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 *

283 related articles for article (PubMed ID: 11873615)

  • 1. [Prions, epidemic of Creutzfeldt-Jakob variant disease and global emergency].
    Bratosiewicz J; Liberski PP
    Neurol Neurochir Pol; 2001; 35(4 Suppl):25-44. PubMed ID: 11873615
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Human prion diseases: surgical lessons learned from iatrogenic prion transmission.
    Bonda DJ; Manjila S; Mehndiratta P; Khan F; Miller BR; Onwuzulike K; Puoti G; Cohen ML; Schonberger LB; Cali I
    Neurosurg Focus; 2016 Jul; 41(1):E10. PubMed ID: 27364252
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Creutzfeldt-Jakob disease.
    Sikorska B; Knight R; Ironside JW; Liberski PP
    Adv Exp Med Biol; 2012; 724():76-90. PubMed ID: 22411235
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II].
    Zaborowski A
    Psychiatr Pol; 2004; 38(2):297-309. PubMed ID: 15307294
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y; Shinagawa M
    Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biochemical and strain properties of CJD prions: complexity versus simplicity.
    Haïk S; Brandel JP
    J Neurochem; 2011 Oct; 119(2):251-61. PubMed ID: 21790605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. The prion diseases.
    Prusiner SB
    Brain Pathol; 1998 Jul; 8(3):499-513. PubMed ID: 9669700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prionoses--neurodegenerative diseases caused by prions, offectious proteinaceous molecules].
    Ferencík M; Novák M; Mikula I; Sokol J
    Bratisl Lek Listy; 1998; 99(8-9):486-98. PubMed ID: 9810774
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Transmission of spongiform encephalopathies (prion diseases)].
    Federspil P; Federspil PA
    HNO; 2002 Apr; 50(4):316-26. PubMed ID: 12063689
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biology and genetics of prion diseases.
    Prusiner SB
    Annu Rev Microbiol; 1994; 48():655-86. PubMed ID: 7826022
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.
    Sikorska B; Liberski PP
    Subcell Biochem; 2012; 65():457-96. PubMed ID: 23225013
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.
    Liberski PP; Barcikowska M; Cervenakova L; Bratosiewicz J; Marczewska M; Brown P; Gajdusek DC
    Acta Neuropathol; 1998 Oct; 96(4):425-30. PubMed ID: 9797009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. BSE: can we predict the future?
    Plum J
    Bull Mem Acad R Med Belg; 1997; 152(6):264-73. PubMed ID: 9581370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Strain-specific viral properties of variant Creutzfeldt-Jakob disease (vCJD) are encoded by the agent and not by host prion protein.
    Manuelidis L; Liu Y; Mullins B
    J Cell Biochem; 2009 Feb; 106(2):220-31. PubMed ID: 19097123
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.
    Collins S; McLean CA; Masters CL
    J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular approaches to mechanisms of prion diseases.
    Bratosiewicz-Wasik J; Wasik TJ; Liberski PP
    Folia Neuropathol; 2004; 42 Suppl A():33-46. PubMed ID: 15449458
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.