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Sustained translational repression by eIF2α–P mediates prion neurodegeneration
The mechanisms leading to neuronal death in neurodegenerative disease are poorly understood. Many of these disorders, including Alzheimer’s (AD), Parkinson’s (PD) and prion diseases, are associated with the accumulation of misfolded disease-specific proteins. The unfolded protein response (UPR) is a...
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| Main Authors: | , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2012
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3378208/ https://ncbi.nlm.nih.gov/pubmed/22622579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature11058 |
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