Redefining Oxidative Stress

[49] Determination of carbonyl content in oxidatively modified proteins

Levine, R. L., Garland, D. L., Oliver, C. N., Amici, A., Climent, I., Lenz, A.-G., Ahn, B. W., Shaltiel, S., & Stadtman, E. R. (1990) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(90)86141-h · Cited by 5,895

A Randomized, Placebo-Controlled, Clinical Trial of High-Dose Supplementation With Vitamins C and E, Beta Carotene, and Zinc for Age-Related Macular Degeneration and Vision Loss: AREDS Report No. 8

(2001) · Archives of Ophthalmology · doi:10.1001/archopht.119.10.1417 · Cited by 3,285

Role of Oxidative Modifications in Atherosclerosis

Stocker, R., & Keaney, J. F. (2004) · Physiological Reviews · doi:10.1152/physrev.00047.2003 · Cited by 2,651

Oxidative Stress and Vascular Disease

Madamanchi, N. R., Vendrov, A., & Runge, M. S. (2005) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000150649.39934.13 · Cited by 1,618 · cited 1×

Risk Factors for Lung Cancer and for Intervention Effects in CARET, the Beta-Carotene and Retinol Efficacy Trial

Omenn, G. S., Goodman, G. E., Thornquist, M. D., Balmes, J., Cullen, M. R., Glass, A., Keogh, J. P., Meyskens, F. L., Valanis, B., Williams, J. H., et al. (1996) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/88.21.1550 · Cited by 1,255

Effects of Long-term Vitamin E Supplementation on Cardiovascular Events and Cancer: A Randomized Controlled Trial

(2005) · JAMA · doi:10.1001/jama.293.11.1338 · Cited by 1,209 · cited 1×

Oxidative Stress: Introductory Remarks

Sies, H. (1985) · Elsevier eBooks · doi:10.1016/b978-0-12-642760-8.50005-3 · Cited by 1,037

[11] Redox potential of GSH/GSSG couple: Assay and biological significance

Jones, D. P. (2002) · Methods in Enzymology · doi:10.1016/s0076-6879(02)48630-2 · Cited by 812

Evidence that Peroxidation of Lysosomal Membranes Is Initiated by Hydroxyl Free Radicals Produced during Flavin Enzyme Activity

Fong, K.-L., McCay, P. B., Poyer, J. L., Keele, B. B., & Misra, H. P. (1973) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)43258-4 · Cited by 650

Distinct Roles of Thioredoxin in the Cytoplasm and in the Nucleus

Hirota, K., Murata, M., Sachi, Y., Nakamura, H., Takeuchi, J. S., Mori, K., & Yodoi, J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.39.27891 · Cited by 615

Thiol/Redox Metabolomic Profiling Implicates GSH Dysregulation in Early Experimental Graft versus Host Disease (GVHD)

Suh, J. H., Sathi, B. K., Shenvi, S. V., Guo, H., Zhou, A., Tiwana, A., Kuypers, F. A., Ames, B. N., & Walters, M. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088868 · Cited by 25

Mechanisms Underlying Chemopreventive Effects of Flavonoids via Multiple Signaling Nodes within Nrf2-ARE and AhR-XRE Gene Regulatory Networks

Xiao, H., Lu, F.-L., Stewart, D., & Zhang, Y. (2013) · Current Chemical Biology · doi:10.2174/2212796811307020008 · Cited by 25

Differential sensitivity to pro-oxidant exposure in two populations of killifish (Fundulus heteroclitus)

Harbeitner, R. C., Hahn, M. E., & Timme‐Laragy, A. R. (2013) · Ecotoxicology · doi:10.1007/s10646-012-1033-x · Cited by 25

Quinic Acid Could Be a Potential Rejuvenating Natural Compound by Improving Survival of Caenorhabditis elegans under Deleterious Conditions

Zhang, L., Zhang, J., Zhao, B., & Zhao-Wilson, X. (2012) · Rejuvenation Research · doi:10.1089/rej.2012.1342 · Cited by 24

Peroxisomes and Cellular Oxidant/Antioxidant Balance: Protein Redox Modifications and Impact on Inter-organelle Communication

Fransen, M., & Lismont, C. (2018) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-981-13-2233-4_19 · Cited by 25

The Effect of Exhaustive Exercise on Plasma Metabolic Profiles of Male and Female Rats.

(2019) · PubMed Central · Cited by 25

Role of MicroRNAs in the Regulation of Redox-Dependent Processes

Kalinina, E. V., Иванова-Радкевич, В. И., & Чернов, Н. Н. (2019) · Biochemistry (Moscow) · doi:10.1134/s0006297919110026 · Cited by 25

Low glucose and high pyruvate reduce the production of 2-oxoaldehydes, improving mitochondrial efficiency, redox regulation, and stallion sperm function†

Ortiz-Rodriguez, J. M., Martín‐Cano, F. E., Gaitskell‐Phillips, G., Silva, A., Ortega‐Ferrusola, C., Gil, M. C., & Peña, F. J. (2021) · Biology of Reproduction · doi:10.1093/biolre/ioab073 · Cited by 27

The Interplay between Endogenous and Foodborne Pro-Oxidants and Antioxidants in Shaping Redox Homeostasis

Jakubek, P., Parchem, K., Wieckowski, M. R., & Bartoszek, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147827 · Cited by 25

Oxidative Cysteine Post Translational Modifications Drive the Redox Code Underlying Neurodegeneration and Amyotrophic Lateral Sclerosis

Percio, A., Cicchinelli, M., Masci, D., Summo, M., Urbani, A., & Greco, V. (2024) · Antioxidants · doi:10.3390/antiox13080883 · Cited by 24

The effect of acute physical exercise on the antioxidant status of the skeletal and cardiac muscle in the Wistar rat

Radu, M.-D., Schiopu, S., & Coprean, D. (2010) · Cited by 24

The Metabolomic Underpinnings of Symptom Burden in Patients With Multiple Chronic Conditions

Corwin, E. J., Brewster, G. S., Dunbar, S. B., Wells, J., Hertzberg, V., Holstad, M. M., Song, M., & Jones, D. P. (2020) · Biological Research For Nursing · doi:10.1177/1099800420958196 · Cited by 25

Live cell imaging of oxidative stress in human airway epithelial cells exposed to isoprene hydroxyhydroperoxide

Masood, S. S. M. E., Pennington, E. R., Simmons, S. O., Bromberg, P. A., Shaikh, S. R., Rice, R. L., Gold, A. R., Zhang, Z., & Samet, J. M. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102281 · Cited by 24

Emerging roles of oxidative stress in the pathogenesis of pseudoexfoliation syndrome (Review)

Mastronikolis, S. N., Pagkalou, M., Plotas, P., Kagkelaris, K., & Georgakopoulos, C. D. (2022) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2022.11539 · Cited by 24

Markers of Oxidative Stress in Obstetrics and Gynaecology—A Systematic Literature Review

Drejza, M. A., Rylewicz, K., Majcherek, E., Gross-Tyrkin, K., Mizgier, M., Plagens-Rotman, K., Wójcik, M., Panecka-Mysza, K., Pisarska-Krawczyk, M., Kędzia, W., et al. (2022) · Antioxidants · doi:10.3390/antiox11081477 · Cited by 24

Redox-Regulation in Cancer Stem Cells

Lendeckel, U., & Wolke, C. (2022) · Biomedicines · doi:10.3390/biomedicines10102413 · Cited by 24

Redox imbalance influence in the myocardial Akt activation in aged rats treated with DHEA

Jacob, M., Janner, D. D. R., Araújo, A. S. D. R., Jahn, M. P., Kucharski, L. C., Moraes, T. B., Dutra‐Filho, C. S., Ribeiro, M. F. M., & Belló‐Klein, A. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.08.017 · Cited by 24

Hepatoprotective Effect of Thymol on Chemical-induced Hepatotoxicity in Rodents

Janbaz, K. H., Saeed, S. A., & Gilani, A. H. (2003) · Pakistan Journal of Biological Sciences · doi:10.3923/pjbs.2003.448.451 · Cited by 24

Chlorogenic Acid Differentially Alters Hepatic and Small Intestinal Thiol Redox Status Without Protecting Against Azoxymethane-Induced Colon Carcinogenesis in Mice

Park, H. J., Davis, S. R., Liang, H., Rosenberg, D. W., & Bruno, R. S. (2010) · Nutrition and Cancer · doi:10.1080/01635580903407239 · Cited by 24

Förster resonance energy transfer-based sensor targeting endoplasmic reticulum reveals highly oxidative environment

Kolossov, V. L., Leslie, M. T., Chatterjee, A., Sheehan, B. M., Kenis, P. J. A., & Gaskins, H. R. (2012) · Experimental Biology and Medicine · doi:10.1258/ebm.2012.011436 · Cited by 25

Antioxidant intake among Brazilian adults - The Brazilian Osteoporosis Study (BRAZOS): a cross-sectional study

Pinheiro, M. M., Ciconelli, R. M., Chaves, G. V., de Aquino, L. A., Juzwiak, C. R., Genaro, P. D. S., & Ferraz, M. B. (2011) · Nutrition Journal · doi:10.1186/1475-2891-10-39 · Cited by 24

Badge Size Reflects Sperm Oxidative Status within Social Groups in the House Sparrow Passer domesticus

Mora, A. R., Meniri, M., Glauser, G., Vallat, A., & Helfenstein, F. (2016) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2016.00067 · Cited by 24

Taurine treatment prevents derangement of the hepatic γ‐glutamyl cycle and methylglyoxal metabolism in a mouse model of classical homocystinuria: regulatory crosstalk between thiol and sulfinic acid metabolism

Maclean, K. N., Jiang, H., Aivazidis, S., Kim, E., Shearn, C. T., Harris, P. S., Petersen, D. R., Allen, R. H., Stabler, S. P., & Roede, J. R. (2017) · The FASEB Journal · doi:10.1096/fj.201700586r · Cited by 24

Impacts of isopyrazam exposure on the development of early-life zebrafish (Danio rerio)

Yao, H., Xu, X. L., Zhou, Y., & Xu, C. (2018) · Environmental Science and Pollution Research · doi:10.1007/s11356-018-2449-5 · Cited by 24

Monolluma quadrangula Protects against Oxidative Stress and Modulates LDL Receptor and Fatty Acid Synthase Gene Expression in Hypercholesterolemic Rats

Bin-Jumah, M. N. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/3914384 · Cited by 24

Biological Markers of Oxidative Stress in Cardiovascular Diseases: After so Many Studies, What do We Know?

Fontana, J., Zima, M., & Větvička, V. (2018) · Immunological Investigations · doi:10.1080/08820139.2018.1523925 · Cited by 24

Natural gypenosides: targeting cancer through different molecular pathways

Ahmad, B., Khan, S., Nabi, G., Gamallat, Y., Su, P., Jamalat, Y., Duan, P., & Yao, L. (2019) · Cancer Management and Research · doi:10.2147/cmar.s185232 · Cited by 24

Glutathione Deficiency and Alterations in the Sulfur Amino Acid Homeostasis during Early Postnatal Development as Potential Triggering Factors for Schizophrenia-Like Behavior in Adult Rats

Górny, M., Wnuk, A., Kamińska, A., Kamińska, K., Chwatko, G., Bilska‐Wilkosz, A., Iciek, M., Kajta, M., Rogóż, Z., & Lorenc‐Koci, E. (2019) · Molecules · doi:10.3390/molecules24234253 · Cited by 24

Oxidative Stress and Antioxidant Therapy in Chronic Kidney and Cardiovascular Disease

David, M., & Glenda, C. (2013) · InTech eBooks · doi:10.5772/51923 · Cited by 25

Substituent position influence on the electrochemical properties and antioxidant activity of tetra(aminophenyl)porphyrins

Kuzmin, S. M., Chulovskaya, S. A., & Parfenyuk, V. I. (2014) · Journal of Porphyrins and Phthalocyanines · doi:10.1142/s108842461450031x · Cited by 24

Development of models for prediction of the antioxidant activity of derivatives of natural compounds

Martinčič, R., Kuzmanovski, I., Wagner, A., & Novič, M. (2015) · Analytica Chimica Acta · doi:10.1016/j.aca.2015.01.050 · Cited by 24

Changes in the Proteome of Functional and Regressing Corpus Luteum During Pregnancy and Lactation in the Rat1

González-Fernández, R., Martı́nez-Galisteo, E., Gaytán, F., Bárcena, J. A., & Sánchez‐Criado, J. E. (2008) · Biology of Reproduction · doi:10.1095/biolreprod.107.065474 · Cited by 23

Redox Metabolism During Tropical Diapause in a Lepidoptera Larva

Moreira, D. C., Paula, D. P., & Hermes‐Lima, M. (2012) · Springer eBooks · doi:10.1007/978-3-642-28678-0_35 · Cited by 23

Research progress on the regulation of oxidative stress by phenolics: the role of gut microbiota and Nrf2 signaling pathway

Liu, Y., Wang, X., Podio, N. S., Wang, X., Xu, S., Jiang, S., Wei, X., Han, Y., Cai, Y., Chen, X., et al. (2023) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.13062 · Cited by 23

The Role of Reductive Stress in the Pathogenesis of Endocrine-Related Metabolic Diseases and Cancer

Mladenov, M. I., Sazdova, I., Hadzi‐Petrushev, N., Konakchieva, R., & Gagov, H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26051910 · Cited by 23

Renal protective effect of Rosa laevigata Michx. by the inhibition of oxidative stress in streptozotocin-induced diabetic rats

He, G. (2012) · Molecular Medicine Reports · doi:10.3892/mmr.2012.855 · Cited by 23

The Role of Selenium in Oxidative Stress and in Nonthyroidal Illness Syndrome (NTIS): An Overview

Silvestrini, A., Mordente, A., Martino, G., Bruno, C., Vergani, E., Meucci, E., & Mancini, A. (2018) · Current Medicinal Chemistry · doi:10.2174/0929867325666180201111159 · Cited by 25

Oxidative stress under general intravenous and inhalation anaesthesia

Alavuk, S., Rašić, D., Popović, L., Peraica, M., & Črnjar, K. (2020) · Archives of Industrial Hygiene and Toxicology · doi:10.2478/aiht-2020-71-3437 · Cited by 23

The role of TXNL1 in disease: treatment strategies for cancer and diseases with oxidative stress

Zhao, J., & Qi, T. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06241-z · Cited by 23

A Pilot Study of the Effect of Lactobacillus casei Obtained from Long-Lived Elderly on Blood Biochemical, Oxidative, and Inflammatory Markers, and on Gut Microbiota in Young Volunteers

Lihua, M. E. I., Zheng, W.-X., Zhao, Z., Meng, N., Zhang, Q., Zhu, W., Li, R.-D., Liang, X., & Li, Q.-Y. (2021) · Nutrients · doi:10.3390/nu13113891 · Cited by 23

Potential toxicity and safety evaluation of nanomaterials for the respiratory system and lung cancer

Valavanidis, A., Vlachogianni, T., Fiotakis, K., Loridas, S., & Perdicaris, S. (2013) · Lung Cancer Targets and Therapy · doi:10.2147/lctt.s23216 · Cited by 23

Antihepatotoxic Effect of Tadehaginoside, Extracted from Tadehagi triquetrum (L.), Against CCl4-Lesioned Rats Through Activating the Nrf2 Signaling Pathway and Attenuating the Inflammatory Response

Tang, A., Chen, X., Lu, Q., Zheng, N., Wei, Y., & Wu, X. (2014) · Inflammation · doi:10.1007/s10753-014-9821-5 · Cited by 23

In vitro exposure to fullerene C60 influences redox state and lipid peroxidation in brain and gills from Cyprinus carpio (Cyprinidae)

Ferreira, J. L. R., Barros, D. M., Geracitano, L. A., Fillmann, G., Fossa, C. E., de Almeida, E. A., Prado, M. C., Neves, B. R. A., Pinheiro, M. V. B., & Monserrat, J. M. (2012) · Environmental Toxicology and Chemistry · doi:10.1002/etc.1792 · Cited by 23

Effects of a novel cystine-based glutathione precursor on oxidative stress in vascular smooth muscle cells

Sinha‐Hikim, I., Shen, R., Lee, W.-N. N. P., Crum, A., Vaziri, N. D., & Norris, K. C. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00434.2009 · Cited by 23

Frying oils with high natural or added antioxidants content, which protect against postprandial oxidative stress, also protect against DNA oxidation damage

Rangel-Zúñiga, O. A., Haro, C., Tormos, C., Pérez‐Martínez, P., Delgado‐Lista, J., Marı́n, C., Quintana‐Navarro, G. M., Cerdá, C., Sáez, G. T., Lopez‐Segura, F., et al. (2016) · European Journal of Nutrition · doi:10.1007/s00394-016-1205-1 · Cited by 25

Cell-free Xenopus egg extracts for studying DNA damage response pathways

Cupello, S., Richardson, C. A., & Yan, S. (2016) · The International Journal of Developmental Biology · doi:10.1387/ijdb.160113sy · Cited by 24

Antioxidant Activity Evaluation Involving Hemoglobin-Related Free Radical Reactivity

Mot, A. C., Bischin, C., Damian, G., & Silaghi-Dumitrescu, R. L. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1441-8_18 · Cited by 23

Glutathione maintenance mitigates age-related susceptibility to redox cycling agents

Thomas, N. O., Shay, K. P., Kelley, A., Butler, J. A., & Hagen, T. M. (2016) · Redox Biology · doi:10.1016/j.redox.2016.09.010 · Cited by 23

Artificial placenta: Analysis of recent progress

Bird, S. D. (2016) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2016.11.005 · Cited by 23

Pediatric Multiple Organ Dysfunction Syndrome: Promising Therapies

Doctor, A., Zimmerman, J. J., Agus, M. S. D., Rajasekaran, S., Wardenburg, J. B., Fortenberry, J. D., Zajicek, A., Mairson, E., & Typpo, K. (2017) · Pediatric Critical Care Medicine · doi:10.1097/pcc.0000000000001053 · Cited by 23

Oxidative stress affects sperm performance and ejaculate redox status in subordinate House Sparrows

Mora, A. R., Firth, A. G., Blareau, S., Vallat, A., & Helfenstein, F. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.154799 · Cited by 23

Hypoxia acclimation alters reactive oxygen species homeostasis and oxidative status in estuarine killifish (Fundulus heteroclitus)

Borowiec, B. G., & Scott, G. R. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.222877 · Cited by 23

Disturbance of redox homeostasis as a contributing underlying pathomechanism of brain and liver alterations in 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency

Leipnitz, G., Vargas, C. R., & Wajner, M. (2015) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-015-9863-3 · Cited by 23

Interaction between sexual steroids and immune response in affecting oxidative status of birds

Casagrande, S., Costantini, D., & Groothuis, T. G. G. (2012) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2012.07.018 · Cited by 23

Grape antioxidant dietary fibre prevents mitochondrial apoptotic pathways by enhancing Bcl-2 and Bcl-xLexpression and minimising oxidative stress in rat distal colonic mucosa

López‐Oliva, M. E., Pozuelo, M. J., Rotger, R., Muñoz-Martínez, E., & Goñi, I. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512000517 · Cited by 24

Gene and Protein Responses of Human Monocytes to Extracellular Cysteine Redox Potential

Go, Y., Craige, S. M., Orr, M. L., Gernert, K. M., & Jones, D. P. (2009) · Toxicological Sciences · doi:10.1093/toxsci/kfp205 · Cited by 24

Exposure to phthalates and their alternatives in relation to biomarkers of inflammation and oxidative stress in adults: evidence from NHANES 2017–2018

Jin, S., Cui, S., Mu, X., Liu, Z., Han, Y., Cui, T., Xiong, W., Wei, X., & Zhang, X. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-30924-8 · Cited by 21

Transplantation of SNAP-treated adipose tissue-derived stem cells improves cardiac function and induces neovascularization after myocardium infarct in rats

Berardi, G. R. M., Rebelatto, C. L. K., Tavares, H. F., Ingberman, M., Shigunov, P., Barchiki, F., de Aguiar, A. M., Miyague, N. I., Francisco, J. C., Correa, A., et al. (2010) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2010.11.005 · Cited by 22

Extracellular Superoxide Dismutase, the Endothelial Basement Membrane, and the WNT Pathway: New Players in Vascular Normalization and Tumor Infiltration by T-Cells

Martínez-Rey, D., Carmona‐Rodríguez, L., Fernández‐Aceñero, M. J., Mira, E., & Mañes, S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.579552 · Cited by 21

Toxicity Evaluation of the Naphthalen-2-yl 3,5-Dinitrobenzoate: A Drug Candidate for Alzheimer Disease

Anwar, F., Saleem, U., Rehman, A.-U., Ahmad, B., Froeyen, M., Mirza, M. U., Kee, L. Y., Abdullah, I., & Ahmad, S. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.607026 · Cited by 22

Ethyl Acetate Fractions of Papaver rhoeas L. and Papaver nudicaule L. Exert Antioxidant and Anti-Inflammatory Activities

Kim, H., Han, S., Song, K., Lee, M. Y., Park, B., Ha, I. J., & Lee, S. (2021) · Antioxidants · doi:10.3390/antiox10121895 · Cited by 23

Is Nucleoredoxin a Master Regulator of Cellular Redox Homeostasis? Its Implication in Different Pathologies

Idelfonso-García, O. G., Alarcón‐Sánchez, B. R., Vásquez-Garzón, V. R., Baltiérrez‐Hoyos, R., Villa‐Treviño, S., Muriel, P., Serrano, H., Pérez‐Carreón, J. I., & Arellanes‐Robledo, J. (2022) · Antioxidants · doi:10.3390/antiox11040670 · Cited by 24

Bromelain Ameliorates Atherosclerosis by Activating the TFEB-Mediated Autophagy and Antioxidant Pathways

Chen, C.-H., Hsia, C.-C., Hu, P.-A., Yeh, C., Chen, C.-T., Peng, C., Wang, C., & Lee, T. (2022) · Antioxidants · doi:10.3390/antiox12010072 · Cited by 22

Antioxidants for adults with chronic kidney disease

Colombijn, J. M. T., Hooft, L., Jun, M., Webster, A. C., Bots, M. L., Verhaar, M. C., & Vernooij, R. W. M. (2023) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd008176.pub3 · Cited by 23

Chapter 2 Biochemical Biomarkers of Oxidative Collagen Damage

Henrotin, Y. E., Deberg, M. A., Mathy-Hartert, M., & Deby-Dupont, G. P. (2009) · Advances in clinical chemistry · doi:10.1016/s0065-2423(09)49002-4 · Cited by 22

Necrosis is increased in lymphoblastoid cell lines from children with autism compared with their non-autistic siblings under conditions of oxidative and nitrosative stress

Main, P. A. E., Thomas, P., Esterman, A., & Fenech, M. F. (2013) · Mutagenesis · doi:10.1093/mutage/get025 · Cited by 22

The Relation Between Low-Level Lead Exposure and Oxidative Stress: a Review of the Epidemiological Evidence in Children and Non-Occupationally Exposed Adults

Roy, A., & Kordas, K. (2016) · Current Environmental Health Reports · doi:10.1007/s40572-016-0115-y · Cited by 22

Promoting a pro-oxidant state in skeletal muscle: Potential dietary, environmental, and exercise interventions for enhancing endurance-training adaptations

Jordan, A., Perry, C. G. R., & Cheng, A. J. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.09.014 · Cited by 23

Antioxidant activity and protective effect of Turnera ulmifolia Linn. var. elegans against carbon tetrachloride-induced oxidative damage in rats

de Brito, N. J. N., López, J. A., do Nascimento, M. A., Macedo, J. B. M., Araújo‐Silva, G., Oliveira, C. N., de Rezende, A. A., Brandão‐Neto, J., Schwarz, A., & Almeida, M. D. G. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.08.003 · Cited by 22

Assessment of food toxicology

Gosslau, A. (2016) · Food Science and Human Wellness · doi:10.1016/j.fshw.2016.05.003 · Cited by 23

Oxidative stress during courtship affects male and female reproductive effort differentially in a wild bird with biparental care

Montoya, B., Valverde, M., Rojas, E., & Torres, R. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.141325 · Cited by 22

Effect of patchouli alcohol on the regulation of heat shock-induced oxidative stress in IEC-6 cells

Liu, X., Jiang, L., Liu, F., Chen, Y., Xu, L., Li, D., Ma, Y., Li, H., & Xu, J. (2016) · International Journal of Hyperthermia · doi:10.3109/02656736.2016.1147617 · Cited by 21

Modulation of Cellular Redox Parameters for Improving Therapeutic Responses in Multiple Myeloma

Allegra, A., Petrarca, C., Gioacchino, M. D., Casciaro, M., Musolino, C., & Gangemi, S. (2022) · Antioxidants · doi:10.3390/antiox11030455 · Cited by 21

Effects of green tea polyphenols against metal-induced genotoxic damage: underlying mechanistic pathways

García‐Rodríguez, M. D. C., Hernández‐Cortés, L. M., Mendoza-Núñez, V. M., & Arenas‐Huertero, F. (2023) · Journal of Toxicology and Environmental Health Part B · doi:10.1080/10937404.2023.2224119 · Cited by 21

Click chemistry-based thiol redox proteomics reveals significant cysteine reduction induced by chronic ethanol consumption

Harris, P. S., McGinnis, C. D., Michel, C. R., Marentette, J., Reisdorph, R. M., Roede, J. R., & Fritz, K. S. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102792 · Cited by 21

50 shades of oxidative stress: A state-specific cysteine redox pattern hypothesis

Cobley, J. N. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102936 · Cited by 24

Sulfur quantum dots as sustainable materials for biomedical applications: Current trends and future perspectives

Priyadarshi, R., Pourmoslemi, S., Khan, A., Riahi, Z., & Rhim, J. (2024) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2024.113863 · Cited by 22

Advancements in Engineering Tetrahedral Framework Nucleic Acids for Biomedical Innovations

Fan, Q., Sun, B., & Chao, J. (2024) · Small Methods · doi:10.1002/smtd.202401360 · Cited by 21

Comparative Proteomic Analysis of Carbonylated Proteins from the Striatum and Cortex of Pesticide-Treated Mice

Coughlan, C. M., Walker, D. I., Lohr, K. M., Richardson, J. R., Saba, L. M., Caudle, W. M., Fritz, K. S., & Roede, J. R. (2015) · Parkinson s Disease · doi:10.1155/2015/812532 · Cited by 21

Effects of β-alanine administration on selected parameters of oxidative stress and phosphoryltransfer network in cerebral cortex and cerebellum of rats

Gemelli, T., de Andrade, R. B., Rojas, D. B., Bonorino, N. F., Mazzola, P. N., Tortorelli, L. S., Funchal, C., Filho, C. S. D., & Wannmacher, C. M. D. (2013) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1669-8 · Cited by 21

A new metabolomic assay to examine inflammation and redox pathways following LPS challenge

Suh, J. H., Kim, R. Y., & Lee, D. S. (2012) · Journal of Inflammation · doi:10.1186/1476-9255-9-37 · Cited by 22

Dietary methylsulfonylmethane supplementation and oxidative stress in broiler chickens

Rasheed, M. S. A., Oelschlager, M. L., Smith, B. N., Bauer, L. L., Whelan, R., & Dilger, R. N. (2020) · Poultry Science · doi:10.1016/j.psj.2019.12.010 · Cited by 21

Oxidative Stress Is Associated With Diastolic Dysfunction in Women With Ischemia With No Obstructive Coronary Artery Disease

Raad, M., AlBadri, A., Wei, J., Mehta, P. K., Maughan, J., Gadh, A., Thomson, L., Jones, D. P., Quyyumi, A. A., Pepine, C. J., et al. (2020) · Journal of the American Heart Association · doi:10.1161/jaha.119.015602 · Cited by 21

Redox Buffer Capacity of the Cell: Theoretical and Experimental Approach

Мартинович, Г. Г., Martinovich, I. V., Cherenkevich, S. N., & Sauer, H. (2010) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-010-9090-3 · Cited by 21

Cellular polarity in aging: role of redox regulation and nutrition

Soares, H., Marinho, H. S., Real, C., & Antunes, F. (2013) · Genes & Nutrition · doi:10.1007/s12263-013-0371-5 · Cited by 21

Altered glutathione system is associated with the presence of distal symmetric peripheral polyneuropathy in type 2 diabetic subjects

Méndez, M. M., Folgado, J., Tormo, C., Artero, A., Ascaso, M., Martínez‐Hervás, S., Chaves, F. J., Ascaso, J. F., & Real, J. T. (2015) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2015.05.023 · Cited by 21

Dietary Sulfur Amino Acid Supplementation Reduces Small Bowel Thiol/Disulfide Redox State and Stimulates Ileal Mucosal Growth after Massive Small Bowel Resection in Rats

Shyntum, Y., Iyer, S. S., Tian, J. J., Li, H., Mannery, Y. O., Jones, D. P., & Ziegler, T. R. (2009) · Journal of Nutrition · doi:10.3945/jn.109.105130 · Cited by 21

Pro-oxidant–antioxidant balance (PAB) as a prognostic index in assessing the cardiovascular risk factors: A narrative review

Ghazizadeh, H., Saberi‐Karimian, M., Aghasizadeh, M., Sahebi, R., Ghazavi, H., Khedmatgozar, H., Timar, A., Rohban, M., Javandoost, A., & Ghayour‐Mobarhan, M. (2020) · Obesity Medicine · doi:10.1016/j.obmed.2020.100272 · Cited by 20

Non-immune Traits Triggered by Blood Intake Impact Vectorial Competence

Talyuli, O. A. C., Bottino-Rojas, V., Polycarpo, C. R., de Oliveira, P. L., & Paiva‐Silva, G. O. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.638033 · Cited by 19

Evaluation of Thiol Homeostasis in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorders

Arslan, B., Arslan, G. A., Tuncer, A., Karabudak, R., & Dinçel, A. S. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.716195 · Cited by 21

Redox organization of living systems

Jones, D. P. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.03.008 · Cited by 22

Use of Land Snails (Pulmonata) for Monitoring Copper Pollution in Terrestrial Ecosystems

Nica, D. V., Bordean, D.-M., Borozan, A. B., Gergen, I., Bura, M., & Banatean-Dunea, I. (2013) · Reviews of Environmental Contamination and Toxicology · doi:10.1007/978-1-4614-6470-9_4 · Cited by 20

On the vasoprotective mechanisms underlying novel β-phosphorylated nitrones: Focus on free radical characterization, scavenging and NO-donation in a biological model of oxidative stress

Cassien, M., Petrocchi, C., Laurent, S., Robin, M., Ricquebourg, E., Kandouli, C., Asteian, A., Rockenbauer, A., Mercier, A., Culcasi, M., et al. (2016) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2016.04.067 · Cited by 20

Inflammation and airway hyperresponsiveness after chlorine exposure are prolonged by Nrf2 deficiency in mice

Ano, S., Panariti, A., Allard, B., O’Sullivan, M. J., McGovern, T. K., Hamamoto, Y., Ishii, Y., Yamamoto, M. P., Powell, W. S., & Martin, J. G. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.017 · Cited by 20

A novel fluorescent probe for imaging the process of HOCl oxidation and Cys/Hcy reduction in living cells

Liu, Z., Li, G., Wang, Y., Li, J., Mi, Y., Guo, L., Xu, W., Zou, D., Li, T., & Wu, Y. (2018) · RSC Advances · doi:10.1039/c7ra13419c · Cited by 20

Cabbage (Brassica oleracea var. capitata) Protects against H2O2‐Induced Oxidative Stress by Preventing Mitochondrial Dysfunction in H9c2 Cardiomyoblasts

Yang, D. K. (2018) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2018/2179021 · Cited by 20

Supplementation with omega-3 fatty acids potentiates oxidative stress in human airway epithelial cells exposed to ozone

Corteselli, E., Gold, A. R., Surratt, J. D., Cui, T., Bromberg, P. A., Dailey, L. A., & Samet, J. M. (2020) · Environmental Research · doi:10.1016/j.envres.2020.109627 · Cited by 20

Oxidative Stress and Its Association with COVID-19: A Narrative Review

Baqi, H. R., Farag, H. A. M., Bilbeisi, A. H. E., Askandar, R. H., & Afifi, A. M. E. (2020) · Kurdistan Journal of Applied Research · doi:10.24017/covid.11 · Cited by 20

Chapter 8 Use of Transgenic Plants to Uncover Strategies for Maintenance of Redox Homeostasis During Photosynthesis

HANKE, G. T., Holtgrefe, S., König, N., Strodtkötter, I., Voß, I., & Scheibe, R. (2009) · Advances in botanical research · doi:10.1016/s0065-2296(10)52008-1 · Cited by 20

The Role of Direct and Indirect Polyphenolic Antioxidants in Protection Against Oxidative Stress

Christensen, L. P., & Christensen, K. B. (2013) · Polyphenols in Human Health and Disease · doi:10.1016/b978-0-12-398456-2.00023-2 · Cited by 20

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

Modulation and Determination of Cellular Glutathione Concentrations

Klotz, L. (2008) · CRC Press eBooks · doi:10.3109/9781420044348-5

Radical-free biology of oxidative stress

Jones, D. P. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00283.2008 · Cited by 1,213

Redox analysis of human plasma allows separation of pro-oxidant events of aging from decline in antioxidant defenses

Jones, D. P., Mody, V. C., Carlson, J. L., Lynn, M. J., & Sternberg, P. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01040-7 · Cited by 392

Glutathione and Thiols

Brown, L. A. S., & Jones, D. P. (2015) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-19096-9_7 · Cited by 2