ANIMAL TISSUE;
ARTICLE;
BILE DUCT;
DRUG ABSORPTION;
DRUG BIOAVAILABILITY;
DRUG CLEARANCE;
DRUG DISPOSITION;
DRUG DISTRIBUTION;
DRUG ELIMINATION;
DRUG EXCRETION;
DRUG FECES LEVEL;
DRUG HALF LIFE;
DRUG METABOLISM;
FEMALE;
MALE;
MAXIMUM PLASMA CONCENTRATION;
NONHUMAN;
PLASMA CONCENTRATION-TIME CURVE;
QUANTITATIVE ANALYSIS;
RADIOACTIVITY;
RAT;
STEADY STATE;
STOMACH SECRETION;
WHOLE BODY AUTORADIOGRAPHY;
Expression profiles of 50 xenobiotic transporter genes in humans and pre-clinical species: A resource for investigations into drug disposition
Bleasby K, Castle JC, Roberts CJ, et al. (2006). Expression profiles of 50 xenobiotic transporter genes in humans and pre-clinical species: a resource for investigations into drug disposition. Xenobiotica 36: 963-88.
Impaired nociception and pain sensation in mice lacking the capsaicin receptor
Caterina MJ, Leffler A, Malmberg AB, et al. (2000). Impaired nociception and pain sensation in mice lacking the capsaicin receptor. Science 288: 306-13.
Distinct pharmacological properties and distribution in neurons and endocrine cells of two isoforms of the human vesicular monoamine transporter
Erickson JD, Schäfer MKH, Bonner TI, et al. (1996). Distinct pharmacological properties and distribution in neurons and endocrine cells of two isoforms of the human vesicular monoamine transporter. Proc Natl Acad Sci USA 93: 5166-71.
Sex differences in pharmacokinetics and pharmacodynamics
Gandhi M, Aweeka F, Greenblatt RM, Blaschke TF. (2004). Sex differences in pharmacokinetics and pharmacodynamics. Annu Rev Pharmacol Toxicol 44: 499-523.