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Familial Parkinson's point mutation abolishes multiple system atrophy prion replication.
Woerman, Amanda L; Kazmi, Sabeen A; Patel, Smita; Aoyagi, Atsushi; Oehler, Abby; Widjaja, Kartika; Mordes, Daniel A; Olson, Steven H; Prusiner, Stanley B.
Affiliation
  • Woerman AL; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Kazmi SA; Department of Neurology, University of California, San Francisco, CA 94158.
  • Patel S; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Aoyagi A; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Oehler A; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Widjaja K; Daiichi Sankyo Co., Ltd., Tokyo 140-8710, Japan.
  • Mordes DA; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Olson SH; Institute for Neurodegenerative Diseases, Weill Institute for Neurosciences, University of California, San Francisco, CA 94158.
  • Prusiner SB; C. S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital, Boston, MA 02114.
Proc Natl Acad Sci U S A ; 115(2): 409-414, 2018 01 09.
Article in En | MEDLINE | ID: mdl-29279394
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Full text: 1 Database: MEDLINE Main subject: Parkinson Disease / Prions / Point Mutation / Multiple System Atrophy Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2018 Type: Article
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Parkinson Disease / Prions / Point Mutation / Multiple System Atrophy Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2018 Type: Article