FUS colocalizes with polyglutamine, but not with TDP-43 in neuronal intranuclear inclusions in spinocerebellar ataxia type 2.

FUS colocalizes with polyglutamine, but not with TDP-43 in neuronal intranuclear inclusions in spinocerebellar ataxia type 2.
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在 2 型脊髓小脑共济失调的神经元核内包涵体中,FUS 与聚谷氨酰胺共定位,但不与 TDP-43 共定位。

DOI:
10.1111/nan.12075
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发表时间:
2014
期刊:
Neuropathol Appl Neurobiol
影响因子:
--
通讯作者:
Wakabayashi K.
Wakabayashi K.
中科院分区:
--
文献类型:
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作者:
Mori F;Toyoshima Y;Tanji K;Kakita A;Takahashi H;Wakabayashi K.

文献摘要

相似文献

本文提供了FUS的特性信息,FUS是多聚谷氨酰胺(polyQ)疾病中神经元核内包涵体(NIIs)的一种成分,与TDP-43(一种结合人类免疫缺陷病毒的细胞蛋白)具有相互关系。它讨论了几个事实,其中包括类别的额颞叶变性(FTLD),FUS免疫组化和核质和细胞质的包涵体轴承神经元,提出零FUS免疫反应。
The article offers information on the properties of FUS which is a component of neuronal intranuclear inclusions (NIIs) in polyglutamine (polyQ) diseases which has reciprocal relationship with TDP-43, a cellular protein that binds human immunodeficiency virus. It discusses several facts which includes categories of frontotemporal lobar degeneration (FTLD), FUS immunohistochemistry and nucleoplasm and cytoplasm of inclusion-bearing neurones that presents zero FUS immunoreactivity.