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Journal Abstract Search

335 related items for PubMed ID: 20064152

  • 1. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.
    Foster N, Paulsson K, Sales M, Cunningham J, Groves M, O'Connor N, Begum S, Stubbs T, McMullan DJ, Griffiths M, Pratt N, Tauro S.
    Br J Haematol; 2010 Mar; 148(6):938-43. PubMed ID: 20064152
    [Abstract] [Full Text] [Related]

  • 2. A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42.
    Paulsson K, Békássy AN, Olofsson T, Mitelman F, Johansson B, Panagopoulos I.
    Leukemia; 2006 Feb; 20(2):224-9. PubMed ID: 16357831
    [Abstract] [Full Text] [Related]

  • 3. 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 Feb; 40(1):80-4. PubMed ID: 20124335
    [Abstract] [Full Text] [Related]

  • 4. Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
    Dai H, Xue Y, Pan J, Wu Y, Wang Y, Shen J, Zhang J.
    Cancer Genet Cytogenet; 2007 Sep; 177(2):120-4. PubMed ID: 17854666
    [Abstract] [Full Text] [Related]

  • 5. Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript.
    Park TS, Choi JR, Yoon SH, Song J, Kim J, Kim SJ, Kwon O, Min YH.
    Cancer Genet Cytogenet; 2008 Dec; 187(2):61-73. PubMed ID: 19027486
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Microhomologies and topoisomerase II consensus sequences identified near the breakpoint junctions of the recurrent t(7;21)(p22;q22) translocation in acute myeloid leukemia.
    Giguère A, Hébert J.
    Genes Chromosomes Cancer; 2011 Apr; 50(4):228-38. PubMed ID: 21319259
    [Abstract] [Full Text] [Related]

  • 8. PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
    Zhang Y, Emmanuel N, Kamboj G, Chen J, Shurafa M, Van Dyke DL, Wiktor A, Rowley JD.
    Genes Chromosomes Cancer; 2004 Aug; 40(4):365-70. PubMed ID: 15188461
    [Abstract] [Full Text] [Related]

  • 9. CLCA2, a novel RUNX1 partner gene in a therapy-related leukemia with t(1;21)(p22;q22).
    Giguère A, Hébert J.
    Cancer Genet Cytogenet; 2010 Oct 15; 202(2):94-100. PubMed ID: 20875871
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 50(1):51-8. PubMed ID: 20967878
    [Abstract] [Full Text] [Related]

  • 11. A novel RUNX1-C11orf41 fusion gene in a case of acute myeloid leukemia with a t(11;21)(p14;q22).
    Abe A, Katsumi A, Kobayashi M, Okamoto A, Tokuda M, Kanie T, Yamamoto Y, Naoe T, Emi N.
    Cancer Genet; 2012 Nov 15; 205(11):608-11. PubMed ID: 23102734
    [Abstract] [Full Text] [Related]

  • 12. Complex translocation (8;12;21): a new variant of t(8;21) in acute myeloid leukemia.
    Farra C, Awwad J, Valent A, Lozach F, Bernheim A.
    Cancer Genet Cytogenet; 2004 Dec 15; 155(2):138-42. PubMed ID: 15571799
    [Abstract] [Full Text] [Related]

  • 13. Acute myeloid leukemia associated with variant t(8;21) detected by conventional cytogenetic and molecular studies: a report of four cases and review of the literature.
    Huang L, Abruzzo LV, Valbuena JR, Medeiros LJ, Lin P.
    Am J Clin Pathol; 2006 Feb 15; 125(2):267-72. PubMed ID: 16393685
    [Abstract] [Full Text] [Related]

  • 14. Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia.
    Nguyen TT, Ma LN, Slovak ML, Bangs CD, Cherry AM, Arber DA.
    Genes Chromosomes Cancer; 2006 Oct 15; 45(10):918-32. PubMed ID: 16858696
    [Abstract] [Full Text] [Related]

  • 15. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
    De Braekeleer E, Douet-Guilbert N, Le Bris MJ, Morel F, Férec C, De Braekeleer M.
    Cancer Genet Cytogenet; 2008 Aug 15; 185(1):47-50. PubMed ID: 18656694
    [Abstract] [Full Text] [Related]

  • 16. Identification of a potential "hotspot" DNA region in the RUNX1 gene targeted by mitoxantrone in therapy-related acute myeloid leukemia with t(16;21) translocation.
    Ottone T, Hasan SK, Montefusco E, Curzi P, Mays AN, Chessa L, Ferrari A, Conte E, Noguera NI, Lavorgna S, Ammatuna E, Divona M, Bovetti K, Amadori S, Grimwade D, Lo-Coco F.
    Genes Chromosomes Cancer; 2009 Mar 15; 48(3):213-21. PubMed ID: 19023877
    [Abstract] [Full Text] [Related]

  • 17. Marker chromosomes are a significant mechanism of high-level RUNX1 gene amplification in hematologic malignancies.
    Moosavi SA, Sanchez J, Adeyinka A.
    Cancer Genet Cytogenet; 2009 Feb 15; 189(1):24-8. PubMed ID: 19167608
    [Abstract] [Full Text] [Related]

  • 18. Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion.
    Panagopoulos I, Gorunova L, Brandal P, Garnes M, Tierens A, Heim S.
    Oncol Rep; 2013 Oct 15; 30(4):1549-52. PubMed ID: 23877199
    [Abstract] [Full Text] [Related]

  • 19. Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations.
    Harada Y, Harada H.
    J Cell Physiol; 2009 Jul 15; 220(1):16-20. PubMed ID: 19334039
    [Abstract] [Full Text] [Related]

  • 20. A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity.
    Jeandidier E, Gervais C, Radford-Weiss I, Zink E, Gangneux C, Eischen A, Galoisy AC, Helias C, Dano L, Cammarata O, Jung G, Harzallah I, Guérin E, Martzolff L, Drénou B, Lioure B, Tancrédi C, Rimelen V, Mauvieux L.
    Cancer Genet; 2012 Jul 15; 205(7-8):365-72. PubMed ID: 22867997
    [Abstract] [Full Text] [Related]

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