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- 人肝脏药物代谢酶CYP1A2Cytochrome CYPIA2
- 实验感染肝片吸虫对水牛肝脏药物代谢酶的损伤作用Impairment of liver drug metabollzing enzymes in experimental Fascioloses in water buffalo
- 实验感染肝片吸虫对大鼠肝脏药物代谢功能的影响Effects of experimental fascioliasis on the drug-metabolizing function in rat liver
- 贝特类药物治疗不影响人肝脏乙酰化辅酶氧化酶的表达Fibrate treatment does not modify the expression of acyl coenzyme A oxidase in human liver
- 白种人ESRD患者药物代谢酶遗传变异及性别与甲状旁腺素水平关系的研究Genetic variation of detoxifying enzymes and gender are associated with circulating levels of parathyroid hormone in Caucasian ESRD patients
- CYP1A2CYP1 A2
- 人肝脏微粒体human liver microsomes
- 由此认为,3-去酮HMT可能具有刺激肝脏药物转化酶的作用.It seems, therefore, that 3-deoxy-HMT is a potent stimulant of the hepatic microsomal drug-metabolizing enzymes.
- 人肝脏星状细胞human hepatic stellate cells
- 报人journalist
- 酶的enzymatic
- 埃及人Egyptian
- 肝脏liver
- 白种人white
- 强人strong man
- 人肝脏肿瘤细胞SMMU-7721The hominal liver cancer cell SMMU- 7721
- CYP1A2可通过影响甲基试卤灵-O-脱甲基酶(methoxyresorufin-O-demethylase,MROD),而选择性地催化7-甲基试卤灵脱甲基反应。In this work, we have examined the role of numerous PCBs as inhibitors of the demethylation of 7-methoxyresorufin, a process that is selectively catalyzed by CYP1A2. 2,3,7,8-Tetrachlorobenzo-p-dioxin (TCDD), 3,3?
- 人渣scouring
- 爱尔兰人Irish
