Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J. R. Bunn"'
Publikováno v:
Review of Scientific Instruments. 94:035101
This paper describes the hardware and software upgrades, operation, and performance of the high intensity diffractometer for residual stress analysis (HIDRA) instrument, a residual stress mapping neutron diffractometer located at the High Flux Isotop
Autor:
James W. Ironside, Gabor G. Kovacs, Herbert Budka, Johannes A. Hainfellner, L. McCardle, Helga Flicker, Mark Head, Tristan J. R. Bunn, Lajos László, Ivan Hegyi, Christa Jarius
Publikováno v:
Brain Pathol
Demonstration of the abnormal form of the prion protein (PrP) in the brain confirms the diagnosis of human prion disease (PrD). Using immunohistochemistry, we have compared ten monoclonal antibodies in PrD subtypes including sporadic and variant Creu
Autor:
Frederik Barkhof, Wouter Kamphorst, James W. Ironside, Philip Scheltens, Bernard M. J. Uitdehaag, Tristan J. R. Bunn, Mark Head, Gerrit Tissingh
Publikováno v:
Annals of Neurology, 50(2), 258-261. John Wiley and Sons Inc.
Head, M W, Tissingh, G, Uitdehaag, B M J, Barkhof, F, Bunn, T J R, Ironside, J W, Kamphorst, W & Scheltens, P 2001, ' Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote : Atypical molecular phenotype ', Annals of Neurology, vol. 50, no. 2, pp. 258-261 . https://doi.org/10.1002/ana.1100
Head, M W, Tissingh, G, Uitdehaag, B M J, Barkhof, F, Bunn, T J R, Ironside, J W, Kamphorst, W & Scheltens, P 2001, ' Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote : Atypical molecular phenotype ', Annals of Neurology, vol. 50, no. 2, pp. 258-261 . https://doi.org/10.1002/ana.1100
A case of sporadic Creutzfeldt-Jakob disease (sCJD) is described in a young Dutch protein prion gene (PRNP) codon 129 valine homozygote. Certain clinical and molecular features of this case overlap those of variant CJD. The case highlights possible d
Autor:
Lajos László, Tristan J. R. Bunn, Gabor G. Kovacs, Robert G. Will, James W. Ironside, Mark Head
Publikováno v:
Neuropathology and Applied Neurobiology. 26:463-472
The naturally occurring polymorphism at codon 129 of the human prion protein gene (PRNP) influences susceptibility to sporadic Creutzfeldt-Jakob Disease (CJD); the majority of the patients are methionine homozygotes at this locus, while valine homozy
Publikováno v:
Calcified tissue international. 76(4)
Pleiotrophin (PTN) was found to have potent effects on regulation of osteoblast recruitment, proliferation and differentiation. The present study examined the long-term effects of targeted PTN over-expression on bone development and repair in a trans
Autor:
Clive S. McKimmie, Robert G. Will, Matthew Bishop, Tristan J. R. Bunn, Victoria McLoughlin, James W. Ironside, Suzanne Lowrie, Mark Head, L. McCardle, Michelle C. Williams, Richard Knight, Jan Mackenzie
Publikováno v:
Annals of neurology. 55(6)
Human prion diseases can occur as an idiopathic disorder (sporadic Creutzfeldt–Jakob disease) or can be acquired, as is the case for variant Creutzfeldt–Jakob disease. These disorders are characterized by the accumulation of a protease-resistant
Autor:
Diane Ritchie, Victoria Northcott, Neil McLennan, Kathleen A. Rennison, Tristan J. R. Bunn, Mark Head, James W. Ironside, L. McCardle, Richard Bonshek, Andrew B Tullo
Publikováno v:
Investigative ophthalmologyvisual science. 44(1)
PURPOSE: Creutzfeldt-Jakob disease (CJD) primarily affects the brain. This study was conducted to assess the possible involvement of the eye in sporadic and variant CJD by testing for the presence of the disease-associated, protease-resistant isoform
Autor:
Mark W. Head, Tristan J. R. Bunn, Matthew T. Bishop, Victoria McLoughlin, Suzanne Lowrie, Clive S. McKimmie, Michelle C. Williams, Linda McCardle, Jan MacKenzie, Richard Knight, Robert G. Will, James W. Ironside
Publikováno v:
Annals of Neurology; Jun2004, Vol. 55 Issue 6, p851-859, 9p