Age-associated analysis of oxidative stress parameters in human plasma and erythrocytes

Free Radicals in the Physiological Control of Cell Function

Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855

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

Improved method for the determination of blood glutathione.

Beutler, E., Duron, O., & KELLY, B. M. (1963) · PubMed · Cited by 6,932

Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple

Schafer, F. Q., & Buettner, G. R. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00480-4 · Cited by 4,587

A fluorometric method for determination of oxidized and reduced glutathione in tissues

Hissin, P. J., & Hilf, R. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90326-2 · Cited by 4,116

The Free Radical Theory of Aging Matures

BECKMAN, K. B., & AMES, B. N. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.2.547 · Cited by 3,879

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

Lipoperoxides in plasma as measured by liquid-chromatographic separation of malondialdehyde-thiobarbituric acid adduct.

Wong, S. H., Knight, J. A., Hopfer, S. M., Zaharia, O., Leach, C. N., & Sunderman, F. W. (1987) · Clinical Chemistry · doi:10.1093/clinchem/33.2.214 · Cited by 814

Oxidative damage, mitochondrial oxidant generation and antioxidant defenses during aging and in response to food restriction in the mouse

Sohal, R. S., Ku, H.-H., Agarwal, S., Forster, M. J., & Lal, H. (1994) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(94)90104-x · Cited by 788

Protein Carbonyl Measurement by a Sensitive ELISA Method

Buss, H., Chan, T., Sluis, K. B., Domigan, N. M., & Winterbourn, C. C. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00104-4 · Cited by 687

Reactive Oxygen Species, Toxicity, Oxidative Stress, and Antioxidants: Chronic Diseases and Aging

Jomova, K., Raptova, R., Alomar, S. Y., Alwasel, S. H., Nepovimova, E., Kuca, K., & Valko, M. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03562-9 · Cited by 2,638

Clinical Relevance of Biomarkers of Oxidative Stress

Frijhoff, J., Winyard, P. G., Žarković, N., Davies, S. S., Stocker, R., Cheng, D., Knight, A. R., Taylor, E., Oettrich, J., Ruskovska, T., et al. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6317 · Cited by 918

Measurement and Clinical Significance of Biomarkers of Oxidative Stress in Humans

Marrocco, I., Fabio Altieri, F., & Peluso, I. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/6501046 · Cited by 907

Safety assessment of probiotics for human use

Sanders, M. E., Akkermans, L. M. A., Haller, D., Hammerman, C., Heimbach, J. T., Hörmannsperger, G., & Huys, G. (2010) · Gut Microbes · doi:10.4161/gmic.1.3.12127 · Cited by 816

Pathological aspects of lipid peroxidation

Nègre‐Salvayre, A., Augè, N., Ayala, V., Başağa, H., Boada, J., Brenke, R., Chapple, S. J., Cohen, G., Fehér, J., Grune, T., et al. (2010) · Free Radical Research · doi:10.3109/10715762.2010.498478 · Cited by 465

Markers of Oxidative Stress in Erythrocytes and Plasma During Aging in Humans

Pandey, K. B., & Rizvi, S. I. (2009) · Oxidative Medicine and Cellular Longevity · doi:10.4161/oxim.3.1.10476 · Cited by 444

Oxidative stress and human diseases: Origin, link, measurement, mechanisms, and biomarkers

Giustarini, D., Dalle‐Donne, I., Tsikas, D., & Rossi, R. (2009) · Critical Reviews in Clinical Laboratory Sciences · doi:10.3109/10408360903142326 · Cited by 452

4‐Hydroxynonenal: A membrane lipid oxidation product of medicinal interest

Poli, G., Schaur, R. J., Siems, W. G., & Leonarduzzi, G. (2007) · Medicinal Research Reviews · doi:10.1002/med.20117 · Cited by 439

The ozone paradox: Ozone is a strong oxidant as well as a medical drug

Bocci, V. A., Borrelli, E., Travagli, V., & Zanardi, I. (2009) · Medicinal Research Reviews · doi:10.1002/med.20150 · Cited by 422

Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescence

Höhn, A., Weber, D., Jung, T., Ott, C., Hugo, M., Kochlik, B., Kehm, R., König, J., Grune, T., & Castro, J. P. (2016) · Redox Biology · doi:10.1016/j.redox.2016.12.001 · Cited by 388

Redox Signaling by Reactive Electrophiles and Oxidants

Parvez, S., Long, M. J. C., Poganik, J. R., & Aye, Y. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00698 · Cited by 372

Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases

Kehm, R., Baldensperger, T., Raupbach, J., & Höhn, A. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101901 · Cited by 348

Lipid Peroxidation-Derived Aldehydes, 4-Hydroxynonenal and Malondialdehyde in Aging-Related Disorders

Barrera, G., Pizzimenti, S., Daga, M., Dianzani, C., Arcaro, A., Cetrangolo, G. P., Giordano, G., Cucci, M. A., Graf, M. E., & Gentile, F. (2018) · Antioxidants · doi:10.3390/antiox7080102 · Cited by 338

Health Effects with Consumption of the Flax Lignan Secoisolariciresinol Diglucoside

Adolphe, J. L., Whiting, S. J., Juurlink, B. H. J., Thorpe, L. U., & Alcorn, J. (2010) · British Journal of Nutrition · doi:10.1017/s0007114509992753 · Cited by 314

FECUNDITY AND SURVIVAL IN RELATION TO RESISTANCE TO OXIDATIVE STRESS IN A FREE‐LIVING BIRD

Bize, P., Devevey, G., Monaghan, P., Doligez, B., & Christe, P. (2008) · Ecology · doi:10.1890/07-1135.1 · Cited by 240

4-Hydroxy-nonenal—A Bioactive Lipid Peroxidation Product

Schaur, R. J., Siems, W., Bresgen, N., & Eckl, P. (2015) · Biomolecules · doi:10.3390/biom5042247 · Cited by 231

Markers of oxidant stress that are clinically relevant in aging and age-related disease

Jacob, K. D., Hooten, N. N., Trzeciak, A. R., & Evans, M. K. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.02.008 · Cited by 240

MARK-AGE biomarkers of ageing

Bürkle, A., Moreno‐Villanueva, M., Bernhard, J., Blasco, M. A., Zondag, G. C. M., Hoeijmakers, J. H. J., Toussaint, O., Grubeck‐Loebenstein, B., Mocchegiani, E., Collino, S., et al. (2015) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2015.03.006 · Cited by 239

An experimental demonstration that early-life competitive disadvantage accelerates telomere loss

Nettle, D., Monaghan, P., Gillespie, R., Brilot, B., Bedford, T., & Melissa Bateson, B. (2014) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2014.1610 · Cited by 202

Antioxidants and HNE in redox homeostasis

Łuczaj, W., Gęgotek, A., & Skrzydlewska, E. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.033 · Cited by 201

Effects of 4-hydroxynonenal on vascular endothelial and smooth muscle cell redox signaling and function in health and disease

Chapple, S., Cheng, X.-H., & Mann, G. (2013) · Redox Biology · doi:10.1016/j.redox.2013.04.001 · Cited by 183

Regulation of proteasome-mediated protein degradation during oxidative stress and aging

Breusing, N., & Grune, T. (2008) · Biological Chemistry · doi:10.1515/bc.2008.029 · Cited by 195

Air pollution and circulating biomarkers of oxidative stress

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

Modulation of oxidative stress and mitochondrial function by the ketogenic diet

Milder, J. B., & Patel, M. (2011) · Epilepsy Research · doi:10.1016/j.eplepsyres.2011.09.021 · Cited by 181

Inborn defects in the antioxidant systems of human red blood cells

van Zwieten, R., Verhoeven, A. J., & Roos, D. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.11.022 · Cited by 179

Markers of Oxidative Stress in Erythrocytes during Aging in Humans

Rizvi, S. I., & Maurya, P. K. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1395.041 · Cited by 179

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

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

The lipid peroxidation product 4-hydroxynonenal inhibits NLRP3 inflammasome activation and macrophage pyroptosis

Hsu, C. G., Chávez, C. L., Zhang, C., Sowden, M. P., Chen, Y., & Berk, B. C. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-00966-5 · Cited by 174

Oxidative and reductive metabolism of lipid-peroxidation derived carbonyls

Singh, M., Kapoor, A., & Bhatnagar, A. (2015) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2014.12.028 · Cited by 165

Why should neuroscientists worry about iron? The emerging role of ferroptosis in the pathophysiology of neuroprogressive diseases

Morris, G., Berk, M., Carvalho, A. F., Maes, M. H. J., Walker, A. J., & Puri, B. K. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.12.036 · Cited by 155

Potential biomarkers of ageing

Simm, A., Naß, N., Bartling, B., Hofmann, B., Silber, R., & Santos, A. N. (2008) · Biological Chemistry · doi:10.1515/bc.2008.034 · Cited by 153

The Role of Oxidative Stress in Amyotrophic Lateral Sclerosis and Parkinson’s Disease

Baillet, A. C., Chanteperdrix, V., Trocmé, C., Casez, P., Garrel, C., & Besson, G. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0212-5 · Cited by 149

Lipid Oxidation Derived Aldehydes and Oxysterols Between Health and Disease

Sottero, B., Leonarduzzi, G., Testa, G., Gargiulo, S., Poli, G., & Biasi, F. (2018) · European Journal of Lipid Science and Technology · doi:10.1002/ejlt.201700047 · Cited by 145

Clinical oxidation parameters of aging

Voß, P., & Siems, W. (2006) · Free Radical Research · doi:10.1080/10715760600953859 · Cited by 134

Erythrocyte Plasma Membrane Redox System in Human Aging

Rizvi, S. I., Jha, R., & Maurya, P. K. (2006) · Rejuvenation Research · doi:10.1089/rej.2006.9.470 · Cited by 134

The antioxidative effects of probiotic Lactobacillus casei Zhang on the hyperlipidemic rats

Zhang, Y., Du, R., Wang, L., & Zhang, H. (2010) · European Food Research and Technology · doi:10.1007/s00217-010-1255-1 · Cited by 129

Measurement of HNE-protein adducts in human plasma and serum by ELISA—Comparison of two primary antibodies

Weber, D., Milković, L., Bennett, S. J., Griffiths, H. R., Žarković, N., & Grune, T. (2013) · Redox Biology · doi:10.1016/j.redox.2013.01.012 · Cited by 121

Protective effects of probiotic Lactobacillus casei Zhang against endotoxin- and d-galactosamine-induced liver injury in rats via anti-oxidative and anti-inflammatory capacities

Wang, Y., Li, Y., Xie, J., Zhang, Y., Wang, J., Sun, X., & Zhang, H. (2012) · International Immunopharmacology · doi:10.1016/j.intimp.2012.10.026 · Cited by 116

4-hydroxynonenal-mediated signaling and aging

Zhang, H., & Forman, H. J. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.032 · Cited by 114

Cysteinylation and homocysteinylation of plasma protein thiols during ageing of healthy human beings

Rossi, R., Giustarini, D., Milzani, A., & Dalle‐Donne, I. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00417.x · Cited by 112

Alterations in Antioxidant Enzymes During Aging in Humans

Rizvi, S. I., & Maurya, P. K. (2007) · Molecular Biotechnology · doi:10.1007/s12033-007-0048-7 · Cited by 111

Embryonal erythropoiesis and aging exploit ferroptosis

Zheng, H., Jiang, L., Tsuduki, T., Conrad, M., & Toyokuni, S. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102175 · Cited by 109

When It Comes to an End: Oxidative Stress Crosstalk with Protein Aggregation and Neuroinflammation Induce Neurodegeneration

Michalska, P., & Leon, R. M. (2020) · Antioxidants · doi:10.3390/antiox9080740 · Cited by 119

Redox-related biomarkers in human cardiovascular disease - classical footprints and beyond

Daiber, A., Hahad, O., Andreadou, I., Steven, S., Daub, S., & Münzel, T. F. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101875 · Cited by 110

Protective role of tea catechins on erythrocytes subjected to oxidative stress during human aging

Maurya, P. K., & Rizvi, S. I. (2008) · Natural Product Research · doi:10.1080/14786410802267643 · Cited by 106

Markers of oxidative stress in ICU clinical settings: present and future

Grune, T., & Berger, M. M. (2007) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3282f0c97c · Cited by 96

Age and Breeding Effort as Sources of Individual Variability in Oxidative Stress Markers in a Bird Species

Alonso‐Álvarez, C., Pérez‐Rodríguez, L., García, J. T., Viñuela, J., & Mateo, R. (2009) · Physiological and Biochemical Zoology · doi:10.1086/605395 · Cited by 94

Protective effects of sea buckthorn polysaccharide extracts against LPS/d-GalN-induced acute liver failure in mice via suppressing TLR4-NF-κB signaling

Liu, H., Zhang, W., Dong, S., Song, L., Zhao, S., Wu, C., Wang, X., Liu, F., Xie, J., Wang, J., et al. (2015) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2015.10.029 · Cited by 94

Red blood cells open promising avenues for longitudinal studies of ageing in laboratory, non-model and wild animals

Stier, A., Reichert, S., Criscuolo, F., & Bize, P. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.09.001 · Cited by 93

Reactive Aldehyde Modification of Thioredoxin-1 Activates Early Steps of Inflammation and Cell Adhesion

Go, Y., Halvey, P. J., Hansen, J. M., Reed, M., Pohl, J., & Jones, D. P. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.070218 · Cited by 89

Probiotic Lactobacillus casei Zhang ameliorates high-fructose-induced impaired glucose tolerance in hyperinsulinemia rats

Zhang, Y., Wang, L., Zhang, J., Li, Y., He, Q., Li, H., Guo, X., Guo, J., & Zhang, H. (2013) · European Journal of Nutrition · doi:10.1007/s00394-013-0519-5 · Cited by 91

Malondialdehyde (MDA) – product of lipid peroxidation as marker of homeostasis disorders and aging

Całyniuk, B., Grochowska‐Niedworok, E., Walkiewicz, K. W., Kawecka, S., Popiołek, E., & Fatyga, E. (2016) · Annales Academiae Medicae Silesiensis · doi:10.18794/aams/65697 · Cited by 92

Aging and cardioprotection

Jahangir, A., Sagar, S., & Terzic, A. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00647.2007 · Cited by 88

Inflammatory and redox status of ponies with a history of pasture-associated laminitis

Treiber, K. H., Carter, R., Gay, L., Williams, C. A., & Geor, R. J. (2008) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2008.11.004 · Cited by 88

Donor‐variation effect on red blood cell storage lesion: A close relationship emerges

Tzounakas, V. L., Kriebardis, A. G., Papassideri, I. S., & Antonelou, M. H. (2016) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201500128 · Cited by 87

Melatonin improves oxidative stress parameters measured in the blood of elderly type 2 diabetic patients

Kędziora–Kornatowska, K., Szewczyk‐Golec, K., Kozakiewicz, M., Pawluk, H., Czuczejko, J., Kornatowski, T., Bartosz, G., & Kędziora, J. (2009) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2009.00666.x · Cited by 87

Oxidative stress in aging: Theoretical outcomes and clinical evidences in humans

del Valle, L. G. (2011) · Biomedicine & Aging Pathology · doi:10.1016/j.biomag.2011.03.001 · Cited by 85

Oxidative stress and exceptional human longevity: Systematic review

Belenguer‐Varea, Á., Tarazona‐Santabalbina, F. J., Avellana-Zaragoza, J. A., Martínez-Reig, M., Mas‐Bargues, C., & Inglés, M. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.09.019 · Cited by 86

Protective effect of resveratrol on markers of oxidative stress in human erythrocytes subjected to in vitro oxidative insult

Pandey, K. B., & Rizvi, S. I. (2009) · Phytotherapy Research · doi:10.1002/ptr.2853 · Cited by 82

4-Hydroxynonenal metabolites and adducts in pre-carcinogenic conditions and cancer

Guéraud, F. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.025 · Cited by 86

Plasma Protein Oxidation and Its Correlation with Antioxidant Potential During Human Aging

Pandey, K. B., Mehdi, M. M., Maurya, P. K., & Rizvi, S. I. (2010) · Disease Markers · doi:10.1155/2010/964630 · Cited by 77

Glutathione-Related Antioxidant Defense System in Elderly Patients Treated for Hypertension

Rybka, J., Kupczyk, D., Kędziora–Kornatowska, K., Motyl, J., Czuczejko, J., Szewczyk‐Golec, K., Kozakiewicz, M., Pawluk, H., de Carvalho, L. A., & Kȩdziora, J. (2010) · Cardiovascular Toxicology · doi:10.1007/s12012-010-9096-5 · Cited by 76

The Role of Antioxidants Supplementation in Clinical Practice: Focus on Cardiovascular Risk Factors

Cammisotto, V., Nocella, C., Bartimoccia, S., Sanguigni, V., Francomano, D., Sciarretta, S., Pastori, D., Peruzzi, M., Cavarretta, E., D’Amico, A., et al. (2021) · Antioxidants · doi:10.3390/antiox10020146 · Cited by 77

Biochemical Markers of Aging for Longitudinal Studies in Humans

Engelfriet, P. M., Jansen, E. H. J. M., Picavet, H. S. J., & Dollé, M. E. T. (2013) · Epidemiologic Reviews · doi:10.1093/epirev/mxs011 · Cited by 75

A Review of Oxidative Stress Products and Related Genes in Early Alzheimer’s Disease

Cioffi, F., Adam, R. H. I., Bansal, R., & Broersen, K. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210497 · Cited by 73

Role of the membrane in the formation of heme degradation products in red blood cells

Nagababu, E., Mohanty, J. G., Bhamidipaty‐Pelosi, S., Ostera, G. R., & Rifkind, J. M. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.11.015 · Cited by 71

A randomized, double-blind, placebo-controlled, pilot study to evaluate the effect of whole grape extract on antioxidant status and lipid profile

Evans, M., Wilson, D., & Guthrie, N. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2013.12.017 · Cited by 70

Evaluation of Selenium, Redox Status and Their Association with Plasma Amyloid/Tau in Alzheimer’s Disease

Krishnan, S., & Rani, P. U. (2014) · Biological Trace Element Research · doi:10.1007/s12011-014-9930-x · Cited by 70

Oxidative Modification of Proteins: From Damage to Catalysis, Signaling, and Beyond

Demasi, M., Augusto, O., Bechara, E. J. H., Bicev, R. N., Cerqueira, F. M., da Cunha, F. M., Denicola, A., Gomes, F., Miyamoto, S., Netto, L. E. S., et al. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8176 · Cited by 71

Galacto-oligosaccharides supplementation in prefrail older and healthy adults increased faecal bifidobacteria, but did not impact immune function and oxidative stress

Wilms, E., An, R., Smolinska, A., Stevens, Y., Weseler, A. R., Elizalde, M., Drittij-Reijnders, M.-J., Ioannou, A., van Schooten, F., Smidt, H., et al. (2021) · Clinical Nutrition · doi:10.1016/j.clnu.2020.12.034 · Cited by 72

Acute ingestion of catechin-rich green tea improves postprandial glucose status and increases serum thioredoxin concentrations in postmenopausal women

Takahashi, M., Miyashita, M., Suzuki, K., Bae, S.-R., Kim, H., Wakisaka, T., Matsui, Y., Takeshita, M., & Yasunaga, K. (2014) · British Journal Of Nutrition · doi:10.1017/s0007114514002530 · Cited by 63

Hormetic and regulatory effects of lipid peroxidation mediators in pancreatic beta cells

Maulucci, G., Daniel, B., Cohen, O., Avrahami, Y., & Sasson, S. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.03.001 · Cited by 63

Age-Related Changes in Hepatic Activity and Expression of Detoxification Enzymes in Male Rats

Vyskočilová, E., Szotáková, B., Skálová, L., Bártíková, H., Hlaváčová, J., & Boušová, I. (2013) · BioMed Research International · doi:10.1155/2013/408573 · Cited by 62

Walking the Oxidative Stress Tightrope: A Perspective from the Naked Mole-Rat, the Longest-Living Rodent

Rodriguez, K. A., Wywiał, E., Pérez, V., Lambert, A. J., Edrey, Y. H., Lewis, K. N., Grimes, K. M., Lindsey, M. L., Brand, M. D., & Buffenstein, R. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211797052457 · Cited by 58

Not All Stressors Are Equal: Mechanism of Stressors on RPE Cell Degeneration

Tong, Y., & Wang, S. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.591067 · Cited by 56

Protective Role of Myricetin on Markers of Oxidative Stress in Human Erythrocytes Subjected to Oxidative Stress

Pandey, K. B., Mishra, N., & Rizvi, S. I. (2009) · Natural Product Communications · doi:10.1177/1934578x0900400211 · Cited by 57

Role of oxidative stress on platelet hyperreactivity during aging

Eduardo Fuentes, Q., & Palomo, I. F. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.02.026 · Cited by 57

Safety assessment of two probiotic strains, Lactobacillus coryniformis CECT5711 and Lactobacillus gasseri CECT5714

Lara‐Villoslada, F., Sierra, S., Martı́n, R., Delgado, S., Rodríguez, J. M., Olivares, M. M., & Xaus, J. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.03225.x · Cited by 54

Dietary Polyphenols and Their Effects on Cell Biochemistry and Pathophysiology 2013

Maraldi, T., Vauzour, D., & Angeloni, C. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/576363 · Cited by 55

Inverse correlation of protein oxidation and proteasome activity in liver and lung

Breusing, N., Arndt, J., Voß, P., Bresgen, N., Wiswedel, I., Gardemann, A., Siems, W., & Grune, T. (2009) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2009.09.004 · Cited by 52

Physiological Antioxidative Network of the Bilirubin System in Aging and Age-Related Diseases

Kim, S. Y., & Park, S. C. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2012.00045 · Cited by 53

Redox Parameters as Markers of the Rate of Aging and Predictors of Life Span

de Toda, I. M., Vida, C., Garrido, A., & la Fuente, M. D. (2019) · The Journals of Gerontology Series A · doi:10.1093/gerona/glz033 · Cited by 50

Zearalenone induced oxidative stress in the jejunum in postweaning gilts through modulation of the Keap1–Nrf2 signaling pathway and relevant genes1

Cheng, Q., Jiang, S., Huang, L., Ge, J., Wang, Y., & Yang, W. (2019) · Journal of Animal Science · doi:10.1093/jas/skz051 · Cited by 48

Biomarkers of protein oxidation from a chemical, biological and medical point of view

Breusing, N., & Grune, T. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.04.004 · Cited by 47

l -Cysteine Efflux in Erythrocytes As A Function of Human Age: Correlation with Reduced Glutathione and Total Anti-Oxidant Potential

Kumar, P., & Maurya, P. K. (2013) · Rejuvenation Research · doi:10.1089/rej.2012.1394 · Cited by 47

Maternal age effects on myometrial expression of contractile proteins, uterine gene expression, and contractile activity during labor in the rat

Elmes, M. J., Szyszka, A., Pauliat, C., Clifford, B. L., Daniel, Z. C. T. R., Cheng, Z., Wathes, C., & McMullen, S. (2015) · Physiological Reports · doi:10.14814/phy2.12305 · Cited by 50

Effect of melatonin on the oxidative stress in erythrocytes of healthy young and elderly subjects*

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Iuchi, Y., Kibe, N., Tsunoda, S., Suzuki, S., Mikami, T., Okada, F., Uchida, K., & Fujii, J. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.01.012 · Cited by 46

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Weber, D., Stuetz, W., Toussaint, O., Debacq-Chainiaux, F., Dollé, M. E. T., Jansen, E., Gonos, E. S., Franceschi, C., Sikora, E., Hervonen, A., et al. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/1401452 · Cited by 46

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Iuchi, Y., Okada, F., Takamiya, R., Kibe, N., Tsunoda, S., Nakajima, O., Toyoda, K., Nagae, R., Suematsu, M., Soga, T., et al. (2009) · Biochemical Journal · doi:10.1042/bj20090176 · Cited by 45

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Lara‐Villoslada, F., Sierra, S., Díaz-Ropero, M. P., Olivares, M. M., & Xaus, J. (2007) · Journal of Dairy Science · doi:10.3168/jds.2006-685 · Cited by 42

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Racine, M. L., & Dinenno, F. A. (2019) · The Journal of Physiology · doi:10.1113/jp278338 · Cited by 40

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Lara‐Villoslada, F., Sierra, S., Díaz-Ropero, M. P., Rodríguez, J. M., Xaus, J., & Olivares, M. M. (2009) · Journal of Dairy Research · doi:10.1017/s0022029909004014 · Cited by 39

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Rondanelli, M., d’Eril, G. V. M., Anesi, A., & Ferrari, E. (1997) · Aging Clinical and Experimental Research · doi:10.1007/bf03340153 · Cited by 33

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