The Biotechnology Training Program (BTP) at the University of Wisconsin- Madison seeks to train a new cadre of researchers who use cross- disciplinary approaches from the biological-physical-computational science interface to solve biomedical problems. The BTP is a multi- dimensional program that builds on existing disciplinary excellence across 5 colleges while providing trainees a common set of cross- disciplinary experiences. BTP trainees are admitted to and fulfill the requirements of leading Ph.D. programs such as Bacteriology, Biochemistry, Biomolecular Chemistry, Chemistry, Chemical Engineering, and Pharmacy. The rich history of excellence within these core graduate programs prepares BTP trainees to become future leaders in their respective fields. The common set of cross-disciplinary experiences that distinguished BTP trainees from their peers including a biotechnology oriented minor course program, regular interactions with a BTP minor professor from another discipline, participation in a biotechnology student seminar program, and an industrial internship. These common experiences ensure that BTP trainees will be conversant in the molecular biology, genetics, biochemistry/physiology principles that will be required to function as cross-disciplinary scientists and engineers in the 21st century. UW-Madison is the proud sponsor of the largest BTP in the country, with 33 NIH-funded trainees. In its 9 year history, the BTP has trained 109 Ph.D. students who worked with 68 different faculty in 20 Ph.D. programs. As student interest in the BTP has continued to grow, the opportunities for trainees to partake of all BTP activities is increasingly constrained. Consequently, we are requesting 3 more NIH- funded positions in each of the next 3 years so there will be a total of 42 BTP trainees at steady-state. Increased NIH support will permit more high-quality students to partake of BTP activities and expand the breadth of cross-disciplinary interactions across campus. This expansion of interactions among students and faculty in the biomedical research community will increase the ability of BTP trainees to capitalize on recent technological advances and solve emerging problems at the biological-physical-computational science interface.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008349-15
Application #
6605766
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Jones, Warren
Project Start
1989-09-27
Project End
2004-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
15
Fiscal Year
2003
Total Cost
$1,026,581
Indirect Cost
Name
University of Wisconsin Madison
Department
Microbiology/Immun/Virology
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Cook, Taylor B; Rand, Jacqueline M; Nurani, Wasti et al. (2018) Genetic tools for reliable gene expression and recombineering in Pseudomonas putida. J Ind Microbiol Biotechnol 45:517-527
Lapointe, Christopher P; Stefely, Jonathan A; Jochem, Adam et al. (2018) Multi-omics Reveal Specific Targets of the RNA-Binding Protein Puf3p and Its Orchestration of Mitochondrial Biogenesis. Cell Syst 6:125-135.e6
England, Christopher G; Jiang, Dawei; Ehlerding, Emily B et al. (2018) 89Zr-labeled nivolumab for imaging of T-cell infiltration in a humanized murine model of lung cancer. Eur J Nucl Med Mol Imaging 45:110-120
Venturelli, Ophelia S; Carr, Alex C; Fisher, Garth et al. (2018) Deciphering microbial interactions in synthetic human gut microbiome communities. Mol Syst Biol 14:e8157
Gastfriend, Benjamin D; Palecek, Sean P; Shusta, Eric V (2018) Modeling the blood-brain barrier: Beyond the endothelial cells. Curr Opin Biomed Eng 5:6-12
Pinkert, Michael A; Salkowski, Lonie R; Keely, Patricia J et al. (2018) Review of quantitative multiscale imaging of breast cancer. J Med Imaging (Bellingham) 5:010901
Stebbins, Matthew J; Lippmann, Ethan S; Faubion, Madeline G et al. (2018) Activation of RAR?, RAR?, or RXR? Increases Barrier Tightness in Human Induced Pluripotent Stem Cell-Derived Brain Endothelial Cells. Biotechnol J 13:
DeLaney, Kellen; Sauer, Christopher S; Vu, Nhu Q et al. (2018) Recent Advances and New Perspectives in Capillary Electrophoresis-Mass Spectrometry for Single Cell ""Omics"". Molecules 24:
Hennings, Thomas G; Chopra, Deeksha G; DeLeon, Elizabeth R et al. (2018) In Vivo Deletion of ?-Cell Drp1 Impairs Insulin Secretion Without Affecting Islet Oxygen Consumption. Endocrinology 159:3245-3256
Schaffer, Leah V; Rensvold, Jarred W; Shortreed, Michael R et al. (2018) Identification and Quantification of Murine Mitochondrial Proteoforms Using an Integrated Top-Down and Intact-Mass Strategy. J Proteome Res 17:3526-3536

Showing the most recent 10 out of 524 publications