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.

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Details on Person Gehring, NH

Class:IdPerson:927844
_displayNameGehring, NH
_timestamp2010-08-10 02:14:03
created[InstanceEdit:927892] May, B, 2010-08-10
initialNH
surnameGehring
(author)[LiteratureReference:927758] Interactions between UPF1, eRFs, PABP and the exon junction complex suggest an integrated model for mammalian NMD pathways
[LiteratureReference:927791] The hierarchy of exon-junction complex assembly by the spliceosome explains key features of mammalian nonsense-mediated mRNA decay
[LiteratureReference:927810] Exon-junction complex components specify distinct routes of nonsense-mediated mRNA decay with differential cofactor requirements
[LiteratureReference:927848] Functions of hUpf3a and hUpf3b in nonsense-mediated mRNA decay and translation
[LiteratureReference:927859] Unusual bipartite mode of interaction between the nonsense-mediated decay factors, UPF1 and UPF2
[LiteratureReference:927860] Y14 and hUpf3b form an NMD-activating complex
[LiteratureReference:1295733] Disassembly of exon junction complexes by PYM
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No pathways have been reviewed or authored by Gehring, NH (927844)