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Journal Abstract Search

500 related items for PubMed ID: 19167608

  • 1. Marker chromosomes are a significant mechanism of high-level RUNX1 gene amplification in hematologic malignancies.
    Moosavi SA, Sanchez J, Adeyinka A.
    Cancer Genet Cytogenet; 2009 Feb; 189(1):24-8. PubMed ID: 19167608
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  • 2. Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.
    Jang JH, Yoo EH, Kim HJ, Kim DH, Jung CW, Kim SH.
    Ann Clin Lab Sci; 2010 Feb; 40(1):80-4. PubMed ID: 20124335
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  • 3. High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia.
    García-Casado Z, Cervera J, Verdeguer A, Tasso M, Valencia A, Pajuelo JC, Mena-Duran AV, Barragán E, Blanes M, Bolufer P, Sanz MA.
    Cancer Genet Cytogenet; 2006 Oct 15; 170(2):171-4. PubMed ID: 17011991
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  • 4. 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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  • 5. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
    Dai H, Xue Y, Pan J, Wu Y, Wang Y, Shen J, Zhang J.
    Cancer Genet Cytogenet; 2007 Sep 15; 177(2):120-4. PubMed ID: 17854666
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  • 8. Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?
    Deluche L, Joha S, Corm S, Daudignon A, Geffroy S, Quief S, Villenet C, Kerckaert JP, Laï JL, Preudhomme C, Roche-Lestienne C.
    Genes Chromosomes Cancer; 2008 Dec 15; 47(12):1110-7. PubMed ID: 18767145
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  • 9. Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22).
    Sakai I, Tamura T, Narumi H, Uchida N, Yakushijin Y, Hato T, Fujita S, Yasukawa M.
    Genes Chromosomes Cancer; 2005 Nov 15; 44(3):265-70. PubMed ID: 16015645
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  • 12. 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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  • 18. Amplification of BCR-ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia.
    Phan CL, Megat Baharuddin PJ, Chin LP, Zakaria Z, Yegappan S, Sathar J, Tan SM, Purushothaman V, Chang KM.
    Cancer Genet Cytogenet; 2008 Jan 01; 180(1):60-4. PubMed ID: 18068536
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  • 19. RUNX1 amplification in lineage conversion of childhood B-cell acute lymphoblastic leukemia to acute myelogenous leukemia.
    Podgornik H, Debeljak M, Zontar D, Cernelc P, Prestor VV, Jazbec J.
    Cancer Genet Cytogenet; 2007 Oct 01; 178(1):77-81. PubMed ID: 17889714
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