Origins of individual variability in P4501A induction

被引:42
作者
Ma, Q [1 ]
Lu, AYH
机构
[1] Ctr Dis Control & Prevent, NIOSH, Hlth Effects Lab Div, Toxicol & Mol Biol Branch,Receptor Biol Lab, Morgantown, WV USA
[2] Rutgers State Univ, Coll Pharm, Dept Biol Chem, Canc Res Lab, Piscataway, NJ USA
关键词
D O I
10.1021/tx0200919
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
引用
收藏
页码:249 / 260
页数:12
相关论文
共 124 条
[1]  
ABDELRAZZAK Z, 1994, MOL PHARMACOL, V46, P1100
[2]   Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine [J].
Adachi, J ;
Mori, Y ;
Matsui, S ;
Takigami, H ;
Fujino, J ;
Kitagawa, H ;
Miller, CA ;
Kato, T ;
Saeki, K ;
Matsuda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :31475-31478
[3]  
ALVARES AP, 1973, CLIN PHARMACOL THER, V14, P30
[4]   Pharmacokinetics, metabolism and interactions of acid pump inhibitors - Focus on omeprazole, lansoprazole and pantoprazole [J].
Andersson, T .
CLINICAL PHARMACOKINETICS, 1996, 31 (01) :9-28
[5]   An uncommon phenotype of poor inducibility of CYP1A1 in human lung is not ascribable to polymorphisms in the AHR, ARNT, or CYP1A1 genes [J].
Anttila, S ;
Lei, XD ;
Elovaara, E ;
Karjalainen, A ;
Sun, WM ;
Vainio, H ;
Hankinson, O .
PHARMACOGENETICS, 2000, 10 (08) :741-751
[6]   Flavones and flavonols at dietary levels inhibit a transformation of aryl hydrocarbon receptor induced by dioxin [J].
Ashida, H ;
Fukuda, I ;
Yamashita, T ;
Kanazawa, K .
FEBS LETTERS, 2000, 476 (03) :213-217
[7]   AROCLOR-1254 AS A 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN ANTAGONIST - EFFECTS ON ENZYME-INDUCTION AND IMMUNOTOXICITY [J].
BANNISTER, R ;
DAVIS, D ;
ZACHAREWSKI, T ;
TIZARD, I ;
SAFE, S .
TOXICOLOGY, 1987, 46 (01) :29-42
[8]   6-METHYL-1,3,8-TRICHLORODIBENZOFURAN (MCDF) AS A 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN ANTAGONIST IN C57BL/6 MICE [J].
BANNISTER, R ;
BIEGEL, L ;
DAVIS, D ;
ASTROFF, B ;
SAFE, S .
TOXICOLOGY, 1989, 54 (02) :139-150
[9]  
BOUCHER PD, 1993, J BIOL CHEM, V268, P17384
[10]  
BRADFIELD CA, 1991, MOL PHARMACOL, V39, P13