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Molecular Pathology of Human Prion Diseases

Prion diseases are fatal neurodegenerative conditions in humans and animals. In this review, we summarize the molecular background of phenotypic variability, relation of prion protein (PrP) to other proteins associated with neurodegenerative diseases, and pathogenesis of neuronal vulnerability. PrP...

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Podrobná bibliografie
Hlavní autoři: Kovacs, Gabor G., Budka, Herbert
Médium: Artigo
Jazyk:Inglês
Vydáno: Molecular Diversity Preservation International (MDPI) 2009
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2672014/
https://ncbi.nlm.nih.gov/pubmed/19399233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms10030976
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