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Disease Info Card
Hypoxic-ischaemic Encephalopathy
Information about Hypoxic-ischaemic Encephalopathy: 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 Hypoxic-ischaemic Encephalopathy
Most recent studies have shown that Hypoxic-ischaemic Encephalopathy shares some biological mechanisms with anoxia, asphyxia, asphyxia-neonatorum, brain-diseases, brain-hypoxia, brain-injuries, brain-ischemia, cerebral-palsy, encephalopathies, epilepsy, hemorrhage, hypoxia, hypoxia-ischemia-brain, induced-hypothermia-(finding), infarction, ischemia, nervousness, sequelae-aspects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypoxic-ischaemic Encephalopathy, and have been seen in publications frequently: Angiogenesis, Brain Development, Cell Death, Cell Proliferation, Coagulation, Excretion, Inflammatory Response, Innervation, Myelination, Neurogenesis, Neuroprotection, Oxidative Phosphorylation, Pathogenesis, Programmed Cell Death, Protein Oxidation, Reflex, Regeneration, Swimming, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Hypoxic-ischaemic Encephalopathy, such as ABCC8, AKAP4, BCL2, CA1, CASP3, CSF2, ENO1, ENO2, EPO, GFAP, IGF1, IL6, LAMC2, MBP, SLC10A7, TH, 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.