Carbamoyl-phosphate Synthase I Deficiency Disease: Disease Bioinformatics
Research of Carbamoyl-phosphate Synthase I Deficiency Disease has been linked to Hyperammonemia, Ornithine Carbamoyltransferase Deficiency, Inborn Errors Of Metabolism, Urea Cycle Disorders, Inborn, Comatose. The study of Carbamoyl-phosphate Synthase I Deficiency Disease has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Carbamoyl-phosphate Synthase I Deficiency Disease include Urea Cycle, Excretion, Proteolysis, Translation, Transport. These pathways complement our catalog of research reagents for the study of Carbamoyl-phosphate Synthase I Deficiency Disease including antibodies and ELISA kits against CPS, CARBAMYL PHOSPHATE SYNTHETASE I, AMINO-ACID N-ACETYLTRANSFERASE, CARBAMOYL-PHOSPHATE SYNTHETASE I, ALB.
Top Research Reagents
We have 1501 products for the study of Carbamoyl-phosphate Synthase I Deficiency Disease that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Carbamoyl-phosphate Synthase I Deficiency Disease is also known as Carbamoyl Phosphate Synthetase Deficiency, Carbamoyl Phosphate Synthetase I Deficiency, Carbamoyl-phosphate Synthase, Carbamoyl-phosphate Synthetase I Deficiency, Carbamoylphosphate Synthetase I Deficiency.