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Disease Info Card
Hyperbilirubinemia, Neonatal
Information about Hyperbilirubinemia, 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 Hyperbilirubinemia, Neonatal
Most recent studies have shown that Hyperbilirubinemia, Neonatal shares some biological mechanisms with anemia, blood-group-incompatibility, brain-injuries, encephalopathies, erythroblastosis-fetal, gilbert-disease-(disorder), glucosephosphate-dehydrogenase-deficiency, hemolysis-(disorder), hemolytic-disorder, hyperbilirubinemia, hypoglycemia, icterus, kernicterus, neonatal-jaundice, neurotoxicity-syndromes, pregnancy-complications, sequelae-aspects, systemic-infection, unconjugated-hyperbilirubinemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hyperbilirubinemia, Neonatal, and have been seen in publications frequently: Bilirubin Conjugation, Bilirubin Transport, Cell Death, Coagulation, Conjugation, Cytokine Production, Cytokine Secretion, Excretion, Glucose Homeostasis, Heme Oxidation, Inflammatory Response, Lactation, Neuroprotection, Ossification, Pathogenesis, Pigmentation, Secretion, Sensitization, Superoxide Anion Generation, Transport
Quite a number of genes have been found to play important roles in Hyperbilirubinemia, Neonatal, such as ABO, ABR, AGA, ALB, CFB, F2, G6PD, GLS2, HMOX1, RHCE, RHD, SLC45A2, SLCO1B1, TNF, TNFSF14, UBL4A, UGT1A1. 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.