The University of Iowa Medical Scientist Training Program (MSTP) is a structured, yet flexible Program, with a mission to provide outstanding training in both clinical medicine and scientific investigation for well-qualified students who are interested in pursuing careers as physician-scientists. In its 27-year history, 109 graduates have received MD/PhD degrees. Of these graduates, 77 have completed postgraduate training, with the majority of these individuals engaged in scientific investigation at major academic medical centers or pharmaceutical companies. Our graduates are making important contributions, both by training future physician-scientists and by increasing the understanding of human disease. Iowa MSTP students are selected from a national pool of highly qualified applicants, who have a demonstrated record of scientific involvement. The Iowa MSTP is an integrated training program, such that students are never just medical students or just graduate students. This is accomplished by several thoughtfully designed initiatives that connect scientific investigation with clinical medicine. These activities both enhance the education of our trainees and invigorate the entire scientific community. The MSTP capitalizes on a dynamic training faculty and benefits from the support of the Dean of the Carver College of Medicine, who recognizes the unique role of physician-scientists in academic medical centers. Currently, the Iowa MSTP has 56 trainees (36% women and 7% URM). These students are in various stages of training, including 20 students in the pre-clinical medical school curriculum, 31 students in the graduate phase of training, and 5 students in the clinical phase of training. MSTP students are leaders among their peers in medical and graduate school. Continued support of the Iowa MSTP is requested for years 29 to 33 (2005 to 2010). We request support for 22 trainees in year 29, 24 trainees in year 30, and 26 trainees in each of years 31, 32, and 33. This request reflects an increase from our current level of support of 17 trainees per year. Our request is based on our strong applicant pool, the high quality of our matriculants, the reputation of our outstanding training faculty and the success of our graduates.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
3T32GM007337-33S1
Application #
8099395
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Hagan, Ann A
Project Start
1977-07-01
Project End
2011-06-30
Budget Start
2009-07-01
Budget End
2011-06-30
Support Year
33
Fiscal Year
2010
Total Cost
$353,370
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Velez, Gabriel; Machlab, Daniel A; Tang, Peter H et al. (2018) Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic- and oxidative stress-related diseases. PLoS One 13:e0193250
Hayes, Michael H; Peuchen, Elizabeth H; Dovichi, Norman J et al. (2018) Dual roles for ATP in the regulation of phase separated protein aggregates in Xenopus oocyte nucleoli. Elife 7:
Matasic, Daniel S; Brenner, Charles; London, Barry (2018) Emerging potential benefits of modulating NAD+ metabolism in cardiovascular disease. Am J Physiol Heart Circ Physiol 314:H839-H852
Kolb, Ryan; Kluz, Paige; Tan, Zhen Wei et al. (2018) Obesity-associated inflammation promotes angiogenesis and breast cancer via angiopoietin-like 4. Oncogene :
Grunewald, Matthew E; Fehr, Anthony R; Athmer, Jeremiah et al. (2018) The coronavirus nucleocapsid protein is ADP-ribosylated. Virology 517:62-68
Benavides, Amanda; Metzger, Andrew; Tereshchenko, Alexander et al. (2018) Sex-specific alterations in preterm brain. Pediatr Res :
Roybal, C Nathaniel; Velez, Gabriel; Toral, Marcus A et al. (2018) Personalized Proteomics in Proliferative Vitreoretinopathy Implicate Hematopoietic Cell Recruitment and mTOR as a Therapeutic Target. Am J Ophthalmol 186:152-163
Elliott, Eric I; Miller, Alexis N; Banoth, Balaji et al. (2018) Cutting Edge: Mitochondrial Assembly of the NLRP3 Inflammasome Complex Is Initiated at Priming. J Immunol 200:3047-3052
Genova, Rachel M; Meyer, Kacie J; Anderson, Michael G et al. (2018) Neprilysin inhibition promotes corneal wound healing. Sci Rep 8:14385
Sabree, Shakoora; Berg, Daniel; Sato, Mariko (2018) Treatment of a pediatric patient with MET-amplified signet ring cell adenocarcinoma of the stomach with crizotinib. Pediatr Blood Cancer 65:e26984

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