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 Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease
| Class:Id | LiteratureReference:9034729 |
|---|---|
| _displayName | Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease |
| _timestamp | 2018-01-10 20:21:19 |
| author | [Person:9034731] Werner, Petra [Person:9034728] Paluru, Prasuna [Person:9034725] Simpson, Anisha M [Person:9034732] Latney, Brande [Person:9034726] Iyer, Radhika [Person:9034734] Brodeur, Garrett M [Person:9034724] Goldmuntz, Elizabeth |
| created | [InstanceEdit:9034735] Orlic-Milacic, Marija, 2018-01-10 |
| journal | Hum. Mutat. |
| pages | 1459-68 |
| pubMedIdentifier | 25196463 |
| title | Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease |
| volume | 35 |
| year | 2014 |
| (literatureReference) | [Pathway:9034013] NTF3 activates NTRK3 signaling [Homo sapiens] [Pathway:9034015] Signaling by NTRK3 (TRKC) [Homo sapiens] [Reaction:9034714] NTRK3 dimers trans-autophosphorylate [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Mutations in NTRK3 suggest a novel signaling pathway in human congenital heart disease (9034729)
