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 A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation
| Class:Id | LiteratureReference:4724324 |
|---|
| _displayName | A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation |
|---|
| _timestamp | 2013-10-23 15:24:45 |
|---|
| author | [Person:4722100] Chantret, Isabelle
[Person:3247609] Dancourt, Julia
[Person:4722094] Dupré, Thierry
[Person:4722116] Delenda, Christophe
[Person:4722104] Bucher, Stéphanie
[Person:4724305] Vuillaumier-Barrot, Sandrine
[Person:4724303] Ogier de Baulny, Hélène
[Person:4724329] Peletan, Celine
[Person:4722105] Danos, Olivier
[Person:4722112] Seta, Nathalie
[Person:4722113] Durand, Geneviève
[Person:4722096] Oriol, Rafael
[Person:4722103] Codogno, Patrice
[Person:4722106] Moore, Stuart E H |
|---|
| created | [InstanceEdit:4724314] Jassal, B, 2013-10-23 |
|---|
| journal | J. Biol. Chem. |
|---|
| pages | 9962-71 |
|---|
| pubMedIdentifier | 12480927 |
|---|
| title | A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation |
|---|
| volume | 278 |
|---|
| year | 2003 |
|---|
| (literatureReference) | [Pathway:4724325] Defective ALG8 causes CDG-1h [Homo sapiens]
[FailedReaction:4724330] Defective ALG8 does not add glucose to the N-glycan precursor [Homo sapiens] |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation (4724324)
