This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The Administrative Core is directed by the Principal Investigator (PI) and includes two office staff members (one 0.9 FTE and one 0.7 FTE) who oversee all administrative activities including accounting, travel arrangements, meetings, Steering and External Advisory Committee (EAC) activities, summer student programs, budgets, the INBRE website, and other activities. During the 01 year, all of these activities were carried out according to plan. The Steering Committee met twice independently as well as once in conjunction with an EAC meeting during the 01 year. The EAC met once in the fall of the 01 year and a second meeting is scheduled for June 10 during the final month of the 01 year. Investigators of the ten INBRE research projects have presented, or will present at the June EAC meeting, to each committee at least once during the 01 year. The PI has carried out regular visits to the laboratories of each of the 10 INBRE project scientists. A report has been commissioned by the American Association for the Advancement of Science (AAAS) Research Competitiveness Program to provide an evaluation of the progress of the INBRE and the implementation of the INBRE plan at INBRE undergraduate institutions. The AAAS site visit was carried out April 25-28 of the 01 year. The Administrative Core also supports a project evaluator to conduct ongoing evaluations, including an assessment of biomedical research capacity at the INBRE undergraduate institutions. In the 01 year, this evaluation has been primarily formative to ensure that the impact of the project can be monitored appropriately in subsequent years.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016478-06
Application #
7381656
Study Section
Special Emphasis Panel (ZRR1-RI-7 (02))
Project Start
2006-05-01
Project End
2007-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
6
Fiscal Year
2006
Total Cost
$573,026
Indirect Cost
Name
University of Oklahoma Health Sciences Center
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
878648294
City
Oklahoma City
State
OK
Country
United States
Zip Code
73117
Hu, Zihua; Jiang, Kaiyu; Frank, Mark Barton et al. (2018) Modeling Transcriptional Rewiring in Neutrophils Through the Course of Treated Juvenile Idiopathic Arthritis. Sci Rep 8:7805
Wetherill, Marianna S; Williams, Mary B; Gray, Karen A (2017) SNAP-Based Incentive Programs at Farmers' Markets: Adaptation Considerations for Temporary Assistance for Needy Families (TANF) Recipients. J Nutr Educ Behav 49:743-751.e1
Hannafon, Bethany N; Trigoso, Yvonne D; Calloway, Cameron L et al. (2016) Plasma exosome microRNAs are indicative of breast cancer. Breast Cancer Res 18:90
Wilson, Kevin R; Cannon-Smith, Desiray J; Burke, Benjamin P et al. (2016) Synthesis and structural studies of two pyridine-armed reinforced cyclen chelators and their transition metal complexes. Polyhedron 114:118-127
Trigoso, Yvonne D; Evans, Russell C; Karsten, William E et al. (2016) Cloning, Expression, and Purification of Histidine-Tagged Escherichia coli Dihydrodipicolinate Reductase. PLoS One 11:e0146525
Khandaker, Morshed; Riahinezhad, Shahram; Sultana, Fariha et al. (2016) Peen treatment on a titanium implant: effect of roughness, osteoblast cell functions, and bonding with bone cement. Int J Nanomedicine 11:585-94
Hu, Zihua; Jiang, Kaiyu; Frank, Mark Barton et al. (2016) Complexity and Specificity of the Neutrophil Transcriptomes in Juvenile Idiopathic Arthritis. Sci Rep 6:27453
Seong, Jaehoon; Jeong, Woowon; Smith, Nataliya et al. (2015) Hemodynamic effects of long-term morphological changes in the human carotid sinus. J Biomech 48:956-62
Day, Michael W; Jackson, Lydgia A; Akins, Darrin R et al. (2015) Whole-Genome Sequences of the Archetypal K1 Escherichia coli Neonatal Isolate RS218 and Contemporary Neonatal Bacteremia Clinical Isolates SCB11, SCB12, and SCB15. Genome Announc 3:
Hannafon, Bethany N; Carpenter, Karla J; Berry, William L et al. (2015) Exosome-mediated microRNA signaling from breast cancer cells is altered by the anti-angiogenesis agent docosahexaenoic acid (DHA). Mol Cancer 14:133

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