3406 Receptor tyrosine kinase gene expression analyses of Ewing sarcomas identify ROR1 as a potential therapeutic target in metastatic disease von Berning, P, Tillmanns, A, Korsching, E, Lechtape, B, Schaefer, C, Schleithoff, C, schäfer, L, Dirksen, U, Potratz, J

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GSK-3β controls NF-kappaB activity via IKKγ/NEMO von Medunjanin, Senad, Schleithoff, Lisa, Fiegehenn, Christian, Weinert, Soenke, Zuschratter, Werner, Braun-Dullaeus, Ruediger C.

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Calcitriol Deficiency and 1-Year Mortality in Cardiac Transplant Recipients von ZITTERMANN, Armin, SCHLEITHOFF, Stefanie S, GDTTING, Christian, FUCHS, Uwe, KUHN, Joachim, KLEESIEK, Knut, TENDERICH, Gero, KOERFER, Reiner

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SC30.02 ASSESSING THE PROBABILITY OF NORMAL TISSUE COMPLICATION FOR CHILDHOOD BRAIN TUMORS von Heinzelmann, F., Bäumer, C., Peters, S., Stock, A., Lühr, A., Schulze-Schleithoff, S., Frisch, S., Timmermann, B.

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OC-0248: Proton Beam Therapy in childhood – First 2-years of practice results from the WPE von Mazhari, A.L, Schulze Schleithoff, S, Guntrum, F, Plass, C, Stickan-Verfürth, M, Lambert, J, Blase, C, Fleischhack, G, Christiaens, M, Timmermann, B

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Screening of the Ryanodine Receptor Gene in 105 Malignant Hyperthermia Families: Novel Mutations and Concordance with the in Vitro Contracture Test von Brandt, Annebill, Schleithoff, Lothar, Jurkat-Rott, Karin, Klingler, Werner, Baur, Christoph, Lehmann-Horn, Frank

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A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions von Lerche, H., Biervert, C., Alekov, A. K., Schleithoff, L., Lindner, M., Klingler, W., Bretschneider, F., Mitrovic, N., Jurkat-Rott, K., Bode, H., Lehmann-Horn, F., Steinlein, O. K.

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The dominant chloride channel mutant G200R causing fluctuating myotonia: Clinical findings, electrophysiology, and channel pathology von Wagner, Susanne, Deymeer, Feza, Kürz, Lothar L., Benz, Sandra, Schleithoff, Lothar, Lehmann-Horn, Frank, Serdaroğlu, Piraye, Özdemir, Coskun, Rüdel, Reinhardt

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An oncogenic fusion product of the phosphatidylinositol 3-kinase p85beta subunit and HUMORF8, a putative deubiquitinating enzyme von Janssen, J W, Schleithoff, L, Bartram, C R, Schulz, A S

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A Pvull-polymorphism within the AXL gene on chromosome 19q13.1 von Linz, Ute, Schleithoff, Lothar, Janssen, Johannes W.G., Bartram, Claus R., MüIIer, C.R.

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A PvuII-polymorphism within the AXL gene on chromosome 19q13.1 von Linz, U, Schleithoff, L, Janssen, J W, Bartram, C R, Müller, C R

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