Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress.

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作者： Hui,Wang ^[1] ; Yilei,Zheng ^[1] ; Jiaxi,Yu ^[1] ; Lingchao,Meng ^[1] ; Wei,Zhang ^[1] ; Daojun,Hong ^[2] ; Zhaoxia,Wang ^[3] ; Yun,Yuan ^[4] ; Jianwen,Deng ^[5]

作者单位： Department of Neurology, Peking University First Hospital, Beijing 100034, China. ^[1] Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China; Department of Medical Genetics, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China. ^[2] Department of Neurology, Peking University First Hospital, Beijing 100034, China; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing 100034, China. ^[3] Department of Neurology, Peking University First Hospital, Beijing 100034, China; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing 100034, China. Electronic address: yuanyun2002@126.com. ^[4] Department of Neurology, Peking University First Hospital, Beijing 100034, China; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing 100034, China; Key Laboratory for Neuroscience, Ministry of Education/National Health Commission, Peking University, Beijing 100083, China. Electronic address: jianwendeng@pkufh.com. ^[5]

关键词 CGG repeat expansion FUS Intranuclear inclusions NOTCH2NLC Stress granules polyG

主题词人类(Humans);核内包涵体(Intranuclear Inclusion Bodies);RNA结合蛋白质FUS(RNA-Binding Protein FUS);神经母细胞瘤(Neuroblastoma);神经变性疾病(Neurodegenerative Diseases)

DOI 10.1016/j.nbd.2023.106391

PMID 38145851

发布时间 2024-01-08

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