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 *

190 related articles for article (PubMed ID: 7767491)

  • 1. Inherited prion diseases and transmission to rodents.
    Tateishi J; Kitamoto T
    Brain Pathol; 1995 Jan; 5(1):53-9. PubMed ID: 7767491
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents.
    Tateishi J; Kitamoto T; Hoque MZ; Furukawa H
    Neurology; 1996 Feb; 46(2):532-7. PubMed ID: 8614527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.
    Asante EA; Gowland I; Grimshaw A; Linehan JM; Smidak M; Houghton R; Osiguwa O; Tomlinson A; Joiner S; Brandner S; Wadsworth JDF; Collinge J
    J Gen Virol; 2009 Mar; 90(Pt 3):546-558. PubMed ID: 19218199
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations.
    Hill AF; Joiner S; Beck JA; Campbell TA; Dickinson A; Poulter M; Wadsworth JD; Collinge J
    Brain; 2006 Mar; 129(Pt 3):676-85. PubMed ID: 16415305
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.
    Higuma M; Sanjo N; Satoh K; Shiga Y; Sakai K; Nozaki I; Hamaguchi T; Nakamura Y; Kitamoto T; Shirabe S; Murayama S; Yamada M; Tateishi J; Mizusawa H
    PLoS One; 2013; 8(3):e60003. PubMed ID: 23555862
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prion Mutations in Republic of Republic of Korea, China, and Japan.
    Kim DY; Shim KH; Bagyinszky E; An SSA
    Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36614069
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prion disease surveillance in Japan: analysis of 1,241 patients].
    Yamada M; Nozaki I; Hamaguchi T; Noguchi-Shinohara M; Kitamoto T; Nakamura Y; Sato T; Mizusawa H
    Rinsho Shinkeigaku; 2009 Nov; 49(11):939-42. PubMed ID: 20030254
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
    Parchi P; Cescatti M; Notari S; Schulz-Schaeffer WJ; Capellari S; Giese A; Zou WQ; Kretzschmar H; Ghetti B; Brown P
    Brain; 2010 Oct; 133(10):3030-42. PubMed ID: 20823086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
    Ironside JW; Head MW
    Curr Top Microbiol Immunol; 2004; 284():133-59. PubMed ID: 15148991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Prion diseases in Japan: analysis of 918 patients].
    Yamada M
    Rinsho Shinkeigaku; 2007 Nov; 47(11):805-8. PubMed ID: 18210803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
    Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
    J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. 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]  

  • 17. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
    Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

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

  • 20. Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases.
    Jackson WS; Borkowski AW; Watson NE; King OD; Faas H; Jasanoff A; Lindquist S
    Proc Natl Acad Sci U S A; 2013 Sep; 110(36):14759-64. PubMed ID: 23959875
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.