S B Prusiner

发表

Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease

F E Cohen, F. Cohen, S. Prusiner, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Prion protein peptides induce alpha-helix to beta-sheet conformational transitions.

F E Cohen, F. Cohen, S. Prusiner, 1995, Biochemistry.

Prion protein gene variation among primates.

F E Cohen, F. Cohen, S. Prusiner, 1997, Journal of molecular biology.

Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform.

F E Cohen, F. Cohen, S. Prusiner, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Regional mapping of prion proteins in brain.

S. Prusiner, S. DeArmond, D. Serban, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity

S. Prusiner, S. DeArmond, P. Cortelli, 1996, Science.

Structural clues to prion replication.

R J Fletterick, F E Cohen, F. Cohen, 1994, Science.

Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid.

A L Burlingame, S. Prusiner, A. Burlingame, 1992, Biochemistry.

Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein.

D R Burton, H Serban, S. Prusiner, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Folding of prion protein to its native alpha-helical conformation is under kinetic control.

F E Cohen, F. Cohen, S. Prusiner, 2001, The Journal of biological chemistry.

The prion folding problem.

F E Cohen, F. Cohen, S. Prusiner, 1997, Current opinion in structural biology.

A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform.

F E Cohen, D R Burton, R A Houghten, 1997, Journal of molecular biology.

Immunologic and molecular biologic studies of prion proteins in bovine spongiform encephalopathy.

H Serban, S. Prusiner, J. Gabriel, 1993, The Journal of infectious diseases.

Molecular biology and pathogenesis of prion diseases.

S. Prusiner, S B Prusiner, S. B. Prusiner, 1996, Trends in biochemical sciences.

A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice.

F E Cohen, F. Cohen, S. Prusiner, 2000, Journal of molecular biology.

Prion diseases and the BSE crisis.

S. Prusiner, S B Prusiner, 1997, Science.

Attempts to restore scrapie prion infectivity after exposure to protein denaturants.

S. Prusiner, N. Stahl, R. Gabizon, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins

S. Prusiner, D. Westaway, S. DeArmond, 1990, Molecular and cellular biology.

Doxycycline control of prion protein transgene expression modulates prion disease in mice.

S. Prusiner, H. Bujard, S. DeArmond, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Intracellular accumulation of the cellular prion protein after mutagenesis of its Asn-linked glycosylation sites.

S. Prusiner, M. Rogers, A. Taraboulos, 1990, Glycobiology.

Some speculations about prions, amyloid, and Alzheimer's disease.

S. Prusiner, S B Prusiner, 1984, The New England journal of medicine.

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform.

F E Cohen, S Farr-Jones, F. Cohen, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible.

P E Wright, F E Cohen, F. Cohen, 1997, Proceedings of the National Academy of Sciences of the United States of America.

The prion diseases.

S. Prusiner, S B Prusiner, 1998, Brain pathology.

Pathologic conformations of prion proteins.

F E Cohen, F. Cohen, S. Prusiner, 1998, Annual review of biochemistry.

Prion biology and diseases.

S. Prusiner, S B Prusiner, 1999, Harvey lectures.

Complete genomic sequence and analysis of the prion protein gene region from three mammalian species.

Inyoul Y. Lee, L. Hood, S. Prusiner, 1998, Genome research.

Shattuck lecture--neurodegenerative diseases and prions.

S. Prusiner, S B Prusiner, 2001, The New England journal of medicine.