A diverse and well-trained scientific workforce is necessary to advance biomedical research, improve human health and to develop effective remedies for disease. The University of Missouri-Columbia (MU) is the only four-year comprehensive public university in the State of Missouri and has a critical role in training the next generation of scientists. As part of the University of Missouri-Columbia (MU) commitment to scientific training and diversity, and with prior funding from NIH, we have developed a successful and innovative program to prepare underrepresented minority students for biomedical research. We have three objectives for our Initiative to Maximize Student Diversity (IMSD) program. First, to further develop a supportive and engaged peer community of minority undergraduate students that are interested in exploring biomedical research. We will increase the number of MU freshmen/sophomore students who are exploring a career in biomedical research. Second, we will expand a program targeted at MU junior/senior students that involves these advanced undergraduates in independent research experiences and prepares them for graduate study in the biomedical sciences. Third, we will provide a structured and mentored research environment for minority graduate students to develop into independent scientists as they pursue their PhD degree in a biomedical discipline. Further development of our IMSD program will have a substantial impact on diversity at the University and on our nation's scientific workforce.

Public Health Relevance

A robust biomedical research enterprise is required to improve human health and reduce morbidity and mortality from disease. A diverse scientific workforce, which utilizes the talents and skills of all individuals, is a necessary component of a robust research enterprise. The goal of our program is to increase the diversity of PhD scientists trained in biomedical research.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Education Projects (R25)
Project #
5R25GM056901-14
Application #
8523906
Study Section
Minority Programs Review Committee (MPRC)
Program Officer
Janes, Daniel E
Project Start
1999-02-01
Project End
2017-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
14
Fiscal Year
2013
Total Cost
$602,341
Indirect Cost
$37,825
Name
University of Missouri-Columbia
Department
Biochemistry
Type
Schools of Medicine
DUNS #
153890272
City
Columbia
State
MO
Country
United States
Zip Code
65211
Van Gronigen Caesar, Gerialisa; Dale, Jeffrey M; Osman, Erkan Y et al. (2016) Placental development in a mouse model of spinal muscular atrophy. Biochem Biophys Res Commun 470:82-7
Welly, Rebecca J; Liu, Tzu-Wen; Zidon, Terese M et al. (2016) Comparison of Diet versus Exercise on Metabolic Function and Gut Microbiota in Obese Rats. Med Sci Sports Exerc 48:1688-98
Figueroa-Cuilan, Wanda; Daniel, Jeremy J; Howell, Matthew et al. (2016) Mini-Tn7 Insertion in an Artificial attTn7 Site Enables Depletion of the Essential Master Regulator CtrA in the Phytopathogen Agrobacterium tumefaciens. Appl Environ Microbiol 82:5015-25
Harper, Jennifer L; Caesar, Gerialisa A; Pennington, Kathleen A et al. (2015) Placental changes caused by food restriction during early pregnancy in mice are reversible. Reproduction 150:165-72
Wainright, Katherine S; Fleming, Nicholas J; Rowles, Joe L et al. (2015) Retention of sedentary obese visceral white adipose tissue phenotype with intermittent physical activity despite reduced adiposity. Am J Physiol Regul Integr Comp Physiol 309:R594-602
Zhang, Xinyue; Xu, Xiaojun; Yang, Zhiyu et al. (2015) Mimicking Ribosomal Unfolding of RNA Pseudoknot in a Protein Channel. J Am Chem Soc 137:15742-52
Morgan, Brandie R; Coates, Joan R; Johnson, Gayle C et al. (2014) Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis. J Neurosci Res 92:531-41
Swatek, Kirby N; Wilson, Rashaun S; Ahsan, Nagib et al. (2014) Multisite phosphorylation of 14-3-3 proteins by calcium-dependent protein kinases. Biochem J 459:15-25
Roberts, Renee N; Schlarman, Maggie S; Kariuki, Michael M et al. (2013) Expression profile of the Plasmodium falciparum intra-erythrocytic stage protein, PF3D7_1363700. Malar J 12:66
Ahsan, Nagib; Huang, Yadong; Tovar-Mendez, Alejandro et al. (2013) A versatile mass spectrometry-based method to both identify kinase client-relationships and characterize signaling network topology. J Proteome Res 12:937-48

Showing the most recent 10 out of 30 publications