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Journal Abstract Search

173 related items for PubMed ID: 11721958

  • 1. Point mutations of the RUNx1/AML1 gene in sporadic and familial myeloid leukemias.
    Osato M, Yanagida M, Shigesada K, Ito Y.
    Int J Hematol; 2001 Oct; 74(3):245-51. PubMed ID: 11721958
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  • 2. Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia.
    Osato M.
    Oncogene; 2004 May 24; 23(24):4284-96. PubMed ID: 15156185
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  • 3. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
    Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N, Shigesada K, Ito Y, Benson KF, Raskind WH, Rossier C, Antonarakis SE, Israels S, McNicol A, Weiss H, Horwitz M, Scott HS.
    Blood; 2002 Feb 15; 99(4):1364-72. PubMed ID: 11830488
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  • 7. Familial mutations of the transcription factor RUNX1 (AML1, CBFA2) predispose to acute myeloid leukemia.
    Ganly P, Walker LC, Morris CM.
    Leuk Lymphoma; 2004 Jan 15; 45(1):1-10. PubMed ID: 15061191
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  • 8. Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
    Minelli A, Maserati E, Rossi G, Bernardo ME, De Stefano P, Cecchini MP, Valli R, Albano V, Pierani P, Leszl A, Sainati L, Lo Curto F, Danesino C, Locatelli F, Pasquali F.
    Genes Chromosomes Cancer; 2004 Jul 15; 40(3):165-71. PubMed ID: 15138996
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  • 9. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia.
    Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T.
    Blood; 2004 Mar 15; 103(6):2316-24. PubMed ID: 14615365
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  • 14. A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.
    Walker LC, Stevens J, Campbell H, Corbett R, Spearing R, Heaton D, Macdonald DH, Morris CM, Ganly P.
    Br J Haematol; 2002 Jun 15; 117(4):878-81. PubMed ID: 12060124
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  • 15. AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.
    Taketani T, Taki T, Takita J, Tsuchida M, Hanada R, Hongo T, Kaneko T, Manabe A, Ida K, Hayashi Y.
    Genes Chromosomes Cancer; 2003 Sep 15; 38(1):1-7. PubMed ID: 12874780
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  • 18. A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies.
    Buijs A, Poddighe P, van Wijk R, van Solinge W, Borst E, Verdonck L, Hagenbeek A, Pearson P, Lokhorst H.
    Blood; 2001 Nov 01; 98(9):2856-8. PubMed ID: 11675361
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  • 19. Crystallization and preliminary studies of the DNA-binding runt domain of AML1.
    Bäckström S, Huang SH, Wolf-Watz M, Xie XQ, Härd T, Grundström T, Sauer UH.
    Acta Crystallogr D Biol Crystallogr; 2001 Feb 01; 57(Pt 2):269-71. PubMed ID: 11173476
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