A 5-year renewal of the Center for Environmental Genetics (CEG) is proposed. The unifying research focus of the Center is to study the impact of genetic diversity on individual susceptibility to toxic environmental agents. The CEG has a long history (10 years) and broad range of accomplishments in environmental genetics, and this research focus has become increasingly important in environmental health science research.
The Specific Aims are:
Aim 1. Facilitate the identification of susceptibility genes that may interact with environmental agents to induce complex diseases such as type II diabetes, asthma, intracranial strokes, hypertension, and lung cancer.
Aim 2. Facilitate studies to analyze the impact of genetic variants of known genes on individual response to specific environmental agents such as airborne particulates, environmental estrogens, metals, and ionizing radiation.
Aim 3. Facilitate studies to examine signal transduction pathways induced by response to environmental agents whose exposure is associated with a disease or tissue/cellular damage.
Aim 4. Encourage investigators to direct their research toward a focus in environmental genetics.
Aim 5. Develop a partnership with the surrounding community to provide education, awareness of environmental health issues, and public policies through the Community Outreach and Education Program (COEP) Core. We have four highly successful Research Cores that have been in existence for at least 5 year, Ecogenetics, Genetic Toxicology, Respiratory Toxicology, and Signal Transduction. The Human Populations Research Core was initiated to reflect our emphasis to perform human studies related to our research focus. In this renewal application, we will respond to new advances in genomics, proteomics and bioinformatics, and genetic epidemiology by modifying the Facilities and Services Cores to offer the following services to CEG members: 1) Bioinformatic data analysis procedures, 2) Microarray expression and protein analysis methodology, and 3) Procedures for conducting human populations studies. The goal of the Center is to understand and thus, either prevent or intervene in complex human disease by determining the role of gene- environment interaction in the development of diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES006096-12
Application #
6620614
Study Section
Environmental Health Sciences Review Committee (EHS)
Program Officer
Collman, Gwen W
Project Start
1992-06-15
Project End
2007-03-31
Budget Start
2003-04-01
Budget End
2004-03-31
Support Year
12
Fiscal Year
2003
Total Cost
$1,463,403
Indirect Cost
Name
University of Cincinnati
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Isiugo, Kelechi; Newman, Nicholas; Jandarov, Roman et al. (2018) Assessing the accuracy of commercially available gas sensors for the measurement of ambient ozone and nitrogen dioxide. J Occup Environ Hyg 15:782-791
Li, Tao; Hu, Rong; Chen, Zi et al. (2018) Fine particulate matter (PM2.5): The culprit for chronic lung diseases in China. Chronic Dis Transl Med 4:176-186
Zhang, Xue; Biagini Myers, Jocelyn M; Burleson, J D et al. (2018) Nasal DNA methylation is associated with childhood asthma. Epigenomics 10:629-641
Haynes, Erin N; Sucharew, Heidi; Hilbert, Timothy J et al. (2018) Impact of air manganese on child neurodevelopment in East Liverpool, Ohio. Neurotoxicology 64:94-102
Bermúdez, Mei-Ling; Skelton, Matthew R; Genter, Mary Beth (2018) Intranasal carnosine attenuates transcriptomic alterations and improves mitochondrial function in the Thy1-aSyn mouse model of Parkinson's disease. Mol Genet Metab 125:305-313
Reigle, Beverly S; Zhang, Bin (2018) Women's Rehabilitation Experiences Following Breast Cancer Surgery. Rehabil Nurs 43:195-200
Whitt, Jordan; Woo, Vivienne; Lee, Patrick et al. (2018) Disruption of Epithelial HDAC3 in Intestine Prevents Diet-Induced Obesity in Mice. Gastroenterology 155:501-513
Uno, Shigeyuki; Nebert, Daniel W; Makishima, Makoto (2018) Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice. Food Chem Toxicol 113:73-82
Vuong, Ann M; Yolton, Kimberly; Poston, Kendra L et al. (2018) Childhood polybrominated diphenyl ether (PBDE) exposure and executive function in children in the HOME Study. Int J Hyg Environ Health 221:87-94
Lee, Alison G; Le Grand, Blake; Hsu, Hsiao-Hsien Leon et al. (2018) Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects. Respir Res 19:76

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