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Details on Person Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups
| Class:Id | LiteratureReference:9957082 |
| _displayName | Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups |
| _timestamp | 2025-06-17 02:57:42 |
| author | [Person:9758749] Hurler, Lisa [Person:9957115] Szilágyi, Ágnes [Person:9957193] Mescia, Federica [Person:9957168] Bergamaschi, Laura [Person:9758743] Mező, Blanka [Person:9758790] Sinkovits, György [Person:9758783] Réti, Marienn [Person:9758768] Müller, Veronika [Person:9758765] Iványi, Zsolt [Person:9758794] Gál, János [Person:9758799] Gopcsa, László [Person:9758810] Reményi, Péter [Person:9758777] Szathmáry, Beáta [Person:9758781] Lakatos, Botond [Person:9758755] Szlávik, János [Person:9758779] Bobek, Ilona [Person:9758748] Prohászka, Zita Z [Person:9758775] Förhécz, Zsolt [Person:8855290] Csuka, Dorottya [Person:9758811] Kajdácsi, Erika [Person:9758776] Cervenak, László [Person:9758757] Kiszel, Petra [Person:9685422] Masszi, Tamás [Person:9758747] Vályi-Nagy, István [Person:1458601] Wurzner, R [Person:9957186] Cambridge Institute of Therapeutic Immunology and Infectious Disease-National Institute of Health Research (CITIID-NIHR) COVID BioResource Collaboration, - [Person:9957166] Lyons, Paul A [Person:9957177] Toonen, Erik J M [Person:9758782] Prohászka, Zoltán |
| created | [InstanceEdit:9957084] Shamovsky, Veronica, 2025-06-17 |
| journal | Front Immunol |
| pages | 1162171 |
| pubMedIdentifier | 37051252 |
| title | Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups |
| volume | 14 |
| year | 2023 |
| (literatureReference) | [Summation:9957092] Mannose-binding lectin (MBL2), a soluble pattern recognition... [Reaction:9957161] MBL2 binds SARS-CoV-2 S [Homo sapiens] |
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No pathways have been reviewed or authored by Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups (9957082)