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- 人肝臟藥物代謝酶CYP1A2Cytochrome CYPIA2
- 實(shí)驗感染肝片吸蟲(chóng)對水牛肝臟藥物代謝酶的損傷作用Impairment of liver drug metabollzing enzymes in experimental Fascioloses in water buffalo
- 實(shí)驗感染肝片吸蟲(chóng)對大鼠肝臟藥物代謝功能的影響Effects of experimental fascioliasis on the drug-metabolizing function in rat liver
- 貝特類(lèi)藥物治療不影響人肝臟乙?；o酶氧化酶的表達Fibrate treatment does not modify the expression of acyl coenzyme A oxidase in human liver
- 白種人ESRD患者藥物代謝酶遺傳變異及性別與甲狀旁腺素水平關(guān)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
- 人肝臟微粒體human liver microsomes
- 由此認為,3-去酮HMT可能具有刺激肝臟藥物轉化酶的作用.It seems, therefore, that 3-deoxy-HMT is a potent stimulant of the hepatic microsomal drug-metabolizing enzymes.
- 人肝臟星狀細胞human hepatic stellate cells
- 報人journalist
- 酶的enzymatic
- 埃及人Egyptian
- 肝臟liver
- 白種人white
- 強人strong man
- 人肝臟腫瘤細胞SMMU-7721The hominal liver cancer cell SMMU- 7721
- CYP1A2可通過(guò)影響甲基試鹵靈-O-脫甲基酶(methoxyresorufin-O-demethylase,MROD),而選擇性地催化7-甲基試鹵靈脫甲基反應。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
- 愛(ài)爾蘭人Irish
