Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia
Author:
Affiliation:
1. Universidade de Pernambuco, Brazil
2. Universidade Federal Rural de Pernambuco, Brazil
3. FIOCRUZ, Brazil
4. Hospital de Hematologia e Hemoterapia de Pernambuco, Brazil
5. Universidade Federal de Pernambuco, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v40n3/1415-4757-gmb-1678-4685-GMB-2016-0161.pdf
Reference17 articles.
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2. Complement, c1q, and c1q-related molecules regulate macrophage polarization;Bohlson SS;Front Immunol,2014
3. Endothelial oxidative stress activates the lectin complement pathway role of cytokeratin 1;Collard CD;Am J Pathol,2001
4. Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage;Dossou-Yovo OP;Hum Biol,2007
5. C1q and MBL, components of the innate immune system, influence monocyte cytokine expression;Fraser DA;J Leukoc Biol,2006
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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18
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