Pathways Knowlegdes

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Pathway DOIs Note
Dopamine metabolism

Accession ID: WikiPathways:WP3155		 -
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.
Prader-Willi and Angelman syndrome

Accession ID: WikiPathways:WP3998
  • 10.1038/ncb2008
 Bekker-Jensen S, Rendtlew Danielsen J, Fugger K, Gromova I, Nerstedt A, Lukas C, Bartek J, Lukas J, Mailand N. HERC2 coordinates ubiquitin-dependent assembly of DNA repair factors on damaged chromosomes. Nat Cell Biol. 2010 Jan;12(1):80–6; sup pp 1. doi: 10.1038/ncb2008. PMID: 20023648.
Dopamine metabolism

Accession ID: WikiPathways:WP2436
  • 10.1177/1756285613493469
 Jones DR, Moussaud S, McLean P. Targeting heat shock proteins to modulate a-synuclein toxicity. Ther Adv Neurol Disord. 2014 Jan;7(1):33–51. PMID: 24409201; PMCID: PMC3886379.
GPR143 in melanocytes and retinal pigment epithelium cells

Accession ID: WikiPathways:WP4941
  • 10.1155/2019/9827519
 Hwang YS, Oh SW, Park S, Lee J, Yoo JA, Kwon K, Park SJ, Kim J, Yu E, Cho JY, Lee J. Melanogenic Effects of Maclurin Are Mediated through the Activation of cAMP/PKA/CREB and p38 MAPK/CREB Signaling Pathways. Oxidative Medicine and Cellular Longevity. 2019 Dec 23;2019():1–10. doi: 10.1155/2019/9827519.
Alkaptonuria

Accession ID: PathBank:SMP0120674		 -
Dopamine beta-Hydroxylase Deficiency

Accession ID: PathBank:SMP0120782		 -
Hawkinsinuria

Accession ID: PathBank:SMP0000190		 -
Tyrosine Metabolism

Accession ID: PathBank:SMP0087450		 -
Tyrosinemia Type I

Accession ID: PathBank:SMP0120729		 -
Monoamine Oxidase-A Deficiency (MAO-A)

Accession ID: PathBank:SMP0120817		 -
Hawkinsinuria

Accession ID: PathBank:SMP0120491		 -
Alkaptonuria

Accession ID: PathBank:SMP0000169		 -
Disulfiram Action Pathway

Accession ID: PathBank:SMP0000429		 -
Tyrosine Metabolism

Accession ID: PathBank:SMP0063684		 -
Alkaptonuria

Accession ID: PathBank:SMP0120453		 -
Tyrosinemia Type I

Accession ID: PathBank:SMP0120509		 -
Monoamine Oxidase-A Deficiency (MAO-A)

Accession ID: PathBank:SMP0120598		 -
Tyrosinemia Type I

Accession ID: PathBank:SMP0000218		 -
Monoamine Oxidase-A Deficiency (MAO-A)

Accession ID: PathBank:SMP0000533		 -