Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA045234-02
Application #
3188295
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1987-08-01
Project End
1988-08-31
Budget Start
1988-08-01
Budget End
1988-08-31
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Chun, Matthew G H; Mao, Jian-Hua; Chiu, Christopher W et al. (2010) Polymorphic genetic control of tumor invasion in a mouse model of pancreatic neuroendocrine carcinogenesis. Proc Natl Acad Sci U S A 107:17268-73
Ulanet, Danielle B; Hanahan, Douglas (2010) Loss of p19(Arf) facilitates the angiogenic switch and tumor initiation in a multi-stage cancer model via p53-dependent and independent mechanisms. PLoS One 5:e12454
Nolan-Stevaux, Olivier; Truitt, Morgan C; Pahler, Jessica C et al. (2010) Differential contribution to neuroendocrine tumorigenesis of parallel egfr signaling in cancer cells and pericytes. Genes Cancer 1:125-41
Chun, Matthew G H; Hanahan, Douglas (2010) Genetic deletion of the desmosomal component desmoplakin promotes tumor microinvasion in a mouse model of pancreatic neuroendocrine carcinogenesis. PLoS Genet 6:e1001120
Hager, Jeffrey H; Ulanet, Danielle B; Hennighausen, Lothar et al. (2009) Genetic ablation of Bcl-x attenuates invasiveness without affecting apoptosis or tumor growth in a mouse model of pancreatic neuroendocrine cancer. PLoS One 4:e4455
Hanahan, D; Jessee, J; Bloom, F R (1991) Plasmid transformation of Escherichia coli and other bacteria. Methods Enzymol 204:63-113