79 GHz UWB automotive short range radar – Spectrum allocation and technology trends (2009)
A. Sailer, G. Rollmann, J. Dickmann
Automotive UWB (Ultra-Wideband) short range radar (SSR) is on the market as a key technology for novel comfort and safety systems. SiGe based 79 GHz UWB SRR will be a definite candidate for the long...
D. F. Bantz, K. A. Beaty, T. Chefalas, S. Jalan, G. Kar, A. Kochut, ...
IT Autopilot: A flexible IT service management and delivery platform for small and medium business IT Autopilot is a flexible architecture to support the delivery of information technology (IT)...
Executive Summary of the Workshop on Polarization and Beam Energy Measurements at the ILC (2008)
B. Aurand, I. Bailey, C. Bartels, G. Blair, A. Brachmann, ...
Internal report | Preprint
Raeber, A J, Sailer, A, Hegyi, I, Klein, M A, Rülicke, T, Fischer, M B, ...
The cellular form of the Prion protein (PrPC) is necessary for prion replication in mice. To determine whether it is also sufficient, we expressed PrP under the control of various cell- or...
The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. (1998)
Weissmann, C, Fischer, M, Raeber, A, Bueler, H, Sailer, A, Shmerling, D, ...
The prion, the transmissible agent that causes spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease, is believed to be devoid of nucleic acid...
Raeber, A J, Race, R E, Brandner, S, Priola, S A, Sailer, A, Bessen, R A, ...
Transmissible spongiform encephalopathies are characterized by spongiosis, astrocytosis and accumulation of PrPSc, an isoform of the normal host protein PrPC. The exact cell types responsible for...
Brandner, S, Raeber, A, Sailer, A, Blättler, T, Fischer, M B, Weissmann, C, ...
Mice devoid of PrPC (Prnp%) are resistant to scrapie and do not allow propagation of the infectious agent (prion). PrPC-expressing neuroectodermal tissue grafted into Prnp% brains but not the...
Fischer, M B, Rülicke, T, Raeber, A, Sailer, A, Moser, M, Oesch, B, ...
The 'protein only' hypothesis postulates that the prion, the agent causing transmissible spongiform encephalopathies, is PrP(Sc), an isoform of the host protein PrP(C). Protease treatment of prion...
Normal host prion protein necessary for scrapie-induced neurotoxicity. (1996)
Brandner, S, Isenmann, S, Raeber, A, Fischer, M B, Sailer, A, Kobayashi, Y, ...
Accumulation of the prion protein PrPSc, a pathological and protease-resistant isoform of the normal host protein PrPC, is a feature of prion disease such as scrapie. It is still unknown whether...
The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. (1996)
Weissmann, C, Fischer, M, Raeber, A, Büeler, H, Sailer, A, Shmerling, D, ...
The role of PrP in pathogenesis of experimental scrapie. (1996)
Weissmann, C, Fischer, M, Raeber, A, Büeler, H, Sailer, A, Shmerling, D, ...
PrP-deficient mice are resistant to scrapie (1994)
Weissmann, C., Bueler, H., Fischer, M., Sailer, A., Aguzzi, A., Aguet, M.
Prusiner proposed that the infectious agent of scrapie, the prion, is PrPSc, a modified form of the normal host protein PrPC. Prn-p0/0 mice devoid of PrPC showed normal development and behavior. When...
Mice devoid of PrP are resistant to scrapie (1993)
Bueler, H., Aguzzi, A., Sailer, A., Greiner, R. A., Autenried, P., Aguet, M., ...
S.B. Prusiner proposed that the infectious agent of scraple, the prion, is PrPSc, a modified form of the normal host protein PrPC. Prn-p0/0 mice devoid of PrPC showed normal development and behavior....
Role of Prp in Prion Diseases (1993)
Weissmann, C., Bueler, H., Sailer, A., Fischer, M., Aguet, M., Aguzzi, A.
Role of PrP in prion diseases (1993)
Weissmann, C, Büeler, H, Sailer, A, Fischer, M, Aguet, M, Aguzzi, A
Fischer, M, Rülicke, T, Raeber, A, Sailer, A, Moser, M, Oesch, B, ...
The 'protein only' hypothesis postulates that the prion, the agent causing transmissible spongiform encephalopathies, is PrP(Sc), an isoform of the host protein PrP(C). Protease treatment of prion...
Raeber, A J, Race, R E, Brandner, S, Priola, S A, Sailer, A, Bessen, R A, ...
Transmissible spongiform encephalopathies are characterized by spongiosis, astrocytosis and accumulation of PrPSc, an isoform of the normal host protein PrPC. The exact cell types responsible for...
Fischer, M, Rülicke, T, Raeber, A, Sailer, A, Moser, M, Oesch, B, ...
The 'protein only' hypothesis postulates that the prion, the agent causing transmissible spongiform encephalopathies, is PrP(Sc), an isoform of the host protein PrP(C). Protease treatment of prion...
Raeber, A J, Race, R E, Brandner, S, Priola, S A, Sailer, A, Bessen, R A, ...
Transmissible spongiform encephalopathies are characterized by spongiosis, astrocytosis and accumulation of PrPSc, an isoform of the normal host protein PrPC. The exact cell types responsible for...
Schwerer, M, Sailer, A, Kraft, K, Baczako, K, Maier, H
Aims—To clarify p21waf1/cip1 expression in sinonasal lesions.
Büeler, H., Raeber, A., Sailer, A., Fischer, M., Aguzzi, A., Weissmann, C.
BACKGROUND: It has been proposed that the prion, the infectious agent of transmissible spongiform encephalopathies, is PrPSc, a post-translationally modified form of the normal host protein PrPC. We...