Pathogenic human prion protein rescues PrP null phenotype in transgenic mice
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference20 articles.
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2. Aminoacid polymorphism in human prion protein and age at death in inherited prion disease [letter];Baker;Lancet,1991
3. Mice devoid of PrP are resistant to scrapie;Bueler;Cell,1993
4. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein;Bueler;Nature,1992
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2. Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS;PLOS Pathogens;2015-07-02
3. A naturally occurring variant of the human prion protein completely prevents prion disease;Nature;2015-06
4. Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases;Acta Neuropathologica Communications;2013-05-09
5. Possible role for Ca2+ in the pathophysiology of the prion protein?;BioFactors;2011-05
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