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2127 related items for PubMed ID: 24845343

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Distribution of cytogenetic abnormalities in myelodysplastic syndromes, Philadelphia negative myeloproliferative neoplasms, and the overlap MDS/MPN category.
    Bacher U, Schnittger S, Kern W, Weiss T, Haferlach T, Haferlach C.
    Ann Hematol; 2009 Dec; 88(12):1207-13. PubMed ID: 19415278
    [Abstract] [Full Text] [Related]

  • 3. Genomic Landscape of Myelodysplastic/Myeloproliferative Neoplasms: A Multi-Central Study.
    Fei F, Jariwala A, Pullarkat S, Loo E, Liu Y, Tizro P, Ali H, Otoukesh S, Amanam I, Artz A, Ally F, Telatar M, Nakamura R, Marcucci G, Afkhami M.
    Int J Mol Sci; 2024 Sep 23; 25(18):. PubMed ID: 39337700
    [Abstract] [Full Text] [Related]

  • 4. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
    Svobodova K, Zemanova Z, Lhotska H, Novakova M, Podskalska L, Belickova M, Brezinova J, Sarova I, Izakova S, Lizcova L, Berkova A, Siskova M, Jonasova A, Cermak J, Michalova K.
    Leuk Res; 2016 Mar 23; 42():7-12. PubMed ID: 26851439
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  • 7. Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis.
    Huh J, Tiu RV, Gondek LP, O'Keefe CL, Jasek M, Makishima H, Jankowska AM, Jiang Y, Verma A, Theil KS, McDevitt MA, Maciejewski JP.
    Genes Chromosomes Cancer; 2010 Apr 23; 49(4):390-9. PubMed ID: 20095039
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  • 9. Atypical chronic myeloid leukemia is clinically distinct from unclassifiable myelodysplastic/myeloproliferative neoplasms.
    Wang SA, Hasserjian RP, Fox PS, Rogers HJ, Geyer JT, Chabot-Richards D, Weinzierl E, Hatem J, Jaso J, Kanagal-Shamanna R, Stingo FC, Patel KP, Mehrotra M, Bueso-Ramos C, Young KH, Dinardo CD, Verstovsek S, Tiu RV, Bagg A, Hsi ED, Arber DA, Foucar K, Luthra R, Orazi A.
    Blood; 2014 Apr 24; 123(17):2645-51. PubMed ID: 24627528
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  • 11. Numerical gain and structural rearrangements of JAK2, identified by FISH, characterize both JAK2617V>F-positive and -negative patients with Ph-negative MPD, myelodysplasia, and B-lymphoid neoplasms.
    Najfeld V, Cozza A, Berkofsy-Fessler W, Prchal J, Scalise A.
    Exp Hematol; 2007 Nov 24; 35(11):1668-76. PubMed ID: 17976519
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  • 12. Combining metaphase cytogenetics with single nucleotide polymorphism arrays can improve the diagnostic yield and identify prognosis more precisely in myelodysplastic syndromes.
    Qin Y, Zhang H, Feng L, Wei H, Wu Y, Jiang C, Xu Z, Zhu H, Liu T.
    Ann Med; 2022 Dec 24; 54(1):2627-2636. PubMed ID: 36148999
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  • 13. Progression in Myeloid Neoplasms: Beyond the Myeloblast.
    Faria C, Tzankov A.
    Pathobiology; 2024 Dec 24; 91(1):55-75. PubMed ID: 37232015
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  • 14. Myeloid malignancies with acquired trisomy 21 as the sole cytogenetic change are clinically highly variable and display a heterogeneous pattern of copy number alterations and mutations.
    Larsson N, Lilljebjörn H, Lassen C, Johansson B, Fioretos T.
    Eur J Haematol; 2012 Feb 24; 88(2):136-43. PubMed ID: 21933280
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  • 15. Genomics of myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes.
    Patnaik MM, Lasho TL.
    Hematology Am Soc Hematol Educ Program; 2020 Dec 04; 2020(1):450-459. PubMed ID: 33275756
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  • 16. Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
    Kanagal-Shamanna R, Hodge JC, Tucker T, Shetty S, Yenamandra A, Dixon-McIver A, Bryke C, Huxley E, Lennon PA, Raca G, Xu X, Jeffries S, Quintero-Rivera F, Greipp PT, Slovak ML, Iqbal MA, Fang M.
    Cancer Genet; 2018 Dec 04; 228-229():197-217. PubMed ID: 30377088
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  • 17. 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 04; 27(9):1852-60. PubMed ID: 23628959
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  • 18. Diagnosing myelodysplastic/myeloproliferative neoplasms: laboratory testing strategies to exclude other disorders.
    Hall J, Foucar K.
    Int J Lab Hematol; 2010 Dec 04; 32(6 Pt 2):559-71. PubMed ID: 20670271
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  • 19. 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 04; 11(6):425-433. PubMed ID: 27664113
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  • 20. SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.
    Gondek LP, Dunbar AJ, Szpurka H, McDevitt MA, Maciejewski JP.
    PLoS One; 2007 Nov 21; 2(11):e1225. PubMed ID: 18030353
    [Abstract] [Full Text] [Related]

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