BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 15551097)

  • 1. Pericentric chromosome 8 inversion associated with the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases.
    Anelli L; Albano F; Zagaria A; Liso A; Cuneo A; Mancini M; Liso V; Rocchi M; Specchia G
    Ann Hematol; 2005 Apr; 84(4):245-9. PubMed ID: 15551097
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints.
    Specchia G; Albano F; Anelli L; Zagaria A; Liso A; La Starza R; Mancini M; Sebastio L; Giugliano E; Saglio G; Liso V; Rocchi M
    Genes Chromosomes Cancer; 2004 Sep; 41(1):86-91. PubMed ID: 15236320
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Submicroscopic deletions in an acute myeloid leukemia case with a four-way t(8;11;16;21).
    Albano F; Specchia G; Anelli L; Liso A; Zagaria A; Santoro A; Mirto S; Liso V; Rocchi M
    Leuk Res; 2005 Jul; 29(7):855-8. PubMed ID: 15927680
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of AML with ins(21;8)(q22;q22q22) reveals similarity to t(8;21) AML.
    Rücker FG; Bullinger L; Gribov A; Sill M; Schlenk RF; Lichter P; Döhner H; Döhner K
    Genes Chromosomes Cancer; 2011 Jan; 50(1):51-8. PubMed ID: 20967878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two more inv(16) acute myeloid leukemia cases with infrequent CBFbeta-MYH11 fusion transcript: clinical and molecular findings.
    Martinelli G; Ottaviani E; Buonamici S; Isidori A; Malagola M; Piccaluga P; Baccarani M
    Haematologica; 2002 May; 87(5):554-5. PubMed ID: 12010674
    [No Abstract]   [Full Text] [Related]  

  • 6. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
    Tosi S; Ballabio E; Teigler-Schlegel A; Boultwood J; Bruch J; Harbott J
    Genes Chromosomes Cancer; 2005 Nov; 44(3):225-32. PubMed ID: 16028218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication and triplication of der(21)t(8;21)(q22;q22) in acute myeloid leukemia.
    Mikulasovich M; LeBlanc A; Scalise A; Manwani D; Keyzner A; Najfeld V
    Cancer Genet Cytogenet; 2009 Jan; 188(2):83-7. PubMed ID: 19100510
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?
    Deluche L; Joha S; Corm S; Daudignon A; Geffroy S; Quief S; Villenet C; Kerckaert JP; Laï JL; Preudhomme C; Roche-Lestienne C
    Genes Chromosomes Cancer; 2008 Dec; 47(12):1110-7. PubMed ID: 18767145
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pericentric chromosome 8 inversion, inv8(p11.2q22), associated with RUNX1/RUNX1T1 rearrangement in acute myeloid leukemia.
    Yamamoto K; Okamura A; Yakushijin K; Matsuoka H; Minami H
    Ann Hematol; 2013 Mar; 92(3):403-5. PubMed ID: 22926532
    [No Abstract]   [Full Text] [Related]  

  • 10. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
    Ahmad F; Kokate P; Chheda P; Dalvi R; Das BR; Mandava S
    Cancer Genet Cytogenet; 2008 Jan; 180(2):153-7. PubMed ID: 18206543
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A further case of acute myeloid leukaemia with inv(8)(p11q13) and MOZ-TIF2 fusion.
    Billio A; Steer EJ; Pianezze G; Svaldi M; Casin M; Amato B; Coser P; Cross NC
    Haematologica; 2002 May; 87(5):ECR15. PubMed ID: 12010678
    [No Abstract]   [Full Text] [Related]  

  • 13. Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukaemia.
    Ichikawa H; Tanabe K; Mizushima H; Hayashi Y; Mizutani S; Ishii E; Hongo T; Kikuchi A; Satake M
    Br J Haematol; 2006 Nov; 135(3):336-47. PubMed ID: 16989659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 3'CBFbeta deletion associated with inv(16) in acute myeloid leukemia.
    Kelly J; Foot NJ; Conneally E; Enright H; Humphreys M; Saunders K; Neat MJ
    Cancer Genet Cytogenet; 2005 Oct; 162(2):122-6. PubMed ID: 16213359
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of additional cytogenetic and molecular genetic abnormalities in acute myeloid leukaemia with t(8;21)/AML1-ETO.
    Kuchenbauer F; Schnittger S; Look T; Gilliland G; Tenen D; Haferlach T; Hiddemann W; Buske C; Schoch C
    Br J Haematol; 2006 Sep; 134(6):616-9. PubMed ID: 16938118
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Identification of RUNX1/AML1 as a classical tumor suppressor gene.
    Silva FP; Morolli B; Storlazzi CT; Anelli L; Wessels H; Bezrookove V; Kluin-Nelemans HC; Giphart-Gassler M
    Oncogene; 2003 Jan; 22(4):538-47. PubMed ID: 12555067
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of the CBFB/MYH11 fusion gene in de novo acute myeloid leukemia (AML): a single-institution study of 224 Japanese AML patients.
    Monma F; Nishii K; Shiga J; Sugahara H; Lorenzo F; Watanabe Y; Kawakami K; Hosokai N; Yamamori S; Katayama N; Shiku H
    Leuk Res; 2007 Apr; 31(4):471-6. PubMed ID: 17052753
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.