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Journal Abstract Search

167 related items for PubMed ID: 21196244

  • 21. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies.
    Weissmann C, Fischer M, Raeber A, Büeler H, Sailer A, Shmerling D, Rülicke T, Brandner S, Aguzzi A.
    Rev Sci Tech; 1998 Apr; 17(1):278-90. PubMed ID: 9638817
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  • 22. Biology of the prion gene complex.
    Mastrangelo P, Westaway D.
    Biochem Cell Biol; 2001 Apr; 79(5):613-28. PubMed ID: 11716303
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  • 23. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle.
    Prusiner SB.
    Dev Biol Stand; 1991 Apr; 75():55-74. PubMed ID: 1686599
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  • 25. Prion encephalopathies of animals and humans.
    Prusiner SB.
    Dev Biol Stand; 1993 Apr; 80():31-44. PubMed ID: 8270114
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  • 28. Endoproteolytic processing of the mammalian prion glycoprotein family.
    Mays CE, Coomaraswamy J, Watts JC, Yang J, Ko KW, Strome B, Mercer RC, Wohlgemuth SL, Schmitt-Ulms G, Westaway D.
    FEBS J; 2014 Feb; 281(3):862-76. PubMed ID: 24286250
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  • 30. Differential expression of Prnp and Sprn in scrapie infected sheep also reveals Prnp genotype specific differences.
    Gossner AG, Bennet N, Hunter N, Hopkins J.
    Biochem Biophys Res Commun; 2009 Jan 23; 378(4):862-6. PubMed ID: 19070601
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  • 31. Proteasomal Inhibition Redirects the PrP-Like Shadoo Protein to the Nucleus.
    Kang SG, Mays CE, Daude N, Yang J, Kar S, Westaway D.
    Mol Neurobiol; 2019 Nov 23; 56(11):7888-7904. PubMed ID: 31129810
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  • 32. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May 23; 35(5):1177-88. PubMed ID: 24360565
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  • 34. Cloning of the bovine prion-like Shadoo (SPRN) gene by comparative analysis of the predicted genomic locus.
    Uboldi C, Paulis M, Guidi E, Bertoni A, Meo GP, Perucatti A, Iannuzzi L, Raimondi E, Brunner RM, Eggen A, Ferretti L.
    Mamm Genome; 2006 Nov 23; 17(11):1130-9. PubMed ID: 17091316
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  • 36. Prion protein transgenes and the neuropathology in prion diseases.
    DeArmond SJ, Prusiner SB.
    Brain Pathol; 1995 Jan 23; 5(1):77-89. PubMed ID: 7767493
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  • 37. Evolution of vertebrate genes related to prion and Shadoo proteins--clues from comparative genomic analysis.
    Premzl M, Gready JE, Jermiin LS, Simonic T, Marshall Graves JA.
    Mol Biol Evol; 2004 Dec 23; 21(12):2210-31. PubMed ID: 15342797
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  • 38. Genetics of prion disease.
    Lloyd S, Mead S, Collinge J.
    Top Curr Chem; 2011 Dec 23; 305():1-22. PubMed ID: 21528440
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  • 39. The First Report of Polymorphisms and Genetic Characteristics of the Shadow of Prion Protein (SPRN) in Prion Disease-Resistant Animal, Chickens.
    Kim YC, Kim HH, Jeong BH.
    Front Vet Sci; 2022 Dec 23; 9():904305. PubMed ID: 35782543
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