Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Abnormalities and NQO1[original query] |
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CYP1A1*2B (Val) allele is overrepresented in a subgroup of acute myeloid leukemia patients with poor-risk karyotype associated with NRAS mutation, but not associated with FLT3 internal tandem duplication. Blood 2003 Apr 101 (7): 2770-4. Bowen David T, Frew Marion E, Rollinson Sara, Roddam Philippa L, Dring Ann, Smith Martyn T, Langabeer Stephen E, Morgan Gareth |
[Investigation of GSTT1, GSTM1 and NQO1 genes polymorphisms in myelodysplastic syndromes]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2005 Nov 26 (11): 674-7. Yang Lin, Zou Xu, Zhang Mei-rong, Zhang Yue, Hao Yu-shu, Xiao Zhi-ji |
Association of the NQO1, MPO, and XRCC1 polymorphisms and chromosome damage among workers at a petroleum refinery. Journal of toxicology and environmental health. Part A 2008 71 (5): 333-41. Kim Yang Jee, Choi Jun Yeol, Paek Domyung, Chung Hai W |
The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome. Cellular and molecular biology (Noisy-le-Grand, France) 2016 62 (7): 61-5. Bagatir G, Sirma S, Palanduz S, Ozturk S, Cefle K, Ozbek U, Yenerel M, Nalcaci |
Oxidative stress in opium users after using lead-adulterated opium: The role of genetic polymorphism. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 2018 Aug 120 571-577. Shojaeepour Saeedeh, Fazeli Mehdi, Oghabian Zohreh, Pourgholi Leyla, Mandegary A |
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