Unraveling the Biological Roles of Reactive Oxygen Species

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

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

How mitochondria produce reactive oxygen species

Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207

Reconciling the chemistry and biology of reactive oxygen species

Winterbourn, C. C. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.85 · Cited by 2,504

Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader11Mention of a trade name, proprietary product, or specific equipment does not constitute a guarantee by the United States Department of Agriculture and does not imply its approval to the exclusion of other products that may be suitable.

Wang, H., & Joseph, J. A. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00107-0 · Cited by 2,355

Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean?

Halliwell, B., & Whiteman, M. (2004) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705776 · Cited by 2,238

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., et al. (2005) · Science · doi:10.1126/science.1112125 · Cited by 2,165

Molecular mechanisms of N-acetylcysteine actions

Zafarullah, M., Li, W. Q., Sylvester, J., & Ahmad, M. (2003) · Cellular and Molecular Life Sciences (CMLS) · doi:10.1007/s000180300001 · Cited by 1,343

Genetically encoded fluorescent indicator for intracellular hydrogen peroxide

Belousov, V. V., Fradkov, A. F., Lukyanov, K. A., Staroverov, D. B., Shakhbazov, K., Terskikh, A. V., & Lukyanov, S. (2006) · Nature Methods · doi:10.1038/nmeth866 · Cited by 1,286

Investigating Mitochondrial Redox Potential with Redox-sensitive Green Fluorescent Protein Indicators

Hanson, G. T., Aggeler, R., Oglesbee, D., Cannon, M., Capaldi, R. A., Tsien, R. Y., & Remington, S. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312846200 · Cited by 988

Polymerase ζ Is Involved in Mitochondrial DNA Maintenance Processes in Concert with APE1 Activity

Schreier, H. K., Wiehe, R. S., Ricchetti, M., & Wiesmüller, L. (2022) · Genes · doi:10.3390/genes13050879 · Cited by 7

Is Measuring OH. Radical Scavenging a Reasonable Measurement of Antioxidant Properties?

Meyerstein, D. (2014) · Israel Journal of Chemistry · doi:10.1002/ijch.201300123 · Cited by 7

Topical Application of TAT‐Superoxide Dismutase in Acupoints LI 20 on Allergic Rhinitis

Guo, J., Xu, M., Zheng, M., Liu, S., Zhou, J., Ke, L., Chen, T., & Rao, P. (2016) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2016/3830273 · Cited by 7

Mitochondrial Regulation of Cell Death

Liu, D., Perfettini, J., & Brenner, C. (2018) · Springer eBooks · doi:10.1007/978-3-319-73344-9_6 · Cited by 8

Nutraceutical Effect of Trace Elements as Additional Injectable Doses to Modulate Oxidant and Antioxidant Status, and Improves the Quality of Lamb Meat

Cazarotto, C. J., Boito, J. P., Glombowsky, P., Baggio, R. A., Galli, G. M. M., Machado, G., Bottari, N. B., Leal, M. L. R., Kessler, J. D., Baldissera, M. D., et al. (2019) · Biological Trace Element Research · doi:10.1007/s12011-018-1612-7 · Cited by 7

Effects of N-acetylcysteine on isolated skeletal muscle contractile properties after an acute bout of aerobic exercise

Jannig, P. R., Alves, C. R. R., Voltarelli, V. A., Bozi, L. H. M., Vieira, J. S., Brum, P. C., & Bechara, L. R. G. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.10.012 · Cited by 7

Glial metabolism versatility regulates mushroom body–driven behavioral output inDrosophilaPreprint

Basu, R., Préat, T., & Plaçais, P.-Y. (2024) · Learning & Memory · doi:10.1101/lm.053823.123 · Cited by 7

ROS homeostasis and cell wall biosynthesis pathway are involved in female inflorescence development of birch (Betula platyphylla)

Cai, M., Zeng, K., Li, L., Shi, J., Jakada, B. H., Zhang, X., Wang, P., Zhu, H., Jiang, J., & Lan, X. (2025) · BMC Plant Biology · doi:10.1186/s12870-025-06740-2 · Cited by 6

OsSSID6 Negatively Regulates Salt Stress Tolerance in Rice (Oryza Sativa L.) via Metabolic Pathways and ROS Scavenging

Wang, Z., Zan, X., Chen, H., Zhu, J., Zhao, X., Chen, M., Kong, Y., Yang, J., Jia, X., Ye, X., et al. (2025) · Rice · doi:10.1186/s12284-025-00868-3 · Cited by 6

A sequence-activatable fluorescent probe for the simultaneous imaging of hypochlorous acid and peroxynitrite under oxidative stress

Bao, X., Shi, W., Cui, Y., Zhang, J., Liang, B., Zhou, B., & Huo, C. (2025) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2025.139362 · Cited by 6

Self-boosting stimulus activation of a polyprodrug with cascade amplification for enhanced antitumor efficacy

Zong, Q., Xiao, X., Li, J., & Yuan, Y. (2022) · Biomaterials Science · doi:10.1039/d2bm00647b · Cited by 6

The Interaction between Climate Change and Biodiversity Can Be Assessed from a Material Cycle Perspective

Kim, A.-Y., Lee, W., & Son, Y. (2024) · Diversity · doi:10.3390/d16080506 · Cited by 13

A hydrogen peroxide activated near-infrared ratiometric fluorescent probe for ratio imaging in vivo

Zheng, B., Wang, S., Huang, L., Xu, J., Luo, Y., & Zhao, S. (2024) · Chemical Communications · doi:10.1039/d4cc04167d · Cited by 6

Radical Scavenging Activities of Novel Cationic Inulin Derivatives

Chen, Y., Mi, Y., Zhang, J., Dong, F., Li, Q., Ji, N., & Guo, Z. (2018) · Polymers · doi:10.3390/polym10121295 · Cited by 6

Insights on Targeting Small Molecules to the Mitochondrial Matrix and the Preparation of MitoB and MitoP as Exomarkers of Mitochondrial Hydrogen Peroxide

Cairns, A. G., McQuaker, S. J., Murphy, M. P., & Hartley, R. C. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1262-0_6 · Cited by 6

A mitochondria-targeted rhodol fluorescent probe for imaging of hydrogen peroxide in living cells

Lv, L., Luo, W., & Diao, Q. (2022) · Analytical Methods · doi:10.1039/d2ay00522k · Cited by 7

Coexpression within Integrated Mitochondrial Pathways Reveals Different Networks in Normal and Chemically Treated Transcriptomes

Chen, C., Hyun, T. K., Han, X., Feng, Z., Li, Y., Liu, X., & Liu, J. (2014) · International Journal of Genomics · doi:10.1155/2014/452891 · Cited by 7

Sulfenic Acids and Peroxiredoxins in Oxidant Defense and Signaling

Poole, L. B., Nelson, K. J., & Karplus, P. A. (2013) · Springer eBooks · doi:10.1007/978-94-007-5787-5_4 · Cited by 6

New strategy for detection of hydrogen peroxide based on bi-nucleophilic reaction

Mao, C., Tian, Y., Wang, S., Wang, B., & Liu, X. (2021) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2021.120131 · Cited by 6

Intracellular Mechanisms of Oxygen Sensing

Vjotosh, A. N. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920010046 · Cited by 6

Bioengineered ROS-tolerant probiotic reshapes gut microbiota-host axis to ameliorate type 2 diabetes in male mice

Mao, C., Jin, W., Dou, L., Guo, T., Huang, J., Wang, Y., Liu, X., Wu, S., Qiao, W., Xiang, Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70138-3 · Cited by 5

Bioactivity of selenium‐containing pyridinium salts: Prospecting future pharmaceutical constituents to treat liver diseases involving oxidative stress

Castro, E. T., Alves, A. G., Maia, D. D. B., Magalhães, L. S., Paim, M. P., Penteado, F., Gomes, C. S., Lenardao, E. J., Brüning, C. A., & Bortolatto, C. F. (2023) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.23535 · Cited by 5

Effects of pulsed Nd:YAG laser kernel irradiation on maize (Zea mays L.): Insights into germination, gas exchange, photosynthetic pigments, and morphological modifications

Perveen, R., Jamil, Y., AL‐Huqail, A. A., Alsudays, I. M., Alghanem, S. M. S., Ali, Q., Saeed, F., Azeem, M., Rizwan, M., & Al‐Robai, S. A. (2024) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2024.112876 · Cited by 5

The acute toxicity of tripropyl phosphate and tributyl phosphate to Microcystis aeruginosa

Zhang, J., Lu, N., Hou, S., Sun, S., Jia, R., & Wu, D. (2025) · Environmental Geochemistry and Health · doi:10.1007/s10653-025-02411-1 · Cited by 5

Electret‐induced antibacterial response of Mg 1‐ x Ca x Si 1‐ x Zr x O 3 ( x = 0–0.4) bioceramics

Singh, P., & Dubey, A. K. (2024) · Journal of the American Ceramic Society · doi:10.1111/jace.19688 · Cited by 5

Non-invasive methods to assess seed quality based on ultra-weak photon emission and delayed luminescence

Griffo, A., Sehmisch, S., Laager, F., Pagano, A., Balestrazzi, A., Macovei, A., & Börner, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-74207-9 · Cited by 5

The role of oxidative protein modification and the gluthatione system in modulation of the redox status of breast epithelial cells

Stepovaya, E. A., Шахристова, Е. В., Ryazantsevа, N. V., Nosareva, O. L., Yakushina, V. D., Nosova, A. I., Gulaya, V. S., Stepanova, E. A., Chil’chigashev, R. I., & Novitsky, V. V. (2016) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20166201064 · Cited by 5

Live-Cell Assessment of Reactive Oxygen Species Levels Using Dihydroethidine

Grefte, S., & Koopman, W. J. H. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1262-0_18 · Cited by 5

Measuring Mitochondrial Reactive Oxygen Species (ROS) Production

Starkov, A. A. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_8 · Cited by 5

INTERACTION OF OXYGEN-SENSING MECHANISMS IN CELLS

Николаевич, В. А. (2019) · Ulyanovsk Medico-biological Journal · doi:10.34014/2227-1848-2019-3-52-62 · Cited by 5

Measurement of Reactive Oxygen and Nitrogen Species in Living Cells Using the Probe 2',7'-Dichlorodihydrofluorescein

DORNAS, W., & Schuppan, D. (2021) · BIO-PROTOCOL · doi:10.21769/bioprotoc.4279 · Cited by 4

Hydrogen peroxide disrupts the regulatory pathway of saliva secretion in two salivary acinar rat cell lines

Golnarnik, G., Søland, T. M., Galtung, H. K., & Haug, T. M. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1480721 · Cited by 4

Peroxynitrite-Activated Conditional Chemical Probe for the Affinity-Based Protein Modification

Wu, C., Lee, S., Huang, T.-J., Lin, J.-C., Lu, Y., Wu, S., & Tan, K. (2025) · Analytical Chemistry · doi:10.1021/acs.analchem.4c05580 · Cited by 4

Molecular and biological characteristics of laboratory tebuconazole-resistant mutants in Sclerotium rolfsii

Huang, R., Mao, X., Zhang, X., Zhang, J., Lian, Z., Wang, Q., Wang, D., Wang, L., & Zhou, L. (2025) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2025.106766 · Cited by 4

A mitochondria-targeting glutathione fluorescent probe reveals distinct mitochondria-endoplasmic reticulum contact between disulfidptosis and ferroptosis

Chen, S.-L., Yang, L., Xie, Y., Zheng, M., & Jin, J.-Y. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.109437 · Cited by 4

Different Directions of Effects of Polyclonal IgG Antibodies from Patients with Schizophrenia and Healthy Individuals on Cell Death In Vitro: A Pilot Study

Epimakhova, E. V., Smirnova, L. P., Kazantseva, D. V., Kamaeva, D. A., & Ivanova, S. А. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45040206 · Cited by 4

Energy Metabolism Enhance Perylenequinone Biosynthesis in Shiraia sp. Slf14 through Promoting Mitochondrial ROS Accumulation

Wu, X., Meng, X., Xiao, Y., Yang, H., Zhang, Z., & Zhu, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810113 · Cited by 4

Effects of Hydrogen‐Rich Water on Growth, Redox Homeostasis and Hormonal, Histological and Immune Systems in Rats Exposed to High Cage Density Stress

Kuru, B. B., Makav, M., Kuru, M., Aras, Ş., Sarı, E. K., Bulut, M., Alwazeer, D., Bektaşoğlu, F., Ölmez, M., Kırmızıbayrak, T., et al. (2025) · Veterinary Medicine and Science · doi:10.1002/vms3.70305 · Cited by 5

BSA templated cerium/gold nanoclusters as pH and ROS dual sensors

Cang, J. (2018) · Analytical Methods · doi:10.1039/c8ay02527d · Cited by 4

Активные формы кислорода в водных средах (обзор)

Belovolova, L. V. (2020) · Журнал технической физики · doi:10.21883/os.2020.07.49565.64-20 · Cited by 4

Oxidation Responsive PEGylated Polyamino Acid Bearing Thioether Pendants for Enhanced Anticancer Drug Delivery

Sun, Y., Zhang, Y., Guo, X., Wang, Y., He, P., & Xiao, C. (2023) · Macromolecular Bioscience · doi:10.1002/mabi.202200498 · Cited by 4

A ROS-response hyaluronic acid-coated/chitosan polymer prodrug for enhanced tumour targeting efficacy of SN38

Qin, J., Meng, S., Zhen, Y., Li, J., & Wang, D. (2023) · Journal of drug targeting · doi:10.1080/1061186x.2023.2216401 · Cited by 4

Measuring Calcium and ROS by Genetically Encoded Protein Sensors and Fluorescent Dyes

Gibhardt, C. S., Vultur, A., & Bogeski, I. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9018-4_17 · Cited by 4

Phytochemical Evaluation, Antimicrobial and Anticancer Properties of New “Oligo Grapes” Supplement

Milutinović, M. G., Vasić, S., Obradović, A. D., Zuher, A., Jovanović, M., Radovanović, M., Čomić, L. R., & Marković, S. (2019) · Natural Product Communications · doi:10.1177/1934578x19860371 · Cited by 4

A Druglike Ferrostatin‐1 Analogue as a Ferroptosis Inhibitor and Photoluminescent Indicator

Yan, J., Bao, L., Liang, H., Zhao, L., Liu, M., Kong, L., Fan, X., Liang, C., Liu, T., Han, X., et al. (2025) · Angewandte Chemie · doi:10.1002/ange.202502195 · Cited by 3

Efficacy of nutraceutical supplements containing Passiflora incarnata L., Withania somnifera (L.) Dunal and Taraxacum officinale (L.) weber ex F.H.Wigg. on markers of inflammation, oxidative stress and gut microbiota in senior dogs

Ciarcia, R., Longobardi, C., Iervolino, V., Manenti, T., Ferrucci, F., Veneruso, I., D’Argenio, V., Rubino, A., Pelagalli, A., Lombardi, P., et al. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1695881 · Cited by 3

Combatting the antigenicity of common ragweed pollen and its primary allergen Amb a 1 with cold atmospheric pressure air plasma

Hojnik, N., Shvalya, V., Zavašnik, J., Šribar, J., Križaj, I., & Walsh, J. L. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135640 · Cited by 3

Sniffer restricts arboviral brain infections by regulating ROS levels and protecting blood-brain barrier integrity in Drosophila and mosquitoes

Hu, R., Li, M., Chen, S., Wang, M., Tao, X., Zhu, Y., Yan, H., & Liu, Y. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012797 · Cited by 3

Flexibility and Hydration of the Q o Site Determine Multiple Pathways for Proton Transfer in Cytochrome bc 1

Camilo, S. R. G., & Arantes, G. M. (2025) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.5c00655 · Cited by 3

Thiazoles: Synthesis, biological activities and their interaction studies with serum albumins

Maruthi, T., Akash, R. B., Yallur, B. C., & Manjunatha, D. H. (2025) · Total Chemistry · doi:10.1016/j.totche.2025.100006 · Cited by 3

High quantum yield orange-emission carbon dots for rapid mitochondrial-targeted and dynamic tracking in apoptosis and autophagy

Zhang, Y., Ni, C., Zhou, Z., Xiao, J., Cao, J., Pan, J., Li, C., & Zheng, Y. (2025) · Dyes and Pigments · doi:10.1016/j.dyepig.2025.113052 · Cited by 3

Future aspects of biomedical applications of chitin and chitosan in diseases associated with oxidative stress

Anraku, M., Ifuku, S., Iohara, D., Hirayama, F., Otagiri, M., & Gebicki, J. M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817966-6.00018-2 · Cited by 3

Antioxidant and Photoprotective Properties of Neotropical Bamboo Species

Grombone‐Guaratini, M. T., Furlan, C. M., Lopes, P. S., Barsalobra, K. P., Leite‐Silva, V. R., & Moreno, P. R. H. (2021) · Reference series in phytochemistry · doi:10.1007/978-3-030-45299-5_33-1 · Cited by 3

Probing cytoplasmic peroxide metabolism in Shewanella oneidensis

Toporek, Y. J., Pak, D., Snyder, H., Shin, H., & DiChristina, T. J. (2023) · FEMS Microbiology Letters · doi:10.1093/femsle/fnad075 · Cited by 3

FRBM Mini REVIEW: Chemogenetic approaches to probe redox dysregulation in heart failure

Guo, R., Spyropoulos, F., & Michel, T. M. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.03.027 · Cited by 3

Oxidative Stress in Type-2 Diabetes Mellitus

Asim, M., Awan, R., Rashid, H. U., & Hussain, F. (2024) · Springer eBooks · doi:10.1007/978-3-031-69962-7_5 · Cited by 3

Vulnerabilities of the SARS-Cov-2 Virus to Proteotoxicity – Opportunity for Repurposed Chemotherapy of COVID-19 Infection

Rabbani, N., Thornalley, P. J., Al-Motawa, M., & Xue, M. (2020) · University of the Future: Re-Imagining Research and Higher Education · doi:10.29117/quarfe.2020.0291 · Cited by 3

Novel prodrug supramolecular nanoparticles capable of rapid mitochondrial-targeting and ROS-responsiveness for pancreatic cancer therapy

Huang, Z., Gao, L., Guo, F., Li, D., Tang, Y., Hu, H., Luo, Y., Tang, D., Wang, B., & Zhang, Y. (2022) · New Journal of Chemistry · doi:10.1039/d2nj01157c · Cited by 3

Perspectives on avian nests and eggs

(2015) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198718666.003.0018 · Cited by 3

Oxidative Stress: Impact in Neuroscience Research

Sies, H. (2013) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-1-62703-598-9_1 · Cited by 3

The effect of amifostine on lung ischaemia–reperfusion injury in rats

Bougioukas, I., Didilis, V. N., Emigholz, J., Waldmann‐Beushausen, R., Stojanovic, T., Mühlfeld, C., Schöndube, F. A., & Danner, B. C. (2016) · Interactive Cardiovascular and Thoracic Surgery · doi:10.1093/icvts/ivw105 · Cited by 3

THE THIOREDOXIN SYSTEM IN REGULATING MCF-7 CELL PROLIFERATION UNDER REDOX STATUS MODULATION

Stepovaya, E. A., Шахристова, Е. В., Ryazantsevа, N. V., Nosareva, O. L., Chil’chigashev, R. I., & Egorova, M. Y. (2016) · Siberian Journal of Oncology · doi:10.21294/1814-4861-2016-15-4-50-55 · Cited by 3

Co-Cultured Continuously Bioluminescent Human Cells as Bioreporters for the Detection of Prodrug Therapeutic Impact Pre- and Post-Metabolism

Xu, T., Conway, M. K., Frank, A. M., Ripp, S. A., Sayler, G. S., & Close, D. M. (2017) · Sensors · doi:10.3390/s17122827 · Cited by 3

The role of oxidative protein modification and the glutathione system in modulation of the redox status of breast epithelial cells

Stepovaya, E. A., Шахристова, Е. В., Ryazantsevа, N. V., Nosareva, O. L., Yakushina, V. D., Nosova, A. I., Gulaya, V. S., Stepanova, E. A., Chil’chigashev, R. I., & Novitsky, V. V. (2016) · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · doi:10.1134/s1990750816030161 · Cited by 3

Botanical, phytochemical and pharmacological aspects of Livistona chinensis: A traditional Chinese plant

Singh, K., Murti, Y., Sanduja, M., Sharma, A. K., Vibha, Bansal, S., Shukla, K. S., & Kulshreshtha, M. (2023) · Pharmacological Research - Modern Chinese Medicine · doi:10.1016/j.prmcm.2023.100301 · Cited by 3

Oxidative stress in oral cavity: interplay between reactive oxygen species and antioxidants in health, inflammation, and cancer

Battino, M. A., Greabu, M., & Calenic, B. (2016) · doi:10.1002/9781118832431.ch10 · Cited by 3

Antioxidant Nutraceuticals as Novel Neuroprotective Agents

Katiyar, P., Ghosh, S., Saini, S., Ghosh, C., Agrawal, H., Sircar, D., & Roy, P. (2022) · Wiley eBooks · doi:10.1002/9781119746843.ch8 · Cited by 4

Synthesis, Characterization, Molecular Docking Studies and Biological Evaluation of Thiazole Schiff Base Analogs

Rahman, M. Z., Islam, M. D., Haque, M. A., Rahman, M. M., Hossain, M. E., & Sutradhar, R. K. (2024) · Asian Journal of Chemistry · doi:10.14233/ajchem.2024.31077 · Cited by 2

Suppression of glycolysis decreases sugar-induced cell death in Saccharomyces cerevisiae

Valiakhmetov, A. Y. (2025) · FEMS Microbiology Letters · doi:10.1093/femsle/fnaf026 · Cited by 2

Pinitol Improves Lipopolysaccharide-Induced Cellular Damage in Human Dermal Microvascular Endothelial Cells

Go, M. Y., Kim, J., Jeon, C. Y., Kim, M., & Shin, D. W. (2025) · Molecules · doi:10.3390/molecules30071513 · Cited by 2

Cyanobacteria as generators of reactive oxygen species – A review of analysis methods and case studies

Lis, H., Kwidzińska, K., Bethke, K., & Caban, M. (2025) · Talanta · doi:10.1016/j.talanta.2025.128648 · Cited by 2

A Cascade‐Targeting System Delivering Polyphenol Into the Mitochondria of M1 Macrophages for Inflammatory Bowel Disease Therapy

Liu, X., Wang, X., Yue, Z., Miao, Y., Cao, Y., Zhao, X., & Deng, D. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202503377 · Cited by 3

Proteoforms as the true units of physiological function

Cobley, J. N. (2025) · European Journal of Applied Physiology · doi:10.1007/s00421-025-06096-3 · Cited by 5

A critical assessment of fluorescent probes as cellular reporters for thioredoxin system enzyme activities

Scholzen, K., Zeisel, L., & Arnér, E. S. J. (2026) · Chem · doi:10.1016/j.chempr.2025.102868 · Cited by 2

German Chamomile-Derived Extracellular Vesicles for the Transdermal Delivery of Glabridin: A Combined Strategy against UVA-Induced Pigmentation

Qin, H., Wang, S., Peng, M., Zu, Y., Zhang, M., & Liu, K. (2026) · ACS Applied Nano Materials · doi:10.1021/acsanm.6c00026 · Cited by 2

Protein oxidation in crowded environments

Fuentes-Lemus, E. (2026) · Biochemical Journal · doi:10.1042/bcj20250150 · Cited by 2

Redox signals and oxidative stress in the control of mitochondrial protein import

Hasberg, L., Lauterbach, V. K., Ochsenreiter, T., & Riemer, J. (2026) · Protein Science · doi:10.1002/pro.70665 · Cited by 2

Investigating the Impact of Carboxylated Polystyrene Nanoplastics in the Liver Using Cell Lines and Precision‐Cut Liver Slices

Pandey, N., Boeira, P., Clark, N. J., Walker, E. T., Aroori, S., Denson, J., Thompson, R. C., Cramp, M., Chokshi, S., & Dhanda, A. (2026) · Liver International · doi:10.1111/liv.70748 · Cited by 2

Oxygen-Dependent Adaptation Processes in a Human Organism in Normal Living Conditions and during Space Flight

Ларина, И. М., Buravkova, L. B., & Grigoriev, A. I. (2022) · Human Physiology · doi:10.1134/s0362119722070118 · Cited by 2

Developmental Thermal Conditioning Regulates Oxidative State and Beak Coloration in Response to Thermal Stressors in Adulthood

Hoffman, A. J., Finger, J. W., Kavazis, A. N., & Wada, H. (2024) · Ecological and Evolutionary Physiology · doi:10.1086/733518 · Cited by 2

Impacts of Resistance Training on Endogenous Antioxidants in Older Individuals: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Cordeiro, L. D. S., Linhares, D. G., de Castro, J. B. P., dos Santos, A. O. B., dos Santos, L. L., da Silva, G. C. P. S. M., & Vale, R. G. D. S. (2025) · Journal of Physical Activity and Health · doi:10.1123/jpah.2024-0281 · Cited by 2

Influence of Diet on Endothelial Dysfunction

Lottenberg, A. M., Lavrador, M. S. F., Afonso, M. S., & Machado, R. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812348-5.00024-6 · Cited by 2

Monitoring of Hydrogen Peroxide and Other Reactive Oxygen and Nitrogen Species Generated by Skeletal Muscle

Jackson, M. J. (2013) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-405881-1.00017-3 · Cited by 2

Antibiotic-induced oxidative stress and antibiotic resistance

POSTNIKOVA, L. B., Келдибековна, С. С., Klimanov, I. A., Kubysheva, N. I., Afinogenov, K. I., Glukhova, M., & Nikitina, L. Y. (2017) · PULMONOLOGIYA · doi:10.18093/0869-0189-2017-27-5-664-671 · Cited by 2

Perspectives of pharmacological correction and evaluation of mitochondrial dysfunction in neurodegenerative and ischemic brain lesions

Dmitry, P. I. (2021) · Studies in natural products chemistry · doi:10.1016/b978-0-12-819487-4.00018-5 · Cited by 2

[Effect of Ketone Body β-Hydroxybutyrate to Attenuate Inflammation-Induced Mitochondrial Oxidative Stress in Vascular Endothelial Cells].

Ji, L., Deng, Y., & Li, T. (2021) · 四川大学学报：医学版 · doi:10.12182/20211160202 · Cited by 2

When Chemodynamic Therapy Meets Photodynamic Therapy: A Synergistic Combination of Cancer Treatments

Blum, N. T., Fu, L., Lin, J., & Huang, P. (2021) · IEEE Nanotechnology Magazine · doi:10.1109/mnano.2021.3081755 · Cited by 2

Compostos da casca de tucum-do-cerrado (Bactris setosa Mart.) com atividade antioxidante

Dantas, M. B. V. C. (2016) · doi:10.26512/2016.08.d.22168 · Cited by 2

Commentary on “Ascorbate kills breast cancer cells by rewiring metabolism via redox imbalance and energy crisis” by Ghanem et al. [Free Radic. Biol. Med. 163 (2021) 196–209]

Halliwell, B. B. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.04.029 · Cited by 2

Don’t you know that you’re ToxSeq?

Liddelow, S. A. (2020) · Nature Immunology · doi:10.1038/s41590-020-0667-8 · Cited by 1

Reactive Oxygen Species (ROS) and Cancer

Soni, J. P., Sood, R., & Kumar, J. (2024) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-031-66421-2_2 · Cited by 1

Constructing a hollow-cage nanoenzyme sensor for dual detection of thiamine hydrochloride and hydrogen peroxide based on dielectric barrier discharge microplasma etching

Qin, H., Dai, R., Hu, P., Liu, H., Du, C., Huang, K., & Wang, Z. (2024) · Microchemical Journal · doi:10.1016/j.microc.2024.112016 · Cited by 1

Withaferin A ameliorates psoriasis-like skin lesions by suppressing oxidative stress in keratinocytes

Zhang, M.-Y., Liu, Y., Liu, X., Chen, D.-W., Han, C., Shen, X., Ding, Y., Wang, X., & Shi, A. (2025) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2025.2492825 · Cited by 1

Protective effects of sinensetin against oxidative stress damage induced by AAPH in the brain-gut

Jin, T., He, M., Li, N., He, Y., & He, F. (2025) · Free Radical Research · doi:10.1080/10715762.2025.2514799 · Cited by 1

Electrochemical Behavior of Nitrofurazone in Aqueous Media Applying Multi‐Walled Carbon Nanotubes and Cu‐Phthalocyanine

Brito, C. L., Ferreira, E. I., & La-Scalea, M. A. (2025) · Electroanalysis · doi:10.1002/elan.70005 · Cited by 1

Liver metabolomics and gut microbiota analysis reveal the alleviation mechanism of wheat bran polyphenols on alcoholic liver disease

Li, W., Tian, Y., Wen, X., Bi, X., & Sun, Y. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107457 · Cited by 1

Defense Capacities Against Oxidative Stress in Diapause and Post‐Diapause Embryos of Artemia franciscana

Arabie, D. A., & Hand, S. C. (2025) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.70051 · Cited by 1

ROS-scavenging tetrahedral framework nucleic acids: reprogramming the pathological microenvironment for oral tissue regeneration

Xiong, J., Cui, W., Fu, X., Zhao, Z., Zhou, Y., Huang, B., Zhang, M., & Lin, Y. (2026) · Oral Science and Homeostatic Medicine · doi:10.26599/oshm.2026.9610064 · Cited by 1

Making light of stress

Chan, J., & Chang, C. J. (2014) · Nature Biotechnology · doi:10.1038/nbt.2873 · Cited by 1

Mitochondrially-Targeted Ratiometric Redox Probes

Kaur, A. (2018) · Springer theses · doi:10.1007/978-3-319-73405-7_4 · Cited by 1

Reactive oxygen species in biological systems an interdisciplinary approach

Gilbert, D. L. (1999) · Cited by 2

"Measuring ROS and Oxidative Damage in Human Health: Relevance and Methodological Considerations"

Becerra, Á. (2023) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2023.49.007833

Reactive Oxygen Species (ROS)

Gul, T., Balkhi, H. M., & Haq, E. (2018) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9781681087030118010008 · Cited by 1

How to Regulate Reactive Oxygen Species?

Niwano, Y. (2014) · Journal of Biomolecular Research & Therapeutics · doi:10.4172/2167-7956.1000e130

Biological Damages Caused by Reactive Oxygen Species

Kruk, I. (1998) · The handbook of environmental chemistry · doi:10.1007/978-3-540-49571-0_6 · Cited by 3