Biological reactivity and biomarkers of the neutrophil oxidant, hypochlorous acid

Inflammation. Basic principles and clinical correlates

(1989) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(89)90156-x · Cited by 2,388

3-Chlorotyrosine, a specific marker of myeloperoxidase-catalyzed oxidation, is markedly elevated in low density lipoprotein isolated from human atherosclerotic intima.

Hazen, S. L., & Heinecke, J. W. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119379 · Cited by 842

Protein Carbonyl Measurement by a Sensitive ELISA Method

Buss, H., Chan, T., Sluis, K. B., Domigan, N. M., & Winterbourn, C. C. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00104-4 · Cited by 687

Inflammation: Basic Principles and Clinical Correlates

Ehrlich, G. E. (2000) · JAMA · doi:10.1001/jama.283.1.123 · Cited by 621

Presence of hypochlorite-modified proteins in human atherosclerotic lesions.

Hazell, L. J., Arnold, L., Flowers, D., Waeg, G., Malle, E., & Stocker, R. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118576 · Cited by 592

Comparative reactivities of various biological compounds with myeloperoxidase-hydrogen peroxide-chloride, and similarity of oxidant to hypochlorite

Winterbourn, C. C. (1985) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(85)90120-5 · Cited by 463

Kinetics of the reactions of hypochlorous acid and amino acid chloramines with thiols, methionine, and ascorbate

Peskin, A. V., & Winterbourn, C. C. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00506-2 · Cited by 335

Chlorination of Tyrosyl Residues in Peptides by Myeloperoxidase and Human Neutrophils

Domigan, N. M., Charlton, T. S., Duncan, M. W., Winterbourn, C. C., & Kettle, A. J. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.28.16542 · Cited by 330

Oxidation of Low-Density Lipoprotein by Hypochlorite Causes Aggregation That is Mediated by Modification of Lysine Residues Rather Than Lipid Oxidation

Hazell, L. J., van den Berg, J. J. M., & Stocker, R. (1994) · Biochemical Journal · doi:10.1042/bj3020297 · Cited by 267

Chlorohydrin Formation From Unsaturated Fatty Acids Reacted With Hypochlorous Acid

Winterbourn, C. C., van den Berg, J. J. M., Roitman, E., & Kuypers, F. A. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90609-z · Cited by 258

Mass spectrometric analysis of HOCl- and free-radical-induced damage to lipids and proteins

Pitt, A. R., & Spickett, C. M. (2008) · Biochemical Society Transactions · doi:10.1042/bst0361077 · Cited by 35

Recent Advances in Nanomaterials for the Treatment of Acute Kidney Injury

Ba, X., Ye, T., Shang, H., Tong, Y., Huang, Q., He, Y., Wu, J., Deng, W., Zhong, Z., Yang, X., et al. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c19308 · Cited by 37

[MD-16-0004R1] Increased taurine in pre-weaned juvenile mdx mice greatly reduces the acute onset of myofibre necrosis and dystropathology and prevents inflammation

Terrill, J. R., Grounds, M. D., & Arthur, P. G. (2016) · PLoS Currents · doi:10.1371/currents.md.77be6ec30e8caf19529a00417614a072 · Cited by 34

Mitochondria-targeted fluorescent probes for oxidative stress imaging

Niu, H., Chen, K., Xu, J., Zhu, X., Cao, W., Wang, Z., Ye, Y., & Zhao, Y. (2019) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2019.126938 · Cited by 34

Hypochlorous acid oxidizes methionine and tryptophan residues in myoglobin

Szuchman-Sapir, A. J., Pattison, D. I., Ellis, N. A., Hawkins, C. L., Davies, M. J., & Witting, P. K. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.06.010 · Cited by 34

Oxidative Damage to Proteins

Davies, M. J. (2012) · Wiley eBooks · doi:10.1002/9781119953678.rad045 · Cited by 38

Protection of flavonoids against hypochlorite-induced protein modifications

Siwak, J., Lewińska, A., Wnuk, M., & Bartosz, G. (2013) · Food Chemistry · doi:10.1016/j.foodchem.2013.04.018 · Cited by 30

Fine Regulation of Neutrophil Oxidative Status and Apoptosis by Ceruloplasmin and Its Derivatives

Golenkina, E. A., Viryasova, G. M., Galkina, S. I., Gaponova, T. V., Sud’ina, G. F., & Av, S. (2018) · Cells · doi:10.3390/cells7010008 · Cited by 30

Chemistry of Reactive Species

Villamena, F. A. (2013) · Wiley eBooks · doi:10.1002/9781118355886.ch1 · Cited by 31

Insight into the interactions of proteinase inhibitor- alpha-2-macroglobulin with hypochlorite

Siddiqui, T., Zia, M. K., Ali, S. S., Ahsan, H., & Khan, F. H. (2018) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2018.05.112 · Cited by 29

Hydrogen supplemented air inhalation reduces changes of prooxidant enzyme and gap junction protein levels after transient global cerebral ischemia in the rat hippocampus

Hugyecz, M., Mracsko, E. Z., Hertelendy, P., Farkas, E., Domoki, F., & Bari, F. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.068 · Cited by 29

Discrete interplay of gut microbiota L-tryptophan metabolites in host biology and disease

Ranhotra, H. S. (2023) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-023-04867-0 · Cited by 28

Protection of oral hydrogen water as an antioxidant on pulmonary hypertension

He, B., Zhang, Y., Kang, B., Xiao, J., Xie, B., & Wang, Z. (2013) · Molecular Biology Reports · doi:10.1007/s11033-013-2653-9 · Cited by 28

Myeloid cell–derived HOCl is a paracrine effector that trans-inhibits IKK/NF-κB in melanoma cells and limits early tumor progression

Liu, T. W., Gammon, S. T., Yang, P., Fuentes, D., & Piwnica-Worms, D. (2021) · Science Signaling · doi:10.1126/scisignal.aax5971 · Cited by 27

Phagocytosis, Oxidative Burst, and Produced Reactive Species are Affected by Iron Deficiency Anemia and Anemia of Chronic Diseases in Elderly

Paino, I. M. M., Miranda, J. C., Marzocchi-Machado, C. M., Cesarino, E. J., de Castro, F. A., & de Souza, A. M. (2009) · Biological Trace Element Research · doi:10.1007/s12011-008-8303-8 · Cited by 27

Loss of 3-chlorotyrosine by inflammatory oxidants: Implications for the use of 3-chlorotyrosine as a bio-marker in vivo

Whiteman, M., & Spencer, J. P. E. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.03.153 · Cited by 27

A dual-functional NIR fluorescence probe for detecting hypochlorous acid and bisulfite in biosystem

Ma, J., Kong, X., Zhao, M., Jiao, Z., Xie, H., Si, W., Li, H., & Zhang, Z. (2024) · Analytica Chimica Acta · doi:10.1016/j.aca.2024.342993 · Cited by 26

Uncovering an Emerging Group of Halogenated Nucleobase-Derived Disinfection Byproducts in Drinking Water: Prioritization of the Highly Cytotoxic 2-Chloroadenine

Sun, G., Guo, P., Kaw, H. Y., Zhou, M., & Wang, W. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c01484 · Cited by 28

Transient receptor potential A1 receptor‐mediated neural cross‐talk and afferent sensitization induced by oxidative stress: Implication for the pathogenesis of interstitial cystitis/bladder pain syndrome

Furuta, A., Suzuki, Y., Hayashi, N., Egawa, S., & Yoshimura, N. (2012) · International Journal of Urology · doi:10.1111/j.1442-2042.2012.02966.x · Cited by 26

Beneficial effects of high dose taurine treatment in juvenile dystrophic mdx mice are offset by growth restriction

Terrill, J. R., Pinniger, G. J., Nair, K. V., Grounds, M. D., & Arthur, P. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187317 · Cited by 26

Relationship between Protein Oxidation Biomarkers and Uterine Health in Dairy Cows during the Postpartum Period

Gabai, G., Luca, E. D., Miotto, G., Zin, G., Stefani, A., Dalt, L. D., Barberio, A., & Celi, P. (2019) · Antioxidants · doi:10.3390/antiox8010021 · Cited by 26

Myeloperoxidase-catalyzed chlorination: The quest for the active species

Ramos, D. R., García, M. V., Canle, M., Santaballa, J. A., Furtmüller, P. G., & Obinger, C. (2008) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2008.01.003 · Cited by 26

Challenges in Developing DNA and RNA Biomarkers of Inflammation

Dedon, P. C., DeMott, M. S., Elmquist, C. E., Prestwich, E. G., McFaline‐Figueroa, J. L., & Pang, B. (2007) · Biomarkers in Medicine · doi:10.2217/17520363.1.2.293 · Cited by 25

Role of Oxidant Scavengers in the Prevention of Ca2+ Homeostasis Disorders

Galan, C., Jardín, I., Dionisio, N., Salido, G. M., & Rosado, J. A. (2010) · Molecules · doi:10.3390/molecules15107167 · Cited by 25

Advanced oxidation protein products are generated by bovine neutrophils and inhibit free radical production in vitro

Bordignon, M., Dalt, L. D., Marinelli, L., & Gabai, G. (2013) · The Veterinary Journal · doi:10.1016/j.tvjl.2013.10.028 · Cited by 25

Apoptosis‐Inducing High .NO Concentrations Are Not Sustained Either in Nascent or in Developed Cancers

Heller, A. (2008) · ChemMedChem · doi:10.1002/cmdc.200800257 · Cited by 24

Fibrinogen Oxidation and Thrombosis: Shaping Structure and Function

Nencini, F., Giurranna, E., Borghi, S., Taddei, N., Fiorillo, C., & Becatti, M. (2025) · Antioxidants · doi:10.3390/antiox14040390 · Cited by 27

Taurine attenuated methotrexate-induced intestinal injury by regulating NF-κB/iNOS and Keap1/Nrf2/HO-1 signals

Hassanein, E. H. M., Althagafy, H. S., Atwa, A. M., Kozman, M. R., El-Sayed, M. I. K., & Soubh, A. A. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121180 · Cited by 24

Ascorbate and α-tocopherol differentially modulate reactive oxygen species generation by neutrophils in response to FcγR and TLR agonists

Chapple, I., Matthews, J. B., Wright, H. J., Scott, A. E., Griffiths, H. R., & Grant, M. M. (2012) · Innate Immunity · doi:10.1177/1753425912455207 · Cited by 24

A conjugated BODIPY–triphenylamine multi-aldoxime: Sonogashira coupling, ratiometric chemodosimeter and rapid detection of hypochlorite with two-photon excited fluorescence

Xu, C., Qian, Y., Qi, Z., Lü, C., & Cui, Y. (2018) · New Journal of Chemistry · doi:10.1039/c8nj00368h · Cited by 23

The benzene metabolite para-benzoquinone is genotoxic in human, phorbol-12-acetate-13-myristate induced, peripheral blood mononuclear cells at low concentrations

Westphal, G., Bünger, J., Lichey, N., Taeger, D., Mönnich, A., & Hallier, E. (2009) · Archives of Toxicology · doi:10.1007/s00204-009-0402-6 · Cited by 23

Design of a two-photon fluorescent probe for ratiometric imaging of endogenous hypochlorite in mitochondria

Li, L., Wang, X., Sun, C., Xu, T., Yang, Z., Zhang, Z., Feng, Y., Fang, M., Chen, M., Wang, X., et al. (2020) · Dyes and Pigments · doi:10.1016/j.dyepig.2020.108548 · Cited by 22

A large Stokes shift and emission shift ratiometric mitochondria-targeted fluorescent probe for sensing HClO with an ESIPT-ICT integrated platform

Shen, Y., Jin, J., Chen, Y., & Tang, Y. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.109424 · Cited by 21

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

Mapping the modification of histones by the myeloperoxidase-derived oxidant hypochlorous acid (HOCl)

Hallberg, L. A. E., Thorsen, N. W., Hartsema, E. A., Hägglund, P., & Hawkins, C. L. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.09.016 · Cited by 21

Biomarkers of Postpartum Depression: A Narrative Review

Modzelewski, S., Oracz, A. J., Iłendo, K., Sokół, A., & Waszkiewicz, N. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12206519 · Cited by 26

Fluoxetine protects against OVA induced bronchial asthma and depression in rats

Sherkawy, M. M., Abo‐Youssef, A. M., Salama, A., & Ismaiel, I. E.-K. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.08.026 · Cited by 21

Non-immunological toxicological mechanisms of metamizole-associated neutropenia in HL60 cells

Rudin, D., Lanzilotto, A., Bachmann, F., Housecroft, C. E., Constable, E. C., Drewe, J., Haschke, M., & Krähenbühl, S. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.01.011 · Cited by 23

Pathophysiological Role of Transient Receptor Potential Ankyrin 1 in a Mouse Long-Lasting Cystitis Model Induced by an Intravesical Injection of Hydrogen Peroxide

Oyama, S., Dogishi, K., Kodera, M., Kakae, M., Nagayasu, K., Shirakawa, H., Nakagawa, T., & Kaneko, S. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00877 · Cited by 20

Afrormosin, an Isoflavonoid from A mburana cearensis A . C . S mith, Modulates the Inflammatory Response of Stimulated Human Neutrophils

Lopes, A. D. A., Rocha, T. M., Uchoa, D. E. D. A., Silveira, E. R., Azzolini, A. E. C. S., Kabeya, L. M., Lucisano-Valim, Y. M., Vasconcelos, S. M. M., Viana, G. S. D. B., & Leal, L. K. A. M. (2013) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.12106 · Cited by 20

Modulation of the Nitric Oxide/BH4 Pathway Protects Against Irradiation-Induced Neuronal Damage

Thabet, N. M., Rashed, E. R., Abdel-Rafei, M. K., & Moustafa, E. M. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03306-0 · Cited by 20

The antioxidant protection of CELLFOOD® against oxidative damage in vitro

Benedetti, S., Catalani, S., Palma, F., & Canestrari, F. (2011) · Food and Chemical Toxicology · doi:10.1016/j.fct.2011.06.029 · Cited by 19

Chemistry of Reactive Species

Villamena, F. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-420017-3.00005-0 · Cited by 19

Effects of a novel selenium substituted-sugar (1,4-anhydro-4-seleno-d-talitol, SeTal) on human coronary artery cell lines and mouse aortic rings

Zacharias, T., Flouda, K., Jepps, T. A., Gammelgaard, B., Schiesser, C. H., & Davies, M. J. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.113631 · Cited by 18

Variants of the 5′-untranslated region of human NCF2: Expression and translational efficiency

Gauss, K. A., Bunger, P. L., Crawford, M. A., McDermott, B. E., Swearingen, R., Nelson-Overton, L. K., Siemsen, D. W., Kobayashi, S. D., DeLeo, F. R., & Quinn, M. T. (2005) · Gene · doi:10.1016/j.gene.2005.09.012 · Cited by 18

A fluorescence probe for monitoring toxic hypochlorous acid in biosystems and environmental waters with a broad pH adaptation

Ma, J., Jiao, Z., Zhao, M., Kong, X., Xie, H., & Zhang, Z. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117370 · Cited by 17

Sirtuins and Sepsis: Cross Talk between Redox and Epigenetic Pathways

Anugraha, G., Roychowdhury, S., & Vachharajani, V. (2021) · Antioxidants · doi:10.3390/antiox11010003 · Cited by 17

Physiological biomarkers in loggerhead turtles (Caretta caretta) as a tool for monitoring sanitary evolution in marine recovery centres

Pinya, S., Renga, E., Fernández, G., Mateu‐Vicens, G., Tejada, S., Capó, X., & Sureda, A. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.143930 · Cited by 17

Antioxidant supplementation influences the neutrophil tocopherol associated protein expression, but not the inflammatory response to exercise

Sureda, A., Tauler, P., Aguiló, A., Cases, N., Llompart, I., Tur, J. A., & Pons, A. (2007) · Open Life Sciences · doi:10.2478/s11535-007-0006-1 · Cited by 17

Tyrosine can protect against oxidative stress through ferryl hemoglobin reduction

Lu, N., He, Y., Chen, C., Tian, R., Xiao, Q., & Peng, Y. (2014) · Toxicology in Vitro · doi:10.1016/j.tiv.2014.03.014 · Cited by 17

A Blood Biomarker for Duchenne Muscular Dystrophy Shows That Oxidation State of Albumin Correlates with Protein Oxidation and Damage in Mdx Muscle

Al-Mshhdani, B. A., Grounds, M. D., Arthur, P. G., & Terrill, J. R. (2021) · Antioxidants · doi:10.3390/antiox10081241 · Cited by 16

Reduction of oxidative stress may play a role in the anti-inflammatory effect of the novel herbal formulation in a rat model of hydrochloric acid-induced cystitis

Bae, W., Ha, U., Kim, S., Kim, S., Hong, S., Lee, J.-Y., HWANG, T.-K., Hwang, S., Kim, H., & Kim, S.-W. (2013) · Neurourology and Urodynamics · doi:10.1002/nau.22507 · Cited by 16

Aminobenzoic acid hydrazide, a myeloperoxidase inhibitor, alters the adhesive properties of neutrophils isolated from acute myocardial infarction patients

Han, L., Shen, X., Pan, L., Lin, S., Liu, X., Deng, Y., & Pu, X. (2011) · Heart and Vessels · doi:10.1007/s00380-011-0178-5 · Cited by 16

TRPA1 and issues relating to animal model selection for extrapolating toxicity data to humans

Lindsay, C., & Timperley, C. M. (2019) · Human & Experimental Toxicology · doi:10.1177/0960327119877460 · Cited by 16

Fluorescence Technique

Villamena, F. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-420017-3.00003-7 · Cited by 18

N-Chloroamino acids mediate the action of hypochlorite on A549 lung cancer cells in culture

Robaszkiewicz, A., Bartosz, G., & Soszyński, M. (2010) · Toxicology · doi:10.1016/j.tox.2010.02.003 · Cited by 16

Photocytotoxicity of platinum(IV)-chloride surface modified TiO2 irradiated with visible light against murine macrophages

Kyzioł, A., Wolnicka-Głubisz, A., Urbańska, K., Stochel, G., & Macyk, W. (2008) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2008.05.003 · Cited by 15

About the dangers, costs and benefits of living an aerobic lifestyle

Knoefler, D., Leichert, L. I. O., Thamsen, M., Cremers, C. M., Reichmann, D., Gray, M. J., Wholey, W.-Y., & Jakob, U. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140108 · Cited by 15

A Near-Infrared Fluorescent Probe for Recognition of Hypochlorite Anions Based on Dicyanoisophorone Skeleton

Liu, C.-X., Xiao, S.-Y., Gong, X.-L., Zhu, X., Wang, Y., & Peng, Y. (2023) · Molecules · doi:10.3390/molecules28010402 · Cited by 15

Myeloperoxidase impairs the contractile function in isolated human cardiomyocytes

Kalász, J., Pásztor, E. T., Fagyas, M., Balogh, Á., Tóth, A., Csató, V., Edes, I. F., Papp, Z., & Borbély, A. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.02.036 · Cited by 15

Novel 5-aminosalicylic derivatives as anti-inflammatories and myeloperoxidase inhibitors evaluated in silico, in vitro and ex vivo

Pérez, L. C. C., Gutiérrez‐Sánchez, M., Wejebe, J. E. M., Rodríguez, M. H., Fragoso-Vázquez, M. J., Salazar, J. R., Correa‐Basurto, J., Martínez, I. I. P., & Rosales‐Hernández, M. C. (2017) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2016.12.026 · Cited by 15

Interplay between group A Streptococcus and host innate immune responses

Su, M. S., Cheng, Y., Lin, Y., & Wu, J.-J. (2024) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00052-22 · Cited by 15

Probiotic bacteria protect against indomethacin-induced gastric ulcers through modulation of oxidative stress, inflammation, and apoptosis

Gelen, V., Gedikli, S., Gelen, S. U., Şengül, E., & Makav, M. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09627-x · Cited by 14

REMOVED: Protein kinase inhibitors in traumatic brain injury and repair: New roles of nanomedicine

Sharma, H. S., Sahib, S., Tian, Z. R., Muresanu, D. F., Nozari, A., Lafuente, J. V., Wiklund, L., & Sharma, A. (2020) · Progress in brain research · doi:10.1016/bs.pbr.2020.09.009 · Cited by 14

Functionally Active Macrophage-Derived Myeloperoxidase in the Skin of Drug-Induced Toxic Epidermal Necrolysis

Paquet, P., Groote, D. D., & Pierard, G. (2010) · Dermatology · doi:10.1159/000284592 · Cited by 14

Ratiometric fluorescent probe with AIE characteristics for hypochlorite detection and biological imaging

Bi, W., Zhao, X., Yang, X., Yuan, X., Lin, Y., Xu, K., Liu, L., Zeng, H., Du, G., & Zhang, L. (2024) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2024.124904 · Cited by 13

Phagocytosis and nitric oxide levels in rheumatic inflammatory states in elderly women

Paino, I. M. M., Miranda, J. C., Marzocchi-Machado, C. M., Cesarino, E. J., de Castro, F. A., & de Souza, A. M. (2011) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.20429 · Cited by 13

Targeting oxidative stress and inflammation in NSAIDs induced gastropathy: A plausible therapeutic approach

(2015) · Inflammation and Cell Signaling · doi:10.14800/ics.763 · Cited by 13

The effects of fluoxetine on circulating oxidative damage parameters in rats exposed to aortic ischemia–reperfusion

Erman, H., Güner, İ., Yaman, M. O., Uzun, D. D., Gelışgen, R., Aksu, U., Yelmen, N. K., Şahin, G., & Uzun, H. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.01.007 · Cited by 13

Hypochlorous acid-induced modulation of cellular redox status in HeLa cells

Park, S. Y., Shin, S., Lee, S., & Park, J. (2008) · Archives of Pharmacal Research · doi:10.1007/s12272-001-1245-y · Cited by 13

Identification of a novel tumor necrosis factor α-responsive region in the NCF2 promoter

Gauss, K. A., Bunger, P. L., Larson, T., Young, C. J., Nelson-Overton, L. K., Siemsen, D. W., & Quinn, M. T. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.0604329 · Cited by 13

Use of Pyrogallol Red and Pyranine as Probes to Evaluate Antioxidant Capacities towards Hypochlorite

Pérez‐Cruz, F., Cortés, C., Atala, E., Bohle, P., Valenzuela, F. J., Olea‐Azar, C., Speisky, H., Aspée, A., Lissi, E. A., López‐Alarcón, C., et al. (2013) · Molecules · doi:10.3390/molecules18021638 · Cited by 12

Oxidative injury induced by hypochlorous acid to Ca-ATPase from sarcoplasmic reticulum of skeletal muscle and protective effect of trolox

Štrosová, M., Karlovská, J., Spickett, C. M., Grune, T., Orszagova, Z., & Horáková, Ľ. (2009) · General Physiology and Biophysics · doi:10.4149/gpb_2009_02_195 · Cited by 12

Oxidative Stress in Depression

Gałecki, P. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_190 · Cited by 11

Phospholipase A2 Inhibitor from Crotalus durissus terrificus rattlesnake: Effects on human peripheral blood mononuclear cells and human neutrophils cells

Xavier, C. V., Setúbal, S. D. S., Lacouth-Silva, F., Pontes, A. S., Néry, N. M., de Castro, O. B., Fernandes, C. F. C., Soares, A. M., Fortes-Dias, C. L., & Zuliani, J. P. (2017) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2017.07.140 · Cited by 11

A Modern Approach to Disinfection, as Old as the Evolution of Vertebrates

Migliarina, F., & Ferro, S. (2014) · Healthcare · doi:10.3390/healthcare2040516 · Cited by 11

In vitro antibacterial activity of E-101 Solution, a novel myeloperoxidase-mediated antimicrobial, against Gram-positive and Gram-negative pathogens

Denys, G. A., Grover, P., O'Hanley, P. D., & Stephens, J. T. (2010) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkq429 · Cited by 11

Oxidative, Nitrosative, and Chlorinative Stress: Biomarkers

Bartosz, G., & Sadowska‐Bartosz, I. (2014) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-1-4939-0440-2_1 · Cited by 10

Superoxide Anion Production by Human Neutrophils Activated by Trichomonas vaginalis

Song, H.-O., & Ryu, J. (2013) · Korean Journal of Parasitology · doi:10.3347/kjp.2013.51.4.479 · Cited by 10

Mechanism of Microbicidal Action of E-101 Solution, a Myeloperoxidase-Mediated Antimicrobial, and Its Oxidative Products

Denys, G. A., Devoe, N. C., Gudis, P., May, M. A., Allen, R. C., & Stephens, J. T. (2019) · Infection and Immunity · doi:10.1128/iai.00261-19 · Cited by 10

Investigation of the effect of taurine supplementation on muscle taurine content in the mdx mouse model of Duchenne muscular dystrophy using chemically specific synchrotron imaging

Terrill, J. R., Webb, S. M., Arthur, P. G., & Hackett, M. J. (2020) · The Analyst · doi:10.1039/d0an00642d · Cited by 10

An Amperometric Flow Injection Analysis of Dissolved Hydrogen Molecule Using Tightly Immobilized Electrodeposited Platinum Particles on Nitrogen-containing Functional Groups Introduced Glassy Carbon Electrodes

Matsuura, H., Takahashi, T., Sakamoto, S., Kitamura, T., & Uchiyama, S. (2017) · Analytical Sciences · doi:10.2116/analsci.33.703 · Cited by 9

Oxidative damage to urinary proteins from the GRMD dog and mdx mouse as biomarkers of dystropathology in Duchenne muscular dystrophy

Terrill, J. R., Al-Mshhdani, B. A., Duong, M. N., Wingate, C. D., Abbas, Z., Baustista, A. P., Bettis, A. K., Balog-Alvarez, C. J., Kornegay, J. N., Nghiem, P. P., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0240317 · Cited by 9

Hypochlorite-induced oxidation of fibrinogen: Effects on its thermal denaturation and fibrin structure

Rosenfeld, M. A., Wasserman, L. A., Vasilyeva, A. D., Podoplelova, N. A., Panteleev, M. A., & Yurina, L. V. (2021) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2021.129970 · Cited by 9

The effect of hypochlorite- and peroxide-induced oxidation of plasminogen on damage to the structure and biological activity

Vasilyeva, A. D., Yurina, L. V., Ivanov, V. S., Azarova, D. Y., Gavrilina, E. S., Indeykina, M. I., Bugrova, A. E., Kononikhin, A. S., Nikolaev, E., & Rosenfeld, M. A. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.02.128 · Cited by 9

Fluorescent Probes for HOCl Detection in Living Cells

Reut, V. E., Gorudko, I. V., Grigorieva, D. V., Av, S., & Panasenko, O. M. (2022) · Russian Journal of Bioorganic Chemistry · doi:10.1134/s1068162022030165 · Cited by 9

HOCl-modified phosphatidylcholines induce apoptosis and redox imbalance in HUVEC-ST cells

Robaszkiewicz, A., Bartosz, G., Pitt, A. R., Thakker, A., Armstrong, R. A., Spickett, C. M., & Soszyński, M. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.02.013 · Cited by 9

Stimuli-responsive antioxidant nanoprodrugs of NSAIDs

Lee, B., Yuan, X., Xu, Q., McLafferty, F. S., Petersen, B. A., Collette, J. C., Black, K. L., & Yu, J. S. (2009) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2008.12.037 · Cited by 9

Evaluation of amino acids as mediators for the antibacterial activity of iodine-lithium-α-dextrin in vitro and in vivo

Davtyan, T. K., Hakobyan, I. S., Muradyan, R. E., Hovhannisyan, H., & Gabrielyan, E. S. (2007) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkm094 · Cited by 9

Functional Enzyme Mimics for Oxidative Halogenation Reactions that Combat Biofilm Formation

Herget, K., Frerichs, H., Pfitzner, F., Tahir, M. N., & Tremel, W. (2020) · Nanostructure science and technology · doi:10.1007/978-981-15-1490-6_8 · Cited by 9

Neutrophil-Derived Myeloperoxidase and Hypochlorous Acid Critically Contribute to 20-Hydroxyeicosatetraenoic Acid Increases that Drive Postischemic Angiogenesis

Azcona, J. A., Tang, S., Berry, E., Zhang, F. F., Garvey, R., Falck, J. R., Schwartzman, M. L., Yi, T., Jeitner, T. M., & Guo, A. M. (2022) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.121.001036 · Cited by 8

Exploration of Potential Anti‐Inflammatory Cum Anti‐Rheumatoid‐Arthritis Phyto‐Molecule Through Integrated Green Approach: Network Pharmacology, Molecular Docking, Molecular Dynamics, In‐Vitro and Ex‐Vivo Study

Kumar, A., Ikbal, A. M. A., Laskar, M. A., Sarkar, A., Saha, A., Bhardwaj, P., Das, S., Singh, S. K., Ghosh, P., Kargarzadeh, H., et al. (2024) · Chemistry & Biodiversity · doi:10.1002/cbdv.202401137 · Cited by 7

Effect of oxidants and antioxidants on oral health

Dąbrowska, Z. N., Bijowski, K., Dabrowska, E., & Pietruska, M. (2020) · Medycyna Ogólna i Nauki o Zdrowiu · doi:10.26444/monz/122255 · Cited by 7

A new pyrene-based “turn-on” fluorescent probe for highly selective detection of hypochlorite in aqueous solution and in living cells

Jiang, N., Zhou, X., Zhong, T., & Wang, G. (2022) · Chemical Papers · doi:10.1007/s11696-022-02475-8 · Cited by 7

An Anthracene Carboxamide-Based Fluorescent Probe for Rapid and Sensitive Detection of Mitochondrial Hypochlorite in Living Cells

Liu, X., Zhou, G., Wang, Y., & Zhang, W. (2023) · Biosensors · doi:10.3390/bios13090883 · Cited by 7

Association of themyeloperoxidase-468G→A polymorphism with gastric inflammation and duodenal ulcer risk

Hsu, P. (2005) · World Journal of Gastroenterology · doi:10.3748/wjg.v11.i18.2796 · Cited by 7

The location of protein oxidation in dystrophic skeletal muscle from the mdx mouse model of Duchenne muscular dystrophy

Iwasaki, T., Terrill, J. R., Kawarai, K., Miyata, Y., Tagami, T., Maeda, N., Hasegawa, Y., Watanabe, T., Grounds, M. D., & Arthur, P. G. (2022) · Acta Histochemica · doi:10.1016/j.acthis.2022.151959 · Cited by 6

Biomarkers of myeloperoxidase-derived hypochlorous acid

Winterbourn, C. C., & Kettle, A. J. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00204-5 · Cited by 390

5533210 Completely reyclable jacket made of synthetic polymer material

(1996) · Journal of Cleaner Production · doi:10.1016/s0959-6526(97)88858-0

Myeloperoxidase-Derived Oxidants Hypochlorous Acid and Chloramines

Vissers, M. C. M., Pullar, J. M., Peskin, A. V., Hampton, M. B., & Kettle, A. J. (2017) · CRC Press eBooks · doi:10.1201/9781315154831-12

Hypochlorous acid as a precursor of free radicals in living systems

Panasenko, O. M., Gorudko, I. V., & Av, S. (2013) · Biochemistry (Moscow) · doi:10.1134/s0006297913130075 · Cited by 159

Myeloperoxidase: a key regulator of neutrophil oxidant production

Kettle, A. J., & Winterbourn, C. C. (1997) · Redox Report · doi:10.1080/13510002.1997.11747085 · Cited by 671