This project is a continuation of the IDeA INBRE in Idaho. It is a collaborative effort of research-intensive institutions to sponsor research and science educational opportunities with primarily undergraduate institutions (PUIs) and community colleges. Ten Idaho institutions of higher education will participate. The requested funding will provide the next step to build the depth and critical mass of investigators at the PUI and to maintain the change in culture that has been initiated.
Five Specific Aims are proposed: 1. To build on the established Idaho research Network with the scientific focus of 'Cell Signaling' and strengthen the participating Idaho institutions' biomedical research expertise and infrastructure. 2. To build and increase the research base and capacity by providing support to faculty, postdoctoral fellows, and graduate students at the participating Idaho institutions. 3. To provide research opportunities for undergraduate students and serve as a pipeline for these students to continue in health research careers within IDeA states. 4. To enhance science and technology knowledge of Idaho's workforce. 5. To provide research opportunities across the Western IDeA region. The project includes four Cores: Administrative, Bioinformatics, Research Mentoring, and Training, Workforce Development and Diversity. Also, a Developmental Research Project Program is outlined that plans for broad eligibility, a well-advertised opportunity, a competitive selection process, clear expectations, and careful guidance. The process will select the most promising faculty and provide an environment for their success and the success of their students by assuring appropriate research infrastructure, scientific mentoring, and a Network community. To help guide our progress, scientific, financial, and compliance oversight will be in place. We have an experienced Idaho INBRE administrative group, a highly qualified external advisory committee, a statewide steering committee, and well-planned summative and formative evaluations that include external-to-ldaho review.

Public Health Relevance

The INBRE Program will increase Idaho's competitiveness for research funding and will improve the quality of biomedical education. We will deliver unique, innovative, state-of-the-art biomedical research that will contribute to improving human health. We will invigorate faculty careers with collaborative research and provide a rich, intensive, competitive research experience for students who are training as the nation's next generation of biomedical scientists.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103408-16
Application #
9061706
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Arora, Krishan
Project Start
2001-09-30
Project End
2019-04-30
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
16
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Idaho
Department
Type
Schools of Arts and Sciences
DUNS #
075746271
City
Moscow
State
ID
Country
United States
Zip Code
83844
Thyagaraj, Suraj; Pahlavian, Soroush Heidari; Sass, Lucas R et al. (2018) An MRI-Compatible Hydrodynamic Simulator of Cerebrospinal Fluid Motion in the Cervical Spine. IEEE Trans Biomed Eng 65:1516-1523
Misra, N; Pu, X; Holt, D N et al. (2018) Immunoproteomics to identify Staphylococcus aureus antigens expressed in bovine milk during mastitis. J Dairy Sci 101:6296-6309
Bayless-Edwards, Landon; Winston, Vern; Lehmann-Horn, Frank et al. (2018) NaV1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers. Sci Rep 8:10372
Nhu Lam, Mila; Dudekula, Dastagiri; Durham, Bri et al. (2018) Insights into ?-ketoacyl-chain recognition for ?-ketoacyl-ACP utilizing AHL synthases. Chem Commun (Camb) 54:8838-8841
Duan, Mingrui; Hunter, Samuel S; Minnich, Scott A et al. (2018) Complete Genome Sequence of Broad-Host-Range Shiga Toxin-Converting Bacteriophage SH2026Stx1, Isolated from Escherichia coli O157:H7. Genome Announc 6:
Robertson, Jake C; Jorcyk, Cheryl L; Oxford, Julia Thom (2018) DICER1 Syndrome: DICER1 Mutations in Rare Cancers. Cancers (Basel) 10:
Frahs, Stephanie M; Oxford, Julia Thom; Neumann, Erica E et al. (2018) Extracellular Matrix Expression and Production in Fibroblast-Collagen Gels: Towards an In Vitro Model for Ligament Wound Healing. Ann Biomed Eng 46:1882-1895
King, Matthew D; Long, Thomas; Pfalmer, Daniel L et al. (2018) SPIDR: small-molecule peptide-influenced drug repurposing. BMC Bioinformatics 19:138
McGinn, Timothy E; Mitchell, Diana M; Meighan, Peter C et al. (2018) Restoration of Dendritic Complexity, Functional Connectivity, and Diversity of Regenerated Retinal Bipolar Neurons in Adult Zebrafish. J Neurosci 38:120-136
LaFoya, Bryce; Munroe, Jordan A; Pu, Xinzhu et al. (2018) Src kinase phosphorylates Notch1 to inhibit MAML binding. Sci Rep 8:15515

Showing the most recent 10 out of 275 publications