Author:
Bantle John A.,Fort Douglas J.,James Brenda L.
Publisher
Springer Science and Business Media LLC
Reference11 articles.
1. Bantle, J. A. & D. A. Dawson, 1988. Uninduced Rat Liver Microsomes as a Metabolic Activation System for the Frog Embryo Teratogenesis Assay-Xenopus (FETAX). In: W. J. Adams, G. A. Chapman & W. G. Landis, (Eds) Proceedings of the 10th Aquatic Toxicology Symposium ASTM STP-971., pp. 316–326.
2. Bantle, J. A., D. J. Fort & D. A. Dawson, 1988. Bridging the gap from short-term teratogenesis assays to human health hazard assessment by understanding common modes of teratogenic action. In: W. J. Adams, G. A. Chapman & W. G. Landis, (Eds.) Proceedings of the 12th Aquatic Toxicology Symposium ASTM, In Press.
3. Courchesne, C. L. & J. A. Bantle, 1985. Analysis of the activity of DNA, RNA, and protein synthesis inhibitors on Xenopus embryo development. Teratogen. Carcinog. Mutagen. 5: 177–193.
4. Dawson, D. A., C. A. McCormick & J. A. Bantle, 1985. Detection of teratogenic substances in acidic mine water samples using the Frog Embryo Teratogenesis Assay-Xenopus (FETAX). J. Appl. Toxicol. 5: 234–244.
5. Dawson, D. A. & J. A. Bantle, 1987. Development of a reconstituted water medium and preliminary validation of the Frog Embryo Teratogenesis Assay-Xenopus (FETAX). J. Appl. Toxicol. 7: 237–244.
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