Cystatin F is a biomarker of prion pathogenesis in mice.
Misfolding of the cellular prion protein (PrPC) into the scrapie prion protein (PrPSc) results in progressive, fatal, transmissible neurodegenerative conditions termed prion diseases. Experimental and epidemiological evidence point toward a protracted, clinically silent phase in prion diseases, yet...
Saved in:
| Main Authors: | Mario Nuvolone, Nicolas Schmid, Gino Miele, Silvia Sorce, Rita Moos, Christian Schori, Roger R Beerli, Monika Bauer, Philippe Saudan, Klaus Dietmeier, Ingolf Lachmann, Michael Linnebank, Roland Martin, Ulf Kallweit, Veronika Kana, Elisabeth J Rushing, Herbert Budka, Adriano Aguzzi |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2017-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0171923&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Rapid functional cloning of cell adhesion molecules
by: Christiane Ruedl, et al.
Published: (2004-12-01) -
Protective anti‐prion antibodies in human immunoglobulin repertoires
by: Assunta Senatore, et al.
Published: (2020-08-01) -
Prion infections and anti-PrP antibodies trigger converging neurotoxic pathways.
by: Uli S Herrmann, et al.
Published: (2015-02-01) -
Loss of PIKfyve drives the spongiform degeneration in prion diseases
by: Asvin K K Lakkaraju, et al.
Published: (2021-07-01) -
Prion pathogenesis is faithfully reproduced in cerebellar organotypic slice cultures.
by: Jeppe Falsig, et al.
Published: (2012-01-01)