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microRNAs in acute myeloid leukemia: expression patterns, correlations with genetic and clinical parameters, and prognostic significance.
Genes Chromosomes Cancer. 2010 Mar;49(3):193-203. doi: 10.1002/gcc.20740.
Genes Chromosomes Cancer. 2010.
PMID: 20013895
Review.
Loss of RAF kinase inhibitor protein is a somatic event in the pathogenesis of therapy-related acute myeloid leukemias with C-RAF germline mutations.
Zebisch A, Haller M, Hiden K, Goebel T, Hoefler G, Troppmair J, Sill H.
Zebisch A, et al. Among authors: hiden k.
Leukemia. 2009 Jun;23(6):1049-53. doi: 10.1038/leu.2009.68. Epub 2009 Apr 9.
Leukemia. 2009.
PMID: 19357705
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Two transforming C-RAF germ-line mutations identified in patients with therapy-related acute myeloid leukemia.
Zebisch A, Staber PB, Delavar A, Bodner C, Hiden K, Fischereder K, Janakiraman M, Linkesch W, Auner HW, Emberger W, Windpassinger C, Schimek MG, Hoefler G, Troppmair J, Sill H.
Zebisch A, et al. Among authors: hiden k.
Cancer Res. 2006 Apr 1;66(7):3401-8. doi: 10.1158/0008-5472.CAN-05-0115.
Cancer Res. 2006.
PMID: 16585161
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Defective DNA-mismatch repair: a potential mediator of leukemogenic susceptibility in therapy-related myelodysplasia and leukemia.
Olipitz W, Hopfinger G, Aguiar RC, Gunsilius E, Girschikofsky M, Bodner C, Hiden K, Linkesch W, Hoefler G, Sill H.
Olipitz W, et al. Among authors: hiden k.
Genes Chromosomes Cancer. 2002 Jun;34(2):243-8. doi: 10.1002/gcc.10059.
Genes Chromosomes Cancer. 2002.
PMID: 11979558
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High expression of the sister-chromatid separation regulator and proto-oncogene hSecurin occurs in a subset of myeloid leukaemias but is not implicated in the pathogenesis of aneuploidy.
Auner HW, Zebisch A, Schimek MG, Bodner C, Hiden K, Linkesch W, Haas OA, Beham-Schmid C, Sill H.
Auner HW, et al. Among authors: hiden k.
Leukemia. 2004 Feb;18(2):303-8. doi: 10.1038/sj.leu.2403235.
Leukemia. 2004.
PMID: 14671639
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Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy.
Pichler MM, Bodner C, Fischer C, Deutsch AJ, Hiden K, Beham-Schmid C, Linkesch W, Guelly C, Sill H, Wölfler A.
Pichler MM, et al. Among authors: hiden k.
Br J Haematol. 2011 Mar;152(5):669-72. doi: 10.1111/j.1365-2141.2010.08404.x. Epub 2011 Jan 20.
Br J Haematol. 2011.
PMID: 21250968
Free article.
No abstract available.
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