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 *

254 related articles for article (PubMed ID: 9811348)

  • 21. Creutzfeldt-Jakob disease and scrapie prions.
    Prusiner SB
    Alzheimer Dis Assoc Disord; 1989; 3(1-2):52-78. PubMed ID: 2568118
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments.
    Cracco L; Xiao X; Nemani SK; Lavrich J; Cali I; Ghetti B; Notari S; Surewicz WK; Gambetti P
    Acta Neuropathol Commun; 2019 May; 7(1):85. PubMed ID: 31142381
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular classification of sporadic Creutzfeldt-Jakob disease.
    Hill AF; Joiner S; Wadsworth JD; Sidle KC; Bell JE; Budka H; Ironside JW; Collinge J
    Brain; 2003 Jun; 126(Pt 6):1333-46. PubMed ID: 12764055
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes.
    Ward A; Hollister JR; McNally K; Ritchie DL; Zanusso G; Priola SA
    Acta Neuropathol Commun; 2020 Jun; 8(1):83. PubMed ID: 32517816
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein.
    Xie Z; O'Rourke KI; Dong Z; Jenny AL; Langenberg JA; Belay ED; Schonberger LB; Petersen RB; Zou W; Kong Q; Gambetti P; Chen SG
    J Biol Chem; 2006 Feb; 281(7):4199-206. PubMed ID: 16338930
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Prion-induced neuronal damage--the mechanisms of neuronal destruction in the subacute spongiform encephalopathies.
    Giese A; Kretzschmar HA
    Curr Top Microbiol Immunol; 2001; 253():203-17. PubMed ID: 11417136
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease.
    Debatin L; Streffer J; Geissen M; Matschke J; Aguzzi A; Glatzel M
    Neurodegener Dis; 2008; 5(6):347-54. PubMed ID: 18349519
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Truncated forms of the human prion protein in normal brain and in prion diseases.
    Chen SG; Teplow DB; Parchi P; Teller JK; Gambetti P; Autilio-Gambetti L
    J Biol Chem; 1995 Aug; 270(32):19173-80. PubMed ID: 7642585
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.
    Head MW; Bunn TJ; Bishop MT; McLoughlin V; Lowrie S; McKimmie CS; Williams MC; McCardle L; MacKenzie J; Knight R; Will RG; Ironside JW
    Ann Neurol; 2004 Jun; 55(6):851-9. PubMed ID: 15174020
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Toluidine blue-O staining of prion protein deposits.
    Sánchez A; Guzmán A; Ortiz A; Rembao D; Espinosa B; Zenteno E; Guevara J
    Histochem Cell Biol; 2001 Dec; 116(6):519-24. PubMed ID: 11810193
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review.
    Bernardi L; Bruni AC
    Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31340582
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Molecular genetics in Creutzfeldt-Jakob disease].
    Kitamoto T
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1222-3. PubMed ID: 7774117
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic and infectious prion diseases.
    Prusiner SB
    Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann-Sträussler syndrome.
    Kitamoto T; Yamaguchi K; Doh-ura K; Tateishi J
    Neurology; 1991 Feb; 41(2 ( Pt 1)):306-10. PubMed ID: 1671530
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.