? CORE A The overall goals of the Administrative Core of the Program Project Grant (PPG) are to provide general scientific, programmatic and fiscal leadership, facilitate lines of communication between the different researchers involved in the PPG, maintain coherence in the PPG's overall and long-range goals, coordinate data analysis and sharing, monitor human subjects issues and issues related to the use of vertebrate animals, and ensure that resources resulting from the PPG will benefit the scientific community. In the context of the above, the tasks of this Core include effective coordination of activities in the four Research Projects and the Bioinformatics Core to best achieve the overall goal of elucidating the mechanisms through which DNA damage drives important aspects of aging and age-related diseases and how certain genome maintenance genotypes found associated with extreme human longevity can preserve genome integrity over longer periods of time. Well-coordinated activities of the Projects and Cores will promote the mobilization of new human data sources and analysis techniques that will allow us to more specifically test the functional impact of DNA damage and its various end points, providing computational and statistical services to all members of the PPG as needed and providing access by the scientific community to the PPG's resources, information and technologies through the internet.

Public Health Relevance

? CORE A Core A will coordinate the research in this Program Project Grant (PPG), which has its members at different geographical locations. Through its Director, Dr. Jan Vijg, its Administrator, Ms. Stephanie Alfieri, and its Administrative Assistant, Ms. Yolanne Blake, Core A will organized the necessary teleconferences, meetings, exchange visits, etc., to hold this PPG together and create an atmosphere of collegiality, in which the focus is on collaboration, with results interpreted in an integrated manner across all research projects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
2P01AG017242-24
Application #
9718908
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2019-07-01
Budget End
2020-04-30
Support Year
24
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
081266487
City
Bronx
State
NY
Country
United States
Zip Code
10461
Hébert, Jean M; Vijg, Jan (2018) Cell Replacement to Reverse Brain Aging: Challenges, Pitfalls, and Opportunities. Trends Neurosci 41:267-279
Lau, Cia-Hin; Suh, Yousin (2018) In vivo epigenome editing and transcriptional modulation using CRISPR technology. Transgenic Res 27:489-509
Wiley, Christopher D; Schaum, Nicholas; Alimirah, Fatouma et al. (2018) Small-molecule MDM2 antagonists attenuate the senescence-associated secretory phenotype. Sci Rep 8:2410
Quispe-Tintaya, Wilber; Lee, Moonsook; Dong, Xiao et al. (2018) Bleomycin-induced genome structural variations in normal, non-tumor cells. Sci Rep 8:16523
Yu, Bo; Dong, Xiao; Gravina, Silvia et al. (2017) Genome-wide, Single-Cell DNA Methylomics Reveals Increased Non-CpG Methylation during Human Oocyte Maturation. Stem Cell Reports 9:397-407
Vijg, Jan; Dong, Xiao; Zhang, Lei (2017) A high-fidelity method for genomic sequencing of single somatic cells reveals a very high mutational burden. Exp Biol Med (Maywood) 242:1318-1324
Ogrodnik, Mikolaj; Miwa, Satomi; Tchkonia, Tamar et al. (2017) Cellular senescence drives age-dependent hepatic steatosis. Nat Commun 8:15691
Dong, Xiao; Zhang, Lei; Milholland, Brandon et al. (2017) Accurate identification of single-nucleotide variants in whole-genome-amplified single cells. Nat Methods 14:491-493
Olivieri, Fabiola; Capri, Miriam; Bonafè, Massimiliano et al. (2017) Circulating miRNAs and miRNA shuttles as biomarkers: Perspective trajectories of healthy and unhealthy aging. Mech Ageing Dev 165:162-170
Perrott, Kevin M; Wiley, Christopher D; Desprez, Pierre-Yves et al. (2017) Apigenin suppresses the senescence-associated secretory phenotype and paracrine effects on breast cancer cells. Geroscience 39:161-173

Showing the most recent 10 out of 253 publications