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1 rimary role in acute responses to this toxic endobiotic.
2 aged in the metabolism of numerous xeno- and endobiotics.
3 metabolic activation of both xenobiotics and endobiotics.
4 e uptake and secretion of cationic drugs and endobiotics.
5 he hydroxyls and primary amines of xeno- and endobiotics.
11 minate by glucuronidation a broad variety of endobiotic and xenobiotic substrates, which include bili
12 d by an impaired metabolic detoxification of endobiotics and a persistent microbial-induced immune re
14 ontrol glucose production, detoxification of endobiotics and xenobiotics, and the regulation of prost
15 etion and lipophilicity) of a broad range of endobiotics and xenobiotics, which could plausibly have
18 ification and elimination of xenobiotics and endobiotics by modulating the expression of genes encodi
19 metabolism and excretion of xenobiotics and endobiotics by regulating the expression of drug-metabol
21 zes a range of potentially harmful drugs and endobiotic chemicals but must complex with the nuclear r
22 the conjugation of lipophilic exobiotic and endobiotic compounds, which leads to the excretion of hy
25 eptor (CAR) are implicated in xenobiotic and endobiotic detoxification, including the clearance of to
27 ndrostane receptor (CAR) modulates xeno- and endobiotic hepatotoxicity by regulating detoxification p
28 re important in the elimination of xeno- and endobiotics, including the natural biladienone pigment b
29 ane X receptor (PXR) mediates xenobiotic and endobiotic metabolism as well as hepatocyte proliferatio
34 uman carboxylesterase 1 (hCE1) is a drug and endobiotic-processing serine hydrolase that exhibits rel
38 this study, we have uncovered an unexpected endobiotic role of PXR in obesity and type 2 diabetes.
42 o conjugate xenobiotics, including drugs and endobiotics such as metabolic byproducts, hormones, and
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