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Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.
Asante, Emmanuel A; Gowland, Ian; Grimshaw, Andrew; Linehan, Jacqueline M; Smidak, Michelle; Houghton, Richard; Osiguwa, Olufunmilayo; Tomlinson, Andrew; Joiner, Susan; Brandner, Sebastian; Wadsworth, Jonathan D F; Collinge, John.
Afiliação
  • Asante EA; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Gowland I; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Grimshaw A; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Linehan JM; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Smidak M; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Houghton R; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Osiguwa O; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Tomlinson A; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Joiner S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Brandner S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Wadsworth JDF; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
  • Collinge J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.
J Gen Virol ; 90(Pt 3): 546-558, 2009 Mar.
Article em En | MEDLINE | ID: mdl-19218199
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob / Doenças Priônicas / Mutação Puntual Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: J Gen Virol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob / Doenças Priônicas / Mutação Puntual Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: J Gen Virol Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Reino Unido