Reactome: A Curated Pathway Database

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.

Name Email address

Pathways reviewed by Sudol, M (1253348)

DB_ID Name
2028269 Signaling by Hippo
2032785 YAP1- and WWTR1 (TAZ)-stimulated gene expression

Details on Person Sudol, M

Class:IdPerson:1253348
_displayNameSudol, M
_timestamp2017-08-22 20:38:57
affiliation[Affiliation:2085533] Weis Center for Research, Geisinger Clinic
created[InstanceEdit:1253346] Orlic-Milacic, Marija, 2011-04-27
firstnameMarius
initialM
modified[InstanceEdit:2085534] D'Eustachio, P, 2012-02-03
surnameSudol
(author)[InstanceEdit:2085532] Sudol, M, 2012-02-03
[LiteratureReference:1253338] WW domain-containing proteins, WWOX and YAP, compete for interaction with ErbB-4 and modulate its transcriptional function
[LiteratureReference:1254249] WW domain-containing protein YAP associates with ErbB-4 and acts as a co-transcriptional activator for the carboxyl-terminal fragment of ErbB-4 that translocates to the nucleus
[LiteratureReference:2064399] Functional complexes between YAP2 and ZO-2 are PDZ domain-dependent, and regulate YAP2 nuclear localization and signalling
[LiteratureReference:2064419] TAZ interacts with zonula occludens-1 and -2 proteins in a PDZ-1 dependent manner
[LiteratureReference:2085535] Modularity in the Hippo signaling pathway
[LiteratureReference:9009291] RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
[Change default viewing format]