NMR and computational studies of stereoisomeric equine estrogen-derived DNA cytidine adducts in oligonucleotide duplexes: opposite orientations of diastereomeric forms. (17/29)

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Dissecting the paradoxical effects of hydrogen bond mutations in the ketosteroid isomerase oxyanion hole. (18/29)

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Solvation response along the reaction coordinate in the active site of ketosteroid isomerase. (19/29)

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Quantitative detection of 4-hydroxyequilenin-DNA adducts in mammalian cells using an immunoassay with a novel monoclonal antibody. (20/29)

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Redox cycling of catechol estrogens generating apurinic/apyrimidinic sites and 8-oxo-deoxyguanosine via reactive oxygen species differentiates equine and human estrogens. (21/29)

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Unexpected hormonal activity of a catechol equine estrogen metabolite reveals reversible glutathione conjugation. (22/29)

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Specificity of human aldo-keto reductases, NAD(P)H:quinone oxidoreductase, and carbonyl reductases to redox-cycle polycyclic aromatic hydrocarbon diones and 4-hydroxyequilenin-o-quinone. (23/29)

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The naphthol selective estrogen receptor modulator (SERM), LY2066948, is oxidized to an o-quinone analogous to the naphthol equine estrogen, equilenin. (24/29)

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