BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 24045615)

  • 21. Characterizing chromosomal break points of t(12;21)[ETV6-RUNX1]-positive leukaemia using multiple tiling PCR on whole-genome-amplified DNA.
    Lausten-Thomsen U; Madsen HO; Schmiegelow K
    Leukemia; 2010 Jan; 24(1):203-5. PubMed ID: 19710699
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. TEL/AML1-positive patients lacking TEL exon 5 resemble canonical TEL/AML1 cases.
    Zaliova M; Meyer C; Cario G; Vaskova M; Marschalek R; Stary J; Zuna J; Trka J
    Pediatr Blood Cancer; 2011 Feb; 56(2):217-25. PubMed ID: 21157892
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Evidence for a role of RUNX1 as recombinase cofactor for TCRβ rearrangements and pathological deletions in ETV6-RUNX1 ALL.
    Seitz V; Kleo K; Dröge A; Schaper S; Elezkurtaj S; Bedjaoui N; Dimitrova L; Sommerfeld A; Berg E; von der Wall E; Müller U; Joosten M; Lenze D; Heimesaat MM; Baldus C; Zinser C; Cieslak A; Macintyre E; Stocking C; Hennig S; Hummel M
    Sci Rep; 2020 Jun; 10(1):10024. PubMed ID: 32572036
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
    Paulsson K; Jonson T; Ora I; Olofsson T; Panagopoulos I; Johansson B
    Br J Haematol; 2007 Jul; 138(2):196-201. PubMed ID: 17593026
    [TBL] [Abstract][Full Text] [Related]  

  • 26. HLA-DM expression is elevated in ETV6-AML1 translocation-positive pediatric acute lymphoblastic leukemia.
    Jastaniah WA; Alessandri AJ; Reid GS; Schultz KR
    Leuk Res; 2006 Apr; 30(4):487-9. PubMed ID: 16191436
    [TBL] [Abstract][Full Text] [Related]  

  • 27. RUNX1 aberrations in ETV6/RUNX1-positive and ETV6/RUNX1-negative patients: its hemato-pathological and prognostic significance in a large cohort (619 cases) of ALL.
    Pais AP; Amare Kadam PS; Raje GC; Banavali S; Parikh P; Kurkure P; Arora B; Gujral S; Kumar SA; Badrinath Y
    Pediatr Hematol Oncol; 2008 Sep; 25(6):582-97. PubMed ID: 18728978
    [TBL] [Abstract][Full Text] [Related]  

  • 28. ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
    Strehl S; Nebral K; König M; Harbott J; Strobl H; Ratei R; Struski S; Bielorai B; Lessard M; Zimmermann M; Haas OA; Izraeli S
    Clin Cancer Res; 2008 Feb; 14(4):977-83. PubMed ID: 18281529
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A case report of childhood acute lymphoblastic leukemia with intrachromosomal amplification of AML1 gene in chromosome 21 and TEL deletion].
    Yang W; Xiong F; Huang H; Wu Y; Lin Y; Fan X; Liu Z; Zhang X; Xu H; Zeng H; Zeng S
    Zhonghua Xue Ye Xue Za Zhi; 2015 Jul; 36(7):569. PubMed ID: 26304079
    [No Abstract]   [Full Text] [Related]  

  • 30. Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia.
    Busche S; Ge B; Vidal R; Spinella JF; Saillour V; Richer C; Healy J; Chen SH; Droit A; Sinnett D; Pastinen T
    Cancer Res; 2013 Jul; 73(14):4323-36. PubMed ID: 23722552
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. V(D)J-mediated translocations in lymphoid neoplasms: a functional assessment of genomic instability by cryptic sites.
    Marculescu R; Le T; Simon P; Jaeger U; Nadel B
    J Exp Med; 2002 Jan; 195(1):85-98. PubMed ID: 11781368
    [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. Febrile infections in young children do not frequently induce translocation ETV6-RUNX1.
    Olsen M; Nielsen NK; Birkballe S; Hjalgrim H; Madsen HO; Schmiegelow K
    Blood Cells Mol Dis; 2011 Feb; 46(2):175-6. PubMed ID: 21145270
    [No Abstract]   [Full Text] [Related]  

  • 35.
    Junk SV; Klein N; Schreek S; Zimmermann M; Möricke A; Bleckmann K; Alten J; Dagdan E; Cario G; Kratz CP; Schrappe M; Stanulla M
    Haematologica; 2019 Sep; 104(9):e402-e405. PubMed ID: 31289210
    [No Abstract]   [Full Text] [Related]  

  • 36. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
    Ellinghaus E; Stanulla M; Richter G; Ellinghaus D; te Kronnie G; Cario G; Cazzaniga G; Horstmann M; Panzer Grümayer R; Cavé H; Trka J; Cinek O; Teigler-Schlegel A; ElSharawy A; Häsler R; Nebel A; Meissner B; Bartram T; Lescai F; Franceschi C; Giordan M; Nürnberg P; Heinzow B; Zimmermann M; Schreiber S; Schrappe M; Franke A
    Leukemia; 2012 May; 26(5):902-9. PubMed ID: 22076464
    [TBL] [Abstract][Full Text] [Related]  

  • 37. V(D)J recombinase binding and cleavage of cryptic recombination signal sequences identified from lymphoid malignancies.
    Zhang M; Swanson PC
    J Biol Chem; 2008 Mar; 283(11):6717-27. PubMed ID: 18187418
    [TBL] [Abstract][Full Text] [Related]  

  • 38. ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events.
    Haferlach C; Bacher U; Schnittger S; Alpermann T; Zenger M; Kern W; Haferlach T
    Genes Chromosomes Cancer; 2012 Apr; 51(4):328-37. PubMed ID: 22162288
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institution.
    Pérez-Vera P; Montero-Ruiz O; Frías S; Ulloa-Avilés V; Cárdenas-Cardós R; Paredes-Aguilera R; Rivera-Luna R; Carnevale A
    Cancer Genet Cytogenet; 2005 Oct; 162(2):140-5. PubMed ID: 16213362
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
    Karrman K; Forestier E; Andersen MK; Autio K; Borgström G; Heim S; Heinonen K; Hovland R; Kerndrup G; Johansson B;
    Br J Haematol; 2006 Nov; 135(3):352-4. PubMed ID: 16965388
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.