BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 7810298)

  • 1. Gerstmann-Sträussler-Scheinker disease showing beta-protein type cerebellar and cerebral amyloid angiopathy.
    Ikeda SI; Yanagisawa N; Allsop D; Glenner GG
    Acta Neuropathol; 1994; 88(3):262-6. PubMed ID: 7810298
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome.
    Miyazono M; Kitamoto T; Iwaki T; Tateishi J
    Acta Neuropathol; 1992; 83(4):333-9. PubMed ID: 1349451
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene.
    Furukawa F; Sanjo N; Kobayashi A; Hamaguchi T; Yamada M; Kitamoto T; Mizusawa H; Yokota T
    Prion; 2018; 12(5-6):315-319. PubMed ID: 30394185
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.
    Barcikowska M; Liberski PP; Boellaard JW; Brown P; Gajdusek DC; Budka H
    Acta Neuropathol; 1993; 85(6):623-7. PubMed ID: 8337941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid.
    Ishizawa K; Mitsufuji T; Shioda K; Kobayashi A; Komori T; Nakazato Y; Kitamoto T; Araki N; Yamamoto T; Sasaki A
    Brain Behav; 2018 Oct; 8(10):e01117. PubMed ID: 30240140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia.
    Ishizawa K; Komori T; Shimazu T; Yamamoto T; Kitamoto T; Shimazu K; Hirose T
    Acta Neuropathol; 2002 Oct; 104(4):342-50. PubMed ID: 12200619
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Pathology of the vessels in cerebral amyloid angiopathy.
    Liberski PP; Barcikowska M
    Folia Neuropathol; 1995; 33(4):207-14. PubMed ID: 8673428
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Structure of Tau filaments in Prion protein amyloidoses.
    Hallinan GI; Hoq MR; Ghosh M; Vago FS; Fernandez A; Garringer HJ; Vidal R; Jiang W; Ghetti B
    Acta Neuropathol; 2021 Aug; 142(2):227-241. PubMed ID: 34128081
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt-Jakob disease.
    Paquet C; Privat N; Kaci R; Polivka M; Dupont O; Haïk S; Laplanche JL; Hauw JJ; Gray F
    Acta Neuropathol; 2008 Nov; 116(5):567-73. PubMed ID: 18551298
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann-Sträussler-Scheinker Disease.
    Honda H; Sasaki K; Takashima H; Mori D; Koyama S; Suzuki SO; Iwaki T
    J Neuropathol Exp Neurol; 2017 Oct; 76(10):854-863. PubMed ID: 28922846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
    Sasaki K; Doh-ura K; Furuta A; Nakashima S; Morisada Y; Tateishi J; Iwaki T
    Acta Neuropathol; 2003 Jul; 106(1):92-6. PubMed ID: 12682740
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuropathology of Gerstmann-Sträussler-Scheinker disease.
    Bugiani O; Giaccone G; Piccardo P; Morbin M; Tagliavini F; Ghetti B
    Microsc Res Tech; 2000 Jul; 50(1):10-5. PubMed ID: 10871543
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
    Bugiani O; Giaccone G; Verga L; Pollo B; Frangione B; Farlow MR; Tagliavini F; Ghetti B
    J Neuropathol Exp Neurol; 1993 Jan; 52(1):64-70. PubMed ID: 8093899
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.