Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01CA048405-03S1
Application #
3549168
Study Section
Special Emphasis Panel (SRC (44))
Project Start
1988-08-01
Project End
1991-07-31
Budget Start
1990-08-01
Budget End
1991-07-31
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
005436803
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Wahl, G M (2006) Mouse bites dogma: how mouse models are changing our views of how P53 is regulated in vivo. Cell Death Differ 13:973-83
Aladjem, Mirit I; Rodewald, Luo Wei; Lin, Chii Mai et al. (2002) Replication initiation patterns in the beta-globin loci of totipotent and differentiated murine cells: evidence for multiple initiation regions. Mol Cell Biol 22:442-52
Raymond, E; Faivre, S; Weiss, G et al. (2001) Effects of hydroxyurea on extrachromosomal DNA in patients with advanced ovarian carcinomas. Clin Cancer Res 7:1171-80
Aladjem, M I; Rodewald, L W; Kolman, J L et al. (1998) Genetic dissection of a mammalian replicator in the human beta-globin locus. Science 281:1005-9
Aladjem, M I; Spike, B T; Rodewald, L W et al. (1998) ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage. Curr Biol 8:145-55
Aladjem, M I; Brody, L L; O'Gorman, S et al. (1997) Positive selection of FLP-mediated unequal sister chromatid exchange products in mammalian cells. Mol Cell Biol 17:857-61
Aladjem, M I; Wahl, G M (1997) Mapping replication fork direction by leading strand analysis. Methods 13:281-92
Van Den Berg, C; Guan, X Y; Von Hoff, D et al. (1995) DNA sequence amplification in human prostate cancer identified by chromosome microdissection: potential prognostic implications. Clin Cancer Res 1:11-8
Van den Berg, C L; McGill, J R; Kuhn, J G et al. (1994) Pharmacokinetics of hydroxyurea in nude mice. Anticancer Drugs 5:573-8
Nonet, G H; Wahl, G M (1993) Introduction of YACs containing a putative mammalian replication origin into mammalian cells can generate structures that replicate autonomously. Somat Cell Mol Genet 19:171-92

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