Pathways Knowlegdes

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Pathway DOIs Note
Statin pathway

Accession ID: WikiPathways:WP1
  • 10.1291/hypres.23.187
 Chen H, Ikeda U, Shimpo M, Shimada K. Direct effects of statins on cells primarily involved in atherosclerosis. Hypertens Res. 2000 Mar;23(2):187–92. doi: 10.1291/hypres.23.187. PMID: 10770267.
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.
Oxysterols derived from cholesterol

Accession ID: WikiPathways:WP4545
  • 10.1016/j.biochi.2018.06.020
 Abdel-Khalik J, Crick PJ, Yutuc E, DeBarber AE, Duell PB, Steiner RD, Laina I, Wang Y, Griffiths WJ. Identification of 7a,24-dihydroxy-3-oxocholest-4-en-26-oic and 7a,25-dihydroxy-3-oxocholest-4-en-26-oic acids in human cerebrospinal fluid and plasma. Biochimie. 2018 Oct;153():86–98. doi: 10.1016/j.biochi.2018.06.020.
Statin pathway

Accession ID: WikiPathways:WP145
  • 10.1291/hypres.23.187
 Chen H, Ikeda U, Shimpo M, Shimada K. Direct effects of statins on cells primarily involved in atherosclerosis. Hypertens Res. 2000 Mar;23(2):187–92. doi: 10.1291/hypres.23.187. PMID: 10770267.
Congenital Bile Acid Synthesis Defect Type III

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

Accession ID: PathBank:SMP0000318		 -
Bile Acid Direct Signalling Pathway (1)

Accession ID: PathBank:SMP0086608		 -
Bile Acid Direct Signalling Pathway (2)

Accession ID: PathBank:SMP0089751		 -
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		 -