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Number of items: 32.

Julius, C; Hutter, G; Wagner, U; Seeger, H; Kana, V; Kranich, J; Klöhn, P C; Weissmann, C; Miele, G; Aguzzi, A (2008). Transcriptional stability of cultured cells upon prion infection. Journal of Molecular Biology, 375(5):1222-1233.

Montrasio, F; Cozzio, A; Flechsig, E; Rossi, D; Klein, M A; Rülicke, T; Raeber, A J; Vosshenrich, C A; Proft, J; Aguzzi, A; Weissmann, C (2001). B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 98(7):4034-4037.

Weissmann, C; Raeber, A J; Montrasio, F; Hegyi, I; Frigg, R; Klein, M A; Aguzzi, A (2001). Prions and the lymphoreticular system. Philosophical Transactions of the Royal Society B: Biological Sciences, 356(1406):177-184.

Rossi, D; Cozzio, A; Flechsig, E; Klein, M A; Rülicke, T; Aguzzi, A; Weissmann, C (2001). Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain. The EMBO Journal, 20(4):694-702.

Raeber, A J; Montrasio, F; Hegyi, I; Frigg, R; Klein, M A; Aguzzi, A; Weissmann, C (2001). Studies on prion replication in spleen. Developmental Immunology, 8(3-4):291-304.

Brandner, S; Klein, M A; Frigg, R; Pekarik, V; Parizek, P; Raeber, A; Glatzel, M; Schwarz, P; Rülicke, T; Weissmann, C; Aguzzi, A (2000). Neuroinvasion of prions: insights from mouse models. Experimental Physiology, 85(6):705-712.

Flechsig, E; Shmerling, D; Hegyi, I; Raeber, A J; Fischer, M B; Cozzio, A; von Mering, C; Aguzzi, A; Weissmann, C (2000). Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice. Neuron, 27(2):399-408.

Benninger, Y; Marino, S; Hardegger, R; Weissmann, C; Aguzzi, A; Brandner, S (2000). Differentiation and histological analysis of embryonic stem cell-derived neural transplants in mice. Brain Pathology, 10(3):330-341.

Montrasio, F; Frigg, R; Glatzel, M; Klein, M A; Mackay, F; Aguzzi, A; Weissmann, C (2000). Impaired prion replication in spleens of mice lacking functional follicular dendritic cells. Science, 288(5469):1257-1259.

Raeber, A J; Klein, M A; Frigg, R; Flechsig, E; Aguzzi, A; Weissmann, C (1999). PrP-dependent association of prions with splenic but not circulating lymphocytes of scrapie-infected mice. The EMBO Journal, 18(10):2702-2706.

Raeber, A J; Sailer, A; Hegyi, I; Klein, M A; Rülicke, T; Fischer, M B; Brandner, S; Aguzzi, A; Weissmann, C (1999). Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 96(7):3987-3992.

Weissmann, C; Aguzzi, A (1999). Perspectives: neurobiology. PrP's double causes trouble. Science, 286(5441):914-915.

Klein, M A; Frigg, R; Raeber, A J; Flechsig, E; Hegyi, I; Zinkernagel, R M; Weissmann, C; Aguzzi, A (1998). PrP expression in B lymphocytes is not required for prion neuroinvasion. Nature Medicine, 4(12):1429-1433.

Raeber, A J; Brandner, S; Klein, M A; Benninger, Y; Musahl, C; Frigg, R; Roeckl, C; Fischer, M B; Weissmann, C; Aguzzi, A (1998). Transgenic and knockout mice in research on prion diseases. Brain Pathology, 8(4):715-733.

Aguzzi, A; Weissmann, C (1998). Prion diseases. Haemophilia, 4(4):619-627.

Shmerling, D; Hegyi, I; Fischer, M B; Blättler, T; Brandner, S; Götz, J; Rülicke, T; Flechsig, E; Cozzio, A; von Mering, C; Hangartner, C; Aguzzi, A; Weissmann, C (1998). Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell, 93(2):203-214.

Aguzzi, A; Weissmann, C (1998). Spongiform encephalopathies. The prion's perplexing persistence. Nature, 392(6678):763-764.

Weissmann, C; Fischer, M; Raeber, A; Bueler, H; Sailer, A; Shmerling, D; Rülicke, T; Brandner, S; Aguzzi, A (1998). The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. Revue scientifique et technique, 17(1):278-290.

Weissmann, C; Aguzzi, A (1997). Bovine spongiform encephalopathy and early onset variant Creutzfeldt-Jakob disease. Current Opinion in Neurobiology, 7(5):695-700.

Blättler, T; Brandner, S; Raeber, A J; Klein, M A; Voigtländer, T; Weissmann, C; Aguzzi, A (1997). PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain. Nature, 389(6646):69-73.

Aguzzi, A; Blättler, T; Klein, M A; Räber, A J; Hegyi, I; Frigg, R; Brandner, S; Weissmann, C (1997). Tracking prions: the neurografting approach. Cellular and Molecular Life Sciences, 53(6):485-495.

Raeber, A J; Race, R E; Brandner, S; Priola, S A; Sailer, A; Bessen, R A; Mucke, L; Manson, J C; Aguzzi, A; Oldstone, M B; Weissmann, C; Chesebro, B (1997). Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie. EMBO Journal, 16(20):6057-6065.

Aguzzi, A; Raeber, A; Blättler, T; Flechsig, E; Klein, M; Weissmann, C; Brandner, S (1997). Neurotoxicity and neuroinvasiveness of prions. Journal of NeuroVirology, 3(S1):S23-S24.

Aguzzi, A; Weissmann, C (1997). Prion research: the next frontiers. Nature, 389(6653):795-798.

Brandner, S; Raeber, A; Sailer, A; Blättler, T; Fischer, M B; Weissmann, C; Aguzzi, A (1996). Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 93(23):13148-13151.

Fischer, M B; Rülicke, T; Raeber, A; Sailer, A; Moser, M; Oesch, B; Brandner, S; Aguzzi, A; Weissmann, C (1996). Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. The EMBO Journal, 15(6):1255-1264.

Brandner, S; Isenmann, S; Raeber, A; Fischer, M B; Sailer, A; Kobayashi, Y; Marino, S; Weissmann, C; Aguzzi, A (1996). Normal host prion protein necessary for scrapie-induced neurotoxicity. Nature, 379(6563):339-343.

Aguzzi, A; Weissmann, C (1996). Sleepless in Bologna: transmission of fatal familial insomnia. Trends in Microbiology, 4(4):129-132.

Aguzzi, A; Weissmann, C (1996). Spongiform encephalopathies: a suspicious signature. Nature, 383(6602):666-667.

Weissmann, C; Fischer, M; Raeber, A; Büeler, H; Sailer, A; Shmerling, D; Rülicke, T; Brandner, S; Aguzzi, A (1996). The role of PrP in pathogenesis of experimental scrapie. Cold Spring Harbor Symposia on Quantitative Biology, 61:511-522.

Weissmann, C; Fischer, M; Raeber, A; Büeler, H; Sailer, A; Shmerling, D; Rülicke, T; Brandner, S; Aguzzi, A (1996). The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. International Journal of Experimental Pathology, 77(6):283-293.

Basler, K; Oesch, B; Scott, M; Westaway, D; Wälchli, M; Groth, D F; McKinley, M P; Prusiner, S B; Weissmann, C (1986). Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell, 46(3):417-428.

This list was generated on Tue Nov 21 00:42:28 2017 CET.