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 *

689 related articles for article (PubMed ID: 19686205)

  • 1. Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease.
    Zanusso G; Ferrari S; Benedetti D; Sbriccoli M; Rizzuto N; Monaco S
    Ann N Y Acad Sci; 2009 Jul; 1170():637-43. PubMed ID: 19686205
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
    Parchi P; Giese A; Capellari S; Brown P; Schulz-Schaeffer W; Windl O; Zerr I; Budka H; Kopp N; Piccardo P; Poser S; Rojiani A; Streichemberger N; Julien J; Vital C; Ghetti B; Gambetti P; Kretzschmar H
    Ann Neurol; 1999 Aug; 46(2):224-33. PubMed ID: 10443888
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
    Casalone C; Zanusso G; Acutis P; Ferrari S; Capucci L; Tagliavini F; Monaco S; Caramelli M
    Proc Natl Acad Sci U S A; 2004 Mar; 101(9):3065-70. PubMed ID: 14970340
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A traceback phenomenon can reveal the origin of prion infection.
    Kobayashi A; Asano M; Mohri S; Kitamoto T
    Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
    Parchi P; Capellari S; Gambetti P
    Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease.
    Iwasaki Y; Hashizume Y; Yoshida M; Kitamoto T; Sobue G
    Acta Neuropathol; 2005 Jun; 109(6):557-66. PubMed ID: 15933870
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients.
    Kobayashi A; Arima K; Ogawa M; Murata M; Fukuda T; Kitamoto T
    Acta Neuropathol; 2008 Nov; 116(5):561-6. PubMed ID: 18751990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Classification of sporadic Creutzfeldt-Jakob disease revisited.
    Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
    Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
    Zanusso G; Righetti PG; Ferrari S; Terrin L; Farinazzo A; Cardone F; Pocchiari M; Rizzuto N; Monaco S
    Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Redox metals and oxidative abnormalities in human prion diseases.
    Petersen RB; Siedlak SL; Lee HG; Kim YS; Nunomura A; Tagliavini F; Ghetti B; Cras P; Moreira PI; Castellani RJ; Guentchev M; Budka H; Ironside JW; Gambetti P; Smith MA; Perry G
    Acta Neuropathol; 2005 Sep; 110(3):232-8. PubMed ID: 16096758
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
    Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
    Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease.
    Jarius C; Kovacs GG; Belay G; Hainfellner JA; Mitrova E; Budka H
    Acta Neuropathol; 2003 May; 105(5):449-54. PubMed ID: 12677444
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuropathologic characteristics of spinal cord lesions in sporadic Creutzfeldt-Jakob disease.
    Iwasaki Y; Yoshida M; Hashizume Y; Kitamoto T; Sobue G
    Acta Neuropathol; 2005 Nov; 110(5):490-500. PubMed ID: 16175355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
    Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P
    Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob disease.
    Faucheux BA; Privat N; Brandel JP; Sazdovitch V; Laplanche JL; Maurage CA; Hauw JJ; Haïk S
    J Neuropathol Exp Neurol; 2009 Aug; 68(8):892-901. PubMed ID: 19606064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease.
    Herzog C; Rivière J; Lescoutra-Etchegaray N; Charbonnier A; Leblanc V; Salès N; Deslys JP; Lasmézas CI
    J Virol; 2005 Nov; 79(22):14339-45. PubMed ID: 16254368
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variant Creutzfeldt-Jakob disease: immunocytochemical studies and image analysis.
    Nailon WH; Ironside JW
    Microsc Res Tech; 2000 Jul; 50(1):2-9. PubMed ID: 10871542
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting.
    Ritchie DL; Head MW; Ironside JW
    Neuropathol Appl Neurobiol; 2004 Aug; 30(4):360-8. PubMed ID: 15305981
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
    Rodríguez A; Pérez-Gracia E; Espinosa JC; Pumarola M; Torres JM; Ferrer I
    Acta Neuropathol; 2006 Nov; 112(5):573-85. PubMed ID: 16871401
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.
    Schoch G; Seeger H; Bogousslavsky J; Tolnay M; Janzer RC; Aguzzi A; Glatzel M
    PLoS Med; 2006 Feb; 3(2):e14. PubMed ID: 16354106
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 35.