These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

303 related articles for article (PubMed ID: 8105481)

  • 1. Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.
    Tagliavini F; Prelli F; Verga L; Giaccone G; Sarma R; Gorevic P; Ghetti B; Passerini F; Ghibaudi E; Forloni G
    Proc Natl Acad Sci U S A; 1993 Oct; 90(20):9678-82. PubMed ID: 8105481
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
    Giaccone G; Verga L; Bugiani O; Frangione B; Serban D; Prusiner SB; Farlow MR; Ghetti B; Tagliavini F
    Proc Natl Acad Sci U S A; 1992 Oct; 89(19):9349-53. PubMed ID: 1357663
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein.
    Salmona M; Morbin M; Massignan T; Colombo L; Mazzoleni G; Capobianco R; Diomede L; Thaler F; Mollica L; Musco G; Kourie JJ; Bugiani O; Sharma D; Inouye H; Kirschner DA; Forloni G; Tagliavini F
    J Biol Chem; 2003 Nov; 278(48):48146-53. PubMed ID: 12970341
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Sträussler-Scheinker disease peptides in the presence of metal ions.
    Ricchelli F; Buggio R; Drago D; Salmona M; Forloni G; Negro A; Tognon G; Zatta P
    Biochemistry; 2006 May; 45(21):6724-32. PubMed ID: 16716083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.
    Tagliavini F; Prelli F; Porro M; Rossi G; Giaccone G; Farlow MR; Dlouhy SR; Ghetti B; Bugiani O; Frangione B
    Cell; 1994 Nov; 79(4):695-703. PubMed ID: 7954833
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
    Tagliavini F; Lievens PM; Tranchant C; Warter JM; Mohr M; Giaccone G; Perini F; Rossi G; Salmona M; Piccardo P; Ghetti B; Beavis RC; Bugiani O; Frangione B; Prelli F
    J Biol Chem; 2001 Feb; 276(8):6009-15. PubMed ID: 11087738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.
    Piccardo P; Ghetti B; Dickson DW; Vinters HV; Giaccone G; Bugiani O; Tagliavini F; Young K; Dlouhy SR; Seiler C
    J Neuropathol Exp Neurol; 1995 Nov; 54(6):790-801. PubMed ID: 7595652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prion protein amyloidosis.
    Ghetti B; Piccardo P; Frangione B; Bugiani O; Giaccone G; Young K; Prelli F; Farlow MR; Dlouhy SR; Tagliavini F
    Brain Pathol; 1996 Apr; 6(2):127-45. PubMed ID: 8737929
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neurotoxic and gliotrophic activity of a synthetic peptide homologous to Gerstmann-Sträussler-Scheinker disease amyloid protein.
    Fioriti L; Angeretti N; Colombo L; De Luigi A; Colombo A; Manzoni C; Morbin M; Tagliavini F; Salmona M; Chiesa R; Forloni G
    J Neurosci; 2007 Feb; 27(7):1576-83. PubMed ID: 17301166
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. PrP P102L and Nearby Lysine Mutations Promote Spontaneous
    Kraus A; Raymond GJ; Race B; Campbell KJ; Hughson AG; Anson KJ; Raymond LD; Caughey B
    J Virol; 2017 Nov; 91(21):. PubMed ID: 28835493
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A special report I. Prion protein (PrP)--amyloid plaques in the transmissible spongiform encephalopathies, or prion diseases revisited.
    Liberski PP; Bratosiewicz J; Waliś A; Kordek R; Jeffrey M; Brown P
    Folia Neuropathol; 2001; 39(4):217-35. PubMed ID: 11928893
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.
    Piccardo P; Liepnieks JJ; William A; Dlouhy SR; Farlow MR; Young K; Nochlin D; Bird TD; Nixon RR; Ball MJ; DeCarli C; Bugiani O; Tagliavini F; Benson MD; Ghetti B
    Am J Pathol; 2001 Jun; 158(6):2201-7. PubMed ID: 11395398
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prion Protein Prolines 102 and 105 and the Surrounding Lysine Cluster Impede Amyloid Formation.
    Kraus A; Anson KJ; Raymond LD; Martens C; Groveman BR; Dorward DW; Caughey B
    J Biol Chem; 2015 Aug; 290(35):21510-22. PubMed ID: 26175152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Self-Replication of Prion Protein Fragment 89-230 Amyloid Fibrils Accelerated by Prion Protein Fragment 107-143 Aggregates.
    Sneideris T; Ziaunys M; Chu BK; Chen RP; Smirnovas V
    Int J Mol Sci; 2020 Oct; 21(19):. PubMed ID: 33049945
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein.
    Selvaggini C; De Gioia L; Cantù L; Ghibaudi E; Diomede L; Passerini F; Forloni G; Bugiani O; Tagliavini F; Salmona M
    Biochem Biophys Res Commun; 1993 Aug; 194(3):1380-6. PubMed ID: 8102526
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
    Hsiao K; Dlouhy SR; Farlow MR; Cass C; Da Costa M; Conneally PM; Hodes ME; Ghetti B; Prusiner SB
    Nat Genet; 1992 Apr; 1(1):68-71. PubMed ID: 1363810
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.