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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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書誌詳細
主要な著者: Karch, Celeste M., Prudencio, Mercedes, Winkler, Duane D., Hart, P. John, Borchelt, David R.
フォーマット: Artigo
言語:Inglês
出版事項: National Academy of Sciences 2009
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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