244 related articles for article (PubMed ID: 34710372)
61. Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation.
Chiesa R; Pestronk A; Schmidt RE; Tourtellotte WG; Ghetti B; Piccardo P; Harris DA
Neurobiol Dis; 2001 Apr; 8(2):279-88. PubMed ID: 11300723
[TBL] [Abstract][Full Text] [Related]
62. An astrocyte cell line that differentially propagates murine prions.
Tahir W; Abdulrahman B; Abdelaziz DH; Thapa S; Walia R; Schätzl HM
J Biol Chem; 2020 Aug; 295(33):11572-11583. PubMed ID: 32561641
[TBL] [Abstract][Full Text] [Related]
63. Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form.
Zou WQ; Cashman NR
J Biol Chem; 2002 Nov; 277(46):43942-7. PubMed ID: 12161431
[TBL] [Abstract][Full Text] [Related]
64. Pressure-assisted dissociation and degradation of "proteinase K-resistant" fibrils prepared by seeding with scrapie-infected hamster prion protein.
Akasaka K; Maeno A; Murayama T; Tachibana H; Fujita Y; Yamanaka H; Nishida N; Atarashi R
Prion; 2014; 8(4):314-8. PubMed ID: 25482603
[TBL] [Abstract][Full Text] [Related]
65. The role of GPI-anchored PrP C in mediating the neurotoxic effect of scrapie prions in neurons.
Radford HE; Mallucci GR
Curr Issues Mol Biol; 2010; 12(2):119-27. PubMed ID: 19767655
[TBL] [Abstract][Full Text] [Related]
66. Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture.
Lawson VA; Vella LJ; Stewart JD; Sharples RA; Klemm H; Machalek DM; Masters CL; Cappai R; Collins SJ; Hill AF
Int J Biochem Cell Biol; 2008; 40(12):2793-801. PubMed ID: 18590830
[TBL] [Abstract][Full Text] [Related]
67. Cooperative binding of dominant-negative prion protein to kringle domains.
Ryou C; Prusiner SB; Legname G
J Mol Biol; 2003 May; 329(2):323-33. PubMed ID: 12758079
[TBL] [Abstract][Full Text] [Related]
68. 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]
69. Insect cell-derived cofactors become fully functional after proteinase K and heat treatment for high-fidelity amplification of glycosylphosphatidylinositol-anchored recombinant scrapie and BSE prion proteins.
Imamura M; Kato N; Okada H; Yoshioka M; Iwamaru Y; Shimizu Y; Mohri S; Yokoyama T; Murayama Y
PLoS One; 2013; 8(12):e82538. PubMed ID: 24367521
[TBL] [Abstract][Full Text] [Related]
70. Anti-prion Protein Antibody 6D11 Restores Cellular Proteostasis of Prion Protein Through Disrupting Recycling Propagation of PrP
Pankiewicz JE; Sanchez S; Kirshenbaum K; Kascsak RB; Kascsak RJ; Sadowski MJ
Mol Neurobiol; 2019 Mar; 56(3):2073-2091. PubMed ID: 29987703
[TBL] [Abstract][Full Text] [Related]
71. Identifying key components of the PrPC-PrPSc replicative interface.
Abalos GC; Cruite JT; Bellon A; Hemmers S; Akagi J; Mastrianni JA; Williamson RA; Solforosi L
J Biol Chem; 2008 Dec; 283(49):34021-8. PubMed ID: 18826953
[TBL] [Abstract][Full Text] [Related]
72. Seeded fibrillation as molecular basis of the species barrier in human prion diseases.
Luers L; Bannach O; Stöhr J; Wördehoff MM; Wolff M; Nagel-Steger L; Riesner D; Willbold D; Birkmann E
PLoS One; 2013; 8(8):e72623. PubMed ID: 23977331
[TBL] [Abstract][Full Text] [Related]
73. Pathologic prion protein infects cells by lipid-raft dependent macropinocytosis.
Wadia JS; Schaller M; Williamson RA; Dowdy SF
PLoS One; 2008; 3(10):e3314. PubMed ID: 19390657
[TBL] [Abstract][Full Text] [Related]
74. Differential solubility of prions is associated in manifold phenotypes.
Kuczius T; Karch H; Groschup MH
Mol Cell Neurosci; 2009 Nov; 42(3):226-33. PubMed ID: 19607920
[TBL] [Abstract][Full Text] [Related]
75. Conservation of a glycine-rich region in the prion protein is required for uptake of prion infectivity.
Harrison CF; Lawson VA; Coleman BM; Kim YS; Masters CL; Cappai R; Barnham KJ; Hill AF
J Biol Chem; 2010 Jun; 285(26):20213-23. PubMed ID: 20356832
[TBL] [Abstract][Full Text] [Related]
76. Altered prion protein glycosylation in the aging mouse brain.
Goh AX; Li C; Sy MS; Wong BS
J Neurochem; 2007 Feb; 100(3):841-54. PubMed ID: 17144900
[TBL] [Abstract][Full Text] [Related]
77. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C).
Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z
J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483
[TBL] [Abstract][Full Text] [Related]
78. Transfer of scrapie prion infectivity by cell contact in culture.
Kanu N; Imokawa Y; Drechsel DN; Williamson RA; Birkett CR; Bostock CJ; Brockes JP
Curr Biol; 2002 Apr; 12(7):523-30. PubMed ID: 11937020
[TBL] [Abstract][Full Text] [Related]
79. Self-assembly of recombinant prion protein of 106 residues.
Baskakov IV; Aagaard C; Mehlhorn I; Wille H; Groth D; Baldwin MA; Prusiner SB; Cohen FE
Biochemistry; 2000 Mar; 39(10):2792-804. PubMed ID: 10704232
[TBL] [Abstract][Full Text] [Related]
80. 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]
[Previous] [Next] [New Search]