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Disease Info Card
Kernicterus
Information about Kernicterus: 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 Kernicterus
Most recent studies have shown that Kernicterus shares some biological mechanisms with asphyxia, blood-group-incompatibility, brain-diseases, brain-injuries, cerebral-palsy, crigler-najjar-syndrome, encephalopathies, erythroblastosis-fetal, glucosephosphate-dehydrogenase-deficiency, hemolysis-(disorder), hemolytic-disorder, hyperbilirubinemia, hyperbilirubinemia-neonatal, icterus, neonatal-jaundice, nervousness, neurotoxicity-syndromes, sequelae-aspects, systemic-infection, unconjugated-hyperbilirubinemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Kernicterus, and have been seen in publications frequently: Bilirubin Conjugation, Bilirubin Transport, Brain Development, Cell Death, Coagulation, Conjugation, Cytokine Secretion, Excretion, Glycolysis, Inflammatory Response, Lactation, Localization, Myelination, Neuroprotection, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Reflex, Secretion, Transport
Quite a number of genes have been found to play important roles in Kernicterus, such as ABCC1, ABO, ABR, ALB, CFB, CP, G6PD, GLS2, IL6, RHCE, RHD, SERPINF2, SLC35A2, SLC45A2, 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.