Oxidatively modified proteins in aging and disease1, 2 1Guest Editor: Earl Stadtman 2This article is part of a series of reviews on “Oxidatively Modified Proteins in Aging and Disease” The full list of papers may be found on the homepage of the journal

A Controlled Trial of Selegiline, Alpha-Tocopherol, or Both as Treatment for Alzheimer's Disease

Sano, M., Ernesto, C., Thomas, R. G., Klauber, M. R., Schafer, K., Grundman, M., Woodbury, P., Growdon, J., Cotman, C. W., Pfeiffer, E., et al. (1997) · New England Journal of Medicine · doi:10.1056/nejm199704243361704 · Cited by 2,380

Oxidative Damage Linked to Neurodegeneration by Selective α-Synuclein Nitration in Synucleinopathy Lesions

Giasson, B. I., Duda, J. E., Murray, I. V. J., Chen, Q., Souza, J. M., Hurtig, H. I., Ischiropoulos, H., Trojanowski, J. Q., & Lee, V. M. ‐. (2000) · Science · doi:10.1126/science.290.5493.985 · Cited by 1,567

Age-related changes in oxidized proteins.

Oliver, C. N., Ahn, B. W., Moerman, E. J., Goldstein, S., & Stadtman, E. R. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45598-6 · Cited by 1,306

Excess brain protein oxidation and enzyme dysfunction in normal aging and in Alzheimer disease.

Smith, C. D., Carney, J. M., Starke-Reed, P. E., Oliver, C. N., Stadtman, E. R., Floyd, R. A., & Markesbery, W. R. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.23.10540 · Cited by 1,296

Widespread Peroxynitrite-Mediated Damage in Alzheimer’s Disease

Smith, M. A., Richey Harris, P. L., Sayre, L. M., Beckman, J. S., & Perry, G. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02653.1997 · Cited by 1,239

Inducible nitric oxide synthase stimulates dopaminergic neurodegeneration in the MPTP model of Parkinson disease

Liberatore, G. T., Jackson-Lewis, V., Vukosavic, S., Mandir, A. S., Vila, M., McAuliffe, W. G., Dawson, V. L., Dawson, T. M., & Przedborski, S. (1999) · Nature Medicine · doi:10.1038/70978 · Cited by 1,046

Oxidative damage in Alzheimer's

Smith, M. A., Perry, G. L., Richey, P. L., Sayrec, L. M., Anderson, V. E., Beal, M. F., & Kowall, N. W. (1996) · Nature · doi:10.1038/382120b0 · Cited by 897

Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal ganglia

Browne, S. E., Bowling, A. C., Macgarvey, U., Baik, M. J., Berger, S. C., Muquit, M. M. K., Bird, E. D., & Beal, M. F. (1997) · Annals of Neurology · doi:10.1002/ana.410410514 · Cited by 885

Evidence of Increased Oxidative Damage in Both Sporadic and Familial Amyotrophic Lateral Sclerosis

Ferrante, R. J., Browne, S. E., Shinobu, L. A., Bowling, A. C., Baik, M. J., MacGarvey, U. M., Kowall, N. W., Brown, R. H., & Beal, M. F. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.69052064.x · Cited by 808

Oxidative damage, mitochondrial oxidant generation and antioxidant defenses during aging and in response to food restriction in the mouse

Sohal, R. S., Ku, H.-H., Agarwal, S., Forster, M. J., & Lal, H. (1994) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(94)90104-x · Cited by 788

Insulin resistance induced by high-fructose diet potentiates carbon tetrachloride hepatotoxicity

Pooranaperundevi, M., Sumiyabanu, M. S., Viswanathan, P., Sundarapandiyan, R., & Anuradha, C. V. (2010) · Toxicology and Industrial Health · doi:10.1177/0748233709359273 · Cited by 18

The Role of the Oxidative State and Innate Immunity Mediated by TLR7 and TLR9 in Lupus Nephritis

Miranda‐Díaz, A. G., Echavarría, R., Cardona-Muñóz, E. G., Ortiz‐Lazareno, P. C., Sierra, J. A., Gómez-Hermosillo, L. F., Casillas-Moreno, J., Campos-Bayardo, T. I., Román-Rojas, D., & García-Sánchez, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015234 · Cited by 17

Current potential pathogenic mechanisms of copper-zinc superoxide dismutase 1 (SOD1) in amyotrophic lateral sclerosis

Wang, X., Chen, W., Li, C., & Xu, R. (2024) · Reviews in the Neurosciences · doi:10.1515/revneuro-2024-0010 · Cited by 18

Oligomeric Tau-induced oxidative damage and functional alterations in cerebral endothelial cells: Role of RhoA/ROCK signaling pathway

Hossen, F., Sun, G. Y., & Lee, J. C. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.05.044 · Cited by 19

Glabridin protects osteoblastic MC3T3-E1 cells against antimycin A induced cytotoxicity

Choi, E. M. (2011) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2011.05.007 · Cited by 18

Effect of prenatal exposure to ethanol on hepatic elongation factor-2 and proteome in 21 d old rats: protective effect of folic acid

García‐Rodríguez, S., Argüelles, S., Llopis, R., Murillo, M. L. O., Machado, A., Carreras, O., & Ayala, A. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(03)00321-6 · Cited by 18

Identification of nitrated proteins in the normal rat brain using a proteomics approach

Suzuki, Y., Tanaka, M., Sohmiya, M., Ichinose, S., Omori, A., & Okamoto, K. (2005) · Neurological Research · doi:10.1179/016164105x22039 · Cited by 18

Peroxynitrite induced structural changes result in the generation of neo-epitopes on human serum albumin

Ahmad, P., Moinuddin, & Ali, A. (2013) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2013.04.068 · Cited by 17

Garlic and allopurinol attenuate hepatic apoptosis induced by fipronil in male albino rats

Sayed, A. A., El-Desouky, M. A., & Ibrahim, K. A. (2019) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2019.05.025 · Cited by 17

Peroxiredoxin 6 secreted by Schwann-like cells protects neuron against ischemic stroke in rats via PTEN/PI3K/AKT pathway

Tang, B., Wei Min, N. I., Zhou, J., Ling, Y., Niu, D., Lu, X., Chen, T., Ramalingam, M., & Hu, J. (2021) · Tissue and Cell · doi:10.1016/j.tice.2021.101635 · Cited by 17

Modulation of Reactive Oxygen Species Homeostasis as a Pleiotropic Effect of Commonly Used Drugs

Thomas, C., Wurzer, L., Malle, E., Ristow, M., & Madreiter‐Sokolowski, C. T. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.905261 · Cited by 18

Chronic Tempol treatment restores pharmacological preconditioning in the senescent rat heart

Zhu, J., Rebecchi, M. J., Wang, Q., Glass, P. S. A., Brink, P. R., & Liu, L. (2012) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00794.2012 · Cited by 17

CarSite: identifying carbonylated sites of human proteins based on a one-sided selection resampling method

Zuo, Y., & Jia, C. (2017) · Molecular BioSystems · doi:10.1039/c7mb00363c · Cited by 17

Total antioxidant capacity and protein peroxidation intensity in seminal plasma of infertile and fertile dogs

Domosławska, A., Zdunczyk, S., Franczyk, M., Kankofer, M., & Janowski, T. E. (2018) · Reproduction in Domestic Animals · doi:10.1111/rda.13345 · Cited by 17

Racial Differences in the Time-Course Oxidative Stress Responses to Acute Exercise.

Feairheller, D. L., Diaz, K. M., Sturgeon, K. M., Williamson, S. T., & Brown, M. D. (2011) · PubMed · Cited by 17

Association between lens opacities and mortality in the Priverno Eye Study

Nucci, C., Cedrone, C., Culasso, F., Cesareo, M., Regine, F., & Cerulli, L. (2004) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-003-0837-z · Cited by 17

Alcohol stress on cardiac tissue – Ameliorative effects of Thespesia populnea leaf extract

Rajbanshi, S. L., & Pandanaboina, S. C. (2013) · Journal of Cardiology · doi:10.1016/j.jjcc.2013.10.015 · Cited by 17

Polyclonal antibodies inhibit the glycation‐induced inactivation of bovine Cu,Zn‐superoxide dismutase

Jabeen, R., & Saleemuddin, M. (2005) · Biotechnology and Applied Biochemistry · doi:10.1042/ba20040201 · Cited by 17

Suppression in advanced glycation adducts of human serum albumin by bio-enzymatically synthesized gold and silver nanoformulations: A potential tool to counteract hyperglycemic condition

Ahmed, F., & Husain, Q. (2019) · Biochimie · doi:10.1016/j.biochi.2019.04.004 · Cited by 17

Effect of a gastrin-releasing peptide receptor antagonist and a proton pump inhibitor association in an animal model of gastritis

Petronilho, F. C., Araújo, J. H., Steckert, A. V., Rezin, G. T., Ferreira, G. K., Roesler, R., Schwartsmann, G., Dal‐Pizzol, F., & STRECK, E. L. (2009) · Peptides · doi:10.1016/j.peptides.2009.04.026 · Cited by 17

“In vitro” effect of cumene hydroperoxide on hepatic elongation factor-2 and its protection by melatonin

Parrado, J., Absi, E., Machado, A., & Ayala, A. (2003) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2003.10.006 · Cited by 17

Leucine-rich repeat kinase 2: A new player with a familiar theme for Parkinson's disease pathogenesis

Li, C., & Beal, M. F. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508350102 · Cited by 17

Molecular mechanism of ethanol fermentation inhibition via protein tyrosine nitration of pyruvate decarboxylase by reactive nitrogen species in yeast

Eknikom, S., Nasuno, R., & Takagi, H. (2022) · Scientific Reports · doi:10.1038/s41598-022-08568-4 · Cited by 16

Jatamansinol from Nardostachys jatamansi Ameliorates Tau-Induced Neurotoxicity in Drosophila Alzheimer’s Disease Model

Anupama, K. P., Antony, A., Olakkaran, S., Raghu, S. V., & Gurushankara, H. P. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02964-7 · Cited by 16

14 Days of supplementation with blueberry extract shows anti-atherogenic properties and improves oxidative parameters in hypercholesterolemic rats model

Ströher, D. J., Piccoli, J. D. C. E., Güllich, A. A. D. C., Pilar, B. C., Coelho, R. P., Bruno, J. B., Faoro, D., & Manfredini, V. (2015) · International Journal of Food Sciences and Nutrition · doi:10.3109/09637486.2015.1064870 · Cited by 16

The effects of cocoa supplementation, caloric restriction, and regular exercise, on oxidative stress markers of brain and memory in the rat model

Radak, Z. O., Silye, G., Bartha, C., Jakus, J., Stefanovits-Bányai, É., Atalay, M., Marton, O., & Koltai, E. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.01.047 · Cited by 16

Novel Protein-Based Solid-Biosensor for Determining Pro-oxidant Activity of Phenolic Compounds

Akyüz, E., Başkan, K. S., Tütem, E., & Apak, R. (2017) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b01649 · Cited by 16

Antioxidants in the Prevention and Treatment of Alzheimer’s Disease

Singh, S. K., Srikrishna, S., Castellani, R. J., & Perry, G. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-67625-8_20 · Cited by 16

Protective effects of N-(2-mercaptopropionyl)-glycine against ischemia–reperfusion injury in hypertrophied hearts

Fantinelli, J. C., Arbeláez, L. F. G., Núñez, I. A. P., & Mosca, S. M. (2012) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2012.07.004 · Cited by 16

Flavin containing monooxygenase 3 genetic polymorphisms Glu158Lys and Glu308Gly and their relation to ischemic stroke

Özçelik, A. T., Demirdöğen, B. C., Demirkaya, Ş., & Adalı, O. (2013) · Gene · doi:10.1016/j.gene.2013.03.010 · Cited by 16

A novel compound, maltolyl p‐coumarate, attenuates cognitive deficits and shows neuroprotective effects in vitro and in vivo dementia models

Shin, K. Y., Lee, G. H., Park, C. H., Kim, H. J., Park, S., Kim, S., Kim, H., Lee, K., Won, B. Y., Lee, H. G., et al. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21397 · Cited by 16

Radical Acetylation of 2′-Deoxyguanosine and l -Histidine Coupled to the Reaction of Diacetyl with Peroxynitrite in Aerated Medium

Massari, J., Fujiy, D. E., Dutra, F., Vaz, S. M., Costa, A. C. O., Micke, G. A., Tavares, M. F. M., Tokikawa, R., Assunção, N. A., & Bechara, E. J. H. (2008) · Chemical Research in Toxicology · doi:10.1021/tx7002799 · Cited by 16

A spectroscopic study of some of the peptidyl radicals formed following hydroxyl radical attack on β-amyloid and α-synuclein

Tabner, B. J., Turnbull, S., King, J. E., Benson, F. E., El‐Agnaf, O. M. A., & Allsop, D. (2006) · Free Radical Research · doi:10.1080/10715760600632545 · Cited by 16

Alpha-Tocopherol Counteracts Cognitive and Motor Deficits Induced by Repeated Treatment with Reserpine

Silva, A. J. S. (2015) · Biochemistry & Pharmacology Open Access · doi:10.4172/2167-0501.1000153 · Cited by 16

The Chemistry of Selenocysteine

Metanis, N., Beld, J., & Hilvert, D. (2011) · Patai's chemistry of functional groups · doi:10.1002/9780470682531.pat0582 · Cited by 17

Influence of feeding thermally peroxidized lipids on growth performance, lipid digestibility, and oxidative status in nursery pigs

Kerr, B. J., Lindblom, S. C., Zhao, J., & Faris, R. J. (2020) · Journal of Animal Science · doi:10.1093/jas/skaa392 · Cited by 15

Cancer Cachexia: Underlying Mechanisms and Potential Therapeutic Interventions

Directo, D. J., & Lee, S.-R. (2023) · Metabolites · doi:10.3390/metabo13091024 · Cited by 16

Late-Onset Dietary Restriction Modulates Protein Carbonylation and Catalase in Cerebral Hemispheres of Aged Mice

Dkhar, P., & Sharma, R. (2013) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-013-0015-8 · Cited by 15

Reaction of a {Co(NO)}8 complex with superoxide: Formation of a six coordinated [CoII(NO)(O2–)] species followed by peroxynitrite intermediate

Mazumdar, R., Mondal, B., Saha, S., Samanta, B., & Mondal, B. (2021) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2021.111698 · Cited by 15

Differential Measurements of Oxidatively Modified Proteins in Colorectal Adenopolyps

Mehrabi, S., Wallace, L. M., Cohen, S. L., Yao, X., & Aikhionbare, F. O. (2015) · International Journal of Clinical Medicine · doi:10.4236/ijcm.2015.64037 · Cited by 15

Free radical processes in aging, neurodegenerative diseases and other pathological states

Dubinina, E. E., & Васильевна, П. А. (2007) · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · doi:10.1134/s1990750807040026 · Cited by 15

Differential hepatic protein tyrosine nitration of mouse due to aging – Effect on mitochondrial energy metabolism, quality control machinery of the endoplasmic reticulum and metabolism of drugs

Marshall, A., Lutfeali, R., Raval, A., Chakravarti, D. N., & Chakravarti, B. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.10.142 · Cited by 15

Fluorescent detection of α-aminoadipic and γ-glutamic semialdehydes in oxidized proteins

Akagawa, M., Suyama, K., & Uchida, K. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.12.014 · Cited by 15

The adverse effects of smoking on health outcomes in bipolar disorder: a review and synthesis of biological mechanisms

Slyepchenko, A., Brunoni, A. R., McIntyre, R. S., Quevedo, J., & Carvalho, A. F. (2016) · Current Molecular Medicine · doi:10.2174/1566524016666160126144601 · Cited by 14

Glycation Induced Physicochemical Changes in Low-Density Lipoprotein and Its Role in Promoting Cholesterol Accumulation in Macrophages along with Antiglycation Effect of Aminoguanidine

Jairajpuri, D. S., Fatima, S., & Jairajpuri, Z. S. (2015) · Advances in Biological Chemistry · doi:10.4236/abc.2015.55017 · Cited by 14

Effects of nitric oxide synthase-3 overexpression on post-translational modifications and cell survival in HepG2 cells

Aguilar‐Melero, P., Ferrín, G., & Muntané, J. (2011) · Journal of Proteomics · doi:10.1016/j.jprot.2011.09.010 · Cited by 14

Oxidatively damaged proteins in the early stage of testicular toxicities in male rats by orally administered with a synthetic oestrogen, diethylstilbestrol

Li, Y., Okumura, K., Nomura, S., Maeda, N., Miyasho, T., & Yokota, H. (2010) · Reproductive Toxicology · doi:10.1016/j.reprotox.2010.09.007 · Cited by 14

Plasma Protein Hydroperoxides During Aging in Humans: Correlation with Paraoxonase 1 (PON1) Arylesterase Activity and Plasma Total Thiols

Mehdi, M. M., & Rizvi, S. I. (2013) · Archives of Medical Research · doi:10.1016/j.arcmed.2013.01.003 · Cited by 14

ANSID: A Solid-Phase Proteomic Approach for Identification and Relative Quantification of Aromatic Nitration Sites

Nuriel, T., Whitehouse, J., Ma, Y., Mercer, E. J., Brown, N., & Gross, S. S. (2016) · Frontiers in Chemistry · doi:10.3389/fchem.2015.00070 · Cited by 14

Global Protein Oxidation Profiling Suggests Efficient Mitochondrial Proteome Homeostasis During Aging

Guevara, C. R., Philipp, O., Hamann, A., Werner, A., Osiewacz, H. D., Rexroth, S., Rögner, M., & Poetsch, A. (2016) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.055616 · Cited by 14

2’-Deoxyribose Mediated Glycation Leads to Alterations in BSA Structure Via Generation of Carbonyl Species

Rafi, Z., Alouffi, S., Khan, M. S., & Ahmad, S. (2020) · Current Protein and Peptide Science · doi:10.2174/1389203721666200213104446 · Cited by 14

Double roles of hydroxycinnamic acid derivatives in protection against lysozyme oxidation

Zhu, H., Chen, S., Hao, S., Zhang, Z., Wang, W., & Yao, S. (2006) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2006.08.007 · Cited by 14

The conserved Trp155 in human frataxin as a hotspot for oxidative stress related chemical modifications

Correia, A. R., Ow, S. Y., Wright, P. C., & Gomes, C. M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.10.095 · Cited by 14

Nitrosative/oxidative modifications and ageing

Musci, G., Persichini, T., Casadei, M., Mazzone, V., Venturini, G., Polticelli, F., & Colasanti, M. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.012 · Cited by 14

DJ-1/PARK7 in Parkinson’s disease: mechanisms of pathogenesis and therapeutic potential

Bao, W., Ge, Y., Huang, J., Li, Y., Luo, Y., & Huang, N. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.09.025 · Cited by 13

BiGRUD-SA: Protein S-sulfenylation sites prediction based on BiGRU and self-attention

Zhang, T., Jia, J., Chen, C., Zhang, Y., & Yu, B. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.107145 · Cited by 13

Identification of ubiquitin nitration and oxidation using a liquid chromatography/mass selective detector system.

Yi, D., & Perkins, P. D. (2005) · PubMed Central · Cited by 12

L-Arginine Ameliorates Arylesterase/Paraoxonase Activity of Paraoxonase-1 in Hypercholesterolemic Rats

Harisa, G. I. (2011) · Asian Journal of Biochemistry · doi:10.3923/ajb.2011.263.272 · Cited by 13

Assessment of Oxidative Stress Markers and Carotid Artery Intima-Media Thickness in Elderly Patients Without and with Coronary Artery Disease

Madisetty, M. K., Kumaraswami, K., Katkam, S. K., Saumya, K., Raju, Y. S., Chandra, N., Jyotsna, M., Patnaik, S., & Kutala, V. K. (2015) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-015-0530-0 · Cited by 13

Serum Oxidized Protein and Prostate Cancer Risk within the Prostate Cancer Prevention Trial

Hoque, A. M., Ambrosone, C. B., Till, C., Goodman, P. J., Tangen, C. M., Kristal, A. R., Lucia, S. M., Wang, Q., Deyssenroth, M. A., Thompson, I. M., et al. (2010) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-09-0201 · Cited by 13

Selected oxidative stress biomarkers in antenatal diagnosis as 11–14 gestational weeks

Pietryga, M., Dydowicz, P., Toboła-Wróbel, K., Napierała, M., Miechowicz, I., Gąsiorowska, A., Brązert, M., & Florek, E. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.04.020 · Cited by 13

Glycation of hemoglobin leads to the immunogenicity as a result of neo-epitope generation

Siddiqui, Z., Faisal, M., Alatar, A. A., & Ahmad, S. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.11.063 · Cited by 13

Anticancer activity of functional polysuccinates with N-acetyl-cysteine in side chains

Mrówka, M., Jaszcz, K., & Skonieczna, M. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173501 · Cited by 13

Oxidatively Modified Proteins in the Serous Subtype of Ovarian Carcinoma

Mehrabi, S., Partridge, E. E., Seffens, W. S., Yao, X., & Aikhionbare, F. O. (2014) · BioMed Research International · doi:10.1155/2014/585083 · Cited by 13

The amylin peptide implicated in type 2 diabetes stimulates copper-mediated carbonyl group and ascorbate radical formation

Masad, A. A., Tabner, B. J., Mayes, J., & Allsop, D. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.05.033 · Cited by 13

Adaptative response to enhanced basal oxidative damage in sod mutants from Saccharomyces cerevisiae

Manfredini, V., Martins, V., Peralba, M. D. C. R., & Benfato, M. S. (2005) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-005-4058-0 · Cited by 13

Studies on metals in motor neuron disease

Roos, P. M. (2013) · Figshare · doi:10.13140/2.1.3513.8566 · Cited by 13

The Neoepitopes on Methylglyoxal‐ (MG‐) Glycated Fibrinogen Generate Autoimmune Response: Its Role in Diabetes, Atherosclerosis, and Diabetic Atherosclerosis Subjects

Rehman, S., Song, J., Faisal, M., Alatar, A. A., Akhter, F., Ahmad, S., & Hu, B. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6621568 · Cited by 13

Induction of oxidative stress and antioxidant defenses in the livers of sea trout, Salmo trutta L., with ulcerative dermal necrosis

Kurhalyuk, N., & Ткаченко, Г. М. (2011) · Fisheries & Aquatic Life · doi:10.2478/v10086-011-0029-0 · Cited by 12

Developmental Proteomic Profiling of Porcine Skeletal Muscle during Postnatal Development

Kim, N.-K., Lim, J.-H., Song, M.-J., Kim, O.-H., Park, B.-Y., Kim, M.-J., Hwang, I., & Lee, C. (2007) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.2007.1612 · Cited by 12

Posttranslational protein modifications by reactive nitrogen and chlorine species and strategies for their prevention and elimination

Sadowska‐Bartosz, I., Ott, C., Grune, T., & Bartosz, G. (2014) · Free Radical Research · doi:10.3109/10715762.2014.953494 · Cited by 13

Regulators of mitochondrial complex I activity: A review of literature and evaluation in postmortem prefrontal cortex from patients with bipolar disorder

Duong, A., Che, Y., Ceylan, D., Pinguelo, A., Andreazza, A. C., Young, L. T., & Berk, M. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2015.12.015 · Cited by 12

Acid–Base Properties of the (1-4,18-36) Fragments of Neuropeptide K and their Mono- and Polynuclear Copper(II) Complexes Products of Metal-Catalyzed Oxidation

Błaszak, M., Jankowska, E., & Kowalik‐Jankowska, T. (2012) · Inorganic Chemistry · doi:10.1021/ic301476p · Cited by 12

A physical model of axonal damage due to oxidative stress

Counterman, A. E., D’Onofrio, T. G., Andrews, A. M., & Weiss, P. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504134103 · Cited by 12

Nitrosative Stress in Aging – Its Importance and Biological Implications in NF-κB Signaling

Ljubuncic, P., Gochman, E., & Reznick, A. Z. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-602-3_2 · Cited by 12

Dynamic and biphasic modulation of nitrosation reaction by superoxide dismutases

Hu, T., Hayton, W. L., Morse, M. A., & Mallery, S. R. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00820-3 · Cited by 12

Induction of Cyclooxygenase‐2 and Peroxisome Proliferator‐Activated Receptor‐γ during Nitric Oxide‐Induced Apoptotic PC12 Cell Death

LIM, S., Jang, J.-H., & Surh, Y. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1299.119 · Cited by 12

An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study

Haji, S., Fujita, K., Oki, R., Osaki, Y., Miyamoto, R., Morino, H., Nagano, S., Atsuta, N., Kanazawa, Y., Matsumoto, Y., et al. (2022) · JMIR Research Protocols · doi:10.2196/42032 · Cited by 11

Testosterone deficiency worsens mitochondrial dysfunction in APP/PS1 mice

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