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Article

Human Hydroxysteroid Sulfotransferase SULT2B1: Two Enzymes Encoded by a Single Chromosome 19 Gene

1 Nov 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9799594
DOI: 10.1006/geno.1998.5518

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human Hydroxysteroid Sulfotransferase SULT2B1: Two Enzymes Encoded by a Single Chromosome 19 GenePMID 9799594Read ↗

Human hydroxysteroid sulfotransferase SULT2B1 pharmacogenomics: gene sequence variation and functional genomics.Semantic proximity Read ↗

Impact of Genetic Polymorphisms on the Sulfation of Dehydroepiandrosterone and 17-β estradiol by Human Cytosolic Sulfotransferase SULT2B1aSemantic proximity Read ↗

Impact of Genetic Polymorphisms on the Sulfation of Dehydroepiandrosterone and 17-β Estradiol by Human Cytosolic Sulfotransferase SULT2B1aSemantic proximity Read ↗

Resequencing the sulfotransferase SULT1 gene provides new insights, while illuminating challenges that lie ahead for pharmacogenomics.Semantic proximity Read ↗

Impact of genetic polymorphisms on the sulfation of dehydroepiandrosterone and 17-β estradiol by human cytosolic sulfotransferase SULT2B1a.Semantic proximity Read ↗

Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19Semantic proximity Read ↗

Structure, Function and Polymorphism of Human Cytosolic SulfotransferasesSemantic proximity Read ↗

Effects of genetic polymorphisms on the sulfation of dehydroepiandrosterone and pregnenolone by human cytosolic sulfotransferase SULT2A1.Semantic proximity Read ↗

Human Sulfotransferase SULT1C1: cDNA Cloning, Tissue-Specific Expression, and Chromosomal Localization1Semantic proximity Read ↗

Very important pharmacogene summary: sulfotransferase 1A1.Semantic proximity Read ↗

The Human Sulfotransferase SULT1A1 Gene Is Regulated in a Synergistic Manner by Sp1 and GA Binding ProteinSemantic proximity Read ↗

17 -Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo MutationsSemantic proximity Read ↗

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