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Role of mutant SOD1 disulfide oxidation and aggregation in the pathogenesis of familial ALS
Transgenic mice that model familial (f)ALS, caused by mutations in superoxide dismutase (SOD)1, develop paralysis with pathology that includes the accumulation of aggregated forms of the mutant protein. Using a highly sensitive detergent extraction assay, we traced the appearance and abundance of de...
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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
2009
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2675570/ https://ncbi.nlm.nih.gov/pubmed/19416874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0902505106 |
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