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Characterization of Amyloidosis Masahide Yazaki 1,2,3 , Shu-ichi Ikeda 1,3 1Institute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University 2Department of Aging Biology, Institute of Pathogenesis and Disease Prevention, Shinshu University Graduate School of Medicine 3Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine Keyword: アミロイドーシス , 蛋白質ミスフォールディング , βシート構造 , アミロイド代謝回転オーバー , アミロイド退縮 , amyloidosis , protein misfolding , β-sheet , amyloid turnover , amyloid regression pp.723-730
Published Date 2014/7/1
DOI https://doi.org/10.11477/mf.1416101832
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Abstract

Amyloidosis refers to disorders that cause organ failure due to amyloid deposition. Deposited amyloid is clearly stained by Congo red and is detected by apple-green birefringence under polarized light. Amyloid fibril proteins are very stable, but several recent studies have revealed that amyloid deposition and the clearance of fibrils cause the steady turnover of deposited amyloid proteins. Therefore, in several amyloidosis disorders, especially primary AL, reactive AA, and transthyretin-related amyloidosis, effective therapies are expected to cause the regression of tissue-deposited amyloid.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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