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Molecular characterization of UFM1 and exploration of its relationship with hereditary multiple system atrophy

Molecular characterization of UFM1 and exploration of its relationship with hereditary multiple system atrophy
UFM1的分子表征及其与遗传性多系统萎缩的关系探讨
批准号：
197280
负责人：
Duquette Antoine
金额：
$12.57万
依托单位：
Montreal Neurological Institute-Hospital
依托单位国家：
加拿大
项目类别：
Fellowship Programs
财政年份：
2009
资助国家：
加拿大
项目状态：
已结题
起止时间：
2009-10-01 至 2012-10-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=197280&lang=en
关键词：
Drosophila Genetics Multiple System Atrophy Neurodegeneration Parkinsonism Post-Translational Modification Ubiquitination Ufm1

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Multiple system atrophy (MSA) is a severe neurodegenerative disorder similar to Parkinson's disease but complicated by failure of the autonomic nervous system and incoordination. Mutations in ubiquitin-fold modifier 1 (UFM1) were recently identified in a
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