| BioCyc:MOUSE_PWY-6061 |
bile acid biosynthesis, neutral pathway |
| Reactome:R-HSA-400206 |
Regulation of lipid metabolism by PPARalpha |
| Reactome:R-HSA-556833 |
Metabolism of lipids |
| Reactome:R-HSA-1989781 |
PPARA activates gene expression |
| Reactome:R-HSA-1430728 |
Metabolism |
| WikiPathways:WP4545 |
Oxysterols derived from cholesterol |
| WikiPathways:WP5329 |
Cholesterol biosynthesis pathway in hepatocytes |
| PathBank:SMP0120468 |
Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0000318 |
Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120463 |
Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120467 |
Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120495 |
Zellweger Syndrome |
| PathBank:SMP0000035 |
Bile Acid Biosynthesis |
| PathBank:SMP0000314 |
Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0000315 |
Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120652 |
27-Hydroxylase Deficiency |
| PathBank:SMP0120477 |
Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000317 |
Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000316 |
Zellweger Syndrome |
| PathBank:SMP0000720 |
27-Hydroxylase Deficiency |
| PathBank:SMP0063601 |
Bile Acid Biosynthesis |