Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development von BLASCHKE, Rudiger J, HAHURIJ, Nathan D, SCHÖLER, Hans, FEITSMA, Harma, ROTTBAUER, Wolfgang, BLUM, Martin, MEIJLINK, Frits, RAPPOLD, Gudrun, GITTENBERGER-DE GROOT, Adriana C, KUIJPER, Sanne, JUST, Steffen, WISSE, Lambertus J, DEISSLER, Kirsten, MAXELON, Tina, ANASTASSIADIS, Konstantinos, SPITZER, Jessica, HARDT, Stefan E

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Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart von Puskaric, Sandra, Schmitteckert, Stefanie, Mori, Alessandro D., Glaser, Anne, Schneider, Katja U., Bruneau, Benoit G., Blaschke, Rüdiger J., Steinbeisser, Herbert, Rappold, Gudrun

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SHOT, a SHOX-Related Homeobox Gene, is Implicated in Craniofacial, Brain, Heart, and Limb Development von Blaschke, Rudiger J., Monaghan, A. Paula, Schiller, Simone, Schechinger, Birgit, Rao, Ercole, Padilla-Nash, Hesed, Ried, Thomas, Rappold, Gudrun A.

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The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome von CLEMENT-JONES, M, SCHILLER, S, LINDSAY, S, RAPPOLD, G. A, RAO, E, BLASCHKE, R. J, ZUNIGA, A, ZELLER, R, ROBSON, S. C, BINDER, G, GLASS, I, STRACHAN, T

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The Short Stature Homeodomain Protein SHOX Induces Cellular Growth Arrest and Apoptosis and Is Expressed in Human Growth Plate Chondrocytes von Marchini, Antonio, Marttila, Tiina, Winter, Anja, Caldeira, Sandra, Malanchi, Ilaria, Blaschke, Rüdiger J., Häcker, Beate, Rao, Ercole, Karperien, Marcel, Wit, Jan M., Richter, Wiltrud, Tommasino, Massimo, Rappold, Gudrun A.

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Impairment of SHOX nuclear localization as a cause for Léri-Weill syndrome von Sabherwal, Nitin, Schneider, Katja U, Blaschke, Rüdiger J, Marchini, Antonio, Rappold, Gudrun

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SHOX: Growth, Léri–Weill and Turner Syndromes von Blaschke, Rüdiger J, Rappold, Gudrun A

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Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX von Blaschke, Rudiger J, Töpfer, Christine, Marchini, Antonio, Steinbeisser, Herbert, Janssen, Johannes W G, Rappold, Gudrun A

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Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis von Schneider, Katja U., Marchini, Antonio, Sabherwal, Nitin, Röth, Ralph, Niesler, Beate, Marttila, Tiina, Blaschke, Rüdiger J., Lawson, Margaret, Dumic, Miroslav, Rappold, Gudrun

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The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator von Rao, E, Blaschke, R J, Marchini, A, Niesler, B, Burnett, M, Rappold, G A

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Phosphorylation on Ser106 modulates the cellular functions of the SHOX homeodomain protein von Marchini, Antonio, Daeffler, Laurent, Marttila, Tiina, Schneider, Katja U, Blaschke, Rüdiger J, Schnölzer, Martina, Rommelaere, Jean, Rappold, Gudrun

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Impairment of SHOX nuclear localization as a cause for Léri-Weill syndrome von Sabherwal, Nitin, Schneider, Katja U., Blaschke, Rüdiger J., Marchini, Antonio, Rappold, Gudrun

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The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator von Rao, E.

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Phosphorylation on Ser 106 Modulates the Cellular Functions of the SHOX Homeodomain Protein von Marchini, Antonio, Daeffler, Laurent, Marttila, Tiina, Schneider, Katja U., Blaschke, Rüdiger J., Schnölzer, Martina, Rommelaere, Jean, Rappold, Gudrun

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SHOX in Short Stature Syndromes von Blaschke, Rüdiger J., Rappold, Gudrun A.

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Man to mouse--lessons learned from the distal end of the human X chromosome von Blaschke, R J, Rappold, G A

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A Novel Murine PKA-Related Protein Kinase Involved in Neuronal Differentiation von Blaschke, Rüdiger J., Monaghan, A.Paula, Bock, Dagmar, Rappold, Gudrun A.

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