CORE facilities accessible to investigators in vision and ophthalmology will be maintained. A modular organization structure will benefit research projects currently active by allowing access to shared equipment and expertise not otherwise available. New collaborative studies will be facilitated. Existing and new clinical research projects will be enhanced by biosatistical methodology necessary for prospective clinical trials. Proposed modules include BIOCHEMISTRY/IMMUNOLOGY (B/I), ELECTRON MICROSCOPY (EM), HISTOLOGY (H), RESEARCH PHOTOGRAPHY (RP), BIOSTATISTICS AND CLINICAL VISION RESEARCH (B/C) and CORE ADMINISTRATION (CA). Areas of investigation include retinal and choroidal diseases, corneal diseases, cataract, glaucoma, and strabismus, amblyopia, and visual processing. Specific disciplines that are brought to bear on these problems include behavioral studies, biochemistry, biostatistics, cell culture, clinical investigation, immunology, morphology, neurophysiology, and pathology. This project will elucidate basic mechanisms that underlie the function of the eye and visual system and apply this knowledge and other information to the solution of problems in vision and ophthalmology. Collaboration among investigators from the University of Washington and elsewhere will be promoted. Affirmative Action programs will be implemented, maintained, and strengthened. Principles of bioethics will be promulgated. Effectiveness of funding available on research project grants will be maximized.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
2P30EY001730-16
Application #
3102426
Study Section
Vision Research and Training Committee (VSN)
Project Start
1976-06-01
Project End
1996-05-31
Budget Start
1991-06-01
Budget End
1992-05-31
Support Year
16
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Bleckert, Adam; Zhang, Chi; Turner, Maxwell H et al. (2018) GABA release selectively regulates synapse development at distinct inputs on direction-selective retinal ganglion cells. Proc Natl Acad Sci U S A 115:E12083-E12090
Kerov, Vasily; Laird, Joseph G; Joiner, Mei-Ling et al. (2018) ?2?-4 Is Required for the Molecular and Structural Organization of Rod and Cone Photoreceptor Synapses. J Neurosci 38:6145-6160
Pepple, Kathryn L; Wilson, Leslie; Van Gelder, Russell N (2018) Comparison of Aqueous and Vitreous Lymphocyte Populations From Two Rat Models of Experimental Uveitis. Invest Ophthalmol Vis Sci 59:2504-2511
Lee, Cecilia S; Lee, Aaron Y; Akileswaran, Lakshmi et al. (2018) Determinants of Outcomes of Adenoviral Keratoconjunctivitis. Ophthalmology 125:1344-1353
Coates, Daniel R; Levi, Dennis M; Touch, Phanith et al. (2018) Foveal Crowding Resolved. Sci Rep 8:9177
Gordon, Sharona E; Munari, Mika; Zagotta, William N (2018) Visualizing conformational dynamics of proteins in solution and at the cell membrane. Elife 7:
Pedersen, Hilde R; Hagen, Lene A; Landsend, Erlend C S et al. (2018) Color Vision in Aniridia. Invest Ophthalmol Vis Sci 59:2142-2152
Chao, Cecilia; Akileswaran, Lakshmi; Cooke Bailey, Jessica N et al. (2018) Potential Role of Ocular Microbiome, Host Genotype, Tear Cytokines, and Environmental Factors in Corneal Infiltrative Events in Contact Lens Wearers. Invest Ophthalmol Vis Sci 59:5752-5761
Yu, Wan-Qing; El-Danaf, Rana N; Okawa, Haruhisa et al. (2018) Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories. Cell Rep 25:2017-2026.e3
Cabrera, Michelle T; Enyedi, Laura B; Ding, Leona et al. (2018) Sexual Harassment in Ophthalmology: A Survey Study. Ophthalmology :

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