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Disease Info Card
Hepatic Encephalopathy
Information about Hepatic 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 Hepatic Encephalopathy
Most recent studies have shown that Hepatic Encephalopathy shares some biological mechanisms with chronic-liver-disease, comatose, edema, encephalopathies, gastrointestinal-hemorrhage, hemorrhage, hepatic-coma, hepatitis, hepatitis-a, hepatitis-b, hyperammonemia, hypertension-portal, hypertensive-disease, icterus, liver-cirrhosis, liver-diseases, liver-failure, liver-failure-acute, varicosity.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hepatic Encephalopathy, and have been seen in publications frequently: Amino Acid Transport, Blood Coagulation, Cell Death, Coagulation, Cognition, Diuresis, Excretion, Hemostasis, Hypersensitivity, Inflammatory Response, Liver Regeneration, Localization, Locomotion, Pathogenesis, Reflex, Regeneration, Secretion, Transport, Urea Cycle, Vasoconstriction
Quite a number of genes have been found to play important roles in Hepatic Encephalopathy, such as AFP, ALB, ARID4B, BCHE, CD55, CNTN3, CSF2, F2, GFAP, GLUL, IL6, INS, LAMC2, NOS2, SLA2, SLC17A5, TNF, TSPO. 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.