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Disease Info Card
Antiphospholipid Syndrome
Information about Antiphospholipid Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Antiphospholipid Syndrome
Most recent studies have shown that Antiphospholipid Syndrome shares some biological mechanisms with acute-promyelocytic-leukemia, arterial-thrombosis, autoimmune-diseases, autoimmune-reaction, cerebrovascular-accident, hemorrhage, hypertensive-disease, infarction, lupus-anticoagulant-disorder, lupus-erythematosus-systemic, polyendocrinopathies-autoimmune, pregnancy-complications, thromboembolism, thrombophilia, thrombosis, venous-thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Antiphospholipid Syndrome, and have been seen in publications frequently: Blood Coagulation, Cell Activation, Cell Adhesion, Coagulation, Complement Activation, Endothelial Cell Activation, Fertilization, Fibrinolysis, Glomerular Filtration, Hemostasis, Immune Response, Inflammatory Response, Localization, Ovulation, Pathogenesis, Phagocytosis, Platelet Activation, Platelet Aggregation, Secretion, Transport
Quite a number of genes have been found to play important roles in Antiphospholipid Syndrome, such as ANXA5, APOH, C3, CRP, F2, F3, F5, GNPDA1, GPI, KLK3, PLG, PNLIP, SERPINC1, SH2B2, TF, TNF. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.