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Airi Tarutani1, Takashi Nonaka2, Reiko Ohtani2

  • 1Department of Clinical Medical Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, 156-8506, Japan. tarutani-ar@igakuken.or.jp.

Acta neuropathologica communications
|January 4, 2026
PubMed
まとめ

No abstract available in PubMed .

キーワード:
アミオトロフィック・ラテラル・スクレロスアネキシンA11FTLD-TDP について主要な横筋硬化症TDP-43 について

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining, normally used to...