| FBP | femoral blood pressure; fibrin breakdown product; folate-binding protein; fructose-1, 6-biphosphatas... |
|---|---|
| FDP | fibrin degradation product; fibrinogen degradation product; flexor digitorum profundus; frontodextra... |
| FDPase | fructose-1,6-diphosphatase |
| FMP | faculty mentorship program; first menstrual period; fructose monophosphate |
| F1P, | F-1-P fructose-1-phosphate |
| galactose tolerance test | A liver function test, based on the ability of the liver to convert galactose to glycogen, measured by the rate of excretion of galactose following ingestion or intravenous injection of a known amount; normally, less than 3 g appear in the urine within 5 hours after the ingestion of 40 g. (05 Mar 2000) |
|---|---|
| UDPgalactosamine-galactose acetylgalactosaminyltransferase | <enzyme> Transfers sugars from udp-n-acetylgalactosamine to terminal galactose of h substance, producing a antigen; consider also fucosyl galactose alpha-n-acetylgalactosaminyltransferase which is called a-transferase Registry number: EC 2.4.1.- Synonym: blood group a-enzyme, blood group glycosyltransferase a, alpha-3-d-n-acetylgalactosaminyltransferase, alpha-3-n-acetyl-d-galactosaminyltransferase (26 Jun 1999) |
| UDP-galactose 4-O-beta-D-galactosyl-D-xylose galactosyltransferase | <enzyme> Involved in chondroitin sulfate synthesis Registry number: EC 2.4.1.- (26 Jun 1999) |
| UDP-galactose hydrolase | <enzyme> Hydrolyzes udp-galactose to galactose Registry number: EC 3.1.4.- (26 Jun 1999) |
| UDP-galactose-lactosylceramide alpha 1-4-galactosyltransferase | <enzyme> Catalyses transfer of galactose from udp-galactose to lactosylceramide; exclusively an alpha1-4-galactosyltransferase Registry number: EC 2.4.1.- Synonym: udpgal-galactosyl-beta-1-4-glucosylceramide alpha1-4-galactosyltransferase, globotriaosylceramide synthase, udp-glcg-transferase, udp galactose lactosylceramide alpha-galactosyltransferase, udp-gal lcgtase, udp-gal-galactose alpha(1,4)-galactosyltransferase, alpha1,4galt (26 Jun 1999) |
| UDP-galactose-lactosylceramide beta 1-3-galactosyltransferase | <enzyme> Catalyses transfer of galactose from udp-galactose to lactose or lactosylceramide Registry number: EC 2.4.1.- Synonym: udp-galactose-lactose beta 1-3 galactosyltransferase, udp-galactose-lactose (lactosylceramide) beta-3-galactosyltransferase, udpgal-lac-3-transferase (26 Jun 1999) |
| UDP-galactose xylose galactosyltransferase | <enzyme> Involved in chondroitin sulfate synthesis Registry number: EC 2.4.1.- (26 Jun 1999) |
| UDP-GalNAc-beta-galactose beta 1,4-N-acetylgalactosaminyltransferase | <enzyme> Consider also EC 2.4.1.92 Registry number: EC 2.4.1.- Synonym: beta-1,4-n-acetylgalactosaminyltransferase, 4-galnactransferase, udp-n-acetylgalactosamine-beta-galactose beta 1,4-n-acetylgalactosaminyltransferase, (1-4)-n-acetyl-beta-d-galactosaminyltransferase, galnact-1 (26 Jun 1999) |
| UDP-N-acetylglucosamine-galactose(1-6)-N-acetylglucosaminyltransferase | <enzyme> Forms oligosaccharide core class 4(glcnac beta 1-3(glcnac beta 1-6)galnac) in mucins and various glycoproteins Registry number: EC 2.4.1.148 Synonym: udp-nagagf (26 Jun 1999) |
| uridine diphosphate galactose | <chemical> A nucleoside diphosphate sugar which can be epimerised into udpglucose for entry into the mainstream of carbohydrate metabolism. Serves as a source of galactose in the synthesis of lipopolysaccharides, cerebrosides, and lactose. Chemical name: Uridine 5'-(trihydrogen diphosphate), P'-alpha-D-galactopyranosyl ester (12 Dec 1998) |
| 2-amino-2-deoxy-D-galactose | <chemical> Chemical name: D-Galactose, 2-amino-2-deoxy- (12 Dec 1998) |
| fucosyl galactose alpha-n-acetylgalactosaminyltransferase | <enzyme> An enzyme that catalyses the transfer of acetylgalactosamine from udp n-acetylgalactosamine to various 2-fucosylgalactosides as acceptors. Chemical name: UDP-N-acetyl-D-galactosamine:alpha-L-fucosyl-(1,2)-D-galactose 3-N-acetyl-D-galactosaminyltransferase Registry number: EC 2.4.1.40 (12 Dec 1998) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |