The Genetics and Molecular Biology Training Program has as its primary goal the education of carefully selected individuals for the research, teaching, and industrial needs of this country. GMB was established five years ago by the fusion of two long-standing training programs: Genetics and Cell and Molecular Biology at Princeton, and this fusion has been very successful. We receive approximately 300 applications a year, and our success at attracting the best students in the country continues to improve. Currently this program contains a 42-member faculty who serve as mentors for 100 graduate students, 124 postdoctoral fellows, and 97 undergraduate majors. The participating mentors include the faculty of the Department of Molecular Biology (33), six faculty members from Chemistry, two faculty members from the Ecology and Evolutionary Biology, and one faculty from Computer Science. They provide expertise in biological systems ranging from bacteria to humans, and they offer training in areas of molecular biology, cell biology developmental biology, genetics, genomics, immunology, microbiology, neurobiology, structural biology, virology, biophysics, biochemistry and computational biology. Training laboratories are located in four different building complexes that are either nearly complete, newly built or recently renovated. Each of these is well-equipped for modern biological research offering state-of-the-art facilities to all. The training program consists of formal course work, laboratory rotations, teaching experiences, and a wide variety of special activities. While formal training is emphasized in year one, and to a lesser extent in year two, we realize that the PhD is a research degree. Accordingly, we spend considerable effort to assist trainees in finding an appropriate mentor, and to monitor their subsequent progress in the research lab. The success of our program is best judged by the success of our graduates. We have awarded 272 PhD's, and greater than 95% of these remain actively involved in science or science-related fields in exciting and, sometimes novel, ways. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007388-30
Application #
7066094
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Rhoades, Marcus M
Project Start
1977-07-01
Project End
2008-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
30
Fiscal Year
2006
Total Cost
$1,261,319
Indirect Cost
Name
Princeton University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Sonnett, Matthew; Yeung, Eyan; Wühr, Martin (2018) Accurate, Sensitive, and Precise Multiplexed Proteomics Using the Complement Reporter Ion Cluster. Anal Chem 90:5032-5039
Raitman, Irene; Huang, Mia L; Williams, Selwyn A et al. (2018) Heparin-fibronectin interactions in the development of extracellular matrix insolubility. Matrix Biol 67:107-122
Murray, L A; Sheng, X; Cristea, I M (2018) Orchestration of protein acetylation as a toggle for cellular defense and virus replication. Nat Commun 9:4967
Cook, Katelyn C; Cristea, Ileana M (2018) Location is everything: protein translocations as a viral infection strategy. Curr Opin Chem Biol 48:34-43
Kaletsky, Rachel; Yao, Victoria; Williams, April et al. (2018) Transcriptome analysis of adult Caenorhabditis elegans cells reveals tissue-specific gene and isoform expression. PLoS Genet 14:e1007559
Lum, Krystal K; Song, Bokai; Federspiel, Joel D et al. (2018) Interactome and Proteome Dynamics Uncover Immune Modulatory Associations of the Pathogen Sensing Factor cGAS. Cell Syst 7:627-642.e6
Cetera, Maureen; Leybova, Liliya; Joyce, Bradley et al. (2018) Counter-rotational cell flows drive morphological and cell fate asymmetries in mammalian hair follicles. Nat Cell Biol 20:541-552
Eagle, Whitby V I; Yeboah-Kordieh, Daniel K; Niepielko, Matthew G et al. (2018) Distinct cis-acting elements mediate targeting and clustering of Drosophila polar granule mRNAs. Development 145:
Gramespacher, Josef A; Stevens, Adam J; Thompson, Robert E et al. (2018) Improved protein splicing using embedded split inteins. Protein Sci 27:614-619
Hoegler, Kenric J; Hecht, Michael H (2018) Artificial Gene Amplification in Escherichia coli Reveals Numerous Determinants for Resistance to Metal Toxicity. J Mol Evol 86:103-110

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