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 Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance
| Class:Id | LiteratureReference:9824940 |
|---|
| _displayName | Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance |
|---|
| _timestamp | 2023-01-23 18:17:00 |
|---|
| author | [Person:2428807] Takeda, K
[Person:9824930] Takemoto, C
[Person:9824941] Kobayashi, I
[Person:5321242] Watanabe, A
[Person:9824942] Nobukuni, Y
[Person:9824639] Fisher, D E
[Person:9730345] Tachibana, M |
|---|
| created | [InstanceEdit:9824943] Rothfels, Karen, 2023-01-23 |
|---|
| journal | Hum Mol Genet |
|---|
| pages | 125-32 |
|---|
| pubMedIdentifier | 10587587 |
|---|
| title | Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance |
|---|
| volume | 9 |
|---|
| year | 2000 |
|---|
| (literatureReference) | [BlackBoxEvent:9824579] MITF-M-dependent TYR gene expression [Homo sapiens]
[RegulationReference:9824996] Positive gene expression regulation by 'M-MITF dimer:BAF complex:TYR gene [nucleoplasm]' Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance (9824940)
