Division of Genetic and Reproductive Toxicology
National Center for Toxicological Research
U.S. Food and Drug Administration
Nan Mei is a Senior Research Biologist in the Division of Genetic and Molecular Toxicology at the US FDA National Center for Toxicological Research, NCTR. He received his MD in 1984 from Hebei Medical University China and earned his PhD degree in 1997 at the University of Occupational and Environmental Health, Japan. He has published 58 peer reviewed research articles in prestigious journals including The FASEB Journal Nature Biotechnology, Journal of Biological Chemistry, British Journal of Cancer, Cancer Letters, Toxicological Sciences, Toxicology in Vitro Chemical Research in Toxicology Mutation Research Environmental and Molecular Mutagenesis and BMC Bioinformatics. He was author of 7 book chapters. He is a member of the Society of Toxicology and the Environmental Mutagen Society. He served as a reviewer of many peer reviewed journals in the area of genetic toxicology and toxicogenomics. He received many awards including the 2007 FDA Scientific Achievement Award.
Currently he focuses his research on genetic toxicology and toxicogenomics. He utilizes the in vivo and in vitro mutation assays to evaluate a number of high-priority chemicals for their mutagenicity and to determine the mechanisms of chemical-induced genetic toxicity. His interests include the evaluation of the mutagenic effects of direct mutagens, botanical chemicals, herbal dietary supplements, industrial compounds, and ingredients in cosmetics and other retail products. He incorporates toxicogenomic approaches into his research to develop potential biomarkers, create gene signatures, and elucidate molecular mechanisms.
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