Authors:
Hua, YS
Wainhaus, SB
Yang, YN
Shen, LX
Xiong, YS
Xu, XY
Zhang, FG
Bolton, JL
van Breemen, RB
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Authors:
Zhang, FG
Yao, D
Hua, YS
van Breemen, RB
Bolton, JL
Citation: Fg. Zhang et al., Synthesis and reactivity of the catechol metabolites from the equine estrogen, 8,9-dehydroestrone, CHEM RES T, 14(6), 2001, pp. 754-763
Authors:
Chen, YM
Liu, XM
Pisha, E
Constantinou, AI
Hua, YS
Shen, LX
van Breemen, RB
Elguindi, EC
Blond, SY
Zhang, FG
Bolton, JL
Citation: Ym. Chen et al., A metabolite of equine estrogens, 4-hydroxyequilenin, induces DNA damage and apoptosis in breast cancer cell lines, CHEM RES T, 13(5), 2000, pp. 342-350
Citation: Pw. Fan et al., 4-hydroxylated metabolites of the antiestrogens tamoxifen and toremifene are metabolized to unusually stable quinone methides, CHEM RES T, 13(1), 2000, pp. 45-52
Citation: Fg. Zhang et al., Synthesis and reactivity of a potential carcinogenic metabolite of tamoxifen: 3,4-dihydroxytamoxifen-o-quinone, CHEM RES T, 13(1), 2000, pp. 53-62
Citation: Fg. Zhang et Jl. Bolton, Synthesis of the equine estrogen metabolites 2-hydroxyequilin and 2-hydroxyequilenin, CHEM RES T, 12(2), 1999, pp. 200-203
Authors:
Zhang, FG
Chen, YM
Pisha, E
Shen, L
Xiong, YS
van Breemen, RB
Bolton, JL
Citation: Fg. Zhang et al., The major metabolite of equilin, 4-hydroxyequilin, autoxidizes to an o-quinone which isomerizes to the potent cytotoxin 4-hydroxyequilenin-o-quinone, CHEM RES T, 12(2), 1999, pp. 204-213