NEI-supported investigators and their collaborators from Duke University (Duke), The University of North Carolina at Chapel Hill (UNC) and North Carolina State University (NCSU) request continuing support for a Core Grant for Vision Research. These researchers are from Departments of Ophthalmology, Medicine, Neurobiology, Pathology, and Cell Biology. Research areas covered by this group range from deciphering basic mechanisms of signal transduction to delineating functional organization of the visual cortex, and from identifying disease genes to finding effective therapy for specific eye disorders. For the past 20 years, we have used the NEI Core Grant to develop and update our resource modules, thus enhancing the capabilities of individual NEI-supported investigators and our institutions to conduct vision research. The Core Grant effectively provides (1) shared resources and services that are not readily supported by individual research grants and (2) an atmosphere conducive to sharing current techniques;both are critical to the successful research of individual investigators. Furthermore, the same infrastructure facilitates the participation of clinical ophthalmologists at Duke, and especially the development of clinician scientists. It thus supports and facilitates the process of translating the discoveries from basic research into new diagnostic and therapeutic applications directly related to human eye diseases. We request continuing support for three resource modules: Morphology/Image Processing Module, Proteomics/Molecular Biology Module, and Animal Models Module. Support of these shared resources, particularly in the present environment of newly-added research space and faculty at Duke, is vital to the creation of synergy that will give impetus to our vision research group in reaching a level of success that is greater than the sum of the individual investigator's expected achievements.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY005722-25
Application #
7866483
Study Section
Special Emphasis Panel (ZEY1-VSN (03))
Program Officer
Liberman, Ellen S
Project Start
1997-07-01
Project End
2011-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
25
Fiscal Year
2010
Total Cost
$826,770
Indirect Cost
Name
Duke University
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Willoughby, Alex S; Vuong, Vivian S; Cunefare, David et al. (2018) Choroidal Changes After Suprachoroidal Injection of Triamcinolone Acetonide in Eyes With Macular Edema Secondary to Retinal Vein Occlusion. Am J Ophthalmol 186:144-151
Soltanian-Zadeh, Somayyeh; Gong, Yiyang; Farsiu, Sina (2018) Information-Theoretic Approach and Fundamental Limits of Resolving Two Closely Timed Neuronal Spikes in Mouse Brain Calcium Imaging. IEEE Trans Biomed Eng 65:2428-2439
Smit-McBride, Zeljka; Nguyen, Johnny; Elliott, Garrett W et al. (2018) Effects of aging and environmental tobacco smoke exposure on ocular and plasma circulatory microRNAs in the Rhesus macaque. Mol Vis 24:633-646
Lobanova, Ekaterina S; Finkelstein, Stella; Li, Jing et al. (2018) Increased proteasomal activity supports photoreceptor survival in inherited retinal degeneration. Nat Commun 9:1738
Parolini, Barbara; Grewal, Dilraj S; Pinackatt, Sajish J et al. (2018) COMBINED AUTOLOGOUS TRANSPLANTATION OF NEUROSENSORY RETINA, RETINAL PIGMENT EPITHELIUM, AND CHOROID FREE GRAFTS. Retina 38 Suppl 1:S12-S22
Malek, Goldis; Busik, Julia; Grant, Maria B et al. (2018) Models of retinal diseases and their applicability in drug discovery. Expert Opin Drug Discov 13:359-377
Choudhary, Mayur; Safe, Stephen; Malek, Goldis (2018) Suppression of aberrant choroidal neovascularization through activation of the aryl hydrocarbon receptor. Biochim Biophys Acta Mol Basis Dis 1864:1583-1595
Toomey, Christopher B; Landowski, Michael; Klingeborn, Mikael et al. (2018) Effect of Anti-C5a Therapy in a Murine Model of Early/Intermediate Dry Age-Related Macular Degeneration. Invest Ophthalmol Vis Sci 59:662-673
Travis, Amanda M; Heflin, Stephanie J; Hirano, Arlene A et al. (2018) Dopamine-Dependent Sensitization of Rod Bipolar Cells by GABA Is Conveyed through Wide-Field Amacrine Cells. J Neurosci 38:723-732
Toomey, Christopher B; Johnson, Lincoln V; Bowes Rickman, Catherine (2018) Complement factor H in AMD: Bridging genetic associations and pathobiology. Prog Retin Eye Res 62:38-57

Showing the most recent 10 out of 437 publications