BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 36254680)

  • 1. Probing the origin of prion protein misfolding via reconstruction of ancestral proteins.
    Cortez LM; Morrison AJ; Garen CR; Patterson S; Uyesugi T; Petrosyan R; Sekar RV; Harms MJ; Woodside MT; Sim VL
    Protein Sci; 2022 Dec; 31(12):e4477. PubMed ID: 36254680
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Eraña H; Fernández-Borges N; Elezgarai SR; Harrathi C; Charco JM; Chianini F; Dagleish MP; Ortega G; Millet Ó; Castilla J
    J Virol; 2017 Dec; 91(24):. PubMed ID: 28978705
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PrP P102L and Nearby Lysine Mutations Promote Spontaneous
    Kraus A; Raymond GJ; Race B; Campbell KJ; Hughson AG; Anson KJ; Raymond LD; Caughey B
    J Virol; 2017 Nov; 91(21):. PubMed ID: 28835493
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification.
    Camacho MV; Telling G; Kong Q; Gambetti P; Notari S
    Lab Invest; 2019 Nov; 99(11):1741-1748. PubMed ID: 31249376
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers.
    Davenport KA; Henderson DM; Mathiason CK; Hoover EA
    J Virol; 2016 Dec; 90(23):10752-10761. PubMed ID: 27654299
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions.
    Barron RM; King D; Jeffrey M; McGovern G; Agarwal S; Gill AC; Piccardo P
    Acta Neuropathol; 2016 Oct; 132(4):611-24. PubMed ID: 27376534
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Porcine prion protein amyloid.
    Hammarström P; Nyström S
    Prion; 2015; 9(4):266-77. PubMed ID: 26218890
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular dynamics studies on the buffalo prion protein.
    Zhang J; Wang F; Chatterjee S
    J Biomol Struct Dyn; 2016; 34(4):762-77. PubMed ID: 26043781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dissociation of prion protein amyloid seeding from transmission of a spongiform encephalopathy.
    Piccardo P; King D; Telling G; Manson JC; Barron RM
    J Virol; 2013 Nov; 87(22):12349-56. PubMed ID: 24027305
    [TBL] [Abstract][Full Text] [Related]  

  • 10.
    Meyerett-Reid C; Wyckoff AC; Spraker T; Pulford B; Bender H; Zabel MD
    mSphere; 2017; 2(1):. PubMed ID: 28144628
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant Mammalian Prions: The "Correctly" Misfolded Prion Protein Conformers.
    Ma J; Zhang J; Yan R
    Viruses; 2022 Aug; 14(9):. PubMed ID: 36146746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.
    Coleman BM; Harrison CF; Guo B; Masters CL; Barnham KJ; Lawson VA; Hill AF
    J Virol; 2014 Mar; 88(5):2690-703. PubMed ID: 24352465
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterozygosity for cervid S138N polymorphism results in subclinical CWD in gene-targeted mice and progressive inhibition of prion conversion.
    Arifin MI; Kaczmarczyk L; Zeng D; Hannaoui S; Lee C; Chang SC; Mitchell G; McKenzie D; Beekes M; Jackson W; Gilch S
    Proc Natl Acad Sci U S A; 2023 Apr; 120(15):e2221060120. PubMed ID: 37014866
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Species-barrier phenomenon in prion transmissibility from a viewpoint of protein science.
    Hagiwara K; Hara H; Hanada K
    J Biochem; 2013 Feb; 153(2):139-45. PubMed ID: 23284000
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Soluble polymorphic bank vole prion proteins induced by co-expression of quiescin sulfhydryl oxidase in E. coli and their aggregation behaviors.
    Abskharon R; Dang J; Elfarash A; Wang Z; Shen P; Zou LS; Hassan S; Wang F; Fujioka H; Steyaert J; Mulaj M; Surewicz WK; Castilla J; Wohlkonig A; Zou WQ
    Microb Cell Fact; 2017 Oct; 16(1):170. PubMed ID: 28978309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Location of the cross-β structure in prion fibrils: A search by seeding and electron spin resonance spectroscopy.
    Chu BK; Tsai RF; Hung CL; Kuo YH; Chen EH; Chiang YW; Chan SI; Chen RP
    Protein Sci; 2022 Jun; 31(6):e4326. PubMed ID: 35634767
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Protein misfolding cyclic amplification (PMCA): Current status and future directions.
    Saá P; Cervenakova L
    Virus Res; 2015 Sep; 207():47-61. PubMed ID: 25445341
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitro.
    Panza G; Luers L; Stöhr J; Nagel-Steger L; Weiss J; Riesner D; Willbold D; Birkmann E
    PLoS One; 2010 Dec; 5(12):e14283. PubMed ID: 21151607
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prions.
    Nyström S; Hammarström P
    Sci Rep; 2015 May; 5():10101. PubMed ID: 25960067
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prion disease: a deadly disease for protein misfolding.
    Chakraborty C; Nandi S; Jana S
    Curr Pharm Biotechnol; 2005 Apr; 6(2):167-77. PubMed ID: 15853695
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.