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hydroxymethylbilane

Known as: 21H-biline-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)- 
 
National Institutes of Health

Papers overview

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2015
2015
BACKGROUND Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease. Patients with non… Expand
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Review
2013
Review
2013
Porphyrins and metalloporphyrins are the key pigments of life on earth as we know it, because they include chlorophyll (a… Expand
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Molecular characterization of circulating tumor cells (CTCs) is crucial to identify novel diagnostic and therapeutic… Expand
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2010
2010
Gene expression analyses based on messenger RNA (mRNA) profiling require accurate data normalisation. When using endogenous… Expand
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2008
2008
Acute intermittent porphyria (AIP) is an autosomal dominant disorder of heme biosynthesis caused by molecular defects in the… Expand
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Highly Cited
2006
Highly Cited
2006
BackgroundReal-time quantitative PCR (qPCR) is a method for rapid and reliable quantification of mRNA transcription. Internal… Expand
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Highly Cited
2004
Highly Cited
2004
All eight enzymes required for de novo heme biosynthesis have been predicted from the nuclear genome of the human malaria… Expand
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1994
1994
Acute intermittent porphyria (AIP), an autosomal dominant inborn error, results from the half-normal activity of the heme… Expand
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1993
1993
Acute intermittent porphyria (AIP), an autosomal dominant inborn error of heme biosynthesis, results from the half-normal… Expand
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1991
1991
The role of conserved arginine residues in hydroxymethylbilane synthase was investigated by replacing these residues in the… Expand
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