Data files

We compared transcriptomes of qNSCs and aNSCs. Quiscent neural stem cells were isolated 3 days after intraventricular injection of either aCSF or miR204 specific antagomers using described protocol (Fischer et al., 2011) and their transcriptome was analyzed

Examination of cell composition and astrocyte to neuron reprogramming in murine striatal tissue.

We performed gene expression microarray analysis in the whole telencephalon at different time points during the course of regeneration after nostril or skull brain injury

Spatial transcriptomics of the intact and injured mouse cerebral cortex at 3 days post injury (dpi).

Single cell transcriptomics of all cells of the intact and injured mouse cerebral cortex at 3 and 5 days post injury (dpi), in control condition and upon inhibition of the Tlr1/2 and Cxcr3 pathways.

Diencephalic astrocytes from 3 months old Aldh1l1-eGFP mice were ACSA2 MACS sorted and processed using Single Cell Reagent Kits V2 from 10x Genomics (scRNA-seq).

Diencephalic astrocytes from 3 months old Aldh1l1-eGFP mice were ACSA2 MACS sorted and processed using Single Cell 3’ Reagent Kits V2 from 10x Genomics (scRNA-seq).