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glycolaldehyde HOCH2CHO;the simplest (2-carbon) sugar; the aerobic deamination product of ethanolamine.
Synonym: biose, diose.
Active glycoaldehyde, 2-(1,2-dihydroxyethyl)thiamin pyrophosphate;a derivative formed in carbohydrate metabolism.
(05 Mar 2000)
glycolaldehydetransferase transaldolase
glycolate A salt or ester of glycolic acid.
(05 Mar 2000)
glycoleucine <chemical> Chemical name: Norleucine
(12 Dec 1998)
glycolic <chemistry> Pertaining to, or derived from, glycol; as, glycolic ether; glycolic acid.
<chemistry> Glycolic acid, an organic acid, found naturally in unripe grapes and in the leaves of the wild grape (Ampelopsis quinquefolia), and produced artificially in many ways, as by the oxidation of glycol, whence its name. It is a sirupy, or white crystalline, substance, HO.CH2.CO2H, has the properties both of an alcohol and an acid, and is a type of the hydroxy acids.
Synonym: hydroxyacetic acid.
Source: Websters Dictionary
(01 Mar 1998)
glycolic acid <biochemistry> Hydroxyacetic acid, found in young plants and green fruits. Glycolate is formed from ribulose 1,5 bisphosphate in a seemingly wasteful side reaction of photosynthesis, known as photorespiration.
(18 Nov 1997)
glycolic acid dehydrogenase <enzyme> Enzyme from human liver converts glycolate to oxalate, acceptor not identified, not oxygen; free glyoxylate is not an intermediate
Registry number: EC 1.1.-
(26 Jun 1999)
glycolic aciduria Excessive excretion of glycolic acid in the urine; a primary metabolic defect due to deficiency of 2-hydroxy-3-oxoadipate carboxylase, resulting in excretion of glycolic and oxalic acids, leading to the clinical syndrome of oxalosis.
(05 Mar 2000)
glycolide <chemistry> A white amorphous powder, C4H4O, obtained by heating and dehydrating glycolic acid.
Alternative forms: glycollide.
Origin: Glycol + anhydride.
Source: Websters Dictionary
(01 Mar 1998)
glycolipid <biochemistry> Oligosaccharides covalently attached to lipid as in the glycosphingolipids found in plasma membranes of all animal and some plant cells.
The lipid part of glycolipids is sphingosine in which the amino group is acylated by a fatty chain, forming a ceramide. most of the oligosaccharide chains belong to one of four series, the ganglio, globo, lacto type 1 and lacto type 2 series. Blood group antigens are glycolipids.
(18 Nov 1997)
glycolipid lipidosis <disease> Lysosomal storage disease caused by a deficiency of alpha-galactosidase a and resulting in an accumulation of globotriaosylceramide in the renal and cardiovascular systems.
The disease is characterised by telangiectatic skin lesions, renal failure, and disturbances of the cardiovascular, gastrointestinal, and central nervous systems.
Inheritance: x-linked.
(08 Mar 2000)
glycols A generic grouping for dihydric alcohols with the hydroxy groups (-oh) located on different carbon atoms. They are viscous liquids with high boiling points for their molecular weights.
(12 Dec 1998)
glycoluric <chemistry> Pertaining to, derived from, glycol and urea; as, glycoluric acid, which is
Synonym: hydantoic acid.
Origin: Glycol + uric.
Source: Websters Dictionary
(01 Mar 1998)
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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 10
  • Glycogen Storage Disease Type III - »õâ An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent.
    Synonyms : Cori Disease, Deficiency, Debrancher, Coris Disease, Debrancher Deficiencies, Deficiencies, Debrancher, Dextrinoses, Limit, Dextrinosis, Limit, Disease, Cori, Disease, Cori's, Disease, Forbes, Limit Dextrinoses
  • Glycogen Storage Disease Type IV - »õâ An autosomal recessive metabolic disorder due to a deficiency in expression of GLYCOGEN BRANCHING ENZYME 1 (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal GLYCOGEN with long outer branches. Clinical features are MUSCLE HYPOTONIA and CIRRHOSIS. Death from liver disease usually occurs before age 2.
    Synonyms : Andersen's Disease, Deficiency, Brancher, Type IV Glycogenosis, Amylopectinoses, Andersens Disease, Brancher Deficiencies, Deficiencies, Brancher, Disease, Andersen, Disease, Andersen's, Glycogenosis, Type IV
  • Glycogen Storage Disease Type V - »õâ Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
    Synonyms : Deficiency, Muscle Phosphorylase, McArdle Disease, Muscle Phosphorylase Deficiency, 5, Glycogenosis, 5s, Glycogenosis, Deficiencies, Muscle Phosphorylase, Disease, McArdle, Disease, McArdle's, Glycogenosis 5s, McArdles Disease, Muscle Phosphorylase Deficiencies
  • Glycogen Storage Disease Type VI - »õâ A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.
    Synonyms : Glycogenosis Type VI, Glycogenosis VI, Hers' Disease, Disease, Hers, Disease, Hers', Her Disease, Type VI, Glycogenosis
  • 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
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glycoside A compound in which a glycosyl group has been substituted for a hydroxyl group.
Ãâó: www.genpromag.com/Glossary~LETTER~G.html
glycogen A storage form of glucose in the body.
Ãâó: www.peteducation.com/dict_alpha_listing.cfm
glycogen The storage form of carbohydrate in the muscles and the blood, composed of chains of glucose molecules.
Ãâó: members.tripod.com/michellejp1/id12.html
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
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