Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype

Autor: Asante, Emmanuel A., Desbruslais, Melanie, Linehan, Jacqueline M., Joiner, Susan, Gowland, Ian, Welch, Julie, Stone, Lisa, Lloyd, Sarah E., Hill, Andrew F., Brandner, Sebastian, Collinge, John

Publikováno v: Science, 2004 Dec 01. 306(5702), 1793-1796.

Externí odkaz: https://www.jstor.org/stable/3839785

Dissociation of Pathological and Molecular Phenotype of Variant Creutzfeldt-Jakob Disease in Transgenic Human Prion Protein 129 Heterozygous Mice

Autor: Asante, Emmanuel A., Linehan, Jacqueline M., Gowland, Ian, Joiner, Susan, Fox, Katie, Cooper, Sharon, Osiguwa, Olufumilayo, Gorry, Michelle, Welch, Julie, Houghton, Richard, Desbruslais, Melanie, Brandner, Sebastian, Wadsworth, Jonathan D. F., Collinge, John

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 2006 Jul 01. 103(28), 10759-10764.

Externí odkaz: https://www.jstor.org/stable/30049575

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BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.

Autor: Asante, Emmanuel A., Linehan, Jacqueline M., Desbruslais, Melanie, Joiner, Susan, Gowland, Ian, Wood, Andrew L., Welch, Julie, Hill, Andrew F., Lloyd, Sarah E., Wadsworth, Jonathan D. F., Collinge, John

Publikováno v: EMBO Journal; 12/1/2002, Vol. 21 Issue 23, p6358-6366, 9p

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice.

Autor: Lloyd SE; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Linehan JM; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Desbruslais M; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Joiner S; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Buckell J; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Brandner S; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Wadsworth JDF; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK., Collinge J; MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College, London WC1N 3BG, UK.

Publikováno v: The Journal of general virology [J Gen Virol] 2004 Aug; Vol. 85 (Pt 8), pp. 2471-2478.