3 months |
GDP-l-fucose Biosynthesis I (from GDP-d-mannose) |
1.89 |
0.500 |
Methylmalonyl pathway |
1.59 |
0.250 |
2-Oxobutanoate degradation I |
1.49 |
0.200 |
PI3K/AKT signaling |
1.33 |
0.024 |
GM-CSF signaling |
1.08 |
0.027 |
Colanic acid building blocks biosynthesis |
1.06 |
0.071 |
Wnt/β-catenin signaling |
1.01 |
0.018 |
Mitochondrial l-carnitine shuttle pathway |
0.98 |
0.059 |
Bladder cancer signaling |
0.96 |
0.023 |
GADD45 signaling |
0.93 |
0.053 |
Acute myeloid leukemia signaling |
0.92 |
0.022 |
Inflammasome pathway |
0.91 |
0.050 |
Pyrimidine deoxyribonucleotides de novo biosynthesis I |
0.85 |
0.044 |
Estrogen-mediated S-phase entry |
0.81 |
0.039 |
Sonic hedgehog signaling |
0.76 |
0.035 |
Sperm motility |
0.73 |
0.017 |
LXR/RXR activation |
0.73 |
0.017 |
FXR/RXR activation |
0.71 |
0.016 |
Circadian rhythm signaling |
0.70 |
0.029 |
9 months |
GDP-l-fucose biosynthesis I (from GDP-d-mannose) |
1.65 |
0.500 |
Estrogen-mediated S-phase entry |
1.47 |
0.077 |
Glioblastoma multiforme signaling |
1.45 |
0.031 |
p53 signaling |
1.44 |
0.036 |
Methylmalonyl pathway |
1.36 |
0.250 |
PI3K/AKT signaling |
1.30 |
0.033 |
2-Oxobutanoate degradation I |
1.26 |
0.200 |
Cell cycle regulation by BTG family proteins |
1.19 |
0.054 |
NAD biosynthesis from 2-amino-3-carboxymuconate semialdehyde |
1.18 |
0.167 |
nNOS signaling in skeletal muscle cells |
1.13 |
0.050 |
Bladder cancer signaling |
1.13 |
0.035 |
Phosphatidylcholine biosynthesis I |
1.12 |
0.143 |
tRNA splicing |
1.11 |
0.049 |
Ovarian cancer signaling |
1.11 |
0.028 |
Role of p14/p19ARF in tumor suppression |
1.09 |
0.048 |
Phosphatidylethanolamine biosynthesis II |
1.06 |
0.125 |
Gustation pathway |
1.05 |
0.027 |
GABA receptor signaling |
1.05 |
0.032 |
Role of Oct4 in mammalian embryonic stem cell pluripotency |
1.04 |
0.044 |