Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes (Q44765959)

6 December 2017

Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes (English)

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6 December 2017

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A J Shield

1

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6 December 2017

B A Thomae

2

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6 December 2017

B W Eckloff

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6 December 2017

E D Wieben

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6 December 2017

R M Weinshilboum

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6 December 2017

language of work or name

English

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publication date

1 February 2004

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6 December 2017

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6 December 2017

9

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6 December 2017

151-160

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6 December 2017

2

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001386

6 December 2017

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cites work

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Major gene model for the inheritance of catechol-O-methyltransferase activity in five large families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Human liver catechol-O-methyltransferase pharmacogenetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Genetics of red cell COMT activity: Analysis of thermal stability and family data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Pharmacogenetics of catechol-O-methyltransferase: Frequency of low activity allele in a Ghanaian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Analysis of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association with aggressive and antisocial behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Association studies of bipolar disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Neuroscience. Deconstructing schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Consed: a graphical tool for sequence finishing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

A comprehensive set of sequence analysis programs for the VAX

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Site-directed mutagenesis by overlap extension using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Microassay of human erythrocyte catechol-O-methyltransferase: Removal of inhibitory calcium ion with chelating resin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Computer Programmes for Processing Enzyme Kinetic Data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Score tests for association between traits and haplotypes when linkage phase is ambiguous

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Crystal structure of catechol O-methyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

TRANSFAC: an integrated system for gene expression regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Haplotype variation and linkage disequilibrium in 313 human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Human sulfotransferase SULT1C1 pharmacogenetics: gene resequencing and functional genomic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Human sulfotransferase SULT2A1 pharmacogenetics: genotype-to-phenotype studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Human 3'-phosphoadenosine 5'-phosphosulfate synthetase 2 (PAPSS2) pharmacogenetics: gene resequencing, genetic polymorphisms and functional characterization of variant allozymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Characterization of human soluble high and low activity catechol-O-methyltransferase catalyzed catechol estrogen methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

Membrane-bound catechol-O-methyltransferase: a reevaluation of its role in the O-methylation of the catecholamine neurotransmitters

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

The inheritance of human erythrocyte catechol-O-methyltransferase activity

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Human erythrocyte catechol-o-methyltransferase: Correlation with lung and kidney activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Catechol-O-methyltransferase: thermolabile enzyme in erythrocytes of subjects homozygous for allele for low activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Preliminary evidence of an association between bipolar disorder in females and the catechol-O-methyltransferase gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Association between homozygosity at the COMT gene locus and obsessive compulsive disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Meta-analysis of polymorphism of the catechol-O-methyltransferase gene in relation to the etiology of Parkinson's disease in Japan

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Statistical estimations in enzyme kinetics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Human histamine N-methyltransferase pharmacogenetics: common genetic polymorphisms that alter activity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Low catechol-O-methyltransferase activity in a Saami population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Enhanced proteasomal degradation of mutant human thiopurine S-methyltransferase (TPMT) in mammalian cells: mechanism for TPMT protein deficiency inherited by TPMT*2, TPMT*3A, TPMT*3B or TPMT*3C

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Rapid polyubiquitination and proteasomal degradation of a mutant form of NAD(P)H:quinone oxidoreductase 1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001386

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001386

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Dimensions Publication ID

6 December 2017

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