This EHSC Facilities Core provides enhanced and subsidized access to facility cores that have been developed by the University of Rochester Medical Center. The University has provided both capital equipment costs as well as costs for technical and professional personnel and maintenance for these Cores. Because of the costs involved, such cores would not be possible to develop using only EHSC resources. These cores are accessible to all University investigators; however, by subsidizing these facilities or providing funds for EHSC members to use these facilities, the EHSC is able to provide access for its faculty at a reduced cost. Further, this can be provided under the same operating principles that exist for other EHSC Facility Cores, particularly with respect to criteria for use as defined in the Facility Cores Overview. Thus, the goal of this core is to provide Center members with access to a wide range of state-of-the-art technologies and methodologies that would not be possible to duplicate with Center funds or with limited individual research grants. The University-based Cores include the Plasma Source Mass Spectroscopy Laboratory, Flow Cytometry/Cell Sorting Core, Electron Microscope Imaging Core, Transgenic Core, Functional Genomics Center, Confocal Microscope Core, and MicroChemical Protein/Peptide Core. Each of these cores has a director and staff to support the core.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES001247-32
Application #
7311783
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
32
Fiscal Year
2006
Total Cost
$100,653
Indirect Cost
Name
University of Rochester
Department
Type
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Cory-Slechta, D A; Allen, J L; Conrad, K et al. (2018) Developmental exposure to low level ambient ultrafine particle air pollution and cognitive dysfunction. Neurotoxicology 69:217-231
Irwin, Jessica L; Yeates, Alison J; Mulhern, Maria S et al. (2018) Maternal Gestational Immune Response and Autism Spectrum Disorder Phenotypes at 7 Years of Age in the Seychelles Child Development Study. Mol Neurobiol :
Feiler, Marina Oktapodas; Patel, Deven; Li, Huiqi et al. (2018) The association between early-life relative telomere length and childhood neurodevelopment. Neurotoxicology 65:22-27
Duffney, Parker F; McCarthy, Claire E; Nogales, Aitor et al. (2018) Cigarette smoke dampens antiviral signaling in small airway epithelial cells by disrupting TLR3 cleavage. Am J Physiol Lung Cell Mol Physiol 314:L505-L513
Newman, Maureen R; Russell, Steven G; Schmitt, Christopher S et al. (2018) Multivalent Presentation of Peptide Targeting Groups Alters Polymer Biodistribution to Target Tissues. Biomacromolecules 19:71-84
Groves, Angela M; Johnston, Carl J; Williams, Jacqueline P et al. (2018) Role of Infiltrating Monocytes in the Development of Radiation-Induced Pulmonary Fibrosis. Radiat Res 189:300-311
Sobolewski, Marissa; Conrad, Katherine; Marvin, Elena et al. (2018) Endocrine active metals, prenatal stress and enhanced neurobehavioral disruption. Horm Behav 101:36-49
Klocke, Carolyn; Allen, Joshua L; Sobolewski, Marissa et al. (2018) Exposure to fine and ultrafine particulate matter during gestation alters postnatal oligodendrocyte maturation, proliferation capacity, and myelination. Neurotoxicology 65:196-206
McSorley, Emeir M; Yeates, Alison J; Mulhern, Maria S et al. (2018) Associations of maternal immune response with MeHg exposure at 28 weeks' gestation in the Seychelles Child Development Study. Am J Reprod Immunol 80:e13046
Duffney, Parker F; Falsetta, Megan L; Rackow, Ashley R et al. (2018) Key roles for lipid mediators in the adaptive immune response. J Clin Invest 128:2724-2731

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