Pentosuria

Known as: L-XYLULOSE REDUCTASE DEFICIENCY, Xylulosuria, PNTSU 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1946-2015
012319462014

Papers overview

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Review
2013
Review
2013
Dicarbonyl/L-xylulose reductase (DCXR) is a highly conserved and phylogenetically widespread enzyme converting L-xylulose into… (More)
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2011
2011
Pentosuria is one of four conditions hypothesized by Archibald Garrod in 1908 to be inborn errors of metabolism. Mutations… (More)
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1994
1994
One of the book's strengths is to discuss less-cited examples: the Shah of Persia, for instance, whose plans to modernize his… (More)
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1985
1985
Okada, S. and O'Brien, J. S. Tay-Sachs disease: generalized absence of an N-acetyl-[3-D-glucosaminidase component. Science 165… (More)
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1985
1985
Only one of the two main L-xylulose reductases present in human tissue is deficient in individuals with essential pentosuria… (More)
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1985
1985
Essential pentosuria is the result of a partial deficiency of l-xylulose reductase. Red blood cells of normal individuals have… (More)
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1978
1978
The genetic basis of metabolic disorders was recognized long before the structure of DNA, the genetic code, or the biochemical… (More)
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1967
1967
PENTOSURIA, one of Garrod's original four inborn errors of metabolism1, is usually believed to occur almost entirely among people… (More)
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1959
1959
ESSENTIAL pentosuria is a rare, recessive genetic metabolic disorder characterized by the excretion of gram quantities of L… (More)
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