BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 20805702)

  • 41. CBFB/MYH11 fusion transcripts in a case of acute myelogenous leukemia (M1) with partial deletion of the long arm of chromosome 16.
    Usuki K; Nakatsu M; Kitazume K; Endo M; Osawa M; Iki S; Arai M; Urabe A
    Intern Med; 1996 Apr; 35(4):327-30. PubMed ID: 8739792
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Abnormalities of chromosome 16q in myeloid malignancy: 14 new cases and a review of the literature.
    Betts DR; Rohatiner AZ; Evans ML; Rassam SM; Lister TA; Gibbons B
    Leukemia; 1992 Dec; 6(12):1250-6. PubMed ID: 1453770
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. [Study of trisomy 22 and inversion 16 in acute myeloid leukemia].
    Zhou HF; Li JY; Pan JL; Qiu HR; Chen LJ; Hu JY; Shen YF; Xu W; Xue YQ
    Zhonghua Xue Ye Xue Za Zhi; 2007 Jan; 28(1):11-4. PubMed ID: 17649718
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16.
    Abbondanzo SL; Gray RG; Whang-Peng J; Jacobson RJ
    Arch Pathol Lab Med; 1987 Apr; 111(4):330-2. PubMed ID: 3469939
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Lymphoid blastic crisis of chronic myelogenous leukaemia with inv(16)(p13;q22).
    Tsuboi K; Komatsu H; Miwa H; Iida S; Banno S; Wakita A; Nitta M; Ueda R
    Leuk Res; 2002 Aug; 26(8):771-4. PubMed ID: 12191573
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia.
    Lugthart S; Gröschel S; Beverloo HB; Kayser S; Valk PJ; van Zelderen-Bhola SL; Jan Ossenkoppele G; Vellenga E; van den Berg-de Ruiter E; Schanz U; Verhoef G; Vandenberghe P; Ferrant A; Köhne CH; Pfreundschuh M; Horst HA; Koller E; von Lilienfeld-Toal M; Bentz M; Ganser A; Schlegelberger B; Jotterand M; Krauter J; Pabst T; Theobald M; Schlenk RF; Delwel R; Döhner K; Löwenberg B; Döhner H
    J Clin Oncol; 2010 Aug; 28(24):3890-8. PubMed ID: 20660833
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Acute nonlymphocytic leukemia with marrow eosinophilia and chromosome 16 abnormality: a report of 18 cases.
    Bernard P; Dachary D; Reiffers J; Marit G; Wen Z; Jonveaux P; David B; Lacombe F; Broustet A
    Leukemia; 1989 Oct; 3(10):740-5. PubMed ID: 2779289
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Prognosis and chromosomal abnormalities in 79 children with t (8;21) acute myeloid leukemia].
    Chen YM; Liu TF; Ruan M; Zou Y; Chen XJ; Guo Y; Wang SC; Zhu XF
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2009 Oct; 31(5):542-6. PubMed ID: 19968066
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Deletion of chromosome arm 15q in a case of minimally differentiated hypoplastic AML-M0.
    Fujieda A; Masuya M; Kitano S; Miyazaki K; Yazaki A; Sugimoto Y; Usui E; Miyata E; Shibasaki T; Yamamura K; Ohishi K; Nishii K; Nakase K; Takeuchi T; Katayama N
    Cancer Genet Cytogenet; 2008 Jul; 184(1):57-61. PubMed ID: 18558291
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Acute myeloid leukemia with t(16;16) (p13;q22) showing a new CBFB-MYH11 fusion transcript associated with an atypical leukemic blasts morphology.
    Albano F; Anelli L; Zagaria A; Coccaro N; Tota G; Impera L; Minervini CF; Cellamare A; Delia M; Minervini A; Casieri P; Specchia G
    Hum Pathol; 2014 Mar; 45(3):643-7. PubMed ID: 24342433
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Childhood acute myeloid leukemia with bone marrow eosinophilia caused by t(16;21)(q24;q22).
    Kawashima N; Shimada A; Taketani T; Hayashi Y; Yoshida N; Matsumoto K; Takahashi Y; Kojima S; Kato K
    Int J Hematol; 2012 May; 95(5):577-80. PubMed ID: 22403058
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Correlation of cytogenetic findings with clinical features in 18 patients with inv(3)(q21q26) or t(3;3)(q21;q26).
    Fonatsch C; Gudat H; Lengfelder E; Wandt H; Silling-Engelhardt G; Ludwig WD; Thiel E; Freund M; Bodenstein H; Schwieder G
    Leukemia; 1994 Aug; 8(8):1318-26. PubMed ID: 8057667
    [TBL] [Abstract][Full Text] [Related]  

  • 54. t(16;21)(q24;q22) in acute myeloid leukemia: case report and review of the literature.
    Boils CL; Mohamed AN
    Acta Haematol; 2008; 119(2):65-8. PubMed ID: 18285693
    [No Abstract]   [Full Text] [Related]  

  • 55. [Genetic prognostic factors in childhood acute myeloid leukemia].
    Reinhardt D; Von Neuhoff C; Sander A; Creutzig U
    Klin Padiatr; 2012 Oct; 224(6):372-6. PubMed ID: 22821298
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.
    Jang JH; Yoo EH; Kim HJ; Kim DH; Jung CW; Kim SH
    Ann Clin Lab Sci; 2010; 40(1):80-4. PubMed ID: 20124335
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases.
    Haferlach C; Bacher U; Grossmann V; Schindela S; Zenger M; Kohlmann A; Kern W; Haferlach T; Schnittger S
    Genes Chromosomes Cancer; 2012 Dec; 51(12):1079-85. PubMed ID: 22887804
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Inversion of chromosome 16 and bone marrow eosinophilia in a myelomonocytic transformation of chronic myeloid leukemia.
    Asou N; Sanada I; Tanaka K; Hidaka M; Suzushima H; Matsuzaki H; Kawano F; Takatsuki K
    Cancer Genet Cytogenet; 1992 Jul; 61(2):197-200. PubMed ID: 1638503
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Karyotypic evolution in acute myelomonocytic leukemia with pericentric inversion of chromosome 16.
    Taniwaki M; Inazawa J; Horiike S; Misawa S; Abe T; Takino T
    Cancer Genet Cytogenet; 1987 Feb; 24(2):257-62. PubMed ID: 3466677
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Acute myeloid leukemia with inversion of chromosome 16: cytological, immunophenotypic and cytogenetic disruption].
    Mghinia S; Zaidani M; Hda N; Gamraoui K; Oukkache B
    Ann Biol Clin (Paris); 2020 Apr; 78(2):187-190. PubMed ID: 32319947
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.