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APP基因中导致阿尔茨海默病的突变的发现以及“淀粉样蛋白级联假说”的形成。

The discovery of Alzheimer-causing mutations in the APP gene and the formulation of the "amyloid cascade hypothesis".

作者信息

Hardy John

机构信息

Reta Lila Weston Research Laboratories and Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.

出版信息

FEBS J. 2017 Apr;284(7):1040-1044. doi: 10.1111/febs.14004.

Abstract

The cloning of APP and genetic analysis of families with Alzheimer's disease were both reported in 1987 and much present work on the disease is based upon the foundations laid at that time. Progress was not smooth, however, and many errors were made. In this memoir, I lay out both the progress and the errors.

摘要

1987年,APP的克隆以及阿尔茨海默病家族的基因分析均有报道,目前关于该疾病的许多研究工作都是基于当时奠定的基础。然而,进展并不顺利,出现了许多错误。在这本回忆录中,我阐述了进展和错误。

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