The Research Development Core of the Einstein- Nathan Shock Center (E-NSC) has leveraged resources to allow funding of 18 pilot and 3 feasibility (P&F) studies and 3 awards for development of Core technologies. Of these, 5 P&F studies led to NIH funding and 5 have pending funding (some with outstanding scores); in addition, 11 publications, resulted from studies funded before 2013. These P&F studies are designed to and will continue to enhance and support E-NSC science at Einstein and at the Brown University `mini-NSC'. We have expanded the Core to identify new faculty who have potential for `conversion' to aging research and provide continuous mentoring through grant applications and to assist junior faculty and investigators new to aging research. We also provide formal education in the biology of aging to recipients of P&F funding and anyone who wants to benefit from part or all of the formal graduate course. We believe that activities of this Core strengthen the E-NSC community, attract new investigators to aging-related research, and successfully promote new research endeavors in aging-related areas. Aging research is a key component of the Einstein scientific community, as shown by the Institution's commitment to provide up to $150,000 annually in matching funds for pilot grants. This will permit the funding of up to 3 to 5 P&F projects and 3 mini-P&Fs in any given year and provide smaller amounts to investigators in this next grant period for Research Resource Core use to obtain preliminary data before formal P&F application.

Public Health Relevance

The Research Development Core of the Einstein Nathan Shock Center is crucial for recruitment and `conversion' of junior or senior investigators to the field of aging research. The Core will provide pilot and feasibility funding, provide mentoring and help investigators with development of grant proposals. Indeed we exemplified our success in the previous grant period, and have ensured institutional support. This Core is crucial in ensuring that we transform the E-NSC to a national/international resource to facilitate the ultimate goal of delaying human aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG038072-10
Application #
9528368
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
10
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine, Inc
Department
Type
DUNS #
079783367
City
Bronx
State
NY
Country
United States
Zip Code
10461
Sathyan, Sanish; Barzilai, Nir; Atzmon, Gil et al. (2018) Genetic Insights Into Frailty: Association of 9p21-23 Locus With Frailty. Front Med (Lausanne) 5:105
Amengual, Jaume; Guo, Liang; Strong, Alanna et al. (2018) Autophagy Is Required for Sortilin-Mediated Degradation of Apolipoprotein B100. Circ Res 122:568-582
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394
Bejarano, Eloy; Murray, John W; Wang, Xintao et al. (2018) Defective recruitment of motor proteins to autophagic compartments contributes to autophagic failure in aging. Aging Cell :e12777
Gong, Zhenwei; Tasset, Inmaculada; Diaz, Antonio et al. (2018) Humanin is an endogenous activator of chaperone-mediated autophagy. J Cell Biol 217:635-647
Hui, Ken Y; Fernandez-Hernandez, Heriberto; Hu, Jianzhong et al. (2018) Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Sci Transl Med 10:
Caballero, Benjamin; Wang, Yipeng; Diaz, Antonio et al. (2018) Interplay of pathogenic forms of human tau with different autophagic pathways. Aging Cell 17:
Gubbi, Sriram; Quipildor, Gabriela Farias; Barzilai, Nir et al. (2018) 40 YEARS of IGF1: IGF1: the Jekyll and Hyde of the aging brain. J Mol Endocrinol 61:T171-T185
Hudgins, Adam D; Tazearslan, Cagdas; Tare, Archana et al. (2018) Age- and Tissue-Specific Expression of Senescence Biomarkers in Mice. Front Genet 9:59
Justice, Jamie N; Ferrucci, Luigi; Newman, Anne B et al. (2018) A framework for selection of blood-based biomarkers for geroscience-guided clinical trials: report from the TAME Biomarkers Workgroup. Geroscience 40:419-436

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