The Administrative Core provides the umbrella for effective operation of the COBRE program. Nearly every activity will be coordinated from this Core. The overall objective of the Administrative Core is to provide an efficient and effective organizational structure in which to ensure good management, integration, and oversight of our COBRE program.
The specific aims of this facility are: 1. To provide skilled personnel for effective fiscal and administrative management of all components of the COBRE program. 2. To provide vision and guidance to each junior investigator in relation to programmatic and career development. 3. To assess the outcomes and success of our tailored team-mentoring plan. 4. To review the scientific accomplishments of the junior investigators and the status of the overall research program with members ofthe Internal and External Advisory Committees and to construct effective means to resolve weaknesses. 5. To provide the interface with NCRR program staff for optimal achievement of program development and long-term goals of this COBRE program.

Public Health Relevance

This Core will provide oversight for the mentoring that is critical to the success of this program. In addition, it will provide critical advice to our investigators on budgets, grant writing and other administrative activities that are critical for our investigators to develop into independently funded researchers.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103629-02
Application #
8517155
Study Section
Special Emphasis Panel (ZRR1-RI-B)
Project Start
Project End
Budget Start
2013-06-01
Budget End
2014-05-31
Support Year
2
Fiscal Year
2013
Total Cost
$509,462
Indirect Cost
$170,949
Name
Tulane University
Department
Type
DUNS #
053785812
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Guo, Weichao; Saito, Shigeki; Sanchez, Cecilia G et al. (2017) TGF-?1 stimulates HDAC4 nucleus-to-cytoplasm translocation and NADPH oxidase 4-derived reactive oxygen species in normal human lung fibroblasts. Am J Physiol Lung Cell Mol Physiol 312:L936-L944
Liao, Wenjuan; Liu, Hongbing; Zhang, Yiwei et al. (2017) Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid Metabolism. Sci Rep 7:9020
Jazwinski, S Michal; Kim, Sangkyu (2017) Metabolic and Genetic Markers of Biological Age. Front Genet 8:64
Palozola, Katherine C; Donahue, Greg; Liu, Hong et al. (2017) Mitotic transcription and waves of gene reactivation during mitotic exit. Science 358:119-122
Jazwinski, S Michal; Jiang, James C; Kim, Sangkyu (2017) Adaptation to metabolic dysfunction during aging: Making the best of a bad situation. Exp Gerontol :
Motherwell, Jessica M; Azimi, Mohammad S; Spicer, Kristine et al. (2017) Evaluation of Arteriolar Smooth Muscle Cell Function in an Ex Vivo Microvascular Network Model. Sci Rep 7:2195
Sweat, Richard S; Sloas, David C; Stewart, Scott A et al. (2017) Aging is associated with impaired angiogenesis, but normal microvascular network structure, in the rat mesentery. Am J Physiol Heart Circ Physiol 312:H275-H284
Kim, Sangkyu; Myers, Leann; Wyckoff, Jennifer et al. (2017) The frailty index outperforms DNA methylation age and its derivatives as an indicator of biological age. Geroscience 39:83-92
Azimi, Mohammad S; Motherwell, Jessica M; Murfee, Walter L (2017) An Ex Vivo Method for Time-Lapse Imaging of Cultured Rat Mesenteric Microvascular Networks. J Vis Exp :
Molinski, Steven V; Shahani, Vijay M; MacKinnon, Stephen S et al. (2017) Computational proteome-wide screening predicts neurotoxic drug-protein interactome for the investigational analgesic BIA 10-2474. Biochem Biophys Res Commun 483:502-508

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