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
المؤلفون الرئيسيون: | Lennard, L, Cartwright, C, Wade, R, Richards, S, Mitchell, C, Kinsey, S, Eden, T, Lilleyman, J, Vora, A |
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التنسيق: | Conference item |
منشور في: |
2010
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مواد مشابهة
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Detection of Thiopurine S-Methyltransferase (TPMT) Polymorphisms TPMT*3A, TPMT*3B and TPMT*3C in Children with Acute Lymphoblastic Leukemia
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Common Polymorphism’s Analysis of Thiopurine S-Methyltransferase (TPMT) in Iranian Population
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منشور في: (2009-01-01) -
Thiopurine methyltransferase genotype-phenotype discordance and thiopurine active metabolite formation in childhood acute lymphoblastic leukaemia.
حسب: Lennard, L, وآخرون
منشور في: (2013) -
Thiopurine methyltransferase (TPMT), nudix hydrolase 15 (NUDT-15) and methylene tetrahydrofolate reductase (MTHFR)polymorphisms in children with acute lymphoblastic leukaemia
حسب: Srikanth Marda, وآخرون
منشور في: (2022-01-01) -
Positive TPMT genotype-phenotype correlation underscores importance of TPMT genotyping for personalized thiopurine dosing
حسب: Hui-min, Neoh, وآخرون
منشور في: (2012)