Reactive Oxygen Species in Metabolic and Inflammatory Signaling

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351

How mitochondria produce reactive oxygen species

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

Autophagy in the Pathogenesis of Disease

Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069

The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology

Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989

Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal

Ayala, A., Muñoz, M., & Argüelles, S. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/360438 · Cited by 6,837

Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance

Xu, H., Barnes, G. T., Yang, Q., Tan, G., Yang, D., Chou, C. J., Sole, J., Nichols, A., Ross, J. S., Tartaglia, L. A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319451 · Cited by 6,760

Anti-Inflammatory and Antioxidative Potential of Aloe vera on the Cartap and Malathion Mediated Toxicity in Wistar Rats

Gupta, V. K., Kumar, A., Pereira, M. D. L., Siddiqi, N. J., & Sharma, B. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17145177 · Cited by 36

Antioxidant, anti-alzheimer, anti-diabetic, and anti-inflammatory activities of the endemic halophyte Limonium spathulatum (Desf.) kuntze on LPS-stimulated RAW264 macrophages

Mazouz, W., Haouli, N. E. H., Gali, L., Vezza, T., Bensouıcı, C., Mebrek, S., Hamel, T., Gálvez, J., & Djeddi, S. (2020) · South African Journal of Botany · doi:10.1016/j.sajb.2020.08.021 · Cited by 35

Meta-analysis of In Vitro Drug-Release Parameters Reveals Predictable and Robust Kinetics for Redox-Responsive Drug-Conjugated Therapeutic Nanogels

Morgulchik, N., & Kamaly, N. (2021) · ACS Applied Nano Materials · doi:10.1021/acsanm.1c00170 · Cited by 35

Redox regulation of DUBs and its therapeutic implications in cancer

Tyagi, A., Haq, S., & Ramakrishna, S. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102194 · Cited by 35

The Intestinal Redox System and Its Significance in Chemotherapy‐Induced Intestinal Mucositis

Yu, Q., Zhang, H., Guo, Y., Han, B., & Jiang, P. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/7255497 · Cited by 36

Therapeutic strategies for liver diseases based on redox control systems

Lee, J., Kim, J., Lee, R., Lee, E., Choi, T. G., Lee, A. S., Yoon, Y., Park, G., Namgoong, J., Lee, S., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113764 · Cited by 37

Effects of Valproate Monotherapy on the Oxidant‐Antioxidant Status in Mexican Epileptic Children: A Longitudinal Study

Beltrán-Sarmiento, E., Arregoitia-Sarabia, C. K., Floriano-Sánchez, E., Sandoval‐Pacheco, R., Galván-Hernández, D. E., Coballase-Urrutía, E., Carmona‐Aparicio, L., Ramos-Reyna, E., Rodríguez‐Silverio, J., & Cárdenas‐Rodríguez, N. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/7954371 · Cited by 35

Succinylation modification: a potential therapeutic target in stroke

Lian, J., Liu, W., Hu, Q., & Zhang, X. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.382229 · Cited by 36

Ultrasmall Cu2O@His Nanozymes with RONS Scavenging Capability for Anti-inflammatory Therapy

Li, S., Chen, Z., Wang, M., Yang, F., Zhang, S., Qiao, C., Chu, W., & Yue, W. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c15083 · Cited by 34

A Systematic Review of Proteomics in Obesity: Unpacking the Molecular Puzzle

Rodríguez-Muñoz, A., Rad, H. M., Martín-Chaves, L., Benítez‐Porres, J., Rodríguez‐Capitán, J., Gonzalez-Jimenez, A., Insenser, M. R., Tinahones, F. J., & Murri, M. (2024) · Current Obesity Reports · doi:10.1007/s13679-024-00561-4 · Cited by 34

Engineering extracellular vesicles for ROS scavenging and tissue regeneration

Dayem, A. A., Yan, E., Do, M., Kim, Y., Lee, Y. K., Cho, S., & Kim, D. (2024) · Nano Convergence · doi:10.1186/s40580-024-00430-9 · Cited by 34

The role of reactive oxygen species in severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) infection-induced cell death

Xie, J., Yuan, C., Yang, S., Ma, Z., Li, W., Mao, L., Jiao, P., & Liu, W. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-024-00659-6 · Cited by 41

Reductive stress: The key pathway in metabolic disorders induced by overnutrition

Zhang, S., Wang, N., Gao, Z., Gao, Z., Wang, X., Xie, H., Wang, C.-Y., & Zhang, S. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.01.012 · Cited by 40

Oral administration of Momordica charantia-derived extracellular vesicles alleviates ulcerative colitis through comprehensive renovation of the intestinal microenvironment

Gao, B., Huang, X., Fu, J., Chen, L., Deng, Z., Wang, S.-H., Zhu, Y., Xu, C., Zhang, Y., Zhang, M., et al. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03346-6 · Cited by 35

Vanadium Derivative Exposure Promotes Functional Alterations of VSMCs and Consequent Atherosclerosis via ROS/p38/NF-κB-Mediated IL-6 Production

Yeh, C.-C., Wu, J.-Y., Lee, G.-L., Wen, H.-T., Lin, P., & Kuo, C.-C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246115 · Cited by 34

The roles of microRNA in redox metabolism and exercise-mediated adaptation

Torma, F., Gombos, Z., Jókai, M., Berkes, I., Takeda, M., Mimura, T., Radak, Z. O., & Győri, F. J. (2020) · Journal of sport and health science/Journal of Sport and Health Science · doi:10.1016/j.jshs.2020.03.004 · Cited by 37

Antioxidant Effect of Standardized Extract of Propolis (EPP‐AF®) in Healthy Volunteers: A “Before and After” Clinical Study

Diniz, D. P., Lorencini, D. A., Berretta, A. A., Cintra, M., Lia, É. N., Jordão, A. A., & Coelho, E. B. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/7538232 · Cited by 34

The Role Played by Mitochondria in FcεRI-Dependent Mast Cell Activation

Chelombitko, M. A., Chernyak, B. V., Fedorov, A. V., Zinovkin, R. A., Razin, E., & Paruchuru, L. B. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.584210 · Cited by 35

Inhibition of mitochondrial reactive oxygen species improves coronary endothelial function after cardioplegic hypoxia/reoxygenation

Song, Y., Xing, H., He, Y., Zhang, Z., Shi, G., Su, W., Liu, Y., Harrington, E. O., Sellke, F. W., & Feng, J. (2021) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2021.06.029 · Cited by 34

Innate Immunity: A Balance between Disease and Adaption to Stress

Faenza, I., & Blalock, W. L. (2022) · Biomolecules · doi:10.3390/biom12050737 · Cited by 34

The role of immune-mediated alterations and disorders in ALS disease

Rodrigues Lima-Junior, J., Sulzer, D., Lindestam Arlehamn, C. S., & Sette, A. (2021) · Human Immunology · doi:10.1016/j.humimm.2021.01.017 · Cited by 33

Inhibition of NADPH Oxidases Prevents the Development of Osteoarthritis

Han, J., Park, D., Park, J. Y., & Han, S. W. (2022) · Antioxidants · doi:10.3390/antiox11122346 · Cited by 33

Role of Perilipins in Oxidative Stress—Implications for Cardiovascular Disease

Cinato, M., Andersson, L. K., Miljanovic, A., Laudette, M., Kunduzova, O., Borén, J., & Levin, M. C. (2024) · Antioxidants · doi:10.3390/antiox13020209 · Cited by 33

Role of reactive oxygen species in myelodysplastic syndromes

Jing, Q., Zhou, C., Zhang, J., Zhang, P., Wu, Y., Zhou, J., Tong, X., Li, Y., Du, J., & Wang, Y. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-024-00570-0 · Cited by 33

The Role of Nrf2 in the Regulation of Mitochondrial Function and Ferroptosis in Pancreatic Cancer

Baiskhanova, D. M., & Schäfer, H. (2024) · Antioxidants · doi:10.3390/antiox13060696 · Cited by 35

The role of oxidative stress in aortic dissection: a potential therapeutic target

Xu, S., Han, X., Wang, X., Yu, Y., Qu, C., Liu, X., & Yang, B. (2024) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2024.1410477 · Cited by 36

Dynamics of intracellular and intercellular redox communication

Sies, H. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.11.002 · Cited by 35

Pexophagy and Oxidative Stress: Focus on Peroxisomal Proteins and Reactive Oxygen Species (ROS) Signaling Pathways

Wei, X., Manandhar, L., Kim, H., Chhetri, A., Hwang, J., Jang, G., Park, C., & Park, R. (2025) · Antioxidants · doi:10.3390/antiox14020126 · Cited by 39

Self‐Healing Hydrogel Dressing with Solubilized Flavonoids for Whole Layer Regeneration of Diabetic Wound

Zeng, Q., Du, S., Yuan, R., Zeng, Y., Li, X., Wu, Y., Chen, K., Tao, L., Tang, Z., & Deng, X. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202500734 · Cited by 34

Endothelial Dysfunction in Cardiovascular Diseases

Biswas, I., & Khan, G. A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.89365 · Cited by 33

Light-Triggered Electron Transfer between a Conjugated Polymer and Cytochrome C for Optical Modulation of Redox Signaling

Aziz, I. A., Malferrari, M., Roggiani, F., Tullii, G., Rapino, S., & Antognazza, M. R. (2020) · iScience · doi:10.1016/j.isci.2020.101091 · Cited by 33

Energetic, antioxidant, inflammatory and cell death responses in the red muscle of thermally stressed Sparus aurata

Feidantsis, K. G., Georgoulis, I., Zachariou, A., Campaz, B., Christoforou, M., Pörtner, H., & Michaelidis, B. (2020) · Journal of Comparative Physiology B · doi:10.1007/s00360-020-01278-1 · Cited by 33

Time-Dependent Indirect Antioxidative Effects of Oat Beta-Glucans on Peripheral Blood Parameters in the Animal Model of Colon Inflammation

Kopiasz, Ł., Dziendzikowska, K., Gajewska, M., Wilczak, J., Harasym, J., Żyła, E., Kamola, D., Oczkowski, M., Królikowski, T., & Gromadzka-Ostrowska, J. (2020) · Antioxidants · doi:10.3390/antiox9050375 · Cited by 33

Post-transcriptional air pollution oxidation to the cholesterol biosynthesis pathway promotes pulmonary stress phenotypes

Gonzalez‐Rivera, J. C., Baldridge, K. C., Wang, D., Patel, K., Chuvalo-Abraham, J. C. L., Ruiz, L. H., & Contreras, L. M. (2020) · Communications Biology · doi:10.1038/s42003-020-01118-6 · Cited by 35

Signaling Integration of Hydrogen Sulfide and Iron on Cellular Functions

Arif, H. M., Qian, Z., & Wang, R. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0203 · Cited by 33

4‐Octyl Itaconate Prevents Free Fatty Acid‐Induced Lipid Metabolism Disorder through Activating Nrf2‐AMPK Signaling Pathway in Hepatocytes

Chu, X., Li, L., Yan, W., & Ma, H. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/5180242 · Cited by 33

Arterial stiffness and atrial fibrillation: A review

Lage, J. G. B., Bortolotto, A. L., Scanavacca, M., Bortolotto, L. A., & Darrieux, F. (2022) · Clinics · doi:10.1016/j.clinsp.2022.100014 · Cited by 33

Enzymatic Depletion of Mitochondrial Inorganic Polyphosphate (polyP) Increases the Generation of Reactive Oxygen Species (ROS) and the Activity of the Pentose Phosphate Pathway (PPP) in Mammalian Cells

Hambardikar, V. D., Guitart‐Mampel, M., Scoma, E. R., Urquiza, P., Gowda, G. A. N., Raftery, D., Collins, J. A., & Solesio, M. E. (2022) · Antioxidants · doi:10.3390/antiox11040685 · Cited by 33

Good bacteria, oxidative stress and neurological disorders: Possible therapeutical considerations

Soheili, M., Alinaghipour, A., & Salami, M. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120605 · Cited by 33

Extract of Jasminum grandiflorum L. alleviates CCl4-induced liver injury by decreasing inflammation, oxidative stress and hepatic CYP2E1 expression in mice

Sun, L., Zhang, Y., Wen, S., Li, Q., Chen, R., Lai, X., Zhang, Z., Zhou, Z., Xie, Y., Zheng, X., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113255 · Cited by 33

Molecular mechanisms of endothelial dysfunction in coronary microcirculation dysfunction

Zhang, Z., Li, X., He, J., Wang, S., Wang, J., Liu, J., & Wang, Y. (2023) · Journal of Thrombosis and Thrombolysis · doi:10.1007/s11239-023-02862-2 · Cited by 33

Novel Anti-Inflammatory Therapies in Coronary Artery Disease and Acute Coronary Syndromes

Dimitroglou, Y., Aggeli, C., Theofilis, P., Tsioufis, P., Oikonomou, E. K., Chasikidis, C., Tsioufis, K. P., & Tousoulis, D. (2023) · Life · doi:10.3390/life13081669 · Cited by 35

Alleviation of tributyltin-induced toxicity by diet and microplastics in the marine rotifer Brachionus koreanus

Yoon, D.-S., Lee, Y., Park, J. C., Lee, M., & Lee, J. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.123739 · Cited by 33

Improvement of the optical, photocatalytic and antibacterial properties of ZnO semiconductor nanoparticles using different pepper aqueous extracts

Villegas-Fuentes, A., la Torre, A. R.-D., Vilchis-Nestor, A. R., & Luque, P. A. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.139577 · Cited by 32

Histone deacetylase 3-specific inhibitor RGFP966 attenuates oxidative stress and inflammation after traumatic brain injury by activating the Nrf2 pathway

Xu, L., An, T., Jia, B., Wu, Q., Shen, J., Jin, J., Liu, J., & Li, C. (2023) · Burns & Trauma · doi:10.1093/burnst/tkad062 · Cited by 32

Oocytes maintain low ROS levels to support the dormancy of primordial follicles

Qin, S., Chi, X., Zhu, Z., Chen, C., Zhang, T., He, M., Gao, M., Zhao, T., Zhang, J., Zhang, L., et al. (2024) · Aging Cell · doi:10.1111/acel.14338 · Cited by 32

Mitochondrial bioenergetics dysfunction in T2DM: linking oxidative stress to insulin resistance

Feng, Z., Tan, Z., & Lu, D. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1674477 · Cited by 32

Kynurenines and the Endocannabinoid System in Schizophrenia: Common Points and Potential Interactions

Zádor, F., Nagy-Grócz, G., Kékesi, G., Dvorácskó, S., Szűcs, E., Tömböly, C., Horváth, G., Benyhe, S., & Vécsei, L. (2019) · Molecules · doi:10.3390/molecules24203709 · Cited by 33

Combinatory effects of cereulide and deoxynivalenol on in vitro cell viability and inflammation of human Caco-2 cells

Beisl, J., Pahlke, G., Abeln, H., Ehling‐Schulz, M., Favero, G. D., Varga, E., Warth, B., Sulyok, M., Abia, W. A., Ezekiel, C. N., et al. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02658-w · Cited by 32

Resuscitating the Globally Ischemic Brain: TTM and Beyond

Hosseini, M., Wilson, R. H., Crouzet, C., Amirhekmat, A., Wei, K. S., & Akbari, Y. (2020) · Neurotherapeutics · doi:10.1007/s13311-020-00856-z · Cited by 33

Effects of REDOX in Regulating and Treatment of Metabolic and Inflammatory Cardiovascular Diseases

Wang, K., Dong, Y., Liu, J., Qian, L., Wang, T., Gao, X., Wang, K., & Zhou, L. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5860356 · Cited by 34

Conjugate between hydrolyzed collagen from defatted seabass skin and epigallocatechin gallate (EGCG): characteristics, antioxidant activity and in vitro cellular bioactivity

Chotphruethipong, L., Sukketsiri, W., Battino, M. A., & Benjakul, S. (2021) · RSC Advances · doi:10.1039/d0ra07135h · Cited by 32

The Role of Micronutrients to Support Immunity for COVID-19 Prevention

Ahmed, M. H., Hassan, A., & Molnár, J. (2021) · Revista Brasileira de Farmacognosia · doi:10.1007/s43450-021-00179-w · Cited by 33

Engineering chitosan nano-cocktail containing iron oxide and ceria: A two-in-one approach for treatment of inflammatory diseases and tracking of material delivery

Wu, Y., Cowin, G., Moonshi, S. S., Nguyen, D. H. T., Fithri, N. A., Whittaker, A. K., Zhang, R., & Ta, H. T. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.112477 · Cited by 32

Dimethyl phthalate induces blood immunotoxicity through oxidative damage and caspase-dependent apoptosis

Chi, Z., Lin, H., Wang, X., Meng, X., Zhou, J., Xiang, L., Cao, G., Wu, P., Cai, Z., & Zhao, X. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.156047 · Cited by 32

Neurobiological mechanisms of mood disorders: Stress vulnerability and resilience

Pereira, C. M., Castro, F. C. D. A. Q., Barcelos, R. M., Chiepe, K. C. M. B., Rossoni, J. V., Ambrósio, R. P., Chiarelli-Neto, O., & Pesarico, A. P. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1006836 · Cited by 36

Growth Hormone–Releasing Hormone in Endothelial Inflammation

Barabutis, N., Akhter, M. S., Kubra, K., & Jackson, K. E. (2022) · Endocrinology · doi:10.1210/endocr/bqac209 · Cited by 32

Anti-biofilm and bystander effects of antimicrobial photo-sonodynamic therapy against polymicrobial periopathogenic biofilms formed on coated orthodontic mini-screws with zinc oxide nanoparticles

Bahrami, R., Pourhajibagher, M., Parker, S. P. A., Esmaeili, D., & Bahador, A. (2023) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2023.103288 · Cited by 32

Bimetallic Metal–Organic Framework for Mitigating Aseptic Osteolysis

Pan, H., Miao, X., Deng, J., Pan, C., Cheng, X., & Wang, X. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c19449 · Cited by 32

Oxidative Stress in Muscle Diseases: Current and Future Therapy

Serra, A. J., Prokić, M. D., Vasconsuelo, A., & Pinto, J. R. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6439138 · Cited by 32

Effects and Mechanisms of Non-Thermal Plasma-Mediated ROS and Its Applications in Animal Husbandry and Biomedicine

Yang, Y., Wang, Y., Wei, S., Wang, X., & Zhang, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115889 · Cited by 32

Controlling pyroptosis through post-translational modifications of gasdermin D

Zhang, N., & Xu, D. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.02.005 · Cited by 33

Recent progress in ROS-responsive biomaterials for the diagnosis and treatment of cardiovascular diseases

Yuan, Z., Li, Y., Sun, M., Yuan, M., Han, Z., Li, X., Liu, S., Sun, Y., Cao, J., & Fan, L. (2025) · Theranostics · doi:10.7150/thno.106991 · Cited by 33

Salvia miltiorrhiza bunge exerts anti-oxidative effects through inhibiting KLF10 expression in vascular smooth muscle cells exposed to high glucose

Zhou, J., Zhang, L., Zheng, B., Zhang, L., Qin, Y., Zhang, X., Yang, Z., Nie, Z.-Y., Yang, G., Yu, J. Q., et al. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113208 · Cited by 31

Biomolecules and Electrochemical Tools in Chronic Non-Communicable Disease Surveillance: A Systematic Review

de Morais, A. L. F., Rijo, P. M., Batanero, B., & Nicolai, M. (2020) · Biosensors · doi:10.3390/bios10090121 · Cited by 32

Toxicogenicity and mechanistic pathways of aflatoxin B1 induced renal injury

Dlamini, N. Z., Somboro, A. M., Amoako, D. G., Arhin, I., Khumalo, H. M., & Khan, R. B. (2021) · Environmental Toxicology · doi:10.1002/tox.23306 · Cited by 31

The effect of lactoferrin in aging: role and potential

Li, B., Zhang, B., Liu, X., Zheng, Y., Han, K., Liu, H., Wu, C., Li, J., Fan, S., Peng, W., et al. (2021) · Food & Function · doi:10.1039/d1fo02750f · Cited by 32

Thyroid hormone-dependent regulation of metabolism and heart regeneration

Ross, I., Omengan, D. B., Huang, G. N., & Payumo, A. Y. (2021) · Journal of Endocrinology · doi:10.1530/joe-21-0335 · Cited by 32

A sensitive colori/fluorimetric nanoprobe for detection of polyphenols using peroxidase-mimic plasma-modified MoO3 nanoparticles

Rashtbari, S., Dehghan, G., Amini, M., Khorram, S., & Khataee, A. (2022) · Chemosphere · doi:10.1016/j.chemosphere.2022.133747 · Cited by 31

A vicious circle in breast cancer: The interplay between inflammation, reactive oxygen species, and microRNAs

Villarreal‐García, V., Estupiñan‐Jiménez, J. R., Vivas‐Mejía, P. E., González-Villasana, V., Vázquez-Guillén, J. M., & Reséndez‐Pérez, D. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.980694 · Cited by 32

Quercetin Prevents Intestinal Stem Cell Aging via Scavenging ROS and Inhibiting Insulin Signaling in Drosophila

Yan, L., Guo, X., Zhou, J., Zhu, Y., Zhang, Z., & Chen, H. (2022) · Antioxidants · doi:10.3390/antiox12010059 · Cited by 32

Effects of L-Carnitine Intake on Exercise-Induced Muscle Damage and Oxidative Stress: A Narrative Scoping Review

Caballero-García, A., Noriega, D. C., Roche, E., Drobnic, F., & Córdova, A. (2023) · Nutrients · doi:10.3390/nu15112587 · Cited by 34

Mesenchymal stem cells alleviate hypoxia-induced oxidative stress and enhance the pro-survival pathways in porcine islets

Tan, Y., Nie, W., Chen, C., He, X., Xu, Y., Ma, X., Zhang, J., Tan, M., Rong, P., & Wang, W. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219844472 · Cited by 31

Self‐Mineralizing Dnazyme Hydrogel as a Multifaceted Bone Microenvironment Amendment for Promoting Osteogenesis in Osteoporosis

Wu, H., Huang, S., Zhu, Y., Li, J., Pang, X., Tang, Y., Li, S., Ji, P., Ding, S., Cheng, W., et al. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202212669 · Cited by 30

Modulation of neuroinflammation and oxidative stress by targeting GPR55 – new approaches in the treatment of psychiatric disorders

Apweiler, M., Saliba, S. W., Sun, L., Streyczek, J., Normann, C., Hellwig, S., Bräse, S., & Fiebich, B. L. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02614-5 · Cited by 31

Danhong Injection Alleviates Postoperative Intra-abdominal Adhesion in a Rat Model

Wu, Y., Wei, G., Yu, J., Chen, Z., Xu, Z., Shen, R., Liang, T., Zheng, L., Wang, K., Sun, X., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4591384 · Cited by 30

Surface modification of silver nanoparticle (AgNP) by liposomal encapsulation mitigates AgNP-induced inflammation

Yusuf, A., & Casey, A. (2019) · Toxicology in Vitro · doi:10.1016/j.tiv.2019.104641 · Cited by 30

Dicarbonyl Stress and S-Glutathionylation in Cerebrovascular Diseases: A Focus on Cerebral Cavernous Malformations

Antognelli, C., Perrelli, A., Armeni, T., Talesa, V. N., & Retta, S. F. (2020) · Antioxidants · doi:10.3390/antiox9020124 · Cited by 30

Antioxidant and Anti-Inflammatory Effects of NCW Peptide from Clam Worm ( Marphysa sanguinea )

Park, Y. R., Park, C., & Soh, Y. (2020) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2003.03050 · Cited by 31

Psidium guajava Linn leaf ethanolic extract: In vivo giardicidal potential with ultrastructural damage, anti-inflammatory and antioxidant effects

Khedr, S. I., Mokhamer, E.-H. M., Hassan, A. A., El-Feki, A. S., El‐Khodary, G. M., & El-Gerbed, M. S. A. (2020) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2020.10.026 · Cited by 30

Use of Network Pharmacology to Explore the Mechanism of Gegen (Puerariae lobatae Radix) in the Treatment of Type 2 Diabetes Mellitus Associated with Hyperlipidemia

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