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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...

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Bibliographic Details
Published in:J Intern Med
Main Authors: Fändrich, Marcus, Nyström, Sofie, Nilsson, K. Peter R., Böckmann, Anja, LeVine, Harry, Hammarström, Per
Format: Artigo
Language:Inglês
Published: 2018
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Online Access: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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