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Journal Abstract Search

245 related items for PubMed ID: 34710372

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  • 2. The N-terminal, polybasic region of PrP(C) dictates the efficiency of prion propagation by binding to PrP(Sc).
    Turnbaugh JA, Unterberger U, Saá P, Massignan T, Fluharty BR, Bowman FP, Miller MB, Supattapone S, Biasini E, Harris DA.
    J Neurosci; 2012 Jun 27; 32(26):8817-30. PubMed ID: 22745483
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  • 3. 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 27; 88(5):2690-703. PubMed ID: 24352465
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  • 4. The N-Terminal Polybasic Region of Prion Protein Is Crucial in Prion Pathogenesis Independently of the Octapeptide Repeat Region.
    Das NR, Miyata H, Hara H, Chida J, Uchiyama K, Masujin K, Watanabe H, Kondoh G, Sakaguchi S.
    Mol Neurobiol; 2020 Feb 27; 57(2):1203-1216. PubMed ID: 31707632
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  • 5. Identifying critical sites of PrP(c)-PrP(Sc) interaction in prion-infected cells by dominant-negative inhibition.
    Taguchi Y, Schätzl HM.
    Prion; 2013 Feb 27; 7(6):452-6. PubMed ID: 24401595
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  • 6. Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease.
    Meier P, Genoud N, Prinz M, Maissen M, Rülicke T, Zurbriggen A, Raeber AJ, Aguzzi A.
    Cell; 2003 Apr 04; 113(1):49-60. PubMed ID: 12679034
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  • 7. Dissociation of infectivity from seeding ability in prions with alternate docking mechanism.
    Miller MB, Geoghegan JC, Supattapone S.
    PLoS Pathog; 2011 Jul 04; 7(7):e1002128. PubMed ID: 21779169
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  • 8. The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like form.
    Hosszu LL, Tattum MH, Jones S, Trevitt CR, Wells MA, Waltho JP, Collinge J, Jackson GS, Clarke AR.
    Biochemistry; 2010 Oct 12; 49(40):8729-38. PubMed ID: 20718410
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  • 9. Strain-Dependent Prion Infection in Mice Expressing Prion Protein with Deletion of Central Residues 91-106.
    Uchiyama K, Miyata H, Yamaguchi Y, Imamura M, Okazaki M, Pasiana AD, Chida J, Hara H, Atarashi R, Watanabe H, Kondoh G, Sakaguchi S.
    Int J Mol Sci; 2020 Oct 01; 21(19):. PubMed ID: 33019549
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  • 10. The charge structure of helix 1 in the prion protein regulates conversion to pathogenic PrPSc.
    Norstrom EM, Mastrianni JA.
    J Virol; 2006 Sep 01; 80(17):8521-9. PubMed ID: 16912302
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  • 17. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice.
    Hara H, Miyata H, Das NR, Chida J, Yoshimochi T, Uchiyama K, Watanabe H, Kondoh G, Yokoyama T, Sakaguchi S.
    J Virol; 2018 Jan 01; 92(1):. PubMed ID: 29046443
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  • 18. Critical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion protein.
    Taguchi Y, Mistica AM, Kitamoto T, Schätzl HM.
    PLoS Pathog; 2013 Jan 01; 9(6):e1003466. PubMed ID: 23825952
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  • 19. Recombinant human prion protein inhibits prion propagation in vitro.
    Yuan J, Zhan YA, Abskharon R, Xiao X, Martinez MC, Zhou X, Kneale G, Mikol J, Lehmann S, Surewicz WK, Castilla J, Steyaert J, Zhang S, Kong Q, Petersen RB, Wohlkonig A, Zou WQ.
    Sci Rep; 2013 Oct 09; 3():2911. PubMed ID: 24105336
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  • 20. Prion protein self-peptides modulate prion interactions and conversion.
    Rigter A, Priem J, Timmers-Parohi D, Langeveld JP, van Zijderveld FG, Bossers A.
    BMC Biochem; 2009 Nov 30; 10():29. PubMed ID: 19943977
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