Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Unknown (R35)
Project #
5R35AG008967-07
Application #
2334022
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Supattapone, S; Muramoto, T; Legname, G et al. (2001) Identification of two prion protein regions that modify scrapie incubation time. J Virol 75:1408-13
Zulianello, L; Kaneko, K; Scott, M et al. (2000) Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein. J Virol 74:4351-60
Baskakov, I V; Aagaard, C; Mehlhorn, I et al. (2000) Self-assembly of recombinant prion protein of 106 residues. Biochemistry 39:2792-804
Scott, M R; Supattapone, S; Nguyen, H O et al. (2000) Transgenic models of prion disease. Arch Virol Suppl :113-24
Kaneko, K; Ball, H L; Wille, H et al. (2000) A synthetic peptide initiates Gerstmann-Straussler-Scheinker (GSS) disease in transgenic mice. J Mol Biol 295:997-1007
Mastrianni, J A; Nixon, R; Layzer, R et al. (1999) Prion protein conformation in a patient with sporadic fatal insomnia. N Engl J Med 340:1630-8
Supattapone, S; Nguyen, H O; Cohen, F E et al. (1999) Elimination of prions by branched polyamines and implications for therapeutics. Proc Natl Acad Sci U S A 96:14529-34
Scott, M R; Will, R; Ironside, J et al. (1999) Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans. Proc Natl Acad Sci U S A 96:15137-42
Safar, J; Prusiner, S B (1998) Molecular studies of prion diseases. Prog Brain Res 117:421-34
Prusiner, S B (1998) The prion diseases. Brain Pathol 8:499-513

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