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 Characterization of recombinant mannan-binding lectin-associated serine protease (MASP)-3 suggests an activation mechanism different from that of MASP-1 and MASP-2
| Class:Id | LiteratureReference:2173402 |
|---|---|
| _displayName | Characterization of recombinant mannan-binding lectin-associated serine protease (MASP)-3 suggests an activation mechanism different from that of MASP-1 and MASP-2 |
| _timestamp | 2012-03-30 21:11:46 |
| author | [Person:2173398] Zundel, S [Person:2173397] Cseh, S [Person:2173384] Lacroix, M [Person:2173401] Dahl, MR [Person:2172138] Matsushita, M [Person:166682] Andrieu, JP [Person:2173399] Schwaeble, WJ [Person:174545] Jensenius, JC [Person:2172145] Fujita, T [Person:166681] Arlaud, GJ [Person:166679] Thielens, NM |
| created | [InstanceEdit:2173400] Shamovsky, V, 2012-03-30 |
| journal | J Immunol |
| pages | 4342-50 |
| pubMedIdentifier | 15034049 |
| title | Characterization of recombinant mannan-binding lectin-associated serine protease (MASP)-3 suggests an activation mechanism different from that of MASP-1 and MASP-2 |
| volume | 172 |
| year | 2004 |
| (literatureReference) | [Reaction:2132206] MASPs activation [Gallus gallus] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Characterization of recombinant mannan-binding lectin-associated serine protease (MASP)-3 suggests an activation mechanism different from that of MASP-1 and MASP-2 (2173402)
