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Disease Info Card
Hepatic Methionine Adenosyltransferase Deficiency
Information about Hepatic Methionine Adenosyltransferase Deficiency: 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 Methionine Adenosyltransferase Deficiency
Most recent studies have shown that Hepatic Methionine Adenosyltransferase Deficiency shares some biological mechanisms with cholestasis, citrullinemia, cystathionine-beta-synthase-deficiency-disease, demyelination, hepatitis, homocystinuria, hyperhomocysteinemia, hyperphenylalaninemia, hyperplasia, hypoglycemia, inborn-errors-of-metabolism, intrahepatic-cholestasis, liver-cirrhosis, liver-diseases, maple-syrup-urine-disease, metabolic-diseases, phenylketonurias, storage-disease, tyrosinemias.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hepatic Methionine Adenosyltransferase Deficiency, and have been seen in publications frequently: Brain Development, Coagulation, Dna Methylation, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Hepatocyte Proliferation, Immune Response, Lactation, Methylation, Muscle Atrophy, Myelination, Pathogenesis, Regeneration, Skeletal Muscle Atrophy, Transport, Transsulfuration, Urea Cycle
Quite a number of genes have been found to play important roles in Hepatic Methionine Adenosyltransferase Deficiency, such as ACADS, ACHE, ADK, AHCY, ATP8A2, AUH, CAT, CBS, CTH, FMN1, FTCD, GNMT, INS, MAT1A, MTHFR, MTRR, PAH, PPA1, PPY, SLC25A13. 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.