UTP-Hexose-1-Phosphate Uridylyltransferase

Known as: Galactose 1 phosphate uridyl transferase, UDP Galactose Pyrophosphorylase, Uridyltransferase, Galactose-1-Phosphate 
An enzyme that catalyzes the synthesis of UDPgalactose from UTP and galactose-1-phosphate. It is present in low levels in fetal and infant liver, but… (More)
National Institutes of Health

Papers overview

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2011
2011
Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uridyltransferase (GALT) deficiency. Newborn… (More)
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2009
2009
BACKGROUND This prospective study compared extracorporeal shockwave treatment (ESWT) with hyperbaric oxygen therapy (HBO) in… (More)
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Review
2008
Review
2008
The enzymes of the Leloir pathway catalyze the conversion of galactose to a more metabolically useful version, glucose-6… (More)
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Review
2008
Review
2008
The basic biology of the menstrual cycle is a complex, coordinated sequence of events involving the hypothalamus, anterior… (More)
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Highly Cited
2004
Highly Cited
2004
OBJECTIVE Classical galactosemia (McKusick 230400) is an autosomal recessive disorder of galactose metabolism caused by a… (More)
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2003
2003
Microarrays of oligonucleotide expression libraries can be hybridised with either cDNA, generated from mRNA during reverse… (More)
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2001
2001
PURPOSE To determine whether preserved human amniotic membrane can reduce corneal haze and keratocyte apoptosis induced by… (More)
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Highly Cited
1997
Highly Cited
1997
ATP is released from most cell types and functions as an extracellular signaling molecule through activation of members of the… (More)
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1996
1996
The P2Y4 receptor is a new member of the P2Y family which functionally behaves as a pyrimidinergic receptor. The pharmacological… (More)
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1995
1995
Despite restricted ingestion of lactose, patients with galactose-1-phosphate uridyltransferase deficiency have raised… (More)
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