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Rapid genotyping of common deficient thiopurine S-methyltransferase alleles using the DNA-microchip technique.
Eur J Hum Genet. 2006 Sep;14(9):991-8. doi: 10.1038/sj.ejhg.5201647. Epub 2006 May 17.
Eur J Hum Genet. 2006.
PMID: 16724002
Closing the gap between science and clinical practice: the thiopurine S-methyltransferase polymorphism moves forward.
Krynetskiy EY, Evans WE.
Krynetskiy EY, et al.
Pharmacogenetics. 2004 Jul;14(7):395-6. doi: 10.1097/01.fpc.0000114753.08559.e9.
Pharmacogenetics. 2004.
PMID: 15226671
Review.
No abstract available.
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Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells.
Diouf B, Cheng Q, Krynetskaia NF, Yang W, Cheok M, Pei D, Fan Y, Cheng C, Krynetskiy EY, Geng H, Chen S, Thierfelder WE, Mullighan CG, Downing JR, Hsieh P, Pui CH, Relling MV, Evans WE.
Diouf B, et al. Among authors: krynetskiy ey.
Nat Med. 2011 Sep 25;17(10):1298-303. doi: 10.1038/nm.2430.
Nat Med. 2011.
PMID: 21946537
Free PMC article.
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Chromatin-associated proteins HMGB1/2 and PDIA3 trigger cellular response to chemotherapy-induced DNA damage.
Krynetskaia NF, Phadke MS, Jadhav SH, Krynetskiy EY.
Krynetskaia NF, et al. Among authors: krynetskiy ey.
Mol Cancer Ther. 2009 Apr;8(4):864-72. doi: 10.1158/1535-7163.MCT-08-0695.
Mol Cancer Ther. 2009.
PMID: 19372559
Free PMC article.
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