282 related articles for article (PubMed ID: 9667781)
1. A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.
Furukawa H; Doh-ura K; Kikuchi H; Tateishi J; Iwaki T
J Neurol Sci; 1998 Jun; 158(1):71-5. PubMed ID: 9667781
[TBL] [Abstract][Full Text] [Related]
2. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
[TBL] [Abstract][Full Text] [Related]
3. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.
Liberski PP; Barcikowska M; Cervenakova L; Bratosiewicz J; Marczewska M; Brown P; Gajdusek DC
Acta Neuropathol; 1998 Oct; 96(4):425-30. PubMed ID: 9797009
[TBL] [Abstract][Full Text] [Related]
4. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
Di Fede G; Giaccone G; Limido L; Mangieri M; Suardi S; Puoti G; Morbin M; Mazzoleni G; Ghetti B; Tagliavini F
J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
Piccardo P; Dlouhy SR; Lievens PM; Young K; Bird TD; Nochlin D; Dickson DW; Vinters HV; Zimmerman TR; Mackenzie IR; Kish SJ; Ang LC; De Carli C; Pocchiari M; Brown P; Gibbs CJ; Gajdusek DC; Bugiani O; Ironside J; Tagliavini F; Ghetti B
J Neuropathol Exp Neurol; 1998 Oct; 57(10):979-88. PubMed ID: 9786248
[TBL] [Abstract][Full Text] [Related]
6. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.
Liberski PP; Bratosiewicz J; Barcikowska M; Cervenakova L; Marczewska M; Brown P; Gajdusek DC
Acta Neuropathol; 2000 Aug; 100(2):233-4. PubMed ID: 10963373
[No Abstract] [Full Text] [Related]
7. Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
Piccardo P; Seiler C; Dlouhy SR; Young K; Farlow MR; Prelli F; Frangione B; Bugiani O; Tagliavini F; Ghetti B
J Neuropathol Exp Neurol; 1996 Nov; 55(11):1157-63. PubMed ID: 8939199
[TBL] [Abstract][Full Text] [Related]
8. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
Sikorska B; Liberski PP; Sobów T; Budka H; Ironside JW
Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
[TBL] [Abstract][Full Text] [Related]
9. Towards authentic transgenic mouse models of heritable PrP prion diseases.
Watts JC; Giles K; Bourkas ME; Patel S; Oehler A; Gavidia M; Bhardwaj S; Lee J; Prusiner SB
Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
[TBL] [Abstract][Full Text] [Related]
10. A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland.
Bratosiewicz J; Barcikowska M; Cervenakowa L; Brown P; Gajdusek DC; Liberski PP
Folia Neuropathol; 2000; 38(4):164-6. PubMed ID: 11693719
[TBL] [Abstract][Full Text] [Related]
11. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].
Udaka F; Fujisawa M; Kameyama M
Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904
[TBL] [Abstract][Full Text] [Related]
12. Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease.
Schmitz M; Schlomm M; Hasan B; Beekes M; Mitrova E; Korth C; Breil A; Carimalo J; Gawinecka J; Varges D; Zerr I
Eur J Neurosci; 2010 Jun; 31(11):2024-31. PubMed ID: 20529115
[TBL] [Abstract][Full Text] [Related]
13. [A trend of molecular genetics on prion diseases and prion protein].
Muramatsu Y; Shinagawa M
Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
[TBL] [Abstract][Full Text] [Related]
14. Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients.
Cardone F; Liu QG; Petraroli R; Ladogana A; D'Alessandro M; Arpino C; Di Bari M; Macchi G; Pocchiari M
Brain Res Bull; 1999 Aug; 49(6):429-33. PubMed ID: 10483920
[TBL] [Abstract][Full Text] [Related]
15. The diagnosis of human prion diseases.
Kordek R
Folia Neuropathol; 2000; 38(4):151-60. PubMed ID: 11693717
[TBL] [Abstract][Full Text] [Related]
16. Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism.
Areškeviciute A; Melchior LC; Broholm H; Krarup LH; Lindquist SG; Johansen P; McKenzie N; Green A; Nielsen JE; Laursen H; Lund EL
J Neuropathol Exp Neurol; 2018 Aug; 77(8):673-684. PubMed ID: 29889261
[TBL] [Abstract][Full Text] [Related]
17. Isolation of infectious, non-fibrillar and oligomeric prions from a genetic prion disease.
Vanni I; Pirisinu L; Acevedo-Morantes C; Kamali-Jamil R; Rathod V; Di Bari MA; D'Agostino C; Marcon S; Esposito E; Riccardi G; Hornemann S; Senatore A; Aguzzi A; Agrimi U; Wille H; Nonno R
Brain; 2020 May; 143(5):1512-1524. PubMed ID: 32303068
[TBL] [Abstract][Full Text] [Related]
18. Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.
Zaidi SI; Richardson SL; Capellari S; Song L; Smith MA; Ghetti B; Sy MS; Gambetti P; Petersen RB
J Alzheimers Dis; 2005 Apr; 7(2):159-71; discussion 173-80. PubMed ID: 15851854
[TBL] [Abstract][Full Text] [Related]
19. [Prion diseases, update].
Kitamoto T
Rinsho Shinkeigaku; 2001 Dec; 41(12):1223-5. PubMed ID: 12235843
[TBL] [Abstract][Full Text] [Related]
20. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP.
Yang W; Cook J; Rassbach B; Lemus A; DeArmond SJ; Mastrianni JA
J Neurosci; 2009 Aug; 29(32):10072-80. PubMed ID: 19675240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
