换一批Comparison of the induction profile for drug disposition proteins by typical nuclear receptor activators in human hepatic and intestinal cells.
第一作者：
P,Martin
第一单位：
Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
作者：
医学主题词
ATP结合匣式转运子(ATP-Binding Cassette Transporters);芳基烃羟化酶类(Aryl Hydrocarbon Hydroxylases);Caco-2细胞(Caco-2 Cells);细胞培养技术(Cell Culture Techniques);细胞, 培养的(Cells, Cultured);鹅脱氧胆酸(Chenodeoxycholic Acid);细胞色素P-450 CYP3A(Cytochrome P-450 CYP3A);细胞色素P450酶系统(Cytochrome P-450 Enzyme System);DNA结合蛋白质类(DNA-Binding Proteins);地塞米松(Dexamethasone);剂量效应关系, 药物(Dose-Response Relationship, Drug);酶诱导(Enzyme Induction);上皮细胞(Epithelial Cells);肝细胞(Hepatocytes);人类(Humans);肠黏膜(Intestinal Mucosa);膜转运蛋白质类(Membrane Transport Proteins);多药耐药相关蛋白质类(Multidrug Resistance-Associated Proteins);氧化还原酶类, N-脱甲基(Oxidoreductases, N-Demethylating);苯巴比妥(Phenobarbital);孕烯诺龙酮腈(Pregnenolone Carbonitrile);RNA, 信使(RNA, Messenger);受体, 胞质和核(Receptors, Cytoplasmic and Nuclear);受体, 类固醇(Receptors, Steroid);研究设计(Research Design);利福平(Rifampin);转录因子(Transcription Factors);增量调节(Up-Regulation)
DOI
10.1038/sj.bjp.0707601
PMID
18037906
发布时间
2021-12-03
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