A hypothesis on prion disorders: are infectious, inherited, and sporadic causes so distinct?
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The ubiquitin-proteasome system in spongiform degenerative disordersMolecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disordersThe variant Creutzfeldt-Jakob Disease: Risk, uncertainty or safety in the use of blood and blood derivatives?Transmission of prions within the gut and towards the central nervous system.The role of autophagy in epileptogenesis and in epilepsy-induced neuronal alterations.Changing the solvent accessibility of the prion protein disulfide bond markedly influences its trafficking and effect on cell function.Protein aggregation and polyasparagine-mediated cellular toxicity in Saccharomyces cerevisiae.Structural basis for the complete resistance of the human prion protein mutant G127V to prion disease
P2860
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P2860
A hypothesis on prion disorders: are infectious, inherited, and sporadic causes so distinct?
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2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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A hypothesis on prion disorder ...... d sporadic causes so distinct?
@ast
A hypothesis on prion disorder ...... d sporadic causes so distinct?
@en
type
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A hypothesis on prion disorder ...... d sporadic causes so distinct?
@ast
A hypothesis on prion disorder ...... d sporadic causes so distinct?
@en
prefLabel
A hypothesis on prion disorder ...... d sporadic causes so distinct?
@ast
A hypothesis on prion disorder ...... d sporadic causes so distinct?
@en
P2093
P50
P1476
A hypothesis on prion disorder ...... d sporadic causes so distinct?
@en
P2093
Bandettini di Poggio A
Paparelli A
P304
P356
10.1016/J.BRAINRESBULL.2005.12.005
P577
2006-01-04T00:00:00Z