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Amyloid fibril polymorphism - a challenge for molecular imaging and therapy
The accumulation of misfolded proteins (MP), both unique and common, for different diseases is central for many chronic degenerative diseases. In certain patients MP accumulation is systemic (e.g. TTR amyloid) and in others this is localized to a specific cell type (e.g. Alzheimer’s disease). In neu...
Uloženo v:
| Vydáno v: | J Intern Med |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5820168/ https://ncbi.nlm.nih.gov/pubmed/29360284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/joim.12732 |
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