SYNPO ( p = 0.062), HSPA4 ( p = 0.100) and VDAC1 ( p = 0.168) showed a decreasing trend unlike ferritin ( p = 0.192), PEA15 ( p = 0.114) and ICAM5 ( p = 0.578) that showed an increasing trend in the VaD group.
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Novel pathophysiological markers are revealed by iTRAQ-based quantitative clinical proteomics approach in vascular dementia.
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