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用于神经退行性疾病研究的转基因模型的价值。

The value of transgenic models for the study of neurodegenerative diseases.

作者信息

Price D L, Wong P C, Markowska A L, Lee M K, Thinakaren G, Cleveland D W, Sisodia S S, Borchelt D R

机构信息

Division of Neuropathology, Johns Hopkins University School of Medicine, 558 Ross Research Building, 720 Rutland Avenue, Baltimore, Maryland 21205-2196, USA.

出版信息

Ann N Y Acad Sci. 2000;920:179-91. doi: 10.1111/j.1749-6632.2000.tb06920.x.

Abstract

Transgenic animal models are useful in studying the features of APP- and PS1-linked FAD and SOD1-linked FALS. These models help to investigate the nature of the cellular/biochemical/molecular alterations in neural tissue; the character and evolution of neuronal and/or glial abnormalities; the ways mutant proteins cause damage to neurons; and the biochemical pathways associated with cell death. New technologies will help to define changes in a variety of genes/gene products and the events and conformational changes in mutant proteins that are implicated in pathogenic cascades. It is hoped such study will result in novel treatments for testing in transgenic models that can then be translated into new treatments for human neurodegenerative diseases.

摘要

转基因动物模型有助于研究与淀粉样前体蛋白(APP)和早老素1(PS1)相关的家族性阿尔茨海默病(FAD)以及与超氧化物歧化酶1(SOD1)相关的家族性肌萎缩侧索硬化症(FALS)的特征。这些模型有助于研究神经组织中细胞/生化/分子改变的本质;神经元和/或胶质细胞异常的特征及演变;突变蛋白对神经元造成损伤的方式;以及与细胞死亡相关的生化途径。新技术将有助于确定各种基因/基因产物的变化,以及参与致病级联反应的突变蛋白中的事件和构象变化。人们希望此类研究将产生新的治疗方法,先在转基因模型中进行测试,然后转化为针对人类神经退行性疾病的新疗法。

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