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221 related items for PubMed ID: 9136917

  • 1. Tandem duplication of the MLL gene in myelodysplastic syndrome-derived overt leukemia with trisomy 11.
    Yamamoto K, Hamaguchi H, Nagata K, Kobayashi M, Taniwaki M.
    Am J Hematol; 1997 May; 55(1):41-5. PubMed ID: 9136917
    [Abstract] [Full Text] [Related]

  • 2. Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML.
    Schnittger S, Kinkelin U, Schoch C, Heinecke A, Haase D, Haferlach T, Büchner T, Wörmann B, Hiddemann W, Griesinger F.
    Leukemia; 2000 May; 14(5):796-804. PubMed ID: 10803509
    [Abstract] [Full Text] [Related]

  • 3. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents.
    Andersen MK, Christiansen DH, Kirchhoff M, Pedersen-Bjergaard J.
    Genes Chromosomes Cancer; 2001 May; 31(1):33-41. PubMed ID: 11284033
    [Abstract] [Full Text] [Related]

  • 4. Trisomy 11 and a complex t(11;11;22) in a patient with acute myelomonocytic leukemia (AML-M4) following myelodysplasia (MDS): a cytogenetic study of a mechanism of leukemogenesis.
    Bernasconi P, Cavigliano PM, Boni M, Malcovati L, Astori C, Castagnola C, Pagnucco G, Vanelli L, Calatroni S, Caresana M, Lazzarino M, Bernasconi C.
    Cancer Genet Cytogenet; 2000 Jan 15; 116(2):111-8. PubMed ID: 10640142
    [Abstract] [Full Text] [Related]

  • 5. Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11.
    Smith A, Robson L, Heaps LS, Sharma P, Dunlop L, Bhave A, Bradstock K.
    Cancer Genet Cytogenet; 2001 Sep 15; 129(2):173-6. PubMed ID: 11566351
    [Abstract] [Full Text] [Related]

  • 6. Partial duplication of the MLL gene in acute myelogenous leukemia without karyotypic aberration.
    Kwong YL.
    Cancer Genet Cytogenet; 1997 Aug 15; 97(1):20-4. PubMed ID: 9242213
    [Abstract] [Full Text] [Related]

  • 7. Clinical and biological implications of partial tandem duplication of the MLL gene in acute myeloid leukemia without chromosomal abnormalities at 11q23.
    Shiah HS, Kuo YY, Tang JL, Huang SY, Yao M, Tsay W, Chen YC, Wang CH, Shen MC, Lin DT, Lin KH, Tien HF.
    Leukemia; 2002 Feb 15; 16(2):196-202. PubMed ID: 11840285
    [Abstract] [Full Text] [Related]

  • 8. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
    Super HG, Strissel PL, Sobulo OM, Burian D, Reshmi SC, Roe B, Zeleznik-Le NJ, Diaz MO, Rowley JD.
    Genes Chromosomes Cancer; 1997 Oct 15; 20(2):185-95. PubMed ID: 9331569
    [Abstract] [Full Text] [Related]

  • 9. Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.
    Zatkova A, Ullmann R, Rouillard JM, Lamb BJ, Kuick R, Hanash SM, Schnittger S, Schoch C, Fonatsch C, Wimmer K.
    Genes Chromosomes Cancer; 2004 Apr 15; 39(4):263-76. PubMed ID: 14978788
    [Abstract] [Full Text] [Related]

  • 10. All patients with the T(11;16)(q23;p13.3) that involves MLL and CBP have treatment-related hematologic disorders.
    Rowley JD, Reshmi S, Sobulo O, Musvee T, Anastasi J, Raimondi S, Schneider NR, Barredo JC, Cantu ES, Schlegelberger B, Behm F, Doggett NA, Borrow J, Zeleznik-Le N.
    Blood; 1997 Jul 15; 90(2):535-41. PubMed ID: 9226152
    [Abstract] [Full Text] [Related]

  • 11. Acute myeloid leukemia with trisomy 11: a molecular cytogenetic study.
    Kwong YL, Wong KF.
    Cancer Genet Cytogenet; 1997 Nov 15; 99(1):19-23. PubMed ID: 9352791
    [Abstract] [Full Text] [Related]

  • 12. Absence of MLL gene rearrangement in de novo myelodysplastic syndromes (MDS).
    Pappa V, Young BD, Economopoulos T, Papageorgiou E, Panani A, Lilington D, Bollas G, Stamouli M, Kontsioti F, Tsiotra P, Vessalas G, Dervenoulas J, Raptis S.
    Ann Hematol; 2004 Mar 15; 83(3):170-5. PubMed ID: 15064866
    [Abstract] [Full Text] [Related]

  • 13. Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23).
    Matsuo Y, MacLeod RA, Uphoff CC, Drexler HG, Nishizaki C, Katayama Y, Kimura G, Fujii N, Omoto E, Harada M, Orita K.
    Leukemia; 1997 Sep 15; 11(9):1469-77. PubMed ID: 9305600
    [Abstract] [Full Text] [Related]

  • 14. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11.
    Caligiuri MA, Strout MP, Schichman SA, Mrózek K, Arthur DC, Herzig GP, Baer MR, Schiffer CA, Heinonen K, Knuutila S, Nousiainen T, Ruutu T, Block AW, Schulman P, Pedersen-Bjergaard J, Croce CM, Bloomfield CD.
    Cancer Res; 1996 Mar 15; 56(6):1418-25. PubMed ID: 8640834
    [Abstract] [Full Text] [Related]

  • 15. Clonal evolution to acute myeloblastic leukemia with MLL gene rearrangement from trisomy 8 clone.
    Katayama Y, Takimoto H, Fujii N, Kimura G, Omoto E, Harada M.
    Leukemia; 1997 Aug 15; 11(8):1380-2. PubMed ID: 9264397
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetic and molecular analysis of the acute monocytic leukemia cell line THP-1 with an MLL-AF9 translocation.
    Odero MD, Zeleznik-Le NJ, Chinwalla V, Rowley JD.
    Genes Chromosomes Cancer; 2000 Dec 15; 29(4):333-8. PubMed ID: 11066077
    [Abstract] [Full Text] [Related]

  • 17. Trisomy 11 in myelodysplastic syndromes defines a unique group of disease with aggressive clinicopathologic features.
    Wang SA, Jabbar K, Lu G, Chen SS, Galili N, Vega F, Jones D, Raza A, Kantarjian H, Garcia-Manero G, McDonnell TJ, Medeiros LJ.
    Leukemia; 2010 Apr 15; 24(4):740-7. PubMed ID: 20072149
    [Abstract] [Full Text] [Related]

  • 18. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias.
    von Bergh A, Emanuel B, van Zelderen-Bhola S, Smetsers T, van Soest R, Stul M, Vranckx H, Schuuring E, Hagemeijer A, Kluin P.
    Genes Chromosomes Cancer; 2000 May 15; 28(1):14-22. PubMed ID: 10738298
    [Abstract] [Full Text] [Related]

  • 19. A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein.
    Wechsler DS, Engstrom LD, Alexander BM, Motto DG, Roulston D.
    Genes Chromosomes Cancer; 2003 Jan 15; 36(1):26-36. PubMed ID: 12461747
    [Abstract] [Full Text] [Related]

  • 20. Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings.
    Watanabe N, Kobayashi H, Ichiji O, Yoshida MA, Kikuta A, Komada Y, Sekine I, Ishida Y, Horiukoshi Y, Tsunematsu Y, Yano M, Nakadate H, Kaneko Y.
    Leukemia; 2003 May 15; 17(5):876-82. PubMed ID: 12750700
    [Abstract] [Full Text] [Related]

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