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Journal Abstract Search

147 related items for PubMed ID: 17690704

  • 1. Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region.
    Lilljebjörn H, Heidenblad M, Nilsson B, Lassen C, Horvat A, Heldrup J, Behrendtz M, Johansson B, Andersson A, Fioretos T.
    Leukemia; 2007 Oct; 21(10):2137-44. PubMed ID: 17690704
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  • 4. Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia.
    Jalali GR, An Q, Konn ZJ, Worley H, Wright SL, Harrison CJ, Strefford JC, Martineau M.
    Leukemia; 2008 Jan; 22(1):114-23. PubMed ID: 17972957
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  • 5. Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia.
    Kjeldsen E.
    Exp Mol Pathol; 2016 Aug; 101(1):38-43. PubMed ID: 27215399
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  • 6. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
    Lundin C, Hjorth L, Behrendtz M, Nordgren A, Palmqvist L, Andersen MK, Biloglav A, Forestier E, Paulsson K, Johansson B.
    Genes Chromosomes Cancer; 2012 Feb; 51(2):196-206. PubMed ID: 22072402
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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 Feb; 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; 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; 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; 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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  • 16. Fluorescence in situ hybridization study of TEL/AML1 fusion and other abnormalities involving TEL and AML1 genes. Correlation with cytogenetic findings and prognostic value in children with acute lymphocytic leukemia.
    Martínez-Ramírez A, Urioste M, Contra T, Cantalejo A, Tavares A, Portero JA, López-Ibor B, Bernacer M, Soto C, Cigudosa JC, Benítez J.
    Haematologica; 2001 Dec 15; 86(12):1245-53. PubMed ID: 11726315
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  • 17. Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
    Paulsson K, Heidenblad M, Mörse H, Borg A, Fioretos T, Johansson B.
    Leukemia; 2006 Nov 15; 20(11):2002-7. PubMed ID: 16990785
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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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