Myeloperoxidase, a catalyst for lipoprotein oxidation, is expressed in human atherosclerotic lesions.

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394

The pathogenesis of atherosclerosis: a perspective for the 1990s

Ross, R. (1993) · Nature · doi:10.1038/362801a0 · Cited by 10,618

Beyond Cholesterol

Epstein, F. H., Steinberg, D. I., Parthasarathy, S., Carew, T. E., Khoo, J. C., & Witztum, J. L. (1989) · New England Journal of Medicine · doi:10.1056/nejm198904063201407 · Cited by 6,425

The Pathogenesis of Atherosclerosis — An Update

Ross, R. (1986) · New England Journal of Medicine · doi:10.1056/nejm198602203140806 · Cited by 4,885

Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent

Babior, B. M., Kipnes, R. S., & Curnutte, J. T. (1973) · Journal of Clinical Investigation · doi:10.1172/jci107236 · Cited by 2,931

Oxygen-Dependent Microbial Killing by Phagocytes

BABIOR, B. M. (1978) · New England Journal of Medicine · doi:10.1056/nejm197803232981205 · Cited by 2,483

Binding site on macrophages that mediates uptake and degradation of acetylated low density lipoprotein, producing massive cholesterol deposition

Goldstein, J. L., Ho, Y. K., Basu, S. K., & Brown, M. S. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.333 · Cited by 2,447

Evidence for the presence of oxidatively modified low density lipoprotein in atherosclerotic lesions of rabbit and man.

Ylä‐Herttuala, S., Palinski, W., Rosenfeld, M. E., Parthasarathy, S., Carew, T. E., Butler, S. S., Witztum, J. L., & Steinberg, D. H. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114271 · Cited by 1,877

Modification of low density lipoprotein by endothelial cells involves lipid peroxidation and degradation of low density lipoprotein phospholipids.

Steinbrecher, U. P., Parthasarathy, S., Leake, D. S., Witztum, J. L., & Steinberg, D. I. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.12.3883 · Cited by 1,626

Low density lipoprotein undergoes oxidative modification in vivo.

Palinski, W., Rosenfeld, M. E., Ylä‐Herttuala, S., Gurtner, G. C., Socher, S. S., Butler, S. W., Parthasarathy, S., Carew, T. E., Steinberg, D. H., & Witztum, J. L. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.4.1372 · Cited by 1,514

Free Radical Lipid Peroxidation Induced by Reactive Halogen Species

Panasenko, O. M., Vladimirov, Y. A., & Сергиенко, В. И. (2024) · Biochemistry (Moscow) · doi:10.1134/s0006297924140098 · Cited by 15

Pathophysiology of Lipoprotein Oxidation

Jairam, V., Uchida, K., & Narayanaswami, V. (2012) · InTech eBooks · doi:10.5772/50622 · Cited by 15

Passive Immunization with Hypochlorite-oxLDL Specific Antibodies Reduces Plaque Volume in LDL Receptor-Deficient Mice

van Leeuwen, M., Kemna, M. J., de Winther, M. P. J., Boon, L., Duijvestijn, A. M., Henatsch, D., Bos, N. A., Gijbels, M. J., & Tervaert, J. W. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068039 · Cited by 15

A pivotal role for NF-κB in the macrophage inflammatory response to the myeloperoxidase oxidant hypothiocyanous acid

Pan, G. J., Rayner, B. S., Zhang, Y., van Reyk, D. M., & Hawkins, C. L. (2018) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2018.01.016 · Cited by 15

Specific detection of hypochlorite: a cyanine based turn-on fluorescent sensor

Samanta, S., Halder, S., Manna, U., & Das, G. C. (2019) · Journal of Chemical Sciences · doi:10.1007/s12039-019-1612-y · Cited by 15

Melatonin rescues swim stress induced gastric ulceration by inhibiting matrix metalloproteinase-3 via down-regulation of inflammatory signaling cascade

Choudhary, P., Roy, T., Chatterjee, A., Mishra, V. K., Pant, S., & Swarnakar, S. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120426 · Cited by 16

Tracking HOCl by an incredibly simple fluorescent probe with AIE plus ESIPT in vitro and in vivo

Qu, W., Guo, T., Yang, B., Tian, R., Qiu, S., Chen, X., Geng, Z., & Wang, Z. (2022) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2022.121649 · Cited by 15

Validation of an Integrated Genetic‐Epigenetic Test for the Assessment of Coronary Heart Disease

Philibert, R. A., Dogan, T., Knight, S., Ahmad, F., Lau, S. K., Miles, G., Knowlton, K. U., & Dogan, M. V. (2023) · Journal of the American Heart Association · doi:10.1161/jaha.123.030934 · Cited by 15

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

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

Oximes as inhibitors of low density lipoprotein oxidation

Portella, R. D. L., Barcelos, R. P., Bem, A. F. D., Carratu, V. S., Bresolin, L., da Rocha, J. B. T., & Soares, F. A. A. (2008) · Life Sciences · doi:10.1016/j.lfs.2008.10.005 · Cited by 15

Native low density lipoprotein promotes lipid raft formation in macrophages

Song, J., Ping, L., Duong, D. M., Gao, X., HE, C.-Y., Wei, L., & WU, J.-Z. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.4781 · Cited by 15

Role of Myeloperoxidase Oxidants in the Modulation of Cellular Lysosomal Enzyme Function: A Contributing Factor to Macrophage Dysfunction in Atherosclerosis?

Ismael, F. O., Barrett, T. J., Sheipouri, D., Brown, B. E., Davies, M. J., & Hawkins, C. L. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168844 · Cited by 15

Matrix Metalloproteinase-9 (MMP-9) and Myeloperoxidase (MPO) Levels in Patients with Nonobstructive Coronary Artery Disease Detected by Coronary Computed Tomographic Angiography

Hou, Z., Lü, B., Gao, Y., Cao, H., Yu, F.-F., Jing, N., Chen, X., Cong, X., Roy, S. K., & Budoff, M. J. (2012) · Academic Radiology · doi:10.1016/j.acra.2012.07.014 · Cited by 15

Hypochlorous acid-modified low-density lipoprotein inactivates the lysosomal protease cathepsin B: protection by ascorbic and lipoic acids

Carr, A. C. (2001) · Redox Report · doi:10.1179/135100001101536526 · Cited by 15

Differential apoptotic pathways activated in response to Cu-induced or HOCl-induced LDL oxidation in U937 monocytic cell line

Ermak, N., Lacour, B., Goirand, F., Drüeke, T. B., & Vicca, S. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.02.082 · Cited by 15

Identification of the human analog of SR‐BI and LOX‐1 as receptors for hypochlorite‐modified high‐density lipoprotein on human umbilical venous endothelial cells

Marsche, G., Levak‐Frank, S., Quehenberger, O., Heller, R., Sattler, W., & Malle, E. (2001) · The FASEB Journal · doi:10.1096/fsb2fj000532fje · Cited by 15

Differential dysregulation of granule subsets in WASH-deficient neutrophil leukocytes resulting in inflammation

Johnson, J. L., Meneses‐Salas, E., Ramadass, M., Monfregola, J., Rahman, F., Gontijo, R. C., Kiosses, W. B., Pestonjamasp, K. N., Allen, D., Zhang, J., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33230-y · Cited by 14

Intraplaque Myeloperoxidase Activity as Biomarker of Unstable Atheroma and Adverse Clinical Outcomes in Human Atherosclerosis

Nadel, J., Tumanov, S., Kong, S. M. Y., Chen, W., Giannotti, N., Sivasubramaniam, V., Rashid, I., Ugander, M., Jabbour, A., & Stocker, R. (2023) · JACC Advances · doi:10.1016/j.jacadv.2023.100310 · Cited by 14

A cyanine based fluorescent probe for detecting hypochlorite in vitro and in vivo

Tang, X. G., Zhou, B., Su, Z., Wu, R., Qiu, X., & Liu, L. (2024) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2024.124826 · Cited by 14

Oxidative Stress in Aortas of Patients with Advanced Occlusive and Aneurysmal Diseases

Lucas, M. L., Carraro, C. C., Belló‐Klein, A., Kalil, A. N., Aerts, N. R., Carvalho, F. B., Fernandes, M. D. C., & Zettler, C. G. (2018) · Annals of Vascular Surgery · doi:10.1016/j.avsg.2018.02.027 · Cited by 14

Role of myeloperoxidase-derived oxidants in the induction of vascular smooth muscle cell damage

Flouda, K., Mercer, J. R., Davies, M. J., & Hawkins, C. L. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.02.021 · Cited by 14

Positive association between plasma levels of oxidized low‐density lipoprotein and myeloperoxidase after hemodialysis in patients with diabetic end‐stage renal disease

Kitabayashi, C., Naruko, T., Sugioka, K., Yunoki, K., Nakagawa, M., Inaba, M., Ohsawa, M., Konishi, Y., Imanishi, M., Inoue, T., et al. (2013) · Hemodialysis International · doi:10.1111/hdi.12049 · Cited by 14

Copper ions and hypochlorite are mainly responsible for oxidative inactivation of paraoxon-hydrolyzing activity in human high density lipoprotein

Nguyen, S. H. V., Kim, J. R., Kim, M. R., Jung, T.-S., & Sok, D.-E. (2004) · Toxicology Letters · doi:10.1016/j.toxlet.2003.12.011 · Cited by 14

Cross-sectional correlates of myeloperoxidase and alpha-1-acid glycoprotein with adiposity, atherogenic and hematological indices in metabolic syndrome patients with or without diabetes

Alquoqa, R. S., Kasabri, V. N., Naffa, R. G., Akour, A. A., & Bustanji, Y. K. (2018) · Therapeutic Advances in Endocrinology and Metabolism · doi:10.1177/2042018818779742 · Cited by 14

NET-associated citrullinated histones promote LDL aggregation and foam cell formation in vitro

Haritha, V., George, A., Shaji, B. V., & Anie, Y. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112320 · Cited by 14

BIOMARKERS OF MYELOPEROXIDASE-DERIVED HYPOCHLOROUS ACID

Winterbourn, C. C., & Kettle, A. J. (2001) · Elsevier eBooks · doi:10.1016/b978-0-444-50957-4.50027-2 · 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

Granulocytic Phagocytes

Nauseef, W. M., & Clark, R. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-443-06839-3.00008-4 · Cited by 13

Sequential detection of hypochlorous acid and sulfur dioxide derivatives by a red-emitting fluorescent probe and bioimaging applications in vitro and in vivo

Liu, J., Yin, H., Shang, Z., Gu, P., He, G., Meng, Q., Zhang, R., & Zhang, Z. (2022) · RSC Advances · doi:10.1039/d2ra01048h · Cited by 13

The Role of Neutrophils in Lower Limb Peripheral Artery Disease: State of the Art and Future Perspectives

Buso, G., Faggin, E., Rosenblatt‐Velin, N., Pellegrin, M., Galliazzo, S., Calanca, L., Rattazzi, M., & Mazzolai, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021169 · Cited by 13

Biomarkers of Neutrophil Activation in Patients with Symptomatic Chronic Peripheral Artery Disease Predict Worse Cardiovascular Outcome

Buso, G., Faggin, E., Bressan, A., Galliazzo, S., Cinetto, F., Felice, C., Fusaro, M., Erdmann, A. A., Pauletto, P., Rattazzi, M., et al. (2023) · Biomedicines · doi:10.3390/biomedicines11030866 · Cited by 13

Accurate detection depression cell model with a dual-locked fluorescence probe in response to noradrenaline and HClO

Xiong, X., Qiu, J., Fu, S., Gu, B., Zhong, C., Zhao, L., & Gao, Y. M. (2024) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2024.107296 · Cited by 14

A PET based colorimetric/fluorescent dual-signal probe for selective detection of hypochlorite in real water samples

Zhang, Y., Liu, J., Xiao, J., Li, F., Li, F., Yang, M., & Liu, J. (2024) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2024.140568 · Cited by 13

Myeloperoxidase Modulates Hydrogen Peroxide Mediated Cellular Damage in Murine Macrophages

Guo, C., Sileikaite, I., Davies, M. J., & Hawkins, C. L. (2020) · Antioxidants · doi:10.3390/antiox9121255 · Cited by 15

Dietary organosulfur compounds from garlic and cruciferous vegetables as potent hypochlorite scavengers

Wang, H., & Huang, D. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2014.07.001 · Cited by 13

A novel quinone derived from 5-hydroxyindoleacetic acid reacts with protein: Possible participation of oxidation of serotonin and its metabolite in the development of atherosclerosis

Kato, Y., Oki, K., Suga, N., Ono, S., Ishisaka, A., Miura, Y., Kanazawa, S., Naito, M., Kitamoto, N., & Kettle, A. J. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.023 · Cited by 13

Two highly sensitive and selective coumarin-based fluorometric probes for the detection of ClO − and cell imaging

Jin, L., Tan, X., Zhao, C., & Wang, Q. (2019) · Analytical Methods · doi:10.1039/c9ay00105k · Cited by 13

A water-soluble colorimetric and fluorescent probe for rapidly sensing of ClO− in organisms

Tang, Y. C., Li, Y., Liu, L., Ni, H., Han, J., Wang, L., Mao, Y., Ni, L., & Wang, Y. (2019) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2019.112166 · Cited by 13

Effect of myeloperoxidase modified LDL on bovine and human aortic endothelial cells

Elsamad, G., Bazzi, S. I., Karam, M., Boudjeltia, K. Z., Vanhamme, L., & Daher, J. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.8109 · Cited by 13

Imino-thiolate-templated synthesis of a chloride-selective neutral macrocyclic host with a specific “turn-off–on” fluorescence response for hypochlorite (ClO − )

Dąbrowa, K., Lindner, M., Tyszka‐Gumkowska, A., & Jurczak, J. (2021) · Organic Chemistry Frontiers · doi:10.1039/d1qo00504a · Cited by 13

A Mitochondria‐Targeted Fluorescence Probe for Visualizing Detection of Hypochlorite in Living Cells

Luo, P., Xu, J., Shen, B., & Xu, P. (2021) · ChemistrySelect · doi:10.1002/slct.202102377 · Cited by 13

The Role of Oxidatively Modified Lipoproteins in Lipid Nephropathy

Gröne, H., Walli, A. K., & Gr�ne, E. F. (1997) · KARGER eBooks · doi:10.1159/000059835 · Cited by 13

Oxidized plasma high-density lipoprotein is decreased in Alzheimer's disease

Bergt, C., Nakano, T., Ditterich, J., DeCarli, C. S., & Eiserich, J. P. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.08.019 · Cited by 13

Urate attenuates oxidation of native low-density lipoprotein by hypochlorite and the subsequent lipoprotein-induced respiratory burst activities of polymorphonuclear leukocytes

Kopprasch, S., Richter, K., Leonhardt, W., Pietzsch, J., & Grßler, J. (2000) · Molecular and Cellular Biochemistry · doi:10.1023/a:1007025318306 · Cited by 13

Myeloperoxidase-mediated oxidation of edaravone produces an apparent non-toxic free radical metabolite and modulates hydrogen peroxide-mediated cytotoxicity in HL-60 cells

Suh, L. Y. K., Babu, D., Tonoyan, L., Reiz, B., Whittal, R. M., Dakhili, S. A. T., Morgan, A. G. M., Velázquez‐Martínez, C. A., & Siraki, A. G. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.08.021 · Cited by 12

The myeloperoxidase gene and its influence on myocardial infarction in a Swedish population: protective role of the −129A allele in women

Zotova, E., Lyrenäs, L., Fairé, U. D., Morgenstern, R., Gigante, B., & Bennet, A. M. (2009) · Coronary Artery Disease · doi:10.1097/mca.0b013e32832da06d · Cited by 12

Unraveling the Complexity of HDL Remodeling: On the Hunt to Restore HDL Quality

Schoch, L., Badimón, L., & Vilahur, G. (2021) · Biomedicines · doi:10.3390/biomedicines9070805 · Cited by 12

IFE based nanosensor composed of UCNPs and Fe(II)-phenanthroline for detection of hypochlorous acid and periodic acid

Song, H., Zhou, H., Zhuang, Q., Li, Z., Sun, F., Yuan, Z., Lou, Y., Zhou, G., & Zhao, Y. (2022) · Journal of Rare Earths · doi:10.1016/j.jre.2022.04.005 · Cited by 12

Sequence analysis, characterization and tissue distribution of channel catfish (Ictalurus punctatus Rafinesque, 1818) myeloperoxidase cDNA

Yeh, H., & Klesius, P. H. (2009) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2009.12.007 · Cited by 12

(1→3)-β-d-Glucan inhibits a dual mechanism of peroxynitrite stroke

Saluk, J., Królewska‐Golińska, K., & Wachowicz, B. (2011) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2011.01.010 · Cited by 11

Pentoxifylline Inhibits Epidural Fibrosis in Post-Laminectomy Rats

Kelten, B., Erdogan, H., Antar, V., Şanel, S., Tunçdemi̇r, M., Kutnu, M., Karaoğlan, A., & Örki, T. (2016) · Medical Science Monitor · doi:10.12659/msm.897668 · Cited by 12

Identification of a novel advanced glycation end product derived from lactaldehyde

Fujimoto, S., Murakami, Y., Miyake, H., Hayase, F., & Watanabe, H. (2019) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2019.1585745 · Cited by 12

Carbazole-conjugated-coumarin by enone realizing ratiometric and colorimetric detection of hypochlorite ions and its application in plants and animals

Chao, J., Duan, Y., Liu, Y., Xu, M., Zhang, Y., Huo, F., Zhang, T., Wang, J., & Yin, C. (2020) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2020.118813 · Cited by 12

Proliferation of macrophages due to the inhibition of inducible nitric oxide synthesis by oxidized low-density lipoproteins

Brunner, M., Gruber, M., Schmid, D., Baran, H., & Moeslinger, T. (2015) · EXCLI journal · doi:10.17179/excli2015-151 · Cited by 12

The Formation of Some Antigenic Epitopes in Oxidized Human Low-Density Lipoprotein Is Inhibited by Nitric Oxide

Seccia, M., Perugini, C., & Bellomo, G. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6148 · Cited by 12

Myeloperoxidase G-463A polymorphism and susceptibility to coronary artery disease: A meta-analysis

Tang, N., Wang, Y., & Mei, Q. (2013) · Gene · doi:10.1016/j.gene.2013.03.131 · Cited by 12

8-Nitroxanthine, a product of myeloperoxidase, peroxynitrite, and activated human neutrophils, enhances generation of superoxide by xanthine oxidase

Yeh, G. C., Henderson, J. P., Byun, J., d’Avignon, D. A., & Heinecke, J. W. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/s0003-9861(03)00256-x · Cited by 12

An oxygen-induced but protein F-independent fibronectin-binding pathway in Streptococcus pyogenes

Lee, J. Y., & Caparon, M. G. (1996) · Infection and Immunity · doi:10.1128/iai.64.2.413-421.1996 · Cited by 12

Association of myeloperoxidase G-463A gene polymorphism with diabetic nephropathy in Japanese type 2 diabetic subjects

Katakami, N., Kume, S., Kaneto, H., Uzu, T., Kashiwagi, A., Yamasaki, Y., Maegawa, H., & Shimomura, I. (2012) · Endocrine Journal · doi:10.1507/endocrj.ej12-0345 · Cited by 11

Head-to-Head Comparison of Oxidative Stress Biomarkers for All-Cause Mortality in Hemodialysis Patients

Zuo, J., Chaykovska, L., Chu, C., Chen, X., Hasan, A. A., Krämer, B. K., Tepel, M., & Hocher, B. (2022) · Antioxidants · doi:10.3390/antiox11101975 · Cited by 12

Role of myeloperoxidase-mediated modification of human blood lipoproteins in atherosclerosis development

Panasenko, O. M., Vakhrusheva, T. V., Vlasova, I. I., Chekanov, A. V., Baranov, Y. V., & Сергиенко, В. И. (2007) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-007-0346-x · Cited by 11

Rational drug design applied to myeloperoxidase inhibition

Antwerpen, P. V., & Boudjeltia, K. Z. (2015) · Free Radical Research · doi:10.3109/10715762.2015.1027201 · Cited by 11

Effects of Quercetin on Improving the Damage Caused by Free Radicals in the Rat Models of Multiple Sclerosis

Mirzazadeh, E., Khezri, S., & Froushani, S. M. A. (2019) · Iranian South Medical Journal · doi:10.29252/ismj.22.1.1 · Cited by 11

HDL from apoA1 transgenic mice expressing the 4WF isoform is resistant to oxidative loss of function

Berisha, S. Z., Brubaker, G., Kasumov, T., Hung, K. T., DiBello, P. M., Huang, Y. R., Li, L., Willard, B. B., Pollard, K. A., Nagy, L. E., et al. (2015) · Journal of Lipid Research · doi:10.1194/jlr.m056754 · Cited by 11

Effects of atorvastatin on serum lipids, lipoproteins, and hemostasis

Kushiya, F., Wada, H., Ooi, K., Sakurai, Y., Sakaguchi, A., Noda, M., Abe, Y., Nakasaki, T., Tsukada, T., Shiku, H., et al. (2004) · American Journal of Hematology · doi:10.1002/ajh.20191 · Cited by 11

Neutrophils, Hypercholesterolemia, and Atherogenesis

Hazen, S. L. (2010) · Circulation · doi:10.1161/circulationaha.110.984062 · Cited by 11

The role of myeloperoxidase as a biomarker in atherosclerotic cardiovascular disease

Amirfakhryan, H., & New, K. J. (2024) · Cardiology Plus · doi:10.1097/cp9.0000000000000097 · Cited by 10

Chronic mineral oil administration increases hepatic inflammation in wild type mice compared to lipocalin 2 null mice

Borkham‐Kamphorst, E., Haas, U., Pinoé-Schmidt, M., Abdallah, A. T., & Weiskirchen, R. (2021) · Laboratory Investigation · doi:10.1038/s41374-021-00672-9 · Cited by 10

Generation and Detection of Levuglandins and Isolevuglandins In Vitro and In Vivo

Zhang, M., Li, W., & Li, T. (2011) · Molecules · doi:10.3390/molecules16075333 · Cited by 11

Biomarkers in ROS and Role of Isoprostanes in Oxidative Stress

Chandra, M., Panchatcharam, M., & Miriyala, S. (2016) · InTech eBooks · doi:10.5772/64706 · Cited by 13

Development of a selective reaction-based turn-on fluorosensor and biomarker for hypochlorite ions in aqueous media

Ahmmed, E., Lohar, S., Ghatak, S. K., Hira, S. K., Manna, P. P., & Chattopadhyay, P. (2019) · Analytical Methods · doi:10.1039/c9ay00325h · Cited by 10

Randomized clinical trial of the effect of intraoperative humidified carbon dioxide insufflation in open laparotomy for colorectal resection

Cheong, J. Y., Chami, B., Fong, G., Wang, X. S., Keshava, A., Young, C. J., & Witting, P. K. (2019) · BJS Open · doi:10.1002/bjs5.50227 · Cited by 10

The Peroxisome Proliferator-Activated Receptor γ Agonist Pioglitazone Protects Vascular Endothelial Function in Hypercholesterolemic Rats by Inhibiting Myeloperoxidase

Zhang, D., Wang, Y., Yi, M., Zhang, S., & Wu, Y. (2020) · Cardiology Research and Practice · doi:10.1155/2020/1845969 · Cited by 10

Deletion of bone marrow myeloperoxidase attenuates chronic kidney disease accelerated atherosclerosis

Mathew, A. V., Zeng, L., Atkins, K. B., Sadri, K. N., Byun, J., Fujiwara, H., Reddy, P. R., & Pennathur, S. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.014095 · Cited by 11

Oxidative modification of human low-density lipoprotein by horseradish peroxidase in the absence of hydrogen peroxide

Natella, F., Nardini, M., Ursini, F., & Scaccini, C. (1998) · Free Radical Research · doi:10.1080/10715769800300471 · Cited by 10

Shift of the interconnection from the reaction system of paraoxonase 1 to the peroxidation reaction system of myeloperoxidase with HDL-C levels: A marker of atherosclerosis in patients with normal cholesterol levels

Wang, F., Liu, Y., Cong, Y., Li, P., Li, Y., Yan, Z., Tang, Y., Cheng, Y., & Zheng, Y. (2014) · Clinica Chimica Acta · doi:10.1016/j.cca.2014.09.020 · Cited by 10

New insights into the effects of the protein moiety of oxidized LDL (oxLDL)

Vicca, S., Massy, Z. A., Hennequin, C., Rihane, D., Nguyen‐Khoa, T., Drüeke, T. B., & Lacour, B. (2003) · Kidney International · doi:10.1046/j.1523-1755.63.s84.44.x · Cited by 10

The mast cell as a pluripotent HDL-modifying effector in atherogenesis

Lee‐Rueckert, M., & Kovanen, P. T. (2015) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000224 · Cited by 10

Determination of myeloperoxidase-induced apoAI-apoAII heterodimers in high-density lipoprotein.

Kameda, T., Usami, Y., Shimada, S., Haraguchi, G., Matsuda, K., Sugano, M., Kurihara, Y., Isobe, M., & Tozuka, M. (2012) · PubMed · Cited by 10

Modified Low-Density Lipoproteins and High-Density Lipoproteins

Koller, E., Volf, I., Gurvitz, A., & Koller, F. (2006) · Pathophysiology of Haemostasis and Thrombosis · doi:10.1159/000093225 · Cited by 10

Myeloperoxidase and Hypochlorite, but Not Copper Ions, Oxidize Heparin-Bound LDL Particles and Release Them From Heparin

Pentikäinen, M. O., Öörni, K., & Kovanen, P. T. (2001) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/hq1201.099423 · Cited by 10

Isoflavones Effects on Vascular and Endothelial Outcomes: How Is the Gut Microbiota Involved?

Laudani, S., Godos, J., Romano, G. L., Gozzo, L., Domenico, F. D., Azpíroz, I. D., Diaz, R. M., Giampieri, F., Quiles, J. L., Battino, M. A., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17020236 · Cited by 10

Development of a near-infrared fluorescence probe for hypochlorous acid based on the phenyl-induced twisted intramolecular charge transfer (p-TICT) mechanism

Ohno, H., Sumitani, S., Chuluun-Erdene, A., Kuchimaru, T., Yamada, S., Sasaki, E., & Hanaoka, K. (2025) · Chemical Communications · doi:10.1039/d5cc02212f · Cited by 9

Binding of lactoferrin to the surface of low-density lipoproteins modified by myeloperoxidase prevents intracellular cholesterol accumulation by human blood monocytes

Vasilyev, V. B., Av, S., Kostevich, V. A., Elizarova, A. Y., Gorbunov, N., & Panasenko, O. M. (2020) · Biochemistry and Cell Biology · doi:10.1139/bcb-2020-0141 · Cited by 9

A BODIPY‐Based Far‐Red‐Absorbing Fluorescent Probe for Hypochlorous Acid Imaging

Wan, Z., Yu, S., Wang, Q., Tobia, J., Chen, H., Li, Z., Liu, X., & Zhang, Y. (2021) · ChemPhotoChem · doi:10.1002/cptc.202100250 · Cited by 9

Plasma Concentrations of New Biochemical Markers of Atherosclerosis in Patients with Dyslipidemia—A Pilot Study

Kosowski, M., Basiak, M., Hachuła, M., & Okopień, B. (2022) · Medicina · doi:10.3390/medicina58060717 · Cited by 9

Novel ultra-sensitive and highly selective cyanine sensors based on solvent-free microwave synthesis for the detection of trace hypochlorite ions in drinking water

Hafez, N. S., Amer, W. A., Okba, E. A., Sakr, M. A. S., Alganzory, H. H., & Ebeid, E. M. (2023) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2023.123116 · Cited by 9

An effective and rapid determination by MALDI/TOF/TOF of methionine sulphoxide content of ApoA‐I in type 2 diabetic patients

Seraglia, R., Sartore, G., Marin, R., Burlina, S., Manzato, E., Ragazzi, E., Traldi, P., & Lapolla, A. (2013) · Journal of Mass Spectrometry · doi:10.1002/jms.3113 · Cited by 9

Oxidative Stress and Cardiovascular Diseases

Hristova, M., & Penev, M. (2014) · Trakia Journal of Sciences · doi:10.15547/tjs.2014.03.012 · Cited by 9

Spectroscopic studies on free radical coalescing antioxidants and brain protein cystatin

Amin, F., & Bano, B. (2018) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2018.1500946 · Cited by 9

Hypochlorite, Oxidative Modification of Plasma Lipoproteins, and Atherosclerosis

Panasenko, O. M., & Сергиенко, В. И. (2001) · Bulletin of Experimental Biology and Medicine · doi:10.1023/a:1017926309665 · Cited by 9

Hypochlorite-oxidized low density lipoproteins reduce production and bioavailability of nitric oxide in RAW 264.7 macrophages by distinct mechanisms

Schmid, W., Lee, A., Son, J., Koller, E., & Volf, I. (2008) · Life Sciences · doi:10.1016/j.lfs.2008.05.002 · Cited by 10

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

Beta-blockers inhibit the modification of low-density lipoproteins by sodium hypochlorite in vitro

Seifert‐Held, T., Zschörnig, O., Arnhold, J., & Arnold, K. (1997) · Chemistry and Physics of Lipids · doi:10.1016/s0009-3084(96)02637-0 · Cited by 9

Exposure of aconitase to smoking-related oxidants results in iron loss and increased iron response protein-1 activity: potential mechanisms for iron accumulation in human arterial cells

Talib, J., & Davies, M. J. (2016) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-016-1340-4 · Cited by 9

Autophagy, Oxidative Stress, and Redox Regulation

Ma, J., Yang, L., Ren, J. T., & Yang, J. Z. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805253-2.00020-1 · Cited by 10

Antioxidantes: importancia biológica y métodos para medir su actividad

Londoño‐Londoño, J. (2012) · Corporación Universitaria Lasallista eBooks · Cited by 9

Oxidative tyrosylation of high density lipoprotein impairs biliary sterol secretion in rats

Guertin, F. (1997) · Atherosclerosis · doi:10.1016/s0021-9150(97)06085-1 · Cited by 9

The paradoxical relationship of aerobic exercise and the oxidative theory of atherosclerosis

Shern-Brewer, R., Santanam, N., Wetzstein, C. J., White-Welkley, J. E., Price, L., & Parthasarathy, S. (2000) · Elsevier eBooks · doi:10.1016/b978-044482650-3/50036-5 · Cited by 9

Myeloperoxidase-generated oxidants and atherosclerosis

Podrez, E. A., Abu‐Soud, H. M., & Hazen, S. L. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00229-x · Cited by 607

Pathways for oxidation of low density lipoprotein by myeloperoxidase: tyrosyl radical, reactive aldehydes, hypochlorous acid and molecular chlorine

Heinecke, J. W. (1997) · BioFactors · doi:10.1002/biof.5520060208 · Cited by 78

Myeloperoxidase Production by Macrophage and Risk of Atherosclerosis

Karakas, M., & Köenig, W. (2012) · Current Atherosclerosis Reports · doi:10.1007/s11883-012-0242-3 · Cited by 55

Modification of low-density lipoprotein by myeloperoxidase-derived oxidants and reagent hypochlorous acid

Malle, E., Marsche, G., Arnhold, J., & Davies, M. J. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.03.024 · Cited by 184

Role of myeloperoxidase in inflammation and atherosclerosis (Review)

Frangie, C., & Daher, J. (2022) · Biomedical Reports · doi:10.3892/br.2022.1536 · Cited by 121