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Results 1 - 10 of 17 for UDP
  1. ... genes that provide instructions for making enzymes called UDP-glucuronosyltransferases. These enzymes perform a chemical reaction called ... already impaired bilirubin-UGT enzyme function. BILIQTL1 bilirubin UDP-glucuronosyltransferase 1-1 bilirubin-specific UDPGT isozyme 1 ...
  2. ... gene provides instructions for making an enzyme called UDP-galactose translocator (UGT). This enzyme is involved in ... About This Health Condition solute carrier family 35 (UDP-galactose transporter), member 2 solute carrier family 35 ( ...
  3. ... gene provides instructions for making an enzyme called UDP-galactose-4-epimerase. This enzyme enables the body ... in all dairy products and many baby formulas.UDP-galactose-4-epimerase converts a modified form of ...
  4. ... acid. It first converts a molecule known as UDP-GlcNAc (UDP-N-acetylglucosamine) to a similar molecule called ManNAc ( ... has also been reported in some individuals. Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase DMRV ...
  5. ... polypeptide GalNAc-transferase T3 pp-GaNTase 3 protein-UDP acetylgalactosaminyltransferase 3 UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 3 ...
  6. ... chemical reaction also produces another form of galactose (UDP-galactose) that is used to build galactose-containing ... Gal-1-P uridylyltransferase Galactosephosphate Uridylyltransferase GALT_HUMAN UDP Galactose Pyrophosphorylase UTP-Hexose-1-Phosphate Uridylyltransferase UTP: ...
  7. Galactosemia is a condition in which the body is unable to use ( metabolize ) the simple sugar galactose. ... Galactosemia is an inherited ...
  8. ... deficiency disease GALE deficiency GALK deficiency GALT deficiency UDP-galactose-4-epimerase deficiency disease UTP hexose-1- ...
  9. ... acetylglucosamine-1-phosphate transferase, alpha and beta subunits UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosamine uridine 5'- ...
  10. ... Rust S, Marquardt T. A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical ... H. De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy. Hum ...
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