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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Progress in transthyretin fibrillogenesis research strengthens the amyloid hypothesis
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Progress in transthyretin fibrillogenesis research strengthens the amyloid hypothesis

机译:运甲状腺素蛋白原纤维形成研究的进展加强了淀粉样蛋白假说

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摘要

The amyloidoses are diseases of protein conformation, in which a particular soluble innocuous protein transforms and aggregates into an insoluble fibrillar struc- ture that deposits in extracellular spaces of specific organs (reviewed in refs. 1-4). Organ dysfunction accompanies fibrillar deposition, and the amyloid hypothesis proposes a cause and effect relationship between deposition and dysfunction (re- viewed in refs. 4-7). Transthyretin (TTR) is one of 20 proteins that are known currently to form fibrillar deposits in hu- man amyloidoses (1,8).
机译:淀粉样蛋白是蛋白质构象的疾病,其中特定的可溶性无毒蛋白质转化并聚集为不溶性纤维状结构,该结构沉积在特定器官的细胞外空间中(参见参考文献1-4)。器官功能障碍伴随着原纤维沉积,淀粉样蛋白假说提出了沉积与功能障碍之间的因果关系(参见参考文献4-7)。运甲状腺素蛋白(TTR)是目前已知在人淀粉样蛋白中形成纤维状沉积物的20种蛋白之一(1,8)。

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