Human Genome Epidemiology Literature Finder
|
Records 1 - 5 (of 5 Records) |
| Query Trace: Syndrome and MASP1[original query] |
|---|
| A novel mannose-binding lectin-associated serine protease 1/3 gene variant. Scandinavian journal of immunology 2007 May 65 (5): 430-4. Weiss G, Madsen H O, Garred |
| Association of Polymorphisms of MASP1/3, COLEC10, and COLEC11 Genes with 3MC Syndrome. International journal of molecular sciences 2020 8 21 (15): . Gajek Gabriela, ?wierzko Anna S, Cedzy?ski Maci |
Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome.
RMD open 2021 12 7 (3): . Norheim Katrine Brække, Imgenberg-Kreuz Juliana, Alexsson Andrei, Johnsen Svein Joar Auglænd, Bårdsen Kjetil, Brun Johan Gorgas, Dehkordi Rezvan Kiani, Theander Elke, Mandl Thomas, Jonsson Roland, Ng Wan-Fai, Lessard Christopher J, Rasmussen Astrid, Sivilis Kathy, Ronnblom Lars, Omdal Roa |
| Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection. Current issues in molecular biology 2022 7 44 (7): 2811-2824. Gavriilaki Eleni, Tsiftsoglou Stefanos A, Touloumenidou Tasoula, Farmaki Evangelia, Panagopoulou Paraskevi, Michailidou Elissavet, Koravou Evaggelia-Evdoxia, Mavrikou Ioulia, Iosifidis Elias, Tsiatsiou Olga, Papadimitriou Eleni, Papadopoulou-Alataki Efimia, Papayanni Penelope Georgia, Varelas Christos, Kokkoris Styliani, Papalexandri Apostolia, Fotoulaki Maria, Galli-Tsinopoulou Assimina, Zafeiriou Dimitrios, Roilides Emmanuel, Sakellari Ioanna, Anagnostopoulos Achilles, Tragiannidis Athanasi |
| Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation. Frontiers in immunology 2023 9 14 1249958. Lilli Leimi, Jessica R Koski, Outi Kilpivaara, Kim Vettenranta, A Inkeri Lokki, Seppo Me |
- Page last reviewed:Feb 1, 2024
- Content source: