Antioxidant protection against organic and inorganic oxygen radicals by normal human plasma: the important primary role for iron-binding and iron-oxidising proteins

[1] Role of free radicals and catalytic metal ions in human disease: An overview

Halliwell, B., & Gutteridge, J. M. C. (1990) · Methods in Enzymology · doi:10.1016/0076-6879(90)86093-b · Cited by 4,994 · see citing works

Oxygen-Dependent Microbial Killing by Phagocytes

BABIOR, B. M. (1978) · New England Journal of Medicine · doi:10.1056/nejm197803232981205 · Cited by 2,483 · see citing works

Oxygen free radicals and iron in relation to biology and medicine: Some problems and concepts

Halliwell, B., & Gutteridge, J. M. C. (1986) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(86)90305-x · Cited by 2,038 · see citing works

Superoxide Radical: An Endogenous Toxicant

Fridovich, I. (1983) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.23.040183.001323 · Cited by 1,168 · see citing works

A compilation of specific bimolecular rate constants for the reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals with inorganic and organic compounds in aqueous solution

Anbar, M., & Neta, P. (1967) · The International Journal of Applied Radiation and Isotopes · doi:10.1016/0020-708x(67)90115-9 · Cited by 982 · see citing works

The relative contributions of vitamin E, urate, ascorbate and proteins to the total peroxyl radical-trapping antioxidant activity of human blood plasma

Wayner, D. D. M., Burton, G. W., Ingold, K. U., Barclay, L. R. C., & Locke, S. J. (1987) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(87)90155-3 · Cited by 871 · see citing works

Formation of a thiobarbituric‐acid‐reactive substance from deoxyribose in the presence of iron salts

Halliwell, B. B., & Gutteridge, J. M. C. (1981) · FEBS Letters · doi:10.1016/0014-5793(81)80114-7 · Cited by 832 · see citing works

Antioxidant activity of albumin-bound bilirubin.

Stocker, R., Glazer, A. N., & Ames, B. N. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.16.5918 · Cited by 769 · see citing works

The possible significance of the ferrous oxidase activity of ceruloplasmin in normal human serum.

Osaki, S., Johnson, D. A., & Frieden, E. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96527-0 · Cited by 679 · see citing works

HYPOFERRÆMIA IN OBESE ADOLESCENTS

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Quantitative measurement of the total, peroxyl radical‐trapping antioxidant capability of human blood plasma by controlled peroxidation

Wayner, D. D. M., Burton, G. W., Ingold, K. U., & Locke, S. J. (1985) · FEBS Letters · doi:10.1016/0014-5793(85)81208-4 · Cited by 634 · see citing works

Radioprotectors and anticarcinogens

Anticarcinogens, Nygaard, O. F., Simic, M. G., & Hauber, J. N. (1983) · Academic Press eBooks · Cited by 610 · see citing works

Antioxidant and co-antioxidant activity of vitamin C. The effect of vitamin C, either alone or in the presence of vitamin E or a water-soluble vitamin E analogue, upon the peroxidation of aqueous multilamellar phospholipid liposomes

Doba, T., Burton, G. W., & Ingold, K. U. (1985) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(85)90285-1 · Cited by 428 · see citing works

A methodology for analysis of tissue sulfhydryl components

Boyne, A. F., & Ellman, G. L. (1972) · Analytical Biochemistry · doi:10.1016/0003-2697(72)90335-1 · Cited by 423 · see citing works

Modification of human serum low density lipoprotein by oxidation — Characterization and pathophysiological implications

Jürgens, G., Hoff, H. F., Chisolm, G. M., & Esterbauer, H. (1987) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(87)90070-3 · Cited by 398 · see citing works

FIRST PROOF THAT VITAMIN E IS MAJOR LIPID-SOLUBLE, CHAIN-BREAKING ANTIOXIDANT IN HUMAN BLOOD PLASMA

Burton, G. W., Joyce, A., & Ingold, K. U. (1982) · The Lancet · doi:10.1016/s0140-6736(82)90293-8 · Cited by 298 · see citing works

Thiobarbituric acid‐reactivity following iron‐dependent free‐radical damage to amino acids and carbohydrates

Gutteridge, J. M. C. (1981) · FEBS Letters · doi:10.1016/0014-5793(81)80113-5 · Cited by 284 · see citing works

EPR spin-trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen peroxide

Yamazaki, I., & Piette, L. H. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00020a021 · Cited by 276 · see citing works

Ferrous-salt-promoted damage to deoxyribose and benzoate. The increased effectiveness of hydroxyl-radical scavengers in the presence of EDTA

Gutteridge, J. M. C. (1987) · Biochemical Journal · doi:10.1042/bj2430709 · Cited by 271 · see citing works

Low-molecular-weight iron complexes and oxygen radical reactions in idiopathic haemochromatosis

Gutteridge, J. M. C., Rowley, D. A., Griffiths, E., & Halliwell, B. B. (1985) · Clinical Science · doi:10.1042/cs0680463 · Cited by 269 · see citing works

Inhibition of lipid peroxidation by the iron-binding protein lactoferrin

Gutteridge, J. M. C., Paterson, S., Segal, A. W., & Halliwell, B. B. (1981) · Biochemical Journal · doi:10.1042/bj1990259 · Cited by 252 · see citing works

Rates of reaction of the hydroxyl radical

Thomas, J. K. (1965) · Transactions of the Faraday Society · doi:10.1039/tf9656100702 · Cited by 249 · see citing works

Caeruloplasmin: Physiological and Pathological Perspectives

Gutteridge, J. M. C., & Stocks, J. (1981) · CRC Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408368109105866 · Cited by 217 · see citing works

Antioxidant properties of the proteins caeruloplasmin, albumin and transferrin. A study of their activity in serum and synovial fluid from patients with rheumatoid arthritis

Gutteridge, J. M. C. (1986) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/0167-4838(86)90286-4 · Cited by 216 · see citing works

The Inhibition of Lipid Autoxidation by Human Serum and its Relation to Serum Proteins and α-Tocopherol

Stocks, J., Gutteridge, J. M. C., Sharp, R. J., & Dormandy, T. L. (1974) · Clinical Science · doi:10.1042/cs0470223 · Cited by 187 · see citing works

Mannitol as an OH· Scavenger in Aqueous Solutions and in Biological Systems

Goldstein, S., & Czapski, G. (1984) · International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine · doi:10.1080/09553008414551961 · Cited by 175 · see citing works

In vitro oxidation of ascorbic acid and its prevention by GSH

Winkler, B. S. (1987) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(87)90190-5 · Cited by 165 · see citing works

Reactions of ferrioxamine and desferrioxamine with the hydroxyl radical

Hoe, S. T., Rowley, D. A., & Halliwell, B. B. (1982) · Chemico-Biological Interactions · doi:10.1016/0009-2797(82)90018-7 · Cited by 149 · see citing works

Reactions of the hydroxyl radical. Part 2.—Determination of absolute rate constants

ADAMS, G. E., Boag, J. W., & Michael, B. D. (1965) · Transactions of the Faraday Society · doi:10.1039/tf9656101417 · Cited by 147 · see citing works

Thiol-dependent lipid peroxidation

Tien, M., Bucher, J. R., & Aust, S. D. (1982) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(82)91701-6 · Cited by 144 · see citing works

Formation of hydroxyl radicals in the presence of ferritin and haemosiderin. Is haemosiderin formation a biological protective mechanism?

O'Connell, M., Halliwell, B. B., Moorhouse, C. P., Aruoma, O. I., Baum, H., & Peters, T. J. (1986) · Biochemical Journal · doi:10.1042/bj2340727 · Cited by 141 · see citing works

Antioxidant properties of caeruloplasmin towards iron‐ and copper‐dependent oxygen radical formation

Gutteridge, J. M. C. (1983) · FEBS Letters · doi:10.1016/0014-5793(83)81111-9 · Cited by 137 · see citing works

The role of superoxide and hydroxyl radicals in phospholipid peroxidation catalysed by iron salts

Gutteridge, J. M. C. (1982) · FEBS Letters · doi:10.1016/0014-5793(82)80788-6 · Cited by 135 · see citing works

The ability of scavengers to distinguish OH· production in the iron-catalyzed Haber-Weiss reaction: Comparison of four assays for OH·

Winterbourn, C. C. (1987) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(87)90037-2 · Cited by 133 · see citing works

Oxygen Radicals Acting as Chemical Messengers: A Hypothesis

Sarán, M., & Bors, W. (1989) · Free Radical Research Communications · doi:10.3109/10715768909087944 · Cited by 129 · see citing works

NON‐TRANSFERRIN PLASMA IRON

Hershko, C., & Peto, T. (1987) · British Journal of Haematology · doi:10.1111/j.1365-2141.1987.tb01291.x · Cited by 125 · see citing works

Oxygen free‐radicals and lipid peroxidation: inhibition by the protein caeruloplasmin

Gutteridge, J. M. C., Richmond, R., & Halliwell, B. B. (1980) · FEBS Letters · doi:10.1016/0014-5793(80)80195-5 · Cited by 114 · see citing works

The measurement of malondialdehyde in peroxidised ox-brain phospholipid liposomes

Gutteridge, J. M. C. (1977) · Analytical Biochemistry · doi:10.1016/0003-2697(77)90136-1 · Cited by 97 · see citing works

Bleomycin‐detectable iron in serum from leukaemic patients before and after chemotherapy Therapeutic implications for treatment with oxidant‐generating drugs

Halliwell, B. B., Aruoma, O. I., Mufti, G. J., & Bomford, A. B. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)81061-5 · Cited by 90 · see citing works

Inhibition of the Fenton reaction by the protein caeruloplasmin and other copper complexes. Assessment of ferroxidase and radical scavenging activities

Gutteridge, J. M. C. (1985) · Chemico-Biological Interactions · doi:10.1016/0009-2797(85)90043-2 · Cited by 85 · see citing works

Fat-soluble vitamins : their biochemistry and applications

Diplock, A. T. (1985) · Technomic Pub. Co. eBooks · Cited by 84 · see citing works

On the Specificity of Allopurinol and Oxypurinol as Inhibitors of Xanthine Oxidase. A Pulse Radiolysis Determination of Rate Constants for Reaction of Allopurinol and Oxypurinol with Hydroxyl Radicals

Hoey, B. M., Butler, J., & Halliwell, B. B. (1988) · Free Radical Research Communications · doi:10.3109/10715768809055151 · Cited by 57 · see citing works

Copper and iron complexes catalytic for oxygen radical reactions in sweat from human athletes

Gutteridge, J. M. C., Rowley, D. A., Halliwell, B. B., Cooper, D., & Heeley, D. M. (1985) · Clinica Chimica Acta · doi:10.1016/0009-8981(85)90033-6 · Cited by 53 · see citing works

Fate of oxygen free radicals in extracellular fluids

Gutteridge, J. M. C. (1982) · Biochemical Society Transactions · doi:10.1042/bst0100072 · Cited by 48 · see citing works

Plasma ascorbate levels and inhibition of the antioxidant activity of caeruloplasmin

Gutteridge, J. M. C. (1991) · Clinical Science · doi:10.1042/cs0810413 · Cited by 46 · see citing works

A simple method for the determination of serum iron

Tokuro, I., Osaka, T., & Kojima, K. (1968) · Clinica Chimica Acta · doi:10.1016/0009-8981(68)90367-7 · Cited by 32 · see citing works

Acute Kidney Injury Associated with Cardiac Surgery

Rosner, M. H., & Okusa, M. D. (2005) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.00240605 · Cited by 1,061 · see citing works

The characterization of antioxidants

Halliwell, B. B., Aeschbach, R., Löliger, J., & Aruoma, O. I. (1995) · Food and Chemical Toxicology · doi:10.1016/0278-6915(95)00024-v · Cited by 973 · see citing works

Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases

Kell, D. B. (2009) · BMC Medical Genomics · doi:10.1186/1755-8794-2-2 · Cited by 554 · see citing works

Copper, iron, and zinc imbalances in severely degenerated brain regions in Alzheimer’s disease: possible relation to oxidative stress.

Deibel, M. A., Ehmann, W. D., & Markesbery, W. R. (1996) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(96)00203-1 · Cited by 540 · see citing works

The definition and measurement of antioxidants in biological systems

Halliwell, B. B., & Gutteridge, J. M. C. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(95)91457-3 · Cited by 539 · see citing works

Commentary: Vitamin C: Antioxidant or Pro-Oxidant In Vivo?

Halliwell, B. (1996) · Free Radical Research · doi:10.3109/10715769609149066 · Cited by 531 · see citing works

Intracellular iron transport and storage: from molecular mechanisms to health implications

Mackenzie, E. L., Iwasaki, K., & Tsuji, Y. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2007.1893 · Cited by 526 · see citing works

Reactive oxygen species in acute lung injury

Chabot, F., Mitchell, J., Gutteridge, J. M. C., & Evans, T. (1998) · European Respiratory Journal · doi:10.1183/09031936.98.11030745 · Cited by 351 · see citing works

Importance of Iron Chelation in Free Radical-Induced Oxidative Stress and Human Disease

Jomová, K., & Valko, M. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211798072463 · Cited by 271 · see citing works

Antioxidants: The Basics-what they are and how to Evaluate them

Halliwell, B. B. (1996) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60976-x · Cited by 270 · see citing works

Progression of human breast cancers to the metastatic state is linked to hydroxyl radical-induced DNA damage.

Malins, D. C., Polissar, N. L., & Gunselman, S. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2557 · Cited by 222 · see citing works

Free Radicals and Brain Damage in the Newborn

Buonocore, G., Perrone, S., & Bracci, R. (2001) · Neonatology · doi:10.1159/000047088 · Cited by 216 · see citing works

Oxidative damage to extracellular matrix and its role in human pathologies

Rees, M. D., Kennett, E. C., Whitelock, J. M., & Davies, M. J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.03.016 · Cited by 206 · see citing works

Redox imbalance in the critically ill

Gutteridge, J. M. C., & Mitchell, J. (1999) · British Medical Bulletin · doi:10.1258/0007142991902295 · Cited by 209 · see citing works

Albumin is a major serum survival factor for renal tubular cells and macrophages through scavenging of ROS

Iglesias, J. I., Abernethy, V. E., Wang, Z., Lieberthal, W., Koh, J. S., & Levine, J. S. (1999) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.1999.277.5.f711 · Cited by 162 · see citing works

Oxidative stress generated by dietary Zn-deficiency: studies in rainbow trout (Oncorhynchus mykiss)

Hidalgo, M. C., Expósito, A., Palma, J. M., & de la Higuera, M. (2002) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(01)00105-4 · Cited by 139 · see citing works

Immobilization stress-induced antioxidant defense changes in rat plasma: Effect of treatment with reduced glutathione

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Crosslinking of DNA and proteins induced by protein hydroperoxides

Gebicki, S., & Gebicki, J. M. (1999) · Biochemical Journal · doi:10.1042/bj3380629 · Cited by 127 · see citing works

Abnormal iron parameters in the pregnancy syndrome preeclampsia

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

Antioxidants and the Comet assay

Cemeli, E., Baumgartner, A., & Anderson, D. C. (2008) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2008.05.002 · Cited by 123 · see citing works

Analytic Reviews: Cardiac Surgery as a Cause of Acute Kidney Injury: Pathogenesis and Potential Therapies

Rosner, M. H., Portilla, D., & Okusa, M. D. (2008) · Journal of Intensive Care Medicine · doi:10.1177/0885066607309998 · Cited by 115 · see citing works

Redox Balance Mechanisms in Schistosoma mansoni Rely on Peroxiredoxins and Albumin and Implicate Peroxiredoxins as Novel Drug Targets

Sayed, A. A., Cook, S. K., & Williams, D. L. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512601200 · Cited by 114 · see citing works

Cryopreservation of primary human hepatocytes: The benefit of trehalose as an additional cryoprotective agent

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Beneficial impact of term labor: Nonenzymatic antioxidant reserve in the human fetus

Buhimschi, I. A., Buhimschi, C. S., PUPKIN, M. J., & Weiner, C. P. (2003) · American Journal of Obstetrics and Gynecology · doi:10.1067/mob.2003.357 · Cited by 108 · see citing works

Human suction blister interstitial fluid prevents metal ion-dependent oxidation of low density lipoprotein by macrophages and in cell-free systems.

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Increased Expression of Iron-Regulating Genes in Monkey and Human Glaucoma

Farkas, R. H. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-0872 · Cited by 101 · see citing works

The inhibitory effects of coffee on radical-mediated oxidation and mutagenicity

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Increased Iron and Ferritin Content of Sputum From Patients With Cystic Fibrosis or Chronic Bronchitis

Stites, S. W., Walters, B., O'Brien-Ladner, A. R., Bailey, K., & Wesselius, L. (1998) · CHEST Journal · doi:10.1378/chest.114.3.814 · Cited by 95 · see citing works

Antioxidant status and lipoprotein peroxidation in chronic fatigue syndrome

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Decreased transferrin and increased transferrin saturation in sera of women with preeclampsia: implications for oxidative stress

Hubel, Kozlov, Kagan, Evans, Davidge, McLaughlin, & Roberts (1996) · American Journal of Obstetrics and Gynecology · doi:10.1053/ob.1996.v175.a74252 · Cited by 91 · see citing works

Nonprotein-bound Iron in Postasphyxial Reperfusion Injury of the Newborn

Dorrepaal, C. A., Berger, H. M., Benders, M. J. N. L., van Zoeren‐Grobben, D., van de Bor, M., & van Bel, F. (1996) · PEDIATRICS · doi:10.1542/peds.98.5.883 · Cited by 85 · see citing works

Iron-Binding Antioxidant Potential of Plasma Albumin

Loban, A., Kime, R., & Powers, H. J. (1997) · Clinical Science · doi:10.1042/cs0930445 · Cited by 83 · see citing works

Albumin Microbubble Persistence During Myocardial Contrast Echocardiography Is Associated With Microvascular Endothelial Glycocalyx Damage

Lindner, J. R., Ismail, S., Spotnitz, W. D., Skyba, D. M., Jayaweera, A. R., & Kaul, S. (1998) · Circulation · doi:10.1161/01.cir.98.20.2187 · Cited by 82 · see citing works

Is the endogenous peroxyl-radical scavenging capacity of plasma protective in systemic inflammatory disorders in humans?

Tsai, K. K., Hsu, T.-G., Kong, C., Lin, K., & Lu, F. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00180-5 · Cited by 77 · see citing works

Oxidative Stress of Vertebrates and Invertebrates

Felton, G. W. (1995) · Springer eBooks · doi:10.1007/978-1-4615-9689-9_10 · Cited by 72 · see citing works

Antioxidant Mechanisms of Enzymes and Proteins

Ahmad, S. (1995) · Springer eBooks · doi:10.1007/978-1-4615-9689-9_7 · Cited by 71 · see citing works

Transferrin Modifications and Lipid Peroxidation: Implications in Diabetes Mellitus

Campenhout, A. V., Campenhout, C. M. V., Lagrou, A., & Manuel‐y‐Keenoy, B. (2003) · Free Radical Research · doi:10.1080/10715760310001600390 · Cited by 67 · see citing works

Systematic parameter optimization of a Me2SO- and serum-free cryopreservation protocol for human mesenchymal stem cells

Salzig, D., Sehl, C., Weber, C., Hudel, K., Czermak, P., Hofmann, N., Spindler, R., & Glasmacher, B. (2011) · Cryobiology · doi:10.1016/j.cryobiol.2011.05.002 · Cited by 67 · see citing works

Antioxidant Activity of Diethyldithiocarbamate

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Lipoperoxidation Induced by Hydrogen Peroxide in Human Erythrocyte Membranes

Köse, K., & Doğan, P. (1995) · Journal of International Medical Research · doi:10.1177/030006059502300102 · Cited by 64 · see citing works

Effect of Sodium Butyrate on Reactive Oxygen Species Generation by Human Neutrophils

Liu, Q., Shimoyama, T., Suzuki, K., Umeda, T., Nakaji, S., & Sugawara, K. (2001) · Scandinavian Journal of Gastroenterology · doi:10.1080/003655201300192012 · Cited by 61 · see citing works

The reactions of copper proteins with nitric oxide

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Iron and the redox status of the lungs

Quinlan, G. J., Evans, T. W., & Gutteridge, J. M. C. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00903-6 · Cited by 57 · see citing works

Clotting Dysfunction in Sepsis: A Role for ROS and Potential for Therapeutic Intervention

Pires, M. E. L., Frade-Guanaes, J. O., & Quinlan, G. J. (2021) · Antioxidants · doi:10.3390/antiox11010088 · Cited by 51 · see citing works

Microscopic and Thermal Characterization of Hydrogen Peroxide Killing and Lysis of Spores and Protection by Transition Metal Ions, Chelators, and Antioxidants

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Oxidative Stress and Antioxidant Defenses in Plasma of Patients with Behcet's Disease.

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Iron-binding antioxidant capacity is impaired in diabetes mellitus

Campenhout, A. V., Campenhout, C. V., Lagrou, A., Moorkens, G. H., Block, C. E. M. D., & Manuel‐y‐Keenoy, B. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.01.010 · Cited by 51 · see citing works

Oxidation-Related Analytes and Lipid and Lipoprotein Concentrations in Healthy Subjects

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Chelatable iron and copper can be released from extracorporeally circulated blood during cardiopulmonary bypass

Moat, N. E., Evans, T. W., Quinlan, G. J., & Gutteridge, J. M. C. (1993) · FEBS Letters · doi:10.1016/0014-5793(93)80974-y · Cited by 49 · see citing works

Role of antioxidants on the erythrocytes resistance to lipid peroxidation after acute iron overload in rats

Galleano, M., & Puntarulo, S. (1995) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/0925-4439(95)00049-a · Cited by 48 · see citing works

Elevated metals compromise repair of oxidative DNA damage via the base excision repair pathway: implications of pathologic iron overload in the brain on integrity of neuronal DNA

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Contaminant concentrations, biochemical and hematological biomarkers in blood of West Indian manatees Trichechus manatus from Brazil

Anzolin, D. G., Sarkis, J. E. D. S., Diaz, E., Soares, D. G., Serrano, I. L., Borges, J. C. G., Souto, A., Taniguchi, S., Montone, R. C., Bainy, A. C. D., et al. (2012) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2012.04.018 · Cited by 45 · see citing works

Supplementation with α-tocopherol or a combination of α-tocopheroland ascorbic acid protects the gastrointestinal tract of iron-deficientrats against iron-induced oxidative damage during iron repletion

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