This project has two purposes. As the statistics core, the project will provide statistical support to other superfund projects. This will typically involve assistance in experimental design or in the analysis and interpretation of data. In addition, this project proposes the development and refinement of statistical methods and algorithms for the analysis of toxics measurement data and for the creation of new and improved measurement techniques. Many analytical methods can be made more efficient and effective by careful statistical design and analysis of the data. This may be important to human health since it allows more frequent monitoring of hazardous sites for the same cost, and since it aids in the development and use of analytical techniques to detect toxic substances both clinically and in the field at lower levels and with greater accuracy than existing methods. A particular emphasis is on statistical contributions to the development of improved ELISA protocols and to the better analysis of data from existing protocols. Techniques such as empirical Bayes estimation, nonlinear optimal design, maximum pseudo-likelihood, and M-estimation will allow these methods to deal with complex problems of nonlinear calibration, nonconstant variance, possible outliers, and values near or below detection limits.
Specific Aims I. Develop and test new and improved statistical methodologies addressing statistical problems typically encountered in the analysis of toxics measurement data using ELISA and other analytical methods. II. Apply state-of-the-art techniques in numerical analysis and numerical optimization to develop efficient, fast, and reliable computer algorithms to solve problems in implementing statistical methods from I. III. Collaborate with other Superfund projects on statistical and mathematical problems of importance to those projects. Test and validate the methods and algorithms derived from I and II using data from other projects. Specific current collaborations are with Hammock's immunochemical project and with Jones's analytical core. IV. Develop software that incorporates the developments in statistical methodology and numerical methods that arise from this project so that they can be used by other scientists in a laboratory setting.

Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Harris, Todd R; Kodani, Sean; Rand, Amy A et al. (2018) Celecoxib Does Not Protect against Fibrosis and Inflammation in a Carbon Tetrachloride-Induced Model of Liver Injury. Mol Pharmacol 94:834-841
Bever, Candace S; Rand, Amy A; Nording, Malin et al. (2018) Effects of triclosan in breast milk on the infant fecal microbiome. Chemosphere 203:467-473
Zheng, Jing; McKinnie, Shaun M K; El Gamal, Abrahim et al. (2018) Organohalogens Naturally Biosynthesized in Marine Environments and Produced as Disinfection Byproducts Alter Sarco/Endoplasmic Reticulum Ca2+ Dynamics. Environ Sci Technol 52:5469-5478
Lakkappa, Navya; Krishnamurthy, Praveen T; Yamjala, Karthik et al. (2018) Evaluation of antiparkinson activity of PTUPB by measuring dopamine and its metabolites in Drosophila melanogaster: LC-MS/MS method development. J Pharm Biomed Anal 149:457-464
Guedes, A G P; Aristizabal, F; Sole, A et al. (2018) Pharmacokinetics and antinociceptive effects of the soluble epoxide hydrolase inhibitor t-TUCB in horses with experimentally induced radiocarpal synovitis. J Vet Pharmacol Ther 41:230-238
Heikenfeld, J; Jajack, A; Rogers, J et al. (2018) Wearable sensors: modalities, challenges, and prospects. Lab Chip 18:217-248
Minaz, Nathani; Razdan, Rema; Hammock, Bruce D et al. (2018) An inhibitor of soluble epoxide hydrolase ameliorates diabetes-induced learning and memory impairment in rats. Prostaglandins Other Lipid Mediat 136:84-89
Lassabe, Gabriel; Kramer, Karl; Hammock, Bruce D et al. (2018) Noncompetitive Homogeneous Detection of Small Molecules Using Synthetic Nanopeptamer-Based Luminescent Oxygen Channeling. Anal Chem 90:6187-6192
?ertíková Chábová, V?ra; Kujal, Petr; Škaroupková, Petra et al. (2018) Combined Inhibition of Soluble Epoxide Hydrolase and Renin-Angiotensin System Exhibits Superior Renoprotection to Renin-Angiotensin System Blockade in 5/6 Nephrectomized Ren-2 Transgenic Hypertensive Rats with Established Chronic Kidney Disease. Kidney Blood Press Res 43:329-349
Kodani, Sean D; Bhakta, Saavan; Hwang, Sung Hee et al. (2018) Identification and optimization of soluble epoxide hydrolase inhibitors with dual potency towards fatty acid amide hydrolase. Bioorg Med Chem Lett 28:762-768

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