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

Protective effects of N-acetyl cysteine against oxidative stress in ibuprofen-induced hepatotoxicity in rats

Satvati, M., Salehi-Vanani, N., Nouri, A., & Heidarian, E. (2022) · Comparative Clinical Pathology · doi:10.1007/s00580-022-03332-6 · Cited by 9

Oxidative stress measured by carbonyl groups level in postmenopausal women after oral and transdermal hormone therapy

Połać, I., Borowiecka, M., Wilamowska, A., & Nowak, P. (2012) · Journal of obstetrics and gynaecology research · doi:10.1111/j.1447-0756.2011.01842.x · Cited by 9

Protein Quality Control by the Ubiquitin Proteolytic Pathway: Roles in Resistance to Oxidative Stress and Disease

Shang, F., Dudek, E. J., Liu, Q. L., Boulton, M. E., & Taylor, A. (2006) · Israel Journal of Chemistry · doi:10.1560/a8aa-y8rp-9drw-y8ax · Cited by 9

Song Bu Li Decoction, a Traditional Uyghur Medicine, Protects Cell Death by Regulation of Oxidative Stress and Differentiation in Cultured PC12 Cells

Maiwulanjiang, M., Zhu, K. Y., Chen, J., Miernisha, A., Xu, S. L., Du, C. Y. Q., Lau, K. K. M., Choi, R. C. Y., Dong, T. T.-X., Aisa, H. A., et al. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/687958 · Cited by 9

Biomarkers of Oxidative and Mitochondrial Stress Are Associated With Accelerated Pace of Aging at Midlife in a Birth Cohort

King-Hudson, T.-R., Pearson, A. G., Dunstan‐Harrison, C., Powell, M. A., Magon, N. J., Edwards, T. S., Paton, L. N., Tang, J. S., Kettle, A. J., Pearson, J. F., et al. (2025) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaf105 · Cited by 9

CBR1 decreases protein carbonyl levels via the ROS /Akt/ CREB pathway to extend lifespan in the cotton bollworm, Helicoverpa armigera

Geng, S., Li, H., Zhang, X., Wang, T., Zhou, S., & Xu, W. (2022) · FEBS Journal · doi:10.1111/febs.16691 · Cited by 8

The protective effect of salicylic acid on lysozyme against riboflavin-mediated photooxidation

Li, K., Wang, H., Cheng, L., Zhu, H., Wang, M., & Wang, S. (2010) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2010.12.008 · Cited by 8

Mitochondrial Defects and Oxidative Stress in Alzheimer Disease

Abraki, S. B., & Chavoshinezhad, S. (2014) · The Neuroscience Journal of Shefaye Khatam · doi:10.18869/acadpub.shefa.2.1.85 · Cited by 9

Prothrombin and fibrinogen carbonylation: How that can affect the blood clotting

Harutyunyan, H. A. (2016) · Redox Report · doi:10.1080/13510002.2016.1200289 · Cited by 8

Comparison of Pre- and Post-translational Expressions of COXIV-1 and MT-ATPase 6 Genes in Colorectal Adenoma-Carcinoma Tissues [NIH-NIGMS]

Wallace, L. M., Cherian, A. M., Adamson, P., Bari, S., Banerjee, S., Flood, M., Simien, M., Yao, X., & Aikhionbare, F. O. (2018) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.1000319 · Cited by 8

Protective effect of ethyl vanillin against Aβ‑induced neurotoxicity in PC12 cells via the reduction of oxidative stress and apoptosis

Zhong, L., Tong, Y., Chuan, J., Bai, L., Shi, J., & Zhu, Y. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7242 · Cited by 8

The polyphenol quercetin protects from glucotoxicity depending on the aggresome in Caenorhabditis elegans

Civelek, M., Flory, S., Meloh, H., Fitzenberger, E., & Wenzel, U. (2019) · European Journal of Nutrition · doi:10.1007/s00394-019-01917-6 · Cited by 8

Age-Dependent Myocardial Dysfunction in Critically Ill Patients: Role of Mitochondrial Dysfunction

Lautz, A. J., & Zingarelli, B. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20143523 · Cited by 8

Ameliorative effect of pioglitazone on glucose induced glycation of α-crystallin: Management of complications associated with diabetic retinopathy

Ren, Z., & Song, J. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.03.202 · Cited by 8

Redox Biology of Aging: Focus on Novel Biomarkers

Pandey, K. B., & Rizvi, S. I. (2014) · Springer eBooks · doi:10.1007/978-81-322-2035-0_18 · Cited by 8

Cytosolic Calcium Homeostasis in Neurons — Control Systems, Modulation by Reactive Oxygen and Nitrogen Species, and Space and Time Fluctuations

Gutiérrez‐Merino, C., Marques‐da‐Silva, D., Fortalezas, S., & Alejandro, K. (2014) · InTech eBooks · doi:10.5772/57576 · Cited by 8

Apolipoprotein, C-Reactive Protein and Oxidative Stress Parameters in Dyslipidemic Type 2 Diabetic Patients Treated or Not with Simvastatin

Manfredini, V., Biancini, G. B., Vanzin, C. S., Vesco, A. M. R. D., Wayhs, C. A. Y., Peralba, M. D. C. R., & Vargas, C. R. (2010) · Archives of Medical Research · doi:10.1016/j.arcmed.2010.03.006 · Cited by 8

CNTF and Related Neurokines

Halvorsen, S. W., & Kaur, N. (2006) · Springer eBooks · doi:10.1007/978-0-387-30381-9_3 · Cited by 8

Developmental changes in the response of murine cerebellar granule cells to nitric oxide

Oldreive, C., Gaynor, S., & Doherty, G. H. (2008) · Neurochemistry International · doi:10.1016/j.neuint.2008.02.010 · Cited by 8

Antitumor activity of Tigerinin-1: Necroptosis mediates toxicity in A549 cells

Antony, A., Olakkaran, S., Anupama, K. P., Shekh, S., Gowd, K. H., & Gurushankara, H. P. (2022) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2022.130182 · Cited by 7

Deficiency in Heat Shock Factor 1 (HSF-1) Expression Exacerbates Sepsis-induced Inflammation and Cardiac Dysfunction

Zang, Q. S. (2014) · SOJ Surgery · doi:10.15226/2376-4570/1/1/00103 · Cited by 7

Novel insights into multitargeted potential of N′-(4-benzylpiperidin-1-yl)alkylamine derivatives in the management of Alzheimer's disease associated pathogenesis

Meena, P., Manral, A., Nemaysh, V., Saini, V., Siraj, F., Luthra, P. M., & Tiwari, M. (2016) · RSC Advances · doi:10.1039/c6ra24017h · Cited by 7

The BK activator NS11021 partially protects rat kidneys from cold storage and transplantation-induced mitochondrial and renal injury

Shrum, S., Tobacyk, J., Lo, S., Parajuli, N., & MacMillan-Crow, L. A. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108410 · Cited by 7

Effect of Rosemary on Stabilization of Proteins during Frozen Storage of Mackerel (Scomber scombrus)

Kvangarsnes, K., Rustad, T., Barnung, T. N., Larssen, W. E., & Hansen, G. (2021) · Journal of Aquatic Food Product Technology · doi:10.1080/10498850.2020.1869128 · Cited by 7

Heme and Cu2+-induced vasoactive intestinal peptide (VIP) tyrosine nitration: A possible molecular mechanism for the attenuated anti-inflammatory effect of VIP in inflammatory diseases

Zeng, L., Zhang, X., Xia, M., Ye, H., Li, H., & Gao, Z. (2023) · Biochimie · doi:10.1016/j.biochi.2023.07.011 · Cited by 7

Characterization of in vitro protein oxidation using mass spectrometry: A time course study of oxidized alpha-amylase

Silva, A. M. N., Marçal, S. L., Vitorino, R. M. P., Domingues, M. R., & Domingues, P. M. (2012) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2012.12.010 · Cited by 7

In Vitro Aging of Human Skin Fibroblasts: Age-Dependent Changes in 4-Hydroxynonenal Metabolism

Petković, I., Bresgen, N., Gilardoni, E., Regazzoni, L., Uchida, K., Aldini, G., Siems, W., & Eckl, P. (2020) · Antioxidants · doi:10.3390/antiox9020150 · Cited by 7

Therapeutic strategies for Parkinson’s disease: promising agents in early clinical development

Fabbri, M., Perez‐Lloret, S., & Rascol, O. (2020) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2020.1814252 · Cited by 7

A Cross-Sectional Study on Assessment of Oxidative Stress in Coronary Heart Disease Patients in Bangladesh

Kamruzzaman, M., Choudhury, T. Z., Rahman, T., & Islam, L. N. (2019) · World Journal of Cardiovascular Diseases · doi:10.4236/wjcd.2019.95029 · Cited by 7

PARP‐1‐dependent 3‐nitrotyrosine protein modification after DNA damage

Siles, E., Martínez‐Lara, E., Núñez, M. I., Muñoz‐Gámez, J. A., Martín‐Oliva, D., Valenzuela, M. T., Peinado, M. Á., de Almodóvar, J. M. R., & Oliver, F. J. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20570 · Cited by 7

Site specificity of the αCH bond dissociation energy for a naturally occurring β‐hairpin peptide—An ab initio study

Cheng, W., Jang, S., Wu, C., Lin, R., Lu, H., & Li, F. (2008) · Journal of Computational Chemistry · doi:10.1002/jcc.21066 · Cited by 7

Oxidative Stress and Neurotrophin Signaling in Autism

Sajdel, E. M. (2009) · CRC Press eBooks · doi:10.1201/9781420068870-c3 · Cited by 7

Oxidative Stress and Protein Oxidation

Grune, T., Catalgol, B., & Jung, T. (2012) · Wiley eBooks · doi:10.1002/9781118493038.ch1 · Cited by 7

The Bioactive Components of Brassicaceae

Ross, I. A. (2024) · Springer eBooks · doi:10.1007/978-3-031-63681-3_2 · Cited by 6

Insulin resistance: fueling oxidative stress and neurodegeneration

Chamorro, L. B., Zulli, B., & Barone, E. (2025) · Journal of Neural Transmission · doi:10.1007/s00702-025-02956-6 · Cited by 8

Oxidative stress biomarkers in assisted reproductive technologies: From follicular redox biology to clinical translation

Lin, N., van Zomeren, K. C., Plösch, T., Hofsink, N., Zhou, X., Tietge, U. J. F., Cantineau, A. E., Schirhagl, R., & Hoek, A. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104167 · Cited by 6

Lithium Benzoate Exerts Neuroprotective Effect by Improving Mitochondrial Function, Attenuating Reactive Oxygen Species, and Protecting Cognition and Memory in an Animal Model of Alzheimer’s Disease

Lu, L.-P., Chang, W.-H., Huang, J., Peng, T., & Tsai, G. E. (2022) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-220025 · Cited by 6

Post-Translational Oxidative Modifications of Hemostasis Proteins: Structure, Function, and Regulation

Rosenfeld, M. A., Yurina, L. V., Gavrilina, E. S., & Vasilyeva, A. D. (2024) · Biochemistry (Moscow) · doi:10.1134/s0006297924140025 · Cited by 6

Garlic and allopurinol alleviate the apoptotic pathway in rats’ brain following exposure to fipronil insecticide

Bakr, A. A., Ali, M., & Ibrahim, K. A. (2022) · Environmental Analysis Health and Toxicology · doi:10.5620/eaht.2022037 · Cited by 6

Butein Inhibits the Glycation of α-Crystallin: An Approach in Prevention of Retinopathy

Liu, J., & Wang, X. (2023) · Journal of Fluorescence · doi:10.1007/s10895-023-03147-w · Cited by 6

Short Survey on the Protein Modifications in Plasma during SARS-CoV-2 Infection

Gęgotek, A., Žarković, N., Orehovec, B., Jaganjac, M., Šunjić, S. B., & Skrzydlewska, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814109 · Cited by 6

Protective roles of some natural and synthetic aromatase inhibitors in testicular insufficiency caused by Bisphenol A exposure

Berköz, M., Yalın, S., & Türkmen, Ö. (2024) · International Journal of Environmental Health Research · doi:10.1080/09603123.2024.2362810 · Cited by 6

Antioxidant properties of hydroxytyrosyl acetate compared with hydroxytyrosol and their protective capacity against oxidative stress in human neuroblastoma cells

Ammendola, S., Giusti, A. M., Masci, A., Mosca, L., Saso, L., & Bovicelli, P. (2011) · IRIS Research product catalog (Sapienza University of Rome) · Cited by 6

Protective potential of Opuntia microdasys flower decoction on fructose-alloxan-induced diabetic rats on kidney and pancreas: chemical and immunohistochemical analyses

Chahdoura, H., Khlifi, A., Lamine, J. B., Ziani, B. E. C., Adouni, K., El-Bok, S., Haouas, Z., Neffati, F., Zakhama, A., Flamini, G., et al. (2018) · Environmental Science and Pollution Research · doi:10.1007/s11356-018-3290-6 · Cited by 6

Future Treatment of Alzheimer Disease

Keskin, A. O., Durmaz, N., Uncu, G., Erzurumluoglu, E., Yıldırım, Z., Tuncer, N., & Adapınar, D. Ö. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.85096 · Cited by 6

N-nitrosodiethylamine induced redox imbalance in rat liver: Protective role of polyphenolic extract of Blighia sapida arilli

Oloyede, O. B., Ajiboye, T. O., & Komolafe, Y. O. (2013) · Free Radicals and Antioxidants · doi:10.1016/j.fra.2013.03.002 · Cited by 6

Familial amyotrophic lateral sclerosis (FALS): Emerging hints from redox proteomics.

Dalle-Donne, I. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.03.029 · Cited by 5

Protective effect of capsaicin against methyl methanesulphonate induced toxicity in the third instar larvae of transgenic Drosophila melanogaster (hsp70-lacZ)Bg9

Khanam, S., Fatima, A., Jyoti, R. S., Ali, F. R., Naz, F., Shakya, B., & Siddique, Y. H. (2017) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(17)30044-4 · Cited by 5

Inhibition of non-enzymatic glycation by capsaicin: targeting AGE-induced diabetic complications

Xu, P., Yang, X., & Wang, Y. (2021) · New Journal of Chemistry · doi:10.1039/d1nj01783g · Cited by 5

Oxidative stress in rat heart mitochondria under a rotenone model of Parkinson’ disease: a corrective effect of capicor treatment

Gonchar, O. O., Klymenko, O. О., Drevytska, T., Bratus, L. V., & Im, M. (2021) · The Ukrainian Biochemical Journal · doi:10.15407/ubj93.05.021 · Cited by 5

Electrochemical micro- and nanobiosensors for in vivo reactive oxygen/nitrogen species measurement in the brain

Beigloo, F., Khoshkar-Vandi, S. A., Pourmand, E., Heydari, M., Molaabasi, F., Gharib, N., Zare, Y., Rhee, K. Y., & Park, S. (2023) · Nanotechnology Reviews · doi:10.1515/ntrev-2023-0124 · Cited by 6

Photosensitized oxidation of tryptophan and tyrosine by aromatic ketones: A laser flash photolysis study

Tang, R., Zhang, P., Li, H., Liu, Y., & Wang, W. (2012) · Science China Chemistry · doi:10.1007/s11426-011-4472-y · Cited by 5

Alkohol a stres oksydacyjny

Świderska-Kołacz, G., Kumański, K., & Parka, B. (2012) · Cited by 5

Oxidative protein damage in patients with colorectal cancer

Murlikiewicz, Ł., Sygut, A., Trzciński, R., Grzegorczyk, K., Rutkowski, M., & Dziki, A. J. (2010) · Polish Journal of Surgery · doi:10.2478/v10035-010-0065-2 · Cited by 5

Modulation of oxidative stress mediators in the liver of adjuvant induced arthritic rats by Nyctanthes arbor tristis

Lad, H., & Bhatnagar, D. (2017) · Clinical Phytoscience · doi:10.1186/s40816-016-0041-4 · Cited by 5

Predictive value of some pro-oxidants in type 2 diabetes mellitus with vascular complications

Goycheva, P., Nikolova, G., Ivanova, M., Kundurdzhiev, T., & Gadjeva, V. (2019) · BioScience Trends · doi:10.5582/bst.2019.01020 · Cited by 5

Assessment of lipid and protein peroxidation markers in non-pregnant and pregnant female dogs

Szczubiał, M., Kankofer, M., Dąbrowski, R., Bochniarz, M., & Urban‐Chmiel, R. (2015) · Polish Journal of Veterinary Sciences · doi:10.1515/pjvs-2015-0022 · Cited by 5

Detection of HNE Modification of Proteins in Aging Mouse Tissues: A Western Blot-Based Approach

Zhang, H., Lyn, N., Haghani, A., & Forman, H. J. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0592-9_21 · Cited by 5

Induced Pluripotent Stem Cells Without c-Myc Ameliorate Retinal Oxidative Damage via Paracrine Effects and Reduced Oxidative Stress in Rats

Fang, I., Yang, C., Chiou, S.-H., & Yang, C.-M. (2014) · Journal of Ocular Pharmacology and Therapeutics · doi:10.1089/jop.2014.0020 · Cited by 5

Untargeted Discovery of Nitric Oxide-Modified Proteins

Deeb, R. S., Nuriel, T., & Gross, S. S. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-373866-0.00010-1 · Cited by 5

Age-Related Neuronal and Behavioral Deficits are Improved by Polyphenol-Rich Blueberry Supplementation

Lau, F. C., Joseph, J. A., & Shukitt‐Hale, B. (2005) · Oxidative stress and disease · doi:10.1201/9781420026559.ch22 · Cited by 5

Influences of different space allowance on reproductive performances in buffalo

Salzano, A., Spagnuolo, M. S., Lombardi, P., Vecchio, D., Limone, A., Censi, S. B., Balestrieri, A., Pelagalli, A., & Neglia, G. (2017) · Animal Reproduction · doi:10.21451/1984-3143-ar799 · Cited by 5

α-Tocotrienol Protects Neurons by Preventing Tau Hyperphosphorylation via Inhibiting Microtubule Affinity-Regulating Kinase Activation

Liu, Y., Chen, Y., & Fukui, K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158428 · Cited by 5

Inhibitory effect of silibinin on Amadori-albumin in diabetes mellitus: A multi-spectroscopic and biochemical approach

Neelofar, K., Arif, Z., Ahmad, J., & Alam, K. (2018) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2018.10.044 · Cited by 4

Zinc Signaling in Aging Heart Function

Turan, B., Billur, D., & Olğar, Y. (2019) · Springer eBooks · doi:10.1007/978-981-15-0557-7_8 · Cited by 4

Oxidative Stress in Depression and Other Comorbid Disorders

Bhatt, S., Pandey, D. K., Patil, C. R., & Nagappa, A. N. (2020) · Springer eBooks · doi:10.1007/978-981-15-1568-2_9 · Cited by 5

Saccharomyces cerevisiae quiescent cells: cadmium resistance and adaptive response

Pisareva, E. I., Tomova, I., & Petrova, V. Y. (2021) · Biotechnology & Biotechnological Equipment · doi:10.1080/13102818.2021.1980106 · Cited by 4

Oxydative stress in type 2 diabetic patients: involvement of HIF-1 alpha AND mTOR genes expression

Saienko, Y. A., Gonchar, O. O., Im, M., Drevytska, T., Bratus, L. V., & Mankovsky, B. (2023) · The Ukrainian Biochemical Journal · doi:10.15407/ubj95.02.048 · Cited by 4

Oxidative Stress and Neuronal Zinc Signaling

Hara, H., & Aizenman, E. (2014) · Springer eBooks · doi:10.1007/978-4-431-55114-0_4 · Cited by 4

Influence of Therapy on Some Important Final Products of Oxidation of Lipids, Proteins and Nucleic Acids in Patients with Parkinson’s Diseases

Nikolova, G., Grigorov, B., Zheleva, A. M., & Gadjeva, V. G. (2014) · Advances in Biological Chemistry · doi:10.4236/abc.2014.44031 · Cited by 3

Protein carbonyl groups in trained subjects

Presti, R. L., Canino, B., Montana, M., Calandrino, V., & Caimi, G. (2012) · Clinical Hemorheology and Microcirculation · doi:10.3233/ch-2011-1518 · Cited by 4

Protective action of fenugreek (Trigonella foenum graecum) seed polyphenols against alcohol-induced protein and lipid damage in rat liver

Kaviarasan, S., Sundarapandiyan, R., & Anuradha, C. V. (2007) · Springer eBooks · doi:10.1007/978-1-4020-9056-1_9 · Cited by 4

The Role of Reactive Nitrogen Species (RNS) in the Activation of Nuclear Factor Kappa B (NFkB) and Its Implications for Biological Systems: The Question of Balance

Ljubuncic, P., Bar‐Shai, M., & Reznick, A. Z. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8399-0_4 · Cited by 4

The histochemistry and cell biology vade mecum: a review of 2005–2006

Taatjes, D. J., Zuber, C., & Roth, J. (2006) · Histochemistry and Cell Biology · doi:10.1007/s00418-006-0253-7 · Cited by 4

Membrane Lipid Replacement for reconstituting mitochondrial function and moderating cancer-related fatigue, pain and other symptoms while counteracting the adverse effects of cancer cytotoxic therapy

Nicolson, G. L., & Ferreira, G. (2024) · Clinical & Experimental Metastasis · doi:10.1007/s10585-024-10290-6 · Cited by 4

Neuro-protective effects of Ligustri Fructus by suppression of oxidative stress in mouse model of Parkinson’s disease

Ye, M., Kim, M. H., & Bae, H. (2016) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-016-0223-0 · Cited by 3

Phytotherapeutics Attenuation of Oxidative Stress, Inflammation and Lipid Peroxidation in Severe and Chronic Diseases

Mavondo, G. A., Ncube, N., Sibanda, A., Dube, D., Chikuse, F. F., & Makoni, P. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.99832 · Cited by 6

The WMI Rat of Premature Cognitive Aging Presents Intrinsic Vulnerability to Oxidative Stress in Primary Neurons and Astrocytes Compared to Its Nearly Isogenic WLI Control

Ferreira, A., Harter, A. M., Afreen, S., Kánai, K., Bátori, S., & Redei, E. E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031692 · Cited by 3

Effect of Glycyrrhiza uralensis crude water extract on the expression of Nitric Oxide Synthase 2 gene during myogenesis

Qadri, A. F., Shaikh, S., Hwang, Y. C., Ahmad, K., Choi, I., & Lee, E. J. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e34747 · Cited by 3

A study on Astragalus mongholicus heterosaccharides affecting contractions of isolated bladder detrusor strips

Zhang, X.-J., Chen, G., Ke, M., Han, H., Lu, Z., Wang, T., Sun, F.-H., & Yu, H. (2011) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2011.02.012 · Cited by 4

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