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1481por Menzel, Ralph, Swain, Suresh C, Hoess, Sebastian, Claus, Evelyn, Menzel, Stefanie, Steinberg, Christian EW, Reifferscheid, Georg, Stürzenbaum, Stephen R“…Beside chemical analysis, three standard bioassays were performed: reproduction of C. elegans, genotoxicity (Comet assay) and endocrine disruption (YES test). …”
Publicado 2009
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1482“…Damage of an individual cell was quantified as a comet tail moment. The proportion of non-zero values compared to the total number of observations was referred to as “amount of DNA damage” expressed in arbitrary units (AU). …”
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1483“…Cellular DNA damage induced by 100 µM H(2)O(2) was measured using Comet assay and quantified by TL. There were no differences in age (61.4 ± 1.7 years vs 62.0 ± 2.2 years) between the two groups. …”
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1484por Inayat-Hussain, S.H., Wong, L.T., Chan, K.M., Rajab, N.F., Din, L.B., Harun, R., Kizilors, A., Saxena, N., Mourtada-Maarabouni, M., Farzaneh, F., Williams, G.T.“…Assessment of DNA damage by Comet assay revealed goniothalamin-induced DNA strand breaks as early as 1 h in vector control but this effect was inhibited in RACK-1 and pc3n3 stably transfected W7.2 cells. …”
Publicado 2009
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1485“…We found that phagosomes formed by engagement of integrins that serve as complement receptors (CR3) undergo secondary waves of actin polymerization, leading to the formation of “comet tails” that propel the vacuoles inside the cells. …”
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1486“…The control group consisted of normal volunteers (blood donors) qualified during standard examinations at Regional Centers of Blood Donation and Blood Therapy. The comet assay was used for determination of DNA damages. …”
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1487“…The compound induced DNA damage evaluated by the alkaline, neutral, and pH 12.1 version of the comet assay. This damage included oxidative modifications of the DNA bases, as checked by DNA repair enzymes EndoIII and Fpg, alkali-labile sites and DNA double-strand breaks. …”
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1488“…These changes were accompanied by increased extent of DNA breaks as measured by the comet assay, and increased levels of the AGE product, carboxymethyl-lysine (CML). …”
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1489“…Genotoxic and cytotoxic activity were determined by DNA fragmentation, comet, and MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assays. …”
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1490por Acosta-Torres, Laura Susana, Mendieta, Irasema, Nuñez-Anita, Rosa Elvira, Cajero-Juárez, Marcos, Castaño, Víctor M“…Cells were cultured for 24 or 72 hours in the presence or absence of the polymer formulations and analyzed using three different tests, ie, cellular viability by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and cell proliferation by enzyme-linked immunosorbent assay BrdU, and genomic DNA damage (Comet assay). Finally, the samples were evaluated mechanically, and the polymer-bearing silver nanoparticles were analyzed microscopically to evaluate dispersion of the nanoparticles. …”
Publicado 2012
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1491“…The control group was treated as the exposed one with the sole difference that the rats were not exposed to magnetic field. Comet assay was used to quantify the level of DNA damage in isolated brain cells. …”
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1492“…RESULTS: In the current study, we investigated the effect of melatonin on DNA strand breaks using the alkaline DNA comet assay in breast cancer (MCF-7) and colon cancer (HCT-15) cell lines. …”
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1493“…Statistically significant (P < 0.01) induction of DNA damage was observed by the comet assay in cells exposed to arsenic trioxide. …”
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1494por Tonini, Clarissa L., Campagnaro, Bianca P., Louro, Lis P. S., Pereira, Thiago M. C., Vasquez, Elisardo C., Meyrelles, Silvana S.“…In the present study, we evaluated the influence of aging and hypercholesterolemia on oxidative stress, DNA damage and apoptosis in bone marrow cells from young and aged apoE(−/−) mice compared with age-matched wild-type C57BL/6 (C57) mice, using the comet assay and flow cytometry. The production of both superoxide and hydrogen peroxide in bone marrow cells was higher in young apoE(−/−) mice than in age-matched C57 mice, and reactive oxygen species were increased in aged C57 and apoE(−/−) mice. …”
Publicado 2013
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1495por Czarny, Piotr, Kasprzak, Ewelina, Wielgorski, Mariusz, Udziela, Monika, Markiewicz, Beata, Blasiak, Janusz, Szaflik, Jerzy, Szaflik, Jacek P.“…To quantify DNA damage and repair we used the alkaline comet assay technique with the enzymes recognizing oxidative DNA damage, hOGG1 and EndoIII. …”
Publicado 2012
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1496por Haug, Kristiane, Azqueta, Amaya, Johnsen-Soriano, Siv, Shahdadfar, Aboulghassem, Drolsum, Liv K, Moe, Morten C, Røger, Magnus T, Romero, Francisco J, Collins, Andrew R, Nicolaissen, Bjørn“…METHODS: Morphology was monitored by light and electron microscopy, expression of phenotypic and genotypic markers by immunohistochemistry and RT-PCR and changes in oxidative lipid and DNA damage by ELISA and COMET assay. RESULTS: A prominent loss of cells was observed after storage in Optisol GS. …”
Publicado 2013
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1497por Ouédraogo, M., Da, F. L., Fabré, A., Konaté, K., Dibala, C. I., Carreyre, H., Thibaudeau, S., Coustard, J.-M., Vandebrouck, C., Bescond, J., Belemtougri, R. G.“…Animals were pretreated with the extract, then liver comet assay was performed. AECal and its chloroformic fractions (CF-AECal) relaxed the contraction induced by Ach, but both were significantly less potent in inhibiting contraction induced by KCl (30 mM; 80 mM). …”
Publicado 2013
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1498“…Single Cell Gel Electrophoresis Assay (Comet Assay) was applied to peripheral blood lymphocytes of five groups of children between six and 15 years of age. …”
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1499por Han, Sang Mi, Park, Kwan Kyu, Nicholls, Young Mee, Macfarlane, Nicola, Duncan, Greig“…To assess BV genotoxicity, damage to human epidermal keratinocyte (HEK) was evaluated using the Comet assay. HEK migration was evaluated using a commercial wound healing kit. …”
Publicado 2013
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1500“…Oral administration of GA (100 mg/kg body weight), one hour prior to whole body gamma radiation exposure (2–8 Gy; 6 animals/group), reduced the radiation-induced cellular DNA damage in mouse peripheral blood leukocytes, bone marrow cells, and spleenocytes as revealed by comet assay. The GA administration also prevented the radiation-induced decrease in the levels of the antioxidant enzyme, glutathione peroxidise (GPx), and nonprotein thiol glutathione (GSH) and inhibited the peroxidation of membrane lipids in these animals. …”
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