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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
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7 relations
Galactose 1 phosphate uridyl transferase phenotype:Type:Pt:Bld:Nom
Galactose 1 phosphate uridyl transferase:CCnc:Pt:Bld.dot:Qn
Galactose 1 phosphate uridyl transferase:CCnt:Pt:WBC:Qn
Galactose 1 phosphate uridyl transferase:PrThr:Pt:Bld.dot:Ord
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase
A. E. Carney
,
Rebecca D. Sanders
,
+7 authors
J. Fridovich-Keil
Human Molecular Genetics
2009
Corpus ID: 2824777
Duarte galactosemia is a mild to asymptomatic condition that results from partial impairment of galactose-1-phosphate…
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1995
1995
In vivo oxidation of [13C]galactose in patients with galactose-1-phosphate uridyltransferase deficiency.
Gerard T. Berry
,
Itzhak Nissim
,
+6 authors
Stanton Segal
Biochemical and Molecular Medicine
1995
Corpus ID: 39949209
We developed an intravenous and oral [13C]galactose breath test for the in vivo study of galactose metabolism. Following an…
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1995
1995
Characterization of the N314D allele of human galactose-1-phosphate uridylyltransferase using a yeast expression system.
J. Fridovich-Keil
,
B. Quimby
,
L. Wells
,
L. Mazur
,
J. Elsevier
Biochemical and Molecular Medicine
1995
Corpus ID: 36688180
Transferase-deficiency galactosemia is an inborn error of metabolism resulting from impairment of the enzyme galactose-1…
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Highly Cited
1991
Highly Cited
1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase.
J. Reichardt
,
S. Packman
,
S. Woo
American Journal of Human Genetics
1991
Corpus ID: 26558865
Galactosemia is an autosomal recessive disorder of human galactose metabolism caused by deficiency of the enzyme galactose-1…
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Highly Cited
1981
Highly Cited
1981
Galactosaemia: a new severe variant due to uridine diphosphate galactose-4-epimerase deficiency.
J. Holton
,
M. Gillett
,
R. Macfaul
,
R. Young
Archives of Disease in Childhood
1981
Corpus ID: 19705352
A baby presented on day 5 with symptoms of classical galactosaemia which are believed to be owing to a lack of uridine…
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Highly Cited
1973
Highly Cited
1973
A new variant of galactose‐1‐phosphate uridyltransferase in man: the Los Angeles variant
W. Ng
,
W. Bergren
,
G. Donnell
Annals of Human Genetics
1973
Corpus ID: 22699183
The first known variant of human erythrocyte galactose1 -phosphate uridyltransferase (E.C. 2 .7 .7 .12 ) , the Duarte variant…
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1969
1969
Formation of Galactose-1-Phosphate from Uridine Diphosphate Galactose in Erythrocytes from Patients with Galactosemia[31]
R. Gitzelmann
Pediatric Research
1969
Corpus ID: 873957
Extract: Erythrocyte lysates of galactosemic patients were found to form galactose-1-phosphate from uridine diphosphate galactose…
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Highly Cited
1966
Highly Cited
1966
Electrophoretic Variation of Galactose-1-Phosphate Uridyltransferase
C. Mathai
,
E. Beutler
Science
1966
Corpus ID: 41850371
A specific method for starch-gel electrophoresis of galactose-1-phosphate uridyltransferase has been developed. Electrophoresis…
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1958
1958
Interference with growth of certain Escherichia coli mutants by galactose.
K. Kurahashi
,
A. Wahba
Biochimica et Biophysica Acta
1958
Corpus ID: 29061293
Review
1943
Review
1943
The fermentation of galactose and galactose-1-phosphate.
H. Kosterlitz
Biochemical Journal
1943
Corpus ID: 5186861
During a survey of the natural sources of ascorbic acid, three reactions have been observed that may be of analytical value: (1…
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