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Journal Abstract Search

147 related items for PubMed ID: 17690704

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  • 2. Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3.
    Davidsson J, Andersson A, Paulsson K, Heidenblad M, Isaksson M, Borg A, Heldrup J, Behrendtz M, Panagopoulos I, Fioretos T, Johansson B.
    Hum Mol Genet; 2007 Sep 15; 16(18):2215-25. PubMed ID: 17613536
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  • 7. CpG island methylator phenotype redefines the prognostic effect of t(12;21) in childhood acute lymphoblastic leukemia.
    Roman-Gomez J, Jimenez-Velasco A, Agirre X, Castillejo JA, Navarro G, Calasanz MJ, Garate L, San Jose-Eneriz E, Cordeu L, Prosper F, Heiniger A, Torres A.
    Clin Cancer Res; 2006 Aug 15; 12(16):4845-50. PubMed ID: 16914570
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  • 10. ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications.
    Martineau M, Jalali GR, Barber KE, Broadfield ZJ, Cheung KL, Lilleyman J, Moorman AV, Richards S, Robinson HM, Ross F, Harrison CJ.
    Genes Chromosomes Cancer; 2005 May 15; 43(1):54-71. PubMed ID: 15704129
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  • 11. A Double Negative Loop Comprising ETV6/RUNX1 and MIR181A1 Contributes to Differentiation Block in t(12;21)-Positive Acute Lymphoblastic Leukemia.
    Yang YL, Yen CT, Pai CH, Chen HY, Yu SL, Lin CY, Hu CY, Jou ST, Lin DT, Lin SR, Lin SW.
    PLoS One; 2015 May 15; 10(11):e0142863. PubMed ID: 26580398
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  • 12. Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.
    Lo KC, Chalker J, Strehl S, Neat M, Smith O, Dastugue N, Kearney L, Izraeli S, Kempski H, Cowell JK.
    Br J Haematol; 2008 Sep 15; 142(6):934-45. PubMed ID: 18557744
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  • 13. Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.
    Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S.
    Cancer Genet Cytogenet; 2008 Aug 15; 185(1):43-6. PubMed ID: 18656693
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  • 14. RUNX1 aberrations in ETV6/RUNX1-positive and ETV6/RUNX1-negative patients: its hemato-pathological and prognostic significance in a large cohort (619 cases) of ALL.
    Pais AP, Amare Kadam PS, Raje GC, Banavali S, Parikh P, Kurkure P, Arora B, Gujral S, Kumar SA, Badrinath Y.
    Pediatr Hematol Oncol; 2008 Sep 15; 25(6):582-97. PubMed ID: 18728978
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  • 15. Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institution.
    Pérez-Vera P, Montero-Ruiz O, Frías S, Ulloa-Avilés V, Cárdenas-Cardós R, Paredes-Aguilera R, Rivera-Luna R, Carnevale A.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):140-5. PubMed ID: 16213362
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  • 19. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
    von Bergh AR, van Drunen E, van Wering ER, van Zutven LJ, Hainmann I, Lönnerholm G, Meijerink JP, Pieters R, Beverloo HB.
    Genes Chromosomes Cancer; 2006 Aug 15; 45(8):731-9. PubMed ID: 16646086
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  • 20. ETV6-RUNX1 fusion gene and additional genetic changes in infant leukemia: a genome-wide analysis.
    Emerenciano M, Bungaro S, Cazzaniga G, Dorea MD, Coser VM, Magalhães IQ, Biondi A, Pombo-de-Oliveira MS.
    Cancer Genet Cytogenet; 2009 Sep 15; 193(2):86-92. PubMed ID: 19665068
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