The MIT Center for Environmental Health Sciences is a multidisciplinary research organization which has taken as its primary mission the discovery of the relationship between human exposure to environmental chemicals, mutation, and genetic diseases such as cancer and birth defects. The Center faculty are integrated in six multidisciplinary research programs which address the sources, environmental movement and genetic effects of chemicals borne to humans by food, air and water. One of these, the Superfund Basic Research Program, involves study of chemical exposure and genetic change in the population of the nearby Aberjona River Basin. This major effort began with four years of public outreach activities and which continue in a public education program to explain the basis, potential value and limitations of our studies in this community in which many of our faculty and staff reside. The MIT academic departments represented by Center faculty include Toxicology (7), Civil Engineering (7), Chemical Engineering (5), Mechanical Engineering (7), Chemistry (2), Biology (2) and Earth and Planetary Sciences (1). Joining these several disciplines together are the shared Core Laboratories in Analytical Chemistry and Toxicology which permit analysis, testing and identification of the most important human mutagens in complex environmental mixtures. Key technologies developed at the Center include means to measure and identify chemicals in human tissue proteins and measurement of mutations and mutational spectra in human cells or tissues. These technologies now drive a transmutation of present core facilities and faculty research toward direct measurement of chemicals and patterns of genetic changes in human cells and tissues. Through these studies we hope to fulfill our primary mission and make a contribution to public health that will justify public support of work.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
3P30ES002109-19S1
Application #
2660568
Study Section
Special Emphasis Panel (SRC)
Project Start
1978-07-01
Project End
1999-03-31
Budget Start
1997-04-01
Budget End
1998-03-31
Support Year
19
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
Organized Research Units
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Wadduwage, Dushan N; Kay, Jennifer; Singh, Vijay Raj et al. (2018) Automated fluorescence intensity and gradient analysis enables detection of rare fluorescent mutant cells deep within the tissue of RaDR mice. Sci Rep 8:12108
Jackson, Megan N; Oh, Seokjoon; Kaminsky, Corey J et al. (2018) Strong Electronic Coupling of Molecular Sites to Graphitic Electrodes via Pyrazine Conjugation. J Am Chem Soc 140:1004-1010
Chen, Percival Yang-Ting; Funk, Michael A; Brignole, Edward J et al. (2018) Disruption of an oligomeric interface prevents allosteric inhibition of Escherichia coli class Ia ribonucleotide reductase. J Biol Chem 293:10404-10412
Lieberman, Mia T; Madden, Carolyn M; Ma, Eric J et al. (2018) Evaluation of 6 Methods for Aerobic Bacterial Sanitization of Smartphones. J Am Assoc Lab Anim Sci 57:24-29
Edington, Collin D; Chen, Wen Li Kelly; Geishecker, Emily et al. (2018) Interconnected Microphysiological Systems for Quantitative Biology and Pharmacology Studies. Sci Rep 8:4530
Mannion, Anthony; Shen, Zeli; Feng, Yan et al. (2018) Gamma-glutamyltranspeptidase expression by Helicobacter saguini, an enterohepatic Helicobacter species isolated from cotton top tamarins with chronic colitis. Cell Microbiol :e12968
Tajai, Preechaya; Fedeles, Bogdan I; Suriyo, Tawit et al. (2018) An engineered cell line lacking OGG1 and MUTYH glycosylases implicates the accumulation of genomic 8-oxoguanine as the basis for paraquat mutagenicity. Free Radic Biol Med 116:64-72
Neumann, Wilma; Nolan, Elizabeth M (2018) Evaluation of a reducible disulfide linker for siderophore-mediated delivery of antibiotics. J Biol Inorg Chem 23:1025-1036
Pereira, Gavin C; Sanchez, Laura; Schaughency, Paul M et al. (2018) Properties of LINE-1 proteins and repeat element expression in the context of amyotrophic lateral sclerosis. Mob DNA 9:35
Wang, Lianrong; Jiang, Susu; Deng, Zixin et al. (2018) DNA phosphorothioate modification - a new multi-functional epigenetic system in bacteria. FEMS Microbiol Rev :

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