| HCD | health care delivery; heavy-chain disease; high-calorie diet; high-carbohydrate diet; homologous can... |
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| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| HEP | hemolysis end point; hepatoerythropoietic porphyria; high egg passage [virus]; high-energy phosphate... |
| HFD | hemorrhagic fever of deer; high-fiber diet; high forceps delivery; hospital field director; human fa... |
| HFHV | high frequency, high volume |
| glycerol-3-phosphate - glucose phosphotransferase | <enzyme> Catalyses the formation of glycerol and glucose-6-phosphate Registry number: EC 2.7.1.142 Synonym: gro3p-glucose transphorylase, glycerol 3-phosphate-glucose transphorylase (26 Jun 1999) |
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| phosphoenolpyruvate-glucose phosphotransferase | <enzyme> Specific for glucose and nonmetabolizable analogs methyl alpha glucoside, beta-d-thioglucose and 5-thioglucose Registry number: EC 2.7.1.- Synonym: II-b(glc) peppts, enzyme II-b(glc) phosphoenolpyruvate phosphotransferase system, enzyme II (glucose), glucose-specific permease, phosphotransferase system, beta-glucosidase permease, beta-glucoside permease, glucose permease, enzyme II(glc), bglp gene product, syta gene product (26 Jun 1999) |
| deficiency, glucose-6-phosphate dehydrogenase | Deficiency of G6PD is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anaemia due to breakup of their red blood cells when they are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans. (12 Dec 1998) |
| d-glucose | D-Glucose;a dextrorotatory monosaccharide (hexose) found in the free state in fruits and other parts of plants, and combined in glucosides, disaccharides (often with fructose in sugars), oligosaccharides, and polysaccharides; it is the product of complete hydrolysis of cellulose, starch, and glycogen. Free glucose also occurs in the blood (normal human concentration, 70 to 110 mg per 100 ml); in diabetes mellitus, it appears in the urine. The epimers of d-glucose are d-allose, d-mannose, d-galactose, and l-idose. Dextrose should not be confused with the l-isomer which is sinistrose. Synonym: cellohexose. (05 Mar 2000) |
| d-glucose 1,6-bisphosphate | A bisphosphorylated derivative of d-glucose that is a required intermediate in the interconversion of d-glucose 1-phosphate and d-glucose-6-phosphate. (05 Mar 2000) |
| d-glucose 1-phosphate | An important intermediate in glycogenesis and glycogenolysis. Synonym: Cori ester. (05 Mar 2000) |
| d-glucose-6-phosphate | A key intermediate in glycolysis, glycogenolysis, pentose phosphate shunt, etc.; elevated levels inhibit brain hexokinase and glycolysis. Synonym: Robison ester, Robison-Embden ester. (05 Mar 2000) |
| dolichol phosphate glucose-dolichol diphosphate oligosaccharide glucosyltransferase | <enzyme> Can also use dolichol-p-galactose as donor Registry number: EC 2.4.1.- Synonym: dolichol-p-glucose-dolichol-p-p-oligosaccharide glucosyltransferase, dolichol-pp-oligosaccharide glucosyltransferase (ii), dolichol-p-p-oligosaccharide glucosyltransferase (i), dol-p-p-oligosaccharide glycosyltransferase, dppo-glucosyltransferase, dolichyl-p-glucose-man(9)(glcnac)2-pp-dolichol glucosyltransferase (26 Jun 1999) |
| dTDP-D-glucose synthase | <enzyme> Catalyses the formation of dtdp-d-glucose by using glucose-1-phosphate and dttp as substrates; rfba is a dual function enzyme; rfba is also a phosphomannose isomerase-guanosine diphosphomannose pyrophosphorylase; see record of pmi-GMP Registry number: EC 2.7.7.- Synonym: rfba protein, deltatdp-glucose synthase, tyla1 gene product, rfba gene product (26 Jun 1999) |
| impaired glucose tolerance | Blood glucose (sugar) levels higher than normal but not high enough to be called diabetes. People with impaired glucose tolerance may or may not develop diabetes. Other names (no longer used) for impaired glucose tolerance are borderline, subclinical, chemical, or latent diabetes. (30 Mar 1998) |
| test, glucose tolerance | After fasting, a specific amount (100 grams) of glucose is given by mouth, and the blood levels of this sugar are measured every hour. Normally, the blood glucose should return to normal within 2 to 2 1/2 hours. The gtt is considered a classic test of carbohydrate metabolism. It is much used in the diagnosis of diabetes. The gtt depends on a number of factors including the ability of the intestine to absorb glucose, the power of the liver to take up and store glucose, the capacity of the pancreas to produce insulin, and the amount of active insulin. (12 Dec 1998) |
| UDP-glucose cyanidin-3-rhamnosyl-(1-6)-glucoside-5-O- glucosyltransferase | <enzyme> Chemical name: glucosyltransferase, uridine diphosphoglucose-cyanidin 3-rhamnosylglucoside 5-o- Registry number: EC 2.4.1.- (26 Jun 1999) |
| UDP-glucose diosgenin-tigogenin glucosyltransferase | <enzyme> Catalyses the glycosylation of steroid saponins; from leaves of eggplant, solanum melongena Registry number: EC 2.4.1.- Synonym: udpglc-diosgenin-tigogenin glc-tase, udpglc-dt-glctase, diosgenin glucosyltransferase (26 Jun 1999) |
| UDPglucose-glycogen glucose 1-phosphotransferase | <enzyme> Catalyses the transfer of glucose 1-phosphate onto c-6 of glucose residues in glycogen to form a phosphodiester Registry number: EC 2.7.8.- Synonym: ugg-glcptase (26 Jun 1999) |
| UDPglucose-glycoprotein glucose-1-phosphotransferase | <enzyme> From embryonic chicken neural retina; glucose is linked by phosphodiester bonds to mannose of a cell surface glycoprotein; catalyses the transfer of alpha glc-1-p from udp-glc to mannose residues on acceptor glycoproteins Registry number: EC 2.7.8.19 Synonym: glcptase, glc-phosphotransferase (26 Jun 1999) |