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Journal Abstract Search

116 related items for PubMed ID: 22867997

  • 1. 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; 205(7-8):365-72. PubMed ID: 22867997
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  • 2. 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
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  • 4. Acute myeloid leukemia (AML-M2) associated with variant t(8;21): report of three cases.
    Bae SY, Kim JS, Ryeu BJ, Lee KN, Lee CK, Kim YK, Lim CS, Cho Y, Choi CW, Ryu SW, Yoon SY.
    Cancer Genet Cytogenet; 2010 May; 199(1):31-7. PubMed ID: 20417866
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  • 5. 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; 30(4):1549-52. PubMed ID: 23877199
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  • 8. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype.
    Kokate P, Ahmad F, Dalvi R, Das BR, Mandava S.
    Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290
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  • 12. An unusual three-way translocation t(21;8;1)(q22;q22;q32) in a case of acute myeloid leukemia (M2).
    Gmidène A, Sennana H, Frikha R, Elloumi M, Belaaj H, Saad A.
    Ann Biol Clin (Paris); 2012 Jul; 70(2):213-6. PubMed ID: 22484534
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  • 13. 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
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  • 14. A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
    Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S.
    Cancer Genet Cytogenet; 2008 Feb; 181(1):36-9. PubMed ID: 18262051
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  • 17. 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
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  • 18. A novel variant translocation t(6;8;21)(p22;q22;q22) leading to AML/ETO fusion in acute myeloid leukemia.
    Al Bahar S, Adriana Z, Pandita R.
    Gulf J Oncolog; 2009 Jan; (5):56-9. PubMed ID: 20084788
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  • 19. [Application of dual-color fluorescence in situ hybridization in acute myeloid leukemia with t (8; 21)].
    Li CW, Bo LJ, Dai Y, Liu XP, Qin S, Liu SH, Wang JX.
    Zhonghua Xue Ye Xue Za Zhi; 2006 Jan; 27(1):32-5. PubMed ID: 16732938
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  • 20. Coexistent t(8;21)(q22;q22) Translocation and 5q Deletion in Acute Myeloid Leukemia.
    Yamamoto K, Yakushijin K, Sanada Y, Kawamoto S, Matsuoka H, Minami H.
    J Clin Exp Hematop; 2015 Jan; 55(3):181-5. PubMed ID: 26763368
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