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Glial fibrillary acidic protein exhibits altered turnover kinetics in a mouse model of alexander disease

Mutations in the astrocyte-specific intermediate filament glial fibrillary acidic protein (GFAP) lead to the rare and fatal disorder, Alexander disease (AxD). A prominent feature of the disease is aberrant accumulation of GFAP. It has been proposed that this accumulation occurs because of an increas...

詳細記述

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書誌詳細
出版年:J Biol Chem
主要な著者: Moody, Laura R., Barrett-Wilt, Gregory A., Sussman, Michael R., Messing, Albee
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Biochemistry and Molecular Biology 2017
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5392575/
https://ncbi.nlm.nih.gov/pubmed/28223355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M116.772020
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