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Disease Info Card
Encephalopathy Neonatal
Information about Encephalopathy Neonatal: 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 Encephalopathy Neonatal
Most recent studies have shown that Encephalopathy Neonatal shares some biological mechanisms with acidosis, asphyxia, asphyxia-neonatorum, brain-diseases, brain-hypoxia, brain-injuries, cerebral-palsy, developmental-disabilities, encephalopathies, fetal-distress, fetal-hypoxia, hypoxia, hypoxia-ischemia-brain, hypoxic-ischaemic-encephalopathy, induced-hypothermia-(finding), malnutrition, pregnancy-complications.
Among the many pathways, these few ones have gauged particular interests from scientists studying Encephalopathy Neonatal, and have been seen in publications frequently: Brain Development, Cell Death, Cell Differentiation, Cell Migration, Coagulation, Diuresis, Gliogenesis, Glucose Homeostasis, Immune Response, Inflammatory Response, Myelination, Neuroprotection, Oxidative Phosphorylation, Pathogenesis, Reflex, Response To Hypoxia, Sensitization, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Encephalopathy Neonatal, such as ABCC8, ADSL, AKAP4, CALB2, CD55, CP, CR2, DHRS4, ELANE, ENO2, EPO, IKBKG, JUN, LCT, MECP2, NTS, TDGF1. 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.