Administrative Core Program Lead: Kathrin Plath, PhD. The Reprogramming P01 Administrative Core will support all of the Projects of this Program. Kathrin Plath, Program PI, will be the Leader of the Administrative Core, with support from Drs. Zaret and Hochedlinger as Co-Investigators. This Core will enable the scientific components of the Program to interact by providing the structure and financial support for regular planning, data sharing, and evaluation of the research. The Core will be responsible for ensuring that the investigators act as a cohesive and interactive group by providing the planning and leadership required for regular and frequent interactions among the Projects. In addition, the Core will ensure efficient collaborations with the existing genomics, computational, and stem cell research centers at UCLA, UPenn, and MGH to provide optimal access to basic resources and infrastructure and leverage existing high-throughput sequencing, bioinformatics, and stem cell resources at the respective institutions. The Core will recruit additional investigators to the study of pluripotency and reprogramming through the distribution of pilot projects. The Administrative Core will also provide centralized grant administration, reporting to the NIGMS, budget oversight and management, and will ensure compliance with all governing IBC and ESCRO regulations and policies. Program interactions and oversight will be facilitated and evaluated by a Scientific Advisory Board composed of both internal and external experts in stem cell biology, reprogramming, and epigenetics. Through all of its activities, the Administrative Core will provide the infrastructure for the Program Project mechanism to enhance synergism and productivity in our thematically linked proposals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM099134-08
Application #
9692706
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2019-05-01
Budget End
2020-04-30
Support Year
8
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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Ohashi, Minori; Korsakova, Elena; Allen, Denise et al. (2018) Loss of MECP2 Leads to Activation of P53 and Neuronal Senescence. Stem Cell Reports 10:1453-1463
Kaeding, Kelsey E; Zaret, Kenneth S (2018) Microsatellite enhancers can be targeted to impair tumorigenesis. Genes Dev 32:991-992
Allison, Thomas F; Smith, Andrew J H; Anastassiadis, Konstantinos et al. (2018) Identification and Single-Cell Functional Characterization of an Endodermally Biased Pluripotent Substate in Human Embryonic Stem Cells. Stem Cell Reports 10:1895-1907
Sereti, Konstantina-Ioanna; Nguyen, Ngoc B; Kamran, Paniz et al. (2018) Analysis of cardiomyocyte clonal expansion during mouse heart development and injury. Nat Commun 9:754
Di Stefano, Bruno; Ueda, Mai; Sabri, Shan et al. (2018) Reduced MEK inhibition preserves genomic stability in naive human embryonic stem cells. Nat Methods 15:732-740
Sun, Fei; Chronis, Constantinos; Kronenberg, Michael et al. (2018) Promoter-Enhancer Communication Occurs Primarily within Insulated Neighborhoods. Mol Cell :
Bar-Nur, Ori; Gerli, Mattia F M; Di Stefano, Bruno et al. (2018) Direct Reprogramming of Mouse Fibroblasts into Functional Skeletal Muscle Progenitors. Stem Cell Reports 10:1505-1521
Xie, Yuan; Lowry, William E (2018) Manipulation of neural progenitor fate through the oxygen sensing pathway. Methods 133:44-53
Brumbaugh, Justin; Di Stefano, Bruno; Wang, Xiuye et al. (2018) Nudt21 Controls Cell Fate by Connecting Alternative Polyadenylation to Chromatin Signaling. Cell 172:629-631

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