Idaho State University and the University of Idaho have both created biomedical research core facilities with the assistance of a previous (1994) Institutional Development Award (NIH IDeA) (RR 10231) and matching funds from the state of Idaho. The core facilities have proven to be highly successful in providing the greatest number of biomedical investigators at both institutions with critically needed research resources and have demonstrated that shared instrumentation in a managed facility is a highly efficient means of utilizing increasingly valuable research funds. Strong evidence exists that research initiatives by investigators at both Idaho universities have been signifcantIy strengthened, expanded in scope, and more competitive for major funding. Biomedical investigators at both universities have now identified research technologies whose availability on campus or modernization would considerably improve biomedical investigation at the respective locations. Therefore, the project proposed here is to enhance existing biomedical research core laboratories at Idaho State University and the University of Idaho by (1) acquisition of new instrumentation, (2) upgrading of existing major core facility instrumentation, (3) development of programs under the direction of the present core laboratories to evaluate research progress, and (4) implementing programs created by core facility users and university administrators to sustain and expand the core facilities far into the future. Achievement of the proposal objectives will be subject to the overall strategic plans of both units.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR011833-03
Application #
2772046
Study Section
Special Emphasis Panel (ZRR1-IDEA-1 (01))
Project Start
1996-09-30
Project End
1999-08-31
Budget Start
1998-09-01
Budget End
1999-08-31
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Idaho State University
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
078341468
City
Pocatello
State
ID
Country
United States
Zip Code
83209
Demboski, John R; Sullivan, Jack (2003) Extensive mtDNA variation within the yellow-pine chipmunk, Tamias amoenus (Rodentia: Sciuridae), and phylogeographic inferences for northwest North America. Mol Phylogenet Evol 26:389-408
Good, Jeffrey M; Demboski, John R; Nagorsen, David W et al. (2003) Phylogeography and introgressive hybridization: chipmunks (genus Tamias) in the northern Rocky Mountains. Evolution 57:1900-16
Hayssen, V; Harper, J M; DeFina, R (2002) Fecal corticosteroids in agouti and non-agouti deer mice (Peromyscus maniculatus). Comp Biochem Physiol A Mol Integr Physiol 132:439-46
Nielson, M; Lohman, K; Sullivan, J (2001) Phylogeography of the tailed frog (Ascaphus truei): implications for the biogeography of the Pacific Northwest. Evolution 55:147-60
Good, J M; Sullivan, J (2001) Phylogeography of the red-tailed chipmunk (Tamias ruficaudus), a northern Rocky Mountain endemic. Mol Ecol 10:2683-95
Harris, D; Rogers, D S; Sullivan, J (2000) Phylogeography of Peromyscus furvus (Rodentia; muridae) based on cytochrome b sequence data. Mol Ecol 9:2129-35
Nagler, J J; Krisfalusi, M; Cyr, D G (2000) Quantification of rainbow trout (Oncorhynchus mykiss) estrogen receptor-alpha messenger RNA and its expression in the ovary during the reproductive cycle. J Mol Endocrinol 25:243-51
Harper, J M; Austad, S N (2000) Fecal glucocorticoids: a noninvasive method of measuring adrenal activity in wild and captive rodents. Physiol Biochem Zool 73:22-Dec
Krisfalusi, M; Nagler, J J (2000) Induction of gonadal intersex in genotypic male rainbow trout (Oncorhynchus mykiss) embryos following immersion in estradiol-17beta. Mol Reprod Dev 56:495-501
Passavant, C; Zhao, X; Das, S K et al. (2000) Changes in uterine expression of leukemia inhibitory factor receptor gene during pregnancy and its up-regulation by prolactin in the western spotted skunk. Biol Reprod 63:301-7

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