检索结果 - Michael A. McDevitt
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TP53 mutations in myeloid malignancies are either homozygous or hemizygous due to copy number-neutral loss of heterozygosity or deletion of 17p 由 Monika Jasek, Lukasz P. Gondek, Nelli Bejanyan, Ramón V. Tiu, Ji Young Huh, Karl S. Theil, C. O'Keefe, Michael A. McDevitt, Jaroslaw P. Maciejewski
出版 2009Carta -
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Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms 由 A. Jankowska, Hadrian Szpurka, Ramón V. Tiu, Hideki Makishima, Manuel Afable, Jungwon Huh, Christine L. O’Keefe, Rebecca Ganetzky, Michael A. McDevitt, Jaroslaw P. Maciejewski
出版 2009Artigo -
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250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of <i>c-Cbl</i>, in My... 由 Andrew Dunbar, Lukasz P. Gondek, Christine L. O’Keefe, Hideki Makishima, Manjot Rataul, Hadrian Szpurka, Mikkael A. Sekeres, Xiaofei Wang, Michael A. McDevitt, Jaroslaw P. Maciejewski
出版 2008Artigo -
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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera:... 由 Barry Stein, Donna M. Williams, C. O'Keefe, Ophelia Rogers, Roxann Ingersoll, Jerry L. Spivak, Amit Verma, Jaroslaw P. Maciejewski, Michael A. McDevitt, Alison R. Moliterno
出版 2011Artigo -
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Telomerase Inhibitor Imetelstat in Patients with Essential Thrombocythemia 由 Gabriela M. Baerlocher, Elisabeth Oppliger Leibundgut, Oliver G. Ottmann, Gary Spitzer, Olatoyosi Odenike, Michael A. McDevitt, Alexander Röth, Michael Daskalakis, Bart Burington, Monic J. Stuart, David S. Snyder
出版 2015Artigo
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Biology
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Biochemistry
Karyotype
Myelodysplastic syndromes
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Uniparental disomy
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