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Disease Info Card
Intrauterine Hypoxia
Information about Intrauterine Hypoxia: 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 Intrauterine Hypoxia
Most recent studies have shown that Intrauterine Hypoxia shares some biological mechanisms with anoxia, asphyxia, asphyxia-neonatorum, brain-injuries, congenital-abnormality, diabetes-mellitus, fetal-death, fetal-diseases, fetal-distress, fetal-growth-retardation, fetal-hypoxia, growth-retardation, hemorrhage, hypertensive-disease, hypoxia, pre-eclampsia, pregnancy-complications, respiratory-distress, stillbirth.
Among the many pathways, these few ones have gauged particular interests from scientists studying Intrauterine Hypoxia, and have been seen in publications frequently: Blood Circulation, Brain Development, Coagulation, Cortisol Secretion, Embryo Development, Fibrinolysis, Lung Development, Mrna Processing, Neurogenesis, Parturition, Pathogenesis, Platelet Aggregation, Reflex, Response To Hypoxia, Response To Stress, Secretion, Tissue Development, Translation, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Intrauterine Hypoxia, such as AGA, CRP, EDN1, EPO, HPX, IL4, IL6, ISYNA1, MAS1, MMP2, NAGA, NOS1, NOS2, S100B, THPO, TNF, VEGFA. 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.