Deficiency of Mitochondrial Aspartate-Glutamate Carrier 1 Leads to Oligodendrocyte Precursor Cell Proliferation Defects Both In Vitro and In Vivo

Aspartate-Glutamate Carrier 1 (AGC1) deficiency is a rare neurological disease caused by mutations in the solute carrier family 25, member 12 (SLC25A12) gene, encoding for the mitochondrial aspartate-glutamate carrier isoform 1 (AGC1), a component of the malate–aspartate NADH shuttle (MAS), expresse...

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書誌詳細
出版年:Int J Mol Sci
主要な著者: Petralla, Sabrina, Peña-Altamira, Luis Emiliano, Poeta, Eleonora, Massenzio, Francesca, Virgili, Marco, Barile, Simona Nicole, Sbano, Luigi, Profilo, Emanuela, Corricelli, Mariangela, Danese, Alberto, Giorgi, Carlotta, Ostan, Rita, Capri, Miriam, Pinton, Paolo, Palmieri, Ferdinando, Lasorsa, Francesco Massimo, Monti, Barbara
フォーマット: Artigo
言語:Inglês
出版事項: MDPI 2019
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6769484/
https://ncbi.nlm.nih.gov/pubmed/31514314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184486
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