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Hypercholesterolemia-Induced Erectile Dysfunction: Endothelial Nitric Oxide Synthase (eNOS) Uncoupling in the Mouse Penis by NAD(P)H Oxidase

Musicki, B., Liu, T., Lagoda, G. A., Strong, T. D., Sezen, S. F., Johnson, J. M., & Burnett, A. L. “. (2010) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2010.01880.x · Cited by 114 · see citing works

The Advanced Lipoxidation End-Product Malondialdehyde-Lysine in Aging and Longevity

Jové, M., Mota‐Martorell, N., Pradas, I., Martin‐Garí, M., Ayala, V., & Pamplona, R. (2020) · Antioxidants · doi:10.3390/antiox9111132 · Cited by 115 · see citing works

Mitochondrial respiratory chain dysfunction variably increases oxidant stress in Caenorhabditis elegans

Dingley, S. D., Polyák, E., Lightfoot, R. T., Ostrovsky, J., Rao, M., Greco, T. M., Ischiropoulos, H., & Falk, M. J. (2009) · Mitochondrion · doi:10.1016/j.mito.2009.11.003 · Cited by 115 · see citing works

The Multifaceted Regulation of Mitochondria in Ferroptosis

Wu, H., Wang, F., Ta, N., Zhang, T., & Gao, W. (2021) · Life · doi:10.3390/life11030222 · Cited by 111 · see citing works

Differential responses to copper-induced oxidative stress in the marine macroalgae Lessonia nigrescens and Scytosiphon lomentaria (Phaeophyceae)

Porcia, L. C., Mella–Flores, D., Moenne, A., & Correa, J. A. (2009) · Aquatic Toxicology · doi:10.1016/j.aquatox.2009.06.004 · Cited by 111 · see citing works

Obesity in a model of gpx4 haploinsufficiency uncovers a causal role for lipid-derived aldehydes in human metabolic disease and cardiomyopathy

Katunga, L. A., Gudimella, P., Efird, J. T., Abernathy, S., Mattox, T. A., Beatty, C., Darden, T. M., Thayne, K. A., Alwair, H., Kypson, A. P., et al. (2015) · Molecular Metabolism · doi:10.1016/j.molmet.2015.04.001 · Cited by 111 · see citing works

Iron oxide nanoparticles induced cytotoxicity, oxidative stress and DNA damage in lymphocytes

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Inflammation-related gene expression by lipid oxidation-derived products in the progression of atherosclerosis

Leonarduzzi, G., Gamba, P., Gargiulo, S., Biasi, F., & Poli, G. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.09.031 · Cited by 110 · see citing works

Membrane lipid unsaturation as physiological adaptation to animal longevity

Naudí, A., Jové, M., Ayala, V., Portero‐Otín, M., Barja, G., & Pamplona, R. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00372 · Cited by 107 · see citing works

Oxidative damage in synovial tissue is associated with in vivo hypoxic status in the arthritic joint

Biniecka, M., Kennedy, A., Fearon, U., Ng, C. T., Veale, D. J., & O'Sullivan, J. N. (2009) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2009.111211 · Cited by 108 · see citing works

Diet and cognition

Gómez‐Pinilla, F., & Tyagi, E. (2013) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328365aae3 · Cited by 110 · see citing works

Does oxidative stress contribute to the pathology of Friedreich's ataxia? A radical question

Armstrong, J. S., Khdour, O., & Hecht, S. M. (2010) · The FASEB Journal · doi:10.1096/fj.09-143222 · Cited by 107 · see citing works

F2-isoprostane formation, measurement and interpretation: The role of exercise

Nikolaidis, M. G., Kyparos, A., & Vrabas, I. S. (2010) · Progress in Lipid Research · doi:10.1016/j.plipres.2010.10.002 · Cited by 106 · see citing works

A novel fluorescent probe with high sensitivity and selective detection of lipid hydroperoxides in cells

Yamanaka, K., Saito, Y., Sakiyama, J., Ohuchi, Y., Oseto, F., & Noguchi, N. (2012) · RSC Advances · doi:10.1039/c2ra20816d · Cited by 107 · see citing works

Lipoic acid mitigates bisphenol A-induced testicular mitochondrial toxicity in rats

El-Beshbishy, H. A., Aly, H. A. A., & Elshafey, M. M. (2012) · Toxicology and Industrial Health · doi:10.1177/0748233712446728 · Cited by 103 · see citing works

A Zn‐Doped CuO Nanocomposite Shows Enhanced Antibiofilm and Antibacterial Activities Against Streptococcus Mutans Compared to Nanosized CuO

Eshed, M., Lellouche, J., Gedanken, A., & Banin, E. (2013) · Advanced Functional Materials · doi:10.1002/adfm.201302425 · Cited by 98 · see citing works

Oxidative stress and antioxidant mechanisms of obligate anaerobes involved in biological waste treatment processes: A review

Li, J., Ran, X., Zhou, M., Wang, K., Wang, H., & Wang, Y. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.156454 · Cited by 98 · see citing works

Peroxidase Activity of Hemoglobin·Haptoglobin Complexes

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Heat Stress-Mediated Constraints in Maize (Zea mays) Production: Challenges and Solutions

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Anti-oxidative stress regulator NF-E2-related factor 2 mediates the adaptive induction of antioxidant and detoxifying enzymes by lipid peroxidation metabolite 4-hydroxynonenal

Huang, Y. S., Li, W., & Kong, A. T. (2012) · Cell & Bioscience · doi:10.1186/2045-3701-2-40 · Cited by 96 · see citing works

Urinary 8-isoprostane as a biomarker for oxidative stress. A systematic review and meta-analysis

Graille, M., Wild, P. P., Sauvain, J., Hemmendinger, M., Canu, I. G., & Hopf, N. B. (2020) · Toxicology Letters · doi:10.1016/j.toxlet.2020.04.006 · Cited by 93 · see citing works

Cyanidin‐3‐glucoside and its phenolic acid metabolites attenuate visible light‐induced retinal degeneration in vivo via activation of Nrf2/HO‐1 pathway and NF‐κB suppression

Wang, Y., Huo, Y., Zhao, L., Lu, F. L., Wang, O., Yang, X., Ji, B., & Zhou, F. L. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201501048 · Cited by 93 · see citing works

Evaluation of mechanical, antimicrobial, and antioxidant properties of vanillic acid induced chitosan/poly (vinyl alcohol) active films to prolong the shelf life of green chilli

Eelager, M. P., Masti, S. P., Chougale, R. B., Hiremani, V. D., Narasagoudr, S. S., Dalbanjan, N. P., & Kumar, S. K. P. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.123499 · Cited by 92 · see citing works

Forever Young: Mechanisms of Natural Anoxia Tolerance and Potential Links to Longevity

Krivoruchko, A., & Storey, K. B. (2010) · Oxidative Medicine and Cellular Longevity · doi:10.4161/oxim.3.3.12356 · Cited by 92 · see citing works

Lead-induced oxidative stress and antioxidant response provide insight into the tolerance of Phanerochaete chrysosporium to lead exposure

Huang, C., Lai, C., Xu, P., Zeng, G., Huang, D., Zhang, J., Zhang, C., Cheng, M., Wan, J., & Wang, R. (2017) · Chemosphere · doi:10.1016/j.chemosphere.2017.08.104 · Cited by 89 · see citing works

Oxidative stress is associated with migraine and migraine‐related metabolic risk in females

Bernecker, C., Ragginer, C., Fauler, G., Horejsi, R., Möller, R., Zelzer, S., Lechner, A., Wallner-Blazek, M., Weiss, S., Fazekas, F., et al. (2011) · European Journal of Neurology · doi:10.1111/j.1468-1331.2011.03414.x · Cited by 89 · see citing works

Microbial oxidative stress response: Novel insights from environmental facultative anaerobic bacteria

Fu, H., Yuan, J., & Gao, H. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.08.012 · Cited by 88 · see citing works

Survival kit of Saccharomyces cerevisiae for anhydrobiosis

Dupont, S., Rapoport, A. I., Gervais, P., & Beney, L. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6028-5 · Cited by 87 · see citing works

Signaling and cytotoxic functions of 4-hydroxyalkenals

Riahi, Y., Cohen, G., Shamni, O., & Sasson, S. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00508.2010 · Cited by 200 · see citing works

Impact of Lipid Peroxidation on the Physiology and Pathophysiology of Cell Membranes

Pizzimenti, S., Ciamporcero, E. S., Daga, M., Pettazzoni, P., Alessia, A., Cetrangolo, G., Minelli, R., Dianzani, C., Lepore, A., GENTILE, F., et al. (2017) · Frontiers research topics · doi:10.3389/978-2-88945-082-4 · Cited by 15 · see citing works

Genotoxicity of lipid oxidation compounds

Eckl, P., & Bresgen, N. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.02.002 · Cited by 88 · see citing works

Immunochemical Detection of Lipid Hydroperoxide- and Aldehyde-Modified Proteins in Diseases

Sugiyama, A., & Sun, J. F. (2013) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-7920-4_10 · Cited by 22 · see citing works

Interaction of aldehydes derived from lipid peroxidation and membrane proteins

Pizzimenti, S., Ciamporcero, E. S., Daga, M., Pettazzoni, P., Arcaro, A., Cetrangolo, G., Minelli, R., Dianzani, C., Lepore, A., Gentile, F., et al. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00242 · Cited by 383 · see citing works