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Uroporphyrinogen III Synthetase

Known as: Uroporphyrinogen-III Synthase, Cosynthase, Cosynthetase, Uroporphyrinogen III 
An enzyme that catalyzes the cyclization of hydroxymethylbilane to yield UROPORPHYRINOGEN III and water. It is the fourth enzyme in the 8-enzyme… Expand
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Congenital erythropoietic porphyria (CEP), an autosomal recessive disorder, is due to mutations of uroporphyrinogen III synthase… Expand
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Review
1997
Review
1997
Congenital erythropoietic porphyria is a rare autosomal-recessive disorder of the porphyrin metabolism caused by the homozygous… Expand
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Highly Cited
1992
Highly Cited
1992
Congenital erythropoietic porphyria (CEP), an inborn error of heme biosynthesis, results from the deficient activity of… Expand
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Highly Cited
1992
Highly Cited
1992
The molecular basis of an inherited defect of ferrochelatase in a patient with erythropoietic protoporphyria (EPP) was… Expand
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Highly Cited
1990
Highly Cited
1990
Congenital erythropoietic porphyria (Günther's disease) is a rare disorder of heme biosynthesis inherited in an autosomal… Expand
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Highly Cited
1990
Highly Cited
1990
A 3.8-kilobase DNA fragment from Bacillus subtilis containing the hemA gene has been cloned and sequenced. Four open reading… Expand
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Highly Cited
1988
Highly Cited
1988
Uroporphyrinogen III synthase [URO-synthase; hydroxymethylbilane hydro-lyase (cyclizing), EC 4.2.1.75], the fourth enzyme in the… Expand
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Highly Cited
1986
Highly Cited
1986
CONGENITAL erythropoietic porphyria is a rare autosomal recessive disorder of heme biosynthesis that is secondary to reduced (10… Expand
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1979
1979
Abstract Acute intermittent porphyria (AIP) is a hereditary disease characterized biochemically by a defect in the heme pathway… Expand
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1969
1969
Abstract 1. 1.|Porphobilinogenase has been isolated and purified from cow liver and its components, porphobilinogen deaminase and… Expand
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