The Pluripotent Stem Cell Core (Core A) is located in the Paul P. Coverdell Center for Biomedical and Health Sciences, adjacent to the Palton lab and the Administrative Core (Core C) for the Program. The Core will have two Specific Aims: 1. Stem cell resources and technical support for the Program's Projects This involves culturing of pluripotent cells, their differentiation into lineages of the three embryonic germ layers and distribution to the three Projects that make up the Program. Cells will be subject to stringent quality control by the Core. The Core will provide analytical and technical support for the Projects, will coordinate purchasing of reagents for the Program and will act as a repository for reagents and materials generated by the Program. The Core will also generate key reagents and modified cell lines for general use. 2.
This aim will provide a similar range of services to that described in Aim 1 but these will be specifically directed towards assisting the Pilot Projects. Additional support will be available on a more limited basis to investigators in the Southeast region with meritorious projects that provide additional synergy to the Program. Over the last 5 years the Core has developed technologies and expertise that will be essential for the success ofthe Projects and Pilot Projects in the upcoming renewal period. In addition to providing continuity of Project support, the Core will continually evolve by introducing new technologies that will accelerate progress.

Public Health Relevance

Pluripotent stem cells are at the forefront of a new revolution in biomedical research and serve important roles in drug screening, disease modeling and regenerative medicine. This Core is focused on providing support for important research on the basic understanding of pluripotent stem cells so that in the future, they can be more effectively and safely used in clinical applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
2P01GM085354-06
Application #
8641831
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-02-28
Support Year
6
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Georgia
Department
Type
DUNS #
City
Athens
State
GA
Country
United States
Zip Code
30602
Sima, Jiao; Bartlett, Daniel A; Gordon, Molly R et al. (2018) Bacterial artificial chromosomes establish replication timing and sub-nuclear compartment de novo as extra-chromosomal vectors. Nucleic Acids Res 46:1810-1820
Singh, Amar M; Dalton, Stephen (2018) What Can 'Brown-ing' Do For You? Trends Endocrinol Metab 29:349-359
Dixon, Jesse R; Xu, Jie; Dileep, Vishnu et al. (2018) Integrative detection and analysis of structural variation in cancer genomes. Nat Genet 50:1388-1398
Xu, Chenhuan; Corces, Victor G (2018) Genome-Wide Mapping of Protein-DNA Interactions on Nascent Chromatin. Methods Mol Biol 1766:231-238
Dileep, Vishnu; Gilbert, David M (2018) Single-cell replication profiling to measure stochastic variation in mammalian replication timing. Nat Commun 9:427
Colunga, Thomas; Dalton, Stephen (2018) Building Blood Vessels with Vascular Progenitor Cells. Trends Mol Med 24:630-641
Wang, Tao; Holt, Matthew V; Young, Nicolas L (2018) The histone H4 proteoform dynamics in response to SUV4-20 inhibition reveals single molecule mechanisms of inhibitor resistance. Epigenetics Chromatin 11:29
Xu, Chenhuan; Corces, Victor G (2018) Nascent DNA methylome mapping reveals inheritance of hemimethylation at CTCF/cohesin sites. Science 359:1166-1170
Marchal, Claire; Sasaki, Takayo; Vera, Daniel et al. (2018) Genome-wide analysis of replication timing by next-generation sequencing with E/L Repli-seq. Nat Protoc 13:819-839
Rivera-Mulia, Juan Carlos; Schwerer, Hélène; Besnard, Emilie et al. (2018) Cellular senescence induces replication stress with almost no affect on DNA replication timing. Cell Cycle 17:1667-1681

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