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A Nine Amino Acid Domain Is Essential for Mutant Prion Protein Toxicity

Transgenic mice expressing prion protein (PrP) molecules with several different internal deletions display spontaneous neurodegenerative phenotypes that can be dose-dependently suppressed by coexpression of wild-type PrP. Each of these deletions, including the largest one (Δ32–134), retains 9 aa imm...

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Hlavní autoři: Westergard, Laura, Turnbaugh, Jessie A., Harris, David A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Society for Neuroscience 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3227396/
https://ncbi.nlm.nih.gov/pubmed/21957261
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1243-11.2011
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