The Administrative Core is essential to the Center's success, responsible for the coordination and execution of the mentorship and career development plan for COBRE Project Leaders. In performing this function, the Administrative Core will monitor research progress, and assess the goals and accomplishments of COBRE investigators to ensure that they are on track to attain independent investigator status. It will provide administrative support for COBRE investigators, listen and respond to their needs, and, with the help of the Internal Advisory Committee (lAC), advocate for these needs within the institution. It will coordinate the function and capabilities of the Imaging and Behavioral Cores so that they meet the evolving needs of the COBRE investigators. It will communicate with the grants administrator to provide assistance to COBRE investigators in finding and applying for external funding. It will organize bimonthly meetings of COBRE investigators to share data and to identify potential areas for internal collaboration and synergy. The Administrative Core is also responsible for leading the review process for the COBRE pilot grants program and for faculty recruitment efforts. The Administrative Core will organize COBRE sponsored symposia that will be coordinated with the semi-annual external advisory committee (EAC) meetings. These symposia will offer COBRE investigators a chance to present and receive feedback on their own research findings, as well as an opportunity for them to interact with and hear presentations from leading pain researchers outside the institution. Finally, the Administrative Core will be responsible for the fiscal management of the Center and lead the assessment of all COBRE programs to ensure accomplishment of the Center's long-term goals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103643-03
Application #
8689111
Study Section
Special Emphasis Panel (ZRR1)
Project Start
Project End
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
3
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of New England
Department
Type
DUNS #
City
Biddeford
State
ME
Country
United States
Zip Code
04005
Gjelsvik, Kayla Jane; Follansbee, Taylor Leon; Ganter, Geoffrey Karl (2018) Bone Morphogenetic Protein Glass Bottom Boat (BMP5/6/7/8) and its receptor Wishful Thinking (BMPRII) are required for injury-induced allodynia in Drosophila. Mol Pain 14:1744806918802703
McLane, Virginia D; Kumar, Saurabh; Leeming, Reno et al. (2018) Morphine-potentiated cognitive deficits correlate to suppressed hippocampal iNOS RNA expression and an absent type 1 interferon response in LP-BM5 murine AIDS. J Neuroimmunol 319:117-129
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Remeniuk, Bethany; King, Tamara; Sukhtankar, Devki et al. (2018) Disease modifying actions of interleukin-6 blockade in a rat model of bone cancer pain. Pain 159:684-698
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Cao, Ling; Malon, Jennifer T (2018) Anti-nociceptive Role of CXCL1 in a Murine Model of Peripheral Nerve Injury-induced Neuropathic Pain. Neuroscience 372:225-236
Govea, Rosann M; Barbe, Mary F; Bove, Geoffrey M (2017) Group IV nociceptors develop axonal chemical sensitivity during neuritis and following treatment of the sciatic nerve with vinblastine. J Neurophysiol 118:2103-2109
Havelin, Joshua; Imbert, Ian; Sukhtankar, Devki et al. (2017) Mediation of Movement-Induced Breakthrough Cancer Pain by IB4-Binding Nociceptors in Rats. J Neurosci 37:5111-5122
Lei, Wei; Mullen, Nathan; McCarthy, Sarah et al. (2017) Heat-shock protein 90 (Hsp90) promotes opioid-induced anti-nociception by an ERK mitogen-activated protein kinase (MAPK) mechanism in mouse brain. J Biol Chem 292:10414-10428
Follansbee, Taylor L; Gjelsvik, Kayla J; Brann, Courtney L et al. (2017) Drosophila Nociceptive Sensitization Requires BMP Signaling via the Canonical SMAD Pathway. J Neurosci 37:8524-8533

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