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 #
2T32GM008349-11
Application #
2800243
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Project Start
1989-09-27
Project End
2004-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
11
Fiscal Year
1999
Total Cost
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
Diaz-Garcia, Luis; Schlautman, Brandon; Covarrubias-Pazaran, Giovanny et al. (2018) Massive phenotyping of multiple cranberry populations reveals novel QTLs for fruit anthocyanin content and other important chemical traits. Mol Genet Genomics 293:1379-1392
Boursier, Michelle E; Moore, Joseph D; Heitman, Katherine M et al. (2018) Structure-Function Analyses of the N-Butanoyl l-Homoserine Lactone Quorum-Sensing Signal Define Features Critical to Activity in RhlR. ACS Chem Biol 13:2655-2662
Gordon, Gina C; Cameron, Jeffrey C; Pfleger, Brian F (2018) Distinct and redundant functions of three homologs of RNase III in the cyanobacterium Synechococcus sp. strain PCC 7002. Nucleic Acids Res 46:1984-1997
UmaƱa, Angie C; Iwahori, Satoko; Kalejta, Robert F (2018) Direct Substrate Identification with an Analog Sensitive (AS) Viral Cyclin-Dependent Kinase (v-Cdk). ACS Chem Biol 13:189-199
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

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