Association and dissociation of the Ah locus with the metabolism of aflatoxin B1 by mouse liver. Co-segregation of aflatoxin B1 hydroxylase induction with aryl hydrocarbon (benzo(a)pyrene) hydroxylase induction. - Suppr | 超能文献

Association and dissociation of the Ah locus with the metabolism of aflatoxin B1 by mouse liver. Co-segregation of aflatoxin B1 hydroxylase induction with aryl hydrocarbon (benzo(a)pyrene) hydroxylase induction.

作者信息

Gurtoo H L, Dahms R P, Kanter P, Vaught J B

出版信息

J Biol Chem. 1978 Jun 10;253(11):3952-61.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Association and dissociation of the Ah locus with the metabolism of aflatoxin B1 by mouse liver. Co-segregation of aflatoxin B1 hydroxylase induction with aryl hydrocarbon (benzo(a)pyrene) hydroxylase induction.

J Biol Chem. 1978 Jun 10;253(11):3952-61.

2

Induction of aryl hydrocarbon (benzo[a]pyrene) hydroxylase and 2-acetylaminofluorene N-hydroxylase by polycyclic hydrocarbons in regenerating liver from inbred strains of mice.多环烃对近交系小鼠再生肝中芳烃（苯并[a]芘）羟化酶和2-乙酰氨基芴N-羟化酶的诱导作用。

Biochem Pharmacol. 1977 Aug 15;26(16):1501-5. doi: 10.1016/0006-2952(77)90422-1.

3

Genetic expression of aflatoxin metabolism. Effects of 3-methylcholanthrene and beta-naphthoflavone on hepatic microsomal metabolism and mutagenic activation of aflatoxins.黄曲霉毒素代谢的基因表达。3-甲基胆蒽和β-萘黄酮对肝微粒体黄曲霉毒素代谢及诱变激活的影响。

Biochem Pharmacol. 1983 Dec 15;32(24):3755-63. doi: 10.1016/0006-2952(83)90146-6.

4

Genetic association of increases in naphthalene, acetanilide, and biphenyl hydroxylations with inducible aryl hydrocarbon hydroxylase in mice.小鼠中萘、乙酰苯胺和联苯羟基化增加与诱导型芳烃羟化酶的遗传关联。

Arch Biochem Biophys. 1976 Aug;175(2):495-506. doi: 10.1016/0003-9861(76)90537-3.

5

Genetic regulation of UDP-glucuronosyltransferase induction by polycyclic aromatic compounds in mice. Co-segregation with aryl hydrocarbon (benzo(alpha)pyrene) hydroxylase induction.小鼠中多环芳烃对UDP-葡萄糖醛酸基转移酶诱导的遗传调控。与芳烃（苯并(α)芘）羟化酶诱导的共分离。

J Biol Chem. 1977 May 10;252(9):2827-33.

6

The genetics of aflatoxin B1 metabolism. Association of the induction of aflatoxin B1-4-hydroxylase with the transcriptional activation of cytochrome P3-450 gene.黄曲霉毒素B1代谢的遗传学。黄曲霉毒素B1 - 4 - 羟化酶的诱导与细胞色素P3 - 450基因转录激活的关联。

J Biol Chem. 1988 Sep 5;263(25):12584-95.

7

Genetic regulation of bilirubin-UDP-glucuronosyltransferase induction by polycyclic aromatic compounds and phenobarbital in mice. Association with aryl hydrocarbon (benzo[a]pyrene) hydroxylase induction.多环芳烃和苯巴比妥对小鼠胆红素 - UDP - 葡萄糖醛酸基转移酶诱导的遗传调控。与芳烃（苯并[a]芘）羟化酶诱导的关联。

J Biol Chem. 1981 Sep 25;256(18):9599-604.

8

Genetic differences in the induction of aryl hydrocarbon hydroxylase and benzo(a)pyrene carcinogenesis in C3H/He and DBA/2 strains of mice.C3H/He和DBA/2品系小鼠中芳烃羟化酶诱导及苯并(a)芘致癌作用的遗传差异。

Gan. 1975 Jun;66(3):217-26.

9

[2,3,7,8-Tetrachlorodibenzo-p-dioxin induces the biosynthesis of highly active benzo(a)pyrene hydroxylase in liver microsomes].[2,3,7,8-四氯二苯并-对-二恶英诱导肝微粒体中高活性苯并(a)芘羟化酶的生物合成]

Dokl Akad Nauk SSSR. 1986;290(5):1271-3.

10

Comparison of beta-naphthoflavone and 3-methylcholanthrene as inducers of hepatic cytochrome(s) P-448 and aryl hydrocarbon (benzo[a]pyrene) hydroxylase activity.β-萘黄酮与3-甲基胆蒽作为肝细胞色素P-448及芳烃（苯并[a]芘）羟化酶活性诱导剂的比较

Mol Pharmacol. 1977 Mar;13(2):259-68.

引用本文的文献

1

In vitro cytochrome P450 monooxygenase and prostaglandin H-synthase mediated aflatoxin B1 biotransformation in guinea pig tissues: effects of beta-naphthoflavone treatment.体外细胞色素P450单加氧酶和前列腺素H合成酶介导豚鼠组织中黄曲霉毒素B1的生物转化：β-萘黄酮处理的影响

Arch Toxicol. 1993;67(6):379-85. doi: 10.1007/BF01977398.

2

Peliosis hepatis. Its relationship to chronic alcoholism, aflatoxin B1, and carcinogenesis in male Holtzman rats.肝紫癜。其与雄性霍尔茨曼大鼠慢性酒精中毒、黄曲霉毒素B1及致癌作用的关系。

Dig Dis Sci. 1980 Aug;25(8):587-92. doi: 10.1007/BF01318871.

3

Chromosomal organization of the cytochrome P450-2C gene family in the mouse: a locus associated with constitutive aryl hydrocarbon hydroxylase.小鼠细胞色素P450 - 2C基因家族的染色体组织：一个与组成型芳烃羟化酶相关的基因座。

Proc Natl Acad Sci U S A. 1988 Apr;85(8):2662-6. doi: 10.1073/pnas.85.8.2662.