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Characterization of a panel of monoclonal antibodies recognizing specific epitopes on GFAP

Alexander disease (AxD) is a neurodegenerative disease caused by heterozygous mutations in the GFAP gene, which encodes the major intermediate filament protein of astrocytes. This disease is characterized by the accumulation of cytoplasmic protein aggregates, known as Rosenthal fibers. Antibodies sp...

詳細記述

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書誌詳細
出版年:PLoS One
主要な著者: Lin, Ni-Hsuan, Messing, Albee, Perng, Ming-Der
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2017
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5503259/
https://ncbi.nlm.nih.gov/pubmed/28700643
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0180694
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