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Volumn 49, Issue 3, 2010, Pages 253-259

Cytogenetics of long-term survivors of ETV6-RUNX1 fusion positive acute lymphoblastic leukemia

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR ETV6; TRANSCRIPTION FACTOR RUNX1;

EID: 76649119108     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.20736     Document Type: Article
Times cited : (5)

References (18)
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  • 3
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    • Attarbaschi A, Mann G, Konig M, Dworzak MN, Trebo MM, Muhlegger N, Gadner H, Haas OA. 2004. Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: An interphase FISH analysis. Leukemia 18:1611-1616.
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    • Attarbaschi, A.1    Mann, G.2    Konig, M.3    Dworzak, M.N.4    Trebo, M.M.5    Muhlegger, N.6    Gadner, H.7    Haas, O.A.8
  • 4
    • 33646589709 scopus 로고    scopus 로고
    • Near-tetraploidy in childhood B-cell precursor acute lymphoblastic leukemia is a highly specific feature of ETV6/RUNX1-positive leukemic cases
    • Attarbaschi A, Mann G, Konig M, Steiner M, Dworzak MN, Gadner H, Haas OA. 2006. Near-tetraploidy in childhood B-cell precursor acute lymphoblastic leukemia is a highly specific feature of ETV6/RUNX1-positive leukemic cases. Genes Chromosomes Cancer 45:608-611.
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    • Attarbaschi, A.1    Mann, G.2    Konig, M.3    Steiner, M.4    Dworzak, M.N.5    Gadner, H.6    Haas, O.A.7
  • 5
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    • Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia
    • Attarbaschi A, Mann G, Strehl S, Konig M, Steiner M, Jeitler V, Lion T, Dworzak MN, Gadner H, Haas OA. 2007. Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia. Leukemia 21:584-586.
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    • Attarbaschi, A.1    Mann, G.2    Strehl, S.3    Konig, M.4    Steiner, M.5    Jeitler, V.6    Lion, T.7    Dworzak, M.N.8    Gadner, H.9    Haas, O.A.10
  • 7
    • 0035003350 scopus 로고    scopus 로고
    • The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: A valuable resource for patient management
    • Harrison CJ, Martineau M, Secker-Walker LM. 2001. The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: A valuable resource for patient management. Br J Haematol 113:3-10.
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    • 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. 2008. Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia. Leukemia 22:114-123.
    • (2008) Leukemia , vol.22 , pp. 114-123
    • Jalali, G.R.1    An, Q.2    Konn, Z.J.3    Worley, H.4    Wright, S.L.5    Harrison, C.J.6    Strefford, J.C.7    Martineau, M.8
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    • 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
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    • Raimondi SC, Zhou Y, Shurtleff SA, Rubnitz JE, Pui CH, Behm FG. 2006. Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: Association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable outcome. Cancer Genet Cytogenet 169:50-57.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.