Similar articles for PMID: 16041371

Year	Number of Results
1998	2
2002	2
2003	2
2004	3
2005	3
2006	4
2007	2
2008	1
2009	2
2010	2
2011	2
2012	5
2013	1
2014	3
2024	0

1

Karyotypic abnormalities create discordance of germline genotype and cancer cell phenotypes.

Cheng Q, Yang W, Raimondi SC, Pui CH, Relling MV, Evans WE. Cheng Q, et al. Nat Genet. 2005 Aug;37(8):878-82. doi: 10.1038/ng1612. Epub 2005 Jul 24. Nat Genet. 2005. PMID: 16041371

2

Epigenetic regulation of human gamma-glutamyl hydrolase activity in acute lymphoblastic leukemia cells.

Cheng Q, Cheng C, Crews KR, Ribeiro RC, Pui CH, Relling MV, Evans WE. Cheng Q, et al. Am J Hum Genet. 2006 Aug;79(2):264-74. doi: 10.1086/505645. Epub 2006 Jun 6. Am J Hum Genet. 2006. PMID: 16826517 Free PMC article.

3

Thiopurine S-methyltransferase phenotype-genotype correlation in children with acute lymphoblastic leukemia.

Chrzanowska M, Kuehn M, Januszkiewicz-Lewandowska D, Kurzawski M, Droździk M. Chrzanowska M, et al. Acta Pol Pharm. 2012 May-Jun;69(3):405-10. Acta Pol Pharm. 2012. PMID: 22594254 Free article.

4

[Analysis of genetic polymorphisms of thiopurine S-methyltransferase (TPMT) in Mexican pediatric patients with cancer].

Moreno-Guerrero SS, Ramírez-Pacheco A, Dorantes-Acosta EM, Medina-Sanson A. Moreno-Guerrero SS, et al. Rev Invest Clin. 2013 Mar-Apr;65(2):156-64. Rev Invest Clin. 2013. PMID: 23844534 Spanish.

5

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.

Peregud-Pogorzelski J, Tetera-Rudnicka E, Kurzawski M, Brodkiewicz A, Adrianowska N, Mlynarski W, Januszkiewicz D, Drozdzik M. Peregud-Pogorzelski J, et al. Pediatr Blood Cancer. 2011 Oct;57(4):578-82. doi: 10.1002/pbc.23013. Epub 2011 Feb 11. Pediatr Blood Cancer. 2011. PMID: 21319286

6

Should TPMT genotype and activity be used to monitor 6-mercaptopurine treatment in children with acute lymphoblastic leukaemia?

Fakhoury M, Andreu-Gallien J, Mahr A, Medard Y, Azougagh S, Vilmer E, Jacqz-Aigrain E. Fakhoury M, et al. J Clin Pharm Ther. 2007 Dec;32(6):633-9. doi: 10.1111/j.1365-2710.2007.00858.x. J Clin Pharm Ther. 2007. PMID: 18021342

7

Thiopurine S-methyltransferase genotype-phenotype concordance: used as a quality assurance tool to help control the phenotype assay.

Ford L, Kampanis P, Berg J. Ford L, et al. Ann Clin Biochem. 2009 Mar;46(Pt 2):152-4. doi: 10.1258/acb.2008.008167. Epub 2009 Jan 22. Ann Clin Biochem. 2009. PMID: 19164342

8

Isolation of a human thiopurine S-methyltransferase (TPMT) complementary DNA with a single nucleotide transition A719G (TPMT*3C) and its association with loss of TPMT protein and catalytic activity in humans.

Loennechen T, Yates CR, Fessing MY, Relling MV, Krynetski EY, Evans WE. Loennechen T, et al. Clin Pharmacol Ther. 1998 Jul;64(1):46-51. doi: 10.1016/S0009-9236(98)90021-2. Clin Pharmacol Ther. 1998. PMID: 9695718

9

Genetic polymorphism of thiopurine S-methyltransferase in Argentina.

Laróvere LE, de Kremer RD, Lambooy LH, De Abreu RA. Laróvere LE, et al. Ann Clin Biochem. 2003 Jul;40(Pt 4):388-93. doi: 10.1258/000456303766477039. Ann Clin Biochem. 2003. PMID: 12880540

10

Genetic polymorphism of γ-glutamyl hydrolase in Chinese acute leukemia children and identification of a novel double nonsynonymous mutation.

Chen X, Wen F, Yue L, Li C. Chen X, et al. Pediatr Hematol Oncol. 2012 May;29(4):303-12. doi: 10.3109/08880018.2012.657767. Pediatr Hematol Oncol. 2012. PMID: 22568793 Clinical Trial.

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