S-美芬妥因羟基化的基因多态性。 - Suppr | 超能文献

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1

Genetic polymorphism of S-mephenytoin hydroxylation.S-美芬妥因羟基化的基因多态性。

Pharmacol Ther. 1989;43(1):53-76. doi: 10.1016/0163-7258(89)90047-8.

2

Pharmacogenetics of mephenytoin: a new drug hydroxylation polymorphism in man.美芬妥英的药物遗传学：人类一种新的药物羟基化多态性

Eur J Clin Pharmacol. 1984;26(6):753-9. doi: 10.1007/BF00541938.

3

Mephenytoin hydroxylation in the Cuna Amerindians of Panama.巴拿马库纳美洲印第安人中美芬妥英的羟基化作用

Br J Clin Pharmacol. 1988 Jan;25(1):75-9. doi: 10.1111/j.1365-2125.1988.tb03284.x.

4

Mephenytoin hydroxylation polymorphism: characterization of the enzymatic deficiency in liver microsomes of poor metabolizers phenotyped in vivo.

Clin Pharmacol Ther. 1985 Nov;38(5):488-94. doi: 10.1038/clpt.1985.213.

5

Genetic polymorphism of mephenytoin p(4')-hydroxylation: difference between Orientals and Caucasians.美芬妥因p(4')-羟化作用的基因多态性：东方人与高加索人的差异。

Br J Clin Pharmacol. 1985 Apr;19(4):483-7. doi: 10.1111/j.1365-2125.1985.tb02673.x.

6

Polymorphism in hydroxylation of mephenytoin and hexobarbital stereoisomers in relation to hepatic P-450 human-2.

Clin Pharmacol Ther. 1990 Mar;47(3):313-22. doi: 10.1038/clpt.1990.34.

7

Mephenytoin hydroxylation deficiency in Caucasians: frequency of a new oxidative drug metabolism polymorphism.高加索人中美芬妥英羟化缺乏症：一种新的氧化药物代谢多态性的频率

Clin Pharmacol Ther. 1984 Dec;36(6):773-80. doi: 10.1038/clpt.1984.256.

8

Family studies of mephenytoin hydroxylation deficiency.美芬妥因羟化缺乏症的家系研究。

Am J Hum Genet. 1986 May;38(5):768-72.

9

Oxidative metabolism of hexobarbital in human liver: relationship to polymorphic S-mephenytoin 4-hydroxylation.人肝脏中己巴比妥的氧化代谢：与多态性S-美芬妥因4-羟化的关系。

J Pharmacol Exp Ther. 1988 Jun;245(3):845-9.

10

The molecular mechanisms of two common polymorphisms of drug oxidation--evidence for functional changes in cytochrome P-450 isozymes catalysing bufuralol and mephenytoin oxidation.药物氧化两种常见多态性的分子机制——催化布呋洛尔和美芬妥因氧化的细胞色素P-450同工酶功能改变的证据

Xenobiotica. 1986 May;16(5):449-64. doi: 10.3109/00498258609050251.

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