(From the Applicant?s Description) The scientific focus of the Molecular and Genetic Toxicology Research Core is aimed at understanding the molecular mechanisms used by prokaryotic and eukaryotic cells to maintain the integrity of DNA and the mechanisms of cellular signaling through transduction pathways. The fundamental objective of this Core is to serve as an intellectual resource to facilitate interactive research centered in several areas including: (1) mechanisms of DNA damage and repair; (2) fidelity of DNA synthesis; (3) biosynthesis of deoxyribonucleoside triphosphates and their relationship to mechanisms of mutagenesis; (4) protein DNA binding mechanisms, structure, and function; (5) protein damage and modification; and (6) protein-protein interactions involved in signal transduction, DNA replication, and DNA repair pathways. Investigative approaches used by Core members cover a wide spectrum of techniques including gene cloning, enzyme/protein purification, protein chemistry, enzyme kinetics (steady-state and stopped-flow), nucleic acid manipulation and modification (site-directed mutagenesis and damaged DNA substrates), biosensor analysis of macromolecular interactions, metabolite pool assays, computer modeling, and nuclear magnetic resonance. Research in this Core is allied with the Nucleic Acids and Proteins Facilities and Service Core that is coordinated by Dr. Schimerlik.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES000210-35
Application #
6575644
Study Section
Project Start
2002-04-01
Project End
2003-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
35
Fiscal Year
2002
Total Cost
$78,870
Indirect Cost
Name
Oregon State University
Department
Type
DUNS #
053599908
City
Corvallis
State
OR
Country
United States
Zip Code
97339
Nix, Cassandra E; Harper, Bryan J; Conner, Cathryn G et al. (2018) Toxicological Assessment of a Lignin Core Nanoparticle Doped with Silver as an Alternative to Conventional Silver Core Nanoparticles. Antibiotics (Basel) 7:
Geier, Mitra C; James Minick, D; Truong, Lisa et al. (2018) Systematic developmental neurotoxicity assessment of a representative PAH Superfund mixture using zebrafish. Toxicol Appl Pharmacol 354:115-125
Welch, Barrett; Smit, Ellen; Cardenas, Andres et al. (2018) Trends in urinary arsenic among the U.S. population by drinking water source: Results from the National Health and Nutritional Examinations Survey 2003-2014. Environ Res 162:8-17
Denluck, Lindsay; Wu, Fan; Crandon, Lauren E et al. (2018) Reactive oxygen species generation is likely a driver of copper based nanomaterial toxicity. Environ Sci Nano 5:1473-1481
Ahn, Soyoun; Magaña, Armando Alcazar; Bozarth, Connie et al. (2018) Integrated identification and quantification of cyanobacterial toxins from Pacific Northwest freshwaters by Liquid Chromatography and High-resolution Mass Spectrometry. J Mex Chem Soc 62:
Titaley, Ivan A; Ogba, O Maduka; Chibwe, Leah et al. (2018) Automating data analysis for two-dimensional gas chromatography/time-of-flight mass spectrometry non-targeted analysis of comparative samples. J Chromatogr A 1541:57-62
Geier, Mitra C; Chlebowski, Anna C; Truong, Lisa et al. (2018) Comparative developmental toxicity of a comprehensive suite of polycyclic aromatic hydrocarbons. Arch Toxicol 92:571-586
Bugel, Sean M; Tanguay, Robert L (2018) Multidimensional chemobehavior analysis of flavonoids and neuroactive compounds in zebrafish. Toxicol Appl Pharmacol 344:23-34
Gaulke, Christopher A; Rolshoven, John; Wong, Carmen P et al. (2018) Marginal Zinc Deficiency and Environmentally Relevant Concentrations of Arsenic Elicit Combined Effects on the Gut Microbiome. mSphere 3:
Roper, Courtney; Simonich, Staci L Massey; Tanguay, Robert L (2018) Development of a high-throughput in vivo screening platform for particulate matter exposures. Environ Pollut 235:993-1005

Showing the most recent 10 out of 690 publications