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Journal Abstract Search

595 related items for PubMed ID: 16646086

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  • 4. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
    Tosi S, Hughes J, Scherer SW, Nakabayashi K, Harbott J, Haas OA, Cazzaniga G, Biondi A, Kempski H, Kearney L.
    Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
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  • 5. Graft versus leukemia effect after haploidentical HSCT in a MLL-negative infant AML with HLXB9/ETV6 rearrangement.
    Hauer J, Tosi S, Schuster FR, Harbott J, Kolb HJ, Borkhardt A.
    Pediatr Blood Cancer; 2008 Apr; 50(4):921-3. PubMed ID: 17960638
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  • 6. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
    Murga Penas EM, Cools J, Algenstaedt P, Hinz K, Seeger D, Schafhausen P, Schilling G, Marynen P, Hossfeld DK, Dierlamm J.
    Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
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  • 7. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P, Harrison CJ, Jarosová M, Foroni L.
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
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  • 10. ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
    Strehl S, Nebral K, König M, Harbott J, Strobl H, Ratei R, Struski S, Bielorai B, Lessard M, Zimmermann M, Haas OA, Izraeli S.
    Clin Cancer Res; 2008 Feb 15; 14(4):977-83. PubMed ID: 18281529
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  • 11. MNX1-ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines.
    Taketani T, Taki T, Sako M, Ishii T, Yamaguchi S, Hayashi Y.
    Cancer Genet Cytogenet; 2008 Oct 15; 186(2):115-9. PubMed ID: 18940475
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  • 13. Cytogenetic and molecular heterogeneity of 7q36/12p13 rearrangements in childhood AML.
    Simmons HM, Oseth L, Nguyen P, O'Leary M, Conklin KF, Hirsch B.
    Leukemia; 2002 Dec 15; 16(12):2408-16. PubMed ID: 12454746
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  • 14. Activation of HLXB9 by juxtaposition with MYB via formation of t(6;7)(q23;q36) in an AML-M4 cell line (GDM-1).
    Nagel S, Kaufmann M, Scherr M, Drexler HG, MacLeod RA.
    Genes Chromosomes Cancer; 2005 Feb 15; 42(2):170-8. PubMed ID: 15540222
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  • 16. ETV6-ARNT fusion in a patient with childhood T lymphoblastic leukemia.
    Otsubo K, Kanegane H, Eguchi M, Eguchi-Ishimae M, Tamura K, Nomura K, Abe A, Ishii E, Miyawaki T.
    Cancer Genet Cytogenet; 2010 Oct 01; 202(1):22-6. PubMed ID: 20804916
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  • 18. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.
    Odero MD, Vizmanos JL, Román JP, Lahortiga I, Panizo C, Calasanz MJ, Zeleznik-Le NJ, Rowley JD, Novo FJ.
    Genes Chromosomes Cancer; 2002 Sep 01; 35(1):11-9. PubMed ID: 12203785
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  • 19. Correlation between the ETV6/CBFA2 (TEL/AML1) fusion gene and karyotypic abnormalities in children with B-cell precursor acute lymphoblastic leukemia.
    Fears S, Vignon C, Bohlander SK, Smith S, Rowley JD, Nucifora G.
    Genes Chromosomes Cancer; 1996 Oct 01; 17(2):127-35. PubMed ID: 8913730
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  • 20. A t(12;17)(p13;q12) identifies a distinct TEL rearrangement-negative subtype of precursor-B acute lymphoblastic leukemia.
    Reid AG, Seppa L, von der Weid N, Niggli FK, Betts DR.
    Cancer Genet Cytogenet; 2006 Feb 01; 165(1):64-9. PubMed ID: 16490598
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