UROS gene

Known as: UROS, UROIIIS, congenital erythropoietic porphyria 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1988-2016
0119882016

Papers overview

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2017
2017
Hemolysis occurring in hematologic diseases is often associated with an iron loading anemia. This iron overload is the result of… (More)
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2017
2017
Glioblastoma (GBM) is the most frequent and most malignant primary brain tumour in adults. GBMs have a unique landscape of… (More)
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Review
2016
Review
2016
Congenital erythropoietic porphyria (CEP) is a rare genetic disease resulting from the remarkable deficient activity of… (More)
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2003
2003
Congenital erythropoietic porphyria (CEP) is an inherited disease due to a deficiency in the uroporphyrinogen III synthase, the… (More)
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1996
1996
The molecular basis of the uroporphyrinogen III synthase (UROIIIS) deficiency was investigated in two members of a Japanese… (More)
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1995
1995
We have isolated a genomic DNA fragment that complements the yeast temperature-sensitive cyt mutation, causing respiratory… (More)
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Review
1995
Review
1995
Porphobilinogen deaminase (hydroxymethylbilane synthase) and uroporphyrinogen III synthase (uroporphyrinogen III cosynthase… (More)
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1994
1994
Uroporphyrinogen lII synthase [URO-synthase, also called hydroxymethylbilane hydro-lyase (cyclizing), EC 4.2.175] is the fourth… (More)
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1988
1988
Uroporphyrinogen III synthase [URO-synthase; hydroxymethylbilane hydro-lyase (cyclizing), EC 4.2.1.75], the fourth enzyme in the… (More)
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