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.
Pathways authored by Hentze, MW (157280)
Details on Person Hentze, MW
| Class:Id | Person:157280 |
| _displayName | Hentze, MW |
| _timestamp | 2016-07-20 19:17:08 |
| affiliation | [Affiliation:69898] European Molecular Biology Laboratory |
| created | [InstanceEdit:157277] Matthews, L, 2004-12-20 12:26:45 |
| initial | MW |
| modified | [InstanceEdit:157539] Joshi-Tope, G, 2005-01-01 18:52:19 [InstanceEdit:8932050] D'Eustachio, Peter, 2016-07-20 |
| surname | Hentze |
| (author) | [LiteratureReference:157274] Molecular mechanisms of translational control [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:927794] Phosphorylation of hUPF1 induces formation of mRNA surveillance complexes containing hSMG-5 and hSMG-7 [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 [LiteratureReference:1295734] NMD: RNA biology meets human genetic medicine |
|
[Change default viewing format]
|