This proposal describes a predoctoral genetics training program on the La Jolla Mesa including the University of California, San Diego (UCSD) School of Medicine, the UCSD Division of Biology, and The Salk Institute for Biological Studies. The goal of this program is to train graduate students for future careers as academic or industrial scientists investigating genetic phenomena, or using genetic methods to understand biological problems important for human health. Our training faculty have joined together to create a common vision of contemporary genetics training in which we first build a foundation of basic biological and biomedical science. This foundation will then support a tripod of integrated educational principles of genetics and genomics including: 1) rigorous education in the classical principles and intellectual methods of genetics; 2) research training in the newest methods of classical and molecular genetics including genomics; and 3) development of an appreciation of the problems, outlooks, and ethical issues associated with modem clinical and medical genetics. The development of this unique program is tied to continued expansion of our graduate programs based on substantial new faculty recruitment in genetics and genomics and as a companion to the integration of previously distinct training efforts at UCSD. Thus, we are requesting financial support for 20 trainees in the first year phasing into 26 trainees after four years to be educated in genetics laboratories at UCSD and the Salk Institute.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008666-08
Application #
6898146
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Rhoades, Marcus M
Project Start
1998-07-01
Project End
2008-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
8
Fiscal Year
2005
Total Cost
$412,899
Indirect Cost
Name
University of California San Diego
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Hsu, Cynthia L; Lee, Elian X; Gordon, Kara L et al. (2018) MAP4K3 mediates amino acid-dependent regulation of autophagy via phosphorylation of TFEB. Nat Commun 9:942
Cowell, Annie N; Istvan, Eva S; Lukens, Amanda K et al. (2018) Mapping the malaria parasite druggable genome by using in vitro evolution and chemogenomics. Science 359:191-199
Wheeler, Emily C; Van Nostrand, Eric L; Yeo, Gene W (2018) Advances and challenges in the detection of transcriptome-wide protein-RNA interactions. Wiley Interdiscip Rev RNA 9:
Buckley, Alexandra R; Ideker, Trey; Carter, Hannah et al. (2018) Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Genome Med 10:69
Veevers, Jennifer; Farah, Elie N; Corselli, Mirko et al. (2018) Cell-Surface Marker Signature for Enrichment of Ventricular Cardiomyocytes Derived from Human Embryonic Stem Cells. Stem Cell Reports 11:828-841
Lindsay, Scott A; Lin, Samuel J H; Wasserman, Steven A (2018) Short-Form Bomanins Mediate Humoral Immunity in Drosophila. J Innate Immun 10:306-314
Brandler, William M; Antaki, Danny; Gujral, Madhusudan et al. (2018) Paternally inherited cis-regulatory structural variants are associated with autism. Science 360:327-331
Wortham, Matthew; Benthuysen, Jacqueline R; Wallace, Martina et al. (2018) Integrated In Vivo Quantitative Proteomics and Nutrient Tracing Reveals Age-Related Metabolic Rewiring of Pancreatic ? Cell Function. Cell Rep 25:2904-2918.e8
Solomon, Terry; Lapek Jr, John D; Jensen, Søren Beck et al. (2018) Identification of Common and Rare Genetic Variation Associated With Plasma Protein Levels Using Whole-Exome Sequencing and Mass Spectrometry. Circ Genom Precis Med 11:e002170
Ghosh, Shereen G; Becker, Kerstin; Huang, He et al. (2018) Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. Am J Hum Genet 103:431-439

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