The undergraduate component of the proposed USCIMSD program will seek to build on our already-existing programs by offering under-represented minority (URM) students a more extensive exposure to biomedical research than can be obtained during a single undergraduate summer laboratory rotation. The IMSD program will increase the level of qualified URM applicants to our graduate programs by offering minority students the opportunity to work as research assistants for two or three years in biomedical research laboratories while preparing for Graduate School. Students who complete the undergraduate portion of the USC IMSD program with a strong recommendation from their mentor and who have an undergraduate GPA of 3.0 or higher will be guaranteed admission into one of the graduate programs in the biomedical sciences at USC. The cooperating HBCUs will provide additional applicants to our graduate programs and to the USC PREP program. The IMSD undergraduates, students completing the PREP program, and well qualified students from the HCBUs will provide the core of the USC IMSD graduate program. The IMSD graduate program will begin with a graduate transition program in July so that the IMSD students are fully prepared for the start of their graduate coursework in August. In addition, the IMSD program will provide participants with a graduate research assistantship during the first year of their graduate program and will pay their tuition for up to 4 years during their graduate training. The specific goals of the USC IMSD program are: (1) To recruit qualified underrepresented minority undergraduates to participate in funded biomedical research programs throughout the remainder of their undergraduate career. (2) To improve research skills of IMSD participants through work as an undergraduate research assistant in a mentored relationship with both a faculty member and a graduate students or postdoctoral fellow. (3) To help the students establish relationships among peers and faculty at USC and elsewhere in the research community so that the students have well-defined career goals and a support system that helps them achieve their goals. (4) To provide a smooth transition from undergraduate science programs at USC and the cooperating HCBUs to biomedical graduate programs at USC. The success of this program will increase the diversity of scientists with careers in biomedical research. This increased diversity will provide a more balanced perspective on research issues and contribute towards soloutions for the correction of health disparities.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Education Projects (R25)
Project #
5R25GM076277-03
Application #
7388867
Study Section
Special Emphasis Panel (ZGM1-MBRS-6 (IM))
Program Officer
Gaillard, Shawn R
Project Start
2006-04-12
Project End
2010-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
3
Fiscal Year
2008
Total Cost
$286,562
Indirect Cost
Name
University of South Carolina at Columbia
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
041387846
City
Columbia
State
SC
Country
United States
Zip Code
29208
Ely, Bert; Wilson, Kiesha; Ross, Keshawn et al. (2018) Genome Comparisons of Wild Isolates of Caulobacter crescentus Reveal Rates of Inversion and Horizontal Gene Transfer. Curr Microbiol :
Berrios, Louis; Ely, Bert (2018) Achieving Accurate Sequence and Annotation Data for Caulobacter vibrioides CB13. Curr Microbiol 75:1642-1648
Woappi, Yvon; Hosseinipour, Maria; Creek, Kim E et al. (2018) Stem Cell Properties of Normal Human Keratinocytes Determine Transformation Responses to Human Papillomavirus 16 DNA. J Virol 92:
Ash, Kurt T; Drake, Kristina M; Gibbs, Whitney S et al. (2017) Genomic Diversity of Type B3 Bacteriophages of Caulobacter crescentus. Curr Microbiol 74:779-786
Callahan, Courtney T; Wilson, Kiesha M; Ely, Bert (2016) Characterization of the Proteins Associated with Caulobacter crescentus Bacteriophage CbK Particles. Curr Microbiol 72:75-80
Scott, Derrick; Ely, Bert (2016) Conservation of the Essential Genome Among Caulobacter and Brevundimonas Species. Curr Microbiol 72:503-10
Velázquez, Kandy T; Enos, Reilly T; McClellan, Jamie L et al. (2016) MicroRNA-155 deletion promotes tumorigenesis in the azoxymethane-dextran sulfate sodium model of colon cancer. Am J Physiol Gastrointest Liver Physiol 310:G347-58
Enos, Reilly T; Velázquez, Kandy T; McClellan, Jamie L et al. (2015) Lowering the dietary omega-6: omega-3 does not hinder nonalcoholic fatty-liver disease development in a murine model. Nutr Res 35:449-59
Ely, Bert; Gibbs, Whitney; Diez, Simon et al. (2015) The Caulobacter crescentus transducing phage Cr30 is a unique member of the T4-like family of myophages. Curr Microbiol 70:854-8
Smith, Sherika N; Paige, Candler; Velazquez, Kandy T et al. (2015) Injury-specific promoters enhance herpes simplex virus-mediated gene therapy for treating neuropathic pain in rodents. J Pain 16:283-90

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