S
Stacey L. Dial
Researcher at National Center for Toxicological Research
Publications - 29
Citations - 2670
Stacey L. Dial is an academic researcher from National Center for Toxicological Research. The author has contributed to research in topics: Gene expression & Receptor. The author has an hindex of 22, co-authored 29 publications receiving 2499 citations. Previous affiliations of Stacey L. Dial include Food and Drug Administration.
Papers
More filters
Journal ArticleDOI
The Estrogen Receptor Relative Binding Affinities of 188 Natural and Xenochemicals: Structural Diversity of Ligands
R. Blair,Hong Fang,William S. Branham,Bruce S. Hass,Stacey L. Dial,Carrie L. Moland,Weida Tong,Leming Shi,Roger Perkins,Daniel M. Sheehan +9 more
TL;DR: The current study provides the most structurally diverse ER RBA data set with the widest range of RBA values published to date.
Journal ArticleDOI
QSAR models using a large diverse set of estrogens
Leming Shi,Hong Fang,Weida Tong,Jie Wu,Roger Perkins,Robert M. Blair,William S. Branham,Stacey L. Dial,Carrie L. Moland,Daniel M. Sheehan +9 more
TL;DR: If used in conjunction with phases I and II, which reduced the size of the data set dramatically by eliminating most inactive chemicals, the current CoMFA model can be used to predict the RBA of chemicals with sufficient accuracy and to provide quantitative information for priority setting.
Journal ArticleDOI
Similarities and Differences in the Expression of Drug-Metabolizing Enzymes between Human Hepatic Cell Lines and Primary Human Hepatocytes
Lei Guo,Stacey L. Dial,Leming Shi,William S. Branham,Jie Liu,Jia-Long Fang,Bridgett Green,Helen Deng,Jim Kaput,Baitang Ning +9 more
TL;DR: The basal gene expression profiles of 251 drug-metabolizing enzymes in untreated primary human hepatocytes from six donors, four commonly used hepatoma cell lines, and one transfected human liver epithelial cell line are characterized, providing references for researchers to choose carefully appropriate in vitro models for studies of drug metabolism and toxicity.
Journal ArticleDOI
Cross-platform comparison of SYBR® Green real-time PCR with TaqMan PCR, microarrays and other gene expression measurement technologies evaluated in the MicroArray Quality Control (MAQC) study
Emi Arikawa,Yanyang Sun,Jie Wang,Qiong Zhou,Baitang Ning,Stacey L. Dial,Lei Guo,Jingping Yang +7 more
TL;DR: SYBR Green real-time PCR delivers highly comparable results in gene expression measurement with TaqMan PCR and other high-density microarrays, and is evaluated in this study in terms of fold-change correlation and overlap of lists of differentially expressed genes.
Journal ArticleDOI
Phytoestrogens and mycoestrogens bind to the rat uterine estrogen receptor.
William S. Branham,Stacey L. Dial,Carrie L. Moland,Bruce S. Hass,R. Blair,Hong Fang,Leming Shi,Weida Tong,Roger Perkins,Daniel M. Sheehan +9 more
TL;DR: Estrogen receptor relative binding affinities can be utilized before animal testing to rank order estimates of the potential for in vivo estrogenic activity of a wide range of untested plant chemicals (as well as other chemicals) based on ER binding.