Cell fusion-independent differentiation of neural stem cells to the endothelial lineage von Gage, Fred H, Wurmser, Andrew E, Nakashima, Kinichi, Summers, Robert G, Toni, Nicolas, D'Amour, Kevin A, Lie, Dieter C

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CNTF and its receptor subunits in human gliomas von Weis, J, Schönrock, L M, Züchner, S L, Lie, D C, Sure, U, Schul, C, Stögbauer, F, Ringelstein, E B, Halfter, H

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Cell fusion-independent differentiation of neural stem cells to the endowelial lineage von WURMSER, Andrew E, NAKASHIMA, Kinichl, SUMMERS, Robert G, TONI, Nicolas, D'AMOUR, Kevin A, LIE, Dieter C, GAGE, Fred H

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Wnt signalling regulates adult hippocampal neurogenesis von Gage, Fred H, Dearie, Alejandro R, Lein, Edward S, Lie, Dieter-Chichung, Colamarino, Sophia A, Song, Hong-Jun, Mira, Helena, Lansford, Heather, Jessberger, Sebastian, Désiré, Laurent, Consiglio, Antonella

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Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis von Hov, Johannes R, Keitel, Verena, Laerdahl, Jon K, Spomer, Lina, Ellinghaus, Eva, ElSharawy, Abdou, Melum, Espen, Boberg, Kirsten M, Manke, Thomas, Balschun, Tobias, Schramm, Christoph, Bergquist, Annika, Weismüller, Tobias, Gotthardt, Daniel, Rust, Christian, Henckaerts, Liesbet, Onnie, Clive M, Weersma, Rinse K, Sterneck, Martina, Teufel, Andreas, Runz, Heiko, Stiehl, Adolf, Ponsioen, Cyriel Y, Wijmenga, Cisca, Vatn, Morten H, Stokkers, Pieter C F, Vermeire, Severine, Mathew, Christopher G, Lie, Benedicte A, Beuers, Ulrich, Manns, Michael P, Schreiber, Stefan, Schrumpf, Erik, Häussinger, Dieter, Franke, Andre, Karlsen, Tom H

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Exon‐disrupting deletions of NRXN1 in idiopathic generalized epilepsy von Møller, Rikke S., Weber, Yvonne G., Klitten, Laura L., Trucks, Holger, Muhle, Hiltrud, Kunz, Wolfram S., Mefford, Heather C., Franke, Andre, Kautza, Monika, Wolf, Peter, Dennig, Dieter, Schreiber, Stefan, Rückert, Ina‐Maria, Wichmann, H.‐Erich, Ernst, Jan P., Schurmann, Claudia, Grabe, Hans J., Tommerup, Niels, Stephani, Ulrich, Lerche, Holger, Hjalgrim, Helle, Helbig, Ingo, Sander, Thomas

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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies von Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G, Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C M, Koeleman, Bobby P, Lindhout, Dick, Weber, Yvonne G, Lerche, Holger, Kapser, Claudia, Schankin, Christoph J, Kunz, Wolfram S, Surges, Rainer, Elger, Christian E, Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M, Rosenow, Felix, Neubauer, Bernd A, Reinthaler, Eva M, Zimprich, Fritz, Feucht, Martha, Møller, Rikke S, Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas

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Autophagy and Adult Neurogenesis: Discoveries Made Half a Century Ago Yet in their Infancy of being Connected von Dhaliwal, Jagroop, Trinkle-Mulcahy, Laura, Lagace, Diane C

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miRNA-Mediated Regulation of Adult Hippocampal Neurogenesis; Implications for Epilepsy von Bielefeld, Pascal, Mooney, Catherine, Henshall, David C, Fitzsimons, Carlos P

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Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy von Lal, Dennis, Trucks, Holger, Møller, Rikke S., Hjalgrim, Helle, Koeleman, Bobby P. C., Kovel, Carolien G. F., Visscher, Frank, Weber, Yvonne G., Lerche, Holger, Becker, Felicitas, Schankin, Christoph J., Neubauer, Bernd A., Surges, Rainer, Kunz, Wolfram S., Zimprich, Fritz, Franke, Andre, Illig, Thomas, Ried, Janina S., Leu, Costin, Nürnberg, Peter, Sander, Thomas

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Genomic Imprinting and the Regulation of Postnatal Neurogenesis von Lozano-Ureña, Anna, Montalbán-Loro, Raquel, Ferguson-Smith, Anne C, Ferrón, Sacri R

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16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy von Reinthaler, Eva M, Lal, Dennis, Lebon, Sebastien, Hildebrand, Michael S, Dahl, Hans-Henrik M, Regan, Brigid M, Feucht, Martha, Steinböck, Hannelore, Neophytou, Birgit, Ronen, Gabriel M, Roche, Laurian, Gruber-Sedlmayr, Ursula, Geldner, Julia, Haberlandt, Edda, Hoffmann, Per, Herms, Stefan, Gieger, Christian, Waldenberger, Melanie, Franke, Andre, Wittig, Michael, Schoch, Susanne, Becker, Albert J, Hahn, Andreas, Männik, Katrin, Toliat, Mohammad R, Winterer, Georg, Lerche, Holger, Nürnberg, Peter, Mefford, Heather, Scheffer, Ingrid E, Berkovic, Samuel F, Beckmann, Jacques S, Sander, Thomas, Jacquemont, Sebastien, Reymond, Alexandre, Zimprich, Fritz, Neubauer, Bernd A

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Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10 von Bierbaum, Sibylle, Forster, Johannes, Berner, Reinhard, Rücker, Gerta, Rohde, Gernot, Neumann-Haefelin, Dieter, Panning, Marcus

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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies von Leu, Costin, de Kovel, Carolien G.F., Zara, Federico, Striano, Pasquale, Pezzella, Marianna, Robbiano, Angela, Bianchi, Amedeo, Bisulli, Francesca, Coppola, Antonietta, Giallonardo, Anna Teresa, Beccaria, Francesca, Trenité, Dorothée Kasteleijn-Nolst, Lindhout, Dick, Gaus, Verena, Schmitz, Bettina, Janz, Dieter, Weber, Yvonne G., Becker, Felicitas, Lerche, Holger, Kleefuß-Lie, Ailing A., Hallman, Kerstin, Kunz, Wolfram S., Elger, Christian E., Muhle, Hiltrud, Stephani, Ulrich, Møller, Rikke S., Hjalgrim, Helle, Mullen, Saul, Scheffer, Ingrid E., Berkovic, Samuel F., Everett, Kate V., Gardiner, Mark R., Marini, Carla, Guerrini, Renzo, Lehesjoki, Anna-Elina, Siren, Auli, Nabbout, Rima, Baulac, Stephanie, Leguern, Eric, Serratosa, Jose M., Rosenow, Felix, Feucht, Martha, Unterberger, Iris, Covanis, Athanasios, Suls, Arvid, Weckhuysen, Sarah, Kaneva, Radka, Caglayan, Hande, Turkdogan, Dilsad, Baykan, Betul, Bebek, Nerses, Ozbek, Ugur, Hempelmann, Anne, Schulz, Herbert, Rüschendorf, Franz, Trucks, Holger, Nürnberg, Peter, Avanzini, Giuliano, Koeleman, Bobby P.C., Sander, Thomas

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Investigation of GRIN2A in common epilepsy phenotypes von Lal, Dennis, Steinbrücker, Sandra, Schubert, Julian, Sander, Thomas, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Krause, Roland, Lehesjoki, Anna-Elina, Nürnberg, Peter, Palotie, Aarno, Neubauer, Bernd A, Muhle, Hiltrud, Stephani, Ulrich, Helbig, Ingo, Becker, Albert J, Schoch, Susanne, Hansen, Jörg, Dorn, Thomas, Hohl, Christin, Lüscher, Nicole, von Spiczak, Sarah, Lemke, Johannes R

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Correction: Human Cytomegalovirus Entry into Dendritic Cells Occurs via a Macropinocytosis-Like Pathway in a pH-Independent and Cholesterol-Dependent Manner von Haspot, Fabienne, Lavault, Amélie, Sinzger, Christian, Laib Sampaio, Kerstin, Stierhof, York-Dieter, Pilet, Paul, Bressolette-Bodin, Céline, Halary, Franck

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Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis von Hov, Johannes R, Keitel, Verena, Laerdahl, Jon K, Spomer, Lina, Ellinghaus, Eva, ElSharawy, Abdou, Melum, Espen, Boberg, Kirsten M, Manke, Thomas, Balschun, Tobias, Schramm, Christoph, Bergquist, Annika, Weismüller, Tobias, Gotthardt, Daniel, Rust, Christian, Henckaerts, Liesbet, Onnie, Clive M, Weersma, Rinse K, Sterneck, Martina, Teufel, Andreas, Runz, Heiko, Stiehl, Adolf, Ponsioen, Cyriel Y, Wijmenga, Cisca, Vatn, Morten H, Stokkers, Pieter C. F, Vermeire, Severine, Mathew, Christopher G, Lie, Benedicte A, Beuers, Ulrich, Manns, Michael P, Schreiber, Stefan, Schrumpf, Erik, Häussinger, Dieter, Franke, Andre, Karlsen, Tom H

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