The thiopurine methyltransferase TPMT *1/*3A genotype is associated with a better treatment outcome in the UK ALL97 trial for childhood acute lymphoblastic leukaemia; TPMT heterozygosity is not associated with secondary cancers

The thiopurine methyltransferase TPMT 1/3A genotype is associated with a better treatment outcome in the UK ALL97 trial for childhood acute lymphoblastic leukaemia; TPMT heterozygosity is not associated with secondary cancers

Bibliografiska uppgifter
Huvudupphovsmän:	Lennard, L, Cartwright, C, Wade, R, Richards, S, Mitchell, C, Kinsey, S, Eden, T, Lilleyman, J, Vora, A
Materialtyp:	Conference item
Publicerad:	2010

Liknande verk

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Benefit of dexamethasone compared with prednisolone for childhood acute lymphoblastic leukaemia: results of the UK Medical Research Council ALL97 randomized trial.
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TPMT and NUDT15 testing for thiopurine therapy: A major tertiary hospital experience and lessons learned
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TPMT Genetic Variability and Its Association with Hematotoxicity in Indonesian Children with Acute Lymphoblastic Leukemia in Maintenance Therapy
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Thiopurine S-Methyltransferase Polymorphism in Iraqi Paediatric Patients with Acute Lymphoblastic Leukaemia
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The impact of risk stratification by early bone-marrow response in childhood lymphoblastic leukaemia: results from the United Kingdom Medical Research Council trial ALL97 and ALL97/99.
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Implications of Tioguanine Dosing in IBD Patients with a TPMT Deficiency
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Meta-analysis of randomised trials comparing thiopurines in childhood acute lymphoblastic leukaemia
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av: Jeny Bazalar-Montoya, et al.
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NUDT15 and TPMT polymorphisms in three distinct native populations of the Brazilian Amazon
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Pharmacogenetic variants in TPMT alter cellular responses to cisplatin in inner ear cell lines.
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Effects of TPMT, NUDT15, and ITPA Genetic Variants on 6-Mercaptopurine Toxicity for Pediatric Patients With Acute Lymphoblastic Leukemia in Yunnan of China
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