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.
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.
|Sheng, Haiqing; Duan, Mingrui; Hunter, Samuel S et al. (2018) High-Quality Complete Genome Sequences of Three Bovine Shiga Toxin-ProducingEscherichia coliO177:H- (fliCH25) Isolates Harboring Virulentstx2and Multiple Plasmids. Genome Announc 6:|
|Mitchell, Diana M; Lovel, Anna G; Stenkamp, Deborah L (2018) Dynamic changes in microglial and macrophage characteristics during degeneration and regeneration of the zebrafish retina. J Neuroinflammation 15:163|
|Eberle, Sarah; Dezoumbe, Djeneba; McGregor, Rhegan et al. (2018) Hierarchical Assessment of Mutation Properties in Daphnia magna. G3 (Bethesda) 8:3481-3487|
|Gunderson, Mark P; Nguyen, Brandon T; Cervantes Reyes, Juan C et al. (2018) Response of phase I and II detoxification enzymes, glutathione, metallothionein and acetylcholine esterase to mercury and dimethoate in signal crayfish (Pacifastacus leniusculus). Chemosphere 208:749-756|
|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:|
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