Harry-Olatoke, R.; Khan, M.N.; Al-Sarraj, S.; Lantos, P.L.; Anderton, B. and Rezaie, P.
|DOI (Digital Object Identifier) Link:||http://doi.org/10.1111/j.1365-2990.2004.00542.x|
|Google Scholar:||Look up in Google Scholar|
Cellular prion protein (PrPe) is a membrane-bound glycoprotein, reportedly expressed at high levels at synapses. The function of PrPe is uncertain. However, the formation of an abnormal isoform (PrPSe) is considered central to the pathogenesis of Creutzfeldt-Jakob disease (CJD), and synaptic damage has been suggested as an early pathological event in CJD.
|Item Type:||Conference Item|
|Extra Information:||The abstract is published in Neuropathology & Applied Neurobiology, Volume 30 Page 194. See page 195 of PDF at link.
|Academic Unit/Department:||Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
|Interdisciplinary Research Centre:||Biomedical Research Network (BRN)|
|Depositing User:||Payam Rezaie|
|Date Deposited:||14 Jun 2006|
|Last Modified:||04 Oct 2016 09:47|
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