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Disease Info Card
Argininosuccinic Aciduria
Information about Argininosuccinic Aciduria: 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 Argininosuccinic Aciduria
Most recent studies have shown that Argininosuccinic Aciduria shares some biological mechanisms with acidemia, ascorbic-acid-deficiency, ataxia, citrullinemia, comatose, developmental-disabilities, hepatomegaly, hyperammonemia, hyperargininemia, inborn-errors-of-metabolism, leukodystrophy, leukodystrophy-metachromatic, metabolic-diseases, ornithine-carbamoyltransferase-deficiency, phenylketonurias, renal-aminoacidurias, urea-cycle-disorders-inborn.
Among the many pathways, these few ones have gauged particular interests from scientists studying Argininosuccinic Aciduria, and have been seen in publications frequently: Amino Acid Transport, Cell Adhesion, Cell Cycle, Cell Death, Coagulation, Dentinogenesis, Endochondral Ossification, Excretion, Glycosylation, Hyphal Growth, Localization, Ossification, Pathogenesis, Prolactin Secretion, Protein Glycosylation, Regeneration, Secretion, Senescence, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Argininosuccinic Aciduria, such as ADSL, ARSA, ASL, ASS1, CSF2, DEGS1, FH, LAMC2, LYZ, NAGS, NOS1, NOS2, OTC, PEPD, PRL. 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.