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One of the key molecular events in the transmissible spongiform encephalopathies or prion diseases is the conformational conversion of the cellular prion protein PrPC into the misfolded and pathogenic isoform, PrPSc. Prion diseases are fatal neurodeg
Externí odkaz:
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685755
Autor:
Suleiman, Suzanne, McGuire, Lynne, Chong, Angela, Ritchie, Diane, Boyle, Aileen, McManus, Lee, Brydon, Fraser, Smith, Colin, Knight, Richard, Green, Alison J E, Diack, Abigail, Barria Matus, Marcelo
Publikováno v:
Suleiman, S, McGuire, L, Chong, A, Ritchie, D, Boyle, A, McManus, L, Brydon, F, Smith, C, Knight, R, Green, A J E, Diack, A & Barria Matus, M 2023, ' Conservation of vCJD strain properties after extraction and in vitro propagation of PrPSc from archived formalin-fixed brain and appendix tissues using highly sensitive Protein Misfolding Cyclic Amplification ', Molecular Neurobiology . https://doi.org/10.1007/s12035-023-03444-2
Three retrospective lymphoreticular tissue studies (Appendix I, II and III) aimed to estimate the UK prevalence of variant Creutzfeldt-Jakob disease (vCJD), following exposure of the population to the bovine spongiform encephalopathy (BSE) agent, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3094::a53184ea2ed2a5d5f1318f2e49a4427a
https://www.pure.ed.ac.uk/ws/files/365669616/s12035_023_03444_2.pdf
https://www.pure.ed.ac.uk/ws/files/365669616/s12035_023_03444_2.pdf
Autor:
Piconi, Gabriele
Prion diseases are a group of fatal neurodegenerative diseases associated with proteopathy occurring in humans and other mammals. The mechanism of prion replication is thought to be based on the induced misfolding of the host encoded prion protein an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______463::038f240c5d1fb4b6d704a723a0a34b49
https://hdl.handle.net/1842/36901
https://hdl.handle.net/1842/36901