In this resubmission of our renewal application, funding is requested for continued support ofthe NIEHS Center for Environmental Health Sciences (CEHS) at the Massachusetts Institute of Technology (IVIIT). The overall focus ofthe MIT CEHS is to understand how toxic environmental agents perturb biological systems and to determine how such perturbations may affect human health. The MIT CEHS is led by Professor Leona Samson. The current CEHS membership consists of 36 members derived from a total of eight MIT departments in both the Schools of Science and Engineering, plus three members from Harvard University, specifically the Harvard School of Public Health (HSPH) and the Harvard Medical School (HMS). The MIT departments are Biology, Chemistry, Biological Engineering, Chemical Engineering, Civil and Environmental Engineering, Mechanical Engineering, Nuclear Science and Engineering, Electrical Engineering and Computer Science;the HSPH department is Epidemiology, and the HMS faculty are based at the Brigham and Women's Hospital and the Massachusetts General Hospital. The current Facilities Cores are (i) the Bioanalytical Facilities Core, (ii) the Genomics and Imaging Facilities Core, (iii) the Animal Models Facilities Core, (iv) the Integrative Health Sciences Facilities Core. The services available through the four Facilities Cores include sophisticated mass spectrometry, accelerator mass spectrometry, transcriptional profiling, Solexa sequencing, bioinformatics and robotics, transgenic and knock out animal production, pathology services, state-of-the-art microscopy and imaging, and clinical services for translational research. Other units include the Administrative Core, the Pilot Project Program, the Global Environmental Health Science Program, and the Community Outreach and Education Core (COEC). The Center sponsors a wide variety of enrichment activities including specific seminars in the Biological Engineering departmental seminar series, two CEHS specific seminar series, an annual Poster Session, and several other mechanisms designed to nurture interactions among CEHS members and to promote the activities ofthe CEHS at MIT.

Public Health Relevance

The overall mission ofthe MIT CEHS is to contribute to decreasing the burden of environmentally induced disease in human populations. Our mission is approached by studying the biological effects of, and the processes of exposure to, chemical, physical and biological environmental agents with the goals of understanding and predicting how such exposures affect human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES002109-34
Application #
8650828
Study Section
Environmental Health Sciences Review Committee (EHS)
Program Officer
Reinlib, Leslie J
Project Start
1997-04-01
Project End
2016-03-31
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
34
Fiscal Year
2014
Total Cost
$1,568,692
Indirect Cost
$468,692
Name
Massachusetts Institute of Technology
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
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 :
Rothenberg, Daniel A; Taliaferro, J Matthew; Huber, Sabrina M et al. (2018) A Proteomics Approach to Profiling the Temporal Translational Response to Stress and Growth. iScience 9:367-381
Brody, Yehuda; Kimmerling, Robert J; Maruvka, Yosef E et al. (2018) Quantification of somatic mutation flow across individual cell division events by lineage sequencing. Genome Res 28:1901-1918

Showing the most recent 10 out of 970 publications