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200 related items for PubMed ID: 10102274

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  • 3. 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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  • 4. Dominant-negative inhibition of prion replication in transgenic mice.
    Perrier V, Kaneko K, Safar J, Vergara J, Tremblay P, DeArmond SJ, Cohen FE, Prusiner SB, Wallace AC.
    Proc Natl Acad Sci U S A; 2002 Oct 01; 99(20):13079-84. PubMed ID: 12271119
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  • 5. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains.
    Tremblay P, Ball HL, Kaneko K, Groth D, Hegde RS, Cohen FE, DeArmond SJ, Prusiner SB, Safar JG.
    J Virol; 2004 Feb 01; 78(4):2088-99. PubMed ID: 14747574
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  • 12. Propagation of RML prions in mice expressing PrP devoid of GPI anchor leads to formation of a novel, stable prion strain.
    Mahal SP, Jablonski J, Suponitsky-Kroyter I, Oelschlegel AM, Herva ME, Oldstone M, Weissmann C.
    PLoS Pathog; 2012 Feb 01; 8(6):e1002746. PubMed ID: 22685404
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  • 13. Disulfide-crosslink scanning reveals prion-induced conformational changes and prion strain-specific structures of the pathological prion protein PrPSc.
    Taguchi Y, Lu L, Marrero-Winkens C, Otaki H, Nishida N, Schatzl HM.
    J Biol Chem; 2018 Aug 17; 293(33):12730-12740. PubMed ID: 29934306
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  • 14. Mouse-hamster chimeric prion protein (PrP) devoid of N-terminal residues 23-88 restores susceptibility to 22L prions, but not to RML prions in PrP-knockout mice.
    Uchiyama K, Miyata H, Yano M, Yamaguchi Y, Imamura M, Muramatsu N, Das NR, Chida J, Hara H, Sakaguchi S.
    PLoS One; 2014 Aug 17; 9(10):e109737. PubMed ID: 25330286
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  • 15. Self-assembly of recombinant prion protein of 106 residues.
    Baskakov IV, Aagaard C, Mehlhorn I, Wille H, Groth D, Baldwin MA, Prusiner SB, Cohen FE.
    Biochemistry; 2000 Mar 14; 39(10):2792-804. PubMed ID: 10704232
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  • 16. Propagation of ovine prions from "poor" transmitter scrapie isolates in ovine PrP transgenic mice.
    Thackray AM, Hopkins L, Lockey R, Spiropoulos J, Bujdoso R.
    Exp Mol Pathol; 2012 Feb 14; 92(1):167-74. PubMed ID: 22120785
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  • 17. Strain-dependent role of copper in prion disease through binding to histidine residues in the N-terminal domain of prion protein.
    Hara H, Miyata H, Chida J, Sakaguchi S.
    J Neurochem; 2023 Nov 14; 167(3):394-409. PubMed ID: 37777338
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  • 18. Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.
    Fischer M, Rülicke T, Raeber A, Sailer A, Moser M, Oesch B, Brandner S, Aguzzi A, Weissmann C.
    EMBO J; 1996 Mar 15; 15(6):1255-64. PubMed ID: 8635458
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  • 19. Identification of two prion protein regions that modify scrapie incubation time.
    Supattapone S, Muramoto T, Legname G, Mehlhorn I, Cohen FE, DeArmond SJ, Prusiner SB, Scott MR.
    J Virol; 2001 Feb 15; 75(3):1408-13. PubMed ID: 11152514
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  • 20. Prion infection of mouse neurospheres.
    Giri RK, Young R, Pitstick R, DeArmond SJ, Prusiner SB, Carlson GA.
    Proc Natl Acad Sci U S A; 2006 Mar 07; 103(10):3875-80. PubMed ID: 16495413
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