Search Results - Janssen, Johannes WG

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  1. 1
    Body fluid derived exosomes as a novel template for clinical diagnostics

    Body fluid derived exosomes as a novel template for clinical diagnostics by Keller, Sascha, Ridinger, Johannes, Rupp, Anne-Kathleen, Janssen, Johannes W G, Altevogt, Peter

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  2. 2
    Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia

    Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia by Kaiser, Ann-Sophie, Maas, Bianca, Wolff, Anna, Sutter, Christian, Janssen, Johannes W G, Hinderhofer, Katrin, Moog, Ute

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  3. 3
    3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior

    3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior by Dikow, Nicola, Maas, Bianca, Karch, Stephanie, Granzow, Martin, Janssen, Johannes W.G., Jauch, Anna, Hinderhofer, Katrin, Sutter, Christian, Schubert-Bast, Susanne, Anderlid, Britt Marie, Dallapiccola, Bruno, Van der Aa, Nathalie, Moog, Ute

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  4. 4
    Mosaic deletion of EXOC6B: Further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability

    Mosaic deletion of EXOC6B: Further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability by Evers, Christina, Maas, Bianca, Koch, Karin A., Jauch, Anna, Janssen, Johannes W.G., Sutter, Christian, Parker, Michael J., Hinderhofer, Katrin, Moog, Ute

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  5. 5
    Chromosomal instability correlates with poor outcome in patients with myelodysplastic syndromes irrespectively of the cytogenetic risk group

    Chromosomal instability correlates with poor outcome in patients with myelodysplastic syndromes irrespectively of the cytogenetic risk group by Heilig, Christoph E., Löffler, Harald, Mahlknecht, Ulrich, Janssen, Johannes W.G., Ho, Anthony D., Jauch, Anna, Krämer, Alwin

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  6. 6
    The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1: Is it really a reversed sotos syndrome?

    The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1: Is it really a reversed sotos syndrome? by Dikow, Nicola, Maas, Bianca, Gaspar, Harald, Kreiss-Nachtsheim, Martina, Engels, Hartmut, Kuechler, Alma, Garbes, Lutz, Netzer, Christian, Neuhann, Teresa M., Koehler, Udo, Casteels, Kristina, Devriendt, Koen, Janssen, Johannes W.G., Jauch, Anna, Hinderhofer, Katrin, Moog, Ute

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  7. 7
    Duplication Xp11.22-p14 in females: Does X-inactivation help in assessing their significance?

    Duplication Xp11.22-p14 in females: Does X-inactivation help in assessing their significance? by Evers, Christina, Mitter, Diana, Strobl-Wildemann, Gertrud, Haug, Ulrich, Hackmann, Karl, Maas, Bianca, Janssen, Johannes W. G., Jauch, Anna, Hinderhofer, Katrin, Moog, Ute

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  8. 8
    A 15q24 microdeletion in transient myeloproliferative disease (TMD) and acute megakaryoblastic leukaemia (AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/AMKL

    A 15q24 microdeletion in transient myeloproliferative disease (TMD) and acute megakaryoblastic leukaemia (AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/AMKL by Haemmerling, Susanne, Behnisch, Wolfgang, Doerks, Tobias, Korbel, Jan O., Bork, Peer, Moog, Ute, Hentze, Sabine, Grasshoff, Ute, Bonin, Michael, Rieß, Olaf, Janssen, Johannes W. G., Jauch, Anna, Bartram, Claus R., Reinhardt, Dirk, Koch, Karin A., Bandapalli, Obul R., Kulozik, Andreas E.

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  9. 9
    Control of MYEOV Protein Synthesis by Upstream Open Reading Frames

    Control of MYEOV Protein Synthesis by Upstream Open Reading Frames by de Almeida, Rogério Alves, Heuser, Tanja, Blaschke, Rüdiger, Bartram, Claus R., Janssen, Johannes W.G.

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  10. 10
    Activation of gef‐h1, a guanine nucleotide exchange factor for RhoA, by DNA transfection

    Activation of gef‐h1, a guanine nucleotide exchange factor for RhoA, by DNA transfection by Brecht, Marcus, Steenvoorden, Agatha C.M., Collard, John G., Luf, Susanne, Erz, Dorothee, Bartram, Claus R., Janssen, Johannes W.G.

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  11. 11
    Sequencing of a Patient with Balanced Chromosome Abnormalities and Neurodevelopmental Disease Identifies Disruption of Multiple High Risk Loci by Structural Variation: e90894

    Sequencing of a Patient with Balanced Chromosome Abnormalities and Neurodevelopmental Disease Identifies Disruption of Multiple High Risk Loci by Structural Variation: e90894 by Blake, Jonathon, Riddell, Andrew, Theiss, Susanne, Gonzalez, Alexis Perez, Haase, Bettina, Jauch, Anna, Janssen, Johannes WG, Ibberson, David, Pavlinic, Dinko, Moog, Ute

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