Frequency of thiopurine S-methyltransferase mutant alleles in indigenous and admixed Guatemalan patients with acute lymphoblastic leukemia.

Item

http://www.wikidata.org/entity/Q35984724

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@ast

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@en

type

Item

label

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@ast

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@en

prefLabel

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@ast

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@en

P1476

Frequency of thiopurine S-meth ...... acute lymphoblastic leukemia.

@en

P2093

Claudia Garrido

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

Daphney Rigaud Soriano

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

Giovana Bendfeldt Avila

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

Michael Dean

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

Petra Müllers

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

Silvia Jimenez-Morales

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

Veronica Giron Santizo

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

P2860

Clinical Pharmacogenetics Implementation Consortium guidelines for thiopurine methyltransferase genotype and thiopurine dosing

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

Origin of Mayans according to HLA genes and the uniqueness of Amerindians

Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus

Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: preliminary data from the patterns of haplotypic association with two CA repeats.

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

Thiopurine S-methyltransferase (TPMT) polymorphisms in children with acute lymphoblastic leukemia, and the need for reduction or cessation of 6-mercaptopurine doses during maintenance therapy: the Polish multicenter analysis.

Clinical pharmacology and pharmacogenetics of thiopurines.

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

P2888

s12032-013-0474-2

P304

474

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

P31

scholarly article

P356

10.1007/S12032-013-0474-2

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

P433

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

P478

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

P577

2013-02-03T00:00:00Z

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

P5875

235398201

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

P698

23377985

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

P932

4545520

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