Our program's goal remains increasing the diversity of students pursuing PhDs in STEM fields and a research career in biomedical sciences. We have developed activities for high achieving underrepresented (UR) students that are designed to hone their talent and professional skills in preparation for excelling in subsequent PhD (or PhD/MD) programs and careers in biomedical-relevant areas. Our strategy involves recruiting 4 juniors/yr and providing them with advising, academic, and research activities that will enable them to achieve the following: (a) GPAs > 3.5 (honors) in their major & graduation with cumulative GPAs > 3.25; (b) GRE scores in the top 50th percentile; (c) increased scientific research expertise via intensive research experiences, including summer research at another institution, facilitated journal clubs, and interaction with campus and visiting scientists; (d) enhanced oral & written presentation skills via specific assignments, research presentations, and peer & instructor feedback; (e) maintenance/enhanced commitment to biomedical research careers; (f) exposure to the broader scientific community via attendance at visiting scientist presentations and national meetings; (g) increased awareness of graduate school application requirements, & improved interviewing skills via practice and feedback from our Advisory Committee; and (h) entry into PhD or PhD/MD programs within 2 years of graduation at a percentage of 75%. To achieve these goals, we will maintain our successful pre-MARC curriculum (BUSP), funded primarily by campus resources with some augmentation from our NIH-IMSD grant. BUSP provides a rich pool for recruiting MARC Scholars. We will also: (a) expand efforts to recruit outstanding students from those who did not participate in BUSP; (b) enhance MARC components, including refining the advising component by establishing clearer guidelines for academic & research balance during the academic year, assisting students in crafting individual development plans, and increasing emphasis on graduate school application requirements and processes; (c) strengthen the academic/professional skills component of the program through additional writing and oral activities (e.g., NSF fellowship application, additiona research presentations, development of elevator/ airplane explanations of research projects); (d) expand student exposure to research by inviting UR postdoctoral fellows to present a research seminar and discuss their career development/path and by providing MARC seniors with the option of presenting their research at a national conference in their discipline with thei research preceptor (vs. returning to ABRCMS); (e) build connections to the next stage in their academic careers by pairing them with an UR graduate student mentor; and (f) add a community outreach component to broaden the program's impact and enhance the MARC Scholars' leadership skills while encouraging UR students at all levels to participate in science. We anticipate that the long-term outcome of our MARC U-Star activities will be an increased pool of highly competitive, diverse candidates who matriculate into outstanding biomedical PhD and/or dual degree programs.

Public Health Relevance

The goal of our proposal is to increase the diversity of students pursuing a PhD in a STEM field and a research career in the biomedical sciences. To achieve this goal, we have developed a series of activities for high achieving underrepresented students - activities that are designed to facilitate the development of their talent and professional skills in preparation for excelling in their subsequent PhD (or PhD/MD) programs and careers in science areas that have biomedical relevance.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
MARC Undergraduate NRSA Institutional Grants (T34)
Project #
5T34GM083894-09
Application #
9481837
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Koduri, Sailaja
Project Start
2009-06-01
Project End
2020-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
9
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of California Davis
Department
Physiology
Type
Schools of Medicine
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Jiang, Guochun; Nguyen, Don; Archin, Nancie M et al. (2018) HIV latency is reversed by ACSS2-driven histone crotonylation. J Clin Invest 128:1190-1198
Sepulveda, Guadalupe; Antkowiak, Mark; Brust-Mascher, Ingrid et al. (2018) Co-translational protein targeting facilitates centrosomal recruitment of PCNT during centrosome maturation in vertebrates. Elife 7:
Shearer, Peter W; West, Jessica D; Walton, Vaughn M et al. (2016) Seasonal cues induce phenotypic plasticity of Drosophila suzukii to enhance winter survival. BMC Ecol 16:11
Murphy, Kaitlin C; Stilhano, Roberta S; Mitra, Debika et al. (2016) Hydrogel biophysical properties instruct coculture-mediated osteogenic potential. FASEB J 30:477-86
Wang, Bo; Pakpour, Nazzy; Napoli, Eleonora et al. (2015) Anopheles stephensi p38 MAPK signaling regulates innate immunity and bioenergetics during Plasmodium falciparum infection. Parasit Vectors 8:424
Tsang, Felicia; James, Christol; Kato, Michiko et al. (2015) Reduced Ssy1-Ptr3-Ssy5 (SPS) signaling extends replicative life span by enhancing NAD+ homeostasis in Saccharomyces cerevisiae. J Biol Chem 290:12753-64
Horwitz, Barbara A; Chau, Sat M; Hamilton, Jock S et al. (2013) Temporal relationships of blood pressure, heart rate, baroreflex function, and body temperature change over a hibernation bout in Syrian hamsters. Am J Physiol Regul Integr Comp Physiol 305:R759-68
Imai, Denise; Holden, Kevin; Velazquez, Eric M et al. (2013) Influence of arthritis-related protein (BBF01) on infectivity of Borrelia burgdorferi B31. BMC Microbiol 13:100
Stenglein, Mark D; Velazquez, Eric; Greenacre, Cheryl et al. (2012) Complete genome sequence of an astrovirus identified in a domestic rabbit (Oryctolagus cuniculus) with gastroenteritis. Virol J 9:216
Hamilton, Andrew M; Oh, Won Chan; Vega-Ramirez, Hugo et al. (2012) Activity-dependent growth of new dendritic spines is regulated by the proteasome. Neuron 74:1023-30