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Journal Abstract Search

338 related items for PubMed ID: 20124335

  • 1. 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; 40(1):80-4. PubMed ID: 20124335
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  • 3. PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
    Zhang Y, Emmanuel N, Kamboj G, Chen J, Shurafa M, Van Dyke DL, Wiktor A, Rowley JD.
    Genes Chromosomes Cancer; 2004 Aug; 40(4):365-70. PubMed ID: 15188461
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  • 10. Molecular characterization of AML with ins(21;8)(q22;q22q22) reveals similarity to t(8;21) AML.
    Rücker FG, Bullinger L, Gribov A, Sill M, Schlenk RF, Lichter P, Döhner H, Döhner K.
    Genes Chromosomes Cancer; 2011 Jan; 50(1):51-8. PubMed ID: 20967878
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  • 15. Acute myeloid leukemia with a RUNX1-RUNX1T1 t(1;21;8)(q21;q22;q22) novel variant: a case report and review of the literature.
    Kim H, Moon HW, Hur M, Yun YM, Lee MH.
    Acta Haematol; 2011 Jan; 125(4):237-41. PubMed ID: 21325813
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  • 19. Persistent altered fusion transcript splicing identifies RUNX1-RUNX1T1+ AML patients likely to relapse.
    Ommen HB, Ostergaard M, Yan M, Braendstrup K, Zhang DE, Hokland P.
    Eur J Haematol; 2010 Feb 01; 84(2):128-32. PubMed ID: 19891700
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