994 related articles for article (PubMed ID: 33019549)
1. Strain-Dependent Prion Infection in Mice Expressing Prion Protein with Deletion of Central Residues 91-106.
Uchiyama K; Miyata H; Yamaguchi Y; Imamura M; Okazaki M; Pasiana AD; Chida J; Hara H; Atarashi R; Watanabe H; Kondoh G; Sakaguchi S
Int J Mol Sci; 2020 Oct; 21(19):. PubMed ID: 33019549
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.
Moreno JA; Telling GC
Methods Mol Biol; 2017; 1658():219-252. PubMed ID: 28861793
[TBL] [Abstract][Full Text] [Related]
4. Central residues in prion protein PrP
Pasiana AD; Miyata H; Chida J; Hara H; Imamura M; Atarashi R; Sakaguchi S
J Biol Chem; 2022 Sep; 298(9):102381. PubMed ID: 35973512
[TBL] [Abstract][Full Text] [Related]
5. The N-Terminal Polybasic Region of Prion Protein Is Crucial in Prion Pathogenesis Independently of the Octapeptide Repeat Region.
Das NR; Miyata H; Hara H; Chida J; Uchiyama K; Masujin K; Watanabe H; Kondoh G; Sakaguchi S
Mol Neurobiol; 2020 Feb; 57(2):1203-1216. PubMed ID: 31707632
[TBL] [Abstract][Full Text] [Related]
6. Mouse-hamster chimeric prion protein (PrP) devoid of N-terminal residues 23-88 restores susceptibility to 22L prions, but not to RML prions in PrP-knockout mice.
Uchiyama K; Miyata H; Yano M; Yamaguchi Y; Imamura M; Muramatsu N; Das NR; Chida J; Hara H; Sakaguchi S
PLoS One; 2014; 9(10):e109737. PubMed ID: 25330286
[TBL] [Abstract][Full Text] [Related]
7. Recombinant human prion protein inhibits prion propagation in vitro.
Yuan J; Zhan YA; Abskharon R; Xiao X; Martinez MC; Zhou X; Kneale G; Mikol J; Lehmann S; Surewicz WK; Castilla J; Steyaert J; Zhang S; Kong Q; Petersen RB; Wohlkonig A; Zou WQ
Sci Rep; 2013 Oct; 3():2911. PubMed ID: 24105336
[TBL] [Abstract][Full Text] [Related]
8. Amino acid sequence and prion strain specific effects on the in vitro and in vivo convertibility of ovine/murine and bovine/murine prion protein chimeras.
Kupfer L; Eiden M; Buschmann A; Groschup MH
Biochim Biophys Acta; 2007 Jun; 1772(6):704-13. PubMed ID: 17145171
[TBL] [Abstract][Full Text] [Related]
9. Propagation of RML prions in mice expressing PrP devoid of GPI anchor leads to formation of a novel, stable prion strain.
Mahal SP; Jablonski J; Suponitsky-Kroyter I; Oelschlegel AM; Herva ME; Oldstone M; Weissmann C
PLoS Pathog; 2012; 8(6):e1002746. PubMed ID: 22685404
[TBL] [Abstract][Full Text] [Related]
10. Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein.
Tamgüney G; Miller MW; Giles K; Lemus A; Glidden DV; DeArmond SJ; Prusiner SB
J Gen Virol; 2009 Apr; 90(Pt 4):1035-1047. PubMed ID: 19264659
[TBL] [Abstract][Full Text] [Related]
11. Synergistic and strain-specific effects of bovine spongiform encephalopathy and scrapie prions in the cell-free conversion of recombinant prion protein.
Eiden M; Palm GJ; Hinrichs W; Matthey U; Zahn R; Groschup MH
J Gen Virol; 2006 Dec; 87(Pt 12):3753-3761. PubMed ID: 17098995
[TBL] [Abstract][Full Text] [Related]
12. Strain-dependent role of copper in prion disease through binding to histidine residues in the N-terminal domain of prion protein.
Hara H; Miyata H; Chida J; Sakaguchi S
J Neurochem; 2023 Nov; 167(3):394-409. PubMed ID: 37777338
[TBL] [Abstract][Full Text] [Related]
13. Early detection of PrPres in BSE-infected bovine PrP transgenic mice.
Castilla J; Gutiérrez Adán A; Brun A; Pintado B; Ramírez MA; Parra B; Doyle D; Rogers M; Salguero FJ; Sánchez C; Sánchez-Vizcaíno JM; Torres JM
Arch Virol; 2003 Apr; 148(4):677-91. PubMed ID: 12664293
[TBL] [Abstract][Full Text] [Related]
14. Transgenic models of prion disease.
Scott MR; Supattapone S; Nguyen HO; DeArmond SJ; Prusiner SB
Arch Virol Suppl; 2000; (16):113-24. PubMed ID: 11214913
[TBL] [Abstract][Full Text] [Related]
15. Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers.
Davenport KA; Henderson DM; Mathiason CK; Hoover EA
J Virol; 2016 Dec; 90(23):10752-10761. PubMed ID: 27654299
[TBL] [Abstract][Full Text] [Related]
16. Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.
Jaumain E; Quadrio I; Herzog L; Reine F; Rezaei H; Andréoletti O; Laude H; Perret-Liaudet A; Haïk S; Béringue V
J Virol; 2016 Dec; 90(23):10867-10874. PubMed ID: 27681129
[TBL] [Abstract][Full Text] [Related]
17. Transmission barriers for bovine, ovine, and human prions in transgenic mice.
Scott MR; Peretz D; Nguyen HO; Dearmond SJ; Prusiner SB
J Virol; 2005 May; 79(9):5259-71. PubMed ID: 15827140
[TBL] [Abstract][Full Text] [Related]
18. Differences in proteinase K resistance and neuronal deposition of abnormal prion proteins characterize bovine spongiform encephalopathy (BSE) and scrapie strains.
Kuczius T; Groschup MH
Mol Med; 1999 Jun; 5(6):406-18. PubMed ID: 10415165
[TBL] [Abstract][Full Text] [Related]
19. Effects of prion protein devoid of the N-terminal residues 25-50 on prion pathogenesis in mice.
Das NR; Miyata H; Hara H; Uchiyama K; Chida J; Yano M; Watanabe H; Kondoh G; Sakaguchi S
Arch Virol; 2017 Jul; 162(7):1867-1876. PubMed ID: 28255815
[TBL] [Abstract][Full Text] [Related]
20. Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie.
Marín B; Otero A; Lugan S; Espinosa JC; Marín-Moreno A; Vidal E; Hedman C; Romero A; Pumarola M; Badiola JJ; Torres JM; Andréoletti O; Bolea R
Sci Rep; 2021 Aug; 11(1):17428. PubMed ID: 34465826
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
