The mission of the Microarray and Bioinformatics Facility Core (MBFC) is to enhance the research productivity of EHS Center members by providing advanced technologies and expertise that will enable the investigation of global gene expression events associated with environmentally induced diseases. High throughput microarray instrumentation and bioinformatics resources available through the MBFC enable Center members to investigate genome-wide responses to environmental toxins, as well as transcription events associated with disease progression. By providing instrumentation, services, and training dedicated to EHS Center members, the MBFC serves Center members in an efficient and responsive manner. Technology available through the MBFC enhances established research projects of numerous Center members. Additionally, the MBFC enables Center members to broaden their research programs by providing instrumentation and expertise that would otherwise be out of reach for many investigators. While extremely powerful for gene expression studies, microarray technology requires a significant investment in instrumentation, computational equipment and software, and experienced personnel. By providing a common resource for all EHS members, the MBFC overcomes this obstacle and allows investigators to efficiently complete microarray experiments and analyses in a quality manner; with a minimal investment of reagents and consumables. Since microarray technology is extremely helpful in monitoring gene expression changes due to environmental insult, the availability of MBFC resources will also be beneficial in the recruitment of new Center members. EHS Center members benefit greatly from the services available through the bioinformatics component of the MBFC. The MBFC microarray facility has high-throughput capacity and can quickly produce a large volume of data for a given research project. Efficient data management and analyses are essential for successful microarray analysis. The MBFC provides computational resources and expertise that enable Center members to effectively manage the large volume of data generated from a microarray experiment and translate the data into a biologically meaningful result.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES006639-12
Application #
7550912
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
12
Fiscal Year
2005
Total Cost
$319,750
Indirect Cost
Name
Wayne State University
Department
Type
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Nakajima, Kosei; Kho, Dhong Hyo; Yanagawa, Takashi et al. (2016) Galectin-3 Cleavage Alters Bone Remodeling: Different Outcomes in Breast and Prostate Cancer Skeletal Metastasis. Cancer Res 76:1391-402
Dombkowski, Alan A; Batista, Carlos E; Cukovic, Daniela et al. (2016) Cortical Tubers: Windows into Dysregulation of Epilepsy Risk and Synaptic Signaling Genes by MicroRNAs. Cereb Cortex 26:1059-71
Sanders, Matthew A; Madoux, Franck; Mladenovic, Ljiljana et al. (2015) Endogenous and Synthetic ABHD5 Ligands Regulate ABHD5-Perilipin Interactions and Lipolysis in Fat and Muscle. Cell Metab 22:851-60
Zhang, Yi; Chopp, Michael; Liu, Xian Shuang et al. (2015) MicroRNAs in the axon locally mediate the effects of chondroitin sulfate proteoglycans and cGMP on axonal growth. Dev Neurobiol 75:1402-19
Kim, Haejin; Johnson, Christine C (2014) The association between acetaminophen and asthma: is there anything to learn from the upper airways? Curr Opin Allergy Clin Immunol 14:25-8
Wu, Hongli; Yu, Yibo; David, Larry et al. (2014) Glutaredoxin 2 (Grx2) gene deletion induces early onset of age-dependent cataracts in mice. J Biol Chem 289:36125-39
D'Angelo, Rosemarie Chirco; Liu, Xu-Wen; Najy, Abdo J et al. (2014) TIMP-1 via TWIST1 induces EMT phenotypes in human breast epithelial cells. Mol Cancer Res 12:1324-33
Deranieh, Rania M; He, Quan; Caruso, Joseph A et al. (2013) Phosphorylation regulates myo-inositol-3-phosphate synthase: a novel regulatory mechanism of inositol biosynthesis. J Biol Chem 288:26822-33
Dzinic, Sijana H; Kaplun, Alexander; Li, Xiaohua et al. (2013) Identification of an intrinsic determinant critical for maspin subcellular localization and function. PLoS One 8:e74502
Moin, Kamiar; Sameni, Mansoureh; Victor, Bernadette C et al. (2012) 3D/4D functional imaging of tumor-associated proteolysis: impact of microenvironment. Methods Enzymol 506:175-94

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