Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/ initiating cell properties von Fahlbusch, Sera Selina, Keil, Silvia, Epplen, Jörg T, Zänker, Kurt S, Dittmar, Thomas

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Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries von Ocklenburg, Sebastian, Schmitz, Judith, Moinfar, Zahra, Moser, Dirk, Klose, Rena, Lor, Stephanie, Kunz, Georg, Tegenthoff, Martin, Faustmann, Pedro, Francks, Clyde, Epplen, Jörg T, Kumsta, Robert, Güntürkün, Onur

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Activation of NPY-Y2 receptors ameliorates disease pathology in the R6/2 mouse and PC12 cell models of Huntington's disease von Fatoba, Oluwaseun, Kloster, Eugen, Reick, Christiane, Saft, Carsten, Gold, Ralf, Epplen, Jörg T., Arning, Larissa, Ellrichmann, Gisa

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PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness von Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M, Hengstler, Jan G, Falkenstein, Michael, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian

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Pathogenetic and Clinical Aspects of Anti-Neutrophil Cytoplasmic Autoantibody-Associated Vasculitides von Lamprecht, Peter, Kerstein, Anja, Klapa, Sebastian, Schinke, Susanne, Karsten, Christian M, Yu, Xinhua, Ehlers, Marc, Epplen, Jörg T, Holl-Ulrich, Konstanze, Wiech, Thorsten, Kalies, Kathrin, Lange, Tanja, Laudien, Martin, Laskay, Tamas, Gemoll, Timo, Schumacher, Udo, Ullrich, Sebastian, Busch, Hauke, Ibrahim, Saleh, Fischer, Nicole, Hasselbacher, Katrin, Pries, Ralph, Petersen, Frank, Weppner, Gesche, Manz, Rudolf, Humrich, Jens Y, Nieberding, Relana, Riemekasten, Gabriela, Müller, Antje

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Handedness and the X chromosome: The role of androgen receptor CAG-repeat length von Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M., Hengstler, Jan G., Falkenstein, Michael, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Endocannabinergic modulation of central serotonergic activity in healthy human volunteers von Emons, Barbara, Arning, Larissa, Makulla, Vera-Estelle, Suchy, Maria-Theresia, Tsikas, Dimitrios, Lücke, Thomas, Epplen, Jörg T, Juckel, Georg, Roser, Patrik

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rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants von Glas, Jürgen, Seiderer, Julia, Wetzke, Martin, Konrad, Astrid, Török, Helga-Paula, Schmechel, Silke, Tonenchi, Laurian, Grassl, Christine, Dambacher, Julia, Pfennig, Simone, Maier, Kerstin, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T, Schiemann, Uwe, Folwaczny, Christian, Lohse, Peter, Göke, Burkhard, Ochsenkühn, Thomas, Müller-Myhsok, Bertram, Folwaczny, Matthias, Mussack, Thomas, Brand, Stephan

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Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes von Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T, Arning, Larissa

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On the relevance of the NPY2-receptor variation for modes of action cascading processes von Beste, Christian, Stock, Ann-Kathrin, Epplen, Jörg T., Arning, Larissa

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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease von Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa

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Prospective Evaluation of Predictive DNA Testing for Huntington’s Disease in a Large German Center von Ibisler, Aysegül, Ocklenburg, Sebastian, Stemmler, Susanne, Arning, Larissa, Epplen, Jörg T., Saft, Carsten, Hoffjan, Sabine

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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification von Rutsch, Frank, Ruf, Nico, Vaingankar, Sucheta, Toliat, Mohammad R., Suk, Anita, Höhne, Wolfgang, Schauer, Galen, Lehmann, Mandy, Roscioli, Tony, Schnabel, Dirk, Epplen, Jörg T., Knisely, Alex, Superti-Furga, Andrea, McGill, James, Filippone, Marco, Sinaiko, Alan R., Vallance, Hillary, Hinrichs, Bernd, Smith, Wendy, Ferre, Merry, Terkeltaub, Robert, Nürnberg, Peter

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Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults von Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Hengstler, Jan G., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Akkad, Denis A.

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Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization von Ocklenburg, Sebastian, Arning, Larissa, Hahn, Constanze, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

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Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization von Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M, Epplen, Jörg T, Güntürkün, Onur, Beste, Christian

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The genetics of atopic dermatitis : recent findings and future options von HOFFJAN, Sabine, EPPLEN, Jörg T

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Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset von Glas, Jürgen, Seiderer, Julia, Nagy, Melinda, Fries, Christoph, Beigel, Florian, Weidinger, Maria, Pfennig, Simone, Klein, Wolfram, Epplen, Jörg T, Lohse, Peter, Folwaczny, Matthias, Göke, Burkhard, Ochsenkühn, Thomas, Diegelmann, Julia, Müller-Myhsok, Bertram, Roeske, Darina, Brand, Stephan

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Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity von Akkad, Denis A, Olischewsky, Alexandra, Reiner, Franziska, Hellwig, Kerstin, Esser, Sarika, Epplen, Jörg T, Curk, Tomaz, Gold, Ralf, Haghikia, Aiden

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Ccdc66 null mutation causes retinal degeneration and dysfunction von GERDING, Wanda M, SCHREIBER, Sabrina, RÜLICKE, Thomas, IBRAHIM, Saleh, EPPLEN, Jörg T, PETRASCH-PARWEZ, Elisabeth, SCHULTE-MIDDELMANN, Tobias, DE CASTRO MARQUES, Andreia, ATORF, Jenny, AKKAD, Denis A, DEKOMIEN, Gabriele, KREMERS, Jan, DERMIETZEL, Rolf, GAL, Andreas

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