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Disease Info Card
Hellp Syndrome
Information about Hellp 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 Hellp Syndrome
Most recent studies have shown that Hellp Syndrome shares some biological mechanisms with disseminated-intravascular-coagulation, eclampsia, edema, fatty-liver, fetal-death, fetal-growth-retardation, hematoma, hemolysis-(disorder), hemorrhage, hypertension-induced-by-pregnancy, hypertensive-disease, kidney-failure, liver-diseases, pain, pre-eclampsia, pregnancy-complications, pregnancy-complications-cardiovascular, pregnancy-complications-hematologic, proteinuria-of-undiagnosed-cause.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hellp Syndrome, and have been seen in publications frequently: Angiogenesis, Blood Coagulation, Coagulation, Complement Activation, Cytolysis, Diuresis, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Fibrinolysis, Hemostasis, Immune Response, Inflammatory Response, Localization, Pathogenesis, Platelet Activation, Platelet Aggregation, Secretion, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Hellp Syndrome, such as ADAMTS13, AP3B1, ENG, F2, F5, HADHA, HP, IL6, MTHFR, PGF, PREP, SERPINC1, SH3BP4, SLC17A5, SLC25A10, TNF, VEGFA, ZFP36. 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.