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Journal Abstract Search

286 related items for PubMed ID: 19829149

  • 1. Molecular monitoring of 8p11 myeloproliferative syndrome in an infant.
    Zhang WW, Habeebu S, Sheehan AM, Naeem R, Hernandez VS, Dreyer ZE, López-Terrada D.
    J Pediatr Hematol Oncol; 2009 Nov; 31(11):879-83. PubMed ID: 19829149
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  • 2. 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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  • 5. B-lymphoblastic leukemia/lymphoma associated with t(8;13)(p11;q12)/ ZMYM2 (ZNF198)-FGFR1 : rare case and review of the literature.
    Trimaldi J, Carballido EM, Bowers JW, Anguiano AL, Zhang ZJ, Shah BD, Bruno S, List AF, Moscinski LC, Grady T, Agosti SJ, Kang L, Zhang L.
    Acta Haematol; 2013 Jan; 130(3):127-34. PubMed ID: 23594707
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  • 6. 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 Jan; 129(2):83-9. PubMed ID: 23171834
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  • 11. B-cell acute lymphoblastic leukemia as evolution of a 8p11 myeloproliferative syndrome with t(8;22)(p11;q11) and BCR-FGFR1 fusion gene.
    Baldazzi C, Iacobucci I, Luatti S, Ottaviani E, Marzocchi G, Paolini S, Stacchini M, Papayannidis C, Gamberini C, Martinelli G, Baccarani M, Testoni N.
    Leuk Res; 2010 Oct; 34(10):e282-5. PubMed ID: 20594995
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  • 13. A rare case report of 8p11 myeloid and lymphoid neoplasm with FGFR1 abnormality in a young adult.
    Shaaban H, Dabu J, Al-Rabi K, Gauchan D, Guron G.
    Ann Hematol; 2013 Jan; 92(2):285-6. PubMed ID: 22941307
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  • 16. 8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality.
    Park TS, Song J, Kim JS, Yang WI, Song S, Kim SJ, Suh B, Choi JR.
    Cancer Genet Cytogenet; 2008 Mar; 181(2):93-9. PubMed ID: 18295660
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  • 17. A ZMYM2-FGFR1 8p11 myeloproliferative neoplasm with a novel nonsense RUNX1 mutation and tumor lysis upon imatinib treatment.
    Buijs A, van Wijnen M, van den Blink D, van Gijn M, Klein SK.
    Cancer Genet; 2013 Apr; 206(4):140-4. PubMed ID: 23751892
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  • 20. 14-3-3 Integrates prosurvival signals mediated by the AKT and MAPK pathways in ZNF198-FGFR1-transformed hematopoietic cells.
    Dong S, Kang S, Gu TL, Kardar S, Fu H, Lonial S, Khoury HJ, Khuri F, Chen J.
    Blood; 2007 Jul 01; 110(1):360-9. PubMed ID: 17389761
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