-2 · Cited by 130

SOD2: A new type of tumor‐suppressor gene?

Bravard, A., Sabatier, L., Hoffschir, F., Ricoul, M., Luccioni, C., & Dutrillaux, B. (1992) · International Journal of Cancer · doi:10.1002/ijc.2910510323 · Cited by 130

Responses of enzymatic antioxidants and non-enzymatic antioxidants in the cyanobacterium Microcystis aeruginosa to the allelochemical ethyl 2-methyl acetoacetate (EMA) isolated from reed (Phragmites communis)

Hong, Y., Hu, H., Xie, X., & Li, F. (2008) · Journal of Plant Physiology · doi:10.1016/j.jplph.2007.10.007 · Cited by 130

2,4-dichlorophenoxyacetic acid-induced leaf senescence in mung bean (Vigna radiata L. Wilczek) and senescence inhibition by co-treatment with silver nanoparticles

Karuppanapandian, T., Wang, H., Prabakaran, N., Kandhavelu, J., Kwon, M. J., Manoharan, K., & Kim, W. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.11.007 · Cited by 130

New genes involved in chromate resistance inRalstonia metallidurans strain CH34

Juhnke, S., Peitzsch, N., Hübener, N., Große, C., & Nies, D. H. (2002) · Archives of Microbiology · doi:10.1007/s00203-002-0492-5 · Cited by 130

Role of Salmonella typhimurium Mn-superoxide dismutase (SodA) in protection against early killing by J774 macrophages

Tsolis, R. M., Bäumler, A. J., & Heffron, F. (1995) · Infection and Immunity · doi:10.1128/iai.63.5.1739-1744.1995 · Cited by 130

Killing of human malaria parasites by macrophage secretory products

Wozencraft, A. O., Dockrell, H. M., Taverne, J., Targett, G. A. T., & Playfair, J. H. L. (1984) · Infection and Immunity · doi:10.1128/iai.43.2.664-669.1984 · Cited by 130

The effect of experimental warming on leaf functional traits, leaf structure and leaf biochemistry in Arabidopsis thaliana

Jin, B., Wang, L., Wang, J., Jiang, K.-Z., Wang, Y., Jiang, X., Ni, C.-Y., Wang, Y., & Teng, N. (2011) · BMC Plant Biology · doi:10.1186/1471-2229-11-35 · Cited by 129

Na+ and Cl− ions show additive effects under NaCl stress on induction of oxidative stress and the responsive antioxidative defense in rice

Khare, T. R., Kumar, V., & Kishor, P. B. K. (2014) · PROTOPLASMA · doi:10.1007/s00709-014-0749-2 · Cited by 130

Growth, photosynthesis and antioxidant responses of endophyte infected and non-infected rice under lead stress conditions

Li, X., Bu, N., Li, Y., Ma, L., Xin, S., & Zhang, L. (2012) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2012.01.052 · Cited by 129

Bacillus pumilus enhances tolerance in rice (Oryza sativa L.) to combined stresses of NaCl and high boron due to limited uptake of Na+

Khan, A., Uddin, S., Zhao, X. Q., Javed, M. T., Khan, K. S., Bano, A., Shen, R. F., & Masood, S. (2016) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.12.011 · Cited by 129

Effect of lead on oxidative status, antioxidative response and metal accumulation in Coronopus didymus

Sidhu, G. P. S., Singh, H. P., Batish, D. R., & Kohli, R. K. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2016.05.019 · Cited by 129

Study of silicon effects on antioxidant enzyme activities and osmotic adjustment of wheat under drought stress

Ahmad, S. T., & Haddad, R. (2011) · Czech Journal of Genetics and Plant Breeding · doi:10.17221/92/2010-cjgpb · Cited by 129

Physiological and proteomic analyses of the drought stress response in Amygdalus Mira (Koehne) Yü et Lu roots

Cao, Y., Luo, Q., Tian, Y., & Meng, F. (2017) · BMC Plant Biology · doi:10.1186/s12870-017-1000-z · Cited by 131

Superoxide dismutase (SOD) as a selection criterion for triticale grain yield under drought stress: a comprehensive study on genomics and expression profiling, bioinformatics, heritability, and phenotypic variability

Saed‐Moucheshi, A., Sohrabi, F., Fasihfar, E., Baniasadi, F., Riasat, M., & Mozafari, A. A. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-02919-5 · Cited by 129

Safety and Pharmacokinetics of Multiple Doses of Recombinant Human CuZn Superoxide Dismutase Administered Intratracheally to Premature Neonates With Respiratory Distress Syndrome

Davis, J. M., Rosenfeld, W., Richter, S. E., Parad, R. B., Gewolb, I. H., Spitzer, A. R., Carlo, W. A., Couser, R. J., Price, A. P., Flaster, E. R., et al. (1997) · PEDIATRICS · doi:10.1542/peds.100.1.24 · Cited by 129

Role of Salicylic Acid in Promoting Salt Stress Tolerance and Enhanced Artemisinin Production in Artemisia annua L.

Aftab, T., Khan, M. M. A., da Silva, J. A. T., Idrees, M., Naeem, M., & Moinuddin (2011) · Journal of Plant Growth Regulation · doi:10.1007/s00344-011-9205-0 · Cited by 129

Reaction of the desulfoferrodoxin from Desulfoarculus baarsii with superoxide anion. Evidence for a superoxide reductase activity

Lombard, M., Fontecave, M., Touati, D., & Nivière, V. (2014) · PubMed · doi:10.48550/arxiv.1412.5038 · Cited by 129

Pleiotropic Functions of a Streptomyces pristinaespiralis Autoregulator Receptor in Development, Antibiotic Biosynthesis, and Expression of a Superoxide Dismutase

Folcher, M., Gaillard, H., Nguyen, L. T., Nguyen, K. T., Lacroix, P., Bamas-Jacques, N., Rinkel, M., & Thompson, C. J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101109200 · Cited by 129

Lipid peroxidation and concentration of glutathione in erythrocytes from workers exposed to lead.

Sugawara, E., Nakamura, K., Miyake, T., Fukumura, A., & Seki, Y. (1991) · Occupational and Environmental Medicine · doi:10.1136/oem.48.4.239 · Cited by 129

Down-regulation of Manganese-Superoxide Dismutase through Phosphorylation of FOXO3a by Akt in Explanted Vascular Smooth Muscle Cells from Old Rats

Li, M., Chiu, J., Mossman, B. T., & Fukagawa, N. K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606596200 · Cited by 128

Calcium and zinc supplementation protects lead (Pb)‐induced perturbations in antioxidant enzymes and lipid peroxidation in developing mouse brain

Prasanthi, R., Devi, C. B., Davuljigari, C. B., Reddy, N. S., & Reddy, G. R. (2009) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2009.12.002 · Cited by 130

Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress

Bonifácio, A., Martins, M. O., Ribeiro, C., Fontenele, A. V., Carvalho, F. E. L., Margis-Pinheiro, M. M. A. N., & da Silveira, J. A. G. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02366.x · Cited by 130

Manganese superoxide dismutase suppresses hypoxic induction of hypoxia-inducible factor-1α and vascular endothelial growth factor

Wang, M., Kirk, J. S., Venkataraman, S., Domann, F. E., Zhang, H. J., Schafer, F. Q., Flanagan, S. W., Weydert, C. J. D., Spitz, D. R., Buettner, G. R., et al. (2005) · Oncogene · doi:10.1038/sj.onc.1208986 · Cited by 133

Induction of Mn SOD in human monocytes without inflammatory cytokine production by a mutant endotoxin

Tian, L., White, J. E., Lin, H., Haran, V. S., Sacco, J., Chikkappa, G., Davis, F. B., Davis, P. J., & Tsan, M. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.275.3.c740 · Cited by 129

Nitric oxide (NO) counteracts cadmium induced cytotoxic processes mediated by reactive oxygen species (ROS) in Brassica juncea: cross-talk between ROS, NO and antioxidant responses

Verma, K., Mehta, S. K., & Shekhawat, G. S. (2013) · BioMetals · doi:10.1007/s10534-013-9608-4 · Cited by 128

Fumigation with essential oils improves sensory quality and enhanced antioxidant ability of shiitake mushroom (Lentinus edodes)

Jiang, T., Luo, Z., & Ying, T. (2014) · Food Chemistry · doi:10.1016/j.foodchem.2014.09.130 · Cited by 131

Antioxidative potential of folate producing probiotic Lactobacillus helveticus CD6

Ahire, J. J., Mokashe, N. U., Patil, H. J., & Chaudhari, B. L. (2011) · Journal of Food Science and Technology · doi:10.1007/s13197-011-0244-0 · Cited by 131

Accumulation efficiency, genotoxicity and antioxidant defense mechanisms in medicinal plant Acalypha indica L. under lead stress

Venkatachalam, P., Jayalakshmi, N., Geetha, N., Sahi, S. V., Sharma, N. C., Rene, E. R., Sarkar, S. K., & Favas, P. J. C. (2016) · Chemosphere · doi:10.1016/j.chemosphere.2016.12.092 · Cited by 128

Serpentine endophytic bacterium Pseudomonas azotoformans ASS1 accelerates phytoremediation of soil metals under drought stress

Ma, Y., Rajkumar, M., Moreno, A. M., Zhang, C., & Freitas, H. M. D. O. (2017) · Chemosphere · doi:10.1016/j.chemosphere.2017.06.135 · Cited by 128

CRISPR/Cas with ribonucleoprotein complexes and transiently selected telomere vectors allows highly efficient marker-free and multiple genome editing in Botrytis cinerea

Leisen, T., Bietz, F., Werner, J. A., Wegner, A., Schaffrath, U., Scheuring, D., Willmund, F., Mosbach, A., Scalliet, G., & Hahn, M. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008326 · Cited by 121

Superoxide dismutase assay using alkaline dimethylsulfoxide as superoxide anion-generating system

Hyland, Κ., Voisin, E., Banoun, H., & Auclair, C. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90684-x · Cited by 128

Effect of 28-homobrassinolide on the drought stress-induced changes in photosynthesis and antioxidant system of Brassica juncea L.

Fariduddin, Q., Khanam, S., Hasan, S. A., Ali, B., Hayat, S., & Ahmad, A. (2009) · Acta Physiologiae Plantarum · doi:10.1007/s11738-009-0302-7 · Cited by 128

Superoxide dismutase activity in arbuscular mycorrhizal Lactuca sativa plants subjected to drought stress

Ruíz-Lozano, J. M., Azcón, R., & Palma, J. M. (1996) · New Phytologist · doi:10.1111/j.1469-8137.1996.tb04637.x · Cited by 128

A preliminary study of the superoxide dismutase content of some human tumors.

Sykes, J. A., McCormack, F. X., & O’Brien, T. (1978) · PubMed · Cited by 127

Lipid peroxidation and antioxidant enzyme activities of Euphorbia millii hyperhydric shoots

Dewir, Y. H., Chakrabarty, D., Ali, M. B., Hahn, E.-J., & Paek, K. (2005) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2005.06.019 · Cited by 127

Selenium Accumulation in Unicellular Green Alga Chlorella vulgaris and Its Effects on Antioxidant Enzymes and Content of Photosynthetic Pigments

Sun, X. L., Zhong, Y., Huang, Z., & Yang, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112270 · Cited by 127

The Application of ESR Spin-Trapping Technique to the Evaluation of SOD-like Activity of Biological Substances

Mitsuta, K., Mizuta, Y., Kohno, M., Hiramatsu, M., & Mori, A. (1990) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.63.187 · Cited by 127

Assessment of phytochemicals, antioxidant, anti-lipid peroxidation and anti-hemolytic activity of extract and various fractions of Maytenus royleanus leaves

Shabbir, M., Khan, M. R., & Saeed, N. (2013) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-13-143 · Cited by 130

Accumulation of Reactive Oxygen Species and Oxidation of Cytokinin in Germinating Soybean Seeds

Gidrol, X., Lin, W. S., Degousée, N., Yip, S. F., & Kush, A. K. (1994) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1994.tb19990.x · Cited by 127

Inhibition of ultraviolet‐induced formation of reactive oxygen species, lipid peroxidation, erythema and skin photosensitization by Polypodium leucotomos

González, S., & Pathak, M. A. (1996) · Photodermatology Photoimmunology & Photomedicine · doi:10.1111/j.1600-0781.1996.tb00175.x · Cited by 127

Superoxide dismutase in some obligately anaerobic bacteria

Hewitt, J. A. (1975) · FEBS Letters · doi:10.1016/0014-5793(75)80518-7 · Cited by 127

Evidence for the Accumulation of Peroxidized Lipids in Membranes of Senescing Cotyledons

Pauls, K. P., & Thompson, J. E. (1984) · PLANT PHYSIOLOGY · doi:10.1104/pp.75.4.1152 · Cited by 127

Engineering a thermo-stable superoxide dismutase functional at sub-zero to >50°C, which also tolerates autoclaving

Kumar, A., Dutt, S., Bagler, G., Ahuja, P. S., & Kumar, S. (2012) · Scientific Reports · doi:10.1038/srep00387 · Cited by 126

Piperine ameliorates oxidative stress, inflammation and histological outcome in collagen induced arthritis

Umar, S., Sarwar, A. H. M. G., Umar, K., Ahmad, N., Sajad, M., Ahmad, S., Katiyar, C. K., & Khan, H. A. (2013) · Cellular Immunology · doi:10.1016/j.cellimm.2013.07.004 · Cited by 126

Silicon Improves Chilling Tolerance During Early Growth of Maize by Effects on Micronutrient Homeostasis and Hormonal Balances

Moradtalab, N., Weinmann, M., Walker, F., Höglinger, B., Ludewig, U., & Neumann, G. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00420 · Cited by 126

Comparative physiological and biochemical mechanisms of salt tolerance in five contrasting highland quinoa cultivars

Cai, Z.-Q., & Gao, Q. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-2279-8 · Cited by 126

Combined ability of salicylic acid and spermidine to mitigate the individual and interactive effects of drought and chromium stress in maize (Zea mays L.)

Naz, R., Sarfraz, A., Anwar, Z., Yasmin, H., Nosheen, A., Keyani, R., & Roberts, T. H. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.12.022 · Cited by 126

Long-term effects of biochar application on the growth and physiological characteristics of maize

Cong, M., Hu, Y., Sun, X., Yan, H., Yu, G., Tang, G., Xu, W., Chen, S., & Jia, H. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1172425 · Cited by 143

Inactivation and Degradation of CuZn-SOD by Active Oxygen Species in Wheat Chloroplasts Exposed to Photooxidative Stress

Casano, L. M., Gomez, L. D., Lascano, R., Gonzalez, C. A., & Trippi, V. S. (1997) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a029186 · Cited by 128

Investigations on the antioxidative defence responses to NaCl stress in a mangrove, Bruguiera parviflora: Differential regulations of isoforms of some antioxidative enzymes

Parida, A. K., Das, A. B., & Mohanty, P. (2004) · Plant Growth Regulation · doi:10.1023/b:grow.0000026508.63288.39 · Cited by 126

Reactive oxygen species‐mediated enzymatic systems involved in the oxidative action of 2,4‐dichlorophenoxyacetic acid*

Romero‐Puertas, M. C., McCarthy-Suárez, I., GÓMEZ, M., Sandalio, L. M., Corpas, F. J., del Río, L. A., & Palma, J. M. (2004) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2004.01219.x · Cited by 126

Preparation of lacquer polysaccharide sulfates and their antioxidant activity in vitro

Zou, C. W., Du, Y., Li, Y., Yang, J., Feng, T., Zhang, L., & Kennedy, J. F. (2007) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2007.11.035 · Cited by 126

Chloroplast superoxide and hydrogen peroxide scavenging systems from pea leaves: Seasonal variations

Gillham, D. J., & Dodge, A. D. (1987) · Plant Science · doi:10.1016/0168-9452(87)90145-2 · Cited by 124

Copper-Containing Oxidases and Superoxide Dismutase

Malmström, B. G., Andréasson, L., & Reinhammar, B. (1975) · The Enzymes · doi:10.1016/s1874-6047(08)60231-0 · Cited by 126

Antioxidative potentials as a protective mechanism in Catharanthus roseus (L.) G. Don. plants under salinity stress

Jaleel, C. A., Gopi, R., Manivannan, P., & Panneerselvam, R. (2007) · DergiPark (Istanbul University) · Cited by 125

Silicon alleviates nickel toxicity in cotton seedlings through enhancing growth, photosynthesis, and suppressing Ni uptake and oxidative stress

Khaliq, A., Ali, S., Hameed, A., Farooq, M. A., Farid, M., Shakoor, M. B., Mahmood, K., Ishaque, W., & Rizwan, M. (2015) · Archives of Agronomy and Soil Science · doi:10.1080/03650340.2015.1073263 · Cited by 126

Sex-related differences in morphological, physiological, and ultrastructural responses of Populus cathayana to chilling

Zhang, S., Jiang, H., Peng, S., Korpelainen, H., & Li, C. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq306 · Cited by 122

Effects of seawater acidification and salinity alterations on metabolic, osmoregulation and oxidative stress markers in Mytilus galloprovincialis

Freitas, R., Marchi, L. D., Bastos, M., Moreira, A., Velez, C., Chiesa, S., Wrona, F. J., Figueira, E. M. D. A. P., & Soares, A. M. V. M. (2017) · Ecological Indicators · doi:10.1016/j.ecolind.2017.04.003 · Cited by 126

Stress Responses of Aquatic Plants to Silver Nanoparticles

Yuan, L., Richardson, C. J., Ho, M., Willis, C. W., Colman, B. P., & Wiesner, M. R. (2018) · Environmental Science & Technology · doi:10.1021/acs.est.7b05837 · Cited by 125

Postharvest treatments with γ ‐aminobutyric acid, methyl jasmonate, or methyl salicylate enhance chilling tolerance of blood orange fruit at prolonged cold storage

Habibi, F., Ramezanian, A., Rahemi, M., Eshghi, S., Guillén, F., Serrano, M., & Valero, D. (2019) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.9920 · Cited by 124

Polystyrene microplastic interaction with Oryza sativa : toxicity and metabolic mechanism

Wu, J., Liu, W., Zeb, A., Lian, J., Sun, Y., & Sun, H. (2021) · Environmental Science Nano · doi:10.1039/d1en00636c · Cited by 125

Water Stress and Free Radical Mediated Changes in Sunflower Seedlings

Quartacci, M. F., & Navari‐Izzo, F. (1992) · Journal of Plant Physiology · doi:10.1016/s0176-1617(11)80381-0 · Cited by 125

Lead-induced increase in antioxidant enzymes and lipid peroxidation products in developing rat brain

Bokara, K. K., Brown, E. T., McCormick, R., Yallapragada, P. R., Rajanna, S., & Rajanna, B. (2007) · BioMetals · doi:10.1007/s10534-007-9088-5 · Cited by 125

BACE1 Cytoplasmic Domain Interacts with the Copper Chaperone for Superoxide Dismutase-1 and Binds Copper

Angeletti, B., Waldron, K. J., Freeman, K. B., Bawagan, H., Hussain, I., Miller, C. C. J., Lau, K., Tennant, M. E., Dennison, C., Robinson, N. J., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m412034200 · Cited by 126

Bacterial [Cu,Zn]-superoxide dismutase: phylogenetically distinct from the eukaryotic enzyme, and not so rare after all!

Kroll, J. S., Langford, P. R., Wilks, K. E., & Keil, A. D. (1995) · Microbiology · doi:10.1099/13500872-141-9-2271 · Cited by 125

The superoxide dismutase activity of iron complexes

Halliwell, B. B. (1975) · FEBS Letters · doi:10.1016/0014-5793(75)80105-0 · Cited by 125

Redox Regulation of cAMP-responsive Element-binding Protein and Induction of Manganous Superoxide Dismutase in Nerve Growth Factor-dependent Cell Survival

Bedogni, B., Pani, G., Colavitti, R., Riccio, A., Borrello, S., Murphy, M., Smith, R., Eboli, M. L., & Galeotti, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301089200 · Cited by 124

EFFECT OF FLUORIDE INTOXICATION ON LIPID PEROXIDATION AND ANTIOXIDANT SYSTEMS IN RATS

Shivarajashankara, Y., Shivashankara, A., & Bhat, K. M. R. (2001) · Cited by 124

Oxidative damage during chagasic cardiomyopathy development: role of mitochondrial oxidant release and inefficient antioxidant defense

Wen, J.-J., Vyatkina, G., & Garg, N. J. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.08.018 · Cited by 124

Arsenate and arsenite exposure modulate antioxidants and amino acids in contrasting arsenic accumulating rice (Oryza sativa L.) genotypes

Dave, R., Tripathi, R. D., Dwivedi, S., Tripathi, P., Awasthi, G., Sharma, Y. K., Trivedi, P. K., Corpas, F. J., Barroso, J. B., & Chakrabarty, D. (2012) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2012.06.049 · Cited by 124

Exogenous putrescine changes redox regulations and essential oil constituents in field-grown Thymus vulgaris L. under well-watered and drought stress conditions

Mohammadi, H., Ghorbanpour, M., & Brestič, M. (2018) · Industrial Crops and Products · doi:10.1016/j.indcrop.2018.05.064 · Cited by 126

Response of Microcystis to copper stress – Do phenotypes of Microcystis make a difference in stress tolerance?

Wu, Z., Gan, N., Huang, Q., & Song, L. (2006) · Environmental Pollution · doi:10.1016/j.envpol.2006.05.022 · Cited by 122

Antioxidant and hepatoprotective effects of punicalagin and punicalin on acetaminophen‐induced liver damage in rats

Lin, C., Hsu, Y., Lin, T., & Hsu, H. (2001) · Phytotherapy Research · doi:10.1002/ptr.816 · Cited by 124

Oxidative stress causes abnormal accumulation of familial amyotrophic lateral sclerosis-related mutant SOD1 in transgenic Caenorhabditis elegans

Oeda, T. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.19.2013 · Cited by 125

Phytotoxic effects of fluorides

Fornasiero, R. B. (2001) · Plant Science · doi:10.1016/s0168-9452(01)00499-x · Cited by 124

Chronic waterborne zinc and cadmium exposures induced different responses towards oxidative stress in the liver of zebrafish

Zheng, J., Yuan, S.-S., Wu, C., & Li, W.-Y. (2016) · Aquatic Toxicology · doi:10.1016/j.aquatox.2016.06.001 · Cited by 124

Hydroxyl radical-dependent inactivation of guanylate cyclase in cerebral arterioles by methylene blue and by LY83583.

Kontos, H. A., & Wei, E. P. (1993) · Stroke · doi:10.1161/01.str.24.3.427 · Cited by 124

The Physiology of Obligate Anaerobiosis

Morris, J. (1975) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/s0065-2911(08)60282-9 · Cited by 118

Effect of methyl parathion and chlorpyrifos on certain biomarkers in various tissues of guppy fish, Poecilia reticulata

Sharbidre, A. A., Metkari, V., & Patode, P. (2011) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2011.09.002 · Cited by 123

Oxidative stress and arsenic toxicity: Role of NADPH oxidases

Gupta, D. K., Inouhe, M., Rodríguez‐Serrano, M., Romero‐Puertas, M. C., & Sandalio, L. M. (2012) · Chemosphere · doi:10.1016/j.chemosphere.2012.10.066 · Cited by 123

The effect of brassinosteroids on radish (Raphanus sativus L.) seedlings growing under cadmium stress

Anuradha, S. M. J., & Rao, S. (2007) · Plant Soil and Environment · doi:10.17221/2307-pse · Cited by 123

Free radical formation and activity of antioxidant enzymes in lupin roots exposed to lead

Rucińska, R., Waplak, S., & Gwóźdź, E. A. (1999) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(99)80033-3 · Cited by 123

Detection of glutathione transferase activity on polyacrylamide gels

Ricci, G., Bello, M. L., Caccuri, A. M., Galiazzo, F., & Federici, G. (1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90657-2 · Cited by 123

Candida albicans Expresses an Unusual Cytoplasmic Manganese-containing Superoxide Dismutase (SOD3 Gene Product) upon the Entry and during the Stationary Phase

Lamarre, C., LeMay, J.-D., Deslauriers, N., & Bourbonnais, Y. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m108095200 · Cited by 123

Antioxidant defences of the apoplast

Vanacker, H., Harbinson, J., Ruijsch, J., Carver, T. L. W., & Foyer, C. H. (1998) · PROTOPLASMA · doi:10.1007/bf01279303 · Cited by 123

A cell-surface superoxide dismutase is a binding protein for peroxinectin, a cell-adhesive peroxidase in crayfish

Johansson, M. W., Holmblad, T., Thörnqvist, P., Cammarata, M., Parrinello, N., & Söderhäll, K. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.6.917 · Cited by 123

Aortic antioxidant defence mechanisms: time-related changes in cholesterol-fed rabbits

Boccio, G. D., Lapenna, D., Porreca, E., Pennelli, A., Savini, F., Feliciani, P., Ricci, G., & Cuccurullo, F. (1990) · Atherosclerosis · doi:10.1016/0021-9150(90)90019-f · Cited by 123

Characterization of superoxide dismutases in anoxia- and hyperoxia-tolerant symbiotic cnidarians

Richier, S., Merle, P.-L., Furla, P., Pigozzi, D., Sola, F., & Allemand, D. (2003) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(03)00049-7 · Cited by 122

Novel interrelationship between salicylic acid, abscisic acid, and PIP2-specific phospholipase C in heat acclimation-induced thermotolerance in pea leaves

Liu, H.-T. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl098 · Cited by 122

Exogenous application of humic acid mitigates salinity stress in maize ( Zea mays L.) plants by improving some key physico-biochemical attributes

Kaya, C., Akram, N. A., Ashraf, M., & Sönmez, O. (2018) · Cereal Research Communications · doi:10.1556/0806.45.2017.064 · Cited by 123

Novel insight into the inhibitory effects and mechanisms of Fe(II)-mediated multi-metabolism in anaerobic ammonium oxidation (anammox)

Jiang, Y., Chen, Y., Wang, Y., Chen, X., Zhou, X., Qing, K., Cao, W., & Zhang, Y. (2023) · Water Research · doi:10.1016/j.watres.2023.120291 · Cited by 120

Brassinosteroids alleviate chilling-induced oxidative damage by enhancing antioxidant defense system in suspension cultured cells of Chorispora bungeana

Liu, Y., Zhao, Z., Si, J., Di, C., Han, J., & An, L. (2009) · Plant Growth Regulation · doi:10.1007/s10725-009-9405-9 · Cited by 123

Effects of salt on lipid peroxidation and antioxidant enzyme activities of Catharanthus roseus suspension cells

Elkahoui, S., Hernández, J. A., Abdelly, C., Ghrir, R., & Limam, F. (2004) · Plant Science · doi:10.1016/j.plantsci.2004.09.006 · Cited by 122

Superoxide dismutase: “Positive” spectrophotometric assays

Misra, H. P., & Fridovich, I. (1977) · Analytical Biochemistry · doi:10.1016/0003-2697(77)90429-8 · Cited by 122

Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster

Tong, J. J., Schriner, S. E., McCleary, D. F., Day, B. J., & Wallace, D. C. (2007) · Nature Genetics · doi:10.1038/ng2004 · Cited by 122

A comparative study of water distribution, free radical production and activation of antioxidative metabolism in germinating pea seeds

Wojtyla, Ł., Garnczarska, M., Zalewski, T., Bednarski, W., Ratajczak, L., & Jurga, S. (2006) · Journal of Plant Physiology · doi:10.1016/j.jplph.2006.06.014 · Cited by 122

Antioxidant and anticancer activities of 8-hydroxypsoralen isolated from wampee [Clausena lansium (Lour.) Skeels] peel

Prasad, K. N., Xie, H., Hao, J. C., Yang, B. J., Qiu, S., Wei, X., Chen, F., & Jiang, Y. (2009) · Food Chemistry · doi:10.1016/j.foodchem.2009.04.073 · Cited by 122

Superoxide Dismutase Micro Assay in Biological Material

Bohnenkamp, W., & Weser, U. (1975) · Hoppe-Seyler´s Zeitschrift für physiologische Chemie · doi:10.1515/bchm2.1975.356.s1.747 · Cited by 22

A modified spectrophotometric assay of superoxide dismutase.

Kakkar, P., Das, B., & Viswanathan, P. N. (1984) · PubMed · Cited by 3,553

Spectrophotometric assay for superoxide dismutase based on the nitroblue tetrazolium reduction by glucose-glucose oxidase.

Nagi, M. N., Al‐Bekairi, A. M., & Al‐Sawaf, H. A. (1995) · PubMed · Cited by 13

A methodological approach to superoxide dismutase (SOD) activity assay based on inhibition of nitroblue tetrazolium (NBT) reduction

Durak, İ., Yurtarslanl, Z., Canbolat, O., & Akyol, Ö. (1993) · Clinica Chimica Acta · doi:10.1016/0009-8981(93)90307-p · Cited by 388

Radial Diffusion as a Simple and Rapid Method for Screening Superoxide Dismutase Activity

Hunaiti, A. A. (1987) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1177/000456328702400515 · Cited by 2