187 related articles for article (PubMed ID: 36291746)
21. 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]
22. Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation.
Riudavets MA; Sraka MA; Schultz M; Rojas E; Martinetto H; Begué C; Noher de Halac I; Poleggi A; Equestre M; Pocchiari M; Sevlever G; Taratuto AL
Brain Pathol; 2014 Mar; 24(2):142-7. PubMed ID: 23944754
[TBL] [Abstract][Full Text] [Related]
23. Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.
Ghetti B; Dlouhy SR; Giaccone G; Bugiani O; Frangione B; Farlow MR; Tagliavini F
Brain Pathol; 1995 Jan; 5(1):61-75. PubMed ID: 7767492
[TBL] [Abstract][Full Text] [Related]
24. Hereditary prion protein amyloidoses.
Ghetti B; Tagliavini F; Takao M; Bugiani O; Piccardo P
Clin Lab Med; 2003 Mar; 23(1):65-85, viii. PubMed ID: 12733425
[TBL] [Abstract][Full Text] [Related]
25. Extracellular Prion Protein Aggregates in Nine Gerstmann-Sträussler-Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data.
Jankovska N; Matej R; Olejar T
Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34948096
[TBL] [Abstract][Full Text] [Related]
26. Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy.
Pirisinu L; Nonno R; Esposito E; Benestad SL; Gambetti P; Agrimi U; Zou WQ
PLoS One; 2013; 8(6):e66405. PubMed ID: 23826096
[TBL] [Abstract][Full Text] [Related]
27. Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants.
Jodoin J; Misiewicz M; Makhijani P; Giannopoulos PN; Hammond J; Goodyer CG; LeBlanc AC
PLoS One; 2009 Aug; 4(8):e6647. PubMed ID: 19680558
[TBL] [Abstract][Full Text] [Related]
28. Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
Tagliavini F; Prelli F; Ghiso J; Bugiani O; Serban D; Prusiner SB; Farlow MR; Ghetti B; Frangione B
EMBO J; 1991 Mar; 10(3):513-9. PubMed ID: 1672107
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
Alzualde A; Indakoetxea B; Ferrer I; Moreno F; Barandiaran M; Gorostidi A; Estanga A; Ruiz I; Calero M; van Leeuwen FW; Atares B; Juste R; Rodriguez-Martínez AB; López de Munain A
J Neuropathol Exp Neurol; 2010 Aug; 69(8):789-800. PubMed ID: 20613639
[TBL] [Abstract][Full Text] [Related]
31. [(11)C]PiB PET in Gerstmann-Sträussler-Scheinker disease.
Deters KD; Risacher SL; Yoder KK; Oblak AL; Unverzagt FW; Murrell JR; Epperson F; Tallman EF; Quaid KA; Farlow MR; Saykin AJ; Ghetti B
Am J Nucl Med Mol Imaging; 2016; 6(1):84-93. PubMed ID: 27069768
[TBL] [Abstract][Full Text] [Related]
32. Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease.
Ximelis T; Marín-Moreno A; Espinosa JC; Eraña H; Charco JM; Hernández I; Riveira C; Alcolea D; González-Roca E; Aldecoa I; Molina-Porcel L; Parchi P; Rossi M; Castilla J; Ruiz-García R; Gelpi E; Torres JM; Sánchez-Valle R
Alzheimers Res Ther; 2021 Oct; 13(1):176. PubMed ID: 34663460
[TBL] [Abstract][Full Text] [Related]
33. New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.
Furukawa H; Kitamoto T; Tanaka Y; Tateishi J
Brain Res Mol Brain Res; 1995 Jun; 30(2):385-8. PubMed ID: 7637591
[TBL] [Abstract][Full Text] [Related]
34. Variable Protease-Sensitive Prionopathy Transmission to Bank Voles.
Nonno R; Notari S; Di Bari MA; Cali I; Pirisinu L; d'Agostino C; Cracco L; Kofskey D; Vanni I; Lavrich J; Parchi P; Agrimi U; Gambetti P
Emerg Infect Dis; 2019 Jan; 25(1):73-81. PubMed ID: 30561322
[TBL] [Abstract][Full Text] [Related]
35. Gerstmann-Sträussler-Scheinker disease. I. Human diseases.
Liberski PP; Budka H
Folia Neuropathol; 2004; 42 Suppl B():120-40. PubMed ID: 16903147
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. 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]
39. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
Dlouhy SR; Hsiao K; Farlow MR; Foroud T; Conneally PM; Johnson P; Prusiner SB; Hodes ME; Ghetti B
Nat Genet; 1992 Apr; 1(1):64-7. PubMed ID: 1363809
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
