Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
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Author / Creator
Xiao, Xiangzhu , Yuan, Jue , Haïk, Stéphane , Cali, Ignazio , Zhan, Yian , Moudjou, Mohammed , Li, Baiya , Laplanche, Jean-Louis , Laude, Hubert , Langeveld, Jan , Gambetti, Pierluigi , Kitamoto, Tetsuyuki , Kong, Qingzhong , Brandel, Jean-Philippe , Cobb, Brian A. , Petersen, Robert B. and Zou, Wen-Quan
Publisher
United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
The four glycoforms of the cellular prion protein (PrP(C)) variably glycosylated at the two N-linked glycosylation sites are converted into their pathological forms (PrP(Sc)) in most cases of sporadic prion diseases. However, a prominent molecular characteristic of PrP(Sc) in the recently identified variably protease-sensitive prionopathy (VPSPr) i...
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Full title
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease
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TN_cdi_plos_journals_1330889431
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1330889431
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0058786
