| Health / Medical Topics |
Argininemia
A rare autosomal recessive metabolic disorder characterized by a deficiency of the enzyme arginase resulting in accumulation of arginine and urea in the blood and cerebrospinal fluid. Signs and symptoms include developmental delays, spasticity, ataxia, seizures and mental retardation. (NCI Thesaurus)
YOU MAY ALSO LIKE
A specialized enteric nutritional supplement, containing substantial amounts of polyunsaturated fatty acids, arginine, and nucleotides, with potential immunostimulating activity. Compared to traditional…
Glutamine is converted to glutamate by glutaminase, or several other enzymes, by the removal of the amide nitrogen. Proline is first…
This protein is a precursor protein consisting of arginine vasopressin and two associated proteins, neurophysin II and a glycopeptide, copeptin. Arginine vasopressin…
Arginine Vasopressin Receptor 2 is also known as the V2 receptor. The V2 receptor is expressed in the kidney tubule, predominantly in…
Arginine vasopressin receptor 1B protein (441 aa, 48 kD) is a cell communication process protein that is encoded by the human AVPR1B…
This protein acts as receptor for arginine vasopressin. This receptor belongs to the subfamily of G-protein coupled receptors which includes AVPR1B, V2R…
