694 related articles for article (PubMed ID: 26171558)
41. [Mechanisms of prion transmission].
Sakaguchi S
Nihon Rinsho; 2007 Aug; 65(8):1391-5. PubMed ID: 17695274
[TBL] [Abstract][Full Text] [Related]
42. Cyclic amplification of protein misfolding: application to prion-related disorders and beyond.
Soto C; Saborio GP; Anderes L
Trends Neurosci; 2002 Aug; 25(8):390-4. PubMed ID: 12127750
[TBL] [Abstract][Full Text] [Related]
43. Thienyl pyrimidine derivatives with PrP(Sc) oligomer-inducing activity are a promising tool to study prions.
Imberdis T; Ayrolles-Torro A; Verdier JM; Perrier V
Curr Top Med Chem; 2013; 13(19):2477-83. PubMed ID: 24059332
[TBL] [Abstract][Full Text] [Related]
44. Pathogenic mechanisms of prion protein, amyloid-β and α-synuclein misfolding: the prion concept and neurotoxicity of protein oligomers.
Ugalde CL; Finkelstein DI; Lawson VA; Hill AF
J Neurochem; 2016 Oct; 139(2):162-180. PubMed ID: 27529376
[TBL] [Abstract][Full Text] [Related]
45. Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein.
Wong C; Xiong LW; Horiuchi M; Raymond L; Wehrly K; Chesebro B; Caughey B
EMBO J; 2001 Feb; 20(3):377-86. PubMed ID: 11157745
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. The prion's elusive reason for being.
Aguzzi A; Baumann F; Bremer J
Annu Rev Neurosci; 2008; 31():439-77. PubMed ID: 18558863
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked.
Sandberg MK; Al-Doujaily H; Sharps B; De Oliveira MW; Schmidt C; Richard-Londt A; Lyall S; Linehan JM; Brandner S; Wadsworth JD; Clarke AR; Collinge J
Nat Commun; 2014 Jul; 5():4347. PubMed ID: 25005024
[TBL] [Abstract][Full Text] [Related]
50. Molecular architecture of human prion protein amyloid: a parallel, in-register beta-structure.
Cobb NJ; Sönnichsen FD; McHaourab H; Surewicz WK
Proc Natl Acad Sci U S A; 2007 Nov; 104(48):18946-51. PubMed ID: 18025469
[TBL] [Abstract][Full Text] [Related]
51. Unraveling the details of prion (con)formation(s): recent advances by mass spectrometry.
Principe S; Maras B; Schininà ME; Pocchiari M; Cardone F
Curr Opin Drug Discov Devel; 2008 Sep; 11(5):697-707. PubMed ID: 18729021
[TBL] [Abstract][Full Text] [Related]
52. Prion diseases and their biochemical mechanisms.
Cobb NJ; Surewicz WK
Biochemistry; 2009 Mar; 48(12):2574-85. PubMed ID: 19239250
[TBL] [Abstract][Full Text] [Related]
53. Towards cellular receptors for prions.
Lee KS; Linden R; Prado MA; Brentani RR; Martins VR
Rev Med Virol; 2003; 13(6):399-408. PubMed ID: 14625887
[TBL] [Abstract][Full Text] [Related]
54. Charged bipolar suramin derivatives induce aggregation of the prion protein at the cell surface and inhibit PrPSc replication.
Nunziante M; Kehler C; Maas E; Kassack MU; Groschup M; Schätzl HM
J Cell Sci; 2005 Nov; 118(Pt 21):4959-73. PubMed ID: 16219680
[TBL] [Abstract][Full Text] [Related]
55. Breakage of PrP aggregates is essential for efficient autocatalytic propagation of misfolded prion protein.
Piening N; Weber P; Giese A; Kretzschmar H
Biochem Biophys Res Commun; 2005 Jan; 326(2):339-43. PubMed ID: 15582583
[TBL] [Abstract][Full Text] [Related]
56. Prion proteins: a biological role beyond prion diseases.
Hu W; Rosenberg RN; Stüve O
Acta Neurol Scand; 2007 Aug; 116(2):75-82. PubMed ID: 17661791
[TBL] [Abstract][Full Text] [Related]
57. Prion formation, but not clearance, is supported by protein misfolding cyclic amplification.
Shikiya RA; Eckland TE; Young AJ; Bartz JC
Prion; 2014; 8(6):415-20. PubMed ID: 25482601
[TBL] [Abstract][Full Text] [Related]
58. Protein misfolding and disease: the case of prion disorders.
Hetz C; Soto C
Cell Mol Life Sci; 2003 Jan; 60(1):133-43. PubMed ID: 12613663
[TBL] [Abstract][Full Text] [Related]
59. Molecular biology and pathology of prion strains in sporadic human prion diseases.
Gambetti P; Cali I; Notari S; Kong Q; Zou WQ; Surewicz WK
Acta Neuropathol; 2011 Jan; 121(1):79-90. PubMed ID: 21058033
[TBL] [Abstract][Full Text] [Related]
60. A Quick Method to Evaluate the Effect of the Amino Acid Sequence in the Misfolding Proneness of the Prion Protein.
Fernández-Borges N; Eraña H; Elezgarai SR; Harrathi C; Venegas V; Castilla J
Methods Mol Biol; 2017; 1658():205-216. PubMed ID: 28861792
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]