BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 14654972)

  • 21. 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]  

  • 22. Amplified, lost, and fused genes in 11q23-25 amplicon in acute myeloid leukemia, an array-CGH study.
    Tyybäkinoja A; Saarinen-Pihkala U; Elonen E; Knuutila S
    Genes Chromosomes Cancer; 2006 Mar; 45(3):257-64. PubMed ID: 16283618
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies.
    Poppe B; Vandesompele J; Schoch C; Lindvall C; Mrozek K; Bloomfield CD; Beverloo HB; Michaux L; Dastugue N; Herens C; Yigit N; De Paepe A; Hagemeijer A; Speleman F
    Blood; 2004 Jan; 103(1):229-35. PubMed ID: 12946992
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The human LASP1 gene is fused to MLL in an acute myeloid leukemia with t(11;17)(q23;q21).
    Strehl S; Borkhardt A; Slany R; Fuchs UE; König M; Haas OA
    Oncogene; 2003 Jan; 22(1):157-60. PubMed ID: 12527918
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Rearrangement of the MLL gene and a region proximal to the RARalpha gene in a case of acute myelocytic leukemia M5 with a t(11;17)(q23;q21).
    Dubé S; Fetni R; Hazourli S; Champagne M; Lemieux N
    Cancer Genet Cytogenet; 2003 Aug; 145(1):54-9. PubMed ID: 12885463
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) study.
    Cuthbert G; Thompson K; McCullough S; Watmore A; Dickinson H; Telford N; Mugneret F; Harrison C; Griffiths M; Bown N
    Leukemia; 2000 Nov; 14(11):1885-91. PubMed ID: 11069023
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe.
    Dyson MJ; Talley PJ; Reilly JT; Stevenson D; Parsons E; Tighe J
    Cancer Genet Cytogenet; 2003 Nov; 147(1):81-3. PubMed ID: 14580777
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia.
    Arnaud B; Douet-Guilbert N; Morel F; Le Bris MJ; Herry A; Banzakour S; Bourquard P; Morice P; Le Calvez G; Marion V; Abgrall JF; Berthou C; De Braekeleer M
    Cancer Genet Cytogenet; 2005 Sep; 161(2):110-5. PubMed ID: 16102580
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MLL amplification in acute myeloid leukemia.
    Pajuelo-Gámez JC; Cervera J; García-Casado Z; Mena-Durán AV; Valencia A; Barragán E; Such E; Bolufer P; Sanz MA
    Cancer Genet Cytogenet; 2007 Apr; 174(2):127-31. PubMed ID: 17452254
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype: rearrangement of the MLL gene and a region proximal to the RARalpha gene.
    Kang LC; Smith SV; Kaiser-Rogers K; Rao K; Dunphy CH
    Cancer Genet Cytogenet; 2005 Jun; 159(2):168-73. PubMed ID: 15899392
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Malignant hematopoietic cell lines: in vitro models for the study of MLL gene alterations.
    Drexler HG; Quentmeier H; MacLeod RA
    Leukemia; 2004 Feb; 18(2):227-32. PubMed ID: 14671638
    [TBL] [Abstract][Full Text] [Related]  

  • 32. X chromosome insertion in the MLL gene in a case of childhood acute myeloblastic leukemia.
    Arnaud B; Morel F; Douet-Guilbert N; Le Bris MJ; De Braekeleer M
    Cancer Genet Cytogenet; 2004 Jul; 152(2):149-52. PubMed ID: 15262436
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. Cryptic insertion of MLL gene into 9p22 leads to MLL-MLLT3 (AF9) fusion in a case of acute myelogenous leukemia.
    Shago M; Bouman D; Kamel-Reid S; Minden M; Chun K
    Genes Chromosomes Cancer; 2004 Aug; 40(4):349-54. PubMed ID: 15188459
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 36(4):393-401. PubMed ID: 12619163
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Del(5q) and MLL amplification in homogeneously staining region in acute myeloblastic leukemia: a recurrent cytogenetic association.
    Herry A; Douet-Guilbert N; Guéganic N; Morel F; Le Bris MJ; Berthou C; De Braekeleer M
    Ann Hematol; 2006 Apr; 85(4):244-9. PubMed ID: 16425025
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A study on 289 consecutive Korean patients with acute leukaemias revealed fluorescence in situ hybridization detects the MLL translocation without cytogenetic evidence both initially and during follow-up.
    Kim HJ; Cho HI; Kim EC; Ko EK; See CJ; Park SY; Lee DS
    Br J Haematol; 2002 Dec; 119(4):930-9. PubMed ID: 12472570
    [TBL] [Abstract][Full Text] [Related]  

  • 40. MLL translocations with concurrent 3' deletions: interpretation of FISH results.
    Barber KE; Ford AM; Harris RL; Harrison CJ; Moorman AV
    Genes Chromosomes Cancer; 2004 Nov; 41(3):266-71. PubMed ID: 15334550
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.