Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA030246-05
Application #
4691318
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Larson, S M; Antczak, J B; Joklik, W K (1994) Reovirus exists in the form of 13 particle species that differ in their content of protein sigma 1. Virology 201:303-11
Starnes, M C; Joklik, W K (1993) Reovirus protein lambda 3 is a poly(C)-dependent poly(G) polymerase. Virology 193:356-66
Xu, P; Miller, S E; Joklik, W K (1993) Generation of reovirus core-like particles in cells infected with hybrid vaccinia viruses that express genome segments L1, L2, L3, and S2. Virology 197:726-31
Antczak, J B; Joklik, W K (1992) Reovirus genome segment assortment into progeny genomes studied by the use of monoclonal antibodies directed against reovirus proteins. Virology 187:760-76
Hu, F Q; Pickup, D J (1991) Transcription of the terminal loop region of vaccinia virus DNA is initiated from the telomere sequences directing DNA resolution. Virology 181:716-20
Mao, Z X; Joklik, W K (1991) Isolation and enzymatic characterization of protein lambda 2, the reovirus guanylyltransferase. Virology 185:377-86
Owen, R D; Ostrowski, M C (1990) A nuclear factor that binds to ras-responsive enhancer elements is present in human tumor cells. Cell Growth Differ 1:601-6
Owen, R D; Bortner, D M; Ostrowski, M C (1990) ras oncogene activation of a VL30 transcriptional element is linked to transformation. Mol Cell Biol 10:1-9
Owen, R D; Ostrowski, M C (1990) Transcriptional activation of a conserved sequence element by ras requires a nuclear factor distinct from c-fos or c-jun. Proc Natl Acad Sci U S A 87:3866-70
Parsons, B L; Pickup, D J (1990) Transcription of orthopoxvirus telomeres at late times during infection. Virology 175:69-80

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