BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 7903647)

  • 1. Genetics of human prion disease.
    Ridley RM; Baker HF
    Dev Biol Stand; 1993; 80():15-23. PubMed ID: 7903647
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular genetics of human prion diseases.
    Collinge J; Palmer MS
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):371-8. PubMed ID: 7913754
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease.
    Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human prion diseases.
    Prusiner SB; Hsiao KK
    Ann Neurol; 1994 Apr; 35(4):385-95. PubMed ID: 8154865
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction].
    Peoc'h K
    Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969
    [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. The human prion diseases. A review with special emphasis on new variant CJD and comments on surveillance.
    Keohane C
    Clin Exp Pathol; 1999; 47(3-4):125-32. PubMed ID: 10472732
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R; Rosemberg S; Passos-Bueno MR; da Silva LS; Iughetti P; Papadopoulos M; Carrilho PM; Caramelli P; Albrecht S; Zatz M; LeBlanc A
    Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular biology and genetics of prion diseases.
    Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):447-63. PubMed ID: 7913765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prospective 10-year surveillance of human prion diseases in Japan.
    Nozaki I; Hamaguchi T; Sanjo N; Noguchi-Shinohara M; Sakai K; Nakamura Y; Sato T; Kitamoto T; Mizusawa H; Moriwaka F; Shiga Y; Kuroiwa Y; Nishizawa M; Kuzuhara S; Inuzuka T; Takeda M; Kuroda S; Abe K; Murai H; Murayama S; Tateishi J; Takumi I; Shirabe S; Harada M; Sadakane A; Yamada M
    Brain; 2010 Oct; 133(10):3043-57. PubMed ID: 20855418
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E; Kovacs GG; Ströbel T; Koperek O; Voigtländer T; Liberski PP; Budka H
    Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Prion disease].
    Mizusawa H
    Rinsho Shinkeigaku; 2010 Nov; 50(11):797-802. PubMed ID: 21921445
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Prion diseases and a new variant of Creutzfeldt-Jakob disease].
    Doh-ura K; Kitamoto T
    Rinsho Shinkeigaku; 1996 Dec; 36(12):1370-2. PubMed ID: 9128415
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. [The prion diseases].
    Kondo K
    Hokkaido Igaku Zasshi; 1997 Jan; 72(1):27-36. PubMed ID: 9086360
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein.
    Liemann S; Glockshuber R
    Biochemistry; 1999 Mar; 38(11):3258-67. PubMed ID: 10079068
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transmissible and genetic prion diseases share a common pathway of neurodegeneration.
    Hegde RS; Tremblay P; Groth D; DeArmond SJ; Prusiner SB; Lingappa VR
    Nature; 1999 Dec; 402(6763):822-6. PubMed ID: 10617204
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.
    Kitamoto T; Doh-ura K; Muramoto T; Miyazono M; Tateishi J
    Am J Pathol; 1992 Aug; 141(2):271-7. PubMed ID: 1353945
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions.
    Kitamoto T; Mohri S; Ironside JW; Miyoshi I; Tanaka T; Kitamoto N; Itohara S; Kasai N; Katsuki M; Higuchi J; Muramoto T; Shin RW
    Biochem Biophys Res Commun; 2002 Jun; 294(2):280-6. PubMed ID: 12051707
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.