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glycoluril <chemistry> A white, crystalline, nitrogenous substance, obtained by the reduction of allantoin.
Origin: Glycolyl + uric.
Source: Websters Dictionary
(01 Mar 1998)
glycolyl <chemistry> A divalent, compound radical, CO.CH2, regarded as the essential radical of glycolic acid, and a large series of related compounds.
Origin: Glycolic + -yl.
Source: Websters Dictionary
(01 Mar 1998)
glycolylurea <chemistry> A derivative of urea, C3H4N2O2, obtained from allantion, as a white, crystalline substance, with a sweetish taste.
Synonym: glycolyl urea.
Origin: Hydrogen + allantion.
Source: Websters Dictionary
(01 Mar 1998)
glycolysis <biochemistry> The conversion of a monosaccharide (generally glucose) to pyruvate via the glycolytic pathway (i.e. The Embden Meyerhof Parnas pathway) in the cytosol.
Generates ATP without consuming oxygen and is thus anaerobic.
Origin: Gr. Lysis = dissolution
(18 Nov 1997)
glycolytic Relating to glycolysis.
(05 Mar 2000)
glyconeogenesis <biochemistry> The making of the polysaccharide glycogen without using glucose or other carbohydrates and instead using things like fats or proteins.
(09 Oct 1997)
glyconic A glyconic verse.
Origin: Gr. A kind of verse, so called from its inventor, Glycon.
Source: Websters Dictionary
(01 Mar 1998)
glyconic acids Monosaccharide derivatives in which the aldehyde group has been oxidised to a carboxyl group. They may form lactones (e.g., galactonic acid).
Synonym: glyconic acids.
(05 Mar 2000)
glyconin An emulsion of glycerin and the yolk of eggs, used as an ointment, as a vehicle for medicines, etc.
Source: Websters Dictionary
(01 Mar 1998)
glycopenia A deficiency of any or all sugars in an organ or tissue.
Origin: Glyco-+ G. Penia, poverty
(05 Mar 2000)
glycopeptidase <enzyme> Cleaves beta-asparty-glycosylamine linkages in glycopeptides with 3-11 amino acid residues
Registry number: EC 3.5.1.52
Synonym: n-oligosaccharide glycopeptidase, peptide-n4-(acetyl-beta-glucosaminyl)asparagine amidase, glycopeptidase a, peptide-n-glycanase, glycopeptidase f, n-glycanase, pngase f, pngase a, n-glycosidase a, pngase se, peptide-n(4)-(n-acetylglucosaminyl)asparagine amidase se, n-glycosidase f, pngase at
(26 Jun 1999)
glycopeptide <biochemistry> A peptide covalently linked to a sugar or polysaccharide.
(09 Oct 1997)
glycopeptide alpha-N-acetylgalactosaminidase <enzyme> Hydrolyzes terminal d-galactosyl-n-acetyl-alpha-d-galactosaminide residues from glycopeptides and glycoproteins linked by serine or threonine residues
Registry number: EC 3.2.1.97
Synonym: o-glycanase
(26 Jun 1999)
glycopeptides Proteins which contain carbohydrate groups attached covalently to the polypeptide chain. The protein moiety is the predominant group with the carbohydrate making up only a small percentage of the total weight.
(12 Dec 1998)
Glycophagus A common genus of grain mites, frequently implicated in dermatitis among food handlers.
See: Tyrophagus putrescentiae.
Origin: Glyco-+ G. Phago, to eat
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 11
  • Glycogen Storage Disease Type VII - »õâ An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
    Synonyms : Deficiency, Muscle Phosphofructokinase, Muscle Phosphofructokinase Deficiency, Tarui's Disease, Deficiencies, Muscle Phosphofructokinase, Disease, Tarui, Disease, Tarui's, Muscle Phosphofructokinase Deficiencies, Phosphofructokinase Deficiencies, Muscle
  • Glycogen Storage Disease Type VIII - »õâ An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon.
    Synonyms :
  • Glycogen Synthase - »õâ An enzyme that catalyzes the transfer of D-glucose from UDPglucose into 1,4-alpha-D-glucosyl chains. EC 2.4.1.11.
    Synonyms : Glycogen Synthase I, Synthase D, Synthase I, UDP-Glucose Glycogen Glucosyl Transferase, Synthase, Glycogen, Synthetase, Glycogen, UDP Glucose Glycogen Glucosyl Transferase
  • Glycogen Synthase Kinase 3 - »õâ A glycogen synthase kinase that was originally described as a key enzyme involved in glycogen metabolism. It regulates a diverse array of functions such as CELL DIVISION, microtubule function and APOPTOSIS.
    Synonyms : GSK-3, gsk-3 Gene Product
  • Glycogen Synthase Kinases - »õâ A class of protein-serine-threonine kinases that was originally found as one of the three types of kinases that phosphorylate GLYCOGEN SYNTHASE. Glycogen synthase kinases along with CA(2+)-CALMODULIN DEPENDENT PROTEIN KINASES and CYCLIC AMP-DEPENDENT PROTEIN KINASES regulate glycogen synthase activity.
    Synonyms : Glycogen Synthase Kinase, Kinase, Glycogen Synthase, Kinases, Glycogen Synthase, Synthase Kinase, Glycogen
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glycogen Form of carbohydrate stored in the liver and muscles vital to human metabolism.
Ãâó: www.bdid.com/termsg.htm
glycocalyx [Greek, glykos= sweet + Latin, calix= cup], also called the cell coat. A densely staining zone just out-side most eukaryotic cells.
Ãâó: embryology.med.unsw.edu.au/Notes/Index/G.htm
glycolysis [Greek, glykys = sweet (referring to sugar) + Iyein = to loosen] A set of ten chemical reactions that is the first stage in the metabolism of glucose.
Ãâó: embryology.med.unsw.edu.au/Notes/Index/G.htm
glycogen a large, highly branched polymer (repeating units) of glucose molecules, used to store energy in muscle and liver cells.
Ãâó: www.nutrabio.com/Definitions/definitions_g.htm
glycogenesis The process by which molecules of glucose combine to form a molecule called glycogen.
Ãâó: www.nutrabio.com/Definitions/definitions_g.htm
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