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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/1994, Volume 91, Issue 21, pp. 9936 - 9940
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2012, Volume 30, Issue 14, pp. 1594 - 1600
Journal Article
Virology, ISSN 0042-6822, 2016, Volume 497, pp. 337 - 345
Abstract Prion diseases are infectious neurodegenerative disorders characterised by accumulations of abnormal prion glycoprotein in affected tissues. Following... 
Infectious Disease | Marginal zone | Spleen | Follicular dendritic cell | Prions | Transmissible spongiform encephalopathies | Specific intercellular adhesion molecule-3-grabbing non-integrin related 1 (SIGN-R1) | Macrophage | C-TYPE LECTIN | SCRAPIE | VIROLOGY | TEMPORARY DEPLETION | DC-SIGN | MOUSE MODEL | FOLLICULAR DENDRITIC CELLS | MEDIATES UPTAKE | NEUROINVASION | CREUTZFELDT-JAKOB-DISEASE | Cell Adhesion Molecules - genetics | Disease Susceptibility | Dendritic Cells, Follicular - metabolism | Down-Regulation | Gene Expression Regulation | Receptors, Cell Surface - metabolism | Lectins, C-Type - genetics | Cell Adhesion Molecules - metabolism | Prion Proteins - metabolism | Lectins, C-Type - metabolism | Macrophages - metabolism | Animals | Spleen - metabolism | Prion Diseases - etiology | Mice | Prion Diseases - metabolism | Disease Models, Animal | Receptors, Cell Surface - genetics | Dextran | Lectins | Nervous system diseases | Dendritic cells | Integrins | Immunohistochemistry | Creutzfeldt-Jakob disease | Macrophages | FDC, follicular dendritic cell | IV, intravenous | PK, proteinase K | vCJD, variant Creutzfeldt-Jakob disease | PrP, prion protein | CNS, central nervous system | SIGN-R1, specific intercellular adhesion molecule-3-grabbing non-integrin related 1 | IHC, immunohistochemistry | MZ, splenic marginal zone | MARCO, macrophage receptor with collagenous structure | PET., paraffin-embedded tissue
Journal Article
Science Translational Medicine, ISSN 1946-6234, 01/2016, Volume 8, Issue 322, pp. 322ra9 - 322ra9
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Dementia and Geriatric Cognitive Disorders Extra, ISSN 1664-5464, 03/2012, Volume 2, Issue 1, pp. 81 - 82
Journal Article
The American Journal of Pathology, ISSN 0002-9440, 2005, Volume 167, Issue 6, pp. 1729 - 1738
Creutzfeldt-Jakob disease (CJD), the most common human prion disease, includes sporadic (s) and familial (f) forms. Regardless of etiology, both forms are... 
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 12, p. e15658
Journal Article