Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| 22q11.2 copy number variation syndrome Accession ID: WikiPathways:WP4657 |
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Umeki I, Niihori T, Abe T, Kanno SI, Okamoto N, Mizuno S, Kurosawa K, Nagasaki K, Yoshida M, Ohashi H, Inoue SI, Matsubara Y, Fujiwara I, Kure S, Aoki Y. Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexes. Hum Genet. 2019 Jan;138(1):21–35. doi: 10.1007/s00439-018-1951-7. PMID: 30368668. |
| Flavan-3-ol metabolic pathway Accession ID: WikiPathways:WP4238 |
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Pereira-Caro G, Moreno-Rojas JM, Brindani N, Del Rio D, Lean MEJ, Hara Y, Crozier A. Bioavailability of Black Tea Theaflavins: Absorption, Metabolism, and Colonic Catabolism. J Agric Food Chem. 2017 Jul 05;65(26):5365–74. doi: 10.1021/acs.jafc.7b01707. PMID: 28595385. |
| Dopamine metabolism Accession ID: WikiPathways:WP3155 |
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| Neurotransmitter disorders Accession ID: WikiPathways:WP4220 |
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Nichol CA, Lee CL, Edelstein MP, Chao JY, Duch DS. Biosynthesis of tetrahydrobiopterin by de novo and salvage pathways in adrenal medulla extracts, mammalian cell cultures, and rat brain in vivo. Proc. Natl. Acad. Sci. U.S.A. 1983 Mar;80(6):1546–50. doi: 10.1073/pnas.80.6.1546. |
| Dopamine metabolism Accession ID: WikiPathways:WP2436 |
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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. |
| Alkaptonuria Accession ID: PathBank:SMP0120674 |
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| Dopamine beta-Hydroxylase Deficiency Accession ID: PathBank:SMP0120782 |
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| Hawkinsinuria Accession ID: PathBank:SMP0000190 |
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| Tyrosine Metabolism Accession ID: PathBank:SMP0087450 |
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| Tyrosinemia Type I Accession ID: PathBank:SMP0120729 |
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| Monoamine Oxidase-A Deficiency (MAO-A) Accession ID: PathBank:SMP0120817 |
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| Hawkinsinuria Accession ID: PathBank:SMP0120491 |
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| Alkaptonuria Accession ID: PathBank:SMP0000169 |
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| Disulfiram Action Pathway Accession ID: PathBank:SMP0000429 |
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| Tyrosine Metabolism Accession ID: PathBank:SMP0063684 |
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| Alkaptonuria Accession ID: PathBank:SMP0120453 |
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| Tyrosinemia Type I Accession ID: PathBank:SMP0120509 |
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| Monoamine Oxidase-A Deficiency (MAO-A) Accession ID: PathBank:SMP0120598 |
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| Tyrosinemia Type I Accession ID: PathBank:SMP0000218 |
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| Monoamine Oxidase-A Deficiency (MAO-A) Accession ID: PathBank:SMP0000533 |
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