BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 116(2):111-8. PubMed ID: 10640142
    [TBL] [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; 129(2):173-6. PubMed ID: 11566351
    [TBL] [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; 97(1):20-4. PubMed ID: 9242213
    [TBL] [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; 16(2):196-202. PubMed ID: 11840285
    [TBL] [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; 20(2):185-95. PubMed ID: 9331569
    [TBL] [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; 39(4):263-76. PubMed ID: 14978788
    [TBL] [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; 90(2):535-41. PubMed ID: 9226152
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acute myeloid leukemia with trisomy 11: a molecular cytogenetic study.
    Kwong YL; Wong KF
    Cancer Genet Cytogenet; 1997 Nov; 99(1):19-23. PubMed ID: 9352791
    [TBL] [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; 83(3):170-5. PubMed ID: 15064866
    [TBL] [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; 11(9):1469-77. PubMed ID: 9305600
    [TBL] [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; 56(6):1418-25. PubMed ID: 8640834
    [TBL] [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; 11(8):1380-2. PubMed ID: 9264397
    [TBL] [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; 29(4):333-8. PubMed ID: 11066077
    [TBL] [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; 24(4):740-7. PubMed ID: 20072149
    [TBL] [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; 28(1):14-22. PubMed ID: 10738298
    [TBL] [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; 36(1):26-36. PubMed ID: 12461747
    [TBL] [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; 17(5):876-82. PubMed ID: 12750700
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.