Environmentally induced oxidative stress in aquatic animals

Free radicals in biology and medicine

Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178

Free radicals and antioxidants in normal physiological functions and human disease

Valko, M., Leibfritz, D., Moncol, J., Cronin, M. T. D., Mazur, M., & Telser, J. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.07.001 · Cited by 14,269

Superoxide Dismutase

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

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

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

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor

Palmer, R. M. J., Ferrige, A. G., & Moncada, S. (1987) · Nature · doi:10.1038/327524a0 · Cited by 10,704

Aging: a theory based on free radical and radiation chemistry

Harman, D. (1956) · Journal of Gerontology · doi:10.1093/geronj/11.3.298 · Cited by 8,567

Metals, Toxicity and Oxidative Stress

Valko, M., Morris, H., & Cronin, M. (2005) · Current Medicinal Chemistry · doi:10.2174/0929867053764635 · Cited by 5,018

Free Radicals in Biology and Medicine

Land, E. J. (1990) · International Journal of Radiation Biology · doi:10.1080/09553009014552071 · Cited by 4,871

Malondialdehyde and thiobarbituric acid-reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury

Janero, D. R. (1990) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(90)90131-2 · Cited by 2,735

The Nrf2-antioxidant response element signaling pathway and its activation by oxidative stress

Nguyen, T., Nioi, P., & Pickett, C. B. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.r900010200 · Cited by 2,655

Purification and Characterization of Hypoxia-inducible Factor 1

Wang, G. L., & Semenza, G. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.3.1230 · Cited by 2,094

Free radical-mediated oxidation of free amino acids and amino acid residues in proteins

Stadtman, E. R., & Levine, R. L. (2003) · Amino Acids · doi:10.1007/s00726-003-0011-2 · Cited by 1,968

Contaminant-stimulated Reactive Oxygen Species Production and Oxidative Damage in Aquatic Organisms

Livingstone, D. R. (2001) · Marine Pollution Bulletin · doi:10.1016/s0025-326x(01)00060-1 · Cited by 1,856

Molecular biomarkers of oxidative stress in aquatic organisms in relation to toxic environmental pollutants

Valavanidis, A., Vlahogianni, T., Dassenakis, M., & Scoullos, M. (2006) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2005.03.013 · Cited by 1,795

Hypoxia-Inducible Factor-1 (HIF-1)

Ke, Q., & Costa, M. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.027029 · Cited by 1,689

Biochemistry and pathology of radical-mediated protein oxidation

Dean, R. T., Fu, S., Stocker, R., & Davies, M. J. (1997) · Biochemical Journal · doi:10.1042/bj3240001 · Cited by 1,678

Hydrogen peroxide sensing and signaling

Veal, E. A., Day, A. M., & Morgan, B. A. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.03.016 · Cited by 1,604

Endoplasmic Reticulum Stress and Oxidative Stress: A Vicious Cycle or a Double-Edged Sword?

Malhotra, J. D., & Kaufman, R. J. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1782 · Cited by 1,588

Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications

Foyer, C. H., & Noctor, G. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2177 · Cited by 1,468

Aging, energy, and oxidative stress in neurodegenerative diseases

Beal, M. F. (1995) · Annals of Neurology · doi:10.1002/ana.410380304 · Cited by 1,434

Prooxidant and antioxidant mechanisms in aquatic organisms

Winston, G. W., & Giulio, R. T. D. (1991) · Aquatic Toxicology · doi:10.1016/0166-445x(91)90033-6 · Cited by 1,355

Thiol chemistry and specificity in redox signaling

Winterbourn, C. C., & Hampton, M. B. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.05.004 · Cited by 1,226

Oxidative stress: molecular perception and transduction of signals triggering antioxidant gene defenses

Scandalios, J. G. (2005) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2005000700003 · Cited by 1,142

Molecular Mechanisms Activating the Nrf2-Keap1 Pathway of Antioxidant Gene Regulation

Kobayashi, M., & Yamamoto, M. P. (2005) · Antioxidants and Redox Signaling · doi:10.1089/ars.2005.7.385 · Cited by 1,087

Chemistry and biology of eukaryotic iron metabolism

Aisen, P. (2001) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(01)00063-2 · Cited by 804

Mercury, Fish Oils, and the Risk of Myocardial Infarction

Güallar, E., Sanz-Gallardo, M. I., Veer, P. V., Bode, P., Aro, A., Gómez-Aracena, J., Kark, J. D., Riemersma, R. A., Martin-Moreno, J. M., & Kok, F. J. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa020157 · Cited by 714

The Antioxidant Defense System Keap1-Nrf2 Comprises a Multiple Sensing Mechanism for Responding to a Wide Range of Chemical Compounds

Kobayashi, M., Li, L., Iwamoto, N., Nakajima‐Takagi, Y., Kaneko, H., Nakayama, Y., Eguchi, M., Wada, Y., Kumagai, Y., & Yamamoto, M. P. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01080-08 · Cited by 641

The cytochrome P-450 system in fish, aquatic toxicology and environmental monitoring

Goksøyr, A., & Förlin, L. (1992) · Aquatic Toxicology · doi:10.1016/0166-445x(92)90046-p · Cited by 624

Intake of mercury from fish, lipid peroxidation, and the risk of myocardial infarction and coronary, cardiovascular, and any death in eastern Finnish men

Salonen, J. T., Seppänen, K., Nyyssönen, K., Korpela, H., Kauhanen, J., Kantola, M., Tuomilehto, J., Esterbauer, H., Tatzber, F., & Salonen, R. (1995) · Circulation · doi:10.1161/01.cir.91.3.645 · Cited by 578

Aquatic toxicology. Part 2

Cairns, J. J., & Mount, D. I. (1990) · Environmental Science & Technology · doi:10.1021/es00072a001 · Cited by 550

Nrf2 signaling: An adaptive response pathway for protection against environmental toxic insults

Osburn, W. O., & Kensler, T. W. (2007) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2007.11.006 · Cited by 549

Quantification of lipid peroxidation in tissue extracts based on Fe(III)xylenol orange complex formation

Hermes‐Lima, M., Willmore, W. G., & Storey, K. B. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)00020-x · Cited by 523

Nutritive metal uptake in teleost fish

Bury, N. R., Walker, P., & Glover, C. N. (2002) · Journal of Experimental Biology · doi:10.1242/jeb.00068 · Cited by 522

Glutathione metabolism and its role in hepatotoxicity

DeLeve, L. D., & Kaplowitz, N. (1991) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(91)90029-l · Cited by 495

Ecotoxicological applications and significance of the comet assay

Jha, A. N. (2008) · Mutagenesis · doi:10.1093/mutage/gen014 · Cited by 479

Oxidative stress biomarkers of exposure to deltamethrin in freshwater fish, Channa punctatus Bloch

Sayeed, I., Parvez, S., Pandey, S., Bin-Hafeez, B., Haque, R., & Raisuddin, S. (2003) · Ecotoxicology and Environmental Safety · doi:10.1016/s0147-6513(03)00009-5 · Cited by 474

Reactive oxygen species, mitochondria, apoptosis and aging

Papa, S., & Skulachev, V. P. (1997) · Springer eBooks · doi:10.1007/978-1-4615-6111-8_47 · Cited by 467

Glucose and reactive oxygen species

Bonnefont‐Rousselot, D. (2002) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/00075197-200209000-00016 · Cited by 455

Oxidative stress in toxicology: established mammalian and emerging piscine model systems.

Kelly, K. A., Havrilla, C. M., Brady, T. C., Abramo, K. H., & Levin, E. (1998) · Environmental Health Perspectives · doi:10.1289/ehp.98106375 · Cited by 450

Antioxidant enzyme activities and lipid peroxidation in the freshwater cladoceran Daphnia magna exposed to redox cycling compounds

Barata, C., Varó, I., Navarro, J. C., Arun, S., & Porte, C. (2005) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2005.01.013 · Cited by 418

A method to measure total antioxidant capacity against peroxyl radicals in aquatic organisms: Application to evaluate microcystins toxicity

Amado, L. L., Garcia, M. L., Ramos, P. B., Freitas, R. F., Zafalon, B., Ferreira, J. L. R., Yunes, J. S., & Monserrat, J. M. (2008) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2008.11.038 · Cited by 415

Hypoxia-induced reactive oxygen species formation in skeletal muscle

Clanton, T. L. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01298.2006 · Cited by 401

Hydrogen peroxide is the major oxidant product of xanthine oxidase

Kelley, E. E., Khoo, N. K. H., Hundley, N. J., Malik, U. Z., Freeman, B. Α., & Tarpey, M. M. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.11.012 · Cited by 399

MAPK Signaling Regulates Nitric Oxide and NADPH Oxidase-Dependent Oxidative Bursts inNicotiana benthamiana

Asai, S., Ohta, K., & Yoshioka, H. (2008) · The Plant Cell · doi:10.1105/tpc.107.055855 · Cited by 390

Oxidative stress and antioxidant defenses in goldfishCarassius auratusduring anoxia and reoxygenation

Lushchak, V. I., Lp, L., Mota, A. A., & Hermes‐Lima, M. (2001) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2001.280.1.r100 · Cited by 390

Reactive oxygen species, mitochondria, apoptosis and aging

Papa, S., & Скулачев, В. П. (1997) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006873518427 · Cited by 389

Intracellular Copper Does Not Catalyze the Formation of Oxidative DNA Damage in Escherichia coli

Macomber, L., Rensing, C., & Imlay, J. A. (2007) · Journal of Bacteriology · doi:10.1128/jb.01357-06 · Cited by 356

The role of thiols, dithiols, nutritional factors and interacting ligands in the toxicology of mercury

Rooney, J. P. K. (2007) · Toxicology · doi:10.1016/j.tox.2007.02.016 · Cited by 348

Antioxidant defenses and metabolic depression. The hypothesis of preparation for oxidative stress in land snails

Hermes‐Lima, M., Storey, J. M., & Storey, K. B. (1998) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/s0305-0491(98)10053-6 · Cited by 348

Identification of the interactive interface and phylogenic conservation of the Nrf2‐Keap1 system

Kobayashi, M., Itoh, K., Suzuki, T., Osanai, H., Nishikawa, K., Katoh, Y., Takagi, Y., & Yamamoto, M. P. (2002) · Genes to Cells · doi:10.1046/j.1365-2443.2002.00561.x · Cited by 340

Chronic dietary mercury exposure causes oxidative stress, brain lesions, and altered behaviour in Atlantic salmon (Salmo salar) parr

Berntssen, M. H. G., Aatland, A., & Handy, R. D. (2003) · Aquatic Toxicology · doi:10.1016/s0166-445x(03)00104-8 · Cited by 328

Hypoxia and recovery perturb free radical processes and antioxidant potential in common carp (Cyprinus carpio) tissues

Lushchak, V. I., Bagnyukova, T., Lushchak, O. V., Storey, J. M., & Storey, K. B. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.01.006 · Cited by 321

Effects of human pharmaceuticals on cytotoxicity, EROD activity and ROS production in fish hepatocytes

Laville, N., Aı̈t-Aı̈ssa, S., Góméz, E., Casellas, C., & Porcher, J. (2003) · Toxicology · doi:10.1016/j.tox.2003.11.002 · Cited by 313

Determination of Carbonyl Groups in Oxidized Proteins

Levine, R. L., Wehr, N. B., Williams, J. A., Stadtman, E. R., & Shacter, E. B. (2003) · Humana Press eBooks · doi:10.1385/1-59259-054-3:15 · Cited by 310

Sensitivity of zebrafish to environmental toxins implicated in Parkinson's disease

Bretaud, S., Lee, S., & Guo, S. (2004) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2004.06.014 · Cited by 306

Oxygen-dependent gene expression in fishes

Nikinmaa, M., & Rees, B. B. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00626.2004 · Cited by 300

Oxygen Sensors at the Crossroad of Metabolism

Aragonés, J., Fraisl, P., Baes, M. I., & Carmeliet, P. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2008.10.001 · Cited by 293

Hyperoxia results in transient oxidative stress and an adaptive response by antioxidant enzymes in goldfish tissues

Lushchak, V. I., Bagnyukova, T., Hušák, V., Luzhna, L. I., Lushchak, O. V., & Storey, K. B. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.02.024 · Cited by 292

Oxidants and antioxidants in aquatic animals

Winston, G. W. (1991) · Comparative Biochemistry and Physiology Part C Comparative Pharmacology · doi:10.1016/0742-8413(91)90148-m · Cited by 285

Effects of different environmental oxygen levels on free radical processes in fish

Lushchak, V. I., & Bagnyukova, T. (2006) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2006.02.014 · Cited by 283

Two divergently transcribed genes, soxR and soxS, control a superoxide response regulon of Escherichia coli

Wu, J., & Weiss, B. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.9.2864-2871.1991 · Cited by 279

Cellular iron metabolism

Ponka, P. (1999) · Kidney International · doi:10.1046/j.1523-1755.1999.055suppl.69002.x · Cited by 278

Acute effects of glyphosate herbicide on metabolic and enzymatic parameters of silver catfish (Rhamdia quelen)

Glusczak, L., Miron, D. D. S., Moraes, B. S., Simões, R. R., Schetinger, M. R. C., Morsch, V. M., & Loro, V. L. (2007) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2007.06.004 · Cited by 273

Genotoxic effects of Roundup® on the fish Prochilodus lineatus

Cavalcante, D. G. S. M., Martinez, C. B. D. R., & Sofia, S. H. (2008) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2008.06.010 · Cited by 260

Oxidative stress response and gene expression with acute copper exposure in zebrafish (Danio rerio)

Craig, P. M., Wood, C. M., & McClelland, G. B. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00383.2007 · Cited by 260

Effect of glyphosate herbicide on acetylcholinesterase activity and metabolic and hematological parameters in piava (Leporinus obtusidens)

Glusczak, L., Miron, D. D. S., Crestani, M., da Fonseca, M. B., Pedron, F. D. A., Duarte, M. F., & Loro, V. L. (2005) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2005.07.017 · Cited by 258

Low toxic herbicide Roundup induces mild oxidative stress in goldfish tissues

Lushchak, O. V., Kubrak, O. I., Storey, J. M., Storey, K. B., & Lushchak, V. I. (2009) · Chemosphere · doi:10.1016/j.chemosphere.2009.04.045 · Cited by 245

mRNA expression of antioxidant enzymes (SOD, CAT and GSH-Px) and lipid peroxidative stress in liver of Atlantic salmon (Salmo salar) exposed to hyperoxic water during smoltification

Olsvik, P. A., Kristensen, T., Waagbø, R., Rosseland, B. O., Tollefsen, K. E., Bæverfjord, G., & Berntssen, M. H. G. (2005) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2005.07.009 · Cited by 244

Extracellular Redox State: Refining the Definition of Oxidative Stress in Aging

Jones, D. P. (2006) · Rejuvenation Research · doi:10.1089/rej.2006.9.169 · Cited by 243

Inorganic mercury exposure: toxicological effects, oxidative stress biomarkers and bioaccumulation in the tropical freshwater fish matrinxã, Brycon amazonicus (Spix and Agassiz, 1829)

Monteiro, D. A., Rantin, F. T., & Kalinin, A. L. (2009) · Ecotoxicology · doi:10.1007/s10646-009-0395-1 · Cited by 242

Biochemical markers of oxidative stress in Perna viridis exposed to mercury and temperature

VERLECAR, X. N., Jena, K., & Chainy, G. B. N. (2007) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2007.01.018 · Cited by 238

Role of metallothionein against oxidative stress in the musselMytilus galloprovincialis

Viarengo, A., Burlando, B., Cavaletto, M., Marchi, B., Ponzano, E., & Blasco, J. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.277.6.r1612 · Cited by 236

Antioxidative stress proteins and their gene expression in brown trout (Salmo trutta) from three rivers with different heavy metal levels

Hansen, B. H., Rømma, S., Garmo, Ø. A., Olsvik, P. A., & Andersen, R. A. (2006) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2006.02.010 · Cited by 228

Physiological changes of sturgeon Acipenser naccarii caused by increasing environmental salinity

Martínez-Álvarez, R., Hidalgo, M. C., Domezain, A., Morales, A. E., García-Gallego, M., & Sanz, A. (2002) · Journal of Experimental Biology · doi:10.1242/jeb.205.23.3699 · Cited by 224

Fish antioxidant defenses--a comparative approach.

Filho, D. W. (1996) · PubMed · Cited by 213

In vivo experiments for the evaluation of genotoxic and cytotoxic effects of Triclosan in Zebra mussel hemocytes

Binelli, A., Cogni, D., Parolini, M., Riva, G., & Provini, A. (2008) · Aquatic Toxicology · doi:10.1016/j.aquatox.2008.11.008 · Cited by 208

Effects of dietary vitamin E supplementation on antioxidant enzyme activities in Litopenaeus vannamei (Boone, 1931) exposed to acute salinity changes

Liu, Y., Wang, W.-N., Wang, A., Wang, J., & Sun, R. (2007) · Aquaculture · doi:10.1016/j.aquaculture.2007.02.010 · Cited by 204

Coordinated response of goldfish antioxidant defenses to environmental stress

Bagnyukova, T., Chahrak, O. I., & Lushchak, V. I. (2006) · Aquatic Toxicology · doi:10.1016/j.aquatox.2006.04.005 · Cited by 204

Oxidative stress during stressful heat exposure and recovery in the North Sea eelpoutZoarces viviparusL.

Heise, K., Puntarulo, S., Nikinmaa, M., Abele, D., & Pörtner, H. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.01977 · Cited by 203

Environmental and occupational biomonitoring using the Comet assay

Valverde, M., & Rojas, E. (2008) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2008.11.001 · Cited by 201

Effects of redox cycling compounds on glutathione content and activity of glutathione-related enzymes in rainbow trout liver

Stephensen, E., Sturve, J., & Förlin, L. (2002) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/s1532-0456(02)00129-1 · Cited by 193

Copper-induced oxidative stress in rainbow trout gill cells

Bopp, S. K., Abicht, H. K., & Knauer, K. (2007) · Aquatic Toxicology · doi:10.1016/j.aquatox.2007.10.014 · Cited by 192

Characterization of a Hypoxia-inducible Factor (HIF-1α) from Rainbow Trout

Soitamo, A. J., Råbergh, C. M. I., Gassmann, M., Sistonen, L., & Nikinmaa, M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m009057200 · Cited by 186

Oxygen Radical Production in the Sea Anemone Anthopleura Elegantissima and Its Endosymbiotic Algae

Dykens, J. A., Shick, J. M., Benoit, C., Buettner, G. R., & Winston, G. W. (1992) · Journal of Experimental Biology · doi:10.1242/jeb.168.1.219 · Cited by 186

Organophosphate Effects on Antioxidant System of Carp (Cyprinus carpio) and Catfish (Ictalurus nebulosus)

Hai, D. Q., Varga, S. I., & Matkovics, B. (1997) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/s0742-8413(96)00234-4 · Cited by 185

The effect of chronic chromium exposure on the health of Chinook salmon (Oncorhynchus tshawytscha)

Farag, A. M., May, T. W., Marty, G. D., Easton, M. D. L., Harper, D. D., Little, E. E., & Cleveland, L. (2005) · Aquatic Toxicology · doi:10.1016/j.aquatox.2005.09.011 · Cited by 179

The effects of temperature reduction on gene expression and oxidative stress in skeletal muscle from adult zebrafish

Malek, R. L., Sajadi, H., Abraham, J., Grundy, M. A., & Gerhard, G. S. (2004) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2004.08.014 · Cited by 172

Oxidative stress and genotoxic effects in gill and kidney of Anguilla anguilla L. exposed to chromium with or without pre-exposure to β-naphthoflavone

Ahmad, I., Maria, V. L., Oliveira, M., Pacheco, M., & Santos, M. A. D. J. C. (2006) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2006.04.020 · Cited by 171

Hypoxia induces oxidative stress in tissues of a goby, the rotan Perccottus glenii

Lushchak, V. I., & Bagnyukova, T. (2007) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2007.07.007 · Cited by 170

Temperature regulates hypoxia-inducible factor-1 (HIF-1) in a poikilothermic vertebrate, crucian carp (Carassius carassius)

Rissanen, E., Tranberg, H. K., Sollid, J., Nilsson, G., & Nikinmaa, M. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02103 · Cited by 169

Understanding Hypoxia-Induced Gene Expression in Early Development: In Vitro and In Vivo Analysis of Hypoxia-Inducible Factor 1-Regulated Zebra Fish Insulin-Like Growth Factor Binding Protein 1 Gene Expression

Kajimura, S., Aida, K., & Duan, C. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.3.1142-1155.2006 · Cited by 167

Oxidative stress in fish exposed to model xenobiotics. Oxidatively modified forms of Cu,Zn-superoxide dismutase as potential biomarkers

Pedrajas, J. R., Peinado, J., & López‐Barea, J. (1995) · Chemico-Biological Interactions · doi:10.1016/0009-2797(95)03651-2 · Cited by 164

Free radicals in biology and medicine, second edition

Halliwell, B. B., & Gutteridge, J. M. C. (1991) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(91)90055-8 · Cited by 160

Role of glutathione redox cycle and catalase in defense against oxidative stress induced by endosulfan in adrenocortical cells of rainbow trout (Oncorhynchus mykiss)

Dorval, J. (2003) · Toxicology and Applied Pharmacology · doi:10.1016/s0041-008x(03)00281-3 · Cited by 149

Molecular characterization and mRNA expression of glutathione peroxidase and glutathione S-transferase during osmotic stress in olive flounder (Paralichthys olivaceus)

Choi, C. Y., An, K. W., & An, M. I. (2008) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2008.01.013 · Cited by 143

NF-κB, Nrf2, and HO-1 Interplay in Redox-Regulated VCAM-1 Expression

Banning, A., & Brigelius‐Flohé, R. (2005) · Antioxidants and Redox Signaling · doi:10.1089/ars.2005.7.889 · Cited by 141

Molecular cloning, characterization and expression of two hypoxia-inducible factor alpha subunits, HIF-1α and HIF-2α, in a hypoxia-tolerant marine teleost, Atlantic croaker (Micropogonias undulatus)

Rahman, M. S., & Thomas, P. (2007) · Gene · doi:10.1016/j.gene.2007.03.009 · Cited by 140

Evidence for a fenton-type mechanism for the generation of .OH radicals in the reduction of Cr(VI) in cellular media

Shi, X., & Dalal, N. S. (1990) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(90)90417-w · Cited by 139

Relationship between oxidative stress and HIF-1α mRNA during sustained hypoxia in humans

Pialoux, V., Mounier, R., Brown, A. D., Steinback, C. D., Rawling, J. M., & Poulin, M. J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.10.047 · Cited by 137

Activation of the Mouse Heme Oxygenase-1 Gene by 15-Deoxy-Δ 12,14 -Prostaglandin J 2 Is Mediated by the Stress Response Elements and Transcription Factor Nrf2

Gong, P., Stewart, D., Hu, B., Li, N., Cook, J. L., Nel, A. E., & Alam, J. (2002) · Antioxidants and Redox Signaling · doi:10.1089/152308602753666307 · Cited by 137

Gene expression patterns in rainbow trout, Oncorhynchus mykiss, exposed to a suite of model toxicants

Hook, S. E., Skillman, A. D., Small, J. A., & Schultz, I. R. (2006) · Aquatic Toxicology · doi:10.1016/j.aquatox.2006.01.007 · Cited by 137

Induction and activity of oxidative stress-related proteins during waterborne Cu-exposure in brown trout (Salmo trutta)

Hansen, B. H., Rømma, S., Søfteland, L., Olsvik, P. A., & Andersen, R. A. (2006) · Chemosphere · doi:10.1016/j.chemosphere.2006.04.088 · Cited by 134

Free radical oxidation of proteins and its relationship with functional state of organisms

Lushchak, V. I. (2007) · Biochemistry (Moscow) · doi:10.1134/s0006297907080020 · Cited by 133

Effects of hexachlorobenzene on antioxidant status of liver and brain of common carp (Cyprinus carpio)

Song, S. B., Xu, Y., & Zhou, B. S. (2006) · Chemosphere · doi:10.1016/j.chemosphere.2006.01.033 · Cited by 132

Aspects of the biological redox chemistry of cysteine: from simple redox responses to sophisticated signalling pathways

Jacob, C., Knight, I., & Winyard, P. G. (2006) · Biological Chemistry · doi:10.1515/bc.2006.174 · Cited by 128

The effects of selenium on oxidative stress biomarkers in the freshwater characid fish matrinxã, Brycon cephalus () exposed to organophosphate insecticide Folisuper 600 BR® (methyl parathion)

Monteiro, D. A., Rantin, F. T., & Kalinin, A. L. (2008) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2008.06.012 · Cited by 127

Pro-oxidant processes and antioxidant defence systems in the tissues of the Antarctic scallop (Adamussium colbecki) compared with the Mediterranean scallop (Pecten jacobaeus)

Viarengo, A., Canesi, L., Martinez, P. G., Peters, L. D., & Livingstone, D. R. (1995) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/0305-0491(94)00228-m · Cited by 125

Oxidized proteins: Mechanisms of removal and consequences of accumulation

Dunlop, R. A., Brunk, U. T., & Rodgers, K. J. (2009) · IUBMB Life · doi:10.1002/iub.189 · Cited by 124

Effects of short-term copper exposure on gill structure, metallothionein and hypoxia-inducible factor-1α (HIF-1α) levels in rainbow trout (Oncorhynchus mykiss)

Vosloo, D., Vosloo, A., & Nikinmaa, M. (2004) · Aquatic Toxicology · doi:10.1016/j.aquatox.2004.06.002 · Cited by 120

Hypoxia-induced Synthesis of Hemoglobin in the Crustacean Daphnia magna Is Hypoxia-inducible Factor-dependent

Gorr, T. A., Cahn, J. D., Yamagata, H., & Bunn, H. F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403981200 · Cited by 120

Transcriptional analysis of antioxidant and immune defense genes in disk abalone (Haliotis discus discus) during thermal, low-salinity and hypoxic stress

Zoysa, M. D., Whang, I., Lee, Y., Lee, S., Lee, J., & Lee, J. (2009) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2009.08.002 · Cited by 118

The bioaccumulation of nonyphenol and its adverse effect on the liver of rainbow trout (Onchorynchus mykiss)

Uğuz, C., İşcan, M., Ergüven, A., Işgör, B. S., & Togan, İ. (2003) · Environmental Research · doi:10.1016/s0013-9351(03)00033-1 · Cited by 118

Waterborne vs. dietary copper uptake in rainbow trout and the effects of previous waterborne copper exposure

Kamunde, C., Clayton, C., & Wood, C. M. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00016.2002 · Cited by 117

p23, a simple protein with complex activities

Felts, S. J., & Toft, D. O. (2003) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2003)008 · Cited by 116

Seasonal variations of exposure biomarkers, oxidative stress responses and cell damage in the clams, Tapes philippinarum, and mussels, Mytilus galloprovincialis, from Adriatic sea

Bocchetti, R., Lamberti, C. V., Pisanelli, B., Razzetti, E. M., Maggi, C., Catalano, B., Sesta, G., Martuccio, G., Gabellini, M., & Regoli, F. (2008) · Marine Environmental Research · doi:10.1016/j.marenvres.2008.02.013 · Cited by 116

Effects of North Sea oil and alkylphenols on biomarker responses in juvenile Atlantic cod (Gadus morhua)

Sturve, J., Hasselberg, L., Fälth, H., Celander, M., & Förlin, L. (2006) · Aquatic Toxicology · doi:10.1016/j.aquatox.2006.02.019 · Cited by 113

Physiological modulation of iron metabolism in rainbow trout(Oncorhynchus mykiss) fed low and high iron diets

Carriquiriborde, P., Handy, R. D., & Davies, S. J. (2003) · Journal of Experimental Biology · doi:10.1242/jeb.00712 · Cited by 112

Molecular Evolution of Keap1

Li, L., Kobayashi, M., Kaneko, H., Nakajima‐Takagi, Y., Nakayama, Y., & Yamamoto, M. P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m708702200 · Cited by 111

Anticarcinogenesis by dietary phytochemicals: Cytoprotection by Nrf2 in normal cells and cytotoxicity by modulation of transcription factors NF-κB and AP-1 in abnormal cancer cells

Gopalakrishnan, A., & Kong, A. T. (2007) · Food and Chemical Toxicology · doi:10.1016/j.fct.2007.09.082 · Cited by 110

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Lushchak, O. V., Kubrak, O. I., Lozinsky, O. V., Storey, J. M., Storey, K. B., & Lushchak, V. I. (2009) · Aquatic Toxicology · doi:10.1016/j.aquatox.2009.03.007 · Cited by 109

Glutathione-dependent resistance of the European eel Anguilla anguilla to the herbicide molinate

Peña‐Llopis, S., Peña, J. B., Sancho, E., Fernández-Vega, C., & Ferrando, M. D. (2001) · Chemosphere · doi:10.1016/s0045-6535(00)00500-2 · Cited by 108

Catalase inhibition by amino triazole induces oxidative stress in goldfish brain

Bagnyukova, T., Vasylkiv, O. Y., Storey, K. B., & Lushchak, V. I. (2005) · Brain Research · doi:10.1016/j.brainres.2005.06.002 · Cited by 107

Induction of oxidative stress in Rana ridibunda during recovery from winter hibernation

Bagnyukova, T., Storey, K. B., & Lushchak, V. I. (2002) · Journal of Thermal Biology · doi:10.1016/s0306-4565(02)00031-1 · Cited by 107

Oxidative stress and antioxidant defenses in goldfish liver in response to short‐term exposure to arsenite

Bagnyukova, T., Luzhna, L., Pogribny, I. P., & Lushchak, V. I. (2007) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20328 · Cited by 106

Dietary copper exposure in the African walking catfish, Clarias gariepinus: Transient osmoregulatory disturbances and oxidative stress

Hoyle, I., Shaw, B. J., & Handy, R. D. (2007) · Aquatic Toxicology · doi:10.1016/j.aquatox.2007.03.014 · Cited by 106

Ethylene Sensing and Gene Activation in Botrytis cinerea: A Missing Link in Ethylene Regulation of Fungus-Plant Interactions?

Chagué, V., Danit, L.-V., Siewers, V., Gronover, C. S., Tudzynski, P., Tudzynski, B., & Sharon, A. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-0033 · Cited by 106

Cardio-respiratory function and oxidative stress biomarkers in Nile tilapia exposed to the organophosphate insecticide trichlorfon (NEGUVON®)

Thomaz, J. M., Martins, N. D., Monteiro, D. A., Rantin, F. T., & Kalinin, A. L. (2009) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2008.11.003 · Cited by 105

Oxygen radical generation by microsomes: Role of iron and implications for alcohol metabolism and toxicity

Cederaum, A. I. (1989) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(89)90033-6 · Cited by 104

Molecular characterization of hypoxia inducible factor-1 (HIF-1) from the white shrimp Litopenaeus vannamei and tissue-specific expression under hypoxia

Soñanez‐Organis, J. G., Peregrino-Uriarte, A. B., Gómez‐Jiménez, S., López-Zavala, A. A., Forman, H. J., & Yepiz-Plascencia, G. M. (2009) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2009.06.005 · Cited by 103

Comparison of the cytotoxicity induced by different exposure to sodium arsenite in two fish cell lines

Wang, Y.-C., Chaung, R.-H., & Tung, L. (2004) · Aquatic Toxicology · doi:10.1016/j.aquatox.2004.04.007 · Cited by 102

Pi class glutathione S-transferase genes are regulated by Nrf 2 through an evolutionarily conserved regulatory element in zebrafish

Suzuki, T., Takagi, Y., Osanai, H., Li, L., TAKEUCHI, M., Katoh, Y., Kobayashi, M., & Yamamoto, M. P. (2005) · Biochemical Journal · doi:10.1042/bj20041860 · Cited by 100

A model of O·2 -generation in the complex III of the electron transport chain

Demin, O. V., Kholodenko, B. Ν., & Skulachev, V. P. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5653-4_3 · Cited by 98

Chromium effects on free radical processes in goldfish tissues: Comparison of Cr(III) and Cr(VI) exposures on oxidative stress markers, glutathione status and antioxidant enzymes

Kubrak, O. I., Lushchak, O. V., Lushchak, J. V., Torous, I. M., Storey, J. M., Storey, K. B., & Lushchak, V. I. (2010) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2010.06.003 · Cited by 98

The effect of potassium dichromate on free radical processes in goldfish: Possible protective role of glutathione

Lushchak, O. V., Kubrak, O. I., Nykorak, M. Z., Storey, K. B., & Lushchak, V. I. (2008) · Aquatic Toxicology · doi:10.1016/j.aquatox.2008.01.007 · Cited by 96

A model of O·2 - generation in the complex III of the electron transport chain

Demin, O. V., Kholodenko, B. Ν., & Скулачев, В. П. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006849920918 · Cited by 94

Effects of alkylphenols on CYP1A and CYP3A expression in first spawning Atlantic cod (Gadus morhua)

Hasselberg, L., Meier, S., Svardal, A. M., Hegelund, T., & Celander, M. (2004) · Aquatic Toxicology · doi:10.1016/j.aquatox.2003.12.007 · Cited by 93

Cloning of hif-1α and hif-2α and mRNA expression pattern during development in zebrafish

Rojas, D., Perez-Munizaga, D. A., Centanin, L., Antonelli, M., Wappner, P., Allende, M. L., & Reyes, A. E. (2006) · Gene Expression Patterns · doi:10.1016/j.modgep.2006.08.002 · Cited by 93

Effects of seasonal and latitudinal cold on oxidative stress parameters and activation of hypoxia inducible factor (HIF-1) in zoarcid fish

Heise, K., Estevez, M. S., Puntarulo, S., Galleano, M., Nikinmaa, M., Pörtner, H., & Abele, D. (2007) · Journal of Comparative Physiology B · doi:10.1007/s00360-007-0173-4 · Cited by 93

Ingestion of sub-lethal levels of iron sulphate by African catfish affects growth and tissue lipid peroxidation

Baker, R. T. M., Martin, P., & Davies, S. J. (1997) · Aquatic Toxicology · doi:10.1016/s0166-445x(97)00047-7 · Cited by 92

Seasonal variation of antioxidant and biotransformation enzymes in barnacle, Balanus balanoides, and their relation with polyaromatic hydrocarbons

Niyogi, S., Biswas, S., Sarker, S., & Datta, A. G. (2001) · Marine Environmental Research · doi:10.1016/s0141-1136(00)00257-9 · Cited by 91

Hydroxyl radical generation and oxidative stress in Carassius auratus liver, exposed to pyrene

Sun, Y., Yin, Y., Zhang, J., Yu, H., Wang, X., Wu, J., & Xue, Y. (2008) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2007.12.016 · Cited by 90

Redox Control of the DNA Damage-inducible Protein DinG Helicase Activity via Its Iron-Sulfur Cluster

Ren, B., Duan, X., & Ding, H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m807943200 · Cited by 87

Stimulation of oxyradical production of hepatic microsomes of flounder (Platichthys flesus) and perch (Perca fluviatilis) by model and pollutant xenobiotics

Lemaire, P., Matthews, A., F�rlin, L., & Livingstone, D. R. (1994) · Archives of Environmental Contamination and Toxicology · doi:10.1007/bf00224804 · Cited by 86

Hypoxia enhances CXCR4 expression favoring microglia migration via HIF-1α activation

Wang, X., Li, C., Chen, Y., Hao, Y., Zhou, W., Chen, C., & Yu, Z. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.04.055 · Cited by 86

Reactive oxygen species as mediators of tissue protection and injury.

Bauer, V., & Bauer, F. (1999) · PubMed · Cited by 86

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Vasylkiv, O. Y., Kubrak, O. I., Storey, K. B., & Lushchak, V. I. (2010) · Chemosphere · doi:10.1016/j.chemosphere.2010.05.023 · Cited by 84

Adaptive response of antioxidant enzymes to catalase inhibition by aminotriazole in goldfish liver and kidney

Bagnyukova, T., Storey, K. B., & Lushchak, V. I. (2005) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2005.08.003 · Cited by 82

Lipid peroxidation and ascorbic acid status in respiratory organs of male and female freshwater catfish Heteropneustes fossilis exposed to temperature increase

Parihar, M. S., & Dubey, A. K. (1995) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/0742-8413(95)02025-x · Cited by 81

Chronic dietary exposure to copper affects growth, tissue lipid peroxidation, and metal composition of the grey mullet, Chelon labrosus

Baker, R. T. M., Handy, R. D., Davies, S. J., & Snook, J. C. (1998) · Marine Environmental Research · doi:10.1016/s0141-1136(98)00098-1 · Cited by 80

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Brouwer, M. H., & Brouwer, T. H. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0568 · Cited by 78

Oxidative stress and HIF-1 DNA binding during stressful cold exposure and recovery in the North Sea eelpout (Zoarces viviparus)

Heise, K., Puntarulo, S., Nikinmaa, M., Lucassen, M., Pörtner, H., & Abele, D. (2006) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2006.01.014 · Cited by 78

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Widmer, R., Ziaja, I., & Grune, T. (2006) · Free Radical Research · doi:10.1080/10715760600911154 · Cited by 76

Effects of alkylphenols on redox status in first spawning Atlantic cod (Gadus morhua)

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Sollid, J., Rissanen, E., Tranberg, H. K., Thorstensen, T., Vuori, K. A. M., Nikinmaa, M., & Nilsson, G. (2005) · Journal of Comparative Physiology B · doi:10.1007/s00360-005-0059-2 · Cited by 71

Influence of temperature, pH, oxygenation, water-type and substrate on biomarker responses in the freshwater clam Corbicula fluminea (Müller)

Vidal, M.-L., Bassères, A., & Narbonne, J. (2002) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/s1532-0456(02)00051-0 · Cited by 70

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Neto, F. F., Zanata, S. M., de Assis, H. C. S., Nakao, L. S., Randi, M. A. F., & Ribeiro, C. A. D. O. (2008) · Toxicology in Vitro · doi:10.1016/j.tiv.2008.07.006 · Cited by 69

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Ruiz, M.-J., & George, S. (2004) · Marine Environmental Research · doi:10.1016/j.marenvres.2004.03.054 · Cited by 67

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Li, T., & Brouwer, M. H. (2007) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2006.12.018 · Cited by 66

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Falfushynska, H., & Stoliar, O. B. (2008) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2008.04.006 · Cited by 66

Effects of copper and its ethylenediaminetetraacetate complex on the antioxidant defenses of the goldfish, Carassius auratus

Liu, H., Wang, W., Zhang, J., & Wang, X. (2005) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2005.09.002 · Cited by 64

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Teixeira, M. C., Telo, J. P., Duarte, N. F., & Sá‐Correia, I. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.09.158 · Cited by 63

Effect of arsenite, arsenate, and the herbicide monosodium methyl arsonate (MSMA) on hepatic metallothionein expression and lipid peroxidation in channel catfish

Schlenk, D., Wolford, L., Chelius, M. K., Steevens, J. A., & Chan, K. M. (1997) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/s0742-8413(97)00083-2 · Cited by 63

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Parvez, S., & Raisuddin, S. (2006) · Archives of Environmental Contamination and Toxicology · doi:10.1007/s00244-005-5083-4 · Cited by 63

Carbonylation of mitochondrial proteins in Drosophila melanogaster during aging

Toroser, D., Orr, W. C., & Sohal, R. S. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.08.193 · Cited by 60

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Coen, W. M. D., & Janssen, C. R. (2003) · Environmental Toxicology and Chemistry · doi:10.1897/02-223 · Cited by 59

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Poljšak, B., Gazdag, Z., Jenko-Brinovec, Š., Fujs, Š., Pesti, M., Belágyi, J., Plesničar, S., & Raspor, P. (2005) · Journal of Applied Toxicology · doi:10.1002/jat.1093 · Cited by 58

Detection of oxidative DNA damage in isolated marine bivalve hemocytes using the comet assay and formamidopyrimidine glycosylase (Fpg)

Gielazyn, M. L., Ringwood, A. H., Piegorsch, W. W., & Stancyk, S. E. (2003) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2003.07.010 · Cited by 58

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Hoogewijs, D., Terwilliger, N. B., Webster, K. A., Powell‐Coffman, J. A., Tokishita, S.-I., Yamagata, H., Hankeln, T., Burmester, T., Rytkönen, K. T., Nikinmaa, M., et al. (2007) · Integrative and Comparative Biology · doi:10.1093/icb/icm072 · Cited by 58

Different responses of biochemical markers in frogs (Rana ridibunda) from urban and rural wetlands to the effect of carbamate fungicide

Falfushynska, H., Romanchuk, L. D., & Stoliar, O. B. (2008) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2008.05.018 · Cited by 57

Genotoxic effects of produced waters in mosquito fish (Gambusia affinis)

Caliani, I., Porcelloni, S., Mori, G., Frenzilli, G., Ferraro, M., Marsili, L., Casini, S., & Fossi, M. C. (2008) · Ecotoxicology · doi:10.1007/s10646-008-0259-0 · Cited by 56

Effect of Trivalent and Hexavalent Chromium on Antioxidant Enzyme Activities and Lipid Peroxidation in a Freshwater Field Crab, Barytelphusa guerini

Sridevi, B. V., REDDY, K. V., & Reddy, S. L. N. (1998) · Bulletin of Environmental Contamination and Toxicology · doi:10.1007/s001289900774 · Cited by 56

Trivalent chromium induces oxidative stress in goldfish brain

Lushchak, O. V., Kubrak, O. I., Torous, I. M., Nazarchuk, T., Storey, K. B., & Lushchak, V. I. (2009) · Chemosphere · doi:10.1016/j.chemosphere.2008.11.052 · Cited by 56

Antioxidant system breakdown in brain of feral golden grey mullet (Liza aurata) as an effect of mercury exposure

Mieiro, C. L., Ahmad, I., Pereira, E., Duarte, A. C., & Pacheco, M. (2010) · Ecotoxicology · doi:10.1007/s10646-010-0485-0 · Cited by 56

Increased recovery of brain acetylcholinesterase activity in dichlorvos-intoxicated European eels Anguilla anguilla by bath treatment with N-acetylcysteine

Peña‐Llopis, S., Ferrando, M., & Peña, J. (2003) · Diseases of Aquatic Organisms · doi:10.3354/dao055237 · Cited by 55

MafT, a new member of the small Maf protein family in zebrafish

Takagi, Y., Kobayashi, M., Li, L., Suzuki, T., Nishikawa, K., & Yamamoto, M. P. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.05.131 · Cited by 54

Biochemical mechanisms leading to tryptophan 2,3‐dioxygenase activation

Li, J. S., Han, Q., Fang, J., Rizzi, M., James, A. A., & Li, J. (2007) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.20159 · Cited by 52

DNA-Strand Breaks Induced by Dimethylarsinic Acid, a Metabolite of Inorganic Arsenics, Are Strongly Enhanced by Superoxide Anion Radicals.

Ken, R. I. N., Kawaguchi, K., Yamanaka, K., Tezuka, M., Oku, N., & Okada, S. (1995) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.18.45 · Cited by 50

Levels of cellular glutathione and metallothionein affect the toxicity of oxidative stressors in an established carp cell line

Wright, J., George, S. G., Martínez‐Lara, E., Carpenè, E., & Kindt, M. (2000) · Marine Environmental Research · doi:10.1016/s0141-1136(00)00125-2 · Cited by 50

Wide diversity in structure and expression profiles among members of the Caenorhabditis elegans globin protein family

Hoogewijs, D., Geuens, E., Dewilde, S., Vierstraete, A. R., Moens, L. J., Vinogradov, S. N., & Vanfleteren, J. R. (2007) · BMC Genomics · doi:10.1186/1471-2164-8-356 · Cited by 50

Waterborne and dietary hexavalent chromium exposure causes DNA-protein crosslink (DPX) formation in erythrocytes of largemouth bass (Micropterus salmoides)

Kuykendall, J. R., Miller, K. L., Mellinger, K. M., & Cain, A. V. (2006) · Aquatic Toxicology · doi:10.1016/j.aquatox.2006.01.019 · Cited by 49

Millimeter Wave-induced Vibrational Modes in DNA as a Possible Alternative to Animal Tests to Probe for Carcinogenic Mutations

WOOLARD, D. L., Koscica, T. E., Rhodes, D. L., Cui, H., Pastore, R., Jensen, J., Jensen, J. L., Loerop, W. R., Jacobsen, R. H., Mittleman, D. M., et al. (1997) · Journal of Applied Toxicology · doi:10.1002/(sici)1099-1263(199707)17:4 · Cited by 47

Oxidative stress and expression of chaperones in aging mollusks

Ivanina, A. V., Sokolova, I. M., & Sukhotin, A. A. (2008) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2008.01.005 · Cited by 47

Measurement of relative antioxidant activityof compounds: a methodological note

Mira, L., Silva, M., Rocha, R., & Manso, C. (1999) · Redox Report · doi:10.1179/135100099101534666 · Cited by 46

Hypoxia-induced oxidative base modifications in the VEGF hypoxia-response element are associated with transcriptionally active nucleosomes

Ruchko, M. V., Gorodnya, O. M., Pastukh, V. M., Swiger, B. M., Middleton, N. S., Wilson, G. L., & Gillespie, M. N. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.09.038 · Cited by 45

Specific antioxidant reactions to oxidative stress promoted by natural organic matter in two amphipod species from Lake Baikal

Timofeyev, M. A., Shatilina, Z. M., Колесниченко, А. В., Колесниченко, В. В., & Steinberg, C. E. W. (2006) · Environmental Toxicology · doi:10.1002/tox.20161 · Cited by 45

Proteomics of Juvenile Senegal Sole (Solea senegalensis) Affected by Gas Bubble Disease in Hyperoxygenated Ponds

Salas-Leitón, E., Cánovas-Conesa, B., Zerolo, R., López‐Barea, J., Cañavate, J. P., & Alhama, J. (2008) · Marine Biotechnology · doi:10.1007/s10126-008-9168-8 · Cited by 44

Effects of chromium(VI) and vanadium(V) on the lifespan of fish

Perez‐Benito, J. F. (2006) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2006.04.001 · Cited by 43

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Detection of hypoxia-related proteins in medaka (Oryzias latipes) brain tissue by difference gel electrophoresis and de novo sequencing of 4-sulfophenyl isothiocyanate-derivatized peptides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

Oehlers, L. P., Perez, A. N., & Walter, R. B. (2006) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2006.06.005 · Cited by 43

Influence of Carbohydrate Ingestion on Oxidative Stress and Plasma Antioxidant Potential Following a 3 h Run

McAnulty, S. R., McAnulty, L. S., Nieman, D. C., Morrow, J. D., Utter, A. C., Henson, D. A., Dumke, C. L., & Vinci, D. M. (2003) · Free Radical Research · doi:10.1080/1071576031000136559 · Cited by 42

Mechanisms of Promotion and Progression of Preneoplastic Lesions in Hepatocarcinogenesis by DDT in F344 Rats

Harada, T., Yamaguchi, S., Ohtsuka, R., Takeda, M., Fujisawa, H., Yoshida, T., Enomoto, A., Chiba, Y., Fukumori, J., Kojima, S., et al. (2003) · Toxicologic Pathology · doi:10.1080/01926230390173941 · Cited by 42

Heat shock induces oxidative stress in rotan Perccottus glenii tissues

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The metal-responsive transcription factor-1 contributes to HIF-1 activation during hypoxic stress

Murphy, B. J., Sato, B., Dalton, T. P., & Laderoute, K. R. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.09.124 · Cited by 40

Effects of 17-β estradiol and 4-nonylphenol on phase II electrophilic detoxification pathways in largemouth bass (Micropterus salmoides) liver

Hughes, E. M., & Gallagher, E. P. (2004) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2004.01.006 · Cited by 39

2-chlorophenol induced hydroxyl radical production in mitochondria in Carassius auratus and oxidative stress – An electron paramagnetic resonance study

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Effect of prochloraz fungicide on biotransformation enzymes and oxidative stress parameters in three-spined stickleback ( Gasterosteus aculeatus L.)

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Hypoxic Preconditioning with Cobalt Attenuates Hypobaric Hypoxia-Induced Oxidative Damage in Rat Lungs

Shukla, D., Saxena, S., Jayamurthy, P., Sairam, M., Singh, M., Jain, S. K., Bansal, A., & Ilavazaghan, G. (2009) · High Altitude Medicine & Biology · doi:10.1089/ham.2008.1028 · Cited by 37

Validation of oxidative stress responses in two populations of frogs from Western Ukraine

Falfushynska, H., Loumbourdis, N., Romanchuk, L. D., & Stoliar, O. B. (2008) · Chemosphere · doi:10.1016/j.chemosphere.2008.07.060 · Cited by 37

Metabolism of iron by normal and iron deficient rainbow trout

Walker, R. L., & Fromm, P. O. (1976) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(76)90052-9 · Cited by 35

Diethyldithiocarbamate injection induces transient oxidative stress in goldfish tissues

Lushchak, V. I., Bagnyukova, T., Lushchak, O. V., Storey, J. M., & Storey, K. B. (2007) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2007.06.033 · Cited by 34

Free radicals, reactive oxygen species, oxidative stress and its classification

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Glutathione Homeostasis and Functions: Potential Targets for Medical Interventions

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Pesticide toxicity

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Blue mussels (Mytilus edulis spp.) as sentinel organisms in coastal pollution monitoring: A review

Beyer, J., Green, N. W., Brooks, S., Allan, I. J., Ruus, A., Gomes, T., Bråte, I. L. N., & Schøyen, M. (2017) · Marine Environmental Research · doi:10.1016/j.marenvres.2017.07.024 · Cited by 555

Heavy-Metal-Induced Reactive Oxygen Species: Phytotoxicity and Physicochemical Changes in Plants

Shahid, M. A. R., Pourrut, B., Dumat, C., Nadeem, M., Aslam, M., & Pinelli, É. (2014) · Reviews of Environmental Contamination and Toxicology · doi:10.1007/978-3-319-06746-9_1 · Cited by 550

Research Progress on Mechanisms of Oxidative Stress Generation in Water Body

Qiu-j, W. (2014) · China Animal Husbandry & Veterinary Medicine · Cited by 1

Research on the Oxidative Stress of Fishes under Environmental Stress Factors

Lin-jun, Y. (2012) · Anhui nongye kexue

Cellular Oxidant/Antioxidant Network: Update on the Environmental Effects Over Marine Organisms

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Contaminant-induced oxidative stress in fish: a mechanistic approach

Lushchak, V. I. (2015) · Fish Physiology and Biochemistry · doi:10.1007/s10695-015-0171-5 · Cited by 392

Sucul Organizmalarda Çevresel Şartlara Karşı Geliştirilen Oksidatif Stres Mekanizmaları ve Adaptif Yanıtlar

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