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Disease Info Card
Citrullinemia
Information about Citrullinemia: 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 Citrullinemia
Most recent studies have shown that Citrullinemia shares some biological mechanisms with acidemia, acidemia, argininosuccinic-aciduria, argininosuccinic-aciduria, brain-edema, brain-edema, cholestasis, cholestasis, citrullinemia, citrullinemia-type-ii-neonatal-onset, citrullinemia-type-ii-neonatal-onset, comatose, comatose, complete-argininosuccinic-acid-synthetase-deficiency-disease, complete-argininosuccinic-acid-synthetase-deficiency-disease, edema, edema, encephalopathies, encephalopathies, fatty-liver, hepatic-encephalopathy, hepatic-encephalopathy, hyperammonemia, hyperammonemia, inborn-errors-of-metabolism, inborn-errors-of-metabolism, intrahepatic-cholestasis, intrahepatic-cholestasis, liver-diseases, liver-diseases, metabolic-diseases, metabolic-diseases, ornithine-carbamoyltransferase-deficiency, ornithine-carbamoyltransferase-deficiency, urea-cycle-disorders-inborn, urea-cycle-disorders-inborn.
Among the many pathways, these few ones have gauged particular interests from scientists studying Citrullinemia, and have been seen in publications frequently: Brain Development, Carnitine Transport, Cell Migration, Cell Migration, Circadian Rhythm, Coagulation, Coagulation, Excretion, Excretion, Fatty Acid Oxidation, Fatty Acid Oxidation, Gluconeogenesis, Gluconeogenesis, Glycolysis, Insemination, Intestinal Absorption, Localization, Localization, Malate-aspartate Shuttle, Malate-aspartate Shuttle, Ornithine Transport, Pathogenesis, Pathogenesis, Phagocytosis, Phagocytosis, Regeneration, Regeneration, Reverse Transcription, Rna Splicing, Translation, Translation, Transport, Transport, Transposition, Transposition, Tricarboxylic Acid Cycle, Urea Cycle, Urea Cycle, Virulence, Virulence
Quite a number of genes have been found to play important roles in Citrullinemia, such as ACADS, ACADS, ADSL, AFP, AFP, ARSA, ASL, ASL, ASS1, ASS1, CRP, LAMC2, LAMC2, NAGS, OTC, OTC, PAH, PC, PC, PSMD1, PSMD4, SLC25A12, SLC25A12, SLC25A13, SLC25A13, SLC25A15, SLC25A15, SLC25A2, SLC25A2, SPINK1, SPINK1, TTR, UMPS. 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.