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Journal Abstract Search


930 related items for PubMed ID: 10415165

  • 21. Hyperefficient PrP Sc amplification of mouse-adapted BSE and scrapie strain by protein misfolding cyclic amplification technique.
    Fujihara A, Atarashi R, Fuse T, Ubagai K, Nakagaki T, Yamaguchi N, Ishibashi D, Katamine S, Nishida N.
    FEBS J; 2009 May; 276(10):2841-8. PubMed ID: 19459939
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  • 22. Experimental Infection of Cattle With a Novel Prion Derived From Atypical H-Type Bovine Spongiform Encephalopathy.
    Okada H, Masujin K, Miyazawa K, Iwamaru Y, Imamura M, Matsuura Y, Arai S, Fukuda S, Murayama Y, Yokoyama T.
    Vet Pathol; 2017 Nov; 54(6):892-900. PubMed ID: 28731378
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  • 23. Experimental transmission of two young and one suspended bovine spongiform encephalopathy (BSE) cases to bovinized transgenic mice.
    Yokoyama T, Masujin K, Yamakawa Y, Sata T, Murayama Y, Shu Y, Okada H, Mohri S, Shinagawa M.
    Jpn J Infect Dis; 2007 Sep; 60(5):317-20. PubMed ID: 17881878
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  • 24. Comparative molecular analysis of the abnormal prion protein in field scrapie cases and experimental bovine spongiform encephalopathy in sheep by use of Western blotting and immunohistochemical methods.
    Lezmi S, Martin S, Simon S, Comoy E, Bencsik A, Deslys JP, Grassi J, Jeffrey M, Baron T.
    J Virol; 2004 Apr; 78(7):3654-62. PubMed ID: 15016886
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  • 25. Detection of prion particles in samples of BSE and scrapie by fluorescence correlation spectroscopy without proteinase K digestion.
    Birkmann E, Schäfer O, Weinmann N, Dumpitak C, Beekes M, Jackman R, Thorne L, Riesner D.
    Biol Chem; 2006 Jan; 387(1):95-102. PubMed ID: 16497169
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  • 26. 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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  • 27. Ovine infection with the agents of scrapie (CH1641 isolate) and bovine spongiform encephalopathy: immunochemical similarities can be resolved by immunohistochemistry.
    Jeffrey M, González L, Chong A, Foster J, Goldmann W, Hunter N, Martin S.
    J Comp Pathol; 2006 Jan 01; 134(1):17-29. PubMed ID: 16324707
    [Abstract] [Full Text] [Related]

  • 28. Transmissibility of H-Type Bovine Spongiform Encephalopathy to Hamster PrP Transgenic Mice.
    Okada H, Masujin K, Miyazawa K, Yokoyama T.
    PLoS One; 2015 Jan 01; 10(10):e0138977. PubMed ID: 26466381
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  • 29. Prion diseases and emerging prion diseases.
    Yokoyama T, Mohri S.
    Curr Med Chem; 2008 Jan 01; 15(9):912-6. PubMed ID: 18473798
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  • 30. Molecular behaviors of "CH1641-like" sheep scrapie isolates in ovine transgenic mice (TgOvPrP4).
    Baron T, Biacabe AG.
    J Virol; 2007 Jul 01; 81(13):7230-7. PubMed ID: 17442721
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  • 31. Evidence for co-infection of ovine prion strains in classical scrapie isolates.
    Thackray AM, Lockey R, Beck KE, Spiropoulos J, Bujdoso R.
    J Comp Pathol; 2012 Jul 01; 147(2-3):316-29. PubMed ID: 22522075
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  • 32. A bovine cell line that can be infected by natural sheep scrapie prions.
    Oelschlegel AM, Geissen M, Lenk M, Riebe R, Angermann M, Schatzl H, Groschup MH.
    PLoS One; 2015 Jul 01; 10(1):e0117154. PubMed ID: 25565633
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  • 33. Early detection of PrPres in BSE-infected bovine PrP transgenic mice.
    Castilla J, Gutiérrez Adán A, Brun A, Pintado B, Ramírez MA, Parra B, Doyle D, Rogers M, Salguero FJ, Sánchez C, Sánchez-Vizcaíno JM, Torres JM.
    Arch Virol; 2003 Apr 01; 148(4):677-91. PubMed ID: 12664293
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  • 34. Stability properties of PrP(Sc) from cattle with experimental transmissible spongiform encephalopathies: use of a rapid whole homogenate, protease-free assay.
    Vrentas CE, Greenlee JJ, Baron T, Caramelli M, Czub S, Nicholson EM.
    BMC Vet Res; 2013 Aug 15; 9():167. PubMed ID: 23945217
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  • 35. Antigen retrieval using sodium hydroxide for prion immunohistochemistry in bovine spongiform encephalopathy and scrapie.
    Okada H, Sato Y, Sata T, Sakurai M, Endo J, Yokoyama T, Mohri S.
    J Comp Pathol; 2011 May 15; 144(4):251-6. PubMed ID: 21112058
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  • 36. Glycosylation deficiency at either one of the two glycan attachment sites of cellular prion protein preserves susceptibility to bovine spongiform encephalopathy and scrapie infections.
    Neuendorf E, Weber A, Saalmueller A, Schatzl H, Reifenberg K, Pfaff E, Groschup MH.
    J Biol Chem; 2004 Dec 17; 279(51):53306-16. PubMed ID: 15448157
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  • 37. Comparison of French natural scrapie isolates with bovine spongiform encephalopathy and experimental scrapie infected sheep.
    Baron TG, Madec JY, Calavas D, Richard Y, Barillet F.
    Neurosci Lett; 2000 Apr 28; 284(3):175-8. PubMed ID: 10773427
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  • 38. Detection and localisation of PrP(Sc) in the liver of sheep infected with scrapie and bovine spongiform encephalopathy.
    Everest SJ, Ramsay AM, Chaplin MJ, Everitt S, Stack MJ, Neale MH, Jeffrey M, Moore SJ, Bellworthy SJ, Terry LA.
    PLoS One; 2011 May 12; 6(5):e19737. PubMed ID: 21589864
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  • 39. Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice.
    Okada H, Masujin K, Miyazawa K, Yokoyama T.
    Vet Res; 2015 Jul 13; 46(1):81. PubMed ID: 26169916
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  • 40. Conventional and State-of-the-Art Detection Methods of Bovine Spongiform Encephalopathy (BSE).
    Olech M.
    Int J Mol Sci; 2023 Apr 12; 24(8):. PubMed ID: 37108297
    [Abstract] [Full Text] [Related]


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