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Titlebook: Biological Reactive Intermediates V; Basic Mechanistic Re Robert Snyder,I. Glenn Sipes,Charlotte M. Witmer Book 1996 The Editor(s) (if appl

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期刊全称Biological Reactive Intermediates V
期刊简称Basic Mechanistic Re
影响因子2023Robert Snyder,I. Glenn Sipes,Charlotte M. Witmer
视频video
学科分类Advances in Experimental Medicine and Biology
图书封面Titlebook: Biological Reactive Intermediates V; Basic Mechanistic Re Robert Snyder,I. Glenn Sipes,Charlotte M. Witmer Book 1996 The Editor(s) (if appl
影响因子Much of organic chemistry is based on the ability of suitably structured chemicals to bind together through the formation of covalent bonds. Biochemistry is replete with exam­ ples of enzymatically catalyzed reactions in which normal body constituents can be linked through covalent bonds during the process of intermediary metabolism. The finding that xenobiotic chemicals that enter the body from the environment, are metabolized to highly reactive species, and then covalently react with cellular macromolecules to induce toxic and carcinogenic effects was an observation that spawned the research featured in the Fifth International Symposium on Biological Reactive Intermediates (BRI V). The group of investigators that became fascinated with this process and its signifi­ cance in terms of human health began their discussions in Turku, Finland (J 975), and continued them at Guildford, England (1980), College Park, Maryland (1985), Tucson, Arizona (1990), and Munich, Germany (1995). Among the results were a series of reports listed below, as well as the book for which this serves as the Preface. • Jollow, DJ., Kocsis, J.J., Snyder, R. and Vainio, H. (eds), Biological Reactive Intermediat
Pindex Book 1996
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Klinik der gynäkologischen Röntgentherapie 1991). The inhibitory effect of both retinoids and carotenoids towards neoplastic transformation correlates with their activity to induce gap junctional communication (Zhang et al., 1991; Bertram et al., 1991).
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https://doi.org/10.1007/978-3-642-95977-6olabeled acetaminophen resulted in covalent binding of radiolabel to protein in the necrotic hepatocytes (5). . experiments revealed that the metabolism was by a cytochrome P-450 dependent mechanism (6). It was postulated that covalent binding of this metabolite to critical proteins was the mechanism of the hepatotoxicity.
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Pathologische Anatomie der Tuberkulose,that it might be feasable to invert the topology of the mEH in the membrane of the endoplasmic reticulum without affecting the catalytic activity of this protein. With this strategy it will be possible to investigate whether the membrane topology of xenobiotic metabolizing enzymes is important for their role in chemical carcinogenesis.
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https://doi.org/10.1007/978-3-662-34539-9gid et al., 1993). There is also growing evidence that endogenous factors such as oxidative stress and DA itself may contribute to the neurodegenerative process (Cohen, 1983; Agid et al., 1993; Zigmond et al., 1992).
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