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Journal Abstract Search

610 related items for PubMed ID: 17854666

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  • 3. 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
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  • 4. 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; 45(10):918-32. PubMed ID: 16858696
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  • 6. t(8;21)(q22;q22) Translocation involving AML1 and ETO in B lymphoblastic leukemia [corrected].
    Wang HY, Tirado CA.
    Hum Pathol; 2010 Feb; 41(2):286-92. PubMed ID: 19896694
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  • 7. LPXN, a member of the paxillin superfamily, is fused to RUNX1 in an acute myeloid leukemia patient with a t(11;21)(q12;q22) translocation.
    Dai HP, Xue YQ, Zhou JW, Li AP, Wu YF, Pan JL, Wang Y, Zhang J.
    Genes Chromosomes Cancer; 2009 Dec; 48(12):1027-36. PubMed ID: 19760607
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  • 9. 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 15; 180(2):153-7. PubMed ID: 18206543
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  • 10. Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant.
    Tirado CA, Chen W, Valdez FJ, Henderson S, Doolittle J, Garcia R, Patel S, Holdridge S, Chastain C, Collins RH.
    Cancer Genet Cytogenet; 2009 Aug 15; 193(1):67-9. PubMed ID: 19602466
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  • 11. 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 Aug 15; 40(1):80-4. PubMed ID: 20124335
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  • 12. 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
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  • 13. A novel t(5;11)(q31;p15) involving the NUP98 gene on 11p15 is associated with a loss of the EGR1 gene on 5q31 in a patient with acute myeloid leukemia.
    Wang Y, Xue Y, Chen S, Wu Y, Pan J, Zhang J, Shen J.
    Cancer Genet Cytogenet; 2010 May 15; 199(1):9-14. PubMed ID: 20417862
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  • 15. Complex t(8;13;21)(q22;q14;q22)--a novel variant of t(8;21) in a patient with acute myeloid leukemia (AML-M2).
    Udayakumar AM, Alkindi S, Pathare AV, Raeburn JA.
    Arch Med Res; 2008 Feb 15; 39(2):252-6. PubMed ID: 18164974
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  • 16. 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
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  • 17. Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation.
    De Braekeleer E, Douet-Guilbert N, Basinko A, Le Bris MJ, Morel F, Berthou C, Férec C, De Braekeleer M.
    Ann Hematol; 2010 Dec 15; 89(12):1277-81. PubMed ID: 20352434
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  • 18. A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement.
    Park KJ, Park HD, Kim HJ, Yoo KH, Koo HH, Kim SH.
    Cancer Genet Cytogenet; 2009 Jul 15; 192(2):90-2. PubMed ID: 19596262
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  • 19. Acute myeloid leukemia with a RUNX1-RUNX1T1 t(1;21;8)(q21;q22;q22) novel variant: a case report and review of the literature.
    Kim H, Moon HW, Hur M, Yun YM, Lee MH.
    Acta Haematol; 2011 Jul 15; 125(4):237-41. PubMed ID: 21325813
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  • 20. 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
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