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1
The significance of drug-induced spectral changes in liver microsomal fraction.药物诱导肝微粒体部分光谱变化的意义。
Biochem J. 1971 Nov;125(2):8P-9P. doi: 10.1042/bj1250008p.
2
The nature of the reverse type I (modified type II) spectral change in liver microsomes.
Biochemistry. 1972 Nov 7;11(23):4243-51. doi: 10.1021/bi00773a008.
3
Kinetic differences in the microsomal metabolism of the isomers of hexobarbital.
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Biochem Soc Symp. 1972;34:55-77.
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[Studies on the hexobarbital difference spectrum with microsomes from 3-methylcholanthrene treated rats].
Yakugaku Zasshi. 1971 Jan;91(1):142.
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Disulfiram impairment of drug metabolism by rat liver microsomes.双硫仑对大鼠肝脏微粒体药物代谢的损害。
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Spectral and kinetic studies of the interaction of imidazole anti-fungal agents with microsomal cytochromes P-450.
Xenobiotica. 1987 Nov;17(11):1315-27. doi: 10.3109/00498258709047162.
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Species differences in the induction of microsomal hemoproteins and 3,4-benzpyrene hydroxylase by phenobarbital and 3-methylcholanthrene.苯巴比妥和3-甲基胆蒽对微粒体血红蛋白和3,4-苯并芘羟化酶诱导作用的种属差异。
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The binding of metyrapone to cytochrome P-450 and its inhibitory action on liver microsomal mixed-function oxidase reactions.甲吡酮与细胞色素P - 450的结合及其对肝微粒体混合功能氧化酶反应的抑制作用。
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本文引用的文献

1
Substrate binding to cytochrome P-450 of liver and adrenal microsomes.底物与肝脏和肾上腺微粒体细胞色素P-450的结合。
FEBS Lett. 1970 Feb 16;6(3):249-252. doi: 10.1016/0014-5793(70)80070-9.
2
Fatty acid interaction with the hydroxylating enzyme system of rat liver microsomes.
Eur J Biochem. 1969 Jun;9(3):415-8. doi: 10.1111/j.1432-1033.1969.tb00624.x.
3
Spectral studies of drug interaction with hepatic microsomal cytochrome.药物与肝微粒体细胞色素相互作用的光谱研究
Mol Pharmacol. 1967 Mar;3(2):113-23.
4
Studies on the nature of the type I and type II spectral changes in liver microsomes.
Biochemistry. 1970 May 12;9(10):2081-91. doi: 10.1021/bi00812a009.

The significance of drug-induced spectral changes in liver microsomal fraction.

作者信息

Orrenius S, Wilson B, Von Bahr C, Schenkman J B

出版信息

Biochem J. 1971 Nov;125(2):8P-9P. doi: 10.1042/bj1250008p.

DOI:10.1042/bj1250008p
PMID:5144764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1178112/
Abstract
摘要