166 related articles for article (PubMed ID: 21107851)
1. Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
Parchi P; Strammiello R; Giese A; Kretzschmar H
Acta Neuropathol; 2011 Jan; 121(1):91-112. PubMed ID: 21107851
[TBL] [Abstract][Full Text] [Related]
2. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
Parchi P; Capellari S; Gambetti P
Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544
[TBL] [Abstract][Full Text] [Related]
3. Phenotypic variability in human prion diseases.
Ironside JW; Ritchie DL; Head MW
Neuropathol Appl Neurobiol; 2005 Dec; 31(6):565-79. PubMed ID: 16281905
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular pathology, classification, and diagnosis of sporadic human prion disease variants.
Parchi P; Saverioni D
Folia Neuropathol; 2012; 50(1):20-45. PubMed ID: 22505361
[TBL] [Abstract][Full Text] [Related]
6. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.
Schoch G; Seeger H; Bogousslavsky J; Tolnay M; Janzer RC; Aguzzi A; Glatzel M
PLoS Med; 2006 Feb; 3(2):e14. PubMed ID: 16354106
[TBL] [Abstract][Full Text] [Related]
7. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
Capellari S; Strammiello R; Saverioni D; Kretzschmar H; Parchi P
Acta Neuropathol; 2011 Jan; 121(1):21-37. PubMed ID: 20978903
[TBL] [Abstract][Full Text] [Related]
8. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
Gelpi E; Kovacs GG; Ströbel T; Koperek O; Voigtländer T; Liberski PP; Budka H
Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763
[TBL] [Abstract][Full Text] [Related]
9. Human prion diseases: molecular and clinical aspects.
Glatzel M; Stoeck K; Seeger H; Lührs T; Aguzzi A
Arch Neurol; 2005 Apr; 62(4):545-52. PubMed ID: 15824251
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Classification of sporadic Creutzfeldt-Jakob disease revisited.
Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
[TBL] [Abstract][Full Text] [Related]
12. [Molecular bases of prion diseases].
Rać M; Rać M
Ann Acad Med Stetin; 2006; 52(3):5-13. PubMed ID: 17385343
[TBL] [Abstract][Full Text] [Related]
13. Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease.
Jeffrey M; McGovern G; Sisó S; González L
Acta Neuropathol; 2011 Jan; 121(1):113-34. PubMed ID: 20532540
[TBL] [Abstract][Full Text] [Related]
14. Strain Typing of Prion Diseases Using In Vivo Mouse Models.
Boyle A; Hogan K; Manson JC; Diack AB
Methods Mol Biol; 2017; 1658():263-283. PubMed ID: 28861795
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type.
Pan T; Li R; Kang SC; Pastore M; Wong BS; Ironside J; Gambetti P; Sy MS
J Neurochem; 2005 Jan; 92(1):132-42. PubMed ID: 15606903
[TBL] [Abstract][Full Text] [Related]
19. Neurotoxic species in prion disease: a role for PrP isoforms?
Harrison CF; Barnham KJ; Hill AF
J Neurochem; 2007 Dec; 103(5):1709-20. PubMed ID: 17944867
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]