References
- Manduzio, H. et al. Characterization of an inducible isoform of the Cu/Zn superoxide dismutase in the blue mussel Mytilus edulis. Aquat Toxicol 64:73-83 (2003) https://doi.org/10.1016/S0166-445X(03)00026-2
- Knigge, T., Monsinjon, T. & Andersen, O. K. Surface -enhanced laser desorption/ionization-time of flightmass spectrometry approach to biomarker discovery in blue mussels (Mytilus edulis) exposed to polyaromatic hydrocarbons and heavy metals under field conditions. Proteomics 4:2722-2727 (2004) https://doi.org/10.1002/pmic.200300828
- Frenzilli, G. et al. DNA damage in eelpout (Zoarces viviparus) from Goteborg harbour. Mutat Res 552: 187-195 (2004) https://doi.org/10.1016/j.mrfmmm.2004.06.018
- Kirso, U. E., Pashin, I., Bakhitova, L. M. & Kiung, A. I. Effect of antioxidants on the carcinogenic and mutagenic activity of benzo[a]pyrene. Vopr Onkol 31:70-75 (1985)
- Stegeman, J. J. & Kloepper-Sams, P. J. Cytochrome P-450 isozymes and mono-oxygenase activity in aquatic animals. Environ Health Perspect 71:87-95 (1987) https://doi.org/10.2307/3430416
- Shaw, J. P., Peters, L. D. & Chipman, J. K. CYP1Aand CYP3A-immunopositive protein levels in digestive gland of the mussel Mytilus galloprovincialis from the Mediterranean Sea. Mar Environ Res 58:649-653 (2004) https://doi.org/10.1016/j.marenvres.2004.03.056
- Miller, K. A., Addison, R. F. & Bandiera, S. M. Hepatic CYP1A levels and EROD activity in English sole: biomonitoring of marine contaminants in Vancouver Harbour. Mar Environ Res 57:37-54 (2004) https://doi.org/10.1016/S0141-1136(03)00059-X
- Boon, J. et al. The expression of CYP1A, vitellogenin and zona radiata proteins in Atlantic salmon (Salmo salar) after oral dosing with two commercial PBDE flame retardant mixtures: absence of short-term responses. Mar Environ Res 54:719-724 (2002) https://doi.org/10.1016/S0141-1136(02)00127-7
- Sies, H. Glutathione and its role in cellular functions. Free Radic Biol Med 27:916-921 (1999) https://doi.org/10.1016/S0891-5849(99)00177-X
- Canpolat, E. & Lynes, M. In vivo manipulation of endogenous metallothionein with a monoclonal antibody enhances a T-dependent humoral immune response. Toxicol Sci 62:61-70 (2001) https://doi.org/10.1093/toxsci/62.1.61
- Klaassen, C. D., Liu, J. & Choudhrui, S. Metallothionein: an intracellular protein to protect against cadmium toxicity. Annu Rev Pharmacol Toxicol 39:267-294 (1999) https://doi.org/10.1146/annurev.pharmtox.39.1.267
- Jenny, M. J. et al. Diversity of metallothioneins in the American oyster, Crassostrea virginica, revealed by transcriptomic and proteomic approaches. Eur J Biochem 271:1702-1712 (2004) https://doi.org/10.1111/j.1432-1033.2004.04071.x
- Manduzio, H. et al. Seasonal variations in antioxidant defenses in blue mussels Mytilus edulis collected from a polluted area: major contributions in gills of an inducible isoform of Cu/Zn-superoxide dismutase and of glutathione S-transferase. Aquat Toxicol 70:83-93 (2004) https://doi.org/10.1016/j.aquatox.2004.07.003
- Fridovich, I. Superoxide radical and superoxide dismutases. Annu Rev Biochem 64:97-112 (1995) https://doi.org/10.1146/annurev.bi.64.070195.000525
- Ciechanover, A., Orian, A. & Schwartz, A. Ubiquitin-mediated proteolysis: biological regulation via destruction. BioEssay 22:442-451 (2000) https://doi.org/10.1002/(SICI)1521-1878(200005)22:5<442::AID-BIES6>3.0.CO;2-Q
- Glickman, M. & Ciechanover, A. The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction. Physiol Rev 82:73-428 (2002)
- Jensen, J. P. et al. Identification of a family of closely related human ubiquitin conjugating enzymes. J Biol Chem 270:30408-30414 (1995) https://doi.org/10.1074/jbc.270.51.30408
- Hicke, L. Ubiquitin-dependent internalization and down-regulation of plasma membrane proteins. Faseb J 11:1215-1226 (1997) https://doi.org/10.1096/fasebj.11.14.9409540
- Pakdel, F. et al. Overexpression of rainbow trout estrogen receptor domains in Escherichia coli: characterization and utilization in the production of antibodies for immunoblotting and immunocytochemistry. Mol Cell Endocrinol 104:81-93 (1994) https://doi.org/10.1016/0303-7207(94)90054-X
- Kime, D. A strategy for assessing the effects of xenobiotics on fish reproduction. Sci Total Environ 225:3-11 (1999) https://doi.org/10.1016/S0048-9697(98)00328-3
- Nimrod, A. C. & Benson, W. H. Environmental estrogenic effects of alkylphenol ethoxylates. Criti Rev Toxicol 26:335-364 (1996) https://doi.org/10.3109/10408449609012527
- Allen, Y. et al. The extent of oestrogenic contamination in the UK estuarine and marine environmentsfurther surveys of flounder. Sci Total Environ 233:5-20 (1999) https://doi.org/10.1016/S0048-9697(99)00175-8
- Matthiessen, P. et al. The impact of oestrogenic and androgenic contamination on marine organisms in the United Kingdom-summary of the EDMAR programme. Endocrine disruption in the marine environment. Mar Environ Res 54:645-649 (2002) https://doi.org/10.1016/S0141-1136(02)00135-6