Reactome: A Curated Pathway Database
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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.

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.

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Details on Person Yamamoto, Atsushi

Class:IdPerson:9629951
_displayNameYamamoto, Atsushi
_timestamp2018-11-26 18:40:22
created[InstanceEdit:9629953] D'Eustachio, Peter, 2018-11-26
firstnameAtsushi
initialA
modified[InstanceEdit:9629969] D'Eustachio, Peter, 2018-11-26
surnameYamamoto
(author)[LiteratureReference:9629949] Optimal translational termination requires C4 lysyl hydroxylation of eRF1
[LiteratureReference:9630772] OGFOD1 catalyzes prolyl hydroxylation of RPS23 and is involved in translation control and stress granule formation
[LiteratureReference:9630963] Oxygenase-catalyzed ribosome hydroxylation occurs in prokaryotes and humans
[LiteratureReference:9685000] Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse
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No pathways have been reviewed or authored by Yamamoto, Atsushi (9629951)