标题
Mutant superoxide dismutase-1 indistinguishable from wild-type causes ALS
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 21, Issue 16, Pages 3568-3574
出版商
Oxford University Press (OUP)
发表日期
2012-05-18
DOI
10.1093/hmg/dds188
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivo
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- (2010) Karin Forsberg et al. PLoS One
- Variation in aggregation propensities among ALS-associated variants of SOD1: Correlation to human disease
- (2009) Mercedes Prudencio et al. HUMAN MOLECULAR GENETICS
- Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse
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- TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations
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- Neuron-Specific Expression of Mutant Superoxide Dismutase Is Sufficient to Induce Amyotrophic Lateral Sclerosis in Transgenic Mice
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