The DOI matches its Crossref record; 121 of the 121 references it cites were found in a registry or an index.
Redox signaling: An evolution from free radicals to aging
Open accessAbstract
Redox biology has evolved from studies of the pathology that involves oxidants to an understanding of how oxidants participate in normal as well as aberrant signal transduction. Although the concept that signal transduction involved changes in the redox state dates from the 1930s, the modern history of redox biology began with the discovery of superoxide dismutase by McCord and Fridovich. The initial focus was on free radicals and damage of macromolecules, which remains an important topic. But, over time it was realized that hydroperoxides, especially H2O2 produced by NADPH oxidases, and electrophiles derived from lipid peroxidation or metabolism, played essential roles in physiologically relevant signaling. The mechanisms through which H2O2 and other electrophiles signal became an important area of study that provided insight into how these reactive molecules were involved in major signaling pathways and regulation of transcription factors. Thus, the field of redox signaling that is the overlap of signal transduction with redox biology was established. Alterations in redox signaling are observed in aging, but we also now know that redox signaling is essential in physiological homeostasis and that sustained deviation from redox homeostasis results in disease. This is a review of the history of redox biology from a personal perspective of nearly fifty years working in this field that hopefully provides some insights for the reader.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, several types of SOD are present in the cytosol and in the mitochondria of human cells, where they convert O 2 •-into H 2 O 2 and molecular oxygen (O 2 ) [164].”
From Sunlight damage to cellular DNA: focus on oxidatively generated lesions (2017) · cites this paper as [164]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
McCord, J. M., & Fridovich, I. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)63504-5 · Cited by 12,952
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
Lung cancer, cardiopulmonary mortality, and long-term exposure to fine particulate air pollution
Pope III, C. A. (2002) · JAMA · doi:10.1001/jama.287.9.1132 · Cited by 8,447
Nanotoxicology: An Emerging Discipline Evolving from Studies of Ultrafine Particles
Oberdörster, G., Oberdörster, E., & Oberdörster, J. (2005) · Environmental Health Perspectives · doi:10.1289/ehp.7339 · Cited by 7,891
Schreck, R., RIEBER, P., & Baeuerle, P. A. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07761.x · Cited by 3,793
Fridovich (1978) · doi:10.1126/science.210504 · Cited by 3,329
Babior, B. M., Kipnes, R. S., & Curnutte, J. T. (1973) · Journal of Clinical Investigation · doi:10.1172/jci107236 · Cited by 2,931
Physiological Roles of Mitochondrial Reactive Oxygen Species
Sena, L. A., & Chandel, N. S. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.09.025 · Cited by 2,632
Mammalian thioredoxin is a direct inhibitor of apoptosis signal‐regulating kinase (ASK) 1
Saitoh, M., Nishitoh, H., Fujii, M., Takeda, K., Tobiume, K., Sawada, Y., Kawabata, M., Miyazono, K., & Ichijo, H. (1998) · The EMBO Journal · doi:10.1093/emboj/17.9.2596 · Cited by 2,377
The reaction of NO with superoxide
Huie, R. E., & Padmaja, S. (1993) · Free Radical Research Communications · doi:10.3109/10715769309145868 · Cited by 2,121
Cited by
Sorted by citations
Chalcone: A Privileged Structure in Medicinal Chemistry
Zhuang, C., Zhang, W., Sheng, C., Zhang, W., Xing, C., & Miao, Z. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00020 · Cited by 1,538
Antioxidant Defence Systems and Oxidative Stress in Poultry Biology: An Update
Surai, P. F., Kochish, I. I., Fisinin, V. I., & Kidd, M. T. (2019) · Antioxidants · doi:10.3390/antiox8070235 · Cited by 721
Sunlight damage to cellular DNA: focus on oxidatively generated lesions
Schuch, A. P., Moreno, N. C., Schuch, N. J., Menck, C. F. M., & Garcia, C. C. M. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.01.029 · Cited by 436
ROS and RNS signalling: adaptive redox switches through oxidative/nitrosative protein modifications
Moldogazieva, N. T., Mokhosoev, I. M., Feldman, N. B., & Lutsenko, S. V. (2018) · Free Radical Research · doi:10.1080/10715762.2018.1457217 · Cited by 297
Fatoki, J. O., & Badmus, J. A. (2022) · Journal of Hazardous Materials Advances · doi:10.1016/j.hazadv.2022.100052 · Cited by 304
Umeno, A., Biju, V., & Yoshida, Y. (2017) · Free Radical Research · doi:10.1080/10715762.2017.1315114 · Cited by 270
Garza-Lombó, C., Posadas, Y., Quintanar, L., Gonsebatt, M. E., & Franco, R. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7272 · Cited by 263
The role of catalases in the prevention/promotion of oxidative stress
Gȩbicka, L., & Krych-Madej, J. (2019) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2019.110699 · Cited by 237
Molecular Mechanism of Arsenic-Induced Neurotoxicity including Neuronal Dysfunctions
Thakur, M., Rachamalla, M., Niyogi, S., Datusalia, A. K., & Flora, S. J. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810077 · Cited by 222
DNA damage by lipid peroxidation products: Implications in cancer, inflammation and autoimmunity
Gentile, F., Arcaro, A., Pizzimenti, S., Daga, M., Cetrangolo, G. P., Dianzani, C., Lepore, A., Graf, M., Ames, P. R. J., & Barrera, G. (2017) · AIMS Genetics · doi:10.3934/genet.2017.2.103 · Cited by 205
Kontoghiorghes, G. J., & Kontoghiorghe, C. (2020) · Cells · doi:10.3390/cells9061456 · Cited by 205
Arsenic: A Review on a Great Health Issue Worldwide
Genchi, G., Lauria, G., Catalano, A. A., Carocci, A., & Sinicropi, M. S. (2022) · Applied Sciences · doi:10.3390/app12126184 · Cited by 205
Liu, Y., Cheng, A., Li, Y.-J., Yang, Y., Kishimoto, Y., Zhang, S., Wang, Y., Wan, R., Raefsky, S. M., Lu, D., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09897-1 · Cited by 176
Arsenic-induced neurotoxicity: a mechanistic appraisal
Garza-Lombó, C., Pappa, A., Panayiotidis, M. I., Gonsebatt, M. E., & Franco, R. (2019) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-019-01740-8 · Cited by 174
Huang, Z., Zhang, Z., Zhou, C., Liu, L., & Huang, C. (2022) · MedComm · doi:10.1002/mco2.144 · Cited by 179
Flor, A. C., Wolfgeher, D., Wu, D., & Kron, S. J. (2017) · Cell Death Discovery · doi:10.1038/cddiscovery.2017.75 · Cited by 149
Zhang, H., Gong, W., Wu, S., & Perrett, S. (2022) · Cells · doi:10.3390/cells11050829 · Cited by 145
Gavia-García, G., Rosado-Pérez, J., Arista-Ugalde, T. L., Aguíñiga-Sánchez, I., Santiago‐Osorio, E., & Mendoza-Núñez, V. M. (2021) · Biology · doi:10.3390/biology10040253 · Cited by 148
Revisiting Oxidative Stress and the Use of Organic Selenium in Dairy Cow Nutrition
Surai, P. F., Kochish, I. I., Fisinin, V. I., & Juniper, D. T. (2019) · Animals · doi:10.3390/ani9070462 · Cited by 195
Oxidative stress: an evolving definition
Ji, L. L., & Yeo, D. (2021) · Faculty Reviews · doi:10.12703/r/10-13 · Cited by 121
The Chemical Reactivity of Membrane Lipids
Duché, G., & Sanderson, J. M. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00608 · Cited by 111
Changes in the blood antioxidant defense of advanced age people
Kozakiewicz, M., Kornatowski, M., Krzywińska, O., & Kędziora–Kornatowska, K. (2019) · Clinical Interventions in Aging · doi:10.2147/cia.s201250 · Cited by 100
Hydrogen Peroxide and Redox Regulation of Developments
Rampon, C., Volovitch, M., Joliot, A., & Vriz, S. (2018) · Antioxidants · doi:10.3390/antiox7110159 · Cited by 101
Godo, S., & Shimokawa, H. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.019 · Cited by 92
Nrf2 Pathway in Age-Related Neurological Disorders: Insights into MicroRNAs
Paladino, S., Conte, A., Caggiano, R., Pierantoni, G. M., & Faraonio, R. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000491465 · Cited by 92
Qin, X., Ni, L., Zhang, M., Lin, S., Zhu, J., Xiao, D., Cui, W., Zhang, T., Lin, Y., & Cai, X. (2019) · Nanoscale · doi:10.1039/c9nr07171g · Cited by 88
Modulation of redox homeostasis: A strategy to overcome cancer drug resistance
Yang, L., Zhang, X., Wang, Z., Li, B., & Zhu, H. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1156538 · Cited by 96
Oxidative stress rapidly stabilizes promoter-proximal paused Pol II across the human genome
Nilson, K. A., Lawson, C. K., Mullen, N. J., Ball, C. B., Spector, B. M., Meier, J. L., & Price, D. H. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx724 · Cited by 85
Zhuang, C., Wu, Z., Xing, C., & Miao, Z. (2017) · MedChemComm · doi:10.1039/c6md00500d · Cited by 84
Oxidative Stress and Bio-Regulation
Yoshikawa, T., & You, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063360 · Cited by 89
Sampson, N., Brunner, E., Weber, A., Puhr, M., Schäfer, G., Szyndralewiez, C., & Klocker, H. (2018) · International Journal of Cancer · doi:10.1002/ijc.31316 · Cited by 85
The Regulatory Effect of Phytochemicals on Chronic Diseases by Targeting Nrf2-ARE Signaling Pathway
He, W., Lv, C., Chen, Z., Shi, M., Zeng, C., Hou, D., & Qin, S. (2023) · Antioxidants · doi:10.3390/antiox12020236 · Cited by 79
Lochhead, J. J., Ronaldson, P. T., & Davis, T. P. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116186 · Cited by 84
Jain, S. K., Parsanathan, R., Levine, S. N., Bocchini, J. A., Holick, M. F., & Vanchiere, J. A. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.002 · Cited by 74
Inflammation and Oxidative Stress in Frailty and Metabolic Syndromes—Two Sides of the Same Coin
Dzięgielewska-Gęsiak, S., & Muc‐Wierzgoń, M. (2023) · Metabolites · doi:10.3390/metabo13040475 · Cited by 62
Lycium barbarum polysaccharides protects retinal ganglion cells against oxidative stress injury
Liu, L., Sha, X.-Y., Wu, Y.-N., Chen, M.-T., & Zhong, J.-X. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.274349 · Cited by 61
Hsp70: A Multifunctional Chaperone in Maintaining Proteostasis and Its Implications in Human Disease
Singh, M. K., Han, S., Ju, S., Ranbhise, J. S., Ha, J., Yeo, S. G., Kim, S. S., & Kang, I. (2025) · Cells · doi:10.3390/cells14070509 · Cited by 57
Kontoghiorghes, G. J., & Kontoghiorghe, C. (2019) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2019.1631284 · Cited by 57
Зенков, Н. К., Kozhin, P. M., Владимирович, Ч. А., Мартинович, Г. Г., Кандалинцева, Н. В., & Брониславовна, М. Е. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917050030 · Cited by 57
Boone, C. H. T., Grove, R. A., Adamcova, D., Seravalli, J., & Adamec, J. (2017) · Redox Biology · doi:10.1016/j.redox.2017.01.025 · Cited by 53
Zhang, H.-T., Zhang, Z., Mo, W., Hu, P., Ding, H., Liu, Y. M., Hua, Q., & He, R. (2017) · Protein & Cell · doi:10.1007/s13238-017-0403-9 · Cited by 52
Protective role of melatonin in early‐stage and end‐stage liver cirrhosis
Hu, C., Zhao, L., Tao, J., & Li, L. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14634 · Cited by 52
Fonseca, S. F., Padilha, N. B., Thurow, S., Roehrs, J. A., Savegnago, L., de Souza, M. N., Fronza, M. G., Collares, T. V., Buss, J. H., Seixas, F. K., et al. (2017) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2017.06.007 · Cited by 51
Han, L., Li, J., Li, J., Pan, C., Xiao, Y., Lan, X., & Wang, M. (2020) · Food & Function · doi:10.1039/c9fo02334h · Cited by 52
Gurunathan, S., Jeyaraj, M., Kang, M.-H., & Kim, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186792 · Cited by 49
Liu, X., Wu, L., Tong, A., Zhen, H., Han, D., Yuan, H., Li, F., Wang, C., & Fan, G. (2022) · Foods · doi:10.3390/foods11233783 · Cited by 48
Dysregulation of redox pathways in liver fibrosis
Torok, N. J. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00050.2016 · Cited by 47
Ishii, T., Warabi, E., & Mann, G. E. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.08.036 · Cited by 45
Antioxidant effects of compound walnut oil capsule in mice aging model induced by D-galactose
Zhao, H., Li, J., Zhao, J., Chen, Y., Ren, C., & Chen, Y. (2018) · Food & Nutrition Research · doi:10.29219/fnr.v62.1371 · Cited by 45
A Tale of Two Concepts: Harmonizing the Free Radical and Antagonistic Pleiotropy Theories of Aging
Golubev, A. G., Hanson, A. D., & Gladyshev, V. N. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7105 · Cited by 43
Nutrient overload, lipid peroxidation and pancreatic beta cell function
Sasson, S. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.09.003 · Cited by 40
Formation of Oxidatively Modified Lipids as the Basis for a Cellular Epilipidome
Spickett, C. M. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.602771 · Cited by 41
Pro-Aging Effects of Xanthine Oxidoreductase Products
Battelli, M. G., Bortolotti, M., Bolognesi, A., & Polito, L. (2020) · Antioxidants · doi:10.3390/antiox9090839 · Cited by 38
Sirtuin 3 (SIRT3) Pathways in Age-Related Cardiovascular and Neurodegenerative Diseases
Silaghi, C. N., Farcas, M. F., & Craciun, A. M. (2021) · Biomedicines · doi:10.3390/biomedicines9111574 · Cited by 37
Aging and atrial fibrillation: A vicious circle
Gao, P., Gao, X., Xie, B., Tse, G., & Liu, T. (2023) · International Journal of Cardiology · doi:10.1016/j.ijcard.2023.131445 · Cited by 40
Moldogazieva, N. T., Mokhosoev, I. M., Melnikova, T. I., Zavadskiy, S. P., Kuzmenko, A. N., & Terentiev, A. A. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920140047 · Cited by 35
Kaga, Y., Kuda, T., Taniguchi, M., Yamaguchi, Y., Takenaka, H., Takahashi, H., & Kimura, B. (2020) · LWT · doi:10.1016/j.lwt.2020.110029 · Cited by 35
Qiu, Y., Ai, P., Song, J., Liu, C., & Li, Z. (2017) · Journal of Medicinal Food · doi:10.1089/jmf.2016.3870 · Cited by 35
Effect of Omega-3 Fatty Acids on Telomeres—Are They the Elixir of Youth?
Ogłuszka, M., Lipiński, P., & Starzyński, R. R. (2022) · Nutrients · doi:10.3390/nu14183723 · Cited by 36
Cysteine Modifications in the Pathogenesis of ALS
Valle, C., & Carrì, M. T. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00005 · Cited by 32
Markiewicz, E., & Idowu, O. C. (2019) · Open Biology · doi:10.1098/rsob.190208 · Cited by 32
Dawes, I. W., & Perrone, G. G. (2019) · FEMS Yeast Research · doi:10.1093/femsyr/foz085 · Cited by 33
Antioxidants and Prooxidants: Effects on Health and Aging
Carocho, M., Ferreira, I. C. F. R., Morales, P., & Sokóvić, M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1472708 · Cited by 31
Melatonin to Rescue the Aged Heart: Antiarrhythmic and Antioxidant Benefits
Segovia‐Roldán, M., Diez, E. R., & Pueyo, E. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8876792 · Cited by 34
Oxidation and Inflammation in the Immune and Nervous Systems, a Link Between Aging and Anxiety
la Fuente, M. D. (2018) · Springer eBooks · doi:10.1007/978-3-319-64597-1_115-1 · Cited by 27
Martinez‐Canton, M., Galván-Álvarez, V., Martín-Rincón, M., Calbet, J. A. L., & Gallego-Selles, Á. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.08.011 · Cited by 29
Zhuang, J., Jiang, Z., Chen, D., Li, J., Crabbe, M. J. C., Qiu, M., Zheng, Y., & Qu, W. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.2c08627 · Cited by 30
NADPH Oxidases and Their Roles in Skin Homeostasis and Carcinogenesis
Rudolf, J., Raad, H., Taı̈eb, A., & Rezvani, H. R. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7282 · Cited by 28
Watson, M. A., Wong, H. S., & Brand, M. D. (2019) · Biochemical Society Transactions · doi:10.1042/bst20190305 · Cited by 27
Effect of yellow rice wine on anti-aging ability in aged mice induced by d-galactose
Liu, R., Fu, Z., Zhang, F., Mao, Q., Luan, C., Han, X., Xue, J., Wang, D., Qin, S., & Hao, F. (2020) · Food Science and Human Wellness · doi:10.1016/j.fshw.2020.02.003 · Cited by 25
Li, N., Lv, S., Ma, Y., Liu, N., Wang, S., & Zhou, D. (2020) · International Journal of Food Properties · doi:10.1080/10942912.2020.1807565 · Cited by 25
Percio, A., Cicchinelli, M., Masci, D., Summo, M., Urbani, A., & Greco, V. (2024) · Antioxidants · doi:10.3390/antiox13080883 · Cited by 24
Khan, I. M., Gul, H., Khan, S., Nassar, N., Khalid, A., Swelum, A. A., & Wang, Z. (2025) · Poultry Science · doi:10.1016/j.psj.2025.105071 · Cited by 30
Kontoghiorghes, G. J. (2023) · Pharmaceuticals · doi:10.3390/ph16071016 · Cited by 27
Jabůrek, M., Průchová, P., Holendová, B., Galkin, A. S., & Ježek, P. (2021) · Antioxidants · doi:10.3390/antiox10050678 · Cited by 24
Pharmacotherapeutic potential of pomegranate in age-related neurological disorders
Kazemabad, M. J. E., Toni, S. A., Tizro, N., Dadkhah, P. A., Amani, H., Rezayat, S. A., Sheikh, Z., Mohammadi, M., Alijanzadeh, D., Alimohammadi, F., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.955735 · Cited by 25
Shear Stress and ROS Dual-Responsive RBC-Hitchhiking Nanoparticles for Atherosclerosis Therapy
Shen, M., Jiang, H., Zhao, Y., Wu, L., Yang, H., Yao, Y., Meng, H., Yang, Q., Liu, L., & Li, Y. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c07371 · Cited by 23
New opportunities for antioxidants in amelioration of neurodegenerative diseases
Bhandari, U. R., Danish, S. M., Ahmad, S., Ikram, M., Nadaf, A., Hasan, N., Kesharwani, P., & Ahmad, F. J. (2024) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2024.111961 · Cited by 24
Santos, I. B. D. S., dos Santos, B. S., de Oliveira, J. R. S., Costa, W. K., Zagmignan, A., da Silva, L. C. N., Ferreira, M. R. A., Lermen, V. L., Lermen, M. S. B. D. S., da Silva, A. G., et al. (2020) · Advances in Pharmacological and Pharmaceutical Sciences · doi:10.1155/2020/1258707 · Cited by 25
de Oliveira, M. R., Peres, A., & Ferreira, G. C. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2140-5 · Cited by 21
Saryono, S., Rahmawati, E., Proverawati, A., & Hisni, D. (2017) · Pakistan Journal of Nutrition · doi:10.3923/pjn.2017.477.481 · Cited by 21
Casella, D., Palumbo, P., Sandroni, S., Caponi, C., Littori, F., Capuano, F., Grimaldi, L., Marcasciano, M., & Cuomo, R. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm11010126 · Cited by 20
Elzainy, A., Sadik, A. E., & Altowayan, W. M. (2024) · Biomolecules · doi:10.3390/biom14030297 · Cited by 19
Approaches for extending human healthspan: from antioxidants to healthspan pharmacology
Gruber, J., & Halliwell, B. B. (2017) · Essays in Biochemistry · doi:10.1042/ebc20160091 · Cited by 20
He, S., Yu, M., Sun, H., Zhang, Z., Zhu, Y., Zhao, J., Tang, M., & Cao, Y. (2018) · Food and Chemical Toxicology · doi:10.1016/j.fct.2018.12.045 · Cited by 19
Attanzio, A., Restivo, I., Tutone, M., Tesoriere, L., Allegra, M., & Livrea, M. A. (2022) · Antioxidants · doi:10.3390/antiox11122364 · Cited by 20
Fiorani, M., Guidarelli, A., Capellacci, V., Cerioni, L., Crinelli, R., & Cantoni, O. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.03.008 · Cited by 18
Bortoluzzi, V. T., Filho, C. S. D., & Wannmacher, C. M. D. (2021) · Metabolic Brain Disease · doi:10.1007/s11011-021-00676-w · Cited by 17
Lemos, C. N., da Silva, L. E. C. M., Faustino, J., Fantucci, M. Z., Murashima, A. D. A. B., Adriano, L., Alves, M., & Rocha, E. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.824726 · Cited by 17
Cell type-specific differences in redox regulation and proliferation after low UVA doses
Ciesielska, S., Bil, P., Gajda, K., Poterała-Hejmo, A., Hudy, D., & Rzeszowska‐Wolny, J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0205215 · Cited by 18
Ricciarelli, R., Azzi, A., & Zingg, J.-M. A. (2020) · BioFactors · doi:10.1002/biof.1636 · Cited by 17
Cuyúl-Vásquez, I., Berríos-Contreras, L., Soto-Fuentes, S., Hunter-Echeverría, K., & Marzuca-Nassr, G. N. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.111012 · Cited by 17
Bai, D., Wang, Z., Xiao, Y., Liu, T., Pu, Y., Sun, H., Wang, M., Guo, C., & Zhang, J. (2024) · Biomaterials Advances · doi:10.1016/j.bioadv.2024.213965 · Cited by 19
Zhang, X., Wang, D.-S., Li, X., Miao, Y.-C., Gao, J., & Zhang, Q. (2023) · Industrial Crops and Products · doi:10.1016/j.indcrop.2023.117207 · Cited by 16
Mutations of the Electron Transport Chain Affect Lifespan and ROS Levels in C. elegans
Ősz, F., Nazir, A., Takács‐Vellai, K., & Farkas, Z. (2025) · Antioxidants · doi:10.3390/antiox14010076 · Cited by 17
Xin, C., Jia, P.-H., Zhao, Y., Cheng, Z., Liu, W., Di, P., Li, W., & Zhu, H. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.139809 · Cited by 16
Wang, J., & Konishi, T. (2018) · Cancer Science · doi:10.1111/cas.13916 · Cited by 17
Alshammari, G. M., Balakrishnan, A., & Chinnasamy, T. (2017) · Inflammation Research · doi:10.1007/s00011-017-1054-2 · Cited by 16
Cardiac Aging – Benefits of Exercise, Nrf2 Activation and Antioxidant Signaling
Narasimhan, M., & Rajasekaran, N. S. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-4307-9_13 · Cited by 17
Fructose-mediated AGE-RAGE axis: approaches for mild modulation
Semchyshyn, H. M. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1500375 · Cited by 15
Metadata
- Authors
- Forman, H. J.
- Affiliations
- University of Southern California (US)
- Corresponding author
- Forman, Henry Jay
- ORCID
- Forman, Henry Jay
- Venue
- Free Radical Biology and Medicine
- Publisher
- Elsevier BV
- Published
- 2016-08
- Volume
- 97
- Pages
- 398-407
- ISSN
- 0891-5849 (ISSN-L)
- PMC
- PMC4996735
- OpenAlex
- W2417395786
- Cited by
- 172
- References
- 121
- Citations by year
- 2026: 7 · 2025: 15 · 2024: 18 · 2023: 15 · 2022: 19 · 2021: 13 · 2020: 19 · 2019: 17 · 2018: 16 · 2017: 27 · 2016: 6
- FWCI
- 1.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Free Radical Biology and Medicine (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- NIH (ES023864)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Keywords
- redox signaling, redox biology, free radicals, superoxide dismutase, hydrogen peroxide, NADPH oxidase, hydroperoxides, electrophiles, lipid peroxidation, signal transduction, transcription factor regulation, aging, redox homeostasis
- MeSH terms
- Animals, Free Radicals, Gene Expression Regulation, Homeostasis, Humans, Lipid Peroxidation, Signal Transduction, Oxidative Stress
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review