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10.1186/s12885-016-2367-1 64 HonjohS.YamamotoT.UnoM.NishidaE

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Sections of the cerebral cortex and hippocampus were fixed in 10% formal saline for 24 h, processed for paraffin wax embedding, dehydration, clearing, and infiltration, sectioned, and then mounted following which they were processed for general histological staining using haematoxylin and eosin as previously described[40]

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