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 He, Langping

Class:IdPerson:6784446
_displayNameHe, Langping
_timestamp2015-06-20 12:55:34
created[InstanceEdit:6784449] May, Bruce, 2015-06-20
firstnameLangping
initialL
surnameHe
(author)[LiteratureReference:6784493] Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA
[LiteratureReference:9906775] Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency
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No pathways have been reviewed or authored by He, Langping (6784446)