437 related articles for article (PubMed ID: 20532540)
1. Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease.
Jeffrey M; McGovern G; Sisó S; González L
Acta Neuropathol; 2011 Jan; 121(1):113-34. PubMed ID: 20532540
[TBL] [Abstract][Full Text] [Related]
2. Abnormal prion protein is associated with changes of plasma membranes and endocytosis in bovine spongiform encephalopathy (BSE)-affected cattle brains.
Ersdal C; Goodsir CM; Simmons MM; McGovern G; Jeffrey M
Neuropathol Appl Neurobiol; 2009 Jun; 35(3):259-71. PubMed ID: 19473293
[TBL] [Abstract][Full Text] [Related]
3. Prion protein self-interactions: a gateway to novel therapeutic strategies?
Rigter A; Langeveld JP; van Zijderveld FG; Bossers A
Vaccine; 2010 Nov; 28(49):7810-23. PubMed ID: 20932496
[TBL] [Abstract][Full Text] [Related]
4. Relationships between ultrastructural scrapie pathology and patterns of abnormal prion protein accumulation.
Ersdal C; Simmons MM; González L; Goodsir CM; Martin S; Jeffrey M
Acta Neuropathol; 2004 May; 107(5):428-38. PubMed ID: 14986027
[TBL] [Abstract][Full Text] [Related]
5. Prions can infect primary cultured neurons and astrocytes and promote neuronal cell death.
Cronier S; Laude H; Peyrin JM
Proc Natl Acad Sci U S A; 2004 Aug; 101(33):12271-6. PubMed ID: 15302929
[TBL] [Abstract][Full Text] [Related]
6. Transmissible and genetic prion diseases share a common pathway of neurodegeneration.
Hegde RS; Tremblay P; Groth D; DeArmond SJ; Prusiner SB; Lingappa VR
Nature; 1999 Dec; 402(6763):822-6. PubMed ID: 10617204
[TBL] [Abstract][Full Text] [Related]
7. The highways and byways of prion protein trafficking.
Campana V; Sarnataro D; Zurzolo C
Trends Cell Biol; 2005 Feb; 15(2):102-11. PubMed ID: 15695097
[TBL] [Abstract][Full Text] [Related]
8. Cellular pathogenesis in prion diseases.
Crozet C; Beranger F; Lehmann S
Vet Res; 2008; 39(4):44. PubMed ID: 18413130
[TBL] [Abstract][Full Text] [Related]
9. Prion channel proteins and their role in vacuolation and neurodegenerative diseases.
Kourie JI
Eur Biophys J; 2002 Sep; 31(5):409-16. PubMed ID: 12202918
[TBL] [Abstract][Full Text] [Related]
10. Classical sheep transmissible spongiform encephalopathies: pathogenesis, pathological phenotypes and clinical disease.
Jeffrey M; González L
Neuropathol Appl Neurobiol; 2007 Aug; 33(4):373-94. PubMed ID: 17617870
[TBL] [Abstract][Full Text] [Related]
11. Binding of disease-associated prion protein to plasminogen.
Fischer MB; Roeckl C; Parizek P; Schwarz HP; Aguzzi A
Nature; 2000 Nov; 408(6811):479-83. PubMed ID: 11100730
[TBL] [Abstract][Full Text] [Related]
12. Development of oligomeric prion-protein aggregates in a mouse model of prion disease.
Sasaki K; Minaki H; Iwaki T
J Pathol; 2009 Sep; 219(1):123-30. PubMed ID: 19479969
[TBL] [Abstract][Full Text] [Related]
13. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
14. Scrapie-specific neuronal lesions are independent of neuronal PrP expression.
Jeffrey M; Goodsir CM; Race RE; Chesebro B
Ann Neurol; 2004 Jun; 55(6):781-92. PubMed ID: 15174012
[TBL] [Abstract][Full Text] [Related]
15. In vivo toxicity of prion protein in murine scrapie: ultrastructural and immunogold studies.
Jeffrey M; Goodsir CM; Bruce ME; McBride PA; Fraser JR
Neuropathol Appl Neurobiol; 1997 Apr; 23(2):93-101. PubMed ID: 9160894
[TBL] [Abstract][Full Text] [Related]
16. Insights into prion strains and neurotoxicity.
Aguzzi A; Heikenwalder M; Polymenidou M
Nat Rev Mol Cell Biol; 2007 Jul; 8(7):552-61. PubMed ID: 17585315
[TBL] [Abstract][Full Text] [Related]
17. The scrapie prion protein is present in flotillin-1-positive vesicles in central- but not peripheral-derived neuronal cell lines.
Pimpinelli F; Lehmann S; Maridonneau-Parini I
Eur J Neurosci; 2005 Apr; 21(8):2063-72. PubMed ID: 15869502
[TBL] [Abstract][Full Text] [Related]
18. Increased immunohistochemical labelling for prion protein occurs in diverse neurological disorders of sheep: relevance for normal cellular PrP function.
Jeffrey M; Scholes SF; Martin S; McGovern G; Sisó S; González L
J Comp Pathol; 2012 Jul; 147(1):46-54. PubMed ID: 22000036
[TBL] [Abstract][Full Text] [Related]
19. Truncated PrP(c) in mammalian brain: interspecies variation and location in membrane rafts.
Laffont-Proust I; Hässig R; Haïk S; Simon S; Grassi J; Fonta C; Faucheux BA; Moya KL
Biol Chem; 2006 Mar; 387(3):297-300. PubMed ID: 16542151
[TBL] [Abstract][Full Text] [Related]
20. Sites of prion protein accumulation in scrapie-infected mouse spleen revealed by immuno-electron microscopy.
Jeffrey M; McGovern G; Goodsir CM; Brown KL; Bruce ME
J Pathol; 2000 Jul; 191(3):323-32. PubMed ID: 10878556
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]