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  • galactose
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  • galactosemia
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  • Galactose
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  • galactose
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  • galactose
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  • galactose breath test
    °¥¶ôÅ佺ȣÈí½ÃÇè
  • galactose tolerance test
    °¥¶ôÅ佺ºÎÇÏ ½ÃÇè.
  • galactose-1-phosphate uridyl tranferase
    °¥¶ôÅ佺-1-Æ÷½ºÆäÀÌÆ®¿ì¸®µôÀüÀÌÈ¿¼Ò
  • Galactosemia
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  • galactosemia
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  • galactosemia
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  • Glucose-galactose malabsorption syndrome
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  • glucose-galactose
    ±Û·çÄÚ¿À½º-°¥¶ôÅ佺
  • glucose-galactose malabsorption
    ±Û·çÄÚ¿À½º-°¥¶ôÅ佺Èí¼öÀå¾Ö
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  • familial fructose and galactose intol
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  • familial fructose and galactose intolerance
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  • glucose-galactose
    ±Û·çÄÚ¿À½º-°¥¶ôÅ佺
  • glucose-galactose malabsorption
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  • galactose tolerance test
    °¶¶ôÅ佺 ³»¼º°Ë»ç(Ò±àõËþÞÛ)
  • galactosemia
    °¶¶ôÅ佺Ç÷Áõ(úìñø)
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GAL galactose; galactosyl; glucuronic acid lactone
Gal galactose
gal galactose; gallon
GALBP galactose-binding protein
GALE galactose epimerase
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Gal D(+)galactose
GO D-galactose oxidase
GEC Galactose elimination capacity
Gal-1-P Galactose-1-phosphate
GALT Galactose-1-phosphate uridyl transferase
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
galactose <biochemistry> Hexose identical to glucose except that orientation of H and OH on carbon 4 are exchanged.
A component of cerebrosides and gangliosides, glycoproteins. Lactose, the disaccharide of milk, consists of galactose joined to glucose by a _(1-4) glycosidic link.
(18 Nov 1997)
galactose 3-O-sulfotransferase <enzyme> Catalyses transfer of sulfate from adenosine 3'-phosphosulfate to methyl galactosides or terminal n-acetyllactosamine-containing carbohydrate chains
Registry number: EC 2.8.2.-
(26 Jun 1999)
galactose binding protein <protein> A bacterial periplasmic protein, most studied in E. Coli, that acts both as a sensory element in the detection of galactose as a chemotactic signal and in the uptake of the sugar.
(18 Nov 1997)
galactose cataract A neonatal cataract associated with intralenticular accumulation of galactose alcohol.
See: galactosaemia.
(05 Mar 2000)
galactose dehydrogenases <enzyme> D-galactose:NAD(p)+ 1-oxidoreductases. Catalyses the oxidation of d-galactose in the presence of NAD+ or NADP+ to d-galactono-gamma-lactone and NADH or NADPH.
Registry number: EC 1.1.1.
(12 Dec 1998)
galactose diabetes <biochemistry> A rare genetic (autosomal recessive) disorder characterised by the inability a defect in the enzyme (galactose 1 phosphate uridyl transferase) that converts galactose 1 phosphate into glucose 1 phosphate is absent.
Excess galactose 1 phosphate accumulates in the blood and a variety of problems result.
Inheritance: autosomal recessive.
Origin: Gr. Haima = blood
(27 Sep 1997)
galactose oxidase <enzyme> An enzyme that oxidises galactose in the presence of molecular oxygen to d-galacto-hexodialdose. It is a copper protein.
Chemical name: D-Galactose:oxygen 6-oxidoreductase
Registry number: EC 1.1.3.9
(12 Dec 1998)
galactose permease <chemical>
(26 Jun 1999)
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)
galactose-1-phosphatase <enzyme> From rat brain; requires mg for activity; phosphate is potent inhibitor
Registry number: EC 3.1.3.-
(26 Jun 1999)
galactose-1-phosphate A phosphorylated derivative of galactose that is key in galactose metabolism; accumulates in certain types of galactosaemia.
(05 Mar 2000)
galactose-1-phosphate uridylyltransferase <enzyme> An enzyme catalyzing the reaction of UTP and alpha-d-galactose 1-phosphate to form UDPgalactose and pyrophosphate, the second and most important step in the metabolism of d-galactose; a deficiency of this enzyme results in an accumulation of galactose, galactose-1-phosphate, and galactitol.
(05 Mar 2000)
galactose-6-phosphate dehydrogenase <enzyme> Possibly a ketoaldose, phosphorylated at primary alcoholic group; found in goat liver cytoplasm, requires nad, has high substrate specificity
Registry number: EC 1.1.1.-
Synonym: hexose-6-phosphate dehydrogenase
(26 Jun 1999)
galactose-6-phosphate isomerase <enzyme> Converts galactose 6-phosphate to tagatose 6-phosphate
Registry number: EC 5.3.1.-
Synonym: galactose 6-phosphate isomerase, gal-6-p isomerase, tagatose-6-phosphate isomerase
(26 Jun 1999)
galactose-6-sulfatase <enzyme> An enzyme that eliminates sulfur from the galactose-6-sulfate residues of certain mucopolysaccharides, producing 3,6-anhydrogalactose residues; it is absent in Morquio's syndrome type A.
Synonym: galactose-6-sulfurase.
(05 Mar 2000)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 11 ÆäÀÌÁö: 1
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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Galactose - »õâ An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood.
    Synonyms : D-Galactose, Galactopyranose, Galactopyranoside, D Galactose
  • Galactose Dehydrogenases - »õâ D-Galactose:NAD(P)+ 1-oxidoreductases. Catalyzes the oxidation of D-galactose in the presence of NAD+ or NADP+ to D-galactono-gamma-lactone and NADH or NADPH. Includes EC 1.1.1.48 and EC 1.1.1.120.
    Synonyms : Dehydrogenases, Galactose, Oxidoreductases, Galactose
  • Galactose Oxidase - »õâ An enzyme that oxidizes galactose in the presence of molecular oxygen to D-galacto-hexodialdose. It is a copper protein. EC 1.1.3.9.
    Synonyms : Oxidase, Galactose
  • Galactosemias - »õâ A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (OVARIAN FAILURE, PREMATURE); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
    Synonyms : Deficiency Disease, Galactokinase, Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase, Deficiency Disease, UDP-Galactose-4-Epimerase, Deficiency Disease, UDPglucose 4-Epimerase, Galactosemia, Classic, UDP-Galactose-4-Epimerase Deficiency Disease
  • Galactosephosphates - »õâ Phosphoric acid esters of galactose.
    Synonyms :
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  • Galactose-1-phosphate uridyl transferase deficiency - »õâ
  • Galactose-1-phosphate uridyltransferase - »õâ
  • Galactose-6-phosphate epimerase deficiency - »õâ
  • Galactosemia - »õâ
  • Galactosemia screen - »õâ
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A08401881 Beta-galactosidase
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galactose a simple sugar found in lactose
Ãâó: wordnet.princeton.edu/perl/webwn
galactosemia a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth
Ãâó: wordnet.princeton.edu/perl/webwn
galactosemic cataract a cataract commonly observed in infants with galactosemia. The opacities look like oil droplets, are bilateral, and are zonular or nuclear.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
galactosemia Galactosemia is a rare genetic metabolic disorder which affects an individual's ability to properly digest the sugar galactose. Lactose in food (such as dairy products) is broken down by the body into glucose and galactose. Normally, galactose is then converted into glucose by the enzyme GALT (galactose-1-phosphate uridylyltransferase). ...
Ãâó: en.wikipedia.org/wiki/Galactosemia
galactose The type of sugar found in sugar beats. This type of sugar is harder for the small intestine to breakdown.
Ãâó: www.gastromd.com/definitionsg.html
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galactose a simple sugar found in lactose
galactose a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent
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