Glutathione peroxidases

Selenium: Biochemical Role as a Component of Glutathione Peroxidase

Rotruck, J. T., Pope, A. L., Ganther, H. E., Swanson, A. B., Hafeman, D. G., & Hoekstra, W. G. (1973) · Science · doi:10.1126/science.179.4073.588 · Cited by 7,815

Association of reactive oxygen species levels and radioresistance in cancer stem cells

Diehn, M., Cho, R. W., Lobo, N. A., Kalisky, T., Dorie, M. J., Kulp, A. N., Qian, D., Lam, J. S., Ailles, L. E., Wong, M., et al. (2009) · Nature · doi:10.1038/nature07733 · Cited by 2,555

Characterization of Mammalian Selenoproteomes

Kryukov, G. V., Castellano, S., Novoselov, S. V., Lobanov, A. V., Zehtab, O., Guigó, R., & Gladyshev, V. N. (2003) · Science · doi:10.1126/science.1083516 · Cited by 2,385

Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis

DeNicola, G. M., Karreth, F. A., Humpton, T. J., Gopinathan, A., Wei, C., Frese, K., Mangal, D., Yu, K. H., Yeo, C. J., Calhoun, E. S., et al. (2011) · Nature · doi:10.1038/nature10189 · Cited by 2,277

Glutathione Peroxidase 4 Senses and Translates Oxidative Stress into 12/15-Lipoxygenase Dependent- and AIF-Mediated Cell Death

Seiler, A., Schneider, M., Förster, H., Roth, S., Wirth, E. K., Culmsee, C., Plesnila, N., Kremmer, E., Rådmark, O., Wurst, W., et al. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.07.005 · Cited by 1,470

Glutathione peroxidase: A selenoenzyme

Flohé, L., Günzler, W. A., & Schock, H. H. (1973) · FEBS Letters · doi:10.1016/0014-5793(73)80755-0 · Cited by 1,389

Obesity and Systemic Oxidative Stress: Clinical Correlates of Oxidative Stress in The Framingham Study

Keaney, J. F., Larson, M. G., Vasan, R. S., Wilson, P. W. F., Lipinska, I., Corey, D., Massaro, J. M., Sutherland, P., Vita, J. A., & Benjamin, E. J. (2003) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000058402.34138.11 · Cited by 1,304

Glutathione Peroxidase-1 in Health and Disease: From Molecular Mechanisms to Therapeutic Opportunities

Lubos, E., Loscalzo, J., & Handy, D. E. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3586 · Cited by 1,280

Tissue-specific functions of individual glutathione peroxidases

Brigelius-Flohé, R. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00173-2 · Cited by 1,114

Circumvention of resistance to photodynamic therapy in doxorubicin-resistant sarcoma by photochemical internalization of gelonin

Olsen, C. E., Berg, K., Selbo, P. K., & Weyergang, A. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.010 · Cited by 25

The Liver, Oxidative Stress, and Antioxidants

Casas‐Grajales, S., & Muriel, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804274-8.00043-6 · Cited by 26

Molecular Characterization and Gene Expression of Glutathione Peroxidase 1 in Tor tambroides Exposed to Temperature Stress

Do, T. D., Mai, N. T., Khoa, T. N. D., Abol‐Munafi, A. B., Liew, H. J., Kim, C.-B., & Wong, L. L. (2019) · Evolutionary Bioinformatics · doi:10.1177/1176934319853580 · Cited by 25

Recent progress in the effect of ferroptosis of HSCs on the development of liver fibrosis

Tang, R., Luo, J., Zhu, X., Miao, P., Tang, H. Y., Jian, Y., Ruan, S., Ling, F., & Tang, M. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1258870 · Cited by 26

Recent progress towards the development of fluorescent probes for the detection of disease-related enzymes

Mishra, L., & Mishra, M. (2024) · Journal of Materials Chemistry B · doi:10.1039/d4tb01960a · Cited by 24

Expression of glutathione peroxidase 1 in the spheno-occipital synchondrosis and its role in ROS-induced apoptosis

Koretsi, V., Kirschneck, C., Proff, P., & Römer, P. (2014) · European Journal of Orthodontics · doi:10.1093/ejo/cju045 · Cited by 24

Alkyl chain modulated cytotoxicity and antioxidant activity of bioinspired amphiphilic selenolanes

Verma, P., Kunwar, A., Arai, K., Iwaoka, M., & Priyadarsini, K. I. (2015) · Toxicology Research · doi:10.1039/c5tx00331h · Cited by 24

Treatment-resistant schizophrenia: focus on the transsulfuration pathway

Berry, T. M., Hamza, E. A., & Moustafa, A. A. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0057 · Cited by 25

New Probucol Analogues Inhibit Ferroptosis, Improve Mitochondrial Parameters, and Induce Glutathione Peroxidase in HT22 Cells

Bueno, D., Canto, R. F. S., de Souza, V., Andreguetti, R. R., Barbosa, F. A. R., Naime, A. A., Dey, P. N., Wüllner, V., Lopes, M. W., Braga, A. L., et al. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-01956-9 · Cited by 24

Relationship between Oxidative Stress and Imatinib Resistance in Model Chronic Myeloid Leukemia Cells

Głowacki, S., Synowiec, E., Szwed, M., Toma, M. M., Skórski, T., & Śliwiński, T. (2021) · Biomolecules · doi:10.3390/biom11040610 · Cited by 24

Dietary Litsea cubeba essential oil supplementation improves growth performance and intestinal health of weaned piglets

Yang, Z., Wang, F., Yin, Y., Huang, P., Jiang, Q., Liu, Z., Yin, Y., & Chen, J. (2022) · Animal nutrition · doi:10.1016/j.aninu.2022.11.004 · Cited by 24

Destroying glutathione peroxidase improves the oxidative stress resistance and pathogenicity of Listeria monocytogenes

Zhang, Y., Guo, Q., Fang, X., Yuan, M., Hu, W., Liang, X., Liu, J. L., Yang, Y., & Fang, C. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1122623 · Cited by 24

Oxidative stress due to Mycobacterium avium subspecies paratuberculosis (MAP) infection upregulates selenium-dependent GPx activity

Qasem, A., Abdel-Aty, A., Abu-Suwa, H., & Naser, S. A. (2016) · Gut Pathogens · doi:10.1186/s13099-016-0090-8 · Cited by 24

Apoptotic transition of senescent cells accompanied with mitochondrial hyper-function

Wang, D., Liu, Y., Zhang, R., Zhang, F., Sui, W., Chen, L., Zheng, R., Chen, X., Wen, F., Ouyang, H., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8536 · Cited by 26

Fluxional Cyclic Seleninate Ester: NMR and Computational Studies, Glutathione Peroxidase-like Behavior, and Unexpected Rearrangement

McNeil, N. M. R., Matz, M. C., & Back, T. G. (2013) · The Journal of Organic Chemistry · doi:10.1021/jo401757m · Cited by 24

Comparison of analytical methods using enzymatic activity, immunoaffinity and selenium-specific mass spectrometric detection for the quantitation of glutathione peroxidase 1

Sonet, J., Bierła, K., Bulteau, A., Łobiński, R., & Chavatte, L. (2018) · Analytica Chimica Acta · doi:10.1016/j.aca.2018.01.068 · Cited by 24

Selenium and iodine in diabetes mellitus with a focus on the interplay and speciation of the elements

Solovyev, N. D., Vanhaecke, F., & Michalke, B. (2019) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2019.07.005 · Cited by 24

Characterization and expression analysis of seven selenoprotein genes in yellow catfish Pelteobagrus fulvidraco to dietary selenium levels

Xu, X., Zhang, D.-G., Zhao, T., Xu, Y., & Luo, Z. (2020) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2020.126600 · Cited by 24

CAR T Cells Engineered to Secrete IFNκ Induce Tumor Ferroptosis via an IFNAR/STAT1/ACSL4 Axis

Gao, Y., Liu, S., Huang, Y., Wang, H., Zhao, Y., Cui, X., Peng, Y., Li, F., & Zhang, Y. (2024) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-24-0130 · Cited by 24

Effects of zearalenone-induced oxidative stress and Keap1–Nrf2 signaling pathway-related gene expression in the ileum and mesenteric lymph nodes of post-weaning gilts

Cheng, Q., Jiang, S., Huang, L., Wang, Y., Yang, W., Yang, Z., & Ge, J. (2019) · Toxicology · doi:10.1016/j.tox.2019.152337 · Cited by 23

Sedaghatian-type spondylometaphyseal dysplasia: Whole exome sequencing in neonatal dry blood spots enabled identification of a novel variant in GPX4

Fedida, A., Harouch, S. B., Kalfon, L., Abunassar, Z., Omari, H., Mandel, H., & Zaccai, T. C. F. (2020) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2020.104020 · Cited by 23

Açaí (Euterpe oleracea Martius) supplementation improves oxidative stress biomarkers in liver tissue of dams fed a high-fat diet and increases antioxidant enzymes’ gene expression in offspring

Barbosa, P. O., de Souza, M. O., Silva, M. P. S., Santos, G. T., Silva, M. E., Bermano, G., & de Freitas, R. N. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111627 · Cited by 23

Self-Activating Therapeutic Nanoparticle: A Targeted Tumor Therapy Using Reactive Oxygen Species Self-Generation and Switch-on Drug Release

Kang, R. H., Kim, Y., Kim, J. H., Kim, N. H., Ko, H. M., Lee, S.-H., Shim, I., Kim, J. S., Jang, H.-J., & Kim, D. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c07037 · Cited by 24

Influence of Oxidative Stress Generated by Smoking during Pregnancy on Glutathione Status in Mother-Newborn Pairs

Chełchowska, M., Gajewska, J., Ambroszkiewicz, J., Mazur, J., Ołtarzewski, M., & Maciejewski, T. (2021) · Antioxidants · doi:10.3390/antiox10121866 · Cited by 23

Synthesis, Reactions, and Antioxidant Properties of Bis(3-amino-1-hydroxybenzyl)diselenide

Yadav, M. K., Kumar, M., Chahal, A., Sodhi, N., Chhillar, B., Alajangi, H. K., Barnwal, R. P., & Singh, V. P. (2023) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.2c02739 · Cited by 23

Membrane Vesicles of Toxigenic Clostridioides difficile Affect the Metabolism of Liver HepG2 Cells

Caballano‐Infantes, E., Ho‐Plagaro, A., Gomez, C. L., Martín‐Reyes, F., Rodríguez‐Pacheco, F., Taminiau, B., Daube, G., Garrido‐Sánchez, L., Alcaín‐Martínez, G., Andrade, R. J., et al. (2023) · Antioxidants · doi:10.3390/antiox12040818 · Cited by 23

Ferritinophagy activation and sideroflexin1-dependent mitochondrial iron overload contribute to patulin-induced cardiac inflammation and fibrosis

Sun, W., Wang, N., Li, R., Sun, X., Liao, J.-W., Yang, G., & Liu, S. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.164472 · Cited by 23

Ferroptosis in Liver Disease: Natural Active Compounds and Therapeutic Implications

Wu, Z., Zhu, Y., Liu, W., Balasubramanian, B., Xu, X. L., Yao, J., & Lei, X. J. (2024) · Antioxidants · doi:10.3390/antiox13030352 · Cited by 26

Arabidopsis mutants affecting oxylipin signaling in photo-oxidative stress responses

Satoh, M., Tokaji, Y., Nagano, A. J., Hara‐Nishimura, I., Hayashi, M., Nishimura, M., Ohta, H., & Masuda, S. (2013) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2013.11.023 · Cited by 23

Low catalase expression confers redox hypersensitivity and identifies an indolent clinical behavior in CLL

Cavallini, C., Chignola, R., Dando, I., Perbellini, O., Mimiola, E., Lovato, O., Laudanna, C., Pizzolo, G., Donadelli, M., & Scupoli, M. T. (2018) · Blood · doi:10.1182/blood-2017-08-800466 · Cited by 23

Alternative approaches to overcome chemoresistance to apoptosis in cancer

Balaji, S., Terrero, D., Tiwari, A. K., Ashby, C. R., & Raman, D. (2021) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2021.01.005 · Cited by 24

The Role of Selenoprotein Tissue Homeostasis in MetS Programming: Energy Balance and Cardiometabolic Implications

Ojeda, M. L., Carreras, O., & Nogales, F. (2022) · Antioxidants · doi:10.3390/antiox11020394 · Cited by 23

NPGPx modulates CPEB2-controlled HIF-1α RNA translation in response to oxidative stress

Chen, P., Weng, J.-Y., Hsu, P., Shew, J., Huang, Y., & Lee, W. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1010 · Cited by 22

Detection of thiol-based redox switch processes in parasites – facts and future

Rahbari, M., Diederich, K., Becker, K., Krauth‐Siegel, R. L., & Jortzik, E. (2015) · Biological Chemistry · doi:10.1515/hsz-2014-0279 · Cited by 22

Electrochemical Methods for Study of Influence of Selenium Nanoparticles on Antioxidant Status of Rats

Horký, P., Ruttkay-Nedecky, B., Nejdl, L., Richtera, L., Cernei, N., Pohanka, M., Kopel, P., Skladanka, J., Hloucalova, P., Slama, P., et al. (2016) · International Journal of Electrochemical Science · doi:10.1016/s1452-3981(23)16142-6 · Cited by 22

Effects of cadmium exposure on expression of glutathione synthetase system genes in Acidithiobacillus ferrooxidans

Zheng, C., Zhang, L., Chen, M., Zhao, X. Q., Duan, Y., Ye, M., Zhang, X., & Shen, R. F. (2018) · Extremophiles · doi:10.1007/s00792-018-1046-3 · Cited by 22

Oxygen conditions oscillating between hypoxia and hyperoxia induce different effects in the pulmonary endothelium compared to constant oxygen conditions

Wohlrab, P., Danhofer, M. J., Schaubmayr, W., Tiboldi, Á., Krenn, K., Markstaller, K., Ullrich, R., Klein, K. U., & Tretter, V. E. (2021) · Physiological Reports · doi:10.14814/phy2.14590 · Cited by 21

Biodegradable copper telluride nanosheets for redox-homeostasis breaking-assisted chemodynamic cancer therapy boosted by mild-photothermal effect

Zhou, G., & Li, M. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.138348 · Cited by 22

Physiology and Proteomic Basis of Lung Adaptation to High-Altitude Hypoxia in Tibetan Sheep

Zhao, P., Li, S., He, Z., Zhao, F., Wang, J., Liu, X., Li, M., Hu, J., Zhao, Z., & Luo, Y. (2022) · Animals · doi:10.3390/ani12162134 · Cited by 23

Silencing TRPM2 enhanced erastin- and RSL3-induced ferroptosis in gastric cancer cells through destabilizing HIF-1α and Nrf2 proteins

Li, D., Wang, T., Lai, J., Zeng, D., Chen, W., Zhang, X., Zhu, X., Zhang, G., & Hu, Z. (2022) · Cytotechnology · doi:10.1007/s10616-022-00545-z · Cited by 22

Molecular mechanism of ferroptosis and its role in the occurrence and treatment of diabetes

Du, G.-H., Zhang, Q., Huang, X., & Wang, Y. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.1018829 · Cited by 22

Follicular fluid exosomes regulate oxidative stress resistance, proliferation, and steroid synthesis in porcine theca cells

Yuan, C., Chen, X., Shen, C., Chen, L., Zhao, Y., Wang, X., Cao, M., Zhao, Z., Chen, T., Zhang, B., et al. (2022) · Theriogenology · doi:10.1016/j.theriogenology.2022.09.024 · Cited by 22

Essential Roles of Peroxiredoxin IV in Inflammation and Cancer

Thapa, P., Ding, N., Hao, Y., Alshahrani, A., Jiang, H., & Wei, Q. (2022) · Molecules · doi:10.3390/molecules27196513 · Cited by 22

Glutathione peroxidase 4 expression predicts poor overall survival in patients with resected lung adenocarcinoma

Liu, C., Liu, C., Li, A. F., Hsu, T.-W., Lin, J.-H., Hung, S., & Hsu, H. (2022) · Scientific Reports · doi:10.1038/s41598-022-25019-2 · Cited by 22

Oxidative stress and inflammation: the root causes of aging

Sobhon, P., Savedvanich, G., & Weerakiet, S. (2023) · Exploration of Medicine · doi:10.37349/emed.2023.00129 · Cited by 26

Modeling Selenoprotein Se-Nitrosation: Synthesis of a Se-Nitrososelenocysteine with Persistent Stability

Masuda, R., Kuwano, S., & Goto, K. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c03394 · Cited by 22

Heme Oxygenase-1 and Its Role in Colorectal Cancer

Fahrer, J., Wittmann, S., Wolf, A., & Kostka, T. (2023) · Antioxidants · doi:10.3390/antiox12111989 · Cited by 27

Glutathione Peroxidase-like Antioxidant Activity of 1,3-Benzoselenazoles: Synthesis and In Silico Molecular Docking Studies as Pancreatic Lipase Inhibitors

Yadav, M., & Singh, V. P. (2023) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.3c01762 · Cited by 22

Competing endogenous RNA networks and ferroptosis in cancer: novel therapeutic targets

Orang, F. N., & Shadbad, M. A. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06732-4 · Cited by 25

Insight into the Role of Ferroptosis in Epilepsy

Huang, L., Liu, H., & Liu, S. (2024) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2306113 · Cited by 22

Oxidative damage repair by glutamine in fish enterocytes

Hu, K., Feng, L., Jiang, W., Liu, Y., Jiang, J., Li, S., & Zhou, X. (2014) · Fish Physiology and Biochemistry · doi:10.1007/s10695-014-9938-3 · Cited by 22

DAPK2 regulates oxidative stress in cancer cells by preserving mitochondrial function

Schlegel, C. R., Georgiou, M. L., Misterek, M. B., Stöcker, S., Chater, E., Munro, C. E., Pardo, O. E., Seckl, M. J., & Costa‐Pereira, A. P. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.31 · Cited by 22

GPX3 methylation in bone marrow predicts adverse prognosis and leukemia transformation in myelodysplastic syndrome

Zhou, J., Lin, J., Zhang, T., Ma, J., Yang, L., Wen, X., Guo, H. Y., Yang, J. C., Deng, Z., & Qian, J. (2016) · Cancer Medicine · doi:10.1002/cam4.984 · Cited by 23

Oxidative status of cardinal ligament in pelvic organ prolapse

Fang, G., Hong, L., Liu, C., Yang, Q. K., Zhang, Q., Li, Y., Li, B., Wu, D., Wu, W., & Shi, H. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.6633 · Cited by 23

Profiling of Alzheimer’s disease related genes in mild to moderate vitamin D hypovitaminosis

Grimm, M. O. W., Lauer, A. A., Grösgen, S., Thiel, A., Lehmann, J., Winkler, J., Janitschke, D., Herr, C., Beißwenger, C., Bals, R., et al. (2019) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.01.015 · Cited by 22

Analysis of Selenoprotein Expression in Response to Dietary Selenium Deficiency During Pregnancy Indicates Tissue Specific Differential Expression in Mothers and Sex Specific Changes in the Fetus and Offspring

Hofstee, P., Cuffe, J. S. M., & Perkins, A. V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062210 · Cited by 22

Glutathione Peroxidase 7 Suppresses Bile Salt-Induced Expression of Pro-Inflammatory Cytokines in Barrett's Carcinogenesis

Peng, D., Hu, T., Soutto, M., Belkhiri, A., & El-Rifai, W. M. (2014) · Journal of Cancer · doi:10.7150/jca.9215 · Cited by 22

Selenoprotein O deficiencies suppress chondrogenic differentiation of ATDC5 cells

Yan, J., Fei, Y., Han, Y., & Lu, S. (2016) · Cell Biology International · doi:10.1002/cbin.10644 · Cited by 22

Inducing ferroptosis by traditional medicines: a novel approach to reverse chemoresistance in lung cancer

Wang, Y., Hu, J., Fleishman, J. S., Li, Y., Zhao, R., Wang, J., Feng, Y., Chen, J., & Wang, H. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1290183 · Cited by 21

A GPX1-OSBPL8 axis mediates noncanonical in vivo ferroptosis and cancer growth suppression

Xia, Z., Yang, X. P., Самович, С. Н., Tyurina, Y. Y., Tyurin, V. A., Kon, N., Zhang, J., Jiang, X., Stockwell, B. R., Jin, J., et al. (2026) · Cell · doi:10.1016/j.cell.2026.01.009 · Cited by 25

DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism

Jabłońska, E., Raimondi, S., Gromadzińska, J., Reszka, E., Wieczorek, E., Król, M. B., Smok-Pieniążek, A., Nocun, M., Stepnik, M., Socha, K., et al. (2015) · Zeitschrift für Ernährungswissenschaft · doi:10.1007/s00394-015-1118-4 · Cited by 21

GPx1 knockdown suppresses chondrogenic differentiation of ATDC5 cells through induction of reductive stress

Yan, J., Guo, Y., Fei, Y., Zhang, R., Han, Y., & Lu, S. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw125 · Cited by 21

The Effect of Selenium on CYP450 Isoform Activity and Expression in Pigs

Jiang, Z., Gu, L.-B., Liang, X., Cao, B., Jingmiao, Z., & Guo, X. (2019) · Biological Trace Element Research · doi:10.1007/s12011-019-01945-7 · Cited by 21

Maternal selenium status plays a crucial role on clinical outcomes of pregnant women with COVID‐19 infection

Erol, S. A., Polat, N., Akdaş, S., Ayral, P. A., Anuk, A. T., Tokalıoğlu, E. Ö., Ayhan, Ş. G., Kesikli, B., Ceylan, M. N., Tanaçan, A., et al. (2021) · Journal of Medical Virology · doi:10.1002/jmv.27064 · Cited by 21

Production and purification of homogenous recombinant human selenoproteins reveals a unique codon skipping event in E. coli and GPX4-specific affinity to bromosulfophthalein

Cheng, Q., Roveri, A., Cozza, G., Bordin, L., Rohn, I., Schwerdtle, T., Kipp, A. P., Ursini, F., Maiorino, M., Miotto, G., et al. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102070 · Cited by 21

Multifunctional Flavonoid‐Silica Nanohydrogel Enables Simultaneous Inhibition of Tumor Recurrence and Bacterial Infection in Post‐Surgical Treatment

Chu, B., Wu, S., Yang, Y., Song, B., Wang, H., & He, Y. (2021) · Small · doi:10.1002/smll.202104578 · Cited by 21

Ferroptosis-related genes involved in animal reproduction: An Overview

Gan, J., Gu, T., Hong, L., & Cai, G. (2022) · Theriogenology · doi:10.1016/j.theriogenology.2022.02.022 · Cited by 22

Model Study on the Catalytic Cycle of Glutathione Peroxidase Utilizing Selenocysteine-Containing Tripeptides: Elucidation of the Protective Bypass Mechanism Involving Selenocysteine Selenenic Acids

Masuda, R., Kuwano, S., Sase, S., Bortoli, M., Madabeni, A., Orian, L., & Goto, K. (2022) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.20220156 · Cited by 21

Effect of selenium nanoparticles (SeNPs) supplementation on the sperm quality of fish after short-term storage

Zhu, C., Li, L., Liu, Q., Li, J., Peng, G., Zhang, L., Qi, M., Yang, F., Ji, H., & Dong, W. (2022) · Aquaculture · doi:10.1016/j.aquaculture.2022.738876 · Cited by 21

The Role of rs713041 Glutathione Peroxidase 4 (GPX4) Single Nucleotide Polymorphism on Disease Susceptibility in Humans: A Systematic Review and Meta-Analysis

Barbosa, P. O., El‐Magd, N. F. A., Hesketh, J. E., & Bermano, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415762 · Cited by 21

New perspectives on ferroptosis and its role in hepatocellular carcinoma

Cong, T., Luo, Y., Fu, Y. H. H., Liu, Y., Li, Y., & Li, X. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002327 · Cited by 21

Targeting critical pathways in ferroptosis and enhancing antitumor therapy of Platinum drugs for colorectal cancer

Wang, G., Wang, J., Zhu, Z., Xu, X.-N., Shi, F., & Fu, X.-L. (2023) · Science Progress · doi:10.1177/00368504221147173 · Cited by 22

Ferroptosis in epithelial ovarian cancer: a burgeoning target with extraordinary therapeutic potential

Ruan, D., Wen, J., Fang, F., Lei, Y., Zhao, Z., & Miao, Y. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01721-6 · Cited by 21

Evidence that oxidative stress is higher in replacement gilts than in multiparous sows

Roy, C., Lavoie, M., Richard, G., Archambault, A., & Lapointe, J. (2016) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12462 · Cited by 21

GPX3 promoter is methylated in chronic myeloid leukemia.

Yao, D., Zhou, J., Zhang, Y., Yang, L., Wen, X., Yang, J. C., Guo, H. Y., Chen, Q., Lin, J., & Qian, J. (2015) · Europe PMC (PubMed Central) · Cited by 21

Tanshinone I Attenuates the Effects of a Challenge with H2O2 on the Functions of Tricarboxylic Acid Cycle and Respiratory Chain in SH-SY5Y Cells

de Oliveira, M. R., Fürstenau, C. R., de Souza, I. C. C., & Ferreira, G. C. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0267-7 · Cited by 21

Colonic and Hepatic Modulation by Lipoic Acid and/or N‐Acetylcysteine Supplementation in Mild Ulcerative Colitis Induced by Dextran Sodium Sulfate in Rats

Moura, F. A., de Andrade, K. Q., de Araújo, O. R. P., Nunes-Souza, V., Santos, J. C. D. F., Rabelo, L. A., & Goulart, M. O. F. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/4047362 · Cited by 21

Oxidative stress and angiogenesis in primary hyperparathyroidism

Deska, M., Romuk, E. B., Segiet, O. A., Buła, G., Truchanowski, W., Stolecka, D., Birkner, E., & Gawrychowski, J. (2016) · European surgery. Supplement/European surgery · doi:10.1007/s10353-016-0457-6 · Cited by 21

Sodium selenite protects from 3-nitropropionic acid-induced oxidative stress in cultured primary cortical neurons

Colle, D., Santos, D. B., de Souza, V., Lopes, M. W., Leal, R. B., Brocardo, P. S., & Farina, M. (2018) · Molecular Biology Reports · doi:10.1007/s11033-018-4531-y · Cited by 21

Quantitative Redox Biology of Exercise

Nikolaidis, M. G., Margaritelis, N. V., & Matsakas, A. (2020) · International Journal of Sports Medicine · doi:10.1055/a-1157-9043 · Cited by 21

The Roles of Oxidative Stress in Regulating Autophagy in Methylmercury-induced Neurotoxicity

Wei, Y., Ni, L., Pan, J., Li, X., Xu, B., Deng, Y. L., Yang, T., & Liu, W. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.06.026 · Cited by 20

An Amphiphilic Selenide Catalyst Behaves Like a Hybrid Mimic of Protein Disulfide Isomerase and Glutathione Peroxidase 7

Arai, K., Moriai, K., Ogawa, A., & Iwaoka, M. (2014) · Chemistry - An Asian Journal · doi:10.1002/asia.201402726 · Cited by 21

Characterization of glutathione peroxidase diversity in the symbiotic sea anemone Anemonia viridis

Pey, A., Zamoum, T., Christen, R., Merle, P.-L., & Furla, P. (2016) · Biochimie · doi:10.1016/j.biochi.2016.10.016 · Cited by 20

Antioxidant activity in vivo and biological safety evaluation of a novel antioxidant peptide from bovine hair hydrolysates

Zeng, W., Sun, Q., Zhang, W., Liao, X., & Shi, B. Q. (2017) · Process Biochemistry · doi:10.1016/j.procbio.2017.02.022 · Cited by 20

Tetrahymena Glutathione Peroxidase Family: A Comparative Analysis of These Antioxidant Enzymes and Differential Gene Expression to Metals and Oxidizing Agents

Cubas-Gaona, L. L., de Francisco, P., Martín‐González, A., & Gutiérrez, J. C. (2020) · Microorganisms · doi:10.3390/microorganisms8071008 · Cited by 20

Maternal selenium deficiency suppresses proliferation, induces autophagy dysfunction and apoptosis in the placenta of mice

Li, M., Cheng, W., & Zhang, L. (2021) · Metallomics · doi:10.1093/mtomcs/mfab058 · Cited by 20

Cytochrome c oxidase mediates labile iron level and radioresistance in glioblastoma

Ali, M. Y., Oliva, C. R., Flor, S., Goswami, P. C., & Griguer, C. E. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.04.012 · Cited by 21

Methylmalonic acid induces inflammatory response and redox homeostasis disruption in C6 astroglial cells: potential glioprotective roles of melatonin and resveratrol

Almeida, R. R. D. S., Bobermin, L. D., Parmeggiani, B., Wartchow, K. M., Souza, D. O., Gonçalves, C., Wajner, M., Leipnitz, G., & Quincozes‐Santos, A. (2022) · Amino Acids · doi:10.1007/s00726-022-03191-z · Cited by 20

Progress in the study of nutritional status and selenium in dialysis patients

Cao, M., Zheng, S., Zhang, W., & Hu, G. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2197296 · Cited by 20

The Role of Amino Acids in Non-Enzymatic Antioxidant Mechanisms in Cancer: A Review

Dyachenko, E. I., & Bel’skaya, L. V. (2023) · Metabolites · doi:10.3390/metabo14010028 · Cited by 21

Redox regulation in lifespan determination

Karagianni, C., & Bazopoulou, D. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.105761 · Cited by 26

A deep insight into ferroptosis in lung disease: facts and perspectives

Zhang, F., Yu, X., Ma, Q., Guo, E., & Zeng, X. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1354859 · Cited by 19

Inducible RPE-specific GPX4 knockout causes oxidative stress and retinal degeneration with features of age-related macular degeneration

Wojciechowski, A. M., Bell, B. A., Song, Y., Anderson, B. D., Conomikes, A., Petruconis, C. R., & Dunaief, J. L. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.110028 · Cited by 20

Treatment with d-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease

Gromadzka, G., Karpińska, A., Przybyłkowski, A. M., Litwin, T., Wierzchowska‐Ciok, A., Dzieżyc, K., Chabik, G., & Członkowska, A. (2013) · BioMetals · doi:10.1007/s10534-013-9694-3 · Cited by 20

Serum selenium levels in patients with respiratory diseases: a prospective observational study

Lee, Y. H., Lee, S. J., Lee, M. K., Lee, W., Yong, S. J., & Kim, S. (2016) · Journal of Thoracic Disease · doi:10.21037/jtd.2016.07.60 · Cited by 20

Glutathione peroxidase 3 is a protective factor against acetaminophen-induced hepatotoxicity in vivo and in vitro

Kanno, S., Tomizawa, A., Yomogida, S., & Hara, A. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3049 · Cited by 20

A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Taurine Distribution in Various Tissues With and Without Taurine Supplementation

Park, E., Park, S., Cho, I. S., Kim, B. S., & Schuller‐Levis, G. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-94-024-1079-2_37 · Cited by 20

Comparative proteomic analysis of seminal plasma proteins in relation to freezability of Dezhou donkey semen

Yu, J., Li, M., Ji, C., Li, X., Li, H., Liu, G., Wang, Y., Liu, G., Wang, T., Che, X., et al. (2021) · Animal Reproduction Science · doi:10.1016/j.anireprosci.2021.106794 · Cited by 20

Changes of the Thioredoxin System, Glutathione Peroxidase Activity and Total Antioxidant Capacity in Rat Brain Cortex During Acute Liver Failure: Modulation by l-histidine

Ruszkiewicz, J. A., & Albrecht, J. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1417-9 · Cited by 21

Strain-Specific Benefits of Bacillus Probiotics in Hybrid Grouper: Growth Enhancement, Metabolic Health, Immune Modulation, and Vibrio harveyi Resistance

Han, C., Song, S., Cui, C., Cai, Y., Zhou, Y., Wang, J., Bei, W., Zhang, D., Guo, W., & Wang, S. (2024) · Animals · doi:10.3390/ani14071062 · Cited by 19

Session 10. Free radicals in biology and medicine Oral Presentations O10.1 Glutathione peroxidases in redox

Brigelius-flohé, R., Flohé, L., Mauri, P., Maiorini, M., & Ursini, F. (2014)

Tissue-specific functions of individual glutathione peroxidases

Brigelius-Flohé, R. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00173-2 · Cited by 1,114

Electrons and Protons | Glutathione Peroxidases

Ursini, F., & Maiorino, M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00572-7

Glutathione peroxidases and redox-regulated transcription factors

Brigelius‐Flohé, R. (2006) · Biological Chemistry · doi:10.1515/bc.2006.166 · Cited by 361

La sélénoprotéine T : un nouvel acteur dans la régulation glycémique

Prévost, G., Arabo, A., Cartier, D., Falluel‐Morel, A., Quelennec, M. E., Hassan, S., Tetsi-Nomigni, M., Lirhmann, I., Gargani, S., Kerr-Conte, J. A., et al. (2013) · Annales d Endocrinologie · doi:10.1016/j.ando.2013.07.116