BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

420 related articles for article (PubMed ID: 18557744)

  • 21. CpG island methylator phenotype redefines the prognostic effect of t(12;21) in childhood acute lymphoblastic leukemia.
    Roman-Gomez J; Jimenez-Velasco A; Agirre X; Castillejo JA; Navarro G; Calasanz MJ; Garate L; San Jose-Eneriz E; Cordeu L; Prosper F; Heiniger A; Torres A
    Clin Cancer Res; 2006 Aug; 12(16):4845-50. PubMed ID: 16914570
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable outcome.
    Raimondi SC; Zhou Y; Shurtleff SA; Rubnitz JE; Pui CH; Behm FG
    Cancer Genet Cytogenet; 2006 Aug; 169(1):50-7. PubMed ID: 16875937
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prevalence of ETV6-RUNX1 fusion gene in children with acute lymphoblastic leukemia in China.
    Gao YJ; Zhu XH; Yang Y; Wu Y; Lu FJ; Zhai XW; Wang HS
    Cancer Genet Cytogenet; 2007 Oct; 178(1):57-60. PubMed ID: 17889709
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prevalence of TEL/AML1 fusion gene in Brazilian pediatric patients with acute lymphoblastic leukemia.
    Zen PR; Lima MC; Coser VM; Silla L; Daudt L; Fernandes MS; Neumann J; Mattevi MS; Ortigara R; Paskulin GA
    Cancer Genet Cytogenet; 2004 May; 151(1):68-72. PubMed ID: 15120912
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.
    Xu W; Lu X; Kim Y; Luo Y; Martin M; Mulvihill JJ; Li S
    Cancer Genet Cytogenet; 2008 Aug; 185(1):43-6. PubMed ID: 18656693
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia.
    García-Casado Z; Cervera J; Verdeguer A; Tasso M; Valencia A; Pajuelo JC; Mena-Duran AV; Barragán E; Blanes M; Bolufer P; Sanz MA
    Cancer Genet Cytogenet; 2006 Oct; 170(2):171-4. PubMed ID: 17011991
    [TBL] [Abstract][Full Text] [Related]  

  • 27. HLA-DPB1 supertype-associated protection from childhood leukaemia: relationship to leukaemia karyotype and implications for prevention.
    Taylor M; Harrison C; Eden T; Birch J; Greaves M; Lightfoot T; Hussain A;
    Cancer Immunol Immunother; 2008 Jan; 57(1):53-61. PubMed ID: 17622527
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The application of conventional cytogenetics, FISH, and RT-PCR to detect genetic changes in 70 children with ALL.
    Soszynska K; Mucha B; Debski R; Skonieczka K; Duszenko E; Koltan A; Wysocki M; Haus O
    Ann Hematol; 2008 Dec; 87(12):991-1002. PubMed ID: 18633615
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Interphase FISH on TEL/AML1 positive acute lymphoblastic leukemia relapses--analysis of clinical relevance of additional TEL and AML1 copy number changes.
    Peter A; Heiden T; Taube T; Körner G; Seeger K
    Eur J Haematol; 2009 Nov; 83(5):420-32. PubMed ID: 19594616
    [TBL] [Abstract][Full Text] [Related]  

  • 30. BCR-ABL, ETV6-RUNX1 and E2A-PBX1: prevalence of the most common acute lymphoblastic leukemia fusion genes in Mexican patients.
    Jiménez-Morales S; Miranda-Peralta E; Saldaña-Alvarez Y; Perez-Vera P; Paredes-Aguilera R; Rivera-Luna R; Velázquez-Cruz R; Ramírez-Bello J; Carnevale A; Orozco L
    Leuk Res; 2008 Oct; 32(10):1518-22. PubMed ID: 18455790
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Co-existence of multiple subclones in TEL-AML1 at diagnosis of acute lymphoblastic leukaemia in association with submicroscopic deletion of AML1.
    Rothman R; Trakhtenbrot L; Bielorai B; Izraeli S; Ishoev G; Amariglio N; Rechavi G; Toren A
    Br J Haematol; 2005 May; 129(4):491-8. PubMed ID: 15877731
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia.
    Brozek I; Babińska M; Kardaś I; Woźniak A; Balcerska A; Hellmann A; Limon J
    J Appl Genet; 2003; 44(3):401-12. PubMed ID: 12923315
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region.
    Lilljebjörn H; Heidenblad M; Nilsson B; Lassen C; Horvat A; Heldrup J; Behrendtz M; Johansson B; Andersson A; Fioretos T
    Leukemia; 2007 Oct; 21(10):2137-44. PubMed ID: 17690704
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1.
    Parker H; An Q; Barber K; Case M; Davies T; Konn Z; Stewart A; Wright S; Griffiths M; Ross FM; Moorman AV; Hall AG; Irving JA; Harrison CJ; Strefford JC
    Genes Chromosomes Cancer; 2008 Dec; 47(12):1118-25. PubMed ID: 18767146
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Acute megakaryoblastic leukaemia (AMKL) and transient myeloproliferative disorder (TMD) in Down syndrome: a multi-step model of myeloid leukaemogenesis.
    Roy A; Roberts I; Norton A; Vyas P
    Br J Haematol; 2009 Oct; 147(1):3-12. PubMed ID: 19594743
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia.
    Attarbaschi A; Mann G; Strehl S; König M; Steiner M; Jeitler V; Lion T; Dworzak MN; Gadner H; Haas OA
    Leukemia; 2007 Mar; 21(3):584-6. PubMed ID: 17215856
    [No Abstract]   [Full Text] [Related]  

  • 37. Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia.
    Kjeldsen E
    Exp Mol Pathol; 2016 Aug; 101(1):38-43. PubMed ID: 27215399
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia.
    von Goessel H; Jacobs U; Semper S; Krumbholz M; Langer T; Keller T; Schrauder A; van der Velden VH; van Dongen JJ; Harbott J; Panzer-Grümayer ER; Schrappe M; Rascher W; Metzler M
    Leuk Res; 2009 Aug; 33(8):1082-8. PubMed ID: 19081626
    [TBL] [Abstract][Full Text] [Related]  

  • 39. GATA1 mutations in patients with down syndrome and acute megakaryoblastic leukaemia do not always confer a good prognosis.
    Ariffin H; Garcia JC; Daud SS; Ibrahim K; Aizah N; Ong GB; Chong LA; Mohamad Z
    Pediatr Blood Cancer; 2009 Jul; 53(1):108-11. PubMed ID: 19260099
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Tiling resolution array-based comparative genomic hybridisation analyses of acute lymphoblastic leukaemias in children with Down syndrome reveal recurrent gain of 8q and deletions of 7p and 9p.
    Lundin C; Davidsson J; Hjorth L; Behrendtz M; Johansson B
    Br J Haematol; 2009 Jun; 146(1):113-5. PubMed ID: 19344409
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.