Peroxynitrite reactivity with amino acids and proteins

Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide

Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029

Peroxynitrite oxidation of sulfhydryls.

Radí, R., Beckman, J. S., Bush, K., & Freeman, B. Α. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,492

The reaction of NO with superoxide

Huie, R. E., & Padmaja, S. (1993) · Free Radical Research Communications · doi:10.3109/10715769309145868 · Cited by 2,121

Peroxynitrite-mediated tyrosine nitration catalyzed by superoxide dismutase

Ischiropoulos, H., Zhu, L., Chen, J., Tsai, M., Martin, J. C., Smith, C. D. L., & Beckman, J. S. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90431-u · Cited by 1,499

Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils

Eiserich, J. P., Hristova, M., Cross, C. E., Jones, A. D., Freeman, B. A., Halliwell, B., & van der Vliet, A. (1998) · Nature · doi:10.1038/34923 · Cited by 1,496

Peroxynitrite, a cloaked oxidant formed by nitric oxide and superoxide

Koppenol, W. H., Moreno, J. J., Pryor, W. A., Ischiropoulos, H., & Beckman, J. S. (1992) · Chemical Research in Toxicology · doi:10.1021/tx00030a017 · Cited by 1,338

Formation of reactive nitrogen species during peroxidase-catalyzed oxidation of nitrite

van der Vliet, A., Eiserich, J. P., Halliwell, B., & Cross, C. E. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.12.7617 · Cited by 780

Nitration and inactivation of manganese superoxide dismutase in chronic rejection of human renal allografts.

MacMillan-Crow, L.-A., Crow, J. P., Kerby, J. D., Beckman, J. S., & Thompson, J. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11853 · Cited by 769

Unraveling peroxynitrite formation in biological systems

Radi, R., Peluffo, G., Alvarez, M. N., Naviliat, M., & Cayota, A. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00373-7 · Cited by 735

Inhibition of Mitochondrial Electron Transport by Peroxynitrite

Radi, R., Rodriguez, M., Castro, L., & Telleri, R. (1994) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1994.1013 · Cited by 693

Post-Translational Oxidative Modifications of Mitochondrial Complex I (NADH: Ubiquinone Oxidoreductase): Implications for Pathogenesis and Therapeutics in Human Diseases

Bharath, M. M. S. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170117 · Cited by 23

Boronate based sensitive fluorescent probe for the detection of endogenous peroxynitrite in living cells

Li, M., Han, H. L., Zhang, H., Song, S., Shuang, S., & Dong, C. (2020) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2020.118683 · Cited by 23

Evaluation of the effects of vitamin A supplementation on adult rat substantia nigra and striatum redox and bioenergetic states: Mitochondrial impairment, increased 3-nitrotyrosine and α-synuclein, but decreased D2 receptor contents

de Oliveira, M. R., Oliveira, M. W. S., Behr, G. A., Hoff, M. L. M., da Rocha, R. F., & Moreira, J. C. F. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.12.020 · Cited by 23

Pepper catalase: a broad analysis of its modulation during fruit ripening and by nitric oxide

González‐Gordo, S., López-Jaramillo, J., Rodríguez-Ruiz, M., Taboada, J., Palma, J. M., & Corpas, F. J. (2024) · Biochemical Journal · doi:10.1042/bcj20240247 · Cited by 22

Biochemical properties of new synthetic carnosine analogues containing the residue of 2,3-diaminopropionic acid: the effect of N-acetylation

Cacciatore, I., Cocco, A., Costa, M., Fontana, M., Lucente, G., Pecci, L., & Pinnen, F. (2005) · Amino Acids · doi:10.1007/s00726-004-0142-0 · Cited by 22

Evaluating the antioxidative activity of diselenide containing compounds in human blood

Saluk, J., Bijak, M., Nowak, P., & Wachowicz, B. (2013) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2013.07.003 · Cited by 22

A maternal low-protein diet and neonatal overnutrition result in similar changes to glomerular morphology and renal cortical oxidative stress measures in male Wistar rats

Pedroza, A. A. D. S., Ferreira, D. J. S., de Santana, D. F., da Silva, P. T., Júnior, F. C. A. D. A., Sellitti, D. F., & Lagranha, C. J. (2018) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2018-0288 · Cited by 22

UVB-induced inactivation of manganese-containing superoxide dismutase promotes mitophagy via ROS-mediated mTORC2 pathway activation

Dhar, S. K., Batinic̈‐Haberle, I., & Clair, D. K. S. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006595 · Cited by 22

Redox control of enzymatic functions: The electronics of life's circuitry

Bonini, M. G., Consolaro, M. E. L., Hart, P. C., Mao, M., de Abreu, A. L. P., & Master, А. M. (2014) · IUBMB Life · doi:10.1002/iub.1258 · Cited by 21

Oxidation of proteins

Heinonen, M., Gürbüz, G., & Ertbjerg, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817380-0.00003-8 · Cited by 21

Central nervous system injury meets nanoceria: opportunities and challenges

Wang, Y., Zhang, M., He, J., Gong, M., Sun, J. H., & Yang, X. (2022) · Regenerative Biomaterials · doi:10.1093/rb/rbac037 · Cited by 21

Plasma-Activated Tap Water Production and Its Application in Atomization Disinfection

Xiao, A., Liu, D., & Li, Y. (2023) · Applied Sciences · doi:10.3390/app13053015 · Cited by 21

The Key Targets of NO-Mediated Post-Translation Modification (PTM) Highlighting the Dynamic Metabolism of ROS and RNS in Peroxisomes

Ergashev, U., Yu, M., Luo, L., Tang, J., & Han, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168873 · Cited by 21

The protective effect of hypotaurine and cysteine sulphinic acid on peroxynitrite-mediated oxidative reactions

Fontana, M., Giovannitti, F., & Pecci, L. (2008) · Free Radical Research · doi:10.1080/10715760801999727 · Cited by 22

Crosslinking of human plasma C-reactive protein to human serum albumin via disulfide bond oxidation

Jiang, S., Hägglund, P., Carroll, L., Rasmussen, L. M., & Davies, M. J. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101925 · Cited by 21

Oxidation of hypotaurine and cysteine sulphinic acid by peroxynitrite

Fontana, M., Amendola, D., ORSINI, E., Boffi, A., & Pecci, L. (2005) · Biochemical Journal · doi:10.1042/bj20041696 · Cited by 21

Estimation of antioxidant capacity against pathophysiologically relevant oxidants using Pyrogallol Red

Robaszkiewicz, A., & Bartosz, G. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.10.023 · Cited by 21

Effects of Peroxynitrite on Relaxation through the NO/sGC/cGMP Pathway in Isolated Rat Iliac Arteries

Tawa, M., Shimosato, T., Iwasaki, H., Imamura, T., & Okamura, T. (2014) · Journal of Vascular Research · doi:10.1159/000371491 · Cited by 21

Peroxynitrite treatment in vitro disables catalytic activity of recombinant p38 MAPK

Webster, R. P., Macha, S. F., Brockman, D. E., & Myatt, L. (2006) · PROTEOMICS · doi:10.1002/pmic.200600176 · Cited by 21

Valsartan reverses post‐translational modifications of the δ‐subunit of ATP synthase during in vivo canine reperfused myocardial infarction

Sawicki, G., & Jugdutt, B. I. (2007) · PROTEOMICS · doi:10.1002/pmic.200601022 · Cited by 21

Relevance of peroxynitrite formation and 3-nitrotyrosine on spermatozoa physiology

Cruz, D. F., & Fardilha, M. (2016) · Porto Biomedical Journal · doi:10.1016/j.pbj.2016.07.004 · Cited by 21

Protein post-translational modifications – A challenge for bioelectrochemistry

Suprun, E. V. (2019) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2019.04.019 · Cited by 20

A comparative study of antioxidative activity of calcium-D-glucarate, sodium-D-gluconate and D-glucono-1,4-lactone in a human blood platelet model

Saluk, J. (2010) · Platelets · doi:10.3109/09537104.2010.512210 · Cited by 20

FeTPPS Reduces Secondary Damage and Improves Neurobehavioral Functions after Traumatic Brain Injury

Bruschetta, G., Impellizzeri, D., Campolo, M., Casili, G., Paola, R. D., Paterniti, I., Esposito, E., & Cuzzocrea, S. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00006 · Cited by 20

Kinetic studies of the reaction of heme-thiolate enzyme chloroperoxidase with peroxynitrite

Gȩbicka, L., & Didik, J. (2006) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2006.09.007 · Cited by 20

The Globins of Cyanobacteria and Algae

Johnson, E. A., & Lecomte, J. T. J. (2013) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-407693-8.00006-6 · Cited by 19

Glutathione Supplementation Attenuates Oxidative Stress and Improves Vascular Hyporesponsiveness in Experimental Obstructive Jaundice

Chen, J., Wu, F., Yue, L., & Yu, W. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/486148 · Cited by 19

Biochemical Strategies to Counter Nitrosative Stress

Alhasawi, A. A., Legendre, F., Jagadeesan, S., Appanna, V. P., & Appanna, V. D. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814849-5.00010-1 · Cited by 19

Oxidant Stress, Antioxidant Defense, and Liver Injury

McGill, M. R., & Jaeschke, H. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-387817-5.00004-2 · Cited by 19

Red Blood Cells as a Model to Differentiate between Direct and Indirect Oxidation Pathways of Peroxynitrite

Minetti, M., Pietraforte, D., Straface, E., Metere, A., Matarrese, P., & Malorni, W. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)00816-6 · Cited by 19

Probing the Hydroxyl Radical-Mediated Reactivity of Peroxynitrite by a Spin-Labeling Fluorophore

Bian, Z., Guo, X.-Q., Zhao, Y., & Du, J. (2005) · Analytical Sciences · doi:10.2116/analsci.21.553 · Cited by 19

Mechanisms of neurodegeneration in Alzheimer’s disease

Jovanović, Z. (2012) · Medicinski pregled · doi:10.2298/mpns1208301j · Cited by 18

Protection against peroxynitrite reactions by flavonoids

Sadowska‐Bartosz, I., Adamczyk, R., & Bartosz, G. (2014) · Food Chemistry · doi:10.1016/j.foodchem.2014.04.105 · Cited by 18

Degradation of extracellular matrix by peroxynitrite/peroxynitrous acid

Kennett, E. C., & Davies, M. J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.05.027 · Cited by 18

DNA polymerase gamma (Polγ) deficiency triggers a selective mTORC2 prosurvival autophagy response via mitochondria-mediated ROS signaling

Dhar, S. K., Bakthavatchalu, V., Dhar, B., Chen, J., Izumi, T., Zhu, H., Gao, T., & Clair, D. K. S. (2018) · Oncogene · doi:10.1038/s41388-018-0404-z · Cited by 18

The short-term consumption of a moderately high-fat diet alters nitric oxide bioavailability in lean female Zucker rats

Huang, K., Huang, Y., Frankel, J., Addis, C., Jaswani, L., Wehner, P. S., Mangiarua, E. I., & McCumbee, W. D. (2011) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y11-016 · Cited by 18

The Effect of the Ala16Val Mutation on the Secondary Structure of the Manganese Superoxide Dismutase Mitochondrial Targeting Sequence

Broz, M., Furlan, V., Lešnik, S., Jukič, M., & Bren, U. (2022) · Antioxidants · doi:10.3390/antiox11122348 · Cited by 17

Photoacoustic probes for inflammation-related biomarker imaging: Mechanisms, design, and applications

Li, G., Zhang, L., Zheng, H., & Lin, W. (2024) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2024.215975 · Cited by 18

Understanding the Reactivity of CO3·– and NO2· Radicals toward S-Containing and Aromatic Amino Acids

Karmakar, S., & Datta, A. (2017) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.7b05186 · Cited by 17

ROS-mediated downregulation of MYPT1 in smooth muscle cells: a potential mechanism for the aberrant contractility in atherosclerosis

Cheng, J., Cheng, H.-P., Tsai, I.-C., & Jiang, M. J. (2013) · Laboratory Investigation · doi:10.1038/labinvest.2013.40 · Cited by 17

Neuroinflammation and demyelination from the point of nitrosative stress as a new target for neuroprotection

Ljubisavljević, S., & Stojanović, I. R. (2014) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0060 · Cited by 19

Inactivation of rabbit muscle glycogen phosphorylase b by peroxynitrite revisited: Does the nitration of Tyr613 in the allosteric inhibition site control enzymatic function?

Sharov, V. S., Galeva, N. A., Dremina, E. S., Williams, T. D., & Schöneich, C. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.12.012 · Cited by 17

Reactive Nitrogen Species and Nitric Oxide

Procházková, D., Wilhelmová, N., & Pavlík, M. (2015) · Springer eBooks · doi:10.1007/978-3-319-17804-2_1 · Cited by 17

Peroxynitrite and nitrosoperoxycarbonate, a tightly connected oxidizing-nitrating couple in the reactive nitrogen-oxygen species family: new perspectives for protection from radical-promoted injury by flavonoids

Pavlović, R., & Santaniello, E. (2007) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.59.12.0011 · Cited by 17

Mitochondrial dysfunction: maternal protein restriction as a trigger of reactive species overproduction and brainstem energy failure in male offspring brainstem

Ferreira, D. J. S., Pedroza, A. A. D. S., Braz, G. R. F., Fernandes, M. P., & Lagranha, C. J. (2018) · Nutritional Neuroscience · doi:10.1080/1028415x.2018.1444543 · Cited by 17

Protein carbonyl determination by a rhodamine B hydrazide-based fluorometric assay

Georgiou, C. D., Zisimopoulos, D., Argyropoulou, V., Kalaitzopoulou, E., Ioannou, P. V., Salachas, G., & Grune, T. (2018) · Redox Biology · doi:10.1016/j.redox.2018.04.017 · Cited by 17

Nitric Oxide Pathways in Toxic Responses

Laskin, J. D., Heck, D. E., & Laskin, D. L. (2009) · General, Applied and Systems Toxicology · doi:10.1002/9780470744307.gat020 · Cited by 17

L‐NAME co‐treatment prevent oxidative damage in the lung of adult Wistar rats treated with vitamin A supplementation

Pasquali, M. A. D. B., de Oliveira, M. R., Bastiani, M. A. D., da Rocha, R. F., Schnorr, C. E., Gasparotto, J., Gelain, D. P., & Moreira, J. C. F. (2011) · Cell Biochemistry and Function · doi:10.1002/cbf.2791 · Cited by 16

ortho ‐Boronic Acid Carbonyl Compounds and Their Applications in Chemical Biology**

Haggett, J. G., & Domaille, D. W. (2023) · Chemistry - A European Journal · doi:10.1002/chem.202302485 · Cited by 16

Peroxynitrite: In vivo and In vitro synthesis and oxidant degradative action on biological systems regarding biomolecular injury and inflammatory processes

Hrabárová, E., Gemeiner, P., & Šoltés, L. (2007) · Chemical Papers · doi:10.2478/s11696-007-0058-8 · Cited by 16

Cross-linking and modification of fibronectin by peroxynitrous acid: Mapping and quantification of damage provides a new model for domain interactions

Mariotti, M., Rogowska-Wrzesińska, A., Hägglund, P., & Davies, M. J. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100360 · Cited by 16

The Pup-Proteasome System of Mycobacteria

Bode, N. J., & Darwin, K. H. (2014) · Microbiology Spectrum · doi:10.1128/microbiolspec.mgm2-0008-2013 · Cited by 17

Electron localization function and electron localizability indicator applied to study the bonding in the peroxynitrous acid HOONO

Berski, S., Latajka, Z., & Gordon, A. J. (2011) · Journal of Computational Chemistry · doi:10.1002/jcc.21731 · Cited by 16

GM-CSF Nitration Is a New Driver of Myeloid Suppressor Cell Activity in Tumors

Calì, B., Agnellini, A. H. R., Cioccarelli, C., Sánchez‐Rodríguez, R., Predonzani, A., Toffolo, G. I., Viola, A., Bronte, V., Arrigoni, G., Zonta, F., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.718098 · Cited by 15

Peroxynitrite is essential for aerenchyma formation in rice roots under waterlogging conditions

Singh, P., Jaiswal, S., Kushwaha, A., Gahlowt, P., Mishra, V., Tripathi, D. K., Singh, S. P., Gupta, R., & Singh, V. P. (2023) · Planta · doi:10.1007/s00425-023-04148-6 · Cited by 15

Game of ‘Somes: Protein Destruction for Mycobacterium tuberculosis Pathogenesis

Samanovic, M. I., & Darwin, K. H. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.10.001 · Cited by 15

Genetic Code Expansion: A Powerful Tool for Understanding the Physiological Consequences of Oxidative Stress Protein Modifications

Porter, J. J., & Mehl, R. A. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/7607463 · Cited by 15

Peroxynitrite supports a metabolic reprogramming in merlin-deficient Schwann cells and promotes cell survival

Pestoni, J. C., Plati, S. K., Camacho, O. D. V., Fuse, M. A., Onatunde, M. O., Sparrow, N. A., Karajannis, M. A., Fernández‐Valle, C., & Franco, M. C. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.007152 · Cited by 15

Comparative Study on High Fat Diet-induced 4-Hydroxy-2E-nonenal Adducts in the Hippocampal CA1 Region of C57BL/6N and C3H/HeN Mice

Hwang, I. K., Kim, I. Y., Kim, Y. N., Yi, S. S., Park, I.-S., Min, B.-H., Doo, H.-K., Ahn, S.-Y., Kim, Y. S., Lee, I. S., et al. (2008) · Neurochemical Research · doi:10.1007/s11064-008-9846-y · Cited by 15

Detrimental effects of hyperandrogenism on uterine functions

Elia, E. M., Vighi, S., Lombardi, E., & Motta, A. B. (2008) · International Immunopharmacology · doi:10.1016/j.intimp.2008.09.002 · Cited by 15

Functional consequences of actin nitration: in vitro and in disease states

Aslan, M. (2010) · Amino Acids · doi:10.1007/s00726-010-0613-4 · Cited by 15

Cross‐linking of serine racemase dimer by reactive oxygen species and reactive nitrogen species

Wang, W., & Barger, S. W. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.22832 · 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

Protein S-Nitrosylation and S-Glutathionylation as Regulators of Redox Homeostasis During Abiotic Stress Response

Begara-Morales, J. C., Sánchez-Calvo, B., Chaki, M., Valderrama, R., Mata-Pérez, C., Corpas, F. J., & Barroso, J. B. (2016) · Springer eBooks · doi:10.1007/978-3-319-44081-1_17 · Cited by 14

Formation of 3-nitrotyrosine by riboflavin photosensitized oxidation of tyrosine in the presence of nitrite

Fontana, M., Blarzino, C., & Pecci, L. (2011) · Amino Acids · doi:10.1007/s00726-011-0905-3 · 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

Separation and characterization of nitrated variants of the major birch pollen allergen by CZE ‐ ESI ‐μ TOF MS

Gusenkov, S., Ackaert, C., & Stutz, H. (2013) · Electrophoresis · doi:10.1002/elps.201300151 · 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

Renal hemodynamic and excretory responses to intra-arterial infusion of peroxynitrite in anesthetized rats

Matavelli, L. C., Kadowitz, P. J., Navar, L. G., & Majid, D. S. A. (2008) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.90487.2008 · Cited by 14

Partial outlet obstruction of the rabbit urinary bladder induces selective protein oxidation

Siflinger-Birnboim, A., Levin, R. M., & Hass, M. A. (2008) · Neurourology and Urodynamics · doi:10.1002/nau.20557 · Cited by 14

Efficacy of treatment with verbascoside, biotechnologically produced by Syringa vulgaris plant cell cultures in an experimental mice model of spinal cord trauma

Genovese, T., Paterniti, I., Mazzon, E., Esposito, E., Paola, R. D., Galuppo, M., Bramanti, P., & Cuzzocrea, S. (2010) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-010-0537-2 · Cited by 13

Peroxynitrite decomposition catalyst enhances respiratory function in isolated brain mitochondria

Albuck, A. L., Sakamuri, S. S. V. P., Sperling, J. A., Evans, W. R., Kolli, L., Sure, V. N. L. R., Mostany, R., & Katakam, P. V. G. (2020) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00389.2020 · Cited by 13

Moderate offspring exercise offsets the harmful effects of maternal protein deprivation on mitochondrial function and oxidative balance by modulating sirtuins

Pedroza, A. A. D. S., Bernardo, E. M., Pereira, A. R., Silva, S. C. A., Lima, T. A., Freitas, C. D. M., da Silva, J. C., Gomes, D. A., Ferreira, D. J. S., & Lagranha, C. J. (2021) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2021.01.006 · Cited by 13

Identification and quantification of protein nitration sites in human coronary artery smooth muscle cells in the absence and presence of peroxynitrous acid/peroxynitrite

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Effect of liquid-dissolved gas components on concentrations of the aqueous reactive oxygen and nitrogen species

Yang, Y. R., Li, Z., Nie, L., & Lu, X. (2019) · Journal of Applied Physics · doi:10.1063/1.5085258 · Cited by 13

Ischemia-Reperfusion Injury

Zingarelli, B. (2008) · Springer eBooks · doi:10.1007/978-1-84800-921-9_20 · Cited by 13

Formation of 6-nitrotryptophan in purified proteins by reactive nitrogen species: A possible new biomarker

Yamakura, F., Ikeda, K., Matsumoto, T., Taka, H., & Kaga, N. (2007) · International Congress Series · doi:10.1016/j.ics.2007.07.045 · Cited by 13

Design, solid phase synthesis and evaluation of cationic ferrocenoyl peptide bioconjugates as potential antioxidant enzyme mimics

Soulère, L., & Bernard, J. (2008) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2008.12.084 · 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

Strategies for comprehensive analysis of amino acid biomarkers of oxidative stress

Ptolemy, A. S., Lee, R., & Britz‐McKibbin, P. (2007) · Amino Acids · doi:10.1007/s00726-007-0542-z · Cited by 13

Ischemia-Reperfusion Injury

Hobson, M. J., & Zingarelli, B. (2014) · Springer eBooks · doi:10.1007/978-1-4471-6362-6_24 · Cited by 13

Novel isophorone fluorescent probe for ratiometric peroxynitrite imaging in vivo

Zhang, D., Lin, B., & Han, Y. (2024) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2024.136490 · Cited by 12

State of the art paper The cardioprotective power of leaves

Dudzińska, D., Boncler, M. A., & Watała, C. W. (2015) · Archives of Medical Science · doi:10.5114/aoms.2015.53303 · 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

Oxidative pathways in response to polyunsaturated aldehydes in the marine diatom Skeletonema marinoi (Bacillariophyceae)

Gallina, A. A., Palumbo, A., & Casotti, R. (2016) · Journal of Phycology · doi:10.1111/jpy.12421 · Cited by 12

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