Abstract

ADMINISTRATIVE CORE ABSTRACT The Administrative Core coordinates the use of Core resources by members of the Atlanta Vision Research Community (AVRC). The Administrative Core is managed by the Program Director (PD), the co-director, an administrative assistant, and the AVRC Core Advisory Committee. The Administrative Core leadership is responsive to the needs of the end-users, the NEI-R01 grant holders, in the context of and as governed by the best interests of innovative vision science in the AVRC and the overall missions of the NEI. The Administrative Core monitors and evaluates the performance of each resource / service Core, monitors the equitable use of the Cores, resolves conflicts over the use of Core resources, assists with the purchasing of Core supplies, manages the finances of the Cores, assists with NIH Public Access Compliance and institutional regulatory compliance, and performs many other tasks as outlined in the Specific Aims:
Aim 1. To assist with development and support of ARVC members? research.
Aim 2. To provide financial oversight and assistance to Core investigators.
Aim 3. To effectively administer the operations of the Core.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY006360-34
Application #
9780505
Study Section
Special Emphasis Panel (ZEY1)
Project Start
Project End
Budget Start
2019-09-01
Budget End
2020-08-31
Support Year
34
Fiscal Year
2019
Total Cost
Indirect Cost

  Institution

Name
Emory University
Department
Type
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322

  Publications

Liu, Yi-Hsia; Corbett, Clare; Klaska, Izabela P et al. (2018) Partial retinal photoreceptor loss in a transgenic mouse model associated with reduced levels of interphotoreceptor retinol binding protein (IRBP, RBP3). Exp Eye Res 172:54-65
Smith, Jesse M; Ward, Laura T; Townsend, Justin H et al. (2018) Rhegmatogenous Retinal Detachment in Children: Clinical Factors Predictive of Successful Surgical Repair. Ophthalmology :
Sankaran, Mathangi; Keeley, Patrick W; He, Li et al. (2018) Dopaminergic amacrine cell number, plexus density, and dopamine content in the mouse retina: Strain differences and effects of Bax gene disruption. Exp Eye Res 177:208-212
Allen, Rachael S; Motz, Cara T; Feola, Andrew et al. (2018) Long-Term Functional and Structural Consequences of Primary Blast Overpressure to the Eye. J Neurotrauma 35:2104-2116
Henneman, Nathaniel F; Foster, Stephanie L; Chrenek, Micah A et al. (2018) Xanthohumol Protects Morphology and Function in a Mouse Model of Retinal Degeneration. Invest Ophthalmol Vis Sci 59:45-53
Wang, Jiaxing; Li, Ying; King, Rebecca et al. (2018) Optic nerve regeneration in the mouse is a complex trait modulated by genetic background. Mol Vis 24:174-186
Kim, Moon K; Aung, Moe H; Mees, Lukas et al. (2018) Dopamine Deficiency Mediates Early Rod-Driven Inner Retinal Dysfunction in Diabetic Mice. Invest Ophthalmol Vis Sci 59:572-581
King, Rebecca; Li, Ying; Wang, Jiaxing et al. (2018) Genomic Locus Modulating IOP in the BXD RI Mouse Strains. G3 (Bethesda) 8:1571-1578
Chakraborty, Ranjay; Ostrin, Lisa A; Nickla, Debora L et al. (2018) Circadian rhythms, refractive development, and myopia. Ophthalmic Physiol Opt 38:217-245
Mui, Amanda M; Yang, Victoria; Aung, Moe H et al. (2018) Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina. PLoS One 13:e0192435

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