Abstract

- Administrative core This proposal describes the Administrative core for the Massachusetts Eye and Ear Infirmary (MEEI) P30 Center Core Grant for Vision Research. The purpose of the Administrative core is to 1) ensure equitable usage of the service cores; 2) manage the P30 budget and resources; 3) integrate core resources and coordinate activity among the core services; and 4) evaluate the core services and revise as user needs evolve. The administrative core is directed by the PI, Dr. Wiggs, with assistance from the resource core directors (Drs. Pierce, Sobrin, and Bujakowska), an Internal Advisory committee that includes the resource core directors and other senior staff, and an External Advisory Committee that includes the resource core directors as well as the PIs of the other two HMS P30s (Drs. Livingstone and Argueso).

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
5P30EY014104-17
Application #
10017264
Study Section
Special Emphasis Panel (ZEY1)
Project Start
2002-09-01
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
17
Fiscal Year
2020
Total Cost
Indirect Cost

  Institution

Name
Massachusetts Eye and Ear Infirmary
Department
Type
DUNS #
073825945
City
Boston
State
MA
Country
United States
Zip Code
02114

  Publications

Cousins, Clara C; Chou, Jonathan C; Greenstein, Scott H et al. (2018) Resting nailfold capillary blood flow in primary open-angle glaucoma. Br J Ophthalmol :
Gupta, Priya R; Pendse, Nachiket; Greenwald, Scott H et al. (2018) Ift172 conditional knock-out mice exhibit rapid retinal degeneration and protein trafficking defects. Hum Mol Genet 27:2012-2024
Laíns, Inês; Kelly, Rachel S; Miller, John B et al. (2018) Human Plasma Metabolomics Study across All Stages of Age-Related Macular Degeneration Identifies Potential Lipid Biomarkers. Ophthalmology 125:245-254
Shiga, Yukihiro; Akiyama, Masato; Nishiguchi, Koji M et al. (2018) Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma. Hum Mol Genet 27:1486-1496
Khawaja, Anthony P; Cooke Bailey, Jessica N; Wareham, Nicholas J et al. (2018) Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. Nat Genet 50:778-782
Tsoka, Pavlina; Matsumoto, Hidetaka; Maidana, Daniel E et al. (2018) Effects of BNN27, a novel C17-spiroepoxy steroid derivative, on experimental retinal detachment-induced photoreceptor cell death. Sci Rep 8:10661
King, Rebecca; Struebing, Felix L; Li, Ying et al. (2018) Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma. PLoS Genet 14:e1007145
Fernandez-Godino, Rosario; Pierce, Eric A (2018) C3a triggers formation of sub-retinal pigment epithelium deposits via the ubiquitin proteasome pathway. Sci Rep 8:9679
Zhu, Ying; Pappas, Anthony C; Wang, Rui et al. (2018) Ultrastructural Morphology of the Optic Nerve Head in Aged and Glaucomatous Mice. Invest Ophthalmol Vis Sci 59:3984-3996
Struebing, Felix L; King, Rebecca; Li, Ying et al. (2018) Genomic loci modulating retinal ganglion cell death following elevated IOP in the mouse. Exp Eye Res 169:61-67

Showing the most recent 10 out of 296 publications