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

Choi, Hee Joo; Wang, Rui; Jakobs, Tatjana C (2018) Single-Cell Dissociation and Characterization in the Murine Retina and Optic Nerve. Methods Mol Biol 1695:311-334
Paschalis, Eleftherios I; Lei, Fengyang; Zhou, Chengxin et al. (2018) Permanent neuroglial remodeling of the retina following infiltration of CSF1R inhibition-resistant peripheral monocytes. Proc Natl Acad Sci U S A 115:E11359-E11368
Iglesias, Adriana I; Mishra, Aniket; Vitart, Veronique et al. (2018) Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nat Commun 9:1864
Chou, Jonathan C; Cousins, Clara C; Miller, John B et al. (2018) Fundus Densitometry Findings Suggest Optic Disc Hemorrhages in Primary Open-Angle Glaucoma Have an Arterial Origin. Am J Ophthalmol 187:108-116
Fan, Bao Jian; Chen, Xueli; Sondhi, Nisha et al. (2018) Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. Invest Ophthalmol Vis Sci 59:2495-2502
Okunuki, Yoko; Mukai, Ryo; Pearsall, Elizabeth A et al. (2018) Microglia inhibit photoreceptor cell death and regulate immune cell infiltration in response to retinal detachment. Proc Natl Acad Sci U S A 115:E6264-E6273
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

Showing the most recent 10 out of 296 publications