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Journal Abstract Search

244 related items for PubMed ID: 34737343

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  • 3. N-Terminal Regions of Prion Protein: Functions and Roles in Prion Diseases.
    Hara H, Sakaguchi S.
    Int J Mol Sci; 2020 Aug 28; 21(17):. PubMed ID: 32872280
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  • 7. Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation.
    Biljan I, Ilc G, Giachin G, Raspadori A, Zhukov I, Plavec J, Legname G.
    J Mol Biol; 2011 Sep 30; 412(4):660-73. PubMed ID: 21839748
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  • 8. In Vitro Approach To Identify Key Amino Acids in Low Susceptibility of Rabbit Prion Protein to Misfolding.
    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 15; 91(24):. PubMed ID: 28978705
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  • 10. Exploring the propensities of helices in PrP(C) to form beta sheet using NMR structures and sequence alignments.
    Dima RI, Thirumalai D.
    Biophys J; 2002 Sep 15; 83(3):1268-80. PubMed ID: 12202354
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  • 12. Mechanism of misfolding of the human prion protein revealed by a pathological mutation.
    Sanz-Hernández M, Barritt JD, Sobek J, Hornemann S, Aguzzi A, De Simone A.
    Proc Natl Acad Sci U S A; 2021 Mar 23; 118(12):. PubMed ID: 33731477
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  • 13. Liquid-liquid phase separation and fibrillation of the prion protein modulated by a high-affinity DNA aptamer.
    Matos CO, Passos YM, do Amaral MJ, Macedo B, Tempone MH, Bezerra OCL, Moraes MO, Almeida MS, Weber G, Missailidis S, Silva JL, Uversky VN, Pinheiro AS, Cordeiro Y.
    FASEB J; 2020 Jan 23; 34(1):365-385. PubMed ID: 31914616
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  • 14. Altered Domain Structure of the Prion Protein Caused by Cu2+ Binding and Functionally Relevant Mutations: Analysis by Cross-Linking, MS/MS, and NMR.
    McDonald AJ, Leon DR, Markham KA, Wu B, Heckendorf CF, Schilling K, Showalter HD, Andrews PC, McComb ME, Pushie MJ, Costello CE, Millhauser GL, Harris DA.
    Structure; 2019 Jun 04; 27(6):907-922.e5. PubMed ID: 30956132
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  • 16. Residue-specific mobility changes in soluble oligomers of the prion protein define regions involved in aggregation.
    Glaves JP, Ladner-Keay CL, Bjorndahl TC, Wishart DS, Sykes BD.
    Biochim Biophys Acta Proteins Proteom; 2018 Sep 04; 1866(9):982-988. PubMed ID: 29935976
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  • 18. Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids.
    Chaves JA, Sanchez-López C, Gomes MP, Sisnande T, Macedo B, de Oliveira VE, Braga CA, Rangel LP, Silva JL, Quintanar L, Cordeiro Y.
    J Biol Inorg Chem; 2014 Aug 04; 19(6):839-51. PubMed ID: 24557708
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  • 19. Local structural plasticity of the prion protein. Analysis of NMR relaxation dynamics.
    Viles JH, Donne D, Kroon G, Prusiner SB, Cohen FE, Dyson HJ, Wright PE.
    Biochemistry; 2001 Mar 06; 40(9):2743-53. PubMed ID: 11258885
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  • 20. X-ray diffraction analysis of scrapie prion: intermediate and folded structures in a peptide containing two putative alpha-helices.
    Inouye H, Kirschner DA.
    J Mol Biol; 1997 May 02; 268(2):375-89. PubMed ID: 9159477
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