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 *

224 related articles for article (PubMed ID: 32516343)

  • 1. Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.
    Asante EA; Linehan JM; Tomlinson A; Jakubcova T; Hamdan S; Grimshaw A; Smidak M; Jeelani A; Nihat A; Mead S; Brandner S; Wadsworth JDF; Collinge J
    PLoS Biol; 2020 Jun; 18(6):e3000725. PubMed ID: 32516343
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.
    Asante EA; Linehan JM; Smidak M; Tomlinson A; Grimshaw A; Jeelani A; Jakubcova T; Hamdan S; Powell C; Brandner S; Wadsworth JD; Collinge J
    PLoS Pathog; 2013; 9(9):e1003643. PubMed ID: 24086135
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.
    Asante EA; Grimshaw A; Smidak M; Jakubcova T; Tomlinson A; Jeelani A; Hamdan S; Powell C; Joiner S; Linehan JM; Brandner S; Wadsworth JD; Collinge J
    PLoS Pathog; 2015 Jul; 11(7):e1004953. PubMed ID: 26135918
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular biology and transgenetics of prion diseases.
    Prusiner SB
    Crit Rev Biochem Mol Biol; 1991; 26(5-6):397-438. PubMed ID: 1684745
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains.
    Tremblay P; Ball HL; Kaneko K; Groth D; Hegde RS; Cohen FE; DeArmond SJ; Prusiner SB; Safar JG
    J Virol; 2004 Feb; 78(4):2088-99. PubMed ID: 14747574
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.
    Nonno R; Angelo Di Bari M; Agrimi U; Pirisinu L
    Prion; 2016 Nov; 10(6):421-433. PubMed ID: 27892798
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prion protein transgenes and the neuropathology in prion diseases.
    DeArmond SJ; Prusiner SB
    Brain Pathol; 1995 Jan; 5(1):77-89. PubMed ID: 7767493
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Description of the first Spanish case of Gerstmann-Sträussler-Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization.
    Eraña H; San Millán B; Díaz-Domínguez CM; Charco JM; Rodríguez R; Viéitez I; Pereda A; Yañez R; Geijo M; Navarro C; Perez de Nanclares G; Teijeira S; Castilla J
    J Neurol; 2022 Aug; 269(8):4253-4263. PubMed ID: 35294616
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prion encephalopathies of animals and humans.
    Prusiner SB
    Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions.
    Barron RM; King D; Jeffrey M; McGovern G; Agarwal S; Gill AC; Piccardo P
    Acta Neuropathol; 2016 Oct; 132(4):611-24. PubMed ID: 27376534
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Cryo-EM structures of prion protein filaments from Gerstmann-Sträussler-Scheinker disease.
    Hallinan GI; Ozcan KA; Hoq MR; Cracco L; Vago FS; Bharath SR; Li D; Jacobsen M; Doud EH; Mosley AL; Fernandez A; Garringer HJ; Jiang W; Ghetti B; Vidal R
    Acta Neuropathol; 2022 Sep; 144(3):509-520. PubMed ID: 35819518
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.