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galactose-1-phosphate

Known as: 1 galactose phosphate, Galactose 1 phosphate, alpha-D-galactopyranose, 1-(dihydrogen phosphate) 
National Institutes of Health

Papers overview

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2009
2009
Duarte galactosemia is a mild to asymptomatic condition that results from partial impairment of galactose-1-phosphate… 
1995
1995
We developed an intravenous and oral [13C]galactose breath test for the in vivo study of galactose metabolism. Following an… 
1995
1995
Transferase-deficiency galactosemia is an inborn error of metabolism resulting from impairment of the enzyme galactose-1… 
Highly Cited
1991
Highly Cited
1991
Galactosemia is an autosomal recessive disorder of human galactose metabolism caused by deficiency of the enzyme galactose-1… 
Highly Cited
1981
Highly Cited
1981
A baby presented on day 5 with symptoms of classical galactosaemia which are believed to be owing to a lack of uridine… 
Highly Cited
1973
Highly Cited
1973
The first known variant of human erythrocyte galactose1 -phosphate uridyltransferase (E.C. 2 .7 .7 .12 ) , the Duarte variant… 
1969
1969
Extract: Erythrocyte lysates of galactosemic patients were found to form galactose-1-phosphate from uridine diphosphate galactose… 
Highly Cited
1966
Highly Cited
1966
A specific method for starch-gel electrophoresis of galactose-1-phosphate uridyltransferase has been developed. Electrophoresis… 
Review
1943
Review
1943
During a survey of the natural sources of ascorbic acid, three reactions have been observed that may be of analytical value: (1…