The Administrative Core will provide the administrative infrastructure support necessary for the SNRP Scientific and Administrative Diredor and SNRP research teams to execute all activities in research, training and evaluation. The SNRP Administrative Diredor and Co-Diredor will strategically allocate the personnel and monetary resources of the Administrative Core to efficiently coordinate administration of budgets, assembly of reports, provide help in procurement for the specific research projects and support cores, as well as help to administer the Enrichment and Evaluation components within the overall SNRP. The Core also senses as a bureaucratic liaison, when necessary, between the Neurosdence Institute and other administrative branches of Morehouse School of Medicine. In addition, the Administrative Core will provide the logistic support necessary to successfully administer the External Advisory Committee and the Steering Committee. The experience and competence of members of the Administrative Core will foster a collegial research environment that encourages a fruitful interchange amongst a multidisdplinary team of scientists and educators.

Public Health Relevance

The success ofthe multi-component SNRP is critically dependent on effective administrative procedures to monitor progress and to guide the investigators, students and postdoctoral fellows in their professional development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54NS083932-02
Application #
8719201
Study Section
Special Emphasis Panel (ZNS1)
Project Start
Project End
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Morehouse School of Medicine
Department
Type
DUNS #
City
Atlanta
State
GA
Country
United States
Zip Code
30310
Piano, Ilaria; Baba, Kenkichi; Claudia Gargini et al. (2018) Heteromeric MT1/MT2 melatonin receptors modulate the scotopic electroretinogram via PKC? in mice. Exp Eye Res 177:50-54
Owino, Sharon; Sánchez-Bretaño, Aida; Tchio, Cynthia et al. (2018) Nocturnal activation of melatonin receptor type 1 signaling modulates diurnal insulin sensitivity via regulation of PI3K activity. J Pineal Res 64:
Huang, Yan; Leng, Tian-Dong; Inoue, Koichi et al. (2018) TRPM7 channels play a role in high glucose-induced endoplasmic reticulum stress and neuronal cell apoptosis. J Biol Chem 293:14393-14406
Morel, Caroline; Sherrin, Tessi; Kennedy, Norman J et al. (2018) JIP1-Mediated JNK Activation Negatively Regulates Synaptic Plasticity and Spatial Memory. J Neurosci 38:3708-3728
Klein, Pavel; Dingledine, Raymond; Aronica, Eleonora et al. (2018) Commonalities in epileptogenic processes from different acute brain insults: Do they translate? Epilepsia 59:37-66
Vann, Kiara T; Xiong, Zhi-Gang (2018) Acid-sensing ion channel 1 contributes to normal olfactory function. Behav Brain Res 337:246-251
Hardy, Jimmaline J; Mooney, Scott R; Pearson, Andrea N et al. (2017) Assessing the accuracy of blood RNA profiles to identify patients with post-concussion syndrome: A pilot study in a military patient population. PLoS One 12:e0183113
Liu, Mingli; Inoue, Koichi; Leng, Tiandong et al. (2017) ASIC1 promotes differentiation of neuroblastoma by negatively regulating Notch signaling pathway. Oncotarget 8:8283-8293
Hernandez-Encarnacion, Luisa; Sharma, Pankaj; Simon, Roger et al. (2017) Condition-specific transcriptional regulation of neuronal ion channel genes in brain ischemia. Int J Physiol Pathophysiol Pharmacol 9:192-201
Sánchez-Bretaño, Aída; Baba, Kenkichi; Janjua, Uzair et al. (2017) Melatonin partially protects 661W cells from H2O2-induced death by inhibiting Fas/FasL-caspase-3. Mol Vis 23:844-852

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