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 Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development
| Class:Id | LiteratureReference:9665800 |
|---|
| _displayName | Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development |
|---|
| _timestamp | 2019-11-01 01:32:01 |
|---|
| author | [Person:9665805] d'Oiron, Roseline
[Person:9665816] Lavergne, Jean-Maurice
[Person:9661624] Lavend'homme, Renaud
[Person:9665797] Benhida, Abdellah
[Person:9665812] Bordet, Jean-Claude
[Person:9665803] Negrier, Claude
[Person:9661586] Peerlinck, Kathelijne
[Person:8936464] Vermylen, Jos
[Person:9661585] Saint-Remy, Jean-Marie
[Person:9661691] Jacquemin, Marc |
|---|
| created | [InstanceEdit:9665826] Shamovsky, Veronica, 2019-11-01 |
|---|
| journal | Blood |
|---|
| pages | 155-7 |
|---|
| pubMedIdentifier | 12969981 |
|---|
| title | Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development |
|---|
| volume | 103 |
|---|
| year | 2004 |
|---|
| (literatureReference) | [EntityWithAccessionedSequence:9665793] F8 A2220del [extracellular region] [Homo sapiens]
[CandidateSet:9665831] FVIII C1, C2 domain variants [extracellular region] [Homo sapiens]
[Summation:9665830] Coagulation factor VIII (FVIII) encoded by the F8 gene is sy...
[FailedReaction:9665809] F8 variant does not bind von Willebrand factor [Homo sapiens]
[Pathway:9672393] Defective F8 binding to von Willebrand factor [Homo sapiens] |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development (9665800)
