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 Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5
| Class:Id | LiteratureReference:5625587 |
|---|---|
| _displayName | Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5 |
| _timestamp | 2014-10-06 10:55:08 |
| author | [Person:5625601] Lee, M P [Person:5625581] Reeves, C [Person:5625568] Schmitt, A [Person:5625600] Su, K [Person:5625570] Connors, T D [Person:5625565] Hu, R J [Person:5625582] Brandenburg, S [Person:5625563] Lee, M J [Person:5625594] Miller, G [Person:5625577] Feinberg, A P |
| created | [InstanceEdit:5625590] Jassal, Bijay, 2014-10-06 |
| journal | Cancer Res. |
| pages | 4155-9 |
| pubMedIdentifier | 9751628 |
| title | Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5 |
| volume | 58 |
| year | 1998 |
| (literatureReference) | [Pathway:5619066] Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1) [Homo sapiens] [FailedReaction:5625574] Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+ [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5 (5625587)
