Neural xenografts contribute to long-term recovery in stroke via molecular graft-host crosstalk.

In the stroke core, we observed 15.1 ± 3% NeuN/caspase-3 double-positive cells in the NPC group and 23.9 ± 8% in the vehicle group, indicating a trend toward a higher proportion of apoptotic neurons in vehicle-treated animals, although this difference did not reach statistical significance (p = 0.34).

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