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 Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
| Class:Id | LiteratureReference:2029809 |
|---|
| _displayName | Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome |
|---|
| _timestamp | 2012-01-04 22:04:08 |
|---|
| author | [Person:2029779] Przylepa, KA
[Person:2029776] Paznekas, W
[Person:2029797] Zhang, M
[Person:2029752] Golabi, M
[Person:2029735] Bias, W
[Person:2029732] Bamshad, MJ
[Person:2029742] Carey, JC
[Person:2029757] Hall, BD
[Person:2029787] Stevenson, R
[Person:2029774] Orlow, S
[Person:2029745] Cohen MM, Jr
[Person:2029761] Jabs, EW |
|---|
| created | [InstanceEdit:2029808] Rothfels, K, 2012-01-04 |
|---|
| journal | Nat Genet |
|---|
| pages | 492-4 |
|---|
| pubMedIdentifier | 8696350 |
|---|
| title | Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome |
|---|
| volume | 13 |
|---|
| year | 1996 |
|---|
| (literatureReference) | [Reaction:2012086] Constitutive dimerization of FGFR4 Y367C mutant [Homo sapiens]
[Pathway:2033519] Activated point mutants of FGFR2 [Homo sapiens]
[EntityWithAccessionedSequence:2029881] FGFR2c Y375C [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2029886] FGFR2c S372C [plasma membrane] [Homo sapiens] |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome (2029809)
