The proposed MARC-USTAR Program represents a continuation of the efforts by St. Mary's University to become a significant producer of underrepresented minority biomedical research scientists. The institutional long-term goal for the Program is to increase the number of underrepresented minority students majoring in biology, chemistry/biochemistry, biophysics and engineering, who enter and complete doctoral research programs in the biomedical sciences. In order to achieve this goal, the following objectives have been established for the proposed funding period: (1) to increase the number of applicants available to the MARC program by providing numerous pre-program opportunities, (2) to increase the number of MARC trainees in our program from 6 to 10 over the next five years, (3) to provide trainees with a strong academic foundation by enrolling students in a specified set of courses, (4) to enhance the ability of trainees to critically read and interpret the scientific literature, (5) to enhance the research skills of trainees by providing both academic year and summer research opportunities, (6) to develop trainee disciplinary socialization skills by enabling trainees to participate in science and service-related activities, (7) to increase the number of trainees entering and completing research doctoral programs, and (8) to increase the opportunities for St. Mary's University faculty members to engage in the academic year research with MARC trainees. Proposed activities include providing trainees with a rigorous science curriculum, performing academic year research, arranging summer research experiences at research-intensive institutions for trainees, developing a Scientific Methods & Analysis course, conducting a biomedical research workshop and seminar series, and arranging trainee attendance at scientific meetings. Students participating in this training program will be qualified to pursue doctoral studies in chemistry, biochemistry, biophysics, cell and molecular biology, physiology, microbiology, epidemiology, and other biomedical sciences. The successful attainment of the stated goal will contribute to the enhancement of the racial and ethnic diversity of the biomedical research community, which in turn will contribute to the eventual elimination of health care disparities. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
MARC Undergraduate NRSA Institutional Grants (T34)
Project #
2T34GM008073-24A1
Application #
7433501
Study Section
Minority Programs Review Committee (MPRC)
Program Officer
Tupas, Jermelina
Project Start
1983-07-01
Project End
2013-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
24
Fiscal Year
2008
Total Cost
$260,947
Indirect Cost
Name
St. Mary's University
Department
Biology
Type
Other Domestic Higher Education
DUNS #
078500725
City
San Antonio
State
TX
Country
United States
Zip Code
78228
Liu, Jinyou; Viswanadhapalli, Suryavathi; Garcia, Lauren et al. (2017) Therapeutic utility of natural estrogen receptor beta agonists on ovarian cancer. Oncotarget 8:50002-50014
Mfuh, Adelphe M; Schneider, Brett D; Cruces, Westley et al. (2017) Metal- and additive-free photoinduced borylation of haloarenes. Nat Protoc 12:604-610
Lane-Donovan, Courtney; Wong, Wen Mai; Durakoglugil, Murat S et al. (2016) Genetic Restoration of Plasma ApoE Improves Cognition and Partially Restores Synaptic Defects in ApoE-Deficient Mice. J Neurosci 36:10141-50
Fu, Jianmin; Blaylock, Morganne; Wickes, Cameron F et al. (2016) Development of a Candida glabrata dominant nutritional transformation marker utilizing the Aspergillus nidulans acetamidase gene (amdS). FEMS Yeast Res 16:
Adkins, Amy; Aleman, Jesus; Boies, Lori et al. (2015) Force Required to Cinch the Tricuspid Annulus: An Ex-Vivo Study. J Heart Valve Dis 24:644-52
Gleason, Julie E; Galaleldeen, Ahmad; Peterson, Ryan L et al. (2014) Candida albicans SOD5 represents the prototype of an unprecedented class of Cu-only superoxide dismutases required for pathogen defense. Proc Natl Acad Sci U S A 111:5866-71
Higgins, Paul B; Rodriguez, Perla J; Voruganti, V Saroja et al. (2014) Body composition and cardiometabolic disease risk factors in captive baboons (Papio hamadryas sp.): sexual dimorphism. Am J Phys Anthropol 153:9-14
Macrini, T E; Coan, H B; Levine, S M et al. (2013) Reproductive status and sex show strong effects on knee OA in a baboon model. Osteoarthritis Cartilage 21:839-48
Daubner, S Colette; Avila, Audrey; Bailey, Johnathan O et al. (2013) Mutagenesis of a specificity-determining residue in tyrosine hydroxylase establishes that the enzyme is a robust phenylalanine hydroxylase but a fragile tyrosine hydroxylase. Biochemistry 52:1446-55
Weiderhold, Kimberly N; Randall-Hlubek, Deborah A; Polin, Lisa A et al. (2006) CB694, a novel antimitotic with antitumor activities. Int J Cancer 118:1032-40