Continuing support is requested for the Yale Predoctoral Training Program in Human Genetics and Genomics. The program involves 43 trainers from 10 departments. The vast majority of trainers are primary and joint appointees in the Department of Genetics at the School of Medicine, and virtually all of the trainees over the last funding period have been matriculated through the Genetics and Development Track of the program in Biological and Biomedical Sciences at Yale University. The focus of the training proposed is the use of genetic and genomic approaches to understand human disease. The main methods used are positional cloning of human and mouse disease genes, complemented by bioinformatics and computational analysis, transgenic and knock-out methods in mouse, as well as use of model organisms including Drosophila, C. elegans, and yeast to define biochemical pathways and permit genetics screening for modifier loci. This integrated program bringing together faculty with diverse backgrounds and expertise provides a rich training environment for students. Admitted students have strong scientific backgrounds and research experience with high academic achievement. Training in the first year includes formal course work and research rotations, leading to selection of the thesis advisor's laboratory. In the second year students complete course work, and take a qualifying exam in which they must demonstrate mastery of genetics and defend two written research proposals. Subsequent years are devoted to dissertation research and preparation of the written thesis. In addition, students engage in supervised teaching experience. Graduates continue in science, both in academia and in industry, most often early-stage biotechnology. With the increasing opportunities in human genetics and increased focus on human disease, there has been a marked increase in the number of applicants to the Genetics and Development Track in the last several years. Support is requested for 10 graduate students per year for a five-year period. ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Institutional National Research Service Award (T32)
Project #
2T32HD007149-26
Application #
6593269
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Vitkovic, Ljubisa
Project Start
1978-07-01
Project End
2008-04-30
Budget Start
2003-05-01
Budget End
2004-04-30
Support Year
26
Fiscal Year
2003
Total Cost
$416,444
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
DeMille, Mellissa M C; Tang, Kevin; Mehta, Chintan M et al. (2018) Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages. Proc Natl Acad Sci U S A 115:4951-4956
Griffin, John N; Sondalle, Samuel B; Robson, Andrew et al. (2018) RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus. Development 145:
Sulkowski, Parker L; Scanlon, Susan E; Oeck, Sebastian et al. (2018) PTEN Regulates Nonhomologous End Joining By Epigenetic Induction of NHEJ1/XLF. Mol Cancer Res 16:1241-1254
van Dijk, David; Sharma, Roshan; Nainys, Juozas et al. (2018) Recovering Gene Interactions from Single-Cell Data Using Data Diffusion. Cell 174:716-729.e27
Scanlon, Susan E; Hegan, Denise C; Sulkowski, Parker L et al. (2018) Suppression of homology-dependent DNA double-strand break repair induces PARP inhibitor sensitivity in VHL-deficient human renal cell carcinoma. Oncotarget 9:4647-4660
Sarro, Richard; Kocher, Acadia A; Emera, Deena et al. (2018) Disrupting the three-dimensional regulatory topology of the Pitx1 locus results in overtly normal development. Development 145:
Endicott, S Joseph; Brueckner, Martina (2018) NUP98 Sets the Size-Exclusion Diffusion Limit through the Ciliary Base. Curr Biol 28:1643-1650.e3
Sondalle, Samuel B; Baserga, Susan J (2017) Ribosomes Need Straight A's to Sleep. Cell 169:565-567
Burclaff, Joseph; Mills, Jason C (2017) Cell biology: Healthy skin rejects cancer. Nature 548:289-290
Adams, Andrew K; Smith, Shelley D; Truong, Dongnhu T et al. (2017) Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. Hum Genet 136:1395-1405

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