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Galactose (/ɡəˈlæktoʊs/, galacto- + -ose, "milk sugar"),
sometimes abbreviated Gal, is a
monosaccharide sugar that is
about as
sweet as glucose, and about...
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Galactose-1-phosphate
uridyltransferase (or GALT, G1PUT) is an
enzyme (EC 2.7.7.12)
responsible for
converting ingested galactose to glucose. Galactose-1-phosphate...
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Galactose-α-1,3-
galactose,
commonly known as
alpha gal and the
Galili antigen, is a
carbohydrate found in most
mammalian cell membranes. It is not found...
- Glucose-
galactose malabsorption is a rare
condition in
which the
cells lining the
intestine cannot take in the
sugars glucose and
galactose,
which prevents...
- galactosaemia, from Gr**** γαλακτόζη + αίμα,
meaning galactose + blood, ac****ulation of
galactose in blood) is a rare
genetic metabolic disorder that affects...
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Galactose 1-dehydrogenase may
refer to: ʟ-
Galactose 1-dehydrogenase ᴅ-
Galactose 1-dehydrogenase
Galactose 1-dehydrogenase (NADP+) This set
index page...
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Galactose-1-phosphate
uridylyltransferase deficiency (classic galactosemia) is the most
common type of galactosemia, an
inborn error of
galactose metabolism...
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Galactose oxidase (D-
galactose:oxygen 6-oxidoreductase, D-
galactose oxidase, beta-
galactose oxidase;
abbreviated GAO, GAOX, GOase; EC 1.1.3.9) is an enzyme...
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hydrolase enzyme that
catalyzes hydrolysis of
terminal non-reducing β-D-
galactose residues in β-D-galactosides. (This
enzyme digests many β-Galactosides...
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Galactose epimerase deficiency, also
known as GALE deficiency,
Galactosemia III and UDP-
galactose-4-epimerase deficiency, is a rare,
autosomal recessive...
