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Molecular control of two novel migratory paths for CGE derived interneurons in the developing mouse brain

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Academic year: 2020

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Figure

Fig. 1. Temporal sequence of the different 5HT3aR-GFP+indicating the plane of horizontal sections shown in C-GGreen arrows highlight the three migratory streams described in the text
Fig. 2. CGE-derived 5HT3aR-GFP+ cells migrate rostrally and caudally. (A) Schematic of the experimental approach in which the CGE is cut from a E13.55HT3aR-GFP horizontal organotypic brain section and homotopically grafted into a non-GFP section of the sam
Fig. 3. Transcription factors expressed along the streams in the subpallium of 5HT3aR-GFPsections of E15.5arrowheads indicate triple-labelled cells; yellow and blue arrowheads point to double-positive cells
Fig. 4. Anatomical and molecular fate of the in utero-grafted CGE-5HT3aR-GFP+ cells in juvenile brains
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