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Zhu, H
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Citation: H. Zhu et al., Analysis of expressed sequence tags from two starvation, time-of-day-specific libraries of Neurospora crassa reveals novel clock-controlled genes, GENETICS, 157(3), 2001, pp. 1057-1065
Authors:
Kraemer, HC
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Citation: Hc. Kraemer et al., How do risk factors work together? Mediators, moderators, and independent,overlapping, and proxy risk factors, AM J PSYCHI, 158(6), 2001, pp. 848-856
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Citation: Sh. Scholle et al., Effect of different recruitment sources on the composition of a bipolar disorder case registry, SOC PSY PSY, 35(5), 2000, pp. 220-227
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Santi, DV
Siani, MA
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Citation: Dv. Santi et al., An approach for obtaining perfect hybridization probes for unknown polyketide synthase genes: a search for the epothilone gene cluster, GENE, 247(1-2), 2000, pp. 97-102
Authors:
Katchamart, S
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Williams, DE
Citation: S. Katchamart et al., Concurrent flavin-containing monooxygenase down-regulation and cytochrome P-450 induction by dietary indoles in rat: Implications for drug-drug interaction, DRUG META D, 28(8), 2000, pp. 930-936
Authors:
Tully, K
Kupfer, D
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Citation: K. Tully et al., A plasticizer released from IV drip chambers elevates calcium levels in neurosecretory terminals, TOX APPL PH, 168(3), 2000, pp. 183-188
Authors:
Gaido, KW
Maness, SC
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Dehal, SS
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Citation: Kw. Gaido et al., Interaction of methoxychlor and related compounds with estrogen receptor alpha and beta, and androgen receptor: structure-activity studies, MOLEC PHARM, 58(4), 2000, pp. 852-858
Authors:
Kraemer, HC
Yesavage, JA
Taylor, JL
Kupfer, D
Citation: Hc. Kraemer et al., How can we learn about developmental processes from cross-sectional studies, or can we?, AM J PSYCHI, 157(2), 2000, pp. 163-171
Citation: Ss. Dehal et D. Kupfer, Cytochrome P-450 3A and 2D6 catalyze ortho hydroxylation of 4-hydroxyamoxifen and 3-hydroxytamoxifen (droloxifene) yielding tamoxifen catechol: Involvement of catechols in covalent binding to hepatic proteins, DRUG META D, 27(6), 1999, pp. 681-688
Citation: Ss. Dehal et al., The aromatase inactivator 4-hydroxyandrostenedione (4-OH-A) inhibits tamoxifen metabolism by rat hepatic cytochrome P-450 3A: Potential for drug-druginteraction of tamoxifen and 4-OH-A in combined anti-breast cancer therapy, DRUG META D, 27(3), 1999, pp. 389-394