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Journal Abstract Search

348 related items for PubMed ID: 9425908

  • 1. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome.
    Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA.
    Nat Genet; 1998 Jan; 18(1):84-7. PubMed ID: 9425908
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  • 4. Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL.
    Fioretos T, Panagopoulos I, Lassen C, Swedin A, Billström R, Isaksson M, Strömbeck B, Olofsson T, Mitelman F, Johansson B.
    Genes Chromosomes Cancer; 2001 Dec; 32(4):302-10. PubMed ID: 11746971
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  • 5. The genomic structure of ZNF198 and location of breakpoints in the t(8;13) myeloproliferative syndrome.
    Kulkarni S, Reiter A, Smedley D, Goldman JM, Cross NC.
    Genomics; 1999 Jan 01; 55(1):118-21. PubMed ID: 9889006
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  • 7. PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder.
    Chen J, Deangelo DJ, Kutok JL, Williams IR, Lee BH, Wadleigh M, Duclos N, Cohen S, Adelsperger J, Okabe R, Coburn A, Galinsky I, Huntly B, Cohen PS, Meyer T, Fabbro D, Roesel J, Banerji L, Griffin JD, Xiao S, Fletcher JA, Stone RM, Gilliland DG.
    Proc Natl Acad Sci U S A; 2004 Oct 05; 101(40):14479-84. PubMed ID: 15448205
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  • 10. The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1.
    Walz C, Chase A, Schoch C, Weisser A, Schlegel F, Hochhaus A, Fuchs R, Schmitt-Gräff A, Hehlmann R, Cross NC, Reiter A.
    Leukemia; 2005 Jun 05; 19(6):1005-9. PubMed ID: 15800673
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  • 12. Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: a review of literature of t(8;13) associated myeloproliferative diseases.
    Wong WS, Cheng KC, Lau KM, Chan NP, Shing MM, Cheng SH, Chik KW, Li CK, Ng MH.
    Leuk Res; 2007 Feb 05; 31(2):235-8. PubMed ID: 16777224
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  • 13. [FGFR1 and MOZ, two key genes involved in malignant hemopathies linked to rearrangements within the chromosomal region 8p11-12].
    Pébusque MJ, Chaffanet M, Popovici C, Birnbaum D.
    Bull Cancer; 2000 Dec 05; 87(12):887-94. PubMed ID: 11174118
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  • 14. Identification of a novel partner gene, TPR, fused to FGFR1 in 8p11 myeloproliferative syndrome.
    Li F, Zhai YP, Tang YM, Wang LP, Wan PJ.
    Genes Chromosomes Cancer; 2012 Sep 05; 51(9):890-7. PubMed ID: 22619110
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  • 15. A case of 8p11 myeloproliferative syndrome with BCR-FGFR1 gene fusion presenting with trilineage acute leukemia/lymphoma, successfully treated by cord blood transplantation.
    Morishige S, Oku E, Takata Y, Kimura Y, Arakawa F, Seki R, Imamura R, Osaki K, Hashiguchi M, Yakushiji K, Mizuno S, Yoshimoto K, Nagafuji K, Ohshima K, Okamura T.
    Acta Haematol; 2013 Sep 05; 129(2):83-9. PubMed ID: 23171834
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  • 16. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1.
    Macdonald D, Reiter A, Cross NC.
    Acta Haematol; 2002 Sep 05; 107(2):101-7. PubMed ID: 11919391
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  • 18. 8p11 myeloproliferative syndrome: a review.
    Jackson CC, Medeiros LJ, Miranda RN.
    Hum Pathol; 2010 Apr 05; 41(4):461-76. PubMed ID: 20226962
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