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.

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.

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Details on Person Feng, XH

Class:IdPerson:202641
_displayNameFeng, XH
_timestamp2007-11-07 13:14:41
created[InstanceEdit:202635] Jassal, B, 2007-11-07 13:11:04
initialXH
surnameFeng
(author)[LiteratureReference:202618] Smurf2 is a ubiquitin E3 ligase mediating proteasome-dependent degradation of Smad2 in transforming growth factor-beta signaling
[LiteratureReference:208080] PPM1A functions as a Smad phosphatase to terminate TGFbeta signaling
[LiteratureReference:208238] Specificity and versatility in tgf-beta signaling through Smads
[LiteratureReference:208300] Protein serine/threonine phosphatase PPM1A dephosphorylates Smad1 in the bone morphogenetic protein signaling pathway
[LiteratureReference:208366] dSmurf selectively degrades decapentaplegic-activated MAD, and its overexpression disrupts imaginal disc development
[LiteratureReference:1181277] Smad2, Smad3 and Smad4 cooperate with Sp1 to induce p15(Ink4B) transcription in response to TGF-beta
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No pathways have been reviewed or authored by Feng, XH (202641)