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.
If you have an ORCID ID that is not listed on this page, please
forward this information to us and we will update your Reactome pathway records.
Details on Person D'Eustachio, Peter, 2024-02-16
| Class:Id | InstanceEdit:9861358 |
| _displayName | D'Eustachio, Peter, 2024-02-16 |
| _timestamp | 2024-02-16 18:12:51 |
| author | [Person:140934] D'Eustachio, Peter |
| dateTime | 2024-02-16 18:12:45 |
| (created) | [InstanceEdit:9861359] Hill, David P, 2024-02-16 |
| (modified) | [CatalystActivity:189412] carbon-carbon lyase activity of 2xUROD [cytosol] [Reaction:189421] CPO transforms COPRO3 to PPGEN9 [Homo sapiens] [Reaction:189425] UROD decarboxylates URO3 to COPRO3 [Homo sapiens] [Reaction:189439] ALAD condenses 2 dALAs to form PBG [Homo sapiens] [Reaction:190141] ALAD binds to Pb2+ [Homo sapiens] [Complex:190145] 8xALAD:Pb2+:Zn2+ [cytosol] [Homo sapiens] [Reaction:190182] UROD decarboxylates URO1 to COPRO1 [Homo sapiens] [PathwayDiagram:421392] Diagram of Metabolism of porphyrins, Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR), Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR), Defective ABCC2 causes DJS, Defective UGT1A1 causes hyperbilirubinemia, and Defective UGT1A4 causes hyperbilirubinemia [Reaction:2995334] COX15 transforms heme O to heme A [Homo sapiens] |
|
[Change default viewing format]
|
No pathways have been reviewed or authored by D'Eustachio, Peter, 2024-02-16 (9861358)