CU is an independent, Jesuit, comprehensive university located in Omaha, Nebraska. The mission of the CUSOM is to develop and promote an understanding of human health and the causes, treatments, and prevention of disease. As biomedical research is key to this understanding, CUSOM is committed to supporting excellence in its research programs. CUSOM recognizes that state-of-the-art research facilities are essential to its success as a research institution. Thus, CUSOM requests matching funds to renovate 13,960 sq. ft. of outdated 1960's-era classroom, research, and administrative space into state-of-the-art research laboratories with shared centralized facilities. The renovation is a critical part of CU's ongoing multi-phased construction of an integrated Science Complex. The long-term objective for the proposed space renovation is to enhance research productivity, collaboration, and training in an evolving program area at the Medical School - the Study of Development and Disease in the Nervous and Immune Systems.
The specific aims of the project are to: 1) relocate six extramurally funded junior and senior investigators with overlapping interests into a modern integrated laboratory space; 2) provide infrastructure, in a flexible open laboratory design, that will promote collaboration and facilitate efficient use of major equipment; 3) provide additional space and opportunities for expansion of National Institutes of Health (NIH)-funded research projects in the areas of neuroscience, immunology, and developmental biology; and 4) promote a flexible and interactive environment for comprehensive training of postdoctoral fellows and students, and to enhance mentoring of junior investigators by established investigators.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Facilities Construction Grant (C06)
Project #
1C06RR017417-01
Application #
6533258
Study Section
Scientific and Technical Review Board on Biomedical and Behavioral Research Facilities (STRB)
Program Officer
Mccullough, Willie
Project Start
2002-06-01
Project End
2004-05-31
Budget Start
2002-06-01
Budget End
2004-05-31
Support Year
1
Fiscal Year
2002
Total Cost
$2,000,000
Indirect Cost
Name
Creighton University
Department
Type
Schools of Medicine
DUNS #
City
Omaha
State
NE
Country
United States
Zip Code
68178
Yuan, Qi; Telling, Glenn; Bartelt-Hunt, Shannon L et al. (2018) Dehydration of Prions on Environmentally Relevant Surfaces Protects Them from Inactivation by Freezing and Thawing. J Virol 92:
Li, Yi; Jia, Shuping; Liu, Huizhan et al. (2018) Characterization of Hair Cell-Like Cells Converted From Supporting Cells After Notch Inhibition in Cultures of the Organ of Corti From Neonatal Gerbils. Front Cell Neurosci 12:73
Schabla, N Max; Perry, Greg A; Palmer, Victoria L et al. (2018) VprBP (DCAF1) Regulates RAG1 Expression Independently of Dicer by Mediating RAG1 Degradation. J Immunol 201:930-939
Rovnak, Joel; Perera, Rushika; Hopken, Matthew W et al. (2017) The 17th Rocky Mountain Virology Association Meeting. Viruses 9:
Nichols, Michael G; Hallworth, Richard (2016) The Single-Molecule Approach to Membrane Protein Stoichiometry. Methods Mol Biol 1427:189-99
Langenfeld, Katie A; Shikiya, Ronald A; Kincaid, Anthony E et al. (2016) Incongruity between Prion Conversion and Incubation Period following Coinfection. J Virol 90:5715-23
Riesberg, Lisa A; Weed, Stephanie A; McDonald, Thomas L et al. (2016) Beyond muscles: The untapped potential of creatine. Int Immunopharmacol 37:31-42
Palmer, Victoria L; Nganga, Vincent K; Rothermund, Mary E et al. (2015) Cd1d regulates B cell development but not B cell accumulation and IL10 production in mice with pathologic CD5(+) B cell expansion. BMC Immunol 16:66
Palmer, Victoria L; Aziz-Seible, Razia; Kassmeier, Michele D et al. (2015) VprBP Is Required for Efficient Editing and Selection of Ig?+ B Cells, but Is Dispensable for Ig?+ and Marginal Zone B Cell Maturation and Selection. J Immunol 195:1524-37
Yuan, Qi; Eckland, Thomas; Telling, Glenn et al. (2015) Mitigation of prion infectivity and conversion capacity by a simulated natural process--repeated cycles of drying and wetting. PLoS Pathog 11:e1004638

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