Search Results - "OCSOVSZKI, Imre"

Chemical composition, antioxidant and anticancer activity of licorice from Fruska Gora locality by Vlaisavljević, Sanja, Šibul, Filip, Sinka, Izabella, Zupko, Istvan, Ocsovszki, Imre, Jovanović-Šanta, Suzana

“…•Phytochemical and biological analysis of licorice from Fruska Gora were investigated.•The highest content of bioactive compounds was observed in the extract…”
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Synthesis and In Vitro Antitumor Activity of Naringenin Oxime and Oxime Ether Derivatives by Latif, Ahmed Dhahir, Gonda, Tímea, Vágvölgyi, Máté, Kúsz, Norbert, Kulmány, Ágnes, Ocsovszki, Imre, Zomborszki, Zoltán Péter, Zupkó, István, Hunyadi, Attila

“…Naringenin is one of the most abundant dietary flavonoids exerting several beneficial biological activities. Synthetic modification of naringenin is of…”
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Investigation of natural phenanthrenes and the antiproliferative potential of juncusol in cervical cancer cell lines by Kuo, Ching-Ying, Schelz, Zsuzsanna, Tóth, Barbara, Vasas, Andrea, Ocsovszki, Imre, Chang, Fang-Rong, Hohmann, Judit, Zupkó, István, Wang, Hui-Chun

“…Phenanthrenes isolated from Juncus species possess different biological activities, including antiproliferative and antimigratory effects. In this study, nine…”
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A versatile transposon-based technology to generate loss- and gain-of-function phenotypes in the mouse liver by Kopasz, Anna Georgina, Pusztai, Dávid Zsolt, Karkas, Réka, Hudoba, Liza, Abdullah, Khaldoon Sadiq Ahmed, Imre, Gergely, Pankotai-Bodó, Gabriella, Migh, Ede, Nagy, Andrea, Kriston, András, Germán, Péter, Drubi, Andrea Bakné, Molnár, Anna, Fekete, Ildikó, Dani, Virág Éva, Ocsovszki, Imre, Puskás, László Géza, Horváth, Péter, Sükösd, Farkas, Mátés, Lajos

“…Understanding the contribution of gene function in distinct organ systems to the pathogenesis of human diseases in biomedical research requires modifying gene…”
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A click approach to novel D-ring-substituted 16α-triazolylestrone derivatives and characterization of their antiproliferative properties by Molnár, Judit, Frank, Éva, Minorics, Renáta, Kádár, Zalán, Ocsovszki, Imre, Schönecker, Bruno, Wölfling, János, Zupkó, István

“…A simple and efficient synthesis of novel, D-ring substituted estrone derivatives containing a 16α-triazolyl moiety is described. Two epimeric azido alcohols…”
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Antiproliferative Properties of Newly Synthesized 19-Nortestosterone Analogs Without Substantial Androgenic Activity by Gyovai, András, Minorics, Renáta, Kiss, Anita, Mernyák, Erzsébet, Schneider, Gyula, Szekeres, András, Kerekes, Erika, Ocsovszki, Imre, Zupkó, István

“…19-Nortestosterone C-17 epimers with prominent antiproliferative properties have been previously described. In our present study, five novel…”
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ACTH- and cortisol-associated neutrophil modulation in coronary artery disease patients undergoing stent implantation by Keresztes, Margit, Horváth, Tamás, Ocsovszki, Imre, Földesi, Imre, Serfőző, Gyöngyi, Boda, Krisztina, Ungi, Imre

“…Psychosocial stress and activation of neutrophil granulocytes are increasingly recognized as major risk factors of coronary artery disease (CAD), but the…”
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Investigation of the Antiproliferative Properties of Natural Sesquiterpenes from Artemisia asiatica and Onopordum acanthium on HL-60 Cells in Vitro by Molnár, Judit, Szebeni, Gábor J, Csupor-Löffler, Boglárka, Hajdú, Zsuzsanna, Szekeres, Thomas, Saiko, Philipp, Ocsovszki, Imre, Puskás, László G, Hohmann, Judit, Zupkó, István

“…Plants and plant extracts play a crucial role in the research into novel antineoplastic agents. Four sesquiterpene lactones, artecanin (1),…”
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Microcirculatory consequences of limb ischemia/reperfusion in ovariectomized rats treated with zoledronic acid by Pócs, Levente, Janovszky, Ágnes, Ocsovszki, Imre, Kaszaki, József, Piffkó, József, Szabó, Andrea

“…Nitrogen-containing bisphosphonates (BIS) are potent therapeutics in osteoporosis, but their use may result in osteonecrotic side-effects in the maxillofacial…”
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Anticancer and multidrug resistance-reversal effects of solanidine analogs synthetized from pregnadienolone acetate by Zupkó, István, Molnár, Judit, Réthy, Borbála, Minorics, Renáta, Frank, Eva, Wölfling, János, Molnár, Joseph, Ocsovszki, Imre, Topcu, Zeki, Bitó, Tamás, Puskás, László G

“…A set of solanidine analogs with antiproliferative properties were recently synthetized from pregnadienolone acetate, which occurs in Nature. The aim of the…”
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Antitumor Activity of Alkaloids Derived from Amaryllidaceae Species by ISTVÁN ZUPKÃ, BORBÁLA RÉTHY, JUDIT HOHMANN, JOSEPH MOLNÁR, IMRE OCSOVSZKI, GEORGE FALKAY

“…The aim of the present study was to investigate the anticancer properties of five alkaloids isolated from Amaryllidaceae, including the inhibitory effect on…”
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Differential Effect of Phenothiazines on MRP1 and P-Glycoprotein Activity by Wesołowska, Olga, Molnar, Joseph, Ocsovszki, Imre, Michalak, Krystyna

“…Background: Overexpression of ATP-binding cassette (ABC) transporters such as P-glycoprotein (P-gp), multidrug resistance-associated protein 1 (MRP1) or breast…”
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Screening of Some Saponins and Phenolic Components of Tribulus terrestris and Smilax excelsa as MDR Modulators by Ivanova, Antoaneta, Serly, Julianna, Dinchev, Dragomir, Ocsovszki, Imre, Kostova, Ivanka, Molnar, Joseph

“…Background: Cytotoxic activity of saponins and phenolic compounds have been described in the literature, but no reports were found on their multidrug…”
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2-(3-Aryl-2-propenoyl)-3-methylquinoxaline-1,4-dioxides: A novel cluster of tumor-specific cytotoxins which reverse multidrug resistance by Das, Umashankar, Pati, Hari N., Panda, Atulya K., Clercq, Erik De, Balzarini, Jan, Molnár, Joseph, Baráth, Zoltán, Ocsovszki, Imre, Kawase, Masami, Zhou, Li, Sakagami, Hiroshi, Dimmock, Jonathan R.

“…The quinoxaline derivatives 3 possess one or more of the following features, namely antiproliferative activities, selective cytotoxicity to neoplasms than…”
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Investigation of cytotoxic activity on human cancer cell lines of arborinine and furanoacridones isolated from Ruta graveolens by Réthy, Borbála, Zupkó, István, Minorics, Renáta, Hohmann, Judit, Ocsovszki, Imre, Falkay, George

“…The cytotoxic effects of a series of furanoacridones isolated from Ruta graveolens L. (Rutaceae) and of two further acridone alkaloids (arborinine and…”
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Antitumour Properties of Acridone Alkaloids on a Murine Lymphoma Cell Line by RETHY, Borbala, HOHMANN, Judit, MINORICS, Renata, VARGA, Andras, OCSOVSZKI, Imre, MOLNAR, Joseph, JUHASZ, Kata, FALKAY, George, ZUPKO, Istvan

“…The aim of the present study was to investigate the anticancer properties of a set of furanoacridone alkaloids, arborinine and evoxanthine, including the…”
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Different administration schedules of darbepoetin alfa affect oxidized and reduced glutathione levels to a similar extent in 5/6 nephrectomized rats by Monostori, Péter, Kocsis, Gabriella F., Ökrös, Zsuzsanna, Bencsik, Péter, Czétényi, Orsolya, Kiss, Zoltán, Gellén, Balázs, Bereczki, Csaba, Ocsovszki, Imre, Pipis, Judit, Pálóczi, János, Sárközy, Márta, Török, Szilvia, Varga, Ilona S., Kiss, István, Fodor, Eszter, Csont, Tamás, Ferdinandy, Péter, Túri, Sándor

“…Background The development of erythropoiesis-stimulating agents (ESAs) with extended serum half-lives has allowed marked prolongation of the administration…”
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MDR-reversal Activity of Chalcones by Ivanova, Antoaneta, Batovska, Daniela, Engi, Helga, Parushev, Stoyan, Ocsovszki, Imre, Kostova, Ivanka, Molnar, Joseph

“…The ability of 11 chalcones with 3,4,5-trimethoxy substitution on ring A to inhibit the transport activity of P-glycoprotein was studied. Flow cytometry was…”
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Flow cytometric analysis of procalcitonin expression in human monocytes and granulocytes by Balog, Attila, Ocsovszki, Imre, Mándi, Yvette

“…Procalcitonin (PCT), a precursor of calcitonin is a useful indicator of severe systemic infection and sepsis. For a better understanding of the…”
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Tumour-specific Cytotoxicity and MDR-reversal Activity of Dihydropyridines by Engi, Helga, Sakagami, Hiroshi, Kawase, Masami, Parecha, Alpesh, Manvar, Dinesh, Kothari, Himanshu, Adlakha, Priti, Shah, Anamik, Motohashi, Noboru, Ocsovszki, Imre, Molnár, Joseph

“…The ability of 41 1,4-diphenyl-1,4-dihydropyridine derivatives to inhibit the transport activity of P-glycoprotein were studied by flow cytometry in a…”
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