TPMT genetic variations in populations of the Russian Federation. - Wikidata - awgldk - TriplyDB

TPMT genetic variations in populations of the Russian Federation.

TPMT genetic variations in populations of the Russian Federation.

http://www.wikidata.org/entity/Q37477625

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Pharmacogenomics in Pediatric Oncology: Review of Gene-Drug Associations for Clinical Use Frequency of thiopurine S-methyltransferase mutant alleles in indigenous and admixed Guatemalan patients with acute lymphoblastic leukemia.Diagnostic microarrays in hematologic oncology: applications of high- and low-density arrays.Therapies on the horizon for childhood acute lymphoblastic leukemia.Analysis of thiopurine S-methyltransferase phenotype-genotype in a Tunisian population with Crohn's disease.Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population.Thiopurine S-Methyltransferase as a Pharmacogenetic Biomarker: Significance of Testing and Review of Major Methods.Genetic Polymorphism of Thiopurine S-methyltransferase in Children with Acute Lymphoblastic Leukemia in Jordan Influence of thiopurine methyltransferase gene polymorphism on Egyptian children with acute lymphoblastic leukaemia.The frequency and distribution of thiopurine S-methyltransferase alleles in south Iranian population.

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TPMT genetic variations in populations of the Russian Federation.

http://www.wikidata.org/entity/Q37477625

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on February 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

TPMT genetic variations in populations of the Russian Federation.

@en

TPMT genetic variations in populations of the Russian Federation.

@nl

type

label

TPMT genetic variations in populations of the Russian Federation.

@en

TPMT genetic variations in populations of the Russian Federation.

@nl

prefLabel

TPMT genetic variations in populations of the Russian Federation.

@en

TPMT genetic variations in populations of the Russian Federation.

@nl

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Pediatric Blood & Cancer

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TPMT genetic variations in populations of the Russian Federation

@en

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Alexander G Roumyantsev

http://www.w3.org/2001/XMLSchema#string

Elena V Samochatova

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Eugene Y Krynetski

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Natalia F Krynetskaia

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Natalia V Chupova

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Olga A Maiorova

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Olga E Fedorova

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Olga Makarova

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Raul C Ribeiro

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Tatyana V Nasedkina

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P2860

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

Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity

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

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

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

Pharmacogenetics as a molecular basis for individualized drug therapy: the thiopurine S-methyltransferase paradigm.

Pharmacogenomics: translating functional genomics into rational therapeutics.

Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus.

Improved outcome in childhood acute lymphoblastic leukemia despite reduced use of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90. German-Austrian-Swiss ALL-BFM Study Group.

Genetic polymorphism of thiopurine S-methyltransferase: molecular mechanisms and clinical importance.

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203-208

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scholarly article

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10.1002/PBC.21837

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2

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52

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Andrey S Glotov

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2009-02-01T00:00:00Z

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23498717

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19034904

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2794198

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