Joseph Landolph Lab

Publications

I. BIBLIOGRAPHY

Peer-Reviewed Publications

  1. Mackay, R.A., Landolph, J.R., and Poziomek, E.J. Experimental Evidence Concerning the Nature of the Two Change-Transfer Bends in Pyridine Iodine. J. Am. Chem. Soc., 93:5015-5030, 1971.
  2. Landolph, J.R., Bartholomew, J.C., and Calvin, M. Quantitative Studies of the Toxicity of Benzo(a)pyrene to a Mouse Liver Epithelial Cell Strain in Culture. Cancer Res., 36:4143-4151, 1976.
  3. Landolph, J.R., Becker, J.F., Gamper, H., Bartholomew, J.C., and Calvin, M. Biochemical Basis for the Acquisition of Resistance to Benzo(a)pyrene in Clones of Mouse Liver Cells in Culture. Chem. Biol. Interactions, 23:331-344, 1978.
  4. Peterson, A.R., Landolph, J.R., Peterson, H., and Heidelberger, C. Mutagenesis of Chinese Hamster Cells is Facilitated by Thymidine and Deoxycytidine. Nature, 276:508-510, 1978.
  5. Landolph, J.R., and Heidelberger, C. Chemical Carcinogens Produce Mutations to Ouabain Resistance in Transformable C3H/10T1/2 Cl 8 Mouse Fibroblasts. Proc. Natl. Acad. Sci. USA, 76:930-934, 1979.
  6. Bartholomew, J.C., Pearlman, A.L., Landolph, J.R., and Straub, K. Modulation of the Cell Cycle of Cultured Mouse Liver Cells by Benzo(a)pyrene and Derivatives. Cancer Res., 39:2538-2543, 1979.
  7. Landolph, J.R., Telfer, N., and Heidelberger, C. Further Evidence that Ouabain-Resistant Variants Induced by Chemical Carcinogens in Transformable C3H/10T1/2 Cl 8 Mouse Fibroblasts are Mutants. Mutation Res., 72:295-310, 1980.
  8. Landolph, J.R., Bhatt, R.B., Telfer, N., and Heidelberger, C. Comparison of Adriamycin- and Ouabain-Induced Cytotoxicity and Inhibition of 86Rubidium Transport in Wild-Type and Ouabain Resistant Mouse Fibroblasts. Cancer Res., 40:4581-4588, 1980.
  9. Peterson, A.R., Landolph, J.R., Peterson, H., Spears, C.P., and Heidelberger, C. Oncogenic Transformation and Mutation of C3H/10T1/2 Cl8 Mouse Embryo Fibroblasts by Alkylating Agents. Cancer Res., 41:3095-3099, 1981.
  10. Gehly, E.B., Landolph, J.R., Heidelberger, C., Nagasawa, H., and Little, J. B. Induction of Cytotoxicity, Mutation, Cytogenetic Changes, and Neoplastic Transformation by Benzo(a)pyrene Derivatives in C3H/10T1/2 Cl 8 Mouse Fibroblasts. Cancer Res., 42:1866-1875, 1982.
  11. Landolph, J.R., and Jones, P. Mutagenicity of 5-Azacytidine and Related Nucleosides in C3H/10T1/2 Clone 8 and V79 Cells. Cancer Res., 42:817-823, 1982.
  12. Landolph, J.R., and Fournier, R.E.K. Microcell-Mediated Transfer of Carcinogen-Induced Ouabain Resistance from C3H/10T1/2 Cl 8 Mouse Fibroblasts to Human Cells. Mutat. Res., 107:447-463, 1983.
  13. Link, K.H., Heidelberger, C., and Landolph, J.R. Induction of Ouabain-Resistant Mutants by Chemical Carcinogens in Rat Prostate Epithelial Cells. Environ. Mutagenesis, 5:33-48, 1983.
  14. Narayan, K.S., Pace, S., Young, R., Heidelberger, C., and Landolph, J.R. Morphological Correlates of Transformation in Cultured C3H/10T1/2 Mouse Embryo Cells. Carcinogenesis, 5:894-895, 1984.
  15. Landolph, J.R. Cytotoxicity and Negligible Genotoxicity of Borax and Borax Ores to Cultured Mammalian Cells. Am. J. Industr. Med., 7:31-43, 1985.
  16. Billings, P.C., Heidelberger, C., and Landolph, J.R. S-9 Metabolic Activation Enhances Aflatoxin-Mediated Transformation of C3H/10T1/2 Cells. Toxicol. Applied Pharmacol., 77:58-65, 1985.
  17. Soe, L.H., Shimizu, R.S., Landolph, J.R., and Roy-Burman, P. Molecular Analysis of Four Classes of Endogenous Feline Leukemia Virus Elements. J. Virol., 56:701-710, 1985.
  18. Von Hofe, E.H., Billings, P., Heidelberger, C., and Landolph, J.R. In Vitro Genotoxicity Studies Using Complex Hydrophobic Mixtures: I. Efficient Delivery of a Petroleum Sample to Cultured C3H/10T1/2 Cells Via Lipid Vesicle Incorporation. Environ. Mutagenesis, 8:589-609, 1986.
  19. Shuin, T., Billings, P.C., Lillehaug, J.R., Patierno, S.A., Roy-Burman, P., and Landolph, J.R. Enhanced Expression of c-myc and Decreased Expression of c-fos Proto-Oncogenes in Chemically and Radiation Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cell Lines. Cancer Res., 46:5302-5311, 1986.
  20. Biedermann, K., and Landolph, J.R. Induction of Anchorage Independence in Human Diploid Foreskin Fibroblasts by Carcinogenic Metal Salts. Cancer Res., 47:3815-3823, 1987.
  21. Billings, P.C., Shuin, T., Lillehaug, J.R., Miura, T., Roy-Burman, P., and Landolph, J.R. Enhanced Expression and State of the c-myc Oncogene in Chemically and X-Ray Transformed C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts. Cancer Res., 47:3643-3649, 1987.
  22. Patierno, S.R., Tuscano, J.M., Kim, K.S., Landolph, J.R., and Lee, A.S. Increased Expression of the Glucose-Regulated Gene Encoding GRP78 in Chemically Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cells. Cancer Res., 47:6220-6224, 1987.
  23. Attalah, A., Landolph, J.R., Ernster, L., and Hochstein, P. DT Diaphorase and the Cytotoxicity of Quinones in Cultured C3H/10T1/2 Mouse Embryo Cells. Biochemical Pharmacol., 37:2451-2459, 1988.
  24. Patierno, S.R., Banh, D., and Landolph, J.R. Transformation of C3H/10T1/2 Mouse Embryo Cells to Focus Formation and Anchorage Independence by Insoluble Lead Chromate but not by Soluble Calcium Chromate: Relationship to Mutagenesis and Internalization of Lead Chromate Particles. Cancer Res., 48:5280-5288, 1988.
  25. Ross, R., Paganini-Hill, A., Landolph, J.R., Gerkens, V., and Henderson, B. Analgesics, Cigarette Smoking, and Other Risk Factors for Cancer of the Renal Pelvis and Ureter. Cancer Res., 49:1045-1048, 1989.
  26. Patierno, S. R., Lehman, N., Henderson, B. E., and Landolph, J.R. Study of the Ability of Phenacetin, Acetaminophen, and Aspirin to Induce Cytotoxicity, Mutation, and Morphological Transformation in C3H/10T1/2 Clone 8 Mouse Embryo Cells. Cancer Res., 49:1038-1044, 1989.
  27. Miura, T., Patierno, S.R., Sakuramoto, T., and Landolph, J.R. Morphological and Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Cells by Insoluble Carcinogenic Nickel Compounds. Environ. Mol. Mutagenesis, 14:65-78, 1989.
  28. Shibuya, M.L., Miura, T., Lillehaug, J.R., Farley, R., and Landolph, J.R. Ouar (Na+,K+)ATPase Enzyme Activity in Chemically Induced Ouabain-Resistant C3H/10T1/2 Cells. Mol. Toxicol., 2:75-98, 1989.
  29. Biederman, K., and Landolph, J.R. Role of Valence State and Solubility of Chromium Compounds on Induction of Cytotoxicity, Mutagenesis, and Anchorage Independence in Diploid Human Fibroblasts. Cancer Res., 50:7835-7842, 1990.
  30. Zou, X.-N., and Landolph, J. R. Cytotoxic and Transforming Activities of Salted Fish Stocks on C3H/10T1/2 Cl 8 Cells. Chinese Journal of Oncology, 13(3): 188-192, l991.
  31. Huang, N., Cerepnalkoski, L., Nwankwo, J., Dews, M.L., and Landolph, J.R. Induction of Chromosomal Aberrations, Cytotoxicity, and Morphological Transformation in Mammalian Cells by the Antiparasitic Drug, Flubendazole, and by the Anti-Neoplastic Drug, Harringtonine. Fundamental Applied Toxicol., 22:304-313, 1994.
  32. Landolph, J.R. Molecular Mechanisms of Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Carcinogenic Metal Salts. Environ. Health Perspect., 102:115-119, 1994.
  33. Landolph, J.R., Verma, A., Ramnath, J., and Clemens, F. Molecular Biology of De-Regulation of Gene Expression in Transformed C3H/10T1/2 Mouse Embryo Cell Lines Induced by Specific Insoluble, Carcinogenic Nickel Compounds. Environ. Health Perspect., 110 (Suppl. 5):845-850, 2002
  34. Clemens, F., and Landolph, J.R. Genotoxicity of Samples of Nickel Refinery Dust. Toxicol. Sci., 73:114-123, 2003.
  35. Verma, A., Ramnath, J., Clemens, F., Kaspin, L. C., and Landolph, J.R. Molecular Biology of Nickel Carcinogenesis: Identification of Differentially Expressed Genes in Morphologically Transformed C3H/10T1/2 Cl 8 Mouse Embryo Fibroblast Cell Lines Induced by Specific Insoluble Nickel Compounds. Mol. Cell. Biochem., 255:203-1216, 2004.
  36. Clemens, F., Verma, R., Ramnath, J., and Landolph, J.R. Amplification of the Ect2 Proto-Oncogene and Over-Expression of Ect-2 mRNA and Protein in Nickel Compound- and Methylcholanthrene-Transformed 10T1/2 Mouse Fibroblast Cell Lines. Toxicol. Applied Pharmacol., 206:138-149, 2005.
  37. DeSilva, A., Verma, R., and Landolph, J. R. Silencing of the Beta Centaurin 2 and the FAD Synthetase Genes in Nickel-Transformed C3H/10T1/2 Cell Lines. Metal Ions in Biology and Medicine, 10: 63-67, 2008. Eds. Ph. Collery, I. Maymard, T. Teophanides, L. Khassanova, and T. Collery. John Libbey Eurotext, Paris, France.
  38. Muggia, F.M., Peters, G. J., and Landolph, J. R., Jr. XIII International Charles Heidelberger Symposium and 50 Years of Fluoropyrimidines in Cancer Therapy Held on September 6 to 8, 2007 at New York University Cancer Institute, Smilow Conference Center. Mol. Cancer Ther., 8(5): 992-999, 2009.
  39. Kacew, S., Alexander, B. H., Bleecker, M. L., Carlson, G. P., Cowan, L. D., Davis, M. E., Frey, R. C., Landolph, J. R., Meek, M. E., McMillan, D. C., Newland, M. C. Quint, J., Rosner, G. L., Rusyn, I., Schule-Hermann, R., Schultz, I . R. Snyder, R., White, R. F., Zhang, L., and Zhu, Y. Review of the Environmental Protection Agency’s Draft IRIS Assessment of Tetrachloroethylene. Committee to Review EPA’s Toxicological Assessment of Tetrachloroethylene, pp. 1-170, 2010. Board of Environmental Studies and Toxicology, Division on Earth and Life Studies. National Research Council of The National Academies of Science, U. S. A. National Academies Press, Washington, D. C.
  40. Tseng, C.-H., Chen, C.-J., and Landolph, J. R. Diabetes and Cancer: Epidemiological, Clinical, and Experimental Perspectives. Experimental Diabetes Research, Vol. 2012, Article ID 101802, 2 pages, 2012. Doi: 10.1155/2012/101802.

Peer-Reviewed Articles in Preparation

  1. Ramnath, J., and Landolph, J.R. Over-Expression of the Calnexin Gene of the mRNA and Protein Levels in Transformed C3H/10T1/2 Cl 8 Mouse Fibroblast Cell Lines Induced by Insoluble, Carcinogenic Nickel Compounds. Planned for Submission to Toxicology and Applied Pharmacology. Manuscript in Preparation.
  2. Verma, A., Ohshima, S., Ramnath, J., and Landolph, J.R. Relative Genotoxicities of Insoluble and Soluble Nickel Compounds in Assays for Induction of Chromosomal Aberrations and Morphological Cell Transformation: Correlations with Carcinogenicity, Predictions of Carcinogenic Potentials, and Implications for Molecular Mechanisms of Nickel Carcinogenesis. Manuscript in Preparation.
  3. Weng, J., Nwankwo, J.O. Pichika, R., Miller, C., and Landolph, J.R. Immortalization and Morphological and Anchorage-Independent Transformation of Normal Human Diploid Human Fibroblasts by SV40 Large T Antigen. Manuscript in Preparation.
  4. Landolph, J.R., and Troesch, C.T. Neoplastic Transformation and Promotion of Methylcholanthrene Initiated Transformation by Sodium Arsenite in C3H/10T1/2 Cells.
  5. Landolph, J.R., and Sanchez, H. C. Aspirin Inhibits Late Stages in Methylcholanthrene Transformation of C3H/10T1/2 Cells. Manuscript in Preparation.
  6. Zho, X.N., Troesch, C.T., Yu, M.C., Henderson, B.H., and Landolph, J.R. Isolation of Fractions of Cantonese Salted Fish that are Mutagenic in CHO Cells and Induce Morphological Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Cells. Manuscript in Preparation.
  7. Dews, M., Ozbun, L., and Landolph, J.R. Increased Steady-State Levels of C-myc Gene Expression on Lead Chromate Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cells. Manuscript in Preparation.
  8. Lillehaug, J.R., Troesch, C.T., Miura, T., and Landolph, J.R. Oncogene Expression in 10T1/2 Mouse Embryo Cell Lines Transformed by Sodium Arsenite. Manuscript in Preparation.
  9. Patierno, S. R., Sakuramoto, T., and Landolph, J.R. Expression and Localization of c-fos Protein in Chemically Transformed and Non-Transformed C3H/10T1/2 Cells. Manuscript in Preparation.
  10. Budroe, J., Cerepnalkoski, L., Meskin, M., Baker, S. M., and Landolph, J.R. Induction of Cytotoxicity and Neoplastic Transformation in the C3H/10T1/2 C1 8 Mouse Embryo Cell Line By Dibenzo(cg)carbazole and its Metabolites. Manuscript in Preparation.

Chapters in Books and Review Articles

  1. Heidelberger, C., Landolph, J. R., Fournier R.E.K., Fernandez, A., and Peterson, A.R. Genetic and Probability Aspects of Cell Transformation by Chemical Carcinogens. In: Progress in Nucleic Acid Research and Molecular Biology, Vol. 29, pp 87-98, 1983.
  2. Landolph, J. R. Chemical Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts: Historical Background, Assessment of the Transformation Assay, and Evolution and Optimization of the Transformation Assay Protocol. In: IARC Scientific Publication No. 67, “Transformation Assay of Established Cell Lines: Mechanisms and Application,” pp. 185-198 International Agency for Research on Cancer, Eds. T. Kakanaga and H. Yamasaki, 1985.
  3. Landolph, J. R. Mechanisms of Chemically, Induced Multi-Step In Vitro Neoplastic Transformation. In: Carcinogenesis, Vol. 10, “Role of Chemicals and Radiation in the Etiology of Neoplasia.” Raven Press, New York, 1985, pp. 211-223, Eds. H. Huberman and S. H. Barr.
  4. Landolph, J. R. Comparisons and Contrasts Between Chemical Transformation in Murine C3H/10T1/2 and Human Fibroblasts In Vitro. In: International Workshop on Carcinogenesis and Mutagenesis, pp. 66-76, Guangzhou Science and Technology Association, Guangzhou, China, January 6-17, 1986.
  5. Attalah, A., Landolph, J. R., and Hochstein, P. DT Diaphorase and Quinone Detoxification. In: Chemica Scripta, 27A, 141-144, 1987 on “DT Diaphorase: A Quinone Reductase with Special Functions in Cell Metabolism and Detoxification.” Eds. L. Ernster, R.W. Estabrook, P. Hochstein, and S. Orrenius.
  6. Landolph, J. R. Molecular and Cellular Mechanisms of Transformation of C3H/10T1/2 Cl 8 and Diploid Human Fibroblasts by Unique Carcinogenic, Non-Mutagenic Metal Compounds: A Review. Biol. Trace Element Research, Vol. 21, 459-467, 1989.
  7. Patierno, S.R., and Landolph, J. R. Soluble Versus Insoluble Hexavalent Chromate: Relationship of Mutation to In Vitro Transformation and Particle Uptake. Biol. Trace Element Research, Vol. 21, 469-474, 1989.
  8. Landolph, J. R. Neoplastic Transformation of Mammalian Cells by Carcinogenic Metal Compounds: Cellular and Molecular Mechanisms. In: Biological Effects of Heavy Metals. Metal Carcinogenesis, CRC Press, Vol. II, pp. 1-18, 1990, Ed. E.C. Foulkes.
  9. Landolph, J. R. Arachidonic Acid Metabolism, Oxygen Radicals, and Chemical Carcinogenesis. In: Biological Oxidants and Anti-Oxidants. Hippokrates and Verlag, Stuttgart, Germany, pp 133-143, 1994, Eds. L. Packer and E. Cadenas.
  10. Landolph, J. R., Dews, M., Ozbun, L., and Evans, D. Chapter 19. Metal-Induced Gene Expression and Neoplastic Transformation. In: Toxicology of Metals, Part I. General and Clinical Aspects, Risk Assessment, and Genotoxicity of Metals. CRC Press, Lewis Publishers Inc., Boca Raton, Florida, pp. 321-329, 1996, Ed. L.W. Chang.
  11. Landolph, J. R. Genotoxicity and Carcinogenicity of Ozone. In: Toxicological Effects of Ozone and Related Photochemical Oxidants, Chapter 6. Vol. III. Air Quality Criteria for Ozone and Related Photochemical Oxidants, U.S. Environmental Protection Agency, pp. 6-103-6-121, 1996.
  12. Landolph, J. R. Mutagenesis. In: Encyclopedia of Toxicology. Academic Press, pp. 95-101, 1997. Ed. P. Wexler.
  13. Landolph, J. R. Role of Free Radicals in Metal-Induced Carcinogenesis, Chapter 14. In: Metal Ions in Biological Systems, Vol. 36, Interrelations Between Free Radicals and Metal Ions in Life Processes. Eds. A. Sigel and H. Sigel. pp 445-483, 1999.
  14. Combes, R., Bells, M., Le Boeuf, R., Curren, R., Fishbach, M., Fusenig, N., Kirkland, D., Losne, C., Landolph, J. R., Marquardt, H., McCormick, J., Rivedal, E., Sabbioni, E., Tanaka, N., Muller, L., Vasseur, P., and Yamasaki, H. Cell Transformation Assays as Predictors of Human Carcinogenicity. The Report and Recommendations of ECVAM Workshop #39. The European Centre for the Validation of Alternative Methods, ATLA 27:745-767, 1999.
  15. Landolph, J. R. The Role of Free Radicals in Chemical Carcinogenesis, Chapter 17. In: Toxicology of the Human Environment: The Critical Role of Free Radicals. Ed. C.J. Rhodes. Taylor and Francis Series in Pharmaceutical Sciences, pp. 339-362, 2000.
  16. Bostwick, D. G., Burke, H. B., Djakiew, D., Euling, S., Ho, S.-M., Landolph, J. R., Morrison, H., Sonawane, B. Shiflett, T., Waters, D. J., and Timms, B. Human Prostate Cancer Risk Factors. Cancer, 101 (Suppl 10):2371-2490, 2004.
  17. Landolph, J. R. Genetic Toxicology. Encyclopedia of Toxicology, 2nd Edition, Volume 2, pp. 421-431, 2005. Elsevier Press, Oxford, United Kingdom. Editor, Philip Wexler.
  18. Landolph, J. R., Xue, W., and Warshawsky, D. Whole Animal Carcinogenicity Biosassays. Chapter 2, pp. 25-44. In: Molecular Carcinogenesis and the Molecular Biology of Human Cancer. Eds. David Warshawsky and Joseph R. Landolph. CRC Press, Taylor and Francis Group, Boca Raton, Florida, U.S.A., 2006.
  19. Warshawsky, D., and Landolph, J. R. Overview of Human Cancer Induction and Human Exposure to Carcinogens. Chapter 13, pp. 280-302. In: Molecular Carcinogenesis and the Molecular Biology of Human Cancer. Eds. David Warshawsky and Joseph R. Landolph, Jr. CRC Press, Taylor and Francis Group, Boca Raton, Florida, U.S.A., 2006.
  20. Landolph, J. R. Chemically Induced Morphological and Neoplastic Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Cells. Chapter 9, pp. 195-219. In: Molecular Carcinogenesis and the Molecular Biology of Human Cancer. Eds. David Warshawsky and Joseph R. Landolph. CRC Press, Taylor and Francis Group, Boca Raton, Florida, U.S.A., 2006.
  21. Landolph, J. R. Genetic Toxicology, Molecular Carcinogenesis, and the Molecular Biology of Carcinogenesis. Field Essay, pp. 1232-1233, 2008. Encyclopedia of Cancer, 2nd Edition, Springer Science and Business Media, New York, New York. Editor, Manfred Schwab.
  22. Landolph, J. R. Chemical Carcinogenesis. Pp. 602-605, 2008. Encyclopedia of Cancer, 2nd Edition, Springer Science and Business Media, New York, New York. Editor, Manfred Schwab.
  23. Landolph, J. R. Chemically Induced Cell Transformation. Pp. 606-608, 2008. Encyclopedia of Cancer, 2nd Edition. Springer Science and Business Media, New York, New York. Editor, Manfred Schwab.
  24. Landolph, J. R. Chromium Carcinogenesis. Pp. 665-668, 2008. Encyclopedia of Cancer, 2nd Edition. Springer Science and Business Media, New York, New York. Editor, Manfred Schwab.
  25. Landolph, J. R. Nickel Carcinogenesis. Pp. 2076-2079, 2008. Encyclopedia of Cancer, 2nd Edition. Springer Science and Business Media, New York, New York. Editor, Manfred Schwab.
  26. Kacew, S., Alexander, B. H., Bleecker, M. L., Carlson, G. P., Cowan, L. D., David, M. E., Frey, H. C., Landolph, J. R., Meek, M. E., McMillan, D. C., Newland, M. C., Quint, J., Rosner, G. L., Rusyn, I., Schulte-Hermann, R., Schultz, I. R., Snyder, R., White, R. F., Zhang, L., and Zhu, Y. Review of the Environmental Protection Agency’s Draft IRIS Assessment of Tetrachloroethylene. National Research Council of the U. S. National Academies of Science, The National Academies Press, Washington, D. C. pp. 1-123, January, 2010.
  27. Landolph, J.R. Genetic Toxicology, pp. 714-725, 2014. In: Wexler, P. (Ed.), Encyclopedia of Toxicology, 3rd Edition, Vol 2. Elsevier Inc., Academic Press.
  28. Fowler, B. A., Landolph, J. R., Sullivan, K., and Hayes, A. W. Organelles as Tools in Toxicology: In Vitro and In Vivo Approaches. Chapter 39. Pp. 1885-1898, 2015. In, Hayes’ Principles and Methods of Toxicology, Sixth Edition. Eds., A. Wallace Hayes and Claire L. Kruger.
  29. Landolph, J. R., Verma, R., Ramnath, J., and Jobling, F. Chapter 13, pp. 599-628. The Cell and Molecular Biology of Nickel Compound-Induced Neoplastic Transformation and Carcinogenesis. In, Toxicology and Risk Assessment. Eds. Anna M. Fan, Elaine M. Khan, and George V. Alexeeff. 2015. Copyright 2015, Pan Stanford Publishing Pte. Ltd. ISBN 978-981-4613-38-5 (Hardcover). www.panstandord.com
  30. Landolph, J. R. Chapter 2385-3, pp. 1-6. Genetic Toxicology. In, Encyclopedia of Cancer, 3nd Edition. Springer Science and Business Media, New York, New York. Editor, Manfred Schwab. 2015. In Press (Proofs just corrected on 6/12/2015 and returned to Editor).

Books

Warshawsky, D., and Landolph, J.R. (editors). Molecular Carcinogenesis and The Molecular Biology of Human Cancer (Textbook). CRC Press, Taylor and Francis Group, Boca Raton, Florida, U.S.A., 2006.

Abstracts – All of these were presented as seminars or posters at scientific conferences by Dr. Landolph, his trainees, or his collaborators.

  1. Landolph, J. R., Bartholomew, J.C., and Calvin, M. Epithelial Cells in Culture and their Growth Response to the Carcinogen Benzo(a)pyrene. J. Cell Biol., 67, 2339, 1975. Presented at the Annual Meeting of the American Society for Cell Biology, held in Puerto Rico, 1975.
  2. Landolph, J. R., Bartholomew, J. C., and Calvin, M. Description of the Toxicity of Benzo(a)pyrene to Mouse Epithelial Cells in Culture. J. Cell Biol., 70, 3269, 1976. Presented at the Annual Meeting of the American Society for Cell Biology, 1976.
  3. Landolph, J. R., Bartholomew, J. C., and Calvin, M. Kinetics of the Toxicity of Benzo(a)pyrene to a Liver Epithelial Cell Line Derived from Namru Mice and the Production of Resistant Variants. Fourth Annual Collaboration Conference, Carcinogenesis Program, February, 1976, pp. 135.
  4. Landolph, J. R., Becker, J. F., Gamper, J., Bartholomew, J. C., and Calvin, M. Basis for Resistance to Benzo(a)pyrene in Mouse Liver Cells. J. Cell Biol., 75, 381, 1977. Presented at the Annual Meeting of the American Society for Cell Biology, 1977.
  5. Bartholomew, J. C., Pearlman, A. L., Landolph, J. R., and Straub, K. M. Cell Cycle Perturbations Caused by Chemical Carcinogens. ICN-UCLA Symposium, February 19, 1977. Presented at this symposium.
  6. Peterson, A. R., Peterson, H., Landolph, J. R., and Heidelberger, C. Facilitation by Pyrimidine Nucleosides and Hypoxanthine of MNNG Mutagenesis in Chinese Hamster Cells. In: Differentiation and Development, Vol. 15, Eleventh Miami Winter Symposium, pg. 114. Eds. F. Ahmad, T.R. Russell, J. Schultz, and R. Werner, 1978. Academic Press.
  7. Landolph, J. R., and Fuchs, R. P. P. Induction of Mutations and Transformation of C3H/10T1/2 Mouse Fibroblasts by Chemical Carcinogens. Proc. Am. Assoc. Cancer Res., 61, (244), 1979. Presented at the Annual Meeting of the American Association for Cancer Research, 1979.
  8. Landolph, J. R. Induction of Ouabain-Resistant Mutants in C3H/10T1/2 Cl 8 Mouse Fibroblasts by Benzo(a)pyrene (BaP) and its Metabolites and Characterization of the Mutants. Proc. Am. Assoc. Cancer Res., 21, 108, 1980. Presented at the Annual Meeting of the American Association for Cancer Research, 1980.
  9. Landolph, J. R. Presentation at National Tissue Culture Association Meeting, June 21, 1980. Correlations Between Chemically Induced Neoplastic Transformation and Chemically Induced Mutagenesis in C3H/10T1/2 Cl8 Mouse Fibroblasts. In: Round Table Discussion Section: “Chemical and Viral Carcinogenesis: Is There A Common Ground?” Presentations not published.
  10. Landolph, J. R. Mutagenicity of 5-Azacytidine and its Analogs in V79 and C3H/10T1/2 Cells. Proc. Am. Assoc. Cancer Res., 22:123, 1981. Presented at the Annual Meeting of the American Association for Cancer Research, 1981.
  11. Landolph, J. R., Heidelberger, C., and Fournier, R. E. K. Microcell-Mediated Chromosome Transfer of Chemical Carcinogen-Induced Ouabain Resistance from Ouabain-Resistant C3H/10T1/2 Cl 8 Cells to Human D98 Cells. J. Cell Biol., 91:384a, Abstract 22020, 1981. Presented at the Annual Meeting of the American Society for Cell Biology, 1981.
  12. Billings, P. C., Uwaifo, A. O., Landolph, J. R., and Heidelberger, C. Faza and FAO-1 Rat Hepatoma Cells Show Extreme Sensitivity to Aflatoxin B1. Proc. Am. Assoc. Cancer Res., 23:79, 1982. Presented at the Annual Meeting of the American Association for Cancer Research, 1982.
  13. Landolph, J. R. Chemical Mutagenesis and Transformation in C3H/10T1/2 Cells. Delivered at Symposium on Therapy-Related Leukemia, Joint Meetings of the American Society for Pharmacology and Experimental Therapeutics and the Society of Toxicology, August 18, 1982, Louisville, Kentucky.
  14. Landolph, J. R., Lee, F. H., and Narayan, K. S. Immunologic and Scanning Electron Microscopy Studies of Chemically and Radiation Transformed C3H/10T1/2 Cells. Environmental Protection Agency Meeting, Chicago, Illinois, presented April 9, 1983.
  15. Landolph, J. R. Transformation of C3H/10T1/2 Mouse Fibroblasts by Carcinogenic Metal Salts in the Absence of Base Substitution Mutations. Proc. Am. Assoc. Cancer Res., 24:100, 1983. Presented at the Annual Meeting of the American Association for Cancer Research, 1983.
  16. Landolph, J. R. Chemical Transformation in C3H/10T1/2 Cells: Review and Critical Assessment of the Transformation Assay. Presented at the International Agency for Cancer Research (IARC), Workshop on Chemical Transformation of Mammalian Cells, Lyon, France, February 18, 1984.
  17. Landolph, J. R. Aspirin Inhibits Late Stages in Methylcholanthrene Transformation of C3H/10T1/2 cells. Proc. Am. Assoc. Cancer Res., 25:126, 1984. Presented at the Annual Meeting of the American Association for Cancer Research, 1984.
  18. Landolph, J. R. Chemical Mutagenesis and Chemical Transformation in C3H/10T1/2 Cells. Presented at the Annual Meeting of the American Society for Microbiology, Southern California Branch, November 2, 1984. Not published.
  19. Landolph, J. R. Chemical Induced Oncogenic Cell Transformation. Presented at the Workshop on Radiation Carcinogenesis, University of California, Irvine, November 10. Not published.
  20. Biedermann, K., and Landolph, J. R. Development of a Soft Agar Assay to Measure Transformation of Human Fibroblasts by Metal Salts. Fed. Proc., 44:927, 1985. Presented at the Annual Meeting of the Federation of the American Societies of Experimental Biology in Anaheim, California.
  21. Landolph, J. R., Shuin, T., and Billings, P. C. Expression of Proto-Oncogenes in Non-Transformed and in Chemically and Radiation Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cell Lines. Proc. Am. Assoc. Cancer Res., 26:65, 1985. Presented at the Annual Meeting of the American Association for Cancer Research, 1985.
  22. Landolph, J. R., Billings, P. C., and Shuin, T. Expression of Proto-Oncogenes in Non-Transformed and in Chemically and Radiation Transformed C3H/10T1/2 Cell Lines. 33rd Meeting of the European Tissue Culture Society, 33, 1985. Presented at this meeting in Bergen, Norway, 1985.
  23. Roy-Burman, P., Soe, L. H., Shimizu, R., and Landolph, J.R. Molecular Analysis of Four Classes of Endogenous Feline Leukemia Virus Elements. American Society for Virology, July 21, 1985. Presented at this meeting.
  24. Landolph, J. R. Comparisons and Contrasts Between Chemical Transformation in Murine C3H/10T1/2 and Human Fibroblasts In Vitro. International Workshop on Carcinogenesis and Mutagenesis. January 6-17, 1986. Guangzhou, China. pp 66-76, 1986. Presented at this International Meeting in Guangzhou, China, 1986, by Dr. Joseph R. Landolph, Jr.
  25. Landolph, J. R., and Sanchez, H. C. Inhibition of Chemical Transformation by Aspirin. II. Proc. Am. Assoc. for Cancer Res., 27:137 (541), 1986. Presented at the Annual Meeting of the American Association for Cancer Research, 1986, as a poster.
  26. Biedermann, K., and Landolph, J. R. Induction of Anchorage Independence in Human Diploid Foreskin Fibroblasts by Metal Salts. Proc. Am. Assoc. for Cancer Res., 27:137 (542), 1986. Presented at the Annual Meeting of the American Association for Cancer Research, 1986.
  27. Landolph, J. R. Molecular Biology of Chemical Transformation by Arsenic Carcinogens in C3H10T1/2 Cells and in Human Fibroblasts. Dr. Landolph was an Invited Symposium speaker, April 15, at the Symposium on Molecular Mechanisms of Cell Transformation and Carcinogenesis by Environmental Carcinogens, Federation Meetings, American Society of Pharmacology and Experimental Therapeutics, St. Louis, Missouri, 1986.
  28. Attalah, A., Landolph, J. R., and Hochstein, P. DT Diaphorase and Quinone Detoxification. In: Symposium on DT Diaphorase in Cell Metabolism and Detoxification. Presented at meeting in Stockholm, Sweden, June 1986. Chemica Scripta, 27A, 141-144, 1987.
  29. Landolph, J. R. Proto-Oncogene Expression in Non-Transformed and in Chemically Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cells. Presented at the Environmental Protection Agency, Symposium on Genetic Toxicology, Rockville, Maryland, July 17, 1986. Symposium organizers did not publish the proceedings of the symposium.
  30. Attalah, A. S., Landolph, J. R., and Hochstein, P. DT Diaphorase and Quinone Detoxification. The Toxicologist, 7, 63, 1987. Presented at the Annual Meeting of the Society of Toxicology, Washington, D.C., 1987.
  31. Landolph, J. R., and Troesch, C. Morphological Transformation and Promotion of Transformation in C3H/10T1/2 C18 Mouse Embryo Cells by Sodium Arsenite. The Toxicologist, 7, 395, 1984. Presented at the Annual Meeting of the Society of Toxicology, Washington, D.C., by Dr. Joseph R. Landolph, Jr.
  32. Miura, T., and Landolph, J. R. Induction of Morphological Transformation in C3H/10T1/2 C1 8 Mouse Embryo Fibroblasts by Carcinogenic Nickel Compounds. Environ. Mutagenesis, 9:(Suppl. 8), 84, 1987. Presented at the Annual Meeting of the Environmental Mutagen Society, 1987.
  33. Patierno, S. R., and Landolph, J. R. Genotoxicity of Aspirin, Phenacetin, and Acetaminophen in C3H/10T1/2 Mouse Embryo Cells. Environ. Mutagenesis, 9:(Suppl. 8), 84, 1987. Presented at the Annual Meeting of the Environmental Mutagen Society, 1987.
  34. Biedermann, K., and Landolph, J. R. Induction of Mutation and Anchorage Independence in Human Fibroblasts by Chromium (VI) and Chromium (III) Compounds. The Toxicologist, 8:193 (#769), 1988. Presented at the Annual Meeting of the Environmental Mutagen Society, 1988.
  35. Biedermann, K., and Landolph, J. R. Modulation of Induction of Anchorage Independence in Human Diploid Fibroblasts: Induction by Tumor Promoters and Inhibition by Aspirin. Proc. Am. Assoc. Cancer Res., 29, 116 (463), 1988. Presented at the Annual Meeting of the American Association for Cancer Research, 1988.
  36. Patierno, S. R., and Landolph, J. R. Transformation of C3H/10T1/2 Cells by Insoluble PbCrO4 but not Soluble CaCrO4: Relationship to Mutation and Particle Disposition. Proc. Am. Assoc. Cancer Res., 29, 117 (464), 1988. Presented at the Annual Meeting of the American Association for Cancer Research, 1988.
  37. Landolph, J. R. Nickel, Chromium, and Arsenic Induced Morphological Transformation in 10T1/2 Mouse Embryo Fibroblasts and Anchorage Independence in Diploid Human Fibroblasts. First International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, p. 57, 1988. Presented at this meeting as an invited talk by Dr. Joseph R. Landolph, Jr.
  38. Patierno, S. R., and Landolph, J. R. Soluble Versus Insoluble Hexavalent Chromate: Relationship of Mutation to In Vitro Transformation and Particle Uptake. First International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, p. 39, 1988. Presented as a symposium talk at this meeting by Dr. Steven R. Patierno.
  39. Patierno, S. R., Sakuramoto, T., and Landolph, J. R. C-Fos Expression in Non-Transformed and Chemically Transformed 10T1/2 Mouse Embryo Cells. J. Cell Biol., 107, 489a (Abst. #2750), 1988. Presented at the Annual Meeting of the American Association for Cell Biology, 1988.
  40. Landolph, J. R., and Lillehaug, J. R. Oncogene Expression in Sodium Arsenite Transformed C3H/10T1/2 Mouse Embryo Cell Lines. Southern California Division of the Society of Toxicologists, Arco Towers, Los Angeles, California, January 21, 1989. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr. Proceedings of this meeting not published.
  41. Patierno, S. R., Landolph, J. R., and Lee, A. S. Over-Expression of the Glucose-Regulated Gene GRP78 in Chemical, Radiation, and Ras-Transformed C3H/10T1/2 Cells. Proc. AACR, 30, 187 (743), 1989. Presented at the Annual Meeting of the American Association for Cancer Research, 1989.
  42. Lillehaug, J. R., and Landolph, J. R. State and Expression of Proto-Oncogenes in Sodium Arsenite Transformed 10T1/2 Mouse Embryo Fibroblasts. Proc. AACR, 30, 426 (1691), 1989. Presented at Annual Meeting of American Association for Cancer Research, 1989.
  43. Landolph, J. R. Chemical Transformation in C3H/10T1/2 and Diploid Human Fibroblasts. 198th American Chemical Society Meeting, Miami Beach, Florida, September 11, 1989. Presented at this meeting as an invited Symposium talk by Dr. Joseph R. Landolph, Jr. Abstracts not published.
  44. Landolph, J. R. Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Carcinogenic Metal Salts. 3rd Charles Heidelberger Symposium: Carcinogenesis and Chemotherapy: Cancer’s Continuing Core Challenges. pg. 69, 1989, in Program Booklet from this meeting. Presented at this meeting as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  45. Shibuya, M. L., Miura, T., Lillehaug, J. R., Farley, R. A., and Landolph, J. R. Ouabain-Resistant (Na+,K+) ATPase Activity in Chemically Induced Ouabain-Resistant C3H/10T1/2 Cells. Society of Toxicology, Southern California Chapter, Annual Meeting, UCLA, January 26, 1990. Presented at this meeting. Abstracts not published.
  46. Landolph, J. R. Chemical Transformation and Chemical Mutagenesis. Program and Abstracts Booklet, 1990 Annual Meeting of the Institute of Food Technologists, Abstract #130, pg. 128, 1990. Presented at this meeting as an invited symposium talk by Dr. Joseph R. Landolph, Jr.
  47. Landolph, J. R., Cerepnalkoski, L., Sakuramoto, T., and Biederman, K. A. Transformation of 10T1/2 Mouse Embryo Cells by Radical-Generating Carcinogens. 5th Biennial Meeting of the International Society for Free Radical Research. Free Radical Biol. Med., 9:163 (17,12), 1990. Presented at this meeting as a poster presentation.
  48. Shibuya, M. L., Miura, T., Lillehaug, J. R., Farley, R. A., and Landolph, J. R. Ouabain-Resistant (Na+,K+) ATPase Enzyme Activity in Chemically Induced Ouabain-Resistant C3H/10T1/2 Cells. The Toxicologist, 11:252 (955), 1991. Presented at the Annual Meeting of the Society of Toxicology, 1991, as a poster.
  49. Sakuramoto, T., Evans, D., Miura, T., Meskin, M., Nwankwo, J., and Landolph, J. R. Oncogene Expression in Nickel-Transformed C3H/10T1/2 Cell Lines. Proc. Am. Assoc. Cancer Res., 32:113 (678), 1991. Presented at the Annual Meeting of the American Association for Cancer Research, 1991.
  50. Landolph, J. R. Molecular and Cellular Mechanisms of Action of Carcinogenic Metal and Polycyclic Aromatic Hydrocarbon Induced Transformation of Mammalian Cells. American Chemical Society, Division of Chemical Health and Safety. Page 2, Abstract #7, 1991. Presented at this meeting as an invited symposium talk by Dr. Joseph R. Landolph, Jr.
  51. Landolph, J. R., Biedermann, K. A., Cerepnalkoski, L., Nwankwo, J. O., and Dews, M. Molecular Mechanisms of Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Metal Salts and Organic Carcinogens. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at the Fourth Charles Heidelberger Conference on Transformation and Chemotherapy, Los Angeles, California, December 7-10, 1991, Marina Del Rey, California. Published on page 11 of abstract booklet.
  52. Cerepnalkoski, L. A., and Landolph, J. R. Inhibition of Methylcholanthrene (MCA)-Induced Neoplastic Transformation in C3H/10T1/2 Cl 8 Cells and Suppression of Transformed Phenotypes of MCA Cl 5 and MCA Cl 16 Cell Lines by Inhibitors of Cyclo-oxygenase, Lipoxygenase, and Phospholipase A2. Presented at the 2nd International Conference on Eicosanoids, and Other Bioactive Lipids in Cancer, Inflammation, and Radiation Injury, and published on pg. 254, of abstract booklet for meeting, 1991, Berlin, West Germany.
  53. Landolph, J. R. Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation of Cultured Murine and Human Fibroblasts. Division of Chemical Health and Safety, American Chemical Society, Extended Abstracts Booklet, Volume II, Number 1, pg. 6, 1992.
  54. Yasin, B., Zou, X.-N., DeGiacomo, M., Yu, M. C., Henderson, B. E., and Landolph, J.R. Induction of Cytotoxicity and Morphological Transformation in C3H/10T1/2 Clone 8 Mouse Embryo Fibroblasts by Chinese Salted Fish. Proc. Am. Assoc. Cancer Res., 33:132 (791), 1992. Presented as a poster at the 83rd Annual Meeting of the Am. Assoc. for Cancer Res., San Diego, California, May 20, 1992.
  55. Landolph, J. R., Dews, M., Evans, D., and Biedermann, K. A. Molecular Mechanisms of Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Carcinogenic Arsenic, Nickel, and Chromium Compounds. Second International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, Abstracts Booklet, pg. 35, 1993. Presented at this meeting in Madonna di Campiglio, Italy, January 14, 1993, as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  56. Landolph, J. R., Cerepnalkoski, L., Biedermann, K., and Weng, J. Involvement of Arachidonic Acid Metabolism in Chemically Induced Neoplastic Transformation. Joint Meeting on Biological Oxidants and Anti-Oxidants: New Developments in Research and Health Effects. Sponsored by the Society for Free Radical Research and the Bay Area Oxygen Club. Abstracts Booklet, pg. 45, March 12-13, 1993. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  57. Dews, M., Ozbun, L., and Landolph, J. R. Enhanced Stability of c-myc RNA Contributes to Increased Steady-State Levels of c-myc RNA in Transformed C3H/10T1/2 Mouse Embryo Cell Lines Induced by Lead Chromate. Mol. Biol. Cell, 5:146a (849), 1994. Presented at the Thirty-Fourth Annual Meeting of the American Society for Cell Biology, December 10-14, 1994.
  58. Landolph, J. R., Budroe, J., Meskin, M., Cerepnalkoski, L., Stong, D., Xue, W., and Warshawsky, D. W. Induction of Cytotoxicity and Morphological Transformation in 10T1/2 Mouse Embryo Fibroblasts by Dibenzo(c,g) carbazole and its Metabolites. Proc. Am. Assoc. Cancer Res., 34:117 (696), 1993. Dr. Joseph R. Landolph, Jr., gave a poster presentation on this Abstract May 19, 1993 at AACR meeting in Orlando, Florida.
  59. Landolph, J. R., Evans, D.P., Tasci, A., and Weng, J. Tobacco Carcinogen-Induced Transformation of Mammalian Cells. First Annual Meeting of the Tobacco-Related Disease Research Program of the State of California, 1993, in Oakland, California. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  60. Dews, M., Ozbun, L., Hayashida, K., and Landolph, J.R. Increased Steady-State Levels of c-myc RNA in Transformed 10T1/2 Mouse Embryo Cell Lines Induced by Lead Chromate. Proc. Am. Assoc. Cancer Res., 35:150 (899), 1994. Dr. Joseph R. Landolph gave a poster presentation on this abstract April 13, 1994 at the AACR meeting in San Francisco, California.
  61. Weng, J., Nwankwo, J. O., Pichika, R., Boone, S., Miller, C. H., and Landolph, J. R. Immortalization and Morphological and Anchorage-Independent Transformation of Diploid Human Fibroblasts by Transfection with SV40 Large T Antigen Encoding Gene and Treatment with MNNG. Proc. Am. Assoc. for Cancer Res., 36:183 (1088), 1995. Presented as a poster at this meeting by Dr. Joseph R. Landolph, Jr.
  62. Weng, J., Nwankwo, J. O., Pichika, R., Miller, C., and Landolph, J. R. Induction of Cellular Immortality, Morphological Transformation and Anchorage-Independence in Diploid Human Fibroblasts Transfected with SV40 Large T Antigen Gene. FASEB J. 9, No. 6, A1280 (141), 1995. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the Annual Meeting of the American Association for Biochemistry and Molecular Biology, San Francisco, California, May 21-25, 1995.
  63. Ozbun, L., Dews, M., Krishnan, K., and Landolph, J. R. c-Myc Activation in Lead Chromate and 3-Methylcholanthrene Transformed 10T1/2 Mouse Embryo Cell Lines. Int. Toxicologist 7:86-P-3, No. 1, 1995. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the VII International Congress of Toxicology, Seattle, Washington, July 6, 1995.
  64. Landolph, J. R., Dews, M., and Ozbun, L. c-Myc Oncogene Activation in Cells Transformed by Lead Chromate. Pg. 14, Abstract 53, 1995. Presented at the Vth COMTOX Symposium on Toxicology and Clinical Chemistry of Metals by Dr. Joseph R. Landolph, Jr., who was invited to give a plenary lecture at this meeting, July 10, 1995, at the University of British Columbia, Vancouver, Canada.
  65. Landolph, J. R., Dews, M. E., and Ozbun L. L. Alterations in a c-Myc Gene, Enhanced Stability of c-Myc mRNA, and Increased c-Myc Protein Levels in Transformed 10T1/2 Cell Lines Induced by Lead Chromate or 3-Methylcholanthrene. Given as a poster presentation by Dr. Joseph R. Landolph, Jr., on November 18, 1995 at: Oxygen ‘95. The Annual Meeting of the Oxygen Society Program and Abstract Booklet, pg. 68, Abstract #2-12, section on Transcriptional Regulation. Meeting held at the Ritz-Carlton Huntington Hotel, Pasadena, California.
  66. Ozbun, L. L., Dews, M. E., and Landolph, J. R. Enhanced Stability/Increased Levels of c-Myc mRNA and Increased c-Myc Protein Levels in Lead Chromate and 3-Methylcholanthrene Transformed 10T1/2 Cell Lines. Fundamental Applied Toxicol., The Toxicologist, 30: No. 1, Part 2, 28 (144), 1996. Presented as a poster at the 35th Annual Meeting of the Society of Toxicology, Anaheim, California, March 11, 1996, by Laurent Ozbun.
  67. Ozbun, L. L., Dews, M. E., and Landolph, J. R. Increased Levels of c-Myc mRNA in Lead Chromate and 3-Methylcholanthrene Transformed 10T1/2 Cell Lines Due to Enhanced Stability of c-Myc RNA. Proc. Am. Assoc. for Cancer Res., 37:145 (1004), 1996. Presented as a poster at the AACR Meeting in Washington, D.C., by Dr. Joseph R. Landolph, Jr.
  68. Landolph, J. R., and Verma, A. Cellular and Molecular Mechanisms of Induction of Morphological/Neoplastic Transformation in 10T1/2 Mouse Embryo Cells and Anchorage Independence in Human Diploid Fibroblasts by Carcinogenic Nickel Compounds. Abstract Booklet of Presentations of the 1996 Nickel Research Workshop, p 4. June 3-6, Rockville, Maryland. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  69. Ozbun, L. L., Dews, M. E., and Landolph, J. R. Biological Significance of Increased Levels of c-Myc mRNA in Lead Chromate and 3-Methylcholanthrene Transformed 10T1/2 Cell lines. Fundamental Applied Toxicol., 36:No. 1, 88 (452), 1997. Presented as a Poster by Dr. Joseph R. Landolph, Jr., in the Session, “Carcinogenesis: Mechanisms and Biotransformation.” Monday 3/10/97, at the 36th Annual Meeting of the Society of Toxicology, Cincinnati, Ohio.
  70. Verma, A., and Landolph, J. R. Molecular Analyses of Transformed C3H/10T1/2 Cl 8 Mouse Embryo Fibroblast Cell lines Induced by Insoluble Nickel Carcinogens. Fundamental Applied Toxicol., 36: No. 1, 88 (453), 1997. Presented in the Session entitled, “Carcinogenesis: Mechanisms and Biotransformation,” Monday 3/10/97 as a poster at the 36th Annual Meeting of the Society of Toxicology, Cincinnati, Ohio, by Dr. Joseph R. Landolph, Jr.
  71. Landolph, J. R., Ozbun, L., and Verma, A. Molecular Biology of Chromium and Nickel-Induced Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. Fundamental Applied Toxicol., 36:No. 1, 202 (1028), 1997. Presented by Dr. Joseph R. Landolph, Jr., as a symposium talk in the Symposium, “Molecular Biology of Metal Carcinogenesis,” Tuesday 3/11/97 at the 36th Annual Meeting of Society of Toxicology, Cincinnati, Ohio.
  72. Landolph, J. R., and Costa, M. The Molecular Biology of Metal Carcinogenesis. Fundamental Applied Toxicol., 36:No. 1, 202 (1025), 1997. Co-Organized and Co-chaired the Symposium on “The Molecular Biology of Metal Carcinogenesis,” 3/11/97 at the 36th Annual Meeting of the Society of Toxicology, Cincinnati, Ohio.
  73. Ozbun, L. L., Dews, M., and Landolph, J. R. Lead Chromate Transformed 10T1/2 Cells Have c-myc RNA with Enhanced Stability but No Point Mutations in Ha-Ras Codons 12, 13, or 61 or Ki-ras Codons 12, 13. Proc. Am. Assoc. Cancer Res., 38:586 (3936), 1997. Presented as a poster on April 17, 1997, at the AACR Meeting in San Diego, California, by Dr. Joseph R. Landolph, Jr.
  74. Landolph, J. R., Verma, A., and Ozbun, L. Molecular and Cellular Mechanisms and Molecular Biology of Chromium and Nickel-Induced Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts. International Association of Environmental Analytical Chemistry, Book of Abstracts, page 58, 1997. Presented as an invited symposium talk by Dr. Joseph R. Landolph, Jr., at the Seventh International Hans Wolfgang Nurnberg Memorial Symposium on Metal Compounds in the Environment and Life, June 4-7, 1997, at the University of Modena, Modena, Italy.
  75. Landolph, J. R., Verma, A., Ozbun, L., and Ramnath, J. Molecular Biology of Chromium and Nickel-Induced Cell Transformation. Abstract Booklet, 7th Charles Heidelberger Meeting on Cancer – Genesis, Detection, and Therapy, 19-21, 1997. Presented as an invited symposium talk by Dr. Joseph R. Landolph, Jr., on July 2-5, 1997, at the 7th Charles Heidelberger Meeting, Reisensburg Castle, Gunzburg, Germany.
  76. Landolph, J. R., Miller, C., Weng, J., Ramnath, J., and Constantinescu, L. Induction of Morphological and Neoplastic Transformation and Promotion of Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells by Sodium Arsenite and Induction of Anchorage Independence in Human Diploid Fibroblasts by Sodium Arsenite and Sodium Arsenate. In the Meeting: Arsenic: Health Effects, Mechanisms of Actions and Research Issues. Presented as a poster by Dr. Joseph R. Landolph, Jr., on September 22-24, 1997, at Marriott’s Hunt Valley Inn, Hunt Valley, Maryland, Poster Section, page 13.
  77. Warshawsky, D., and Landolph, J. R. Molecular and Cellular Biology of Chemical Carcinogenesis. Toxicological Sci., 42, No. 1-5, 234 (#1152), 1998. 37th Annual Meeting of the Society of Toxicology, March 3, 1998, Seattle, Washington. We co-organized and co-chaired this symposium.
  78. Landolph, J. R., Verma, A., Ramnath, J., Miller, C., and Ohshima, S. Molecular Biology of Polycyclic Aromatic Hydrocarbon and Metal-Induced Cell Transformation. Toxicological Sci., 42, No. 1-5, 234 (#1152), 1998. 37th annual meeting of the Society of Toxicology. Presented as invited symposium talk by Dr. Joseph R. Landolph, Jr., on March 3, 1998, Seattle, Washington.
  79. Ramnath, J., Verma, A., Ohshima, S., and Landolph, J. R. Identification and Characterization of Differentially Expressed Genes in Non-Transformed and Nickel Transformed C3H/10T1/2 Mouse Embryo Fibroblasts. Proceedings of the American Association for Cancer Res., 39:329 (2247), 1998. Presented as a poster at the 39th Annual Meeting of the American Association for Cancer Research, New Orleans, Louisiana, March 28-April 1, 1998, by Dr. Joseph R. Landolph, Jr.
  80. Ramnath, J., Verma, A., and Landolph, J. R. Identification of a Candidate Upregulated Gene in Transformed C3H/10T1/2 Mouse Embryo Cell Lines Induced by Carcinogenic Nickel Compounds. The Toxicologist, 48: No. 1-S, page 346, Abstract #1631, 1999. Presented as a poster at the 38th Annual Meeting of the Society of Toxicology, New Orleans, Louisiana, March 17, 1999.
  81. Ohshima, S., Verma, A., Ramnath, J., and Landolph, J. R. Determination of Relative Genotoxicities of Specific Nickel Compounds in Short-Term In Vitro Assays Using C3H/10T1/2 Cells. The Toxicologist, 48: No. 1-S, page 349, Abstract #1648, 1999. Presented as a poster at the 38th Annual Meeting of the Society of Toxicology, New Orleans, Louisiana, March 17, 1999.
  82. Ramnath, J., Verma, A., and Landolph, J. R. Molecular Cloning of a Gene Highly Expressed in Morphologically Transformed C3H/10T1/2 Cells Induced by Carcinogenic Nickel Compounds. Proceedings of the American Association for Cancer Research 40:504(#3329), 1999. Presented as a Poster at the 90th Annual Meeting of the American Association for Cancer Research, Philadelphia, Pennsylvania, April 10-14, 1999.
  83. Thakore, K. N., Verma, A., Ohshima, S., Ramnath, J., Kaspin, L., Clemens, F., and Landolph, J. R. Nickel Compound-Induced Toxicity and Morphological Transformation in 10T1/2 Cells. The Toxicologist, Fundamental and Applied Toxicology 54 (1), 36 (174), 2000. Presented as a Poster at 39th Annual Meeting of the Society of Toxicology.
  84. Ramnath, J., Verma, A., Kaspin, L., Clemens, F., and Landolph, J. R. Characterization of Genes that are Differentially Expressed in Nickel-Induced, Morphologically Transformed C3H/10T1/2 Mouse Embryo Fibroblasts. Proceedings of the American Association for Cancer Research 41:506 (#3234), 2000. Presented as a Poster by Dr. Joseph R. Landolph, Jr., at the 91st Annual Meeting of the American Association for Cancer Research, San Francisco, Calif., April 1-5, 2000
  85. Clemens, F. M., Ramnath, J. R., Verma, A., Kaspin, L., and Landolph, J. R. Studies of the Toxicological Effects of Insoluble Nickel Compounds. Toxicological Sciences, The Toxicologist 60(1):152 (724), 2001. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the 40th Annual Meeting of the Society of Toxicology, San Francisco, California, March 27, 2001.
  86. Landolph, J. R., Ramnath, J., Clemens, F., Verma, A., and Kaspin, L. Molecular Biology of De-Regulation of Gene Expression in Transformed 10T1/2 Mouse Embryo Cell Lines Induced by Specific Insoluble, Carcinogenic Nickel Compounds. Third International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, Stintino, Sardinia, Italy, September 2-5, 2001. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  87. Clemens, F. M., and Landolph, J. R. Genotoxicity Studies of Two Historical Samples of Nickel Refinery Dust. Toxicological Sciences, The Toxicologist, 66, 1-S, 35 (#167), 2002. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the 41st Annual Meeting of the Society of Toxicology, Nashville, Tennessee, March 18, 2002.
  88. Verma, R., Clemens, F., Kaspin, L., Metwally, M., and Landolph, J. R. Genotoxicity of Nickel-Containing Samples in 10T1/2 Mouse Embryo Cells: Predictions of Carcinogenic Potentials and Implications for Mechanisms of Carcinogenesis. Toxicological Sciences, The Toxicologist, 66, 1-S, 71 (#345), 2002. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the 41st Annual Meeting of the Society of Toxicology, Nashville, Tennessee, March 18, 2002.
  89. Clemens, F., Ramnath, J., Verma, R., Kaspin, L., and Landolph, J. R. Increased Expression of the Ect2 Oncogene in Nickel-Induced Transformed 10T1/2 Mouse Embryo Cell Lines. Proc. Am. Assoc. Cancer Res., 43:294 (#1458), 2002. Presented as a poster by Dr. Joseph R. Landolph, Jr., at the 93rd Annual Meeting of the American Association for Cancer Research, April 7, 2002, San Francisco, California.
  90. Ramnath, J. R., and Landolph, J. R. Enhanced Expression of Calnexin, A Molecular Chaperone, in Nickel-Induced Morphologically Transformed 10T1/2 Mouse Embryo Fibroblasts. Proc. Am. Assoc. Cancer Res., 43:1034 (#5122), 2002. Presented as a poster by Dr. Jamuna Ramnath at the 93rd Annual Meeting of the American Association for Cancer Research, April 10, 2002, San Francisco, California.
  91. Verma, R., Clemens, F., Kaspin, L., and Landolph, J.R. Genotoxicity of Insoluble Nickel Compounds: Predictions of Carcinogenic Potential. Environmental and Molecular Mutagenesis, 39(Suppl. 33):65 (#211), 2002. Annual Meeting of the Environmental Mutagen Society, Anchorage Alaska, April 27-May 2, 2002.
  92. Landolph, J. R., Ramnath, J., Verma, R., and Clemens, F. Under-Expression of the DRIP/TRAP-80 Gene and Over-Expression of the Ect-2 Proto-Oncogene and the Calnexin Gene in Nickel Compound-Induced Transformed 10T1/2 Mouse Embryo Cell Lines. Ninth International Charles Heidelberger Symposium on Molecular and Cellular Mechanisms of Carcinogenesis and Cancer Chemotherapy. Os, Norway, Program Meeting Booklet, pg. 12., 2002.
  93. Clemens, F., Ramnath, J., Verma, R., and Landolph, J. R. Increased Expression of the Ect2 Oncogene in Nickel Compound Induced, Transformed 10T1/2 Mouse Embryo Fibroblast Cell Lines. The Toxicologist 72(S1):216 (1047), 2003. Presented as a poster at the Annual Meeting of the Society of Toxicology.
  94. Verma, R., Clemens, F.M., and Landolph, J. R. Genotoxicities of Nickel Samples in C3H/10T1/2 Mouse Embryo Fibroblasts: Predictions of Carcinogenic Potentials of Nickel Carcinogenesis. The Toxicologist 72(S1):217 (1049), 2003. Presented as a poster at the Annual Meeting of the Society of Toxicology.
  95. Landolph, J. R., Verma, R., and Clemens, F. Molecular Biology of Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblast Cells Induced by Carcinogenic, Insoluble Nickel Compounds: Global Disruption of Control of Gene Expression. Presented as an invited Symposium talk a the International Conference on Biomarkers for Toxicology and Molecular Epidemiology. Abstract Booklet, pg. 13, March 15-17, 2004, Atlanta, Georgia. Sponsored by the CDC, NIEHS, NIOSH, AFIP, NCI.
  96. Verma, R. and Landolph, J. R. Genotoxicity of Samples from Nickel Refineries: Prediction of Carcinogenic Potentials. The Toxicologist, 2004. Presented as poster by Dr. Joseph R. Landolph, Jr., at the 42nd Annual Meeting of the Society of Toxicology, March 23, 2004, Baltimore, Maryland.
  97. Landolph, J. R., Verma, R., and Clemens, F. Global Disruption of Control of Gene Expression in Transformed C3H/10T1/2 Mouse Fibroblast Cell Lines Induced by Carcinogenic Nickel Compounds. Presented as an invited Symposium talk at the First International Symposium on Recent Advances in Environmental Health Research. Abstract Booklet, page 66, 2004. Marriott Hotel, Jackson, Mississippi. Sponsored by Jackson State University. Sept. 19-22, 2004. Symposium Coordinator: Dr. Paul Tchounwou, Professor of Biology and Associate Dean for Research, College of Science and Technology, Jackson State University.
  98. Landolph, J. R., Clemens, F., Ramnath, J., and Verma, R. Insoluble Nickel Compound-Induced Morphological Transformation in 10T1/2 Mouse Embryo Cells Accompanied by Global Disruption of Gene Expression in Nickel Transformed 10T1/2 Cell Lines. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at the Third Conference on Metal Toxicity and Carcinogenesis. Sept. 12-15, 2004. National Institute of Occupational Safety and Health (NIOSH), Morgantown, West Virginia. Abstract Booklet, page 57. Conference Organizer: Dr. Xianglin Shi, NIOSH.
  99. Landolph, J. R., Ramnath, J. Verma, R., and Clemens, F. Induction of Morphological Transformation in 10T1/2 Mouse Embryo Cells by Carcinogenic Insoluble Nickel Compounds and Global Disruption of Gene Expression in Nickel Transformed 10T1/2 Cell Lines. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr. Abstract Booklet, 10th International Charles Heidelberger Symposium on Cancer Research, page O-2, Yokohama, Japan, November 4-7, 2004.
  100. Landolph, J. R., Clemens, F., and Verma, R. Morphological Transformation of 10T1/2 Mouse Embryo Cells by Insoluble Nickel Compounds and Global Disruption of Gene Expression in Nickel Transformed 10T1/2 Cell Lines. Abstract Booklet, Second International Symposium on Recent Advances in Environmental Health Research, page 73, Sept. 18-25, 2005. Held at Jackson State University, Jackson State, Mississippi. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  101. Landolph, J. R., Clemens, F. and Verma, R. Molecular/Cellular Biology of Nickel Compound-Induced Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts. Abstract # S-III-04, Abstract Booklet, page 48, The Fifth International Conference on Metals and Metallothionein in Biology and Medicine, Beijing, The People’s Republic of China, October 8-12, 2005. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  102. Landolph, J. R., Verma, R., and Clemens, F. Uptake of Specific Insoluble Nickel Compounds Leads to Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological Transformation in 10T1/2 Mouse Embryo Cells. 11th International Charles Heidelberger Symposium on Cancer Research, Abstract Booklet, pg. 26, held at Naresuan University, Phitsanulok, Thailand, Jan. 26-29, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  103. Landolph, J. R., Andrade, A., Hamirani, A., Vekaria, H., Scheiner, M., Castillo, D., and Norhadian, S. Genotoxicities of Nickel Refinery Samples in 10T1/2 Mouse Embryo Cells. The Toxicologist, 90(1): 427, Abstract #2085, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at the Annual Meeting of the Society of Toxicology, 2006.
  104. Landolph, J. R., Clemens, F., and Verma, R. Induction of Morphological Transformation and Global Disruption of Gene Expression in C3H/10T1/2 Mouse Embryo Cells by Specific Insoluble Nickel Compounds. 2006 Toxicology and Risk Assessment Conference, Marriott Hotel, West Chester, Ohio, April 23-27, 2006. Meeting Abstract Booklet, page 48, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  105. Landolph, J. R., Verma, R. and Jobling, F. C. Phagocytic Uptake of Specific Insoluble Nickel Compounds Followed by Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological Transformation in C3H/10T1/2 Mouse Embryo Cells. Abstract Book, page 84. 9th International Symposium on Metal Ions in Biology and Medicine. Metal Ions: Role in Life: An Integrated View. Lisbon, Portugal, May 21-14, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  106. Landolph, J. R., Verma, R., Jobling, F. C., Castillo, D., Vekaria, H., DeSilva, A. T., and Vanderwall, K. Phagocytic Uptake of Specific Insoluble Nickel Compounds Results in Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological, Anchorage-Independent, and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. Third International Symposium on Recent Advances in Environmental Health Research, Program Booklet, page 77, 2006. Marriott Hotel, Jackson, Mississippi, Sept. 17-20, 2006. Sponsored by Jackson State University, Jackson, Mississippi. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  107. Landolph, J. R., Verma, R., Jobling, F.C., Castillo, D., Vekaria, H., and DeSilva, A. Cellular and Molecular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts. 4th Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis, Morgantown, West Virginia, Sponsored by CDC/NIOSH and U.S.E.P.A. Abstract Booklet, page 65, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  108. Landolph, J. R., Verma, R., Jobling, F.C., Castillo, D., Mathur, M., DeSilva, A., and Vander Wall, K. Phagocytosis of Insoluble Nickel Compounds Into C3H/10T1/2 Mouse Embryo Cells Followed by Cytotoxicity, Chromosomal Aberrations, Disruption of Gene Expression, and Morphological and Neoplastic Transformation. Symposium on Ecotoxicology and Contamination. Sponsored by the Society of Environmental Toxicology and Chemistry, Nov. 29-Dec. 1, 2006, at Los Cocos, Prinvince of Cordoba, Argentina. Abstract Booklet, page 14, 2006. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  109. Castillo, D. C., Mathur, M., Vander Wall, K. Chen, J J., Verma, R., and Landolph, J. R. Higher Uptake, Cytotoxicity, and Cell Transforming Ability of Nickel Subsulfide Compared to Nickel Sulfate in C3H/10T1/2 Mouse Embryo Cells. The Toxicologist (Suppl. To Toxicological Sciences), 403(1955), 2007. Presented as a Poster by Dr. Landolph on March 29, 2007, at 46th Annual Meeting of Society of Toxicology in Charlotte, North Carolina.
  110. Landolph, J. R., DeSilva, A. T., Lee, H. K., Mathur, M. and VanderWall, K. Induction of Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological and Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells Following Phagocytosis of Insoluble Nickel Compounds. 12th International Charles Heidelberger Symposium on Cancer Research, Abstract Booklet, page 24, 2007. Presented at the 12th International Charles Heidelberger Symposium on Cancer Research, held at the Mishkenot Sha’ananim, Jerusalem, Israel, as an invited symposium talk by Dr. Joseph R. Landolph, Jr., on May 8, 2007.
  111. Landolph, J. R., DeSilva, A. T., Lee, H. K., Mathur, M., Garg, N., Chen, J., Torres, H. A., Fleck, D., and Sandhu, T. Insoluble Nickel Compounds Induce a Combination of Genotoxic and Non-Genotoxic Events, That Result in Global Disruption of Gene Expression and Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. The 2nd International Conference on Forensic Science and Medical Science, Abstract Booklet, page 31, 2007. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at The 2nd International Conference on Forensic Science and Medical Science at Naresuan University in Phitsanulok, Thailand, on July 28, 2007.
  112. Landolph, J. R., DeSilva, A. T., Lee, H. K., and Garg, N. Insoluble Nickel Compound-Induced Genotoxic and Epigenetic Events, Global Disruption of Gene Expression, and Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. The 13th International Charles Heidelberger Symposium on Cancer Research, Abstract Booklet, page 6, 2007. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at 13th International Charles Heidelberger Symposium on Cancer Research at the Smilow Cancer Center of the Medical School of New York University in New York City, New York, on Sept. 8, 2007.
  113. Landolph, J. R. Molecular Mechanisms and Molecular Biology of Metal Carcinogenesis. Chemistry, Molecular Genetics, Epigenetics, and Aberrations in Gene Expression. The Toxicologist 102(1), 264, Abstract #1284, 2008. Presented as an invited symposium talk by Dr. Joseph R. Landolph, Jr., at the 47th Annual Meeting of the Society of Toxicology in Seattle Washington, March 18, 2008.
  114. Landolph, J. R., DeSilva, A., Lee, K. K, Garg, N., and Fleck, D. Insoluble Nickel Compounds Induce Genotoxic and Epigenetic Events, Global Disruption of Gene Expression, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. The Toxicologist 102(1), 264-265, Abstract #1287, 2008. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at the 47th Annual Meeting of the Society of Toxicology in Seattle Washington, March 18, 2008.
  115. DeSilva, A. T., Lee, H. K., and Landolph, J. R. Aberrations in Structure/Distribution of Microfilaments in Nickel-MCA Transformed 10T1/2 Mouse Embry Cell Lines Bearing Amplification of ECT-2 Proto-Oncogene. Proceedings of the American Association for Cancer Research, 49: 525 (#2226), 2008. Presented as a poster at the 2008 Annual Meeting of the American Association for Cancer Research in San Diego, California, on Monday, 15, 2008, by Dr. Joseph R. Landolph.
  116. Landolph, J. R., DeSilva, A. T., and Lee, H. K. Insoluble Nickel Compounds Induce Global Disruption of Gene Expression, Increased Levels and Altered Distributions of Microfilaments and Microtubules, and Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts. Program Booklet (Disc Form), The Fifth International Symposium on Recent Advances in Environmental Health Research , page 1, 2008. Marriott Hotel, Jackson State University, Jackson, Mississippi. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  117. Landolph, J. R., DeSilva, A T., and Lee, Hong, K. Insoluble Ni Compounds Generate Intracellular Ni(II) Ions, Inducing Amplification of the ECT-2 Gene, Global Disruption of Gene Expression, Increased Levels/Altered Distribution of Microfilaments, and Microtubules, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. Program Booklet, The 14 International Charles Heidelberger Symposium on Cancer Research, pg. 17, 2008. The Silverstar Hotel, Urumqi, Xinjiang Province, The People’s Republic of China. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  118. Landolph, J. R., DeSilva, A. T. Lee, H. K., Garg, N. and Chang, E. S. Insoluble Nickel
    Compounds, Amplify theECT-2 Gene, Silence the DRIP/TRAP80 Gene, Globally
    Disrupt Gene Expression, Increase Levels of/Alter Distribution of Microfilaments and Microtubules, and Induce Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. Russian Conference on Molecular Oncology With International Participation. Novosibirsk State University, Siberia, Russia, October 1-3, 2008. Meeting Program Booklet, pages 46-47, 2008. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  119. DeSilva, A. T., Lee, H. S., and Landolph, J. R. Higher Levels/Aggregation of Microtubules/Microfilaments and Global Disruption of Gene Expression in Ni-Transformed 10T1/2 Mouse Embryo Cells. The Toxicologist 108(1), 345, Abstract #1666, 2009. Presented as a poster presentation by Dr. Landolph at the 48th Annual Meeting of the Society of Toxicology in the Poster Session: Chemical Carcinogenesis, in Baltimore, Maryland, March 18, 2009.
  120. DeSilva, A. T., Lee, H. S., and Landolph, J. R. Nickel Ions Induce Amplification of the
    Ect-2 Gene/Over-Expression of Microtubules, and Down-Regulation of the Beta-Centaurin-2 Gene/Over-Expression of Microfilaments, Inducing Morphological and Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. Proc. Am. Assoc. of Cancer Res., 428(5049), 2009. 100th Annual Meeting of the American Association for Cancer Research, Denver, Colorado. Presented as a Poster by Ms. Aruni DeSilva.
  121. Landolph, J. R., DeSilva, A. T., Mai, D., Harrison, A., Lee, H., Garg, N., and Kim, E. S.
    Insoluble Nickel Compounds Induce Chromosomal Aberrations, Gene Amplification/Gene Silencing, Global Disruption of Gene Expression, And Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.”
  122. Landolph, J. R., DeSilva, A. T., Samala, P., and Lin, J. Molecular Biology of Nickel Carcinogenesis. Symposium on Cadmium in Food and Human Health and Technologies for Environmental Restoration and Rehabilitation. January 17, 2010. Topland Hotel Convention Center, Phitsnaulok, Thailand. Sponsored by Naresuan University, Phitsanulok, Thailand, January 15-17, 2010. Meeting Program Booklet, page 32, 2010.
    Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  123. Landolph, J. R., DeSilva, A., Lee, H., Mai, D., Samala, P., Lin, J., and Zheng, J. Insoluble Ni Compounds Induce Gene Amplification/Gene Silencing, Global Disruption of Gene Expression, Alterations in Calcium Ion Gradients, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. January 18, 2010. 15th International Charles Heidelberger Symposium on Cancer Research. Held at the Leelawadee Hotel in Phitsanulok, Thailand. Sponsored by Naresuan University in Phitsanulok, Thailand, from January 18-21, 2010. Meeting Program Booklet, Page 5, Oral Presentation No. 18, 2010. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  124. Landolph, J. R., Mai, D., Harrison, A. R., Garg, N., Chang, E., Lin, J. K., Zheng, J., and DeSilva, A.T. Altered Distributions of Calcium(+2) Ions In Nickel and MCA-Transformed 10T1/2 Mouse Embryo Cell Lines. The Toxicologist, 114(1), page 114, #525, 2010. Presented as a poster by Dr. Landolph at 49th Annual Meeting of Society of Toxicology at Salt Lake City Convention Center, Salt Lake City, Utah, March 8, 2010.
  125. Pehl-De Silva, A. T., Samala, P., Lee, H., and Landolph, J. R. Increased Steady-State Levels of Microtubules in Aberrant Distributions in Ni+2 Ion/MCA-Transformed C3H/10T1/2 Mouse Embryo Cell Lines. Proceedings of the 101st Annual Meeting of the American Association for Cancer Research. Apr. 17-21, 2010. Washington, D. C. Abstract No. 3466. Presented as a Poster by Dr. Aruni Pehl-De Silva on April 18, 2010.
  126. Landolph, J. R., DeSilva, A. Mai, D., Samala, P., Lin, J. K., and Zheng., J. Insoluble Ni Compounds Amplify the Ect-2 Proto-Oncogene and Silence the DRIP80 and β-Centaurin-2 Genes, Altering Global Gene Expression the Cytoskeleton, and Ca+2 Gradients, Inducing Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. Presented as an Invited Symposium Talk at the Seventh International Symposium on Recent Advances in Environmental Health Research, Sept. 13, 2010, at Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor and Associate Dean Paul B. Tchounwou. Program Booklet, page 39 and on program computer disc, 2010.
  127. Landolph, J. R., DeSilva, A., Mai, D., Lin, J. K., and Zheng, J. Insoluble Ni Compound-Induced Gene Amplification/Gene Silencing Causes Over-Expression of Microtubules/Microfilaments, Cell Shape Changes, and De-Regulation of Global Gene Expression/Ca+2 Gradients, Inducing Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. Biomed. Central Proceedings, Vol. 4, Suppl. 2, page 3, O6, 2010.
  128. Landolph, J. R., DeSilva, A., Mai, D., Lin, J. K., and Zheng, J. Cell and Molecular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embry Fibroblasts. 6th Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis, Program Booklet, page 50, 2010. Presented as an invited symposium talk by Dr. Landolph on November 17, 2010, at the Hilton Lexington/Downtown Hotel in Lexington, Kentucky. Host: Professor Xianglin Shi, University of Kentucky.
  129. Landolph, J. R., Pehl-DeSilva, A. T., Mai, D, Lin, J.K. and Zheng, J. Global De-Regulation of Gene Expression, Over-Expression of Microtubules/Microfilaments, and Altered Ca+2 Gradients in Ni-Transformed 10T1/2 Mouse Embryo Cells. The Toxicologist 120(S2), 50(236), 2011. Supplement to Toxicological Sciences. Presented by Dr. Landolph on Monday, March 7, as a poster in Poster Session: Carcinogenesis I, Poster Board #418, at the Convention Center in Washington, D. C., at the 50th Annual Meeting of the Society of Toxicology.
  130. Landolph, J. R., Pehl-DeSilva, A. T., Mai, D., Lin, J, K., Samala, P., and Keliipaakaua, S. Molecular Biology of De-Regulation of Gene Expression in Ni(II) Compound
    Transformed C3H/10T1/2 Mouse Fibroblasts. Meeting Abstract Booklet. February 16-18, 2011. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., on February 17, 2011, at the International Conference: Frontiers in Carcinogenesis and Cancer Prevention: Scientific Advances and Public Health Initiatives. Dayananda Sagar Institutions, Bangalore, India. Host: Jagannatha Rao, Ph. D., Professor, C.D. Sagar Centre for Life Sciences, Dayananda Sagar Institutions, Bangalore, India.
  131. Landolph, J. R., Pehl-DeSilva, A. T., Mai, D., Lin, J. K. H., Samala, P. and Keliipaakaua, S. Ni(II) Compounds Globally Disrupt Gene Expression, Inducing Over-Expression of Microtubules/Microfilaments, Altered Ca+2 Gradients, and Morphological and Neoplastic Transformation of C3H/10T1/2 Cells. Meeting Abstract Booklet, International Conference on Recent Advances in Cancer Research, School of Life Sciences, Central Univ. of Gujarat, Gandhinagar (Ahmedabad), India. Feb. 19-20, 2011.
    Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr.
  132. Landolph, J. R., Pehl-DeSilva, A. T., Mai, D., Lin, J. K. H., and Samala, P. Insoluble Nickel Compounds Induce Gene Amplification, Gene Silencing, Global Disruption of Gene Expression, and Morphological/Neoplastic Transformation of C3H/10T1/2 Cells. Meeting Abstract Booklet, page 32, 2011, of The 17th International Charles Heidelberger Symposium on Cancer Research, June 5-10, 2011, Held at the Fourth Military Medical University, in Xi’an, The People’s Republic of China. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., at this meeting.
  133. Landolph, J. R., Pehl-DeSilva, A., Mai, D., Lin, J., and Zheng, J. Systems Biology and Nickel Carcinogenesis: Global Deregulation of Gene Expression and Cytoskeletal Alterations in Ni-Transformed 10T1/2 Mouse Embryo Cells. Invited Symposium Talk presented by Dr. Joseph R. Landolph, Jr., at the Eighth International Symposium on Recent Advances in Environmental Health Research, Sept. 19, 2011, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor and Associate Dean Paul B. Tchounwou. Program Booklet, page 41 and on program computer disc, 2011.
  134. Landolph, J. R., D. Mai, J. D. Zheng, and P. Samala. Insoluble Ni+2 Compounds Silence The DRIP80 Gene, Altering Ca+2 Ion Distributions in Ni+2/MCA-Transformed 10T1/2 Mouse Embryo Cells. The Toxicologist, Abstract #2490, page 537, 2012. Presented as a Poster by Dr. Landolph at the 51st Annual Meeting of the Society of Toxicology, Wednesday, March 21, 2012, in the Session entitled, “Metals,” at the Moscone Convention Center, San Francisco, California.
  135. Landolph, J. R., Samala, P., Keliipaakaua, S., and Guo, J. Nickel Carcinogenesis: Disruption of Control of the Network of Gene Expression in C3H/10T1/2 Cells. The 18th International Charles Heidelberger Symposium on Cancer Research, held at the University of Ulm in Ulm, Germany. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., in Session 1: Cancer Etiology and Epidemiology, June 28, 2012. Final Program Book of Abstracts, Abstract O4, page 2-2, 2012.
  136. Landolph, J. R., Samala, P., Keliipaakaua, S., and Guo, J. Ni+2-Induced Global De-regulation of Gene Expression, Cytoskeletal Alterations, and Ca+2 Ion Distribution Alterations in Ni+2-Transformed 10T1/2 Mouse Embryo Cells. Presented as an Invited Symposium Talk by Dr. Joseph R. Landolph, Jr., at the Ninth International Symposium on Recent Advances in Environmental Health Research, Sept. 17, 2012, in the Plenary Session I-A: Environmental Toxicology and Health Risk Assessment, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Paul Tchounwou. Program Booklet, page 37, Abstract O-01, full abstract on program computer disc, 2012.
  137. Landolph, J. R., Samala, P., Keliilpaakaua, S., and Akinwumi, K.A. Ni+2 Ion-Induced Chromosomal Aberrations, Gene Amplification, and Gene Silencing, Leading to Global De-Regulation of Gene Expression, Cytoskeletal Alterations, and Aberrations in Ca+2 Ion Distribution in Ni+2-Transformed C3H/10T1/2 Mouse Embryo Cells. Presented as an Invited Symposium Talk by Dr. Joseph R. Landolph, Jr., at the 7th Conference on Metal Toxicity and Carcinogenesis, October 25, 2012, in Plenary Session VIII, Omics/Epigenetics, at the Hotel Albuquerque in Albuquerque, New Mexico. Sponsored by the University of Kentucky and the University of New Mexico. Invited by Professors Xianglin Shi and Ke Kian Jim Liu. Published in the Program Booklet for this meeting, page 28, 2012.
  138. Landolph, J. R., Samala, P., Keliipaakaua, S., and Akinwumi, K. A. Ni+2 Induces Chromosome Aberrations, Gene Amplification/Silencing, Global De-Regulation of Gene Expression, Cytoskeletal and Ca+2 Ion Distribution Alterations, and Morphological/-Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. The 19th International Charles Heidelberger Symposium on Cancer Research, held at the Faculty of Medicine of Kagoshima University in Kagoshima, Japan. Presented as an invited Symposium talk by Dr. Joseph R. Landolph, Jr., in Session 2: Carcinogenesis, Feb. 14, 2013. Final Program Book of Abstracts, Abstract #D1-S2-05, page 20.
  139. Landolph, J. R., DeSilva Pehl, A., Samala, P. Keliipaakaua, S., and Akinwumi, K. Ni+2-Induced Chromosome Aberrations/Gene Amplification/Gene Silencing Alter Cytoskeleton, Ca+2 Distribution, and Global Gene Expression, Causing Morphol./-Neolast. Transformation of 10T12/ Mouse Embryo Cells. The Toxicologist, Supplement to Toxicological Sciences, #164, page 34, 2013. Presented as a Poster by Dr. Landolph at the 52st Annual Meeting of the Society of Toxicology, Monday, March 11, 2013, from 9:30 A. M. – 12:30 P. M., in the Session entitled, “Carcinogenesis,” at the Henry B. Gonzalez Convention Center, San Antonio, Texas.
  140. Landolph, J. R., Akinwumi, K., Tseng, F.-H., Trieu, M., and Menon, S. “Ni+2-Induced Gene Amplification, Gene Silencing, and Global De-regulation of Gene Expression, Leading to Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Abstract #O-01. Listed in the Program Booklet, page 42, and on program computer disc, 2013. Presented by Dr. Joseph R. Landolph, Jr., as an Invited Symposium talk presented at the Tenth International Symposium on Recent Advances in Environmental Health Research, Sept. 16, 2013, in the Plenary Session I-A: Environmental Toxicology and Health Risk Assessment, at the Jackson Convention Center in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor and Associate Dean Paul Tchounwou of Jackson State University.
  141. Landolph, J. R., Pehl-DeSilva, A. T., Akinwumi, K. A., Tseng, F.-H., Trieu, M., and Menon, S. Ni+2-Induced Global De-Regulation of Gene Expression and Morphological/-Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells. Abstract #1502. Published in the Program Booklet, page 393. The Toxicologist, Supplement to Toxicological Sciences, Abstract 1502, pg. 383, 2014. Presented by Dr. Joseph R. Landolph as a poster at the 53rd Annual Meeting of the Society of Toxicology, Wednesday, March 26, 2014, from 9:00 A. M. – 12:30 P. M., in the Session entitled, “Carcinogenesis III.”
  142. Shahin, S. A., Liao, W., Tran, L., Akinwumi, Q. A., Tseng, F.-H., Mathew-Joseph, A., and Landolph, J. R. Induction of Cytotoxicity by Soluble Chromim (VI) Compounds in Cultured C3H/10T1/2 Cl 8 Mouse Cells: Effects of Ascorbate and Dehydroascorbate. Proceedings of the American Association of Cancer Research, 380(#1579), 2014. Presented by Ms. Shahin and Dr. Landolph as a poster at the Annual Meeting of the American Association for Cancer Research at the Convention Center in San Diego, California, on Monday, April 7, 2014, in the Session, Carcinogenesis 2: Chemical and Physical Carcinogens.
  143. Landolph, J. R., Pehl-DeSilva, A. T., Akinwumi, K., Shahin, S. A., Tran, L., Oluwawemitan, I., Tseng, F.-H., Liao, W., and Lin, J. “Ni+2-Induced Global De-Regulation of Gene Expression, Leading to Morphological/Neoplastic Transformation of CH/10T1/2 Mouse Embryo Cells; Cr(VI)-Induced Morphological Transformation of 10T1/2 Cells and A. I. in Human Fibroblasts. Abstract #O-43. Listed in the Program Booklet, page 52 and page 60 and on program computer disc, 2014. Presented by Dr. Joseph R. Landolph as A Distinguished Invited Lecture in the Honorary Biomedical Sciences and Health Information Lecture Series at the Combined Eleventh International Symposium on Recent Advances in Environmental Health Research, and the Thirteenth International Symposium on Metal Ions in Biology and Medicine, Sept. 17, 2014, at the Jackson Convention Center in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor and Associate Dean Paul Tchounwou of Jackson State University.
  144. Landolph, J. R., Pehl-Desilva, A. T., and Akinwumi, K. Molecular Biology of Morphological and Neoplastic Transformation Induced by Insoluble Ni+2 Compounds in C3H/10T/2 Mouse Embryo Fibroblasts.” Presented as an invited Symposium talk at the 20th International Charles Heidelberger Symposium on Cancer Research, held at the Instituto de Alta Investigacion, Universidad de Tarapaca, Calle Antofogasta 1520, Casilla 6-D, Arica, Chile. October 8-11, 2014. Program Booklet, page 34, 2014. Invited by Professor Gloria Calaf, Tarapaca University, Host for the Meeting.

Invited Lectures/Scientific Presentations

  1. Presentation at National Tissue Culture Association Meeting. “Correlations Between Chemically Induced Neoplastic Transformation and Chemically Induced Mutagenesis in C3H/10T1/2 Cl 8 Mouse Fibroblasts.” May, 1980.
  2. “Chemical Carcinogenesis and Environmental Toxicology.” To graduate students in Public Health at UCLA at request of Professor John Froines. April, 1982.
  3. “Chemical Mutagenesis and Transformation in C3H/10T1/2 Cells.” Delivered at Symposium on Therapy-Related Leukemia, Joint Meetings of the Society of Toxicology and American Society for Pharmacology and Experimental Therapeutics. l982.
  4. “Chemical Carcinogenesis and Environmental Toxicology.” To graduate students in Public Health at UCLA at the request of Professor John Froines. April, l982.
  5. “Chemical Transformation and Somatic Mutation in C3H/10T1/2 Cells.” USC General Hospital, Oncology Grand Rounds. 1983.
  6. “Chemical Carcinogenesis.” To St. George Society, 3rd and 4th year medical students, USC School of Medicine. l983.
  7. “Chemical Carcinogenesis and Mutagenesis.” To 12th grade high school students, Lincoln High School Magnet Program, Los Angeles, California. 1984.
  8. “Chemical Mutagenesis and Chemical Transformation in C3H/10T1/2 Mouse
    Embryo Fibroblasts.” Centre Nationale de Recherche Sur le Cancer, Paris, France.
    January, l984. Host: Professor Ivan Chourolinkov.
  9. “Molecular Biology of Chemical Carcinogenesis and Environmental Carcinogenesis.” To graduate students in Public Health at UCLA at the request of Professor John Froines. April, l984.
  10. “Chemically Induced Mutagenesis and Transformation in C3H/10T1/2 Cells.” Argonne National Laboratory International Symposium: The Role of Chemicals and Radiation in the Etiology of Cancer, Oak Brook, Illinois. 1984.
  11. “Chemical Mutagenesis and Chemical Transformation in C3H/10T1/2 Cells.” American Society for Microbiology, Southern California Branch, San Diego, California. l984.
  12. “Chemical Induced Oncogenic Cell Transformation.” Workshop on Radiation Carcinogenesis, University of California, Irvine, California. l984.
  13. “Mechanisms of Multi-Step Chemically Induced Neoplastic Transformation.” Department of Biology, University of Southern California, Los Angeles, California. l984.
  14. “Multi-Step Chemical Transformation in Rodent and Human Cells.” Biology Division, City of Hope National Medical Center, Duarte, California. l984.
  15. “Multi-Step Chemical Transformation and Oncogene Expression in Mouse and Human Fibroblasts.” Wistar Institute, University of Pennsylvania, Philadelphia, Pennsylvania. 1985. Host: Dr. Leila Diamond.
  16. “Transformation by Carcinogenic Metal Salts in C3H/10T1/2 and Human Diploid Foreskin Fibroblasts.” Institute of Scientific Research on Cancer, Paris, France.
    Host: Professor Ivan Chourlinkov. 1985.
  17. “Multi-Step Chemical Transformation and Oncogene Expression in Mouse and Human Fibroblasts.” Institute of Cellular and Molecular Biology, National Center for Scientific Research, Strasbourg, France. Host: Dr. Robert P. P. Fuchs. 1985.
  18. “Chemically Induced Multi-Step Neoplastic Transformation in Cultured Mouse and Human Fibroblasts.” Genetisches Institute, University of Giessen, Giessen, West Germany. Host: Professors Fritz Anders and Dr. Karl Heinz Link. 1985.
  19. Plenary Lecture, “Chemically Induced Multi-Step Neoplastic Transformation of C3H/10T1/2 Cl 8 Cells. Inhibition of a Late Step in Transformation by Aspirin and Implications for the Mechanism of Chemical Transformation.” Meeting of the European Tissue Culture Association, Bergen, Norway. March, l985.
  20. “Molecular Biology of Chemically Induced Neoplastic Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts.” University of Texas, Department of Pharmacology, Houston, Texas. July, l985.
  21. “Mechanisms and Molecular Biology of Chemical Transformation in Mouse and Human Fibroblasts.” Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina. Host: Dr. Roger McClellan, Director of CIIT. July 3, l985.
  22. “Mechanisms and Molecular Biology of Multi-Step Chemical Transformation in 10T1/2 Mouse Embryo Fibroblasts and Diploid Human Fibroblasts.” Donner Laboratory Seminar, Lawrence Berkeley Laboratory, Biology and Medicine Division, University of California, Berkeley, California. l985.
  23. “Mechanisms and Molecular Biology of Multi-Step Neoplastic Transformation in C3H/10T1/2 and Human Diploid Foreskin Fibroblasts.” Cancer Center of Hawaii, University of Hawaii at Manoa. Host: Professor John S. Bertram. 1986.
  24. “Comparisons and Contrasts Between Chemical Transformation in Murine C3H/10T1/2 and Human Fibroblasts In Vitro.” International Workshop on Carcinogenesis and Mutagenesis, Guangzhou, China. Host: Professor Du. 1986.
  25. “Mechanisms and Molecular Biology of Multi-Step Neoplastic Transformation in C3H/10T1/2 Cells and Human Diploid Foreskin Fibroblasts.” Department of Oncology, University of Osaka, Osaka, Japan. Host: Professor Yoshinobu Kubota. 1986.
  26. “Mechanisms and Molecular Biology of Multi-Step Neoplastic Transformation in C3H/10T1/2 on Human Diploid Foreskin Fibroblasts.” Department of Cancer Biology, University of Tokyo, Tokyo, Japan. Host: Prof. Toshio Kuroki. 1986.
  27. “Mechanisms and Molecular Biology of Multi-Step Neoplastic Transformation in C3H/10T1/2 and Human Diploid Fibroblasts.” Univer. of Yokohama, Department of Urology, Yokohama, Japan. Host: Professor Yoshinobu Kubota. 1986.
  28. “Chemically Induced Multi-Step Neoplastic Transformation in C3H/10T1/2 and Human Diploid Foreskin Fibroblasts.” Department of Oncology, Harbor General Hospital, Los Angeles, California. Host: Professor Philip Koeffler. 1986.
  29. “Mechanisms and Molecular Biology of Chemically Induced Multi-Step Neoplastic Transformation in C3H/10T1/2 and Human Fibroblasts.” University of Cincinnati, Department of Environmental Health, Kettering Laboratory, Cincinnati, Ohio. Host: Dr. Roy Albert, Professor and Chairman. 1986.
  30. “Molecular Biology of Chemical Transformation by Organic Carcinogens in C3H/10T1/2 Cells in Human Fibroblasts.” Invited symposium talk at Federation Meetings, at symposium on “Molecular Mechanisms of Cell Transformation of Carcinogenesis by Environmental Carcinogens,” St. Louis, Missouri. 1986.
  31. “Chemical Carcinogenesis.” California State University at Los Angeles, Department of Chemistry and Biology, Los Angeles, California. l986.
  32. “Mechanisms and Molecular Biology of Chemical Transformation in C3H/10T1/2 and Human Fibroblasts.” Chemistry Department and Biology Department, Drexel University, Philadelphia, Pennsylvania. Host: Dr. Amar Nath, Professor of Chemistry. 1986.
  33. “Mechanisms of Chemical Transformation in C3H/10T1/2 and Human Fibroblasts.” Life Sciences Division, Allied Chemical Company, Newark, New Jersey. Host: Dr. Richard Zakour, Staff Scientist. 1986.
  34. “Mechanisms and Molecular Biology of Chemical Transformation in C3H/10T1/2 and Human Diploid Fibroblasts.” Department of Environmental Medicine, New York University. Host: Dr. Max Costa, Professor and Chairman. 1986.
  35. “Proto-Oncogene Expression in Nontransformed and in Chemically Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cells.” Life Sciences Division, Hoffmann La-Roche, Nutley, New Jersey. Host: Dr. Anthony Neri, Staff Scientist. 1986.
  36. “Proto-Oncogene Expression in Non-Transformed and in Chemically Transformed C3H/10T1/2 Cl 8 Mouse Embryo Cells.” Environmental Protection Agency Symposium on Genetic Toxicology, Rockville, Maryland. 1986.
  37. “Mechanisms and Molecular Biology of Chemical Transformation in C3H/10T1/2 and Human Diploid Fibroblasts.” Department of Anatomy, USC School of Medicine, Los Angeles, California. 1986.
  38. “Molecular Mechanisms of Chemical Transformation in C3H/10T1/2 and Human Fibroblasts.” Division of Toxicology, School of Pharmacy, University of California of San Francisco. Host: Professors Thomas D. Meehan and Susan P. Hawkes. March 1987.
  39. “Induction of Mutation and Morphological Transformation of Cultured Mammalian Cells by Extracts of Cantonese Salted Fish.” Albert Soiland Cancer Foundation/USC Comprehensive Cancer Symposium. Invited Symposium Speaker. Host: Dr. Colin Hill, USC School of Medicine. May 19, 1987.
  40. “Molecular and Cellular Mechanisms of Chemical Transformation.” Oncology Grand Rounds, USC School of Medicine. Host: Professor Peter Rosen. November 17, l987.
  41. “Molecular and Cellular Mechanisms of Chemical Transformation in C3H/10T1/2 and Diploid Human Fibroblasts.” USC Department of Pharmacology. Host: Dr. Wayne Bidlack, Professor and Chairman. April 7, l988.
  42. “Chemical Transformation of C3H/10T1/2 and Human Diploid Fibroblasts.” Plenary Lecture, California Division of Tissue Culture Association Meeting, Garden Grove, California, April 22, 1988.
  43. “Molecular and Cellular Mechanisms of Chemical Transformation in C3H/10T1/2 and Diploid Human Fibroblasts.” National Institutes of Occupational Safety and Health, University of West Virginia. Host: Dr. Tong-Man Ong, Division Leader. Sept. 14, l988.
  44. “Nickel, Arsenic, and Chromium Induced Morphological Transformation in 10T1/2 Mouse Embryo Fibroblasts and Anchorage Independence in Diploid Human Fibroblasts.” First International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, Collegio Universitario, Urbino, Italy, September 22, 1988.
  45. “Molecular and Cellular Mechanisms of Carcinogen Metal Induced Transformation of C3H/10T1/2 and Human Fibroblasts.” Wistar Institute, University of Pennsylvania, Philadelphia, Pennsylvania. Host: Dr. Leila Diamond. December 20, 1988.
  46. “Molecular Mechanisms of PAH and Metal Induced Transformation of 10T1/2 and Human Fibroblasts.” Lawrence Berkeley Laboratory and Peralta Cancer Hospital, University of California at Berkeley, Berkeley, California. Hosts: Drs. James Bartholomew, Mina Bissell, and Adeline Hackett. February 6, l989.
  47. “Cellular and Molecular Biology of PAH – and Metal Induced Transformation of Murine and Human Fibroblasts.” Department of Pharmacology, George Washington University School of Medicine, Washington, D.C. Host: Professor Steven Patierno. March 2, l989.
  48. “Morphological Transformation of Mammalian Cells by Carcinogenic Metal Compounds.” Department of Chemistry and Department of Biosciences, Drexel University, Philadelphia, Pennsylvania. Hosts: Professors Amar Nath, Wayne Magee, and Robert O. Hutchins. March 3, 1989
  49. “Molecular and Cellular Mechanisms of Chemical Transformation in Murine and Human Fibroblasts.” Division of Environmental/Occupational Health Sciences, School of Public Health, UCLA. Host: Prof. John Froines. Apr. 18, 1989.
  50. “Molecular and Cell Biology of Chemically Induced Neoplastic Transformation.” Department of Anatomy and Physiology, California State University at Long Beach, Long Beach, California. Host: Dr. Frank Shatzlein. April 21, 1989
  51. “Chemically Induced Neoplastic Transformation.” Genetics Division, Department of Pediatrics, USC School of Medicine, Los Angeles, California. Host: Dr. Atsuko Fujimoto. May 9, 1989.
  52. “Chemical Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Cells and Diploid Human Fibroblasts.” Invited talk at Symposium on Genetic Toxicology of the Chemical Pathology and Toxicology Subdivision, American Chemical Society, Miami Beach, Florida, September 11, 1989.
  53. “Metal Induced Neoplastic Transformation of Mammalian Cells.” Division of Pathology, Childrens Hospital of Los Angeles, USC, Los Angeles, California. Host: Professor Paul Pattengale. November 20, 1989.
  54. “Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Carcinogenic Metal Salts.” Charles Heidelberger International Symposium on Carcinogenesis and Chemotherapy, Kyoto Conference Center, Kyoto, Japan. December 12, 1989.
  55. “Metal-Induced Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Department of Urology, Yokohama City University Medical School, Yokohama, Japan. Host: Professor Yoshihobu Kubota. Dec. 15, 1989.
  56. “Cellular and Molecular Biology of Metal and PAH-Induced Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Japanese Cancer Foundation, Tokyo, Japan. Host: Prof. Takatoshi Ishikawa. December 16, 1989.
  57. “Cellular and Molecular Biology of Metal and PAH-Induced Transformation of C3H/10T1/2 Mouse and Diploid Human Fibroblasts.” Division of Radiation Oncology, University of Arizona Health Science Center, Tucson, Arizona, Host: Professor George T. Bowden. January 5, 1990.
  58. “Cellular and Molecular Mechanisms of Chemical Transformation in C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” California State Department of Public Health, Cancer Risk Assessment Branch, Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, Berkeley, California. April 12, 1990. Host: Dr. Andrew Salmon, Staff Toxicologist.
  59. “Chemical Carcinogenesis.” Department of Toxicology, Imperial Chemical Industries (ICI), Richmond, California. Host: Dr. Thomas Castles, Division Chief. April 13, 1990.
  60. “Chemical Carcinogenesis and Chemical Mutagenesis.” Invited Symposium Talk, in Symposium on “A Perspective on Risk, Diet and Cancer.” Sponsored by the Toxicology and Safety Evaluation Division, Institute of Food Technologists, Anaheim, California. Host: Dr. Wayne Bidlack, Symposium Organizer. June 17, 1990.
  61. “Chemical Transformation in 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Department of Pathology, USC School of Medicine, Los Angeles, California. June 19, 1990.
  62. “Chemical Transformation of Murine and Human Fibroblasts: Cellular and Molecular Mechanisms.” Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina. Host: Dr. Roger O. McClellan, Director of CIIT. June 29, 1990.
  63. “Cellular and Molecular Biology of Chemically Induced Neoplastic Transformation in C3H/10T1/2 and Diploid Human Fibroblasts.” Departments of Biology and Chemistry, Drexel University, Philadelphia, Pennsylvania, Host: Professor Amar Nath. July 2, 1990.
  64. “Cellular and Molecular Biology of Chemically Induced Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Central Toxicology Laboratories, Imperial Chemical Industries (ICI), Alderley Park, Macclesfield, England, United Kingdom. Hosts: Director Dr. Iain Purchase and Staff Scientist Dr. Jerry Styles. July 11, 1990.
  65. “Cellular and Molecular Mechanisms of Chemical Transformation of C3H/10T1/2 Mouse Cells and Diploid Human Fibroblasts.” Department of the Environment, Department of Human Health, British Government, London, England, United Kingdom. Hosts: Drs. Robin Fielder and John Steadman. July 16, 1990.
  66. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” Peterson Institute for Cancer Research, Christie Hospital and Holt Radium Institute, Manchester, England, United Kingdom. Host: Dr. Margaret Fox. July 17, 1990.
  67. “Molecular and Cellular Mechanisms of Chemical Transformation of Murine and Human Fibroblasts.” Imperial Cancer Research Fund (ICRF) Laboratories, London, England, United Kingdom. Host: Dr. Eric Sidebottom. July 18, 1990.
  68. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” MRC Toxicology Unit, Carshalton, Surrey, England, United Kingdom. Host: Dr. Don G. E. Neal, Director. July 20, 1990.
  69. “Cellular and Molecular Mechanisms of Chemical Transformation in C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Beatson Institute for Cancer Research, Glasgow, Scotland, United Kingdom. Host: Dr. Alan Balmain. July 23, 1990.
  70. “Chemically Induced Neoplastic Transformation of Murine and Human Fibroblasts: Cellular and Molecular Mechanisms.” Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, England, United Kingdom. Host: Dr. Steven Ward. July 25, 1990.
  71. “Cellular and Molecular Mechanisms of Chemical Transformation in C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Department of Environmental Carcinogenesis, The Fibiger Cancer Research Institute, Copenhagen, Denmark. Host: Dr. Herman C. Autrup. August 30, 1990.
  72. “Molecular Mechanisms of Neoplastic Transformation Induced in Fibroblasts by Radical-Generating Chemical Carcinogens.” Invited Special Cancer Research Campaign Lectures at the 34th Harden Conference, “Free Radicals: Cell Growth, Disease and Repair Mechanisms,” University of London, Conference Center, Wye, England, United Kingdom. Host: Professor Catherine Rice-Evans. September 2, 1990.
  73. “Cellular and Molecular Mechanisms of Chemical Transformation in Cultured Murine and Human Fibroblasts.” Department of Biology, University of York, York, England, United Kingdom. Host: Dr. Colin Garner. September 10, 1990.
  74. “Chemical Transformation in Murine and Human Fibroblasts.” Department of Biochemistry, University of Bergen, Bergen, Norway. Host: Professor John R. Lillehaug. September 14, 1990.
  75. “Cellular and Molecular Mechanisms of Chemical Transformation in Murine and Human Fibroblasts.” Department of Toxicology, Institute of Occupational Health, Oslo, Norway. Host: Dr. Aage Haugen, Chairman of Occupational Toxicology. September 18, 1990.
  76. “Cellular and Molecular Mechanisms of Chemical Transformation in Murine and Human Fibroblasts.” Department of Biochemistry, University of Stockholm, Stockholm, Sweden. Host: Professor Lars Ernster. September 23, 1990.
  77. “Cellular and Molecular Mechanisms of Chemical Transformation in Murine and Human Fibroblasts.” Institute for Cell Biology and Tumor Studies, University of Essen, Essen, Germany. Host: Professor Manfred Rajewsky. Sept. 26, 1990.
  78. “Cellular and Molecular Mechanisms of Chemical Transformation of Murine and Human Fibroblasts.” Deutsche Krebs Forschung Zentrum (German Cancer Research Center), Heidelberg, Germany, Host: Professor Norbert Fusenig. September 27, 1990.
  79. “Impact of Chemical Carcinogens in the Development of Carcinomas.” Department of Surgery, University of Ulm, Ulm, Germany. Host: Dr. Karl Link. Assistant Professor of Surgery. October 1, 1990.
  80. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation in Mouse C3H/10T1/2 and Diploid Human Fibroblasts.” Department of Environmental Health, University of Cincinnati, and the U.S. Environment Protection Agency, Cincinnati, Ohio. Hosts: Professor David Warshawsky and Dr. F. B. Daniel. April 17, 1991.
  81. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” U.S. Army Chemical Research and Development Command, Division of Toxicology, Edgewood Arsenal, Edgewood, Maryland. Hosts: Dr. Harry Salem, Staff Toxicologist, and Dr. Raymond Mackay, Director of the Detection Directorate. April 22, 1991.
  82. “Cellular and Molecular Biology of Chemically Induced Neoplastic Transformation.” Division of Toxicology, School of Public Health, UCLA. Host: Professor John R. Froines. April 5, 1991.
  83. “Molecular and Cellular Mechanisms of Carcinogenic Metal and Polycyclic Aromatic Hydrocarbon Induced Transformation of Mammalian Cells.” Symposium on Molecular Mechanisms of Action of Environmentally Significant Carcinogens and Mutagens. Sponsored by the Division of Chemical Health and Safety, 202nd National Meeting of the American Chemical Society, New York, New York, August 26, 1991.
  84. “Molecular Mechanisms of Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Metal Salts and Organic Carcinogens.” International Charles Heidelberger Memorial Symposium on Carcinogenesis and Chemotherapy, Marina Del Rey, California, December 8, 1991.
  85. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation of Cultured Murine and Human Fibroblasts.” 203rd National Meeting of the American Chemical Society, San Francisco, California. In a Symposium on “DNA Repair, Genotoxicity and Human Cancer Risk Assessment.” April 6, 1992.
  86. “Molecular Mechanisms of Transformation of 10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts by Carcinogenic Arsenic, Nickel, and Chromium Compounds.” Second International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, Madonna di Campiglio, Italy, January 14, 1993.
  87. “Role of Free Radicals in Chemically-Induced Cell Transformation.” Joint Meeting on Biological Oxidants and Anti-Oxidants: New Development in Research and Health Effects. Invited by Dr. Enrique Cadenas, Meeting Organizer. Sponsored by the Society for Free Radical Research at the Bay Area Oxygen Club, Pasadena, California, March 13, 1993.
  88. “Molecular Mechanisms of Chemically Induced Transformation of C3H/10T1/2 Mouse Fibroblasts and Diploid Human Fibroblasts.” U. S. Environmental Protection Agency, Research Triangle Park, North Carolina. Host: Dr. Steven Nesnow, Branch Chief for Chemical Carcinogenesis, United States Environmental Protection Agency. July 6, 1993.
  89. “Molecular Mechanisms of Chemical Transformation.” Department of Molecular Pharmacology and Toxicology, School of Medicine, University of Southern California, September 15, 1993.
  90. “Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” Department of Environmental Toxicology, University of California at Riverside, Riverside, California. Hosts: Professors David Eastmond and Rajesh K. Mehra. October 15, 1993.
  91. “Molecular Mechanisms of Chemically Induced Neoplastic Cell Transformation.” Department of Pathology and the Lineberger Cancer Center, University of North Carolina, Chapel Hill, North, Carolina. Host: Professor Bernard Weissman. November 15, 1993.
  92. “Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” Environmental Carcinogenesis Seminar Program, National Institutes of Environmental Health Sciences (NIEHS/NIH), Research Triangle Park, North Carolina. Host: Dr. Robert Langenbach, Staff Scientist. November 16, 1993.
  93. “Molecular Mechanisms of Chemically Induced Cell Transformation.” Environmental Toxicology Seminar Series, Department of Community and Preventive Medicine, University of California at Irvine, Irvine, California. Host: Professor Deepak Bhalla. November 19, 1993.
  94. “Tobacco Carcinogen-Induced Transformation of Mammalian Cells.” First Annual Meeting at the Tobacco-Related Disease Research Program (TRDRP) of the State of California, San Francisco Airport Hilton Hotel, San Francisco, California. Invited by the TRDRP. December 1-3, 1993.
  95. “Molecular Mechanisms of Chemical Carcinogenesis.” California State University at Los Angeles, Biomedical Science Seminar Series, Departments of Chemistry and Biology. Host: Professor Carlos Gutierrez. January 21, 1994.
  96. “Molecular Mechanisms of Chemically Induced Neoplastic Cell Transformation.” Institute for Toxicology and Environmental Health, University of California at Davis, Davis, California. Host: Professor Hanspeter Witschi. March 3, 1994.
  97. “Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” Department of Pharmaceutical Chemistry, Univ. of California at San Francisco, San Francisco, California. Host: Professor Susan P. Hawkes. May 23, 1994.
  98. “Molecular Mechanisms of PAH and Metal Transformation of Murine and Human Fibroblasts.” Life Sciences Division, Stanford Research Institute International, Menlo Park, California. Host: Dr. James MacGregor, Director of Toxicology. May 24, 1994.
  99. “Molecular Mechanisms of PAH and Metal Salt-Induced Neoplastic Transformation.” Department of Radiation Oncology, Division of Oncology Research, University of Pennsylvania, School of Medicine, Philadelphia, Pennsylvania. Hosts: Professor Paul Billings and Ann R. Kennedy. July 11, 1994.
  100. “Molecular Mechanisms of Chemically Induced Neoplastic Cell Transformation.” Departments of Microbiology and Pharmacology and the Markey Cancer Center, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia. Host: Professors Richard Moran and Shirley Taylor. July 22, 1994.
  101. “Molecular Mechanisms of Chemically Induced Neoplastic Cell Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts and Diploid Human Fibroblasts by Carcinogenic PAH and Metal Salts.” Eppley Institute for Cancer Research, University of Nebraska, Omaha, Nebraska. Host: Professor Ercole Cavalieri. October 20, 1994.
  102. “Genotoxicity and Carcinogenicity of Ozone.” Department of Biology, California State University of Los Angeles, Los Angeles, California. Host: Professor Carlos Robles. November 4, 1994.
  103. “Molecular and Cellular Mechanisms of Chemically Induced Neoplastic Transformation: Insights Into Anti-Cancer Agents.” Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, California. Host: Professor Roger Duncan. December 7, 1994.
  104. “Molecular Mechanisms of Metal-Induced Cell Transformation.” Center for Environmental Exposures, Host Exposures, and Disease, USC School of Medicine, Los Angeles, California. Host: Prof. Duncan Thomas. April 26, 1995.
  105. “c-Myc Activation in Cells Transformed by Lead Chromate.” Invited Plenary Lecture, Vth International COMTOX Symposium on Toxicology and Clinical Chemistry of Metals, Vancouver, British Columbia, Canada. Host: Professor William Sunderman, Meeting Organizer. July 10, 1995.
  106. “Molecular Mechanisms and Molecular Biology of PAH/Carcinogenic Metal Salt Induced Neoplastic Cell Transformation.” Aero-Malignancy Working Group, School of Medicine, University of Southern California, Los Angeles, California. Host: Dr. Isaiah Dimery. November 11, 1995.
  107. “Genotoxicity and Carcinogenicity of Ozone.” Department of Biology, California State University at Los Angeles, Los Angeles, California.. Host: Professor Carlos Robles. October 4, 1995
  108. “Chemical Carcinogenesis and Chemically Induced Neoplastic Cell Transformation.” To the Indo-American Society for Health and Laboratory Professionals, Anaheim, California. Host: Dr. G. Khare, President, Indo-American Society of Health and Laboratory Professionals. December 2, 1995
  109. “Cellular and Molecular Mechanisms of Chemically Induced Neoplastic Transformation.” Department of Radiology and the Cancer Research Centre, Faculty of Medicine, The University of Hong Kong, Hong Kong. Host: Dr Jonathan Sham, Reader in Radiation Oncology. April 19, l996.
  110. “Molecular Mechanisms of Neoplastic Transformation Induced in C3H/10T1/2 Mouse Embryo Cells and in Diploid Human Fibroblasts by Carcinogenic Metal Salts.” Zheijang Academy of Medical Sciences, Hangzhou, The People’s Republic of China. Host: Professor Yong-dan Yu. April 23, 1996.
  111. “Cell and Molecular Biology of PAH and Metal Salt-Induced Neoplastic Transformation in Mouse C3H/10T1/2 Cells and in Human Diploid Fibroblasts.” Department of Toxicology, Second Military Medical University, Shanghai, The People’s Republic of China. Host: Professor Muquan Yin, Department of Toxicology, Second Military Medical University. April 25, l996.
  112. “Molecular Mechanisms of Neoplastic Transformation Induced in C3H/10T1/2 Mouse Embryo Cells and in Diploid Human Fibroblasts by Carcinogenic Metal Salts.” Department of Toxicology, Nanjing Railway Medical College, Nanjing, The People’s Republic of China. Host: Professor Yaopu Pu, Department of Toxicology, Nanjing Railway Medical College. April 29, l996.
  113. “Cellular and Molecular Biology of PAH and Metal Salt-Induced Neoplastic Transformation of Mouse C3H/10T1/2 Cells and of Human Diploid Fibroblasts.” Department of Pathology, School of Medicine, University of Tokyo, Tokyo, Japan. Host: Dr. Takatoshi Ishikawa, Professor and Chairman, Department of Pathology, University of Tokyo Medical School. May 1, l996.
  114. “Cellular and Molecular Biology of PAH and Metal Salt-Induced Neoplastic Transformation in Mouse C3H/10T1/2 Cells and in Human Diploid Fibroblasts.” Department of Urology, Medical School, Yokohama City University, Yokohama, Japan. Host: Professor Yoshinobu Kubota, Department of Urology, Yokohama City University Medical School. May 2, l996.
  115. “Mechanisms of Cell Transformation by Carcinogenic Nickel Compounds.” Nickel Research Workshop, Rockville, Maryland. Host: Dr. Laurence N. Curcio/ Nickel Producers Environmental Research Association (NiPERA). June 3, l996.
  116. “Metal Salt and PAH-Induced Neoplastic Cell Transformation: Cellular and Molecular Mechanisms.” Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Host: Dr. Stuart Yuspa, Head, Laboratory of Cellular Carcinogenesis and Tumor Promotion. June 6, l996.
  117. “Molecular Mechanisms of Cell Transformation by Polycyclic Aromatic Hydrocarbons and Metal Salts.” National Cancer Institute-Frederick Cancer Research and Development Center, National Institutes of Health, Frederick, Maryland. Host: Dr. Kazimierz Kasprzak. June 7, l996.
  118. “Molecular and Cellular Mechanisms of Neoplastic Cell Transformation Induced by Polycyclic Aromatic Hydrocarbons and Carcinogenic Metal Salts.” Workshop on Genotoxicity of Electromagnetic Fields. Motorola Corporation, Santa Fe, New Mexico. Host: Dr. Mays Swicord, Director, Biology Division. July 31-Aug. 1, l996.
  119. “Genotoxicity and Carcinogenicity of Ozone; Regulation of Carcinogens in California.” Department of Biology, California State University at Los Angeles, Los Angeles, California. Host: Professor Carlos Robles. October 10, l996
  120. “Molecular Mechanisms of Chromium and Nickel-Induced Neoplastic Cell Transformation.” Department of Molecular Pharmacology and Toxicology, School of Pharmacy, University of Southern California, Los Angeles, California. Host: Professor Roger Duncan. January 17, 1997.
  121. “Molecular Biology of Chromium and Nickel-Induced Neoplastic Cell Transformation.” Department of Environmental Health, School of Medicine, University of Cincinnati, Cincinnati, Ohio. Host: Professor David Warshawsky. March 5, l997.
  122. “Molecular Biology of Chromium and Nickel Induced Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Symposium presentation in the symposium, “Molecular Biology of Metal Carcinogenesis” at the 36th Annual Meeting of the Society of Toxicology, Cincinnati, Ohio. March 11, 1997.
  123. “Molecular and Cellular Mechanisms and Molecular Biology of Chromium and Nickel-Induced Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells and Diploid Human Fibroblasts.” Seventh International Hans Wolfgang Nurnberg Memorial Symposium on Metal Compounds in the Environment and Life. University of Modena, Modena, Italy. Host: Dr. Mario Baraldi, Professor and Chairman, Department of Pharmacology, University of Modena, Modena, Italy. June 4-7, l997.
  124. “Molecular Biology of Chromium and Nickel-Induced Cell Transformation.” Seventh International Charles Heidelberger Symposium on Cancer Research- Genesis, Detection, and Therapy. Reisensburg Castle, Gunzburg, Germany. Host: Professor Karl-Heinz Link, Department of General Surgery, University of Ulm, Ulm, Germany. June 2-5, l997.
  125. “Molecular Carcinogenesis Induced by Nickel and Chromium Compounds.” Departments of Chemistry and Biology, Drexel University, Philadelphia, Pennsylvania. Hosts: Professors Amar Nath and Yen Wei. January 30, l998.
  126. “Molecular Biology of Polycyclic Aromatic Hydrocarbon and Metal-Induced Cell Transformation.” Invited symposium talk in the symposium, “Molecular and Cellular Biology of Chemical Carcinogenesis,” sponsored by the Carcinogenesis Specialty Section. 37th Annual Meeting of the Society of Toxicology, Seattle, Washington, March 4, 1998.
  127. “Cellular and Molecular Mechanisms of Chromium and Nickel Carcinogenesis.” Department of Molecular Pharmacology and Toxicology, School of Pharmacy. University of Southern California, Los Angeles, California. Host: Professor Roger Duncan. March 27, l998.
  128. “Cellular and Molecular Mechanisms of Chemically Induced Morphological and Neoplastic Transformation in C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts.” Workshop on Use of Cell Transformation Assays in Regulation of Chemical Carcinogens. Angera, Italy. Hosts: Dr. Michael Balls, Director, European Centre for the Validation of Alternative Test Methods (ECVAM), Angera, Italy, and Dr. Robert Combs, Foundation for the Reduction of Animals in Medical Experimentation (FRAME), Nottingham, England. October 12-16, l998.
  129. “Cell and Molecular Biology of Nickel Carcinogenesis.” Invited seminar speaker. Department of Cell Biology, School of Medicine, Georgetown University, Washington, D. C. Host: Dr. Dan Djakiew, Associate Professor of Cell Biology. February 3, l999.
  130. “Nickel Carcinogenesis.” Department of Molecular Pharmacology and Toxicology, School of Pharmacy, University of Southern California, Los Angeles, California. Host: Professor Roger Duncan. Feb. 19, l999.
  131. “Molecular Biology of Nickel-induced Cell Transformation.” Department of Chemistry, Drexel University, Philadelphia, Pennsylvania. Host: Professor Amar Nath. April 15, l999.
  132. “Biochemistry and Molecular Biology of Nickel Carcinogenesis.” Department of Chemistry, Drexel University, Philadelphia, Pennsylvania. Host: Professor Amar Nath. January 2, 2000.
  133. “Identification of Two Genes Differentially Expressed in Transformed 10T1/2 Mouse Embryo Cell Lines Induced by Insoluble Crystalline Nickel Monosulfide and Green Nickel Oxide.” Invited seminar speaker in “Symposium on Molecular Biology of Metal Carcinogenesis,” May 8, 2000, at the 6th International Symposium on Metal Ions in Biology and Medicine, San Juan Puerto Rico, May 7-10, 2000.
  134. “Nickel Compound Uptake, Toxicity, Transformation, and Gene Expression in 10T1/2 Cells.” Invited seminar speaker in “Symposium on Occupational Health Issues for Nickel and Nickel Compounds,” May 8, 2000, at the 6th International Symposium on Metal Ions in Biology and Medicine, San Juan, Puerto Rico, May 7-10, 2000.
  135. “Molecular Biology of Nickel Carcinogenesis,” Dept. of Molecular Pharmacology and Toxicology, School of Pharmacy, University of Southern California, Los Angeles, California, February 16, 2001. Host: Professor Roger Duncan. February 15, 2001.
  136. “Chromium (VI) and its Human Health Implications,” Southern California Coalition for Pollution Prevention Retreat, Hilton Hotel, La Jolla, California. Host: Mr. Campbell. May 10, 2001.
  137. “Toxicology of Chromium and Arsenic Compounds and Current Drinking Water Regulations: Status of the Science,” San Gabriel Council Valley of Governments, Marriott Hotel, City of Industry, May 12, 2001.
  138. “Molecular Biology of De-Regulation of Gene Expression in Transformed 10T1/2 Mouse Embryo Cell Lines Induced by Specific Insoluble, Carcinogenic Nickel Compounds.” Third International Meeting on Molecular Mechanisms of Metal Toxicity and Carcinogenicity, Stintino, Sardinia, Italy, September 3, 2001.
  139. “Under-Expression of the DRIP/TRAP-80 Gene and Over-Expression of the ECT-2 Proto-Oncogene and the Calnexin Gene in Nickel Compound-Induced, Transformed 10T1/2 Mouse Embryo Cell Lines.” Ninth International Charles Heidelberger Symposium on Molecular and Cellular Mechanisms of Carcinogenesis and Cancer Chemotherapy. Solstrand Fjord Hotel, Os, Norway. Host: Professor Johan R. Lillehaug. July 5-8, 2002.
  140. “Molecular and Cellular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation,” Edgewood Chemical and Biological Center, Aberdeen Proving Ground, U.S. Army SBCCOM, Aberdeen, Maryland. Hosts: Dr. Raymond Mackay, Director of The Biology and Chemistry Division, and Dr. Harry Salem, Chief Toxicologist. March 8, 2003.
  141. “Molecular and Cellular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells,” National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Host: Dr. Stuart Yuspa, Chief, Laboratory of Tumor Promotion. March 10, 2003.
  142. “Toxicology of Nanoparticles,” Panel on Nanotechnology, Annual Science Advisory Board Meeting of the U.S. Environmental Protection Agency, Washington, D.C. December 11, 2003.
  143. “Molecular Biology of Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblast Cells Induced by Carcinogenic, Insoluble Nickel Compounds: Global Disruption of Control of Gene Expression.” International Conference on Biomarkers for Toxicology and Molecular Epidemiology, Atlanta, Georgia. Sponsored by the CDC, ATSDR, U.S. EPA, NIOSH, NIEHS, NCI, and AFIP. Host: Dr. Bruce Fowler, Deputy Director for Science, CDC. March 15-17, 2004.
  144. “Genetic Toxicology of Carcinogenic Nickel Compounds and Molecular Biology of Nickel Compound-Induced Morphological and Neoplastic Cell Transformation.” National Institute of Environmental Health Sciences (NIEHS), Research Triangle Park, North Carolina. Host: Dr. Michael Waalkes. March 26, 2004.
  145. “Insoluble Nickel Compound-Induced Morphological Transformation in 10T1/2 Mouse Embryo Cells Accompanied by Global Disruption of Gene Expression in Nickel Transformed 10T12/ Cell Lines.” Third Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis. NIOSH, Morgantown, West Virginia. Host: Dr. Xianglin Shi, NIOSH. Sept. 12-15, 2004.
  146. “Global Disruption of Control of Gene Expression in Transformed C3H/10T1/2 Mouse Fibroblast Cell Lines Induced by Carcinogenic Nickel Compounds.” First International Symposium on Recent Advances in Environmental Health Research. Invited Distinguished Speaker. Meeting sponsored by Jackson State University, Jackson, Mississippi. Host: Dr. Paul Tchounwou, Professor and Chairman, Dept. of Biology, Jackson State University, Jackson, Mississippi. Sept. 19-22, 2004.
  147. “Induction of Morphological Transformation in 10T1/2 Mouse Embryo Cells by Carcinogenic Insoluble Nickel Compounds and Global Disruption of Gene Expression in Nickel Transformed 10T1/2 Cell Lines.” 10Th International Charles Heidelberger Symposium on Cancer Research, Yokohama Conference Center, Yokohama, Japan. Host: Dr. Yoshinobu Kubota, Professor and Chairman, Dept. of Urology, Yokohama City University, School of Medicine, Yokohama, Japan. November 4, 2004.
  148. “Molecular and Cell Biology of Morphological and Neoplastic Transformation Induced in C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts by Insoluble, Carcinogenic Nickel Compounds.” Department of Environmental Toxicology, University of California at Santa Cruz, Santa Cruz, California. Host: Donald Smith, Ph. D., Professor and Chairman, Dept. of Environmental Toxicology, University of California at Santa Cruz, Santa Cruz, California. February 7, 2005.
  149. “Genetic Toxicology of Carcinogenic Insoluble Nickel Compounds.” Faculty of Medical Sciences, Naresuan University, Phitsanulok, Thailand. Host: Dr. Kanungnit Pupatwibul, Dean of the Graduate School, Naresuan University, Muang, Phitsanulok, Thailand. August 18, 2005.
  150. “Molecular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation by Carcinogenic, Insoluble Nickel Compounds. Thailand Society for Free Radical Research, Workshop on Free Radical Research, Naresuan University, Phitsanulok, Thailand. Host: Professor Maitree Suttajit, of Mahasarakham University, Mahasarakham, Thailand. August 18, 2005.
  151. “Molecular and Cell Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation by of C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts by Carcinogenic, Insoluble Nickel Compounds.” School of Medicine, Cheng Mai University, Cheng Mai, Thailand. Host: Dr. Werawan Ruangyuttikarn, Associate Professor, Division of Toxicology, Dept. of Forensic Medicine, Chiang Mai University, Chiang Mai, Thailand. August 22, 2005.
  152. “Molecular and Cell Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts by Carcinogenic Insoluble Compounds.” School of Pharmacy, Chiang Mai University, Chiang Mai, Thailand. Host: Dr. Nasapon Povichit, Associate Professor, Chiang Mai University, Chiang Mai, Thailand. August 23, 2005.
  153. “Molecular and Cell Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts.” National Cancer Institute of Thailand, Bangkok, Thailand. Host: Dr. Suleeporn Sangrajrang, Staff Scientist, and Dr. Porntipa Pichi, Director, Research Division, National Cancer Institute of Thailand, Bangkok, Thailand. August 24, 2005.
  154. “Molecular and Cell Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts.” School of Medicine, Thammasat University, Klong Luang, Phathumthani, Thailand. Host: Treetip Ratanavalachai, Ph. D., Associate Professor, Dept. of Preclinical Sciences, Division of Biochemistry, Faculty of Medicine, Thammasat University, Kong Luang, Phathumthani, Thailand. August 24, 2005.
  155. “Morphological Transformation of 10T1/2 Mouse Embryo Cells by Insoluble Nickel Compounds and Global Disruption of Gene Expression in Nickel Transformed 10T1/2 Cell Lines.” Second International Symposium on Recent Advances in Environmental Health Research. Jackson State University, Jackson, Mississippi. Invited Distinguished Speaker. Host: Dr. Paul Tchounwou, Professor and Chairman, Dept. of Biology, Jackson State University, Jackson, Mississippi. Sept. 20, 2005.
  156. “Molecular/Cellular Biology of Nickel Compound-Induced Morphological/ Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts.” The Fifth International Conference on Metals and Metallothionein in Biology and Medicine. Friendship Hotel, Beijing, The People’s Republic of China. Invited Speaker. Host: Professor Binggen Ru, Dept. of Biology, Peking University, Beijing, The People’s Republic of China. October 8-12, 2005.
  157. “Uptake of Specific, Insoluble Nickel Compounds Leads to Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological Transformation in 10T1/2 Mouse Embryo Cells.” Meeting Abstract Booklet, page 26. The 11th International Charles Heidelberger Symposium on Cancer Research, Naresuan University, Phitsanulok, Thailand. January 26-29, 2006.
  158. “Molecular Biology of Nickel-Induced Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts.” Centers for Disease Control/Agency for Toxic Substances Disease Registry (CDC/ATDSR), Atlanta, Georgia. Host: Dr. Bruce Fowler, Deputy Director for Science, Centers for Disease Control. March 2, 2006.
  159. “Genotoxicities of Nickel Refinery Samples in 10T1/2 Mouse Embryo Cells.” Poster Presentation, in Poster Session, “Carcinogenesis Bioassay,” at 45th Annual Meeting of the Society of Toxicology, San Diego, California. March 8, 2006.
  160. “Genotoxicity of Insoluble Nickel Compounds and the Molecular Biology of Morphological and Neoplastic Transformation Induced by Carcinogenic Nickel Compounds in C3H/10T1/2 Mouse Embryo Fibroblasts.” Department of Otolaryngology, Keck School of Medicine, University of Southern California. Host: Dale Rice, M.D., Professor and Chairman, Department of Otolaryngology, Keck School of Medicine, Univ. of Southern California, Los Angeles, Calif.
    March 24, 2006.
  161. “Induction of Morphological Transformation and Global Disruption of Gene Expression in C3H/10T1/2 Mouse Embryo Cells by Specific Insoluble Nickel Compounds.” In Session on Heavy Metals of Emerging Toxicological Concern, at the 2006 Toxicology and Risk Assessment Conference, Marriott North Hotel, West Chester, Ohio. Host: Dr. Laurie Roszell, U.S. Army Center for Health Promotion and Preventive Medicine. April 26, 2006.
  162. “Nickel-Induced Toxicity, Mutagenesis, and Carcinogenesis.” Short Course in the Session, “IV. Metal Ion Toxicity and Biomedical Research.” 9th International Symposium on Metals Ions In Biology and Medicine. Lisbon, Portugal. Invited by Dr. Paul Tchounwou. Conference Center of the Catholic University of Portugal, Lisbon, Portugal. May 21, 2006.
  163. “Phagocytic Uptake of Specific Insoluble Nickel Compounds Followed by Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological Transformation in C3H/10T1/2 Mouse Embryo Cells.” Session on “Metal Ions: Molecular Toxicity and Carcinogenesis II.” 9th International Symposium on Metal Ions in Biology and Medicine. Hosts: Dr. Maria Carmen Alpoim and Dr. Paula Morais. Conference Center of the Catholic University of Portugal, Lisbon, Portugal. May 23, 2006.
  164. “Phagocytic Uptake of Specific Insoluble Nickel Compounds Results in Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological, Anchorage-Independent, and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented at the Third International Symposium on Recent Advances in Environmental Health Research, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Paul Tchounwou, Chairman of the Dept. of Biology and Associate Dean of the College of Science and Engineering, Jackson State University, Jackson, Mississippi. Sept. 19, 2006.
  165. “Cell and Molecular Biology of Nickel Compound-Induced Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Fibroblasts.” Presented on Sept. 24, 2006, at the 4th Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis, at the Euro-Suites Hotel in Morgantown, West Virginia. Host: Dr. Xianglin Shi. Sponsored by CDC/NIOSH and U.S.E.P.A. Sept. 24-27, 2006.
  166. “Phagocytosis of Insoluble Nickel Compounds into C3H/10T1/2 Mouse Embryo Cells, Followed by Cytotoxicity, Chromosomal Aberrations, Disruption of Gene Expression, and Morphological and Neoplastic Transformation.” Invited Keynote
    Lecture Presented at the Symposium of the Society of Environmental Toxicology and Chemistry, on “Ecotoxicology and Contamination,” in Los Cocos, Cordoba Province, Argentina. Invited by Dr. Jorge Herkovits, M.D., Organizer of the Symposium. November 29, 2006.
  167. “Induction of Cytotoxicity, Chromosomal Aberrations, Global Disruption of Gene Expression, and Morphological and Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells Following Phagocytosis of Insoluble Nickel Compounds.” Presented as a symposium talk at the 12th International Charles Heidelberger Symposium on Cancer Research at the Mishkenot Sha’ananim in Jerusalem, Israel. Invited by Dr. Sara Lavi, Co-Organizer of the Symposium. May 8, 2007.
  168. “Insoluble Nickel Compounds Induce a Combination of Genotoxic and Non-Genotoxic Events, That Result in Global Disruption of Gene Expression and Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented as a symposium talk at The 2nd International Conference on Forensic Science and Medical Science at Naresuan University in Phitsanulok, Thailand. Invited by Dr. Rosarin Wonwilairat, Dean of the Faculty of Medical Science of the School of Medicine at Naresuan University and Organizer and Host of the Conference. July 28, 2007.
  169. “Insoluble Nickel Compound-Induced Genotoxic and Epigenetic Events, Global Disruption of Gene Expression, and Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented as a symposium talk at The 13th International Charles Heidelberger Symposium on Cancer Research, at the Smilow Cancer Center of the Medical School of New York University, in New York City, New York. Invited by Dr. Franco Muggia, Chief Organizer of the meeting, Professor and Director of the Breast Cancer Research Program at the School of Medicine of New York University. Sept. 8, 2007.
  170. “Insoluble Nickel Compounds Cause Both Genotoxic and Non-Genotoxic Events, Resulting in Global Disruption of Gene Expression and Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented as a symposium talk at the Fourth International Symposium on Recent Advances in Environmental Health Research. Invited by Dr. Paul Tchounwou, Professor and Associate Dean of the College of Science, Engineering, and Technology, Jackson State University, and Organizer of the Symposium. Sept. 17, 2007.
  171. “Insoluble Nickel Compound-Induced Genotoxicity and Epigenetic Events, Including Chromosomal Aberrations, Micronuclei, Gene Amplification, and Epigenetic Events, Leading to Global Disruption and Morphological and Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Fibroblasts.” Presented as an invited seminar at the College of Life Science and Technology of Xinjiang University, in Urumqi, Xinjiang Province, The People’s Republic of China. Host: Dr. Fuchan Zhang, Professor and Dean, College of Life Science and Technology, Xinjiang University. October 13, 2007.
  172. “Molecular Mechanisms and Molecular Biology of Metal Carcinogenesis: Chemistry, Molecular Genetics, Epigenetics, and Aberrations in Gene Expression.” Presented as a Symposium Talk at the 47th Annual Meeting of the Society of Toxicology, Washington State Convention Center, Seattle, Washington, March 18, 2008.
  173. “Insoluble Nickel Compounds Induce Genotoxic and Epigenetic Events, Global Disruption of Gene Expression, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells.” In a Symposium on Molecular Mechanisms and Molecular Biology of Metal Carcinogenesis, at the 47th Annual Meeting of the Society of Toxicology, Washington State Convention Center, Seattle, Washington, March 18, 2008.
  174. “Nickel-Induced Toxicity, Mutagenesis, and Carcinogenesis.” Invited Seminar Given at a Workshop on “Metal Ions In Environmental Health and Biomedical Research,” on Sunday, May 18, 2008, at the 10th International Symposium on Metal Ions In Biology and Medicine, at the Conference Hall of the Polyclinique Maymard, in Bastia, Corsica, France. Invited by Professor Paul Tchounwou, Conference Co-Organizer.
  175. “Silencing of Expression of the Beta Centaurin 2 and the FAD Synthetase Genes in Nickel Transformed C3H10T1/2 Cell lines.” Invited Symposium Talk in the Session, “Metal Ions and Cancer (Part I),” at the 10th International Symposium on Metal Ions In Biology and Medicine, Conference Hall of the Conseil General De Haute-Corse , Bastia, Corsica, France, May 20, 2008.
  176. “Insoluble Nickel Compounds Induce Global Disruption of Gene Expression, Increased Levels and Altered Distribution of Microfilaments and Microtubules, And Morphological and Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Invited Symposium Talk presented at the Fifth International Symposium on Recent Advances in Environmental Health Research, Sept. 15, 2008, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Associate Dean and Professor Paul Tchounwou of Jackson State University.
  177. “Insoluble Nickel Compounds Generate Intracellular Ni(II) Ions, Inducing Amplification of the ECT-2 Gene, Global Disruption of Gene Expression, Increased Levels/Altered Distribution of Microfilaments and Microtubules, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells.” Invited Symposium Talk Presented at the 14th International Charles Heidelberger Symposium on Cancer Research at the Silverstar Hotel in Urumqi, Xinjiang Province, The Peoples’ Republic of China, Sept. 20, 2008.
  178. “Molecular Mechanisms of Genotoxicity and Cell Transformation Induced by Carcinogenic Nickel Compounds.” Presented as a Symposium talk at the 1st International School of Molecular Oncology, section on “Hereditary Cancer and Molecular Diagnostics. Sept. 29, 2008, at Novosibirsk State University in Novosibirsk, Siberia Province, Russia. Invited by Professor Lyudmilla Gulyaeva of Novosibirsk State University in Siberia, Russia.
  179. “Insoluble Nickel Compounds Induce Chromosomal Aberrations, Gene Amplification/Gene Silencing, Global Disruption of Gene Expression, And Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Invited Symposium Talk presented at the Sixth International Symposium on Recent Advances in Environmental Health Research, Sept. 14, 2009, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Dr. Paul B. Tchounwou, Professor of Biology and Associate Dean for Research of Jackson State University.
  180. “Nickel-Induced Morphological/Neoplastic Cell Transformation: Global De- Regulation of Gene Expression.” Princess Chulabhorn Research Institute, January 13, 2010, 10:00 A. M., Bangkok, Thailand. Invited by Dr. Chantagran Srisomsap, Laboratory of Biochemistry.
  181. “Nickel-Induced Morphological/Neoplastic Cell Transformation: Global De-Regulation of Gene Expression.” Dept. of Biochemistry, Faculty of Science, Mahidol University, January 13, 2010, 2:00 P. M., Bangkok, Thailand. Invited by Professor Jisnusan Svasti, Dept. of Biochemistry, Mahidol University.
  182. “Molecular Biology of Nickel Carcinogenesis.” Symposium on Cadmium in Food and Human Health and Technologies for Environmental Restoration and Rehabilitation. January 17, 2010. Topland Hotel Convention Center, Phitsnaulok, Thailand. January 15-17, 2010. Sponsored by Naresuan University, Phitsanulok, Thailand. Invited by Professor Soisungwan Satarug, and Dr. Sukkid Yasothornsrikul, Professor of Biology and Associate Dean of the Faculty of Medical Sciences, and Professor Supanpaiboon Wisa of Naresuan University.
  183. “Insoluble Ni Compounds Induce Gene Amplification/Gene Silencing, Global Disruption of Gene Expression, Alterations in Calcium Ion Gradients, and Morphological/Neoplastic Transformation of 10T1/2 Mouse Embryo Cells. January 18, 2010. 15th International Charles Heidelberger Symposium on Cancer Research. Held at the Leelawadee Hotel in Phitsanulok, Thailand. Sponsored by Naresuan University in Phitsanulok, Thailand, from January 18-21, 2010. Invited by Associate Professor/Associate Dean Sukkid Yasothornsrikul, Dean Rosarin Wongvilariat, and Dean Kanungnit Pupatwibul, of the Faculty of Mdedical Sciences of Naresuan University.
  184. “Global De-Regulation of Gene Expression in Nickel Compound-Induced Morphological/Neoplastic Cell Transformation.” Department of Pathology, The Lineberger Cancer Center, and the Graduate Program in Toxicology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Hosts: Professor Buddy Weissman and Professor Jim Swenberg. Wednesday, June 23, 2010.
  185. “Nickel Compounds Cause Gene Amplification, Gene Silencing, and Morphological and Neoplastic Transformation of C3H/10T1/2 Cells.” United States Environmental Protection Agency, Research Triangle Park, North Carolina. Host: Dr. Stephen Nesnow, Acting Deputy Director of the National Health Environmental Effects Laboratory (NHEERL). Thursday, June 24, 2010.
  186. “Insoluble Nickel Compounds Amplify the Ect-2 Proto-Oncogene and Silence DRIP/TRAP80 and β-Centaurin 2 Genes, Altering Global Gene Expression, the Cytoskeleton, and Ca+2 Gradients, Inducing Morphological/Neoplastic Transformation of 10T1/2 Mouse Embry Cells.” Invited Symposium Talk presented at the Seventh International Symposium on Recent Advances in Environmental Health Research, Sept. 13, 2010, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Paul Tchounwou, Associate Dean of the College of Science and Technology at Jackson State University, Jackson, Mississippi.
  187. “Insoluble Ni Compound-Induced Gene Amplification/Gene Silencing Causes
    Over-Expression of Microtubules/Microfilaments, Cell Shape Changes, and Deregulation of Global Gene Expression/Ca+2 Gradients, Inducing Morphological Neoplastic Transformation of 10T1/2 Mouse Embryo Cells.” 16th International Charles Heidelberger Symposium on Cancer Research. Held at the Tryp Hotel in Coimbra, Portugal. Sponsored by The University of Coimbra, from Sept. 26-28, 2010. Invited by Professor Maria Carmen Alpoim, Dept. of Biochemistry, University of Coimbra, Coimbra, Portugal.
  188. “Alterations in the Cytoskeleton and in Calcium Gradients Accompany Ni+2 Ion-Induced Morphological and Neoplastic Transformation.” 6th Conference on Molecular Mechanisms of Metal Toxicity and Carcinogenesis, November 17, 2010, at the Hilton Lexington/Downtown Hotel in Lexington, Kentucky. Sponsored by the University of Kentucky at Lexington in Lexington, Kentucky. Invited by Professor Xianglin Shi, Graduate Center for Toxicology in the College of Medicine at the University of Kentucky at Lexington, Kentucky.
  189. “The Molecular Biology of Nickel Compound-Induced Morphological/ Neoplastic Cell Transformation. February 14, 2011. School of Biological Sciences, Indian Institute of Technology, New Delhi, India. Host: Professor James Gomes.
  190. “Molecular Biology of De-Regulation of Gene Expression in Ni(II) Compound
    Transformed C3H/10T1/2 Mouse Fibroblasts.” February 16-18, 2011. Presented on February 17, 2011, at the International Conference: Frontiers in Carcinogenesis and Cancer Prevention: Scientific Advances and Public Health Initiatives. Dayananda Sagar Institutions, Bangalore, India. Host: Jagannatha Rao, Ph. D., Pofessor, C.D. Sagar Centre for Life Sciences, Dayananda Sagar Institutions, Bangalore, India.
  191. “Ni(II) Compounds Globally Disrupt Gene Expression, Inducing Over-Expression of Microtubules/Microfilaments, Altered Ca+2 Gradients, and Morphological and Neoplastic Transformation of C3H/10T1/2 Cells.” Presented on February 19, 2011, in “Session 3: Novel Mechanisms in Carcinogenesis,” at the International Conference on Recent Advances in Cancer Research: Bench to Bedside. Feb. 19-20, 2011, at the Fortune Inn Haveli, Gandhinagar, India. Sponsored by the Central University of Gujarat in Gandhinagar (Ahmedabad), India. Host: Professor Rana P. Singh, Central University of Gujarat.
  192. “Insoluble Nickel Compounds Induce Gene Amplification, Gene Silencing, Global Disruption of Gene Expression, and Morphologically/Neoplastic Transformation of C3H/10T1/2 Cells.” Presented as an invited Symposium talk In Session III, on June 6, 2011, at the 17th International Charles Heidelberger Symposium on Cancer Research, June 5-10, 2011, at the Fourth Military Medical University in Xi’an, The People’s Republic of China. Host: Professor Libo Yao, Professor and Chairman of the Dept. of Biochemistry and Molecular Biology, TheFourth Military Medical University, Xi’an, The People’s Republic of China.
  193. “Systems Biology and Nickel Carcinogenesis: Global Deregulation of Gene Expression and Cytoskeletal Alterations in Ni-Transformed 10T1/2 Mouse Embryo Cells.” Invited Symposium Talk presented at the Eighth International Symposium on Recent Advances in Environmental Health Research, Sept. 19, 2011, at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Paul Tchounwou. Program Booklet, page 41 and on program computer disc, 2011.
  194. “Nickel-Induced Global Disruption of Gene Expression Results In Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Invited Seminar presented at the Department of Genetics, Research Seminar Series, Rutgers, The State University of New Jersey, New Brunswick, New Jersey, Sept. 26, 2011. Hosts: Prof. Goppali Kovvali and Prof. Amrik Sahota.
  195. “The Proposition 65 Science Advisory Board.” Invited Symposium Talk Presented in the Informational Session entitled, “Proposition 65: Twenty-Five Years of Implementing California’s Unique and Far-Reaching Law Regulating Organic and Metallic Carcinogens and Developmental/Reproductive Toxins.” March 14, 4:30 – 5:30 P. M., 2012. At the 51st Annual Meeting of the Society of Toxicology, at the Moscone Convention Center, San Francisco, California.
  196. “Nickel Carcinogenesis: Disruption of Control of the Network of Gene Expression in C3H/10T1/2 Cells.” Presented as a Symposium talk at the 18th International Charles Heidelberger Symposium on Cancer Research, “Translational Cancer Research: From Bench to Bedside,” held at The University of Ulm, Ulm, Germany, June 28, 2012. Host: Professor Marko Kornmann, University of Ulm, Ulm, Germany.
  197. “Nickel-Induced Genotoxic and Possible Epigenetic Effects Leading to De- Regulation of Gene Expression and Morphological/Neoplastic Transformation in C3H/10T1/2 Mouse Embryo Cells.” Host: Professor Ann Kennedy, Department of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, July 23, 2012.
  198. “Ni+2-Induced Global De-regulation of Gene Expression, Cytoskeletal Alterations, and Ca+2 Ion Distribution Alterations in Ni+2-Transformed 10T1/2 Mouse Embryo Cells.” Invited Symposium Talk presented at the Ninth International Symposium on Recent Advances in Environmental Health Research, Sept. 17, 2012, in the “Plenary Session I-A: Environmental Toxicology and Health Risk Assessment,” at the Marriott Hotel in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Professor Paul Tchounwou, Associate Dean of the College of Science and Technology. Program Booklet, page 37 and on program computer disc, 2012
  199. “Ni+2-Induced Global De-Regulation of Gene Expression.” Invited Symposium Talk presented at the 7th Conference on Metal Toxicity and Carcinogenesis, October 24, 2012, in Plenary Section VIII: Omics/Epigenetics, at the Hotel Albuquerque in Albuquerque, New Mexico. Hosts/Sponsors: Professor Xianglin Shi of the University of Kentucky and Professor Ke Jian (Jim) Liu of the Department of Pharmaceutical Sciences of the University of New Mexico in Albuquerque, New Mexico.
  200. “Ni+2 Induces Chromosome Aberrations, Gene Amplification/Silencing, Global De-Regulation of Gene Expression, Cytoskeletal and Ca+2 Ion Distribution Alterations, and Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented as a Symposium talk at the 19th International Charles Heidelberger Symposium on Cancer Research, “Carcinogenesis and Chemotherapy: Cancer’s Core Challenges,” held at William Willis Hall of the Faculty of Medicine of Kagoshima University, Kagoshima, Japan, February 14- 16, 2013. Host: Professor Suguru Yonezawa, Dept. of Pathology, Kagoshima University, Kagoshima, Japan.
  201. “Ni+2-Induced Chromosomal Aberrations/Gene Amplification/Silencing, Global De-Regulation of Gene Expression, and Cytoskeletal/Ca+2 Ion Distribution Alterations, Resulting in Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Presented on April 10, 2013, at the Environmental Toxicology Seminar Series of the University of California at Riverside, Riverside, California. Invited by Dr. David Eastmond, Professor and Chairman of the Dept. of Cell Biology of the University of California at Riverside.
  202. “Carcinogenic Nickel Compound Induce Global Alterations in Gene Expression, Leading to Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Invited by Professor Kelvin J. A. Davies and Professor Enrique Cadenas of the Free Radical Institute of the University of Southern California, Los Angeles, California, Wednesday, May 15, 2013.
  203. “Ni+2-Induced Gene Amplification, Gene Silencing, and Global De-regulation of Gene Expression, Leading to Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells.” Invited Symposium Talk presented at the Tenth International Symposium on Recent Advances in Environmental Health Research, Sept. 16, 2013, in the “Plenary Session I-A: Environmental Toxicology and Health Risk Assessment,” at the Jackson Convention Center in Jackson, Mississippi. Sponsored by Jackson State University. Invited by Dr. Paul B. Tchounwou, Professor of Biology and Associate Dean, College of Science and Technology. Program Booklet, page 42 and on program computer disc, 2013. Abstract #O-01.
  204. “Ni+2-Induced Genotoxicity and Gene Silencing, Leading to Morphological and
    Neoplastic Transformation of C3H/10T1/2 Cl 8 Mouse Embryo Cells.” Invited Symposium Talk, Given at the Annual Retreat of the Dept. of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California. Held at the Proud Bird Restaurant/Conference Facility, Los Angeles, California, Friday, Sept. 20, 2013.
  205. “Ni+2-Induced Global De-Regulation of Gene Expression, Leading to
    Morphological/Neoplastic Transformation of C3H/10T1/2 Mouse Embryo Cells; Cr(VI)-Induced Morphological Transformation of 10T1/2 cells and A. I. in Human Fibroblasts.” A Distinguished Lecture in the Honorary Biomedical Science and Health Information Lecture Series.” Invited Plenary Symposium Talk presented at the Eleventh International Symposium on Recent Advances in Environmental Health Research and the Thirteenth International Symposium on Metal Ions in Biology and Medicine, Sept. 17, 2013, at the Jackson Convention Center in Jackson, Mississippi. Sponsored by Jackson State University, Jackson, Mississippi. Invited by Dr. Paul B. Tchounwou, Associate Dean for Research of the College of Science, Engineering, and Technology at Jackson State University, Jackson, Mississippi. Program Booklet, pages 52 and 67 and on the program computer disc, 2014. Abstract #O-43.
  206. “Molecular Biology of Morphological and Neoplastic Transformation Induced by Insoluble Ni+2 Compounds in C3H/10T/2 Mouse Embryo Fibroblasts.” Presented as a Symposium talk at the 20th International Charles Heidelberger Symposium on Cancer Research, held at the Instituto de Alta Investigacion, Universidad de Tarapaca, Calle Antofogasta 1520, Casilla 6-D, Arica, Chile. October 8-11, 2014. Host: Dr. Gloria M. Calaf, rofessor of Biology, University of Tarapaca, Arica, Chile.

H. Seminars Given to Public Health Officials and the Public, on The Causes of Human Cancer, To Help the USC/Norris Comprehensive Cancer Reduce Cancer Incidence in Los Angeles County, California

  1. “The Proportional Causes of Human Cancer. How Much Human Cancer Is Preventable?” Invited Symposium Talk, presented at the Access for LA Coalition (Access to Cancer Care Education Services and Support) Monthly Meeting on “Preventing Cancer Through Healthy Communities: A Focus on Policy, Systems, and Environment.” Dec. 3, 2012 at the California Endowment, Alameda Street, Los Angeles, California. Sponsored by the American Cancer Society, Cancer Legal Resource Center, Cancer Support Community Pasadena, USC/Norris Comprehensive Cancer Center, UCLA AANCART, L. A. County Affiliate of Susan G. Komen for the Cure, LA County Dept. of Public Health, Office of Women’s Health, and WINCART Center.
  2. “The Proportional Causes of Human Cancer. How Much Human Cancer Is Preventable?” Invited Symposium Talk, presented to the Vietnamese Community in Orange County, Friday, February 22, 2013, 11:00 A. M. – 12:00 P. M., at the Vietnamese-American Community Center in Westminster, California.
  3. “The Proportional Causes of Human Cancer. How Much Human Cancer Is Preventable?” Invited Symposium Talk, presented to cancer patients at the Tower Cancer Research Foundation, 9090 Wilshire Boulevard, Suite #450, Beverly Hills, California 90211, on Tuesday, Sept. 10, 2013, from 6:30 – 8:30 P. M. Invited by Ms. Phyllis R. Tell, MSW, Director, of Psychosocial Programs.
  4. “The Proportional Causes of Human Cancer. How Much Human Cancer Is Preventable?” Invited Symposium Talk, presented to Physicians, Scientists, and Public Health Officials, at the California Dialog on Cancer’s (CDOC) Biennial Stakeholder Conference, 300 J Street, Holiday Inn, Sacramento, California, Monday, June 9, 2014, 10:50 – 11:20 A. M. Invited by Ms. Shauntay Davis, M. P. H., Program Director, California Dept. of Public Health, Sacramento, California, and Comprehensive Cancer Control Program, CDOC.
  5. “The Proportional Causes of Human Cancer. How Much Human Cancer Is Preventable?” Invited Symposium Talk, presented at Abraham Lincoln High School, at 4501 North Broadway Avenue, to Students, Parents, Teachers and Community Members, Wednesday, July 8, 2014, 10:00 – 10:30 A. M. Invited by the Health Group at Lincoln High School.