NG2 and GFAP co-expression after differentiation in cells transfected with mutant GFAP and in undifferentiated glioma cells
Alexander disease is a rare disorder caused by mutations in the gene coding for glial fibrillary acidic protein (GFAP). In a previous study, differentiation of neurospheres transfected with these mutations resulted in a cell type that expresses both GFAP and NG2. To determine the effect of molecular...
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Veröffentlicht in: | Neurologia (Barcelona, Spain) Spain), 2020-09, Vol.35 (7), p.479-485 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng ; spa |
Online-Zugang: | Volltext |
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