Research Topics
Species | C WeissmannSummaryAffiliation: University College London Country: UK Publications
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Detail Information
Publications
A mouse to rememberCharles Weissmann
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom
Cell 116:S111-3, 2 p following S113. 2004
Approaches to therapy of prion diseasesCharles Weissmann
Department of Neurodegenerative Disease MRC Prion Unit, Institute of Neurology, Queen Square, London WC1N 3BG, UK
Annu Rev Med 56:321-44. 2005....
Transmission of prionsC Weissmann
Medical Research Council Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, UK
J Infect Dis 186:S157-65. 2002..This property, first observed in a clinical setting, is now being investigated in experimental settings, both in animals and in cell culture...
Molecular biology of prionsCharles Weissmann
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, UK
Acta Neurobiol Exp (Wars) 62:153-66. 2002..This property, first observed in a clinical setting, is now being investigated in experimental settings, both in animals and in cell culture...
Transmission of prionsC Weissmann
Medical Research Council Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom
Proc Natl Acad Sci U S A 99:16378-83. 2002..This property, first observed in a clinical setting, is now being investigated in experimental settings, both in animals and in cell culture...
The state of the prionCharles Weissmann
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, UK
Nat Rev Microbiol 2:861-71. 2004..The precise structure of the prion is not yet known, nor are the mechanisms of infection, conformational conversion and pathogenesis understood...
PrP knock-out and PrP transgenic mice in prion researchC Weissmann
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, London, UK
Br Med Bull 66:43-60. 2003..In addition, the availability of PrP knock-out mice provided an approach to carry out reverse genetics on PrP, both in regard to prion disease and to its physiological role...
Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibodyM Enari
Medical Research Council Prion Unit, Neurogenetics, Imperial College School of Medicine at St. Mary's, London W2 1PG, United Kingdom
Proc Natl Acad Sci U S A 98:9295-9. 2001..These findings encourage the belief that passive immunization may provide a therapeutic approach to prion disease...
Ethical issues in human prion diseasesS J Tabrizi
Department of Neurodegenerative Disease/MRC Prion Unit, Institute of Neurology, London, UK
Br Med Bull 66:305-16. 2003..In this chapter, we outline ethical questions posed by research, diagnostic procedures and therapy in the field of prion diseases...
Molecular genetics of transmissible spongiform encephalopathies: an introductionCharles Weissmann
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, Queen Square, London WC1N 3BG, UK
J Toxicol Sci 27:69-77. 2002..How these murine models for human prion-related disease would contribute to the presently ongoing TSE research?..
A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prionsP C Klöhn
Medical Research Council Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, United Kingdom
Proc Natl Acad Sci U S A 100:11666-71. 2003..SC assays performed in a more time-consuming end point titration format extend the sensitivity and show that infectivity titers measured in tissue culture and in the mouse are similar...
Prions and the lymphoreticular systemC Weissmann
Medical Research Council Prion Unit, Imperial College School of Medicine at St Mary s, Norfolk Place, London W2 1PG, UK
Philos Trans R Soc Lond B Biol Sci 356:177-84. 2001....
Transgene-driven expression of the Doppel protein in Purkinje cells causes Purkinje cell degeneration and motor impairmentLucy Anderson
Medical Research Council Prion Unit and Department of Neurodegenerative Disease, and Division of Neuropathology, Institute of Neurology, University College, Queen Square, London WC1N 3BG, United Kingdom
Proc Natl Acad Sci U S A 101:3644-9. 2004..A similar situation was reported for the corresponding TgL7-DeltaPrP mice supporting the concept that Dpl and DeltaPrP cause cell death, possibly by interfering with a common signaling cascade essential for cell survival...
An enzyme-detergent method for effective prion decontamination of surgical steelGraham S Jackson
MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK
J Gen Virol 86:869-78. 2005..The prion-degrading reagents identified in this study are readily available, inexpensive, non-corrosive to instruments, non-hazardous to staff and compatible with current equipment and procedures used in hospital sterilization units...
Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfacesJulie Ann Edgeworth
Medical Research Council Prion Unit, Department of Neurodegenerative Disease, University College London Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom
Proc Natl Acad Sci U S A 106:3479-83. 2009..In addition, its specific application in assay of metal-bound prions allows evaluation of novel prion decontamination methods...
Spontaneous generation of mammalian prionsJulie A Edgeworth
Medical Research Council Prion Unit, Department of Neurodegenerative Disease, University College London Institute of Neurology, London WC1N 3BG, United Kingdom
Proc Natl Acad Sci U S A 107:14402-6. 2010..Alternatively, if prions were naturally present in the brain at levels not detectable by conventional methods, metal surfaces might concentrate them to the extent that they become quantifiable by the scrapie cell assay...
Birth of a prion: spontaneous generation revisitedCharles Weissmann
Scripps Florida, Jupiter 33480, USA
Cell 122:165-8. 2005..Recent work shows that the agent, the prion, can be replicated in a cell-free system, that it can be generated de novo, and that the strain-specific properties of prions are encoded by conformational variations of the underlying protein...
Chronic lymphocytic inflammation specifies the organ tropism of prionsMathias Heikenwalder
Institute of Neuropathology, University Hospital of Zurich, CH 8091 Zurich, Switzerland
Science 307:1107-10. 2005..By expanding the tissue distribution of prions, chronic inflammatory conditions may act as modifiers of natural and iatrogenic prion transmission...
Transcriptional stability of cultured cells upon prion infectionChristian Julius
Institute of Neuropathology, University Hospital of Zurich, Schmelzbergstrasse 12, CH 8091 Zurich, Switzerland
J Mol Biol 375:1222-33. 2008..We conclude that, surprisingly, there are no universal transcriptional changes induced by prion infection of neural cells in vitro...
Assaying prions in cell culture: the standard scrapie cell assay (SSCA) and the scrapie cell assay in end point format (SCEPA)Sukhvir P Mahal
Department of Infectology, Scripps Florida, Jupiter, FL, USA
Methods Mol Biol 459:49-68. 2008..Assays performed in a more time-consuming end point titration format extend the sensitivity and show that infectivity titers measured in tissue culture and in the mouse are similar...
Expression of truncated PrP targeted to Purkinje cells of PrP knockout mice causes Purkinje cell death and ataxiaEckhard Flechsig
Institut fur Molekularbiologie, Universitat Zurich, CH 8057 Zurich, Switzerland
EMBO J 22:3095-101. 2003..Doppel and truncated PrP probably cause Purkinje cell degeneration by the same mechanism...
Prion strain discrimination in cell culture: the cell panel assaySukhvir P Mahal
Department of Infectology, Scripps Florida, 5353 Parkside Drive, Jupiter, FL 33458, USA
Proc Natl Acad Sci U S A 104:20908-13. 2007....
