Endocrine disruption induced by organotin compounds; organotins function as a powerful agonist for nuclear receptors rather than an aromatase inhibitor-Reference-Cited by-同舟云学术

Endocrine disruption induced by organotin compounds; organotins function as a powerful agonist for nuclear receptors rather than an aromatase inhibitor

Published:2008 Issue:3 Volume:33 Page:269-276
ISSN:0388-1350
Container-title:The Journal of Toxicological Sciences
language:en
Short-container-title:J. Toxicol. Sci.

Author:

Nakanishi Tsuyoshi¹²

Affiliation:

1. Laboratory of Hygienics, Gifu Pharmaceutical University

2. Department of Toxicology, Graduate School of Pharmaceutical Sciences, Osaka University

Publisher

Japanese Society of Toxicology

Subject

Toxicology

Link

http://www.jstage.jst.go.jp/article/jts/33/3/33_3_269/_pdf

Reference59 articles.

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3. Bamberger, A.M., Ezzat, S., Cao, B., Wong, M., Parker, K.L., Schulte, H.M. and Asa, S.L. (1996): Expression of steroidogenic factor-1 (SF-1) mRNA and protein in the human placenta. Mol. Hum. Reprod., 2, 457-461.

4. PPAR-RXR Heterodimer Activates a Peroxisome Proliferator Response Element Upstream of the Bifunctional Enzyme Gene

5. TBT-induced imposex in marine neogastropods is mediated by an increasing androgen level

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