Localization of A11-reactive oligomeric species in prion diseases-Reference-Cited by-同舟云学术

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Localization of A11-reactive oligomeric species in prion diseases

Published:2013-04-09 Issue:7 Volume:62 Page:994-1001
ISSN:0309-0167
Container-title:Histopathology
language:en
Short-container-title:Histopathology

Author:

Aidt Frederik H,Hasholt Lis F¹,Christiansen Michael²,Laursen Henning³

Affiliation:

1. Institute of Cellular and Molecular Medicine; Faculty of Health Sciences; University of Copenhagen; Copenhagen; Denmark

2. Section of Molecular Medicine; Department of Clinical Biochemistry, Immunology and Genetics; Statens Serum Institut; Copenhagen; Denmark

3. Neuropathology Laboratory; Rigshospitalet; Copenhagen; Denmark

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/his.12097/fullpdf

Reference52 articles.

1. Novel proteinaceous infectious particles cause scrapie;Prusiner;Science,1982

2. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins;Pan;Proc. Natl Acad. Sci. USA,1993

3. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases);Budka;Brain Pathol.,1995

4. Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol;Ma;Science,2002

5. Interactions between prion protein isoforms: the kiss of death?;Caughey;Trends Biochem. Sci.,2001

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