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 *

726 related articles for article (PubMed ID: 19218199)

  • 1. 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]  

  • 2. Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.
    Takeuchi A; Kobayashi A; Ironside JW; Mohri S; Kitamoto T
    J Biol Chem; 2013 Jul; 288(30):21659-66. PubMed ID: 23792955
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.
    Asante EA; Grimshaw A; Smidak M; Jakubcova T; Tomlinson A; Jeelani A; Hamdan S; Powell C; Joiner S; Linehan JM; Brandner S; Wadsworth JD; Collinge J
    PLoS Pathog; 2015 Jul; 11(7):e1004953. PubMed ID: 26135918
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions.
    Chapuis J; Moudjou M; Reine F; Herzog L; Jaumain E; Chapuis C; Quadrio I; Boulliat J; Perret-Liaudet A; Dron M; Laude H; Rezaei H; Béringue V
    Acta Neuropathol Commun; 2016 Feb; 4():10. PubMed ID: 26847207
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human prion strain selection in transgenic mice.
    Giles K; Glidden DV; Patel S; Korth C; Groth D; Lemus A; DeArmond SJ; Prusiner SB
    Ann Neurol; 2010 Aug; 68(2):151-61. PubMed ID: 20695008
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.
    Wadsworth JD; Joiner S; Linehan JM; Cooper S; Powell C; Mallinson G; Buckell J; Gowland I; Asante EA; Budka H; Brandner S; Collinge J
    Brain; 2006 Jun; 129(Pt 6):1557-69. PubMed ID: 16597650
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene.
    Korth C; Kaneko K; Groth D; Heye N; Telling G; Mastrianni J; Parchi P; Gambetti P; Will R; Ironside J; Heinrich C; Tremblay P; DeArmond SJ; Prusiner SB
    Proc Natl Acad Sci U S A; 2003 Apr; 100(8):4784-9. PubMed ID: 12684540
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H; Huor A; Espinosa JC; Douet JY; Lugan S; Aron N; Vilette D; Delisle MB; Marín-Moreno A; Peran P; Beringue V; Torres JM; Ironside JW; Andreoletti O
    mBio; 2020 Jun; 11(3):. PubMed ID: 32546613
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.
    Hizume M; Kobayashi A; Teruya K; Ohashi H; Ironside JW; Mohri S; Kitamoto T
    J Biol Chem; 2009 Feb; 284(6):3603-9. PubMed ID: 19074151
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.
    Watts JC; Giles K; Saltzberg DJ; Dugger BN; Patel S; Oehler A; Bhardwaj S; Sali A; Prusiner SB
    J Virol; 2016 Nov; 90(21):9558-9569. PubMed ID: 27440899
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Identification of I137M and other mutations that modulate incubation periods for two human prion strains.
    Giles K; De Nicola GF; Patel S; Glidden DV; Korth C; Oehler A; DeArmond SJ; Prusiner SB
    J Virol; 2012 Jun; 86(11):6033-41. PubMed ID: 22438549
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A naturally occurring variant of the human prion protein completely prevents prion disease.
    Asante EA; Smidak M; Grimshaw A; Houghton R; Tomlinson A; Jeelani A; Jakubcova T; Hamdan S; Richard-Londt A; Linehan JM; Brandner S; Alpers M; Whitfield J; Mead S; Wadsworth JD; Collinge J
    Nature; 2015 Jun; 522(7557):478-81. PubMed ID: 26061765
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Prion protein transgenes and the neuropathology in prion diseases.
    DeArmond SJ; Prusiner SB
    Brain Pathol; 1995 Jan; 5(1):77-89. PubMed ID: 7767493
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
    Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
    Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Experimental verification of a traceback phenomenon in prion infection.
    Kobayashi A; Sakuma N; Matsuura Y; Mohri S; Aguzzi A; Kitamoto T
    J Virol; 2010 Apr; 84(7):3230-8. PubMed ID: 20089646
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 37.