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Journal Abstract Search

381 related items for PubMed ID: 20226962

  • 21.
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  • 24. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1.
    Macdonald D, Reiter A, Cross NC.
    Acta Haematol; 2002; 107(2):101-7. PubMed ID: 11919391
    [Abstract] [Full Text] [Related]

  • 25. Rapid transformation of atypical myeloproliferative disorder with consistent t(8;13) to B-cell acute lymphoblastic leukemia: a case report.
    Sahin F, Sercan Z, Ertan Y, Ocakci S, Ay E, Vural F, Yuksel E, Tombuloglu M, Saydam G.
    Hematology; 2007 Dec; 12(6):489-92. PubMed ID: 17852454
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  • 26. 8p11 Myeloproliferative syndrome with BCR-FGFR1 rearrangement presenting with T-lymphoblastic lymphoma and bone marrow stromal cell proliferation: a case report and review of the literature.
    Kim SY, Oh B, She CJ, Kim HK, Jeon YK, Shin MG, Yoon SS, Lee DS.
    Leuk Res; 2011 May; 35(5):e30-4. PubMed ID: 21239058
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  • 27. 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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  • 28. Myeloid and lymphoid neoplasm with abnormalities of FGFR1 presenting with trilineage blasts and RUNX1 rearrangement: a case report and review of literature.
    Kumar KR, Chen W, Koduru PR, Luu HS.
    Am J Clin Pathol; 2015 May; 143(5):738-48. PubMed ID: 25873510
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  • 29. 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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  • 31. 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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  • 32. 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; 19(6):1005-9. PubMed ID: 15800673
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  • 33. The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias.
    Lo Coco F, Pisegna S, Diverio D.
    Haematologica; 1997 Jun; 82(3):364-70. PubMed ID: 9234595
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  • 35. A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review.
    Macdonald D, Aguiar RC, Mason PJ, Goldman JM, Cross NC.
    Leukemia; 1995 Oct; 9(10):1628-30. PubMed ID: 7564500
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  • 36. Diagnostic application of next-generation sequencing in ZMYM2-FGFR1 8p11 myeloproliferative syndrome: A case report.
    Wang Y, Wu X, Deng J, Yu H, Xu R, Zhu Z, Tu S, Hu Y.
    Cancer Biol Ther; 2016 Aug 02; 17(8):785-9. PubMed ID: 27415155
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  • 37. Cytogenetic and molecular aspects of Philadelphia negative chronic myeloproliferative disorders: clinical implications.
    Panani AD.
    Cancer Lett; 2007 Sep 18; 255(1):12-25. PubMed ID: 17383090
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  • 38. Coexistent T-cell lymphoblastic lymphoma and an atypical myeloproliferative disorder associated with t(8;13)(p21;q14).
    Somers GR, Slater H, Rockman S, Ekert H, Southey MC, Chow CW, Armes JE, Venter DJ.
    Pediatr Pathol Lab Med; 1997 Sep 18; 17(1):141-58. PubMed ID: 9050068
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