This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Researchers in the Clemson's Bioengineering Translational Research Program will enhance the clinical applicability of their research through close interaction with Greenville Hospital System (GHS) physicians. Ideas that emerge from these interactions are evaluated in the laboratory and/or bioskills facilities, transferred to the clinic through the GHS clinical-trial program, and optimally will lead to technology transfer and incubation. Such a collaboration between Clemson bioengineering and GHS vascular surgery established CreatiVasc Medical, LLC, in 2004. The Greenville, SC, medical device company delivers innovative vascular technologies that address universal problems of kidney dialysis connectivity. In the program, research informed by clinical collaboration will contribute to containment and reduction of health care costs and improve health care effectiveness. Anticipated outcomes of the program are: 1) Technology development for improved health care?technology licensing, start-up company development, entrepreneurship;2) Economic impact?specialized workforce training, continuing education, commercialization and job creation, regional and state-wide growth;and 3) Increased NIH R01 research funding?innovative data through unique facilities and clinical involvement. This program will serve as a unique resource in the SC INBRE network as a template for translational biomedical. Three projects will be conducted under the auspices of the SC INBRE network. They have been selected because of their clinical applicability and potential data generation for NIH R01 funding, and as challenging opportunities for the integration of under-represented groups in NIH funded biomedical research. These projects are led by three junior faculty members who have demonstrated outstanding skills as researchers, translators, and mentors/role models. The PI will serve as the Program Director. The INBRE activities at CU will be closely monitored by the Clemson University Road Map Council and an external steering committee. Assessment of the program will be performed periodically by the Program Director and Thrust Leaders to monitor research productivity among CBC researchers including target faculty. Measures of success will include publications, awards, grant proposal submission and funding, and educational outcomes.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016461-11
Application #
8360738
Study Section
Special Emphasis Panel (ZRR1-RI-7 (01))
Project Start
2011-07-01
Project End
2012-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
11
Fiscal Year
2011
Total Cost
$181,923
Indirect Cost
Name
University of South Carolina at Columbia
Department
Pathology
Type
Schools of Medicine
DUNS #
041387846
City
Columbia
State
SC
Country
United States
Zip Code
29208
Liang, Jiaxin; Chen, Mengqian; Hughes, Daniel et al. (2018) CDK8 Selectively Promotes the Growth of Colon Cancer Metastases in the Liver by Regulating Gene Expression of TIMP3 and Matrix Metalloproteinases. Cancer Res 78:6594-6606
Emetu, Sophia; Troiano, Morgan; Goldmintz, Jacob et al. (2018) Metabolic Labeling and Profiling of Transfer RNAs Using Macroarrays. J Vis Exp :
Oprisan, Sorinel A; Buhusi, Mona; Buhusi, Catalin V (2018) A Population-Based Model of the Temporal Memory in the Hippocampus. Front Neurosci 12:521
Germany, Edward M; Zahayko, Nataliya; Huebsch, Mason L et al. (2018) The AAA ATPase Afg1 preserves mitochondrial fidelity and cellular health by maintaining mitochondrial matrix proteostasis. J Cell Sci 131:
Krout, Danielle; Pramod, Akula Bala; Dahal, Rejwi Acharya et al. (2017) Inhibitor mechanisms in the S1 binding site of the dopamine transporter defined by multi-site molecular tethering of photoactive cocaine analogs. Biochem Pharmacol 142:204-215
Waddell, Grace L; Gilmer, Caroline R; Taylor, Nicholas G et al. (2017) The eukaryotic enzyme Bds1 is an alkyl but not an aryl sulfohydrolase. Biochem Biophys Res Commun 491:382-387
Oprisan, Ana; Rice, Ashley; Oprisan, Sorinel A et al. (2017) Non-equilibrium concentration fluctuations in superparamagnetic nanocolloids. Eur Phys J E Soft Matter 40:14
Gochez, Alberto M; Shantharaj, Deepak; Potnis, Neha et al. (2017) Molecular characterization of XopAG effector AvrGf2 from Xanthomonas fuscans ssp. aurantifolii in grapefruit. Mol Plant Pathol 18:405-419
Cole, Casey A; Anshari, Dien; Lambert, Victoria et al. (2017) Detecting Smoking Events Using Accelerometer Data Collected Via Smartwatch Technology: Validation Study. JMIR Mhealth Uhealth 5:e189
Oliver, David; Ji, Hao; Liu, Piaomu et al. (2017) Identification of novel cancer therapeutic targets using a designed and pooled shRNA library screen. Sci Rep 7:43023

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