These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
212 related articles for article (PubMed ID: 18585368)
21. BSE infectivity in the absence of detectable PrP(Sc) accumulation in the tongue and nasal mucosa of terminally diseased cattle. Balkema-Buschmann A; Eiden M; Hoffmann C; Kaatz M; Ziegler U; Keller M; Groschup MH J Gen Virol; 2011 Feb; 92(Pt 2):467-76. PubMed ID: 20943888 [TBL] [Abstract][Full Text] [Related]
22. Infectivity of scrapie prion protein (PrPSc) following in vitro digestion with bovine gastrointestinal microbiota. Scherbel C; Pichner R; Groschup MH; Mueller-Hellwig S; Scherer S; Dietrich R; Maertlbauer E; Gareis M Zoonoses Public Health; 2007; 54(5):185-90. PubMed ID: 17542960 [TBL] [Abstract][Full Text] [Related]
24. In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features. Baskakov IV; Bocharova OV Biochemistry; 2005 Feb; 44(7):2339-48. PubMed ID: 15709746 [TBL] [Abstract][Full Text] [Related]
25. The emerging principles of mammalian prion propagation and transmissibility barriers: Insight from studies in vitro. Surewicz WK; Jones EM; Apetri AC Acc Chem Res; 2006 Sep; 39(9):654-62. PubMed ID: 16981682 [TBL] [Abstract][Full Text] [Related]
26. Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitro. Panza G; Luers L; Stöhr J; Nagel-Steger L; Weiss J; Riesner D; Willbold D; Birkmann E PLoS One; 2010 Dec; 5(12):e14283. PubMed ID: 21151607 [TBL] [Abstract][Full Text] [Related]
27. Seeded conversion of recombinant prion protein to a disulfide-bonded oligomer by a reduction-oxidation process. Lee S; Eisenberg D Nat Struct Biol; 2003 Sep; 10(9):725-30. PubMed ID: 12897768 [TBL] [Abstract][Full Text] [Related]
28. Transgenic mouse brains for the evaluation and quality control of BSE tests. Philipp WJ; Groth D; Giles K; Vodrazka P; Schimmel H; Feyssaguet M; Toomik R; Schacher P; Osman AA; Lachmann I; Wear A; Arsac JN; Prusiner SB Biol Chem; 2007 Mar; 388(3):349-54. PubMed ID: 17338644 [TBL] [Abstract][Full Text] [Related]
29. Differences between the prion protein and its homolog Doppel: a partially structured state with implications for scrapie formation. Nicholson EM; Mo H; Prusiner SB; Cohen FE; Marqusee S J Mol Biol; 2002 Feb; 316(3):807-15. PubMed ID: 11866533 [TBL] [Abstract][Full Text] [Related]
30. An unusual soluble beta-turn-rich conformation of prion is involved in fibril formation and toxic to neuronal cells. Kazlauskaite J; Young A; Gardner CE; Macpherson JV; Vénien-Bryan C; Pinheiro TJ Biochem Biophys Res Commun; 2005 Mar; 328(1):292-305. PubMed ID: 15670783 [TBL] [Abstract][Full Text] [Related]
31. The structural transition of the prion protein into its pathogenic conformation is induced by unmasking hydrophobic sites. Leffers KW; Schell J; Jansen K; Lucassen R; Kaimann T; Nagel-Steger L; Tatzelt J; Riesner D J Mol Biol; 2004 Nov; 344(3):839-53. PubMed ID: 15533449 [TBL] [Abstract][Full Text] [Related]
32. Structural insights into alternate aggregated prion protein forms. Polano M; Bek A; Benetti F; Lazzarino M; Legname G J Mol Biol; 2009 Nov; 393(5):1033-42. PubMed ID: 19720066 [TBL] [Abstract][Full Text] [Related]
33. Characterisation of new monoclonal antibodies reacting with prions from both human and animal brain tissues. Cordes H; Bergström AL; Ohm J; Laursen H; Heegaard PM J Immunol Methods; 2008 Sep; 337(2):106-20. PubMed ID: 18657541 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Lactoferrin induces cell surface retention of prion protein and inhibits prion accumulation. Iwamaru Y; Shimizu Y; Imamura M; Murayama Y; Endo R; Tagawa Y; Ushiki-Kaku Y; Takenouchi T; Kitani H; Mohri S; Yokoyama T; Okada H J Neurochem; 2008 Nov; 107(3):636-46. PubMed ID: 18717818 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Two-rung model of a left-handed beta-helix for prions explains species barrier and strain variation in transmissible spongiform encephalopathies. Langedijk JP; Fuentes G; Boshuizen R; Bonvin AM J Mol Biol; 2006 Jul; 360(4):907-20. PubMed ID: 16782127 [TBL] [Abstract][Full Text] [Related]
38. Expansion of the octarepeat domain alters the misfolding pathway but not the folding pathway of the prion protein. Leliveld SR; Stitz L; Korth C Biochemistry; 2008 Jun; 47(23):6267-78. PubMed ID: 18473442 [TBL] [Abstract][Full Text] [Related]
39. Molecular model of an alpha-helical prion protein dimer and its monomeric subunits as derived from chemical cross-linking and molecular modeling calculations. Kaimann T; Metzger S; Kuhlmann K; Brandt B; Birkmann E; Höltje HD; Riesner D J Mol Biol; 2008 Feb; 376(2):582-96. PubMed ID: 18158160 [TBL] [Abstract][Full Text] [Related]
40. Monitoring prion protein stability by NMR. Julien O; Graether SP; Sykes BD J Toxicol Environ Health A; 2009; 72(17-18):1069-74. PubMed ID: 19697241 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]