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 *

229 related articles for article (PubMed ID: 22072968)

  • 1. Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease.
    Friedman-Levi Y; Meiner Z; Canello T; Frid K; Kovacs GG; Budka H; Avrahami D; Gabizon R
    PLoS Pathog; 2011 Nov; 7(11):e1002350. PubMed ID: 22072968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C).
    Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z
    J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483
    [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. The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.
    Bregman N; Shiner T; Kavé G; Alcalay R; Gana-Weisz M; Goldstein O; Glinka T; Aizenstein O; Bashat DB; Alcalay Y; Mirelman A; Thaler A; Giladi N; Omer N
    BMC Neurol; 2023 Apr; 23(1):151. PubMed ID: 37069531
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copper is toxic to PrP-ablated mice and exacerbates disease in a mouse model of E200K genetic prion disease.
    Canello T; Friedman-Levi Y; Mizrahi M; Binyamin O; Cohen E; Frid K; Gabizon R
    Neurobiol Dis; 2012 Mar; 45(3):1010-7. PubMed ID: 22198568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.
    Meiner Z; Gabizon R; Prusiner SB
    Medicine (Baltimore); 1997 Jul; 76(4):227-37. PubMed ID: 9279329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PrP(ST), a soluble, protease resistant and truncated PrP form features in the pathogenesis of a genetic prion disease.
    Friedman-Levi Y; Mizrahi M; Frid K; Binyamin O; Gabizon R
    PLoS One; 2013; 8(7):e69583. PubMed ID: 23922744
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Differential allelic expression of PrP mRNA in carriers of the E200K mutation.
    Rosenmann H; Halimi M; Kahana I; Biran I; Gabizon R
    Neurology; 1997 Sep; 49(3):851-6. PubMed ID: 9305353
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease.
    Kovacs GG; Molnár K; Keller E; Botond G; Budka H; László L
    J Neuropathol Exp Neurol; 2012 Mar; 71(3):223-32. PubMed ID: 22318125
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Towards authentic transgenic mouse models of heritable PrP prion diseases.
    Watts JC; Giles K; Bourkas ME; Patel S; Oehler A; Gavidia M; Bhardwaj S; Lee J; Prusiner SB
    Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
    Mitrová E; Belay G
    Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Roles of methionine oxidation in E200K prion protein misfolding: Implications for the mechanism of pathogenesis in E200K linked familial Creutzfeldt-Jakob disease.
    Wang Z; Feng B; Xiao G; Zhou Z
    Biochim Biophys Acta; 2016 Apr; 1864(4):346-58. PubMed ID: 26779934
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effects of a naturally occurring amino acid substitution in bovine PrP: a model for inherited prion disease in a natural host species.
    Vrentas CE; Greenlee JJ; Foster GH; West J; Jahnke MM; Schmidt MT; Nicholson EM
    BMC Res Notes; 2017 Dec; 10(1):759. PubMed ID: 29262866
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype.
    Ghoshal N; Cali I; Perrin RJ; Josephson SA; Sun N; Gambetti P; Morris JC
    Arch Neurol; 2009 Oct; 66(10):1240-6. PubMed ID: 19822779
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.