89 related articles for article (PubMed ID: 20121218)
1. Assessing the role of oxidized methionine at position 213 in the formation of prions in hamsters.
Silva CJ; Onisko BC; Dynin I; Erickson ML; Vensel WH; Requena JR; Antaki EM; Carter JM
Biochemistry; 2010 Mar; 49(9):1854-61. PubMed ID: 20121218
[TBL] [Abstract][Full Text] [Related]
2. Methionine sulfoxides on PrPSc: a prion-specific covalent signature.
Canello T; Engelstein R; Moshel O; Xanthopoulos K; Juanes ME; Langeveld J; Sklaviadis T; Gasset M; Gabizon R
Biochemistry; 2008 Aug; 47(34):8866-73. PubMed ID: 18680312
[TBL] [Abstract][Full Text] [Related]
3. Reduction of prion infectivity and levels of scrapie prion protein by lithium aluminum hydride: implications for RNA in prion diseases.
Jeong BH; Kim NH; Jin JK; Choi JK; Lee YJ; Kim JI; Choi EK; Carp RI; Kim YS
J Neuropathol Exp Neurol; 2009 Aug; 68(8):870-9. PubMed ID: 19606066
[TBL] [Abstract][Full Text] [Related]
4. Oxidation of methionine 216 in sheep and elk prion protein is highly dependent upon the amino acid at position 218 but is not important for prion propagation.
Silva CJ; Dynin I; Erickson ML; Requena JR; Balachandran A; Hui C; Onisko BC; Carter JM
Biochemistry; 2013 Mar; 52(12):2139-47. PubMed ID: 23458153
[TBL] [Abstract][Full Text] [Related]
5. Generation of genuine prion infectivity by serial PMCA.
Weber P; Giese A; Piening N; Mitteregger G; Thomzig A; Beekes M; Kretzschmar HA
Vet Microbiol; 2007 Aug; 123(4):346-57. PubMed ID: 17493773
[TBL] [Abstract][Full Text] [Related]
6. Spontaneous deamidation and isomerization of Asn108 in prion peptide 106-126 and in full-length prion protein.
Sandmeier E; Hunziker P; Kunz B; Sack R; Christen P
Biochem Biophys Res Commun; 1999 Aug; 261(3):578-83. PubMed ID: 10441469
[TBL] [Abstract][Full Text] [Related]
7. In vitro generation of infectious scrapie prions.
Castilla J; Saá P; Hetz C; Soto C
Cell; 2005 Apr; 121(2):195-206. PubMed ID: 15851027
[TBL] [Abstract][Full Text] [Related]
8. Oxidation of methionine residues in the prion protein by hydrogen peroxide.
Requena JR; Dimitrova MN; Legname G; Teijeira S; Prusiner SB; Levine RL
Arch Biochem Biophys; 2004 Dec; 432(2):188-95. PubMed ID: 15542057
[TBL] [Abstract][Full Text] [Related]
9. Non-genetic propagation of strain-specific properties of scrapie prion protein.
Bessen RA; Kocisko DA; Raymond GJ; Nandan S; Lansbury PT; Caughey B
Nature; 1995 Jun; 375(6533):698-700. PubMed ID: 7791905
[TBL] [Abstract][Full Text] [Related]
10. Prion encephalopathies of animals and humans.
Prusiner SB
Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
[TBL] [Abstract][Full Text] [Related]
11. Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.
Liemann S; Glockshuber R
Biochemistry; 1999 Mar; 38(11):3258-67. PubMed ID: 10079068
[TBL] [Abstract][Full Text] [Related]
12. Immunoaffinity purification and neutralization of scrapie prions.
Gabizon R; McKinley MP; Groth D; Westaway D; DeArmond SJ; Carlson GA; Prusiner SB
Prog Clin Biol Res; 1989; 317():583-600. PubMed ID: 2574871
[TBL] [Abstract][Full Text] [Related]
13. PrP(Sc) of scrapie 263K propagates efficiently in spleen and muscle tissues with protein misfolding cyclic amplification.
Shi S; Dong CF; Wang GR; Wang X; An R; Chen JM; Shan B; Zhang BY; Xu K; Shi Q; Tian C; Gao C; Han J; Dong XP
Virus Res; 2009 Apr; 141(1):26-33. PubMed ID: 19162101
[TBL] [Abstract][Full Text] [Related]
14. Oligomers of the prion protein fragment 106-126 are likely assembled from beta-hairpins in solution, and methionine oxidation inhibits assembly without altering the peptide's monomeric conformation.
Grabenauer M; Wu C; Soto P; Shea JE; Bowers MT
J Am Chem Soc; 2010 Jan; 132(2):532-9. PubMed ID: 20020713
[TBL] [Abstract][Full Text] [Related]
15. Selective oxidation of methionine residues in prion proteins.
Wong BS; Wang H; Brown DR; Jones IM
Biochem Biophys Res Commun; 1999 Jun; 259(2):352-5. PubMed ID: 10362513
[TBL] [Abstract][Full Text] [Related]
16. Scrapie prion protein structural constraints obtained by limited proteolysis and mass spectrometry.
Sajnani G; Pastrana MA; Dynin I; Onisko B; Requena JR
J Mol Biol; 2008 Sep; 382(1):88-98. PubMed ID: 18621059
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Quantitative profiling of the pathological prion protein allotypes in bank voles by liquid chromatography-mass spectrometry.
Cartoni C; Schininà ME; Maras B; Nonno R; Vaccari G; Di Bari M; Conte M; De Pascalis A; Principe S; Cardone F; Pocchiari M; Agrimi U
J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Apr; 849(1-2):302-6. PubMed ID: 17008136
[TBL] [Abstract][Full Text] [Related]
19. Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation.
Breydo L; Bocharova OV; Makarava N; Salnikov VV; Anderson M; Baskakov IV
Biochemistry; 2005 Nov; 44(47):15534-43. PubMed ID: 16300402
[TBL] [Abstract][Full Text] [Related]
20. Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion.
Pan T; Li R; Kang SC; Wong BS; Wisniewski T; Sy MS
J Neurochem; 2004 Sep; 90(5):1205-17. PubMed ID: 15312175
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]