(Q42606037)

English

Human phenol sulfotransferases SULT1A2 and SULT1A1: genetic polymorphisms, allozyme properties, and human liver genotype-phenotype correlations

scientific article published on August 1999

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 November 2017

Human phenol sulfotransferases SULT1A2 and SULT1A1: genetic polymorphisms, allozyme properties, and human liver genotype-phenotype correlations (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Richard Weinshilboum

3

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Weinshilboum RM

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PubMed publication ID

3 November 2017

author name string

Raftogianis RB

1

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3 November 2017

Wood TC

2

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3 November 2017

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publication date

1 August 1999

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3 November 2017

Biochemical Pharmacology

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3 November 2017

58

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3 November 2017

4

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Europe PubMed Central

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3 November 2017

605-616

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3 November 2017

Sulfation and sulfotransferases 1: Sulfotransferase molecular biology: cDNAs and genes

1 reference

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Multiple forms of phenolsulphotransferase in human tissues: selective inhibition by dichloronitrophenol.

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Human liver phenol sulfotransferase: assay conditions, biochemical properties and partial purification of isozymes of the thermostable form

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Localization and characterization of phenol sulfotransferase in human platelets

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Human brain phenol sulfotransferase: biochemical properties and regional localization

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Human platelet phenol sulfotransferase: familial variation in thermal stability of the TS form

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Phenol sulfotransferase pharmacogenetics in humans: association of common SULT1A1 alleles with TS PST phenotype

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Mapping of the phenol sulfotransferase gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7

1 reference

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7 January 2021

Human thermolabile phenol sulfotransferase gene (STM): molecular cloning and structural characterization

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Genomic organization and DNA sequence of the human catecholamine-sulfating phenol sulfotransferase gene (STM)

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Human phenol sulfotransferase gene contains two alternative promoters: Structure and expression of the gene

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Human phenol sulfotransferase STP2 gene: molecular cloning, structural characterization, and chromosomal localization

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Human phenol sulfotransferase pharmacogenetics: STP1 gene cloning and structural characterization

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Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease

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Rat brain phenolsulfotransferase—partial purification and some properties

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Phenolsulphotransferase in human tissue: radiochemical enzymatic assay and biochemical properties

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Platelet phenol sulfotransferase activity: correlation with sulfate conjugation of acetaminophen

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The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression

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Human liver thermolabile phenol sulfotransferase: cDNA cloning, expression and characterization

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High efficiency polyoma DNA transfection of chloroquine treated cells

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Statistical estimations in enzyme kinetics

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Computer Programmes for Processing Enzyme Kinetic Data

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Primary structures and properties of two related forms of aryl sulfotransferases in human liver

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cDNA cloning and expression of a new form of human aryl sulfotransferase

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Identification of two human brain aryl sulfotransferase cDNAs

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Molecular characterisation of a human aryl sulfotransferase cDNA

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7 January 2021

Human platelet phenolsulfotransferases: cDNA cloning, stable expression in V79 cells and identification of a novel allelic variant of the phenol-sulfating form

1 reference

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Genetic polymorphisms in human liver phenol sulfotransferases involved in the bioactivation of N-hydroxy derivatives of carcinogenic arylamines and heterocyclic amines

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Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity

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Identifiers

10.1016/S0006-2952(99)00145-8

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

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