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Journal Abstract Search

278 related items for PubMed ID: 14978793

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  • 7. 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; 36(1):26-36. PubMed ID: 12461747
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  • 8. ABI-1, a human homolog to mouse Abl-interactor 1, fuses the MLL gene in acute myeloid leukemia with t(10;11)(p11.2;q23).
    Taki T, Shibuya N, Taniwaki M, Hanada R, Morishita K, Bessho F, Yanagisawa M, Hayashi Y.
    Blood; 1998 Aug 15; 92(4):1125-30. PubMed ID: 9694699
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  • 9. Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides.
    Langer T, Metzler M, Reinhardt D, Viehmann S, Borkhardt A, Reichel M, Stanulla M, Schrappe M, Creutzig U, Ritter J, Leis T, Jacobs U, Harbott J, Beck JD, Rascher W, Repp R.
    Genes Chromosomes Cancer; 2003 Apr 15; 36(4):393-401. PubMed ID: 12619163
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  • 10. LCX, leukemia-associated protein with a CXXC domain, is fused to MLL in acute myeloid leukemia with trilineage dysplasia having t(10;11)(q22;q23).
    Ono R, Taki T, Taketani T, Taniwaki M, Kobayashi H, Hayashi Y.
    Cancer Res; 2002 Jul 15; 62(14):4075-80. PubMed ID: 12124344
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  • 11. Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5.
    Poirel H, Rack K, Delabesse E, Radford-Weiss I, Troussard X, Debert C, Leboeuf D, Bastard C, Picard F, Veil-Buzyn A, Flandrin G, Bernard O, Macintyre E.
    Blood; 1996 Mar 15; 87(6):2496-505. PubMed ID: 8630416
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  • 12. Molecular analysis of the rearranged genome and chimeric mRNAs caused by the t(6;11)(q27;q23) chromosome translocation involving MLL in an infant acute monocytic leukemia.
    Akao Y, Isobe M.
    Genes Chromosomes Cancer; 2000 Apr 15; 27(4):412-7. PubMed ID: 10719372
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  • 14. Identification of CBL, a proto-oncogene at 11q23.3, as a novel MLL fusion partner in a patient with de novo acute myeloid leukemia.
    Fu JF, Hsu JJ, Tang TC, Shih LY.
    Genes Chromosomes Cancer; 2003 Jun 15; 37(2):214-9. PubMed ID: 12696071
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  • 15. MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature.
    Kim HJ, Ki CS, Park Q, Koo HH, Yoo KH, Kim EJ, Kim SH.
    Genes Chromosomes Cancer; 2003 Sep 15; 38(1):8-12. PubMed ID: 12874781
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  • 16. The CDCREL1 gene fused to MLL in de novo acute myeloid leukemia with t(11;22)(q23;q11.2) and its frequent expression in myeloid leukemia cell lines.
    Tatsumi K, Taki T, Taniwaki M, Nakamura H, Taguchi J, Chen YZ, Bessho F, Yanagisawa M, Hayashi Y.
    Genes Chromosomes Cancer; 2001 Mar 15; 30(3):230-5. PubMed ID: 11170279
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  • 17. The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia.
    Fuchs U, Rehkamp G, Haas OA, Slany R, Kōnig M, Bojesen S, Bohle RM, Damm-Welk C, Ludwig WD, Harbott J, Borkhardt A.
    Proc Natl Acad Sci U S A; 2001 Jul 17; 98(15):8756-61. PubMed ID: 11438682
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  • 18. DNA structural properties of AF9 are similar to MLL and could act as recombination hot spots resulting in MLL/AF9 translocations and leukemogenesis.
    Strissel PL, Strick R, Tomek RJ, Roe BA, Rowley JD, Zeleznik-Le NJ.
    Hum Mol Genet; 2000 Jul 01; 9(11):1671-9. PubMed ID: 10861294
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  • 19. Fusion of the MLL gene with two different genes, AF-6 and AF-5alpha, by a complex translocation involving chromosomes 5, 6, 8 and 11 in infant leukemia.
    Taki T, Hayashi Y, Taniwaki M, Seto M, Ueda R, Hanada R, Suzukawa K, Yokota J, Morishita K.
    Oncogene; 1996 Nov 21; 13(10):2121-30. PubMed ID: 8950979
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