The Genetic Susceptibility Core will combine state-of-the-art research laboratory facilities with population-based epidemiology to improve our understanding of the mechanisms of disease causation and develop strategies for prevention and intervention that can be applied on a population level. The identification of genes that influence the outcomes of exposures to toxic substances in the environment represents an important advance in toxicology and environmental health. Whereas public health researchers traditionally measured average risk of disease for all members of a population, genetic markers can now be used to identify persons who are highly susceptible to environmental hazards. Genetic susceptibility may be especially important for determining the consequences of chronic low-level exposures to environmental radiation and chemical pollutants found in air and water (Vineis and Martone, 1995). The discovery of genetic markers of susceptibility promises not only to increase our knowledge of the health consequences of low-level environmental hazards, but also to provide a more rational basis for risk assessment and public policy (Khoury and Wagner, 1995). The Genetic Susceptibility Core will be established by the UNC Center on Environmental Health and Susceptibility and will have as its aims to: 1) Support and expand collaborative research in genetic susceptibility utilizing state-of-the-art laboratory methods and rigorously designed epidemiologic approaches. 2) Bring together, on a regular basis, researchers in mechanisms of DNA damage and repair and epidemiologists involved in field studies of gene/environment interactions in carcinogenesis and atherogenesis. 3) Promote the integration of molecular genetics into areas of cardiovascular, reproductive and developmental research. 4) Foster dialogue regarding policy implications of genetic-testing technology and results of genetic research. 5) Stimulate collaborations by award of seed grants for pilot studies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
1P30ES010126-01A1
Application #
6458264
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
2001-04-01
Project End
2005-03-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Marrus, Natasha; Eggebrecht, Adam T; Todorov, Alexandre et al. (2018) Walking, Gross Motor Development, and Brain Functional Connectivity in Infants and Toddlers. Cereb Cortex 28:750-763
Burbank, Allison J; Duran, Charity G; Pan, Yinghao et al. (2018) Gamma tocopherol-enriched supplement reduces sputum eosinophilia and endotoxin-induced sputum neutrophilia in volunteers with asthma. J Allergy Clin Immunol 141:1231-1238.e1
Yu, Xiao; Fuller, Ashley M; Blackmon, Richard et al. (2018) Quantification of the Effect of Toxicants on the Intracellular Kinetic Energy and Cross-Sectional Area of Mammary Epithelial Organoids by OCT Fluctuation Spectroscopy. Toxicol Sci 162:234-240
Rappazzo, Kristen M; Warren, Joshua L; Davalos, Angel D et al. (2018) Maternal residential exposure to specific agricultural pesticide active ingredients and birth defects in a 2003-2005 North Carolina birth cohort. Birth Defects Res :
Estes, Annette; Munson, Jeffrey; John, Tanya St et al. (2018) Parent Support of Preschool Peer Relationships in Younger Siblings of Children with Autism Spectrum Disorder. J Autism Dev Disord 48:1122-1132
McClain, Kathleen M; Bradshaw, Patrick T; Khankari, Nikhil K et al. (2018) Fish/shellfish intake and the risk of head and neck cancer. Eur J Cancer Prev :
DeBono, Nathan L; Robinson, Whitney R; Lund, Jennifer L et al. (2018) Race, Menopausal Hormone Therapy, and Invasive Breast Cancer in the Carolina Breast Cancer Study. J Womens Health (Larchmt) 27:377-386
Swanson, Meghan R; Shen, Mark D; Wolff, Jason J et al. (2018) Naturalistic Language Recordings Reveal ""Hypervocal"" Infants at High Familial Risk for Autism. Child Dev 89:e60-e73
van Bömmel, Alena; Love, Michael I; Chung, Ho-Ryun et al. (2018) coTRaCTE predicts co-occurring transcription factors within cell-type specific enhancers. PLoS Comput Biol 14:e1006372
McNeill, Robert S; Stroobant, Emily E; Smithberger, Erin et al. (2018) PIK3CA missense mutations promote glioblastoma pathogenesis, but do not enhance targeted PI3K inhibition. PLoS One 13:e0200014

Showing the most recent 10 out of 1900 publications