Comparison of genomic and cDNA sequences of guinea pig CYP2B18 and rat CYP2B2: Absence of a phenobarbital-responsive enhancer module in the upstream region of theCYP2B18 gene-Reference-Cited by-同舟云学术

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Comparison of genomic and cDNA sequences of guinea pig CYP2B18 and rat CYP2B2: Absence of a phenobarbital-responsive enhancer module in the upstream region of theCYP2B18 gene

Published:2004 Issue:3 Volume:18 Page:124-130
ISSN:1095-6670
Container-title:Journal of Biochemical and Molecular Toxicology
language:en
Short-container-title:J. Biochem. Mol. Toxicol.

Author:

Yamamoto Midori,Mise Masashi,Matsumoto Sanae,Ito Shoich,Gohyama Noriko,Ishida Satoru,Sagara Yasuhiro,Omiecinski Curtis J.,Oguri Kazuta,Yamada Hideyuki

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

Reference19 articles.

1. Enzymology of rat liver cytochrome P-450. In: editor. Mammalian Cytochromes P-450. Boca Raton: CRC Press; 1987, Vol. 1, pp 1-54.

2. Phenobarbital induction of cytochrome P-450 gene expression

3. Localization of a phenobarbital-responsive element (PBRE) in the 5′-flanking region of the rat CYP2B2 gene

4. Characterization of a Phenobarbital-responsive Enhancer Module in Mouse P450 Cyp2b10 Gene

5. The CYP2B2 Phenobarbital Response Unit Contains an Accessory Factor Element and a Putative Glucocorticoid Response Element Essential for Conferring Maximal Phenobarbital Responsiveness

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Induction of the Hepatic Cytochrome P450 2B Subfamily by Xenobiotics: Research History, Evolutionary Aspect, Relation to Tumorigenesis, and Mechanism;Current Drug Metabolism;2006-05-01

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