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Habibi, H. R.
- Modulation of Gene Expression in Gonad and Liver of Male Goldfish Exposed to Bisphenol A
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Authors
Affiliations
1 Faculty of Fisheries and Protection of Waters, South Bohemia Research Center of Aquaculture and Biodiversity of Hydrocenoses, University of South Bohemia in České Budějovice, Zátiší 728/II, Vodnany 389 25, CZ
2 Department of Biological Sciences, University of Calgary, Calgary, Alberta, CA
1 Faculty of Fisheries and Protection of Waters, South Bohemia Research Center of Aquaculture and Biodiversity of Hydrocenoses, University of South Bohemia in České Budějovice, Zátiší 728/II, Vodnany 389 25, CZ
2 Department of Biological Sciences, University of Calgary, Calgary, Alberta, CA
Source
Indian Journal of Science and Technology, Vol 4, No S8 (2011), Pagination: 247-248Abstract
No AbstractReferences
- Kang JH, Aasi D, Katayama Y. 2007. Bishenol A in the aquatic environment and its endocrine-disruptive effects on aquatic organisms. Critical Rev. Toxicol., 37: 607–625.
- Vandenberg LN, Maffini MV, Sonnenschein C, Rubin BS, SOTO AM. 2009. Bisphenol-A and the great divide: A review of controversies in the field of endocrine disruption. Endocrine Rev., 30: 75–95.
- Akingbemi BT, Sottas CM, Koulova AI, Klinefelter GR, Hardy MP. 2004. Inhibition of testicular steroidogenesis by the xenoestrogen bisphenol A is associated with reduced pituitary luteinizing hormone secretion and decreased steroidogenic enzyme gene expression in rat Leydig cells. Endocrinology, 145: 592–603.
- Hatef A, Alavi SMH, Abdulfatah A, Fontaine F, Linhart O. 2011. In vivo effects of Bisphenol A on sex steroids and vitellogenin production in male goldfish (Carassius auratus L.) at environmentally relevant concentrations. Reprod. Biol. Endocrinol. In revision.
- Nelson ER, Habibi HR. 2010. Functional significance of nuclear estrogen receptor subtypes in the liver of goldfish. Endocrinology, 151: 1668–1676.