The goal of the University of Chicago Post-Baccalaureate Research Education Program (PREP) is to provide research training, educational opportunities, and career strategies for underrepresented college graduates so that they will be better prepared to apply, matriculate and succeed in a PhD or MD/PhD program. It is based on the concept that an in-depth mentored research experience enriched by activities which develop scholastic, communication, social and cultural skills is the optimal preparation for graduate studies in the biomedical sciences. The core program encompasses two years of laboratory-based research in a rigorous yet nurturing environment under the guidance and supervision of well-funded, nationally recognized University of Chicago faculty with outstanding records of promoting the training, education and career advancement of biomedical scientists. This research experience will be complemented by a multi-tiered skill enhancement approach for improving oral and written communication, critical thinking and analysis, ethical decision making, and teaching strategies. Training in areas pertinent to the biomedical sciences and didactic preparation for the graduate application process will also be incorporated in stages over the two years with GRE review, application workshops and interviewing skills. Although the Program is highly structured and logically organized, it is still sufficiently flexible that after careful self- and mentored-assessment, an individual development plan will be prepared to serve as the roadmap for each Scholar's course over their tenure as a University of Chicago PREP Scholar. This is illustrated by the Accelerated Program created by rearranging components to accommodate those individuals requiring only one year to transition from undergraduate to graduate student. All of these elements represent definable and readily accessible goals. The ultimate sucess will be the matriculation of Scholars into a PhD or MD/PhD program and their continued success as biomedical scientists. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Education Projects (R25)
Project #
5R25GM066522-04
Application #
7277279
Study Section
Special Emphasis Panel (ZGM1-MARC-7 (PR))
Program Officer
Toliver, Adolphus
Project Start
2004-09-30
Project End
2009-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
4
Fiscal Year
2007
Total Cost
$208,406
Indirect Cost
Name
University of Chicago
Department
Pediatrics
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Domowicz, Miriam; Wadlington, Natasha L; Henry, Judith G et al. (2018) Glial cell responses in a murine multifactorial perinatal brain injury model. Brain Res 1681:52-63
Bhanvadia, Raj R; VanOpstall, Calvin; Brechka, Hannah et al. (2018) MEIS1 and MEIS2 Expression and Prostate Cancer Progression: A Role For HOXB13 Binding Partners in Metastatic Disease. Clin Cancer Res 24:3668-3680
Umana, Iboro C; Daniele, Claire A; Miller, Brooke A et al. (2017) Nicotinic modulation of descending pain control circuitry. Pain 158:1938-1950
Mir-Sanchis, Ignacio; Roman, Christina A; Misiura, Agnieszka et al. (2016) Staphylococcal SCCmec elements encode an active MCM-like helicase and thus may be replicative. Nat Struct Mol Biol 23:891-898
Lamar, Kay-Marie; Bogdanovich, Sasha; Gardner, Brandon B et al. (2016) Overexpression of Latent TGF? Binding Protein 4 in Muscle Ameliorates Muscular Dystrophy through Myostatin and TGF?. PLoS Genet 12:e1006019
Riley, Sean P; Patterson, Jennifer L; Nava, Samantha et al. (2014) Pathogenic Rickettsia species acquire vitronectin from human serum to promote resistance to complement-mediated killing. Cell Microbiol 16:849-61
Goldstein, Jeffery A; Bogdanovich, Sasha; Beiriger, Anastasia et al. (2014) Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy. Hum Mol Genet 23:6722-31
Sittig, Laura J; Jeong, Choongwon; Tixier, Emily et al. (2014) Phenotypic instability between the near isogenic substrains BALB/cJ and BALB/cByJ. Mamm Genome 25:564-72
Skinner, John J; Yu, Wookyung; Gichana, Elizabeth K et al. (2014) Benchmarking all-atom simulations using hydrogen exchange. Proc Natl Acad Sci U S A 111:15975-80
Makinen, Marvin W; Bamba, Ravinder; Ikejimba, Lynda et al. (2013) The vanadyl chelate bis(acetylacetonato)oxovanadium(IV) increases the fractional uptake of 2-(fluorine-18)-2-deoxy-D-glucose by cultured human breast carcinoma cells. Dalton Trans 42:11862-7

Showing the most recent 10 out of 12 publications