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Titlebook: Carcinogenesis: Fundamental Mechanisms and Environmental Effects; Proceedings of the T Bernard Pullman,Paul O. P. Ts’o,Harry Gelboin Confer

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Jerusalem Symposiahttp://image.papertrans.cn/c/image/221694.jpg
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On Euler Buckling and Snap-Through,part of a bay-region of a carcinogenic polycyclic aromatic hydrocarbon. In general, predicted chemical reactivity for positional isomers of benzo-ring diol epoxides of individual hydrocarbons has been paralleled by their respective mutagenicity and/or tumorigenicity. Although relative reactivity of
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J. E. Macías,M. G. Clerc,C. Falcónter embryo cells treated with the hydrocarbon contain adducts arising from the reactions with the nucleic acid of both the ‘bay- region’ .-3,4-diol-1,2-epoxide and the non-‘bay-region’ .-8,9- diol-10,11-epoxide. However, only the 8,9-diol-10,11-epoxide appears to be involved in the reaction of the h
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Z. Liu,F. Leo,S. Coulibaly,M. Takiderivatives, acetylaminofluorene and naphthylamines have been found to be easily converted to free radicals after being activated to the proximate forms. These free radicals were sufficiently reactive to bind covalently with nucleic acid bases. Anthanthrene which lacks bay region and 10-aza-benzo[a)
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N. Slimani,A. Makhoute,M. Tlidire .: positive ions or uncharged molecules with reactive centers at their electron deficient atoms (see e.g. 1,2). This is true both for carcinogens considered as being active . (a number of relatively simple alkylating agents) and those which necessitate a metabolic activation (aromatic hydrocarbon
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Business Cycles: Discrete Time,ar orbital calculations. Of particular interest is the degree to which epoxide ring opening may be facilitated by either or both of two special factors: (1) The proximity, in the molecule, of a double bond, and (2) intramolecular hydrogen bonding between an appropriately oriented hydroxyl group and
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https://doi.org/10.1007/978-3-642-60775-2e hamster cells. Within a series of hydrocarbon epoxides, differences in mutagenic effectiveness and efficiency were related to carcinogenic potency. The cell-mediated mutation system was used to compare the mutagenic efficiency of a series of parent hydrocarbons. Quantitative studies of the mutagen
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https://doi.org/10.1007/978-3-642-60775-2ymerase in the presence of Mn.. When normal hydrogen bonding is blocked by a substituent, total ambiguity results with transcription continuing beyond the modified nucleotide. Examples are 3-MeC, 3-MeU, 1-MeA and O.-MeU. In the case of modifications of the exocyclic amino groups, in addition to the
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