Differential overexpression of SERPINA3 in human prion diseases
Differential overexpression of SERPINA3 in human prion diseases
About this item
Full title
Author / Creator
Vanni, S. , Moda, F. , Zattoni, M. , Bistaffa, E. , De Cecco, E. , Rossi, M. , Giaccone, G. , Tagliavini, F. , Haïk, S. , Deslys, J. P. , Zanusso, G. , Ironside, J. W. , Ferrer, I. , Kovacs, G. G. and Legname, G.
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
Formats
Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
Prion diseases are fatal neurodegenerative disorders with sporadic, genetic or acquired etiologies. The molecular alterations leading to the onset and the spreading of these diseases are still unknown. In a previous work we identified a five-gene signature able to distinguish intracranially BSE-infected macaques from healthy ones, with
SERPINA3<...
Alternative Titles
Full title
Differential overexpression of SERPINA3 in human prion diseases
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5688139
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5688139
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-017-15778-8
