BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 15927680)

  • 61. A cryptic three-way translocation involving chromosomes 8, 14, and 21 in a case of acute myeloid leukemia subtype M1.
    Lau LC; Koh LP; Lim TH; Loo LE; Tien SL
    Cancer Genet Cytogenet; 2005 Nov; 163(1):86-90. PubMed ID: 16271963
    [No Abstract]   [Full Text] [Related]  

  • 62. Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).
    Corral Mdel P; Villa O; Alfaro EM; Alonso CN; Baro C; Felice MS; Rossi J; Solé F; Gallego MS
    Pediatr Blood Cancer; 2008 Mar; 50(3):651-4. PubMed ID: 17405156
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant.
    Tirado CA; Chen W; Valdez FJ; Henderson S; Doolittle J; Garcia R; Patel S; Holdridge S; Chastain C; Collins RH
    Cancer Genet Cytogenet; 2009 Aug; 193(1):67-9. PubMed ID: 19602466
    [No Abstract]   [Full Text] [Related]  

  • 64. Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
    Macedo Silva ML; Raimondi SC; Abdelhay E; Gross M; Mkrtchyan H; de Figueiredo AF; Ribeiro RC; de Jesus Marques-Salles T; Sobral ES; Gerardin Land MP; Liehr T
    Cancer Genet Cytogenet; 2008 Apr; 182(1):56-60. PubMed ID: 18328953
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H; Xue Y; Zhang J; Pan J; Dai H; Wu Y; Wang Y; Chen S; Wu D
    Exp Hematol; 2008 Nov; 36(11):1487-95. PubMed ID: 18715689
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [A favorable clinical course of acute myeloid leukemia with t (6;21;8)(p23;q22;q22)].
    Wada A; Doki N; Otsuka Y; Adachi H; Konuma R; Kishida Y; Konishi T; Yamada Y; Nagata A; Nagata R; Marumo A; Noguchi Y; Mukae J; Toya T; Igarashi A; Najima Y; Kobayashi T; Harada H; Harada Y; Sakamaki H; Ohashi K
    Rinsho Ketsueki; 2022; 63(2):104-107. PubMed ID: 35264498
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A distinct epigenetic signature at targets of a leukemia protein.
    Rossetti S; Hoogeveen AT; Liang P; Stanciu C; van der Spek P; Sacchi N
    BMC Genomics; 2007 Feb; 8():38. PubMed ID: 17266773
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22).
    Sakai I; Tamura T; Narumi H; Uchida N; Yakushijin Y; Hato T; Fujita S; Yasukawa M
    Genes Chromosomes Cancer; 2005 Nov; 44(3):265-70. PubMed ID: 16015645
    [TBL] [Abstract][Full Text] [Related]  

  • 69. A patient with de novo AML M1 and t(16;21) with karyotype evolution.
    Zatkova A; Fonatsch C; Sperr WR; Valent P
    Leuk Res; 2007 Sep; 31(9):1319-21. PubMed ID: 17126398
    [No Abstract]   [Full Text] [Related]  

  • 70. Expression of B cell-specific activator protein/PAX5 in acute myeloid leukemia with t(8;21)(q22;q22).
    Valbuena JR; Medeiros LJ; Rassidakis GZ; Hao S; Wu CD; Chen L; Lin P
    Am J Clin Pathol; 2006 Aug; 126(2):235-40. PubMed ID: 16891199
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Translocation (3;21)(q26;q22) in secondary leukemia. Report of two cases and literature review.
    Schneider NR; Bowman WP; Frenkel EP
    Ann Genet; 1991; 34(3-4):256-63. PubMed ID: 1809236
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo.
    Ohsaka A; Otsubo K; Yokota H; Hisa T; Saito H; Kozaki T
    Cancer Genet Cytogenet; 2008 Jul; 184(2):113-8. PubMed ID: 18617061
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Fluorescence in situ hybridization dissection of a chronic myeloid leukemia case bearing the apparently balanced translocations (9;22)(q34;q11.2) and (11;11)(p15;q13).
    Malvestiti F; Colombo D; Perego D; Rodeschini O; Finelli P; Larizza L; Giardino D
    Cancer Genet Cytogenet; 2009 Jan; 188(1):42-7. PubMed ID: 19061779
    [TBL] [Abstract][Full Text] [Related]  

  • 74. NUP98 is fused to topoisomerase (DNA) IIbeta 180 kDa (TOP2B) in a patient with acute myeloid leukemia with a new t(3;11)(p24;p15).
    Nebral K; Schmidt HH; Haas OA; Strehl S
    Clin Cancer Res; 2005 Sep; 11(18):6489-94. PubMed ID: 16166424
    [TBL] [Abstract][Full Text] [Related]  

  • 75. t(14;22)(q32;q11) in non-Hodgkin lymphoma and myeloid leukaemia: molecular cytogenetic investigations.
    Aamot HV; Bjørnslett M; Delabie J; Heim S
    Br J Haematol; 2005 Sep; 130(6):845-51. PubMed ID: 16156854
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma.
    Lee J; Hopcus-Niccum DJ; Mulvihill JJ; Li S
    Cancer Genet Cytogenet; 2005 Jun; 159(2):177-80. PubMed ID: 15899394
    [TBL] [Abstract][Full Text] [Related]  

  • 77. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
    von Bergh AR; van Drunen E; van Wering ER; van Zutven LJ; Hainmann I; Lönnerholm G; Meijerink JP; Pieters R; Beverloo HB
    Genes Chromosomes Cancer; 2006 Aug; 45(8):731-9. PubMed ID: 16646086
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1.
    de Oliveira FM; Tone LG; Simões BP; Falcão RP; Brassesco MS; Sakamoto-Hojo ET; dos Santos GA; Marinato AF; Jácomo RH; Rego EM
    Cancer Genet Cytogenet; 2007 Jan; 172(2):154-7. PubMed ID: 17213025
    [TBL] [Abstract][Full Text] [Related]  

  • 79. A complex, four-way variant t(15;17) in acute promyelocytic leukemia.
    Yoo SJ; Seo EJ; Lee JH; Seo YH; Park PW; Ahn JY
    Cancer Genet Cytogenet; 2006 Jun; 167(2):168-71. PubMed ID: 16737919
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Acquired Robertsonian translocations in leukemia: two more cases.
    Herring DB; Harbert KA; Wenger SL; Ericson SG
    Cancer Genet Cytogenet; 2005 Apr; 158(2):196-7. PubMed ID: 15796971
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.