Pathways Knowlegdes

Biological pathway database

Pathway DOIs Note
Biochemical pathways: part I

Accession ID: WikiPathways:WP3604
  • 10.1016/s0303-2647(98)00019-7
 Michal G. On representation of metabolic pathways. Biosystems. 1998 Jun;47(1-2):1–7. doi: 10.1016/s0303-2647(98)00019-7. PMID: 9715748.
Drug induction of bile acid pathway

Accession ID: WikiPathways:WP2289		 -
3q29 copy number variation syndrome

Accession ID: WikiPathways:WP4906
  • 10.1146/annurev.nutr.26.061505.111303
 Nemeth E, Ganz T. Regulation of iron metabolism by hepcidin. Annu Rev Nutr. 2006;26():323–42. doi: 10.1146/annurev.nutr.26.061505.111303. PMID: 16848710.
Drug induction of bile acid pathway

Accession ID: WikiPathways:WP3253		 -
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0120468		 -
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0000318		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0120697		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0120463		 -
Congenital Bile Acid Synthesis Defect Type II

Accession ID: PathBank:SMP0120467		 -
Zellweger Syndrome

Accession ID: PathBank:SMP0120495		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0000035		 -
Congenital Bile Acid Synthesis Defect Type II

Accession ID: PathBank:SMP0000314		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0000315		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0087329		 -
27-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120652		 -
Congenital Bile Acid Synthesis Defect Type III

Accession ID: PathBank:SMP0120688		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0120477		 -
Familial Hypercholanemia (FHCA)

Accession ID: PathBank:SMP0000317		 -
Bile Acid Biosynthesis

Accession ID: PathBank:SMP0087236		 -
Cerebrotendinous Xanthomatosis (CTX)

Accession ID: PathBank:SMP0120683		 -