检索结果 - Steininger, Anne

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  1. 1
    GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants

    GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants 由 Tebel, Katrin, Boldt, Vivien, Steininger, Anne, Port, Matthias, Ebert, Grit, Ullmann, Reinhard

    出版 2017
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  2. 2
    Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line

    Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell... 由 Steininger, Anne, Ebert, Grit, Becker, Benjamin V., Assaf, Chalid, Möbs, Markus, Schmidt, Christian A., Grabarczyk, Piotr, Jensen, Lars R., Przybylski, Grzegorz K., Port, Matthias, Kuss, Andreas W., Ullmann, Reinhard

    出版 2018
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  3. 3
    Genomic loss of the putative tumor suppressor gene E2A in human lymphoma

    Genomic loss of the putative tumor suppressor gene E2A in human lymphoma 由 Steininger, Anne, Möbs, Markus, Ullmann, Reinhard, Köchert, Karl, Kreher, Stephan, Lamprecht, Björn, Anagnostopoulos, Ioannis, Hummel, Michael, Richter, Julia, Beyer, Marc, Janz, Martin, Klemke, Claus-Detlev, Stein, Harald, Dörken, Bernd, Sterry, Wolfram, Schrock, Evelin, Mathas, Stephan, Assaf, Chalid

    出版 2011
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  4. 4
    Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7

    Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 由 Ebert, Grit, Steininger, Anne, Weißmann, Robert, Boldt, Vivien, Lind-Thomsen, Allan, Grune, Jana, Badelt, Stefan, Heßler, Melanie, Peiser, Matthias, Hitzler, Manuel, Jensen, Lars R, Müller, Ines, Hu, Hao, Arndt, Peter F, Kuss, Andreas W, Tebel, Katrin, Ullmann, Reinhard

    出版 2014
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  5. 5
    Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

    Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum 由 Thorwarth, Anne, Schnittert-Hübener, Sarah, Schrumpf, Pamela, Müller, Ines, Jyrch, Sabine, Dame, Christof, Biebermann, Heike, Kleinau, Gunnar, Katchanov, Juri, Schuelke, Markus, Ebert, Grit, Steininger, Anne, Bönnemann, Carsten, Brockmann, Knut, Christen, Hans-Jürgen, Crock, Patricia, deZegher, Francis, Griese, Matthias, Hewitt, Jacqueline, Ivarsson, Sten, Hübner, Christoph, Kapelari, Klaus, Plecko, Barbara, Rating, Dietz, Stoeva, Iva, Ropers, Hans-Hilger, Grüters, Annette, Ullmann, Reinhard, Krude, Heiko

    出版 2014
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