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MSA prions exhibit remarkable stability and resistance to inactivation.
Woerman, Amanda L; Kazmi, Sabeen A; Patel, Smita; Freyman, Yevgeniy; Oehler, Abby; Aoyagi, Atsushi; Mordes, Daniel A; Halliday, Glenda M; Middleton, Lefkos T; Gentleman, Steve M; Olson, Steven H; Prusiner, Stanley B.
Afiliação
  • Woerman AL; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Kazmi SA; Department of Neurology, University of California, San Francisco, CA, USA.
  • Patel S; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Freyman Y; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Oehler A; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Aoyagi A; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Mordes DA; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
  • Halliday GM; Daiichi Sankyo Co., Ltd., Tokyo, Japan.
  • Middleton LT; C.S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Gentleman SM; Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, Australia.
  • Olson SH; Faculty of Medicine, School of Medical Science, University of New South Wales, Kensington, Australia.
  • Prusiner SB; Neuroscience Research Australia, Randwick, Australia.
Acta Neuropathol ; 135(1): 49-63, 2018 01.
Article em En | MEDLINE | ID: mdl-28849371
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Atrofia de Múltiplos Sistemas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Acta Neuropathol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Atrofia de Múltiplos Sistemas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Acta Neuropathol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos