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Disease Info Card
Galactosemias
Information about Galactosemias: 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 Galactosemias
Most recent studies have shown that Galactosemias shares some biological mechanisms with cataract, classical-galactosemia, cystic-fibrosis, deficiency-of-galactokinase, diabetes-mellitus, diabetes-mellitus-experimental, diabetic-retinopathy, glycogen-storage-disease, hereditary-fructose-intolerance-syndrome, homocystinuria, hyperglycemia, hypothyroidism, inborn-errors-of-metabolism, liver-diseases, maple-syrup-urine-disease, metabolic-diseases, phenylketonurias, premature-menopause, retinal-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Galactosemias, and have been seen in publications frequently: Aging, Cell Death, Cell Growth, Cell Proliferation, Excretion, Fatty Acid Oxidation, Gluconeogenesis, Glucose Transport, Glycolysis, Glycosylation, Lactation, Localization, Menopause, Myelination, Ovulation, Pathogenesis, Regeneration, Secretion, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Galactosemias, such as ADH1A, ADH1B, ADH1C, ADH4, ADH6, AKR1A1, AKR1B1, ALB, BRD2, BTD, G6PD, GAL, GALE, GALK1, GALT, GLB1, INS, LHCGR, PAH, 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.