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Query Trace: Uniparental Disomy and IDH1[original query]

Frequency, onset and clinical impact of somatic DNMT3A mutations in therapy-related and secondary acute myeloid leukemia. Haematologica 2012 Feb 97 (2): 246-50. Fried Isabella, Bodner Claudia, Pichler Monika M, Lind Karin, Beham-Schmid Christine, Quehenberger Franz, Sperr Wolfgang R, Linkesch Werner, Sill Heinz, Wölfler Albe Similar articles in PubMed
Single nucleotide polymorphism array lesions, TET2, DNMT3A, ASXL1 and CBL mutations are present in systemic mastocytosis. PloS one 2012 7 (8): e43090. Traina Fabiola, Visconte Valeria, Jankowska Anna M, Makishima Hideki, O'Keefe Christine L, Elson Paul, Han Yingchun, Hsieh Fred H, Sekeres Mikkael A, Mali Raghuveer Singh, Kalaycio Matt, Lichtin Alan E, Advani Anjali S, Duong Hien K, Copelan Edward, Kapur Reuben, Olalla Saad Sara T, Maciejewski Jaroslaw P, Tiu Ramon Similar articles in PubMed
CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia. Blood 2011 May 117 (21): e198-206. Makishima Hideki, Jankowska Anna M, McDevitt Michael A, O'Keefe Christine, Dujardin Simon, Cazzolli Heather, Przychodzen Bartlomiej, Prince Courtney, Nicoll John, Siddaiah Harish, Shaik Mohammed, Szpurka Hadrian, Hsi Eric, Advani Anjali, Paquette Ronald, Maciejewski Jaroslaw Similar articles in PubMed