Research Topics
| Jennifer FostelSummaryAffiliation: National Institutes of Health Country: USA Publications
| Collaborators
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Detail Information
Publications
Towards standards for data exchange and integration and their impact on a public database such as CEBS (Chemical Effects in Biological Systems)Jennifer M Fostel
Global Health Sector, SRA International, Inc, LLC, Durham, North Carolina, USA
Toxicol Appl Pharmacol 233:54-62. 2008..The utility and a method for integrating data within and across DNA microarray studies is shown in an example analysis using DrugMatrix data deposited in CEBS by Iconix Pharmaceuticals...
Toward a checklist for exchange and interpretation of data from a toxicology studyJennifer M Fostel
NIEHS, LMIT ITSS Contract, Research Triangle Park, North Carolina 27709 2233, USA
Toxicol Sci 99:26-34. 2007..It is anticipated that once a toxicology checklist is accepted and put into use, then toxicology databases can be configured to require and output these fields, making it straightforward to annotate data for interpretation by others...
Maximizing biomarker discovery by minimizing gene signaturesChang Chang
The Center for Bioinformatics and Institute of Biomedical Sciences, School of Life Science, East China Normal University, 500 Dongchuan Road, Shanghai 200241, China
BMC Genomics 12:S6. 2011....
Transcriptomic analysis of pathways regulated by toll-like receptor 4 in a murine model of chronic pulmonary inflammation and carcinogenesisAlison K Bauer
Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI, USA
Mol Cancer 8:107. 2009..This study was designed to identify TLR4-mediated gene expression pathways that may be used as prognostic indicators of susceptibility to lung tumorigenesis in mice and provide insight into the mechanism...
Modeling biomedical experimental processes with OBIRyan R Brinkman
British Columbia Cancer Agency, Vancouver, Canada
J Biomed Semantics 1:S7. 2010..AVAILABILITY : OBI is available at http://purl.obolibrary.org/obo/obi/2009-11-02/obi.owl...
Gene expression response in target organ and whole blood varies as a function of target organ injury phenotypeEdward K Lobenhofer
Cogenics, Division of Clinical Data, Inc, Morrisville, NC 27560, USA
Genome Biol 9:R100. 2008..The results of the study demonstrate the classification of histopathological differences, likely reflecting differences in mechanisms of cell-specific toxicity, using either liver tissue or blood transcriptomic data...
Sources of variation in baseline gene expression levels from toxicogenomics study control animals across multiple laboratoriesMichael J Boedigheimer
CDER, US FDA, Silver Spring, MD 20993, USA
BMC Genomics 9:285. 2008....
Exploration of the gene expression correlates of chronic unexplained fatigue using factor analysisJennifer Fostel
National Center for Toxicogenomics, NIEHS MD F1 05, 111 Alexander Drive, PO Box 12233, Research Triangle Park, NC 27709 2233, USA
Pharmacogenomics 7:441-54. 2006..To identify biomarkers of chronic fatigue syndrome (CFS) and related disorders through analysis of microarray data, pathology test results and self-report symptom profiles...
Chemical effects in biological systems--data dictionary (CEBS-DD): a compendium of terms for the capture and integration of biological study design description, conventional phenotypes, and 'omics dataJennifer Fostel
LIMT Lockheed Martin Information Technology LMIT, Research Triangle Park, NC 27709, USA
Toxicol Sci 88:585-601. 2005..To illustrate the utility of the CEBS-DD, we present an example of integrating data from two proteomics and transcriptomics studies of the response to acute acetaminophen toxicity (A. N. Heinloth et al., 2004, Toxicol. Sci. 80, 193-202)...
Predictive ADME-Tox London, UK, 27 -- 28 April 2005Jennifer Fostel
US National Center for Toxicogenomics, National Institute for Environmental Health Sciences, Lockheed Martin Information Technology, Research Triangle Park, North Carolina, USA
Expert Opin Drug Metab Toxicol 1:565-70. 2005..In addition, collaboration to apply novel methods such as metabonomics profiling to withdrawn drugs may permit the identification of new safety biomarkers to prevent such costly failures...
Sources of variance in baseline gene expression in the rodent liverJ Christopher Corton
Integrated Systems Toxicology Division, National Health and Environmental Effects Research Lab, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA
Mutat Res 746:104-12. 2012..Identification of batteries of genes that are altered in a variety of background conditions could be used to predict responses to drugs and chemicals in appropriate models of the human liver...
CEBS--Chemical Effects in Biological Systems: a public data repository integrating study design and toxicity data with microarray and proteomics dataMichael Waters
NIEHS, National Center for Toxicogenomics, PO Box 12233, Research Triangle Park, NC 27709, USA
Nucleic Acids Res 36:D892-900. 2008..niehs.nih.gov. BID can be accessed via the user interface from https://dir-apps.niehs.nih.gov/arc/. Requests for a copy of BID and for depositing data into CEBS or BID are available at http://www.niehs.nih.gov/cebs-df/...
Toxicogenomics and systems toxicology: aims and prospectsMichael D Waters
National Center for Toxicogenomics, National Institute of Environmental Health Sciences, PO Box 12233, MD F1 05, 111 Alexander Drive, Research Triangle Park, North Carolina 27709 2233, USA
Nat Rev Genet 5:936-48. 2004....
Comparison of drug transporter levels in normal colon, colon cancer, and Caco-2 cells: impact on drug disposition and discoveryAnna Maria Calcagno
Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
Mol Pharm 3:87-93. 2006..However, the molecular "fingerprint" of Caco-2 was distinctly different from tumor samples, indicating that the Caco-2 model would unlikely predict accurate drug absorption for colon cancer sites...
Modulation of cell adhesion molecules in various epithelial cell lines after treatment with PP2Anna Maria Calcagno
Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas 66047, USA
Mol Pharm 2:170-84. 2005..Overall, our data suggest that E-cadherin is positively regulated by inhibition of Src tyrosine kinases at the functional and protein expression levels within these epithelial cell lines...
Effects of an E-cadherin-derived peptide on the gene expression of Caco-2 cellsAnna Maria Calcagno
Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas 66047, USA
Pharm Res 21:2085-94. 2004..The goal of this study was to determine the effects of exposure to an HAV peptide (Ac-SHAVSS-NH2) on the protein and gene expression in Caco-2 cells, a model for the intestinal mucosa...
Future of toxicogenomics and safety signatures: balancing public access to data with proprietary drug discoveryJennifer M Fostel
Pharmacogenomics 8:425-30. 2007
