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. 2011 Dec 7;31(49):18185–18194. doi: 10.1523/JNEUROSCI.4936-11.2011

Table 1.

Microarray analysis of enriched white matter from the corpus callosum indicates multiple pathways involved in the response to hypoperfusion

Database Biological process Observed Expected p value
GO Regulation of cell proliferation 15 3.66 0.001
GO Angiogenesis 9 1.23 0.001
KEGG Jak–STAT signaling pathway 7 1.06 0.0027
KEGG Complement and coagulation cascades 5 0.54 0.0029
GO Organ development 28 12.89 0.0037
GO Blood vessel morphogenesis 9 1.7 0.0037
GO Blood vessel development 10 2.07 0.0037
GO Vasculature development 10 2.11 0.0037
GO Anatomical structure formation/morphogenesis 12 2.88 0.0037
KEGG Cytokine–cytokine receptor interaction 8 1.79 0.0039
GO Cell adhesion 14 4.34 0.0048
GO Cell proliferation 15 4.99 0.0048
GO Anatomical structure development 32 16.39 0.0048
KEGG Acute myeloid leukemia 4 0.42 0.0058

Genes (n = 129) altered (p < 0.001) were uploaded to WebGestalt enrichment analysis based on Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. Biological processes [adjusted p < 0.01 (Benjamini and Hochberg, 1995)] from both Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases, along with the observed and expected number of molecules represented for each category, are listed.