Pathways Knowlegdes

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Pathway DOIs Note
Trans-sulfuration, one-carbon metabolism and related pathways

Accession ID: WikiPathways:WP2525
  • 10.1016/j.cmet.2016.08.009
 Ducker GS, Rabinowitz JD. One-Carbon Metabolism in Health and Disease. Cell Metabolism. 2017 Jan;25(1):27–42. doi: 10.1016/j.cmet.2016.08.009.
One-carbon metabolism and related pathways

Accession ID: WikiPathways:WP1770		 -
Disorders of bile acid synthesis and biliary transport

Accession ID: WikiPathways:WP5176
  • 10.3748/wjg.v18.i25.3322
 Hadžic N, Bull LN, Clayton PT, Knisely AS. Diagnosis in bile acid-CoA: amino acid N-acyltransferase deficiency. World J Gastroenterol. 2012 Jul 07;18(25):3322–6. PMID: 22783059; PMCID: PMC3391772.
Glucose homeostasis

Accession ID: WikiPathways:WP661
  • 10.1038/msb.2008.50
 Shaham O, Wei R, Wang TJ, Ricciardi C, Lewis GD, Vasan RS, Carr SA, Thadhani R, Gerszten RE, Mootha VK. Metabolic profiling of the human response to a glucose challenge reveals distinct axes of insulin sensitivity. Molecular Systems Biology. 2008 Jan;4(1). doi: 10.1038/msb.2008.50.
One-carbon metabolism and related pathways

Accession ID: WikiPathways:WP3940		 -
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		 -