Rezultati - 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 od Tebel, Katrin, Boldt, Vivien, Steininger, Anne, Port, Matthias, Ebert, Grit, Ullmann, Reinhard

    Izdano 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... od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 2014
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