Search Results - "Handler, N."

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    Milker's nodule: an occupational infection and threat to the immunocompromised by Handler, N.S., Handler, M.Z., Rubins, A., Rubins, S., Septe, M., Janniger, C.K., Schwartz, R.A.

    “…Milker's nodule virus, also called paravaccinia virus, is a DNA virus of the parapoxvirus genus transmitted from infected cows to humans. It results from…”
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    Antitumor Effects of 3,3′,4,4′,5,5′-Hexahydroxystilbene in hl-60 Human Promyelocytic Leukemia Cells by Saiko, P., Horvath, Z., Murias, M., Handler, N., Jaeger, W., Erker, T., Fritzer-Szekeres, M., Szekeres, T.

    Published in Nucleosides, nucleotides & nucleic acids (01-01-2006)
    “…Resveratrol (3,4′,5-trihydroxystilbene, RV) exerts remarkable cytostatic and cytotoxic effects against a multitude of human cancer cell lines. Since the…”
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    New approaches to treating pain by Wolkerstorfer, Andrea, Handler, Norbert, Buschmann, Helmut

    Published in Bioorganic & medicinal chemistry letters (15-02-2016)
    “…After 100years of pain research—old scaffolds, minor improvements? [Display omitted] Pain is the most common reason for patients seeking medical care resulting…”
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    Antioxidant, prooxidant and cytotoxic activity of hydroxylated resveratrol analogues: structure–activity relationship by Murias, Marek, Jäger, Walter, Handler, Norbert, Erker, Thomas, Horvath, Zsuzsanna, Szekeres, Thomas, Nohl, Hans, Gille, Lars

    Published in Biochemical pharmacology (15-03-2005)
    “…Resveratrol ( trans-3,4′,5-trihydroxystilbene), a naturally occurring hydroxystilbene, is considered an essential antioxidative constituent of red wine…”
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    Resveratrol analogues as selective cyclooxygenase-2 inhibitors: synthesis and structure–activity relationship by Murias, Marek, Handler, Norbert, Erker, Thomas, Pleban, Karin, Ecker, Gerhard, Saiko, Philipp, Szekeres, Thomas, Jäger, Walter

    Published in Bioorganic & medicinal chemistry (01-11-2004)
    “…A series of hydroxylated and methoxylated trans-stilbenes were synthesized and evaluated for their ability to inhibit COX-1 and COX-2. Some of the hydroxylated…”
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    Synthesis of Novel Curcumin Analogues and Their Evaluation as Selective Cyclooxygenase-1 (COX-1) Inhibitors by Handler, Norbert, Jaeger, Walter, Puschacher, Helmut, Leisser, Klaus, Erker, Thomas

    “…Curcumin, a major yellow pigment and active component of turmeric, has been shown to possess anti-inflammatory and anti-cancer activities. Recent studies have…”
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    Evaluation of the Onda Correlations for Mass Transfer with Large Random Packings by Dvorak, Bruce I, Lawler, Desmond F, Fair, James R, Handler, Neil E

    Published in Environmental science & technology (01-03-1996)
    “…Although large (≥5 cm) polypropylene packings are frequently used in air stripping towers for environmental applications, few fundamental studies of the mass…”
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    Antioxidant activity of resveratrol, piceatannol and 3,3',4,4',5,5'-hexahydroxy-trans-stilbene in three leukemia cell lines by OVESNA, Zdenka, KOZICS, Katarina, BADER, Yvonne, SAIKO, Philipp, HANDLER, Norbert, ERKER, Thomas, SZEKERES, Thomas

    Published in Oncology reports (01-09-2006)
    “…trans-Resveratrol (t-RES) is one of the most relevant and extensively investigated stilbenes with a broad spectrum of biological activities. In contrast to the…”
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    Novel Resveratrol Derivatives Induce Apoptosis and Cause Cell Cycle Arrest in Prostate Cancer Cell Lines by Horvath, Z, Marihart-Fazekas, S, Saiko, P, Grusch, M, Oezsuey, M, Harik, M, Handler, N, Erker, T, Jaeger, W, Fritzer-Szekeres, M, Djavan, B, Szekeres, T

    Published in Anticancer research (01-09-2007)
    “…Background: Resveratrol (RV), a naturally occurring phytoalexin, exerts manifold biological effects against a variety of human tumor cell lines. In this study,…”
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    Cyclooxygenase-1 and Cyclooxygenase-2 Inhibition of Novel 1,2-Disubtituted Imidazoles by Handler, Norbert, Jaeger, Walter, Kuen-Krismer, Bea, Erker, Thomas

    Published in Archiv der Pharmazie (Weinheim) (01-12-2005)
    “…Novel 1,2‐disubstituted imidazoles were synthesized and tested for COX‐1 and COX‐2 inhibition. A substituted phenyl cycle in position 1 and an alicyclic…”
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