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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Detaylı Bibliyografya
Yayımlandı:Int J Mol Sci
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2019
Konular:
Article
Online Erişim: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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