ANIMAL TISSUE;
ARTICLE;
BLOOD SAMPLING;
CHEMOPROPHYLAXIS;
CONTROLLED STUDY;
DRUG BLOOD LEVEL;
DRUG METABOLISM;
DRUG STABILITY;
HUMAN;
HUMAN TISSUE;
IN VITRO STUDY;
IN VIVO STUDY;
LIQUID CHROMATOGRAPHY;
MICROSOME MEMBRANE;
NONHUMAN;
TANDEM MASS SPECTROMETRY;
ANIMAL;
COMPARATIVE STUDY;
DOG;
DRUG DETOXIFICATION;
FEMALE;
LIVER MICROSOME;
MALE;
METABOLISM;
METHODOLOGY;
PRIMATE;
RAT;
SPECIES DIFFERENCE;
SPRAGUE DAWLEY RAT;
ANIMALS;
CHROMANS;
CHROMATOGRAPHY, LIQUID;
DOGS;
FEMALE;
HUMANS;
ISOENZYMES;
MALE;
METABOLIC DETOXICATION, DRUG;
MICROSOMES, LIVER;
PRIMATES;
RATS;
RATS, SPRAGUE-DAWLEY;
SPECIES SPECIFICITY;
TANDEM MASS SPECTROMETRY;
Ong ASH, Natural sources of tocotrienols. In: Packer L, Fuchs J, eds. Vitamin E in Health and Disease: Biochemistry and Clinical Applications. Florida: CRC Press, 1992: 3-8.
Thompson TA, Wilding G. Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells. Mol Cancer Ther 2003; 8: 797-803.
Thompson TA, Wilding G. Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells. Mol Cancer Ther 2003; 8: 797-803.
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The importance of steroid hormones in prostate cancer
Wilding G. The importance of steroid hormones in prostate cancer. Cancer Surv 1992; 14: 113-130.
Expression and characterization of a novel thyroid hormone-sulfating form of cytosolic sulfotransferase from human liver
Wang J et al. Expression and characterization of a novel thyroid hormone-sulfating form of cytosolic sulfotransferase from human liver. Mol Pharmacol 1998; 53: 274-282.
Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions
Bertz RJ, Granneman GR. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997; 37: 1150-1159.
The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
Obach RS et al. The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J Pharmacol Exp Ther 1997; 283: 46-58.
Cytochrome P450 genes are differently expressed in female and male hepatocyte retinoid X receptor α-deficient mice
Cai Y et al. Cytochrome P450 genes are differently expressed in female and male hepatocyte retinoid X receptor α-deficient mice. Endocrinology 2003; 144: 2311-2318.
Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 caucasians
Shimada T et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 caucasians. J Pharmacol Exp Ther 1994; 270: 414-423.
Human cytochrome P450 2A6 is a major enzyme involved in the metabolism of three alkoxy ethers used as oxyfuels
Le Gal A et al. Human cytochrome P450 2A6 is a major enzyme involved in the metabolism of three alkoxy ethers used as oxyfuels. Toxicol Lett 2001; 124: 47-58.
Quantitative structure activity relationships for the glucuronidation of simple phenols by expressed human UGT1A6 and UGT1A9
Ethell B et al. Quantitative structure activity relationships for the glucuronidation of simple phenols by expressed human UGT1A6 and UGT1A9. Drug Metab Dispos 2002; 30: 734-738.
The expression of UDP-glucuronosyltransferases of the UGT1 family in human liver and kidney and in response to drugs
Sutherland L et al. The expression of UDP-glucuronosyltransferases of the UGT1 family in human liver and kidney and in response to drugs. Biochem Pharmacol 1993; 45: 295-301.
Glucuronidation of catechols by human hepatic, gastric, and intestinal microsomal UDP-glucuronosyltransferases (UGT) and recombinant UGT1A6, UGT1A9, and UGT2B7
Antonio L et al. Glucuronidation of catechols by human hepatic, gastric, and intestinal microsomal UDP-glucuronosyltransferases (UGT) and recombinant UGT1A6, UGT1A9, and UGT2B7. Arch Biochem Biophys 2003; 478: 127-212.