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dc.contributor.authorBarbosa, Cynara Gomes-
dc.contributor.authorSouza, Claudio Lima-
dc.contributor.authorMoura Neto, José Pereira de-
dc.contributor.authorArruda, Maria da Glória Bomfim-
dc.contributor.authorBarreto, José Henrique Silva-
dc.contributor.authorReis, Mitermayer Galvão-
dc.contributor.authorGoncalves, Marilda Souza-
dc.creatorBarbosa, Cynara Gomes-
dc.creatorSouza, Claudio Lima-
dc.creatorMoura Neto, José Pereira de-
dc.creatorArruda, Maria da Glória Bomfim-
dc.creatorBarreto, José Henrique Silva-
dc.creatorReis, Mitermayer Galvão-
dc.creatorGoncalves, Marilda Souza-
dc.date.accessioned2011-09-08T18:54:23Z-
dc.date.available2011-09-08T18:54:23Z-
dc.date.issued2008-
dc.identifier.issn1415-4757-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/2619-
dc.descriptionp.29-32pt_BR
dc.description.abstractMethylenetetrahydrofolate reductase (MTHFR: EC 1.5.1.20) polymorphisms are associated to acute lymphoid leukemia in different populations. We used the polymerase chain reaction and the restriction fragment length polymorphism method (PCR-RFLP) to investigate MTHFR C677T and A1298C polymorphism frequencies in 67 patients with chronic myeloid leukemia (CML), 27 with acute myeloid leukemia FAB subtype M3 (AML-M3) and 100 apparently healthy controls. The MTHFR mutant allele frequencies were as follows: CML = 17.2% for C677T, 21.6% for A1298C; AML-M3 = 22.2% for C677T, 24.1% for A1298C; and controls = 20.5% for C677T, 21% for A1298C. Taken together, our results provide evidence that MTHFR polymorphisms have no influence on the development of CML or AML-M3.pt_BR
dc.language.isoenpt_BR
dc.subjectAMLpt_BR
dc.subjectCMLpt_BR
dc.subjectMTHFR polymorphismspt_BR
dc.titleMethylenetetrahydrofolate reductase polymorphisms in myeloid leukemia patients from Northeastern Brazilpt_BR
dc.title.alternativeGenetics and Molecular Biologypt_BR
dc.typeArtigo de Periódicopt_BR
dc.description.localpubSão paulopt_BR
dc.identifier.number31(1):29-32pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (FAR)

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