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alternate case: galactose—1-phosphate uridylyltransferase
Galactose-1-phosphate uridylyltransferase
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"Entrez Gene: GALT galactose-1-phosphate uridylyltransferase". Wong LJ, Frey PA (September 1974). "Galactose-1-phosphate uridylyltransferase: rate studiesGalactose-1-phosphate uridylyltransferase deficiency (1,280 words) [view diff] no match in snippet view article find links to article
Galactose-1-phosphate uridylyltransferase deficiency (classic galactosemia) is the most common type of galactosemia, an inborn error of galactose metabolismUDP-glucose—hexose-1-phosphate uridylyltransferase (286 words) [view diff] no match in snippet view article find links to article
systematic name of this enzyme class is UDP-glucose:alpha-D-galactose-1-phosphate uridylyltransferase. Other names in common use include uridyl transferaseGalactitol (128 words) [view diff] no match in snippet view article find links to article
other common galactose metabolism defect is a defect in galactose-1-phosphate uridylyltransferase, an autosomal recessive disorder, which also causes aUTP—hexose-1-phosphate uridylyltransferase (280 words) [view diff] no match in snippet view article find links to article
include galactose-1-phosphate uridylyltransferase, galactose 1-phosphate uridylyltransferase, alpha-D-galactose 1-phosphate uridylyltransferase, galactoseGalactose 1-phosphate (380 words) [view diff] no match in snippet view article find links to article
putting patients at higher risk for presenile cataract. Galactose-1-phosphate uridylyltransferase "Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)"Duarte galactosemia (2,820 words) [view diff] no match in snippet view article find links to article
metabolize galactose due to a partial deficiency of the enzyme galactose-1-phosphate uridylyltransferase. DG differs from classic galactosemia in that patientsGal4 transcription factor (2,205 words) [view diff] no match in snippet view article find links to article
(galactokinase), GAL10 (UDP-glucose 4-epimerase), and GAL7 (galactose-1-phosphate uridylyltransferase), three enzymes required for galactose metabolism. ThisProtein dimer (653 words) [view diff] no match in snippet view article find links to article
Cartoon diagram of a dimer of Escherichia coli galactose-1-phosphate uridylyltransferase (GALT) in complex with UDP-galactose (stick models). PotassiumUridine diphosphate galactose (199 words) [view diff] no match in snippet view article find links to article
1-phosphate (5); Glucose 6-phosphate (6). Galactokinase (GK), Galactose-1-phosphate uridylyltransferase (GALT), UDP-glucose 4-epimerase (UGE), phosphoglucomutaseList of diseases (G) (846 words) [view diff] no match in snippet view article
hyperprolactinemia Galactosamine-6-sulfatase deficiency Galactose-1-phosphate uridylyltransferase deficiency Galactosemia Galloway Mowat syndrome Gamborg–NielsenGalactokinase (1,459 words) [view diff] no match in snippet view article find links to article
enzymes are required in the Leloir pathway: galactokinase, galactose-1-phosphate uridylyltransferase, and UDP-galactose 4-epimerase. Galactokinase catalyzesCyclic GMP-AMP synthase (514 words) [view diff] no match in snippet view article find links to article
Nucleotidyltransferase UTP—glucose-1-phosphate uridylyltransferase Galactose-1-phosphate uridylyltransferase Guanylyltransferase mRNA capping enzyme Other RecombinaseInterleukin 11 receptor alpha subunit (1,034 words) [view diff] no match in snippet view article find links to article
(1998). "Cotranscription and intergenic splicing of human galactose-1-phosphate uridylyltransferase and interleukin-11 receptor alpha-chain genes generateChromosome 9 (1,587 words) [view diff] no match in snippet view article find links to article
domain containing 1 FOCAD: focadhesin FXN: frataxin GALT: galactose-1-phosphate uridylyltransferase GAS1: growth arrest-specific protein 1 GCNT1: glucosaminylInborn errors of carbohydrate metabolism (2,783 words) [view diff] no match in snippet view article find links to article
caused by mutations in the gene that makes the enzyme galactose-1-phosphate uridylyltransferase. Approximately 70% of galactosemia-causing alleles haveGalactosemia (1,854 words) [view diff] no match in snippet view article find links to article
people with classic galactosemia (GALT deficiency or Galactose-1-phosphate uridylyltransferase deficiency), galactokinase deficiency, and epimerase deficiencyUTP—glucose-1-phosphate uridylyltransferase (2,932 words) [view diff] no match in snippet view article find links to article
and microorganisms. In galactose metabolism, the enzyme galactose 1-phosphate uridylyltransferase transfers a phosphate from UDP-glucose to galactose 1-phosphateLuis Federico Leloir (2,782 words) [view diff] no match in snippet view article find links to article
in galactosemia, patients lacked the necessary enzyme (Galactose-1-phosphate uridylyltransferase) to convert unusable galactose into usable glucose.Transferase (6,229 words) [view diff] no match in snippet view article find links to article
simple sugar. This deficiency occurs when the gene for galactose-1-phosphate uridylyltransferase (GALT) has any number of mutations, leading to a deficiency