A reduction in the percentage of demyelinating axons was also observed in the CXCR3-KO group, although this did not reach statistical significance ( P > 0.05 WT ICH versus CXCR3-KO ICH; Fig. 4J ).
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CXCR3-mediated natural killer cell infiltration exacerbates white matter injury after intracerebral haemorrhage.
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