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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person D'Eustachio, Peter, 2019-03-25

Class:IdInstanceEdit:9640340
_displayNameD'Eustachio, Peter, 2019-03-25
_timestamp2019-03-25 14:56:30
author[Person:140934] D'Eustachio, Peter
dateTime2019-03-25 18:55:10
(modified)[Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens]
[Pathway:71291] Metabolism of amino acids and derivatives [Homo sapiens]
[Pathway:209776] Metabolism of amine-derived hormones [Homo sapiens]
[Pathway:350562] Regulation of ornithine decarboxylase (ODC) [Homo sapiens]
[Pathway:351202] Metabolism of polyamines [Homo sapiens]
[Pathway:389661] Glyoxylate metabolism and glycine degradation [Homo sapiens]
[Pathway:2408522] Selenoamino acid metabolism [Homo sapiens]
[PathwayDiagram:6788657] Diagram of Metabolism of polyamines
[PathwayDiagram:6788658] Diagram of Branched-chain amino acid catabolism, Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD, Loss-of-function mutations in DBT cause MSUD2, Loss-of-function mutations in DLD cause MSUD3/DLDD, H139Hfs13* PPM1K causes a mild variant of MSUD, Branched-chain ketoacid dehydrogenase kinase deficiency, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency, 3-methylglutaconic aciduria, Beta-ketothiolase deficiency, Mitochondrial short-chain enoyl-CoA hydratase deficiency 1, and 3-hydroxyisobutyryl-CoA hydrolase deficiency
[PathwayDiagram:6788661] Diagram of Metabolism of amine-derived hormones
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No pathways have been reviewed or authored by D'Eustachio, Peter, 2019-03-25 (9640340)