Skip to main content
. Author manuscript; available in PMC: 2018 Oct 15.
Published in final edited form as: Biol Psychiatry. 2017 Apr 4;82(8):594–600. doi: 10.1016/j.biopsych.2017.03.018

Table 3.

Top 10 gene pathways (ranked by p-value) altered in L3 or L5 pyramidal cells for SZ**.

Name of pathway Number of genes in pathway L3 L5

DEGs in pathway* p-value DEGs in pathway* p-value
Oxidative phosphorylation 95 41 (43.2%) < 10-24 27 (28.4%) < 10-10
Mitochondrial dysfunction 155 49 (31.6%) < 10-22 32 (20.6%) < 10-8
EIF2 signaling 182 38 (20.9%) < 10-10 31 (17%) < 10-6
Protein Ubiquitination Pathway 254 34 (13.4%) < 10-5
Regulation of eIF4 and p70S6K Signaling 151 21 (13.9%) <0.001 24 (15.9%) < 10-5
mTOR Signaling 193 24 (12.4%) <0.001 25 (13%) <0.001
CDK5 Signaling 98 15 (15.3%) <0.001
Pyrimidine Deoxyribonucleotides De Novo Biosynthesis I 23 6 (26.1%) <0.01
Pyrimidine Ribonucleotides Interconversion 30 6 (20%) <0.01
Gluconeogenesis I 24 6 (25%) <0.01
Cdc42 Signaling 121 15 (12.4%) <0.01
Endoplasmic Reticulum Stress Pathway 21 5 (23.8%) <0.01
TCA Cycle II (Eukaryotic) 23 5 (21.7%) 0.010 6 (26.1%) <0.01
Pyrimidine Ribonucleotides De Novo Biosynthesis 32 6 (18.8%) 0.011
*

Number and % of differentially expressed genes (DEGs) in each pathway.

**

No significantly altered pathways were detected in either layer for subjects with bipolar or major depressive disorder.