Research of Fructose-1,6-diphosphatase Deficiency has been linked to Hypoglycemia, Acidosis, Hereditary Fructose Intolerance Syndrome, Acidosis, Lactic, Glycogen Storage Disease Type I. The study of Fructose-1,6-diphosphatase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Fructose-1,6-diphosphatase Deficiency include Gluconeogenesis, Excretion, Urea Cycle, Glycolysis, Pyruvate Oxidation. These pathways complement our catalog of research reagents for the study of Fructose-1,6-diphosphatase Deficiency including antibodies and ELISA kits against FBPASE, PHOSPHOENOLPYRUVATE CARBOXYKINASE (GTP), SUCCINIC SEMIALDEHYDE DEHYDROGENASE, FBP1, FOLR1.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Fructose-1,6-diphosphatase Deficiency below!
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We have 1072 products for the study of Fructose-1,6-diphosphatase Deficiency that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Fructose-1,6-diphosphatase Deficiency is also known as Deficiency, Fructose-1,6-bisphosphatase, Deficiency, Fructose-1,6-diphosphatase, Fructose 1,6 Diphosphatase Deficiency, Fructose-1, 6-diphosphatase Deficiency, Fructose-1,6-bisphosphatase Deficiency.