253 related articles for article (PubMed ID: 15229245)
1. Intrinsic resistance of oligodendrocytes to prion infection.
Prinz M; Montrasio F; Furukawa H; van der Haar ME; Schwarz P; Rülicke T; Giger OT; Häusler KG; Perez D; Glatzel M; Aguzzi A
J Neurosci; 2004 Jun; 24(26):5974-81. PubMed ID: 15229245
[TBL] [Abstract][Full Text] [Related]
2. Normal host prion protein necessary for scrapie-induced neurotoxicity.
Brandner S; Isenmann S; Raeber A; Fischer M; Sailer A; Kobayashi Y; Marino S; Weissmann C; Aguzzi A
Nature; 1996 Jan; 379(6563):339-43. PubMed ID: 8552188
[TBL] [Abstract][Full Text] [Related]
3. The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies.
Weissmann C
FEBS Lett; 1996 Jun; 389(1):3-11. PubMed ID: 8682199
[TBL] [Abstract][Full Text] [Related]
4. Truncated prion protein and Doppel are myelinotoxic in the absence of oligodendrocytic PrPC.
Radovanovic I; Braun N; Giger OT; Mertz K; Miele G; Prinz M; Navarro B; Aguzzi A
J Neurosci; 2005 May; 25(19):4879-88. PubMed ID: 15888663
[TBL] [Abstract][Full Text] [Related]
5. Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease.
Meier P; Genoud N; Prinz M; Maissen M; Rülicke T; Zurbriggen A; Raeber AJ; Aguzzi A
Cell; 2003 Apr; 113(1):49-60. PubMed ID: 12679034
[TBL] [Abstract][Full Text] [Related]
6. Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system.
Brandner S; Raeber A; Sailer A; Blättler T; Fischer M; Weissmann C; Aguzzi A
Proc Natl Acad Sci U S A; 1996 Nov; 93(23):13148-51. PubMed ID: 8917559
[TBL] [Abstract][Full Text] [Related]
7. Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.
Raeber AJ; Race RE; Brandner S; Priola SA; Sailer A; Bessen RA; Mucke L; Manson J; Aguzzi A; Oldstone MB; Weissmann C; Chesebro B
EMBO J; 1997 Oct; 16(20):6057-65. PubMed ID: 9321385
[TBL] [Abstract][Full Text] [Related]
8. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice.
Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S
J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443
[TBL] [Abstract][Full Text] [Related]
9. KDEL-tagged anti-prion intrabodies impair PrP lysosomal degradation and inhibit scrapie infectivity.
Vetrugno V; Cardinale A; Filesi I; Mattei S; Sy MS; Pocchiari M; Biocca S
Biochem Biophys Res Commun; 2005 Dec; 338(4):1791-7. PubMed ID: 16288721
[TBL] [Abstract][Full Text] [Related]
10. Antiprion prophylaxis by gene transfer of a soluble prion antagonist.
Genoud N; Ott D; Braun N; Prinz M; Schwarz P; Suter U; Trono D; Aguzzi A
Am J Pathol; 2008 May; 172(5):1287-96. PubMed ID: 18372425
[TBL] [Abstract][Full Text] [Related]
11. Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.
Fischer M; Rülicke T; Raeber A; Sailer A; Moser M; Oesch B; Brandner S; Aguzzi A; Weissmann C
EMBO J; 1996 Mar; 15(6):1255-64. PubMed ID: 8635458
[TBL] [Abstract][Full Text] [Related]
12. Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice.
Pfeifer A; Eigenbrod S; Al-Khadra S; Hofmann A; Mitteregger G; Moser M; Bertsch U; Kretzschmar H
J Clin Invest; 2006 Dec; 116(12):3204-10. PubMed ID: 17143329
[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. Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell types.
Kercher L; Favara C; Chan CC; Race R; Chesebro B
Am J Pathol; 2004 Dec; 165(6):2055-67. PubMed ID: 15579448
[TBL] [Abstract][Full Text] [Related]
15. Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.
Mallucci G; Dickinson A; Linehan J; Klöhn PC; Brandner S; Collinge J
Science; 2003 Oct; 302(5646):871-4. PubMed ID: 14593181
[TBL] [Abstract][Full Text] [Related]
16. Generating Bona Fide Mammalian Prions with Internal Deletions.
Munoz-Montesino C; Sizun C; Moudjou M; Herzog L; Reine F; Chapuis J; Ciric D; Igel-Egalon A; Laude H; Béringue V; Rezaei H; Dron M
J Virol; 2016 Aug; 90(15):6963-6975. PubMed ID: 27226369
[TBL] [Abstract][Full Text] [Related]
17. Dramatic reduction of PrP C level and glycosylation in peripheral nerves following PrP knock-out from Schwann cells does not prevent transmissible spongiform encephalopathy neuroinvasion.
Bradford BM; Tuzi NL; Feltri ML; McCorquodale C; Cancellotti E; Manson JC
J Neurosci; 2009 Dec; 29(49):15445-54. PubMed ID: 20007469
[TBL] [Abstract][Full Text] [Related]
18. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle.
Prusiner SB
Dev Biol Stand; 1991; 75():55-74. PubMed ID: 1686599
[TBL] [Abstract][Full Text] [Related]
19. Cultured peripheral neuroglial cells are highly permissive to sheep prion infection.
Archer F; Bachelin C; Andreoletti O; Besnard N; Perrot G; Langevin C; Le Dur A; Vilette D; Baron-Van Evercooren A; Vilotte JL; Laude H
J Virol; 2004 Jan; 78(1):482-90. PubMed ID: 14671128
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]