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Thus, our findings indicate that unlike IH 30 , the abbreviated duration of IH 10 was not sufficient at driving a measurable increase either in number or in the proliferative activity of the early neural precursor populations
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This review synthesizes post-stroke metabolic landscapes and evaluates how mesenchymal stromal, neural stem/progenitor, endothelial progenitor, cord blood-derived, and mononuclear cells, and extracellular vesicles, may be incorporated into a phase-specific translational framework supported by target-engagement biomarkers and standardized potency assays
