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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...

詳細記述

保存先:
書誌詳細
出版年:J Intern Med
主要な著者: Fändrich, Marcus, Nyström, Sofie, Nilsson, K. Peter R., Böckmann, Anja, LeVine, Harry, Hammarström, Per
フォーマット: Artigo
言語:Inglês
出版事項: 2018
主題:
オンライン・アクセス: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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