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2. Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease. Croes EA; Alizadeh BZ; Bertoli-Avella AM; Rademaker T; Vergeer-Drop J; Dermaut B; Houwing-Duistermaat JJ; Wientjens DP; Hofman A; Van Broeckhoven C; van Duijn CM Eur J Hum Genet; 2004 May; 12(5):389-94. PubMed ID: 14970845 [TBL] [Abstract][Full Text] [Related]
3. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778 [TBL] [Abstract][Full Text] [Related]
4. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction]. Peoc'h K Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969 [TBL] [Abstract][Full Text] [Related]
5. The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations. Scholz SW; Xiromerisiou G; Fung HC; Eerola J; Hellström O; Papadimitriou A; Hadjigeorgiou GM; Tienari PJ; Fernandez HH; Mandel R; Okun MS; Gwinn-Hardy K; Singleton AB Neurosci Lett; 2006 Mar; 395(3):227-9. PubMed ID: 16298483 [TBL] [Abstract][Full Text] [Related]
6. [Spongiform encephalitis]. Domínguez Carmona M; Domínguez de la Calle M An R Acad Nac Med (Madr); 2001; 118(3):633-52. PubMed ID: 11783043 [TBL] [Abstract][Full Text] [Related]
7. Molecular genetics of human prion diseases. Collinge J; Palmer MS Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):371-8. PubMed ID: 7913754 [TBL] [Abstract][Full Text] [Related]
9. Mutations and polymorphisms in the prion protein gene. Palmer MS; Collinge J Hum Mutat; 1993; 2(3):168-73. PubMed ID: 8364585 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetics of human prion disease. Ridley RM; Baker HF Dev Biol Stand; 1993; 80():15-23. PubMed ID: 7903647 [TBL] [Abstract][Full Text] [Related]
12. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129]. Colombier C; Géraud G; Delisle MB; Laplanche JL; Pavy le Traon A; Alizé P; Delpla PA Rev Neurol (Paris); 1997 May; 153(4):239-43. PubMed ID: 9296141 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease. Jarius C; Kovacs GG; Belay G; Hainfellner JA; Mitrova E; Budka H Acta Neuropathol; 2003 May; 105(5):449-54. PubMed ID: 12677444 [TBL] [Abstract][Full Text] [Related]
15. One genetic mutation, two diseases: fatal familial insomnia and Creutzfeldt-Jakob disease. Bellows JG Compr Ther; 1993; 19(1):3. PubMed ID: 8334858 [No Abstract] [Full Text] [Related]
16. One gene, two diseases and three conformations: molecular dynamics simulations of mutants of human prion protein at room temperature and elevated temperatures. Shamsir MS; Dalby AR Proteins; 2005 May; 59(2):275-90. PubMed ID: 15739202 [TBL] [Abstract][Full Text] [Related]
17. Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders. Schröder B; Franz B; Hempfling P; Selbert M; Jürgens T; Kretzschmar HA; Bodemer M; Poser S; Zerr I Hum Genet; 2001 Sep; 109(3):319-25. PubMed ID: 11702213 [TBL] [Abstract][Full Text] [Related]
18. Human prion diseases with variant prion protein. Kitamoto T; Tateishi J Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):391-8. PubMed ID: 7913756 [TBL] [Abstract][Full Text] [Related]
19. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease. Erginel-Unaltuna N; Peoc'h K; Komurcu E; Acuner TT; Issever H; Laplanche JL Eur J Hum Genet; 2001 Dec; 9(12):965-8. PubMed ID: 11840201 [TBL] [Abstract][Full Text] [Related]
20. Loss of glycosylation associated with the T183A mutation in human prion disease. Grasbon-Frodl E; Lorenz H; Mann U; Nitsch RM; Windl O; Kretzschmar HA Acta Neuropathol; 2004 Dec; 108(6):476-84. PubMed ID: 15558291 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]