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Pentosuria
Known as:
L-XYLULOSE REDUCTASE DEFICIENCY
, L-XYLULOSURIA
, Xylulosuria
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National Institutes of Health
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Related topics
Related topics
4 relations
Autosomal recessive inheritance
congenital deficiency
Broader (2)
Sugar Alcohol Dehydrogenases
Xylulose
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Human DCXR – another ‘moonlighting protein’ involved in sugar metabolism, carbonyl detoxification, cell adhesion and male fertility?
B. Ebert
,
M. Kisiela
,
E. Maser
Biological Reviews of The Cambridge Philosophical…
2015
Corpus ID: 5227287
Dicarbonyl/l‐xylulose reductase (DCXR; SDR20C1), a member of the short‐chain dehydrogenase/reductase (SDR) superfamily catalyzes…
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Review
2008
Review
2008
Garrod’s Croonian Lectures (1908) and the charter ‘Inborn Errors of Metabolism’: Albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008
C. Scriver
Journal of Inherited Metabolic Disease
2008
Corpus ID: 10154482
SummaryGarrod presented his concept of ‘the inborn error of metabolism’ in the 1908 Croonian Lectures to the Royal College of…
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1985
1985
On the nature of l-xylulose reductase deficiency in essential pentosuria
A. Lane
Biochemical Genetics
1985
Corpus ID: 23655195
Essential pentosuria is the result of a partial deficiency of l-xylulose reductase. Red blood cells of normal individuals have…
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1970
1970
The enzymatic defect in essential pentosuria.
Y. M. Wang
,
J. van Eys
New England Journal of Medicine
1970
Corpus ID: 35817501
Abstract The enzyme defect in pentosuria has been assumed to be NADP-linked xylitol dehydrogenase, a specific enzyme found in…
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1961
1961
Studies of pentose metabolism in normal subjects and in patients with pentosuria and pentosuria trait.
Y. Kumahara
,
D. Feingold
,
I. Freedberg
,
H. Hiatt
Journal of Clinical Endocrinology and Metabolism
1961
Corpus ID: 9043207
Endogenous serum l-xylulose concentration exceeds 1 mg. per 100 ml. in pontosuric patients, and the level rises several-fold…
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Review
1960
Review
1960
Inheritance of Essential Pentosuria
P. Roberts
British medical journal
1960
Corpus ID: 33359016
Dicusson Hemiatrophy of the body is usually facial, and not always progressive and unilateral. Like other hereditary…
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1959
1959
Essential Pentosuria: Renal or Enzymic Disorder
R. C. Bozian
,
O. Touster
Nature
1959
Corpus ID: 4203224
ESSENTIAL pentosuria is a rare, recessive genetic metabolic disorder characterized by the excretion of gram quantities of L…
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1958
1958
The isolation of L-arabitol from pentosuric urine.
O. Touster
,
S. Harwell
Journal of Biological Chemistry
1958
Corpus ID: 28765752
Highly Cited
1956
Highly Cited
1956
The reduction of L-xylulose to xylitol by guinea pig liver mitochondria.
R. Hutcheson
,
V. H. Reynolds
,
O. Touster
Journal of Biological Chemistry
1956
Corpus ID: 16069817
1956
1956
Nature and Significance of Pentosuria in Neuromuscular Disease
D. B. Tower
,
E. Peters
,
M. A. Pogorelskin
Neurology
1956
Corpus ID: 24664586
2. CHROMATOGRAPHIC STUDIES Examinations by paper chromatography were carried out on 43 specimens of 24-hour urine from 21…
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