Prion diseases and the BSE crisis von Prusiner, S.B

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Compelling Transgenetic Evidence for Transmission of Bovine Spongiform Encephalopathy Prions to Humans von Scott, Michael R., Will, Robert, Ironside, James, Nguyen, Hoang-Oanh B., Tremblay, Patrick, DeArmond, Stephen J., Prusiner, Stanley B.

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Induction of Distinct [URE3] Yeast Prion Strains von Schlumpberger, Martin, Prusiner, Stanley B., Herskowitz, Ira

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A Transmembrane Form of the Prion Protein in Neurodegenerative Disease von Hegde, Ramanujan S., Mastrianni, James A., Scott, Michael R., DeFea, Kathryn A., Tremblay, Patrick, Torchia, Marilyn, DeArmond, Stephen J., Prusiner, Stanley B., Lingappa, Vishwanath R.

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Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity von Telling, Glenn C., Parchi, Piero, DeArmond, Stephen J., Cortelli, Pietro, Montagna, Pasquale, Gabizon, Ruth, Mastrianni, James, Lugaresi, Elio, Gambetti, Pierluigi, Prusiner, Stanley B.

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Branched Polyamines Cure Prion-Infected Neuroblastoma Cells von Supattapone, S, Wille, H, Uyechi, L, Safar, J, Tremblay, P, Szoka, F C, Cohen, F E, Prusiner, S B, Scott, M R

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Transmissible and genetic prion diseases share a common pathway of neurodegeneration von Lingappa, Vishwanath R, Hegde, Ramanujan S, Tremblay, Patrick, Groth, Darlene, DeArmond, Stephen J, Prusiner, Stanley B

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Evidence for synthesis of scrapie prion proteins in the endocytic pathway von Borchelt, D.R. (University of California, San Francisco, CA), Taraboulos, A, Prusiner, S.B

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Molecular biology of prion diseases von Prusiner, S.B. (University of California, San Francisco, CA)

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Local Structural Plasticity of the Prion Protein. Analysis of NMR Relaxation Dynamics von Viles, John H, Donne, David, Kroon, Gerard, Prusiner, Stanley B, Cohen, Fred E, Dyson, H. Jane, Wright, Peter E

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Shattuck lecture: Neurodegenerative diseases and prions von PRUSINER, Stanley B

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Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies von PRUSINER, S. B, GROTH, D, SERBAN, A, KOEHLER, R, FOSTER, D, TORCHIA, M, BURTON, D, SHU-LIAN YANG, DEARMOND, S. J

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Copper binding to octarepeat peptides of the prion protein monitored by mass spectrometry von WHITTAL, RANDY M., BALL, HAYDN L., COHEN, FRED E., BURLINGAME, ALMA L., PRUSINER, STANLEY B., BALDWIN, MICHAEL A.

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Etiology and pathogenesis of prion diseases von DEARMOND, S. J, PRUSINER, S. B

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Chemical chaperones interfere with the formation of scrapie prion protein von Tatzelt, J., Prusiner, S. B., Welch, W. J.

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins von KEH-MING PAN, BALDWIN, M, PRUSINER, S. B, NGUYEN, J, GASSET, M, SERBAN, A, GROTH, D, MEHLHORN, I, ZIWEI HUANG, FLETTERICK, R. J, COHEN, F. E

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Prion Protein Conformation in a Patient with Sporadic Fatal Insomnia von Mastrianni, James A, Nixon, Randal, Layzer, Robert, Telling, Glenn C, Han, Dong, DeArmond, Stephen J, Prusiner, Stanley B

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Prions von Prunsiner, S.B. (University of California, San Francisco, CA.)

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Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein von Büeler, Hansruedi, Fischer, Marek, Lang, Yolande, Bluethmann, Horst, Lipp, Hans-Peter, DeArmond, Stephen J, Prusiner, Stanley B, Aguet, Michel, Weissmann, Charles

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Prion Glycoprotein:  Structure, Dynamics, and Roles for the Sugars von Rudd, Pauline M, Wormald, Mark R, Wing, David R, Prusiner, Stanley B, Dwek, Raymond A

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