(Q44800151)

6 December 2017

title

Phenotype and genotype for thiopurine methyltransferase activity in the French Caucasian population: impact of age. (English)

1 reference

6 December 2017

author

Evelyne Jacqz-Aigrain

8

1 reference

6 December 2017

author name string

Catherine Ganiere-Monteil

1

1 reference

6 December 2017

Yves Medard

2

1 reference

6 December 2017

Corinne Lejus

3

1 reference

6 December 2017

Béatrice Bruneau

4

1 reference

6 December 2017

Alain Pineau

5

1 reference

6 December 2017

Odile Fenneteau

6

1 reference

6 December 2017

Michel Bourin

7

1 reference

6 December 2017

publication date

12 March 2004

1 reference

European Journal of Clinical Pharmacology

6 December 2017

published in

1 reference

6 December 2017

volume

60

1 reference

6 December 2017

issue

2

1 reference

6 December 2017

page(s)

89-96

1 reference

https://scigraph.springernature.com/pub.10.1007/s00228-004-0732-5

6 December 2017

exact match

0 references

cites work

Thiopurine S-methyltransferase activity in human erythrocytes: a new HPLC method using 6-thioguanine as substrate

1 reference

12 December 2020

Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity

1 reference

12 December 2020

Measurement of thiopurine S-methyltransferase activity in human blood samples based on high-performance liquid chromatography: reference values in erythrocytes from children

1 reference

12 December 2020

Pharmacogenetics in pediatrics. Implications for practice

1 reference

12 December 2020

Human erythrocyte thiopurine methyltransferase: radiochemical microassay and biochemical properties

1 reference

12 December 2020

Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms

1 reference

12 December 2020

High incidence of secondary brain tumours after radiotherapy and antimetabolites.

1 reference

12 December 2020

Methylation of 6-mercaptopurine and 6-thioguanine by thiopurine S-methyltransferase. A comparison of activity in red blood cell samples of 199 blood donors

1 reference

12 December 2020

Biotransformation of caffeine in human liver microsomes from foetuses, neonates, infants and adults

1 reference

12 December 2020

Is thiopurine methyltransferase genetic polymorphism a major factor for withdrawal of azathioprine in rheumatoid arthritis patients?

1 reference

12 December 2020

In vitro characterization of four novel non-functional variants of the thiopurine S-methyltransferase

1 reference

12 December 2020

High-performance liquid chromatographic assay of human red blood cell thiopurine methyltransferase activity

1 reference

12 December 2020

Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity

1 reference

12 December 2020

Thiopurine methyl transferase activity: new extraction conditions for high-performance liquid chromatographic assay

1 reference

12 December 2020

Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians

1 reference

12 December 2020

A single point mutation leading to loss of catalytic activity in human thiopurine S-methyltransferase

1 reference

12 December 2020

N-acetylation in healthy and diseased children

1 reference

12 December 2020

Possible carcinogenic effect of 6-mercaptopurine on bone marrow stem cells: relation to thiopurine metabolism

1 reference

12 December 2020

Childhood leukaemia: a relationship between intracellular 6-mercaptopurine metabolites and neutropenia

1 reference

12 December 2020

Genetic determinants of the thiopurine methyltransferase intermediate activity phenotype in British Asians and Caucasians

1 reference

12 December 2020

Thiopurine methyltransferase activity in a French population: h.p.l.c. assay conditions and effects of drugs and inhibitors

1 reference

12 December 2020

Monitoring azathioprine metabolite levels and thiopurine methyl transferase (TPMT) activity in children with inflammatory bowel disease

1 reference

12 December 2020

Thiopurine methyltransferase alleles in British and Ghanaian populations

1 reference

12 December 2020

Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia

1 reference

12 December 2020

Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy

1 reference

12 December 2020

Cytochrome P450-dependent metabolism of dextromethorphan: fetal and adult studies

1 reference

12 December 2020

Thiopurine S-methyltransferase pharmacogenetics: chaperone protein association and allozyme degradation

1 reference

12 December 2020

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

1 reference

12 December 2020

A retrospective evaluation of azathioprine in severe childhood atopic eczema, using thiopurine methyltransferase levels to exclude patients at high risk of myelosuppression

1 reference

12 December 2020

Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine

1 reference

12 December 2020

Thiopurine methyltransferase activity in American white subjects and black subjects

1 reference

12 December 2020

Possible implication of thiopurine S-methyltransferase in occurrence of infectious episodes during maintenance therapy for childhood lymphoblastic leukemia with mercaptopurine.

1 reference

12 December 2020

Characterization of a variable number tandem repeat region in the thiopurine S-methyltransferase gene promoter

1 reference

12 December 2020

Human thiopurine methyltransferase activity varies with red blood cell age

1 reference

12 December 2020

Enhanced proteolysis of thiopurine S-methyltransferase (TPMT) encoded by mutant alleles in humans (TPMT*3A, TPMT*2): mechanisms for the genetic polymorphism of TPMT activity

1 reference

12 December 2020

A novel TPMT missense mutation associated with TPMT deficiency in a 5-year-old boy with ALL.

1 reference

12 December 2020

Genetic variation in response to 6-mercaptopurine for childhood acute lymphoblastic leukaemia

1 reference

12 December 2020

Thiopurine Methyltransferase in Humans: Development and Tissue Distribution

1 reference

12 December 2020

Caffeine acetylator phenotyping during maturation in infants

1 reference

12 December 2020

Human kidney thiopurine methyltransferase. Purification and biochemical properties.

1 reference

12 December 2020

Higher activity of polymorphic thiopurine S-methyltransferase in erythrocytes from neonates compared to adults

1 reference

12 December 2020

Leucopenia resulting from a drug interaction between azathioprine or 6-mercaptopurine and mesalamine, sulphasalazine, or balsalazide

1 reference

12 December 2020

Metabolism of thiopyrimidines and thiopurines. S-Methylation with S-adenosylmethionine transmethylase and catabolism in mammalian tissues

1 reference

12 December 2020

A comparison of molecular and enzyme-based assays for the detection of thiopurine methyltransferase mutations

1 reference

12 December 2020

Renal transplantation in children; the Auckland experience 1980-96.

1 reference

12 December 2020

Polymorphism of the thiopurine S-methyltransferase gene in African-Americans

1 reference

12 December 2020

Pharmacogenetics and development: are infants and children at increased risk for adverse outcomes?

1 reference

12 December 2020

Promoter and intronic sequences of the human thiopurine S-methyltransferase (TPMT) gene isolated from a human PAC1 genomic library

1 reference

12 December 2020

Differences between children and adults in thiopurine methyltransferase activity and metabolite formation during thiopurine therapy: possible role of concomitant methotrexate

1 reference

12 December 2020

Mistaken identity: misclassification of TPMT phenotype following blood transfusion

1 reference

12 December 2020

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance

1 reference

12 December 2020

Variability in the rate of 6-mercaptopurine methylation in the erythrocytes, liver and kidney in an Italian population

1 reference

12 December 2020

10.1007/S00228-004-0732-5

Identifiers

DOI

1 reference

6 December 2017

1 reference