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Journal Abstract Search

683 related items for PubMed ID: 23628959

  • 1. SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations.
    Meggendorfer M, Bacher U, Alpermann T, Haferlach C, Kern W, Gambacorti-Passerini C, Haferlach T, Schnittger S.
    Leukemia; 2013 Sep; 27(9):1852-60. PubMed ID: 23628959
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  • 6. Making sense of the myelodysplastic/myeloproliferative neoplasms overlap syndromes.
    Tiu RV, Sekeres MA.
    Curr Opin Hematol; 2014 Mar; 21(2):131-40. PubMed ID: 24378705
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  • 9. Genomic aberrations of myeloproliferative and myelodysplastic/myeloproliferative neoplasms in chronic phase and during disease progression.
    Hahm C, Huh HJ, Mun YC, Seong CM, Chung WS, Huh J.
    Int J Lab Hematol; 2015 Apr; 37(2):181-9. PubMed ID: 24845343
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  • 10. Myelodysplastic/myeloproliferative neoplasms-unclassifiable with isolated isochromosome 17q represents a distinct clinico-biologic subset: a multi-institutional collaborative study from the Bone Marrow Pathology Group.
    Kanagal-Shamanna R, Orazi A, Hasserjian RP, Arber DA, Reichard K, Hsi ED, Bagg A, Rogers HJ, Geyer J, Darbaniyan F, Do KA, Devins KM, Pozdnyakova O, George TI, Cin PD, Greipp PT, Routbort MJ, Patel K, Garcia-Manero G, Verstovsek S, Medeiros LJ, Wang SA, Bueso-Ramos C.
    Mod Pathol; 2022 Apr; 35(4):470-479. PubMed ID: 34775472
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  • 11. Molecular landscape and clonal architecture of adult myelodysplastic/myeloproliferative neoplasms.
    Palomo L, Meggendorfer M, Hutter S, Twardziok S, Ademà V, Fuhrmann I, Fuster-Tormo F, Xicoy B, Zamora L, Acha P, Kerr CM, Kern W, Maciejewski JP, Solé F, Haferlach C, Haferlach T.
    Blood; 2020 Oct 15; 136(16):1851-1862. PubMed ID: 32573691
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  • 13. An Exercise in Extrapolation: Clinical Management of Atypical CML, MDS/MPN-Unclassifiable, and MDS/MPN-RS-T.
    Talati C, Padron E.
    Curr Hematol Malig Rep; 2016 Dec 15; 11(6):425-433. PubMed ID: 27664113
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  • 17. Activating CBL mutations are associated with a distinct MDS/MPN phenotype.
    Schwaab J, Ernst T, Erben P, Rinke J, Schnittger S, Ströbel P, Metzgeroth G, Mossner M, Haferlach T, Cross NC, Hochhaus A, Hofmann WK, Reiter A.
    Ann Hematol; 2012 Nov 15; 91(11):1713-20. PubMed ID: 23010802
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  • 19. SETBP1 mutations drive leukemic transformation in ASXL1-mutated MDS.
    Inoue D, Kitaura J, Matsui H, Hou HA, Chou WC, Nagamachi A, Kawabata KC, Togami K, Nagase R, Horikawa S, Saika M, Micol JB, Hayashi Y, Harada Y, Harada H, Inaba T, Tien HF, Abdel-Wahab O, Kitamura T.
    Leukemia; 2015 Apr 15; 29(4):847-57. PubMed ID: 25306901
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  • 20. Atypical CML: diagnosis and treatment.
    Breccia M.
    Hematology Am Soc Hematol Educ Program; 2023 Dec 08; 2023(1):476-482. PubMed ID: 38066919
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