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Invited Review: The role of prion‐like mechanisms in neurodegenerative diseases
The prototype of transmissible neurodegenerative proteinopathies is prion diseases, characterized by aggregation of abnormally folded conformers of the native prion protein. A wealth of mechanisms has been proposed to explain the conformational conversion from physiological protein into misfolded, p...
Tallennettuna:
| Julkaisussa: | Neuropathol Appl Neurobiol |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7687189/ https://ncbi.nlm.nih.gov/pubmed/31868945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nan.12592 |
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