关注
david stresser
david stresser
在 abbvie.com 的电子邮件经过验证
标题
引用次数
引用次数
年份
Substrate-dependent modulation of CYP3A4 catalytic activity: analysis of 27 test compounds with four fluorometric substrates
DM Stresser, AP Blanchard, SD Turner, JCL Erve, AA Dandeneau, ...
Drug Metabolism and Disposition 28 (12), 1440-1448, 2000
3462000
Effects of ginseng components on c-DNA-expressed cytochrome P450 enzyme catalytic activity
GL Henderson, MR Harkey, ME Gershwin, RM Hackman, JS Stern, ...
Life sciences 65 (15), PL209-PL214, 1999
2041999
In vitro and pharmacophore insights into CYP3A enzymes
S Ekins, DM Stresser, JA Williams
Trends in pharmacological sciences 24 (4), 161-166, 2003
1972003
Cytochrome P450 fluorometric substrates: identification of isoform-selective probes for rat CYP2D2 and human CYP3A4.
DM Stresser, SD Turner, AP Blanchard, VP Miller, CL Crespi
Drug Metabolism and Disposition 30 (7), 845-852, 2002
1972002
In vitro drug metabolism using liver microsomes
KM Knights, DM Stresser, JO Miners, CL Crespi
Current protocols in pharmacology 74 (1), 7.8. 1-7.8. 24, 2016
1912016
Fluorometric screening for metabolism-based drug–drug interactions
CL Crespi, DM Stresser
Journal of pharmacological and toxicological methods 44 (1), 325-331, 2000
1652000
A high-throughput screen to identify inhibitors of aromatase (CYP19)
DM Stresser, SD Turner, J McNamara, P Stocker, VP Miller, CL Crespi, ...
Analytical biochemistry 284 (2), 427-430, 2000
1612000
Monospecific antipeptide antibody to cytochrome P-450 2B6
DM Stresser, D Kupfer
Drug Metabolism and Disposition 27 (4), 517-525, 1999
1591999
Highly selective inhibition of human CYP3A in vitro by azamulin and evidence that inhibition is irreversible
DM Stresser, MI Broudy, T Ho, CE Cargill, AP Blanchard, R Sharma, ...
Drug Metabolism and Disposition 32 (1), 105-112, 2004
1562004
Indole-3-carbinol and beta-naphthoflavone induction of aflatoxin B1 metabolism and cytochromes P-450 associated with bioactivation and detoxication of aflatoxin B1 in the rat.
DM Stresser, GS Bailey, DE Williams
Drug metabolism and disposition 22 (3), 383-391, 1994
1321994
Mechanisms of tumor modulation by indole-3-carbinol. Disposition and excretion in male Fischer 344 rats.
DM Stresser, DE Williams, DA Griffin, GS Bailey
Drug metabolism and disposition 23 (9), 965-975, 1995
1301995
Fluorometric high‐throughput screening for inhibitors of cytochrome P450
VP Miller, DM Stresser, AP Blanchard, S Turner, CL Crespi
Annals of the New York Academy of Sciences 919 (1), 26-32, 2000
1252000
Evaluation of multiple in vitro systems for assessment of CYP3A4 induction in drug discovery: human hepatocytes, pregnane X receptor reporter gene, and Fa2N-4 and HepaRG cells
DF McGinnity, G Zhang, JR Kenny, GA Hamilton, S Otmani, KR Stams, ...
Drug metabolism and disposition 37 (6), 1259-1268, 2009
1212009
Human cytochrome P450–catalyzed conversion of the proestrogenic pesticide methoxychlor into an estrogen: Role of CYP2C19 and CYP1A2 inO-demethylation
DM Stresser, D Kupfer
Drug Metabolism and disposition 26 (9), 868-874, 1998
1141998
Validation of cytochrome P450 time-dependent inhibition assays: a two-time point IC50 shift approach facilitates kinact assay design
ES Perloff, AK Mason, SS Dehal, AP Blanchard, L Morgan, T Ho, ...
Xenobiotica 39 (2), 99-112, 2009
1022009
Indole-3-carbinol induces a rat liver glutathione transferase subunit (Yc2) with high activity toward aflatoxin B1 exo-epoxide. Association with reduced levels of hepatic …
DM Stresser, DE Williams, LI McLellan, TM Harris, GS Bailey
Drug metabolism and disposition 22 (3), 392-399, 1994
861994
Tissue-specific expression of flavin-containing monooxygenase (FMO) forms 1 and 2 in the rabbit.
SE Shehin-Johnson, DE Williams, S Larsen-Su, DM Stresser, RN Hines
Journal of Pharmacology and Experimental Therapeutics 272 (3), 1293-1299, 1995
851995
The anticarcinogen 3, 3′‐diindolylmethane is an inhibitor of cytochrome P‐450
DM Stresser, GS Bailey, DE Williams, LF Bjeldanes
Journal of biochemical toxicology 10 (4), 191-201, 1995
741995
Concurrent flavin-containing monooxygenase down-regulation and cytochrome P-450 induction by dietary indoles in rat: implications for drug-drug interaction
S Katchamart, DM Stresser, SS Dehal, D Kupfer, DE Williams
Drug Metabolism and Disposition 28 (8), 930-936, 2000
702000
The use of 3-[2-(N, N-diethyl-N-methylammonium) ethyl]-7-methoxy-4-methylcoumarin (AMMC) as a specific CYP2D6 probe in human liver microsomes
N Chauret, B Dobbs, RL Lackman, K Bateman, DA Nicoll-Griffith, ...
Drug metabolism and disposition 29 (9), 1196-1200, 2001
652001
系统目前无法执行此操作,请稍后再试。
文章 1–20