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Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.
- Published in:
- PLoS Biology, 2020, v. 18, n. 6, p. 1, doi. 10.1371/journal.pbio.3000725
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- Article
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 819, doi. 10.1093/brain/aws006
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- Article
Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.
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- PLoS Pathogens, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.ppat.1004953
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- Article
Inherited Prion Disease A117V Is Not Simply a Proteinopathy but Produces Prions Transmissible to Transgenic Mice Expressing Homologous Prion Protein.
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- PLoS Pathogens, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.ppat.1003643
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- Article
A naturally occurring variant of the human prion protein completely prevents prion disease.
- Published in:
- Nature, 2015, v. 522, n. 7557, p. 478, doi. 10.1038/nature14510
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- Article