The Gene Regulation and Genetics Research Core has identified two dynamic focus groups within its membership. These think tanks include scientists with common interests of the role of the environment on human disease mechanisms. Members may participate in one or both focus groups. The hypothesis-based research that has emerged from focus group activities has served as a crucible for environmental scientists from a variety of disciplines. As a consequence of the Gene Regulation and Genetics Research Core, a diverse group of expert scientists has joined forces to understand the effects of environmental factors on gene regulation, cell signaling, and hormonal control networks that underpin the pathogenesis of human heart disease, diabetes, and cancer. For many investigators outside the environmental health sciences field, incorporation of an environmental component with the research objectives would most likely not have taken shape without the benefit of the Gene Regulation and Genetics Research Core activities and EHS Center membership. For faculty members within the IEHS, having the added advantage of EHS Center resources has enabled quantum strides in mechanism-based environmental health sciences research. The evidence of research productivity that is provided in this report, establishes the validity of the Gene Regulation and Genetics Research Core as a functional nexus for intellectual scientific exchange and research synergy. The core has successfully drawn together scientists with diverse interdisciplinary backgrounds and has stimulated working collaborations among investigators who enjoy ready access to shared EHS Center core facilities. The technical and material support in the EHS Center facility cores has enabled core members to apply state-of-the-art approaches to well-integrated studies examining the impact of the environment on molecular and cellular processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES006639-15
Application #
7597138
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
15
Fiscal Year
2008
Total Cost
$41,949
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
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
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
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
Wang, Guohui; Liu, Gang; Wang, Xiaogang et al. (2012) ERLIN2 promotes breast cancer cell survival by modulating endoplasmic reticulum stress pathways. BMC Cancer 12:225

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