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Disease Info Card
Neonatal Hypoglycemia
Information about Neonatal Hypoglycemia: 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 Neonatal Hypoglycemia
Most recent studies have shown that Neonatal Hypoglycemia shares some biological mechanisms with beckwith-wiedemann-syndrome, brain-injuries, congenital-abnormality, diabetes-mellitus, diabetes-mellitus-insulin-dependent, diabetes-mellitus-non-insulin-dependent, fetal-growth-retardation, fetal-macrosomia, gestational-diabetes, hyperbilirubinemia, hyperglycemia, hyperinsulinism, hypertensive-disease, hypoglycemia, nesidioblastosis, pre-eclampsia, pregnancy-complications, pregnancy-in-diabetics, respiratory-distress.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neonatal Hypoglycemia, and have been seen in publications frequently: Cell Proliferation, Detection Of Glucose, Dna Methylation, Electron Transport, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Glucose Homeostasis, Glycolysis, Glycosylation, Habituation, Insulin Secretion, Lactation, Localization, Methylation, Parturition, Pathogenesis, Regulation Of Insulin Secretion, Secretion, Transport
Quite a number of genes have been found to play important roles in Neonatal Hypoglycemia, such as ABCC8, AGA, CDKN1C, G6PC, GCG, GCK, GGH, GH1, GLS2, HNF4A, IGF1, IGF2, IGFBP3, INS, KCNJ11, POMC, PRG4, SST. 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.