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PUBMED FOR HANDHELDS

Journal Abstract Search


635 related items for PubMed ID: 16467864

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  • 4. Mutations of genes in the receptor tyrosine kinase (RTK)/RAS-BRAF signal transduction pathway in therapy-related myelodysplasia and acute myeloid leukemia.
    Christiansen DH, Andersen MK, Desta F, Pedersen-Bjergaard J.
    Leukemia; 2005 Dec; 19(12):2232-40. PubMed ID: 16281072
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  • 5. AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
    Migas A, Savva N, Mishkova O, Aleinikova OV.
    Pediatr Blood Cancer; 2011 Oct; 57(4):583-7. PubMed ID: 21294243
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  • 8. Implications of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome (MDS): future molecular therapeutic directions for MDS.
    Harada H, Harada Y, Kimura A.
    Curr Cancer Drug Targets; 2006 Sep; 6(6):553-65. PubMed ID: 17017876
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  • 9. Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome.
    Nakao M, Horiike S, Fukushima-Nakase Y, Nishimura M, Fujita Y, Taniwaki M, Okuda T.
    Br J Haematol; 2004 Jun; 125(6):709-19. PubMed ID: 15180860
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  • 11. Genetics of therapy-related myelodysplasia and acute myeloid leukemia.
    Pedersen-Bjergaard J, Andersen MK, Andersen MT, Christiansen DH.
    Leukemia; 2008 Feb; 22(2):240-8. PubMed ID: 18200041
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  • 13. Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations.
    Christiansen DH, Desta F, Andersen MK, Pedersen-Bjergaard J.
    Genes Chromosomes Cancer; 2007 Jun; 46(6):517-21. PubMed ID: 17330262
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  • 15. RUNX1 gene mutation in primary myelodysplastic syndrome--the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome.
    Chen CY, Lin LI, Tang JL, Ko BS, Tsay W, Chou WC, Yao M, Wu SJ, Tseng MH, Tien HF.
    Br J Haematol; 2007 Nov; 139(3):405-14. PubMed ID: 17910630
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  • 16. Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
    Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR.
    Eur J Haematol; 2005 Jan; 74(1):47-53. PubMed ID: 15613106
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  • 19. New mechanisms of AML1 gene alteration in hematological malignancies.
    Roumier C, Fenaux P, Lafage M, Imbert M, Eclache V, Preudhomme C.
    Leukemia; 2003 Jan; 17(1):9-16. PubMed ID: 12529654
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