The quest for companions to post-common envelope binaries I. Searching a sample of stars from the CSS and SDSS von BACKHAUS, U, BAUER, S, DETTE, J, DUBBERT, J, MIOSGA, T, ROCHUS VOGEL, A. L, SIMONS, S, BIRIUK, S, DEBRAH, M, GRIEMENS, M, HAHN, A, MÖLLER, T, BEUERMANN, K, PAWLOWSKI, M, SCHWEIZER, M, SPECK, A.-L, ZAPROS, C, BOLLMANN, T, HABERMANN, F. N, HAUSTOVICH, N, LAUSER, M, LIEBING, F, NIEDERSTADT, F, DIESE, J, HOPPEN, K, KINDERMANN, D, KÜPPERS, F, RAUCH, B, ALTHOFF, F, HORSTMANN, M, KELLERMAN, J. N, KIETZ, R, NIENABER, T, SAUER, M, DREIZLER, S, SECCI, A, WÜLLNER, L, HESSMAN, F. V, HUSSER, T.-O, KLAPDOHR, K.-H, MÖLLMANNS, J, SCHÜNECKE, R

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The quest for companions to post-common envelope binaries von Backhaus, U., Bauer, S., Beuermann, K., Diese, J., Dreizler, S., Hessman, F. V., Husser, T.-O., Klapdohr, K.-H., Möllmanns, J., Schünecke, R., Dette, J., Dubbert, J., Miosga, T., Rochus Vogel, A. L., Simons, S., Biriuk, S., Debrah, M., Griemens, M., Hahn, A., Möller, T., Pawlowski, M., Schweizer, M., Speck, A.-L., Zapros, C., Bollmann, T., Habermann, F. N., Haustovich, N., Lauser, M., Liebing, F., Niederstadt, F., Hoppen, K., Kindermann, D., Küppers, F., Rauch, B., Althoff, F., Horstmann, M., Kellerman, J. N., Kietz, R., Nienaber, T., Sauer, M., Secci, A., Wüllner, L.

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Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naïve Parkinson's disease patients von Bedarf, J R, Hildebrand, F, Coelho, L P, Sunagawa, S, Bahram, M, Goeser, F, Bork, P, Wüllner, U

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A53T-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice von Kurz, Alexander, Double, Kay L, Lastres-Becker, Isabel, Tozzi, Alessandro, Tantucci, Michela, Bockhart, Vanessa, Bonin, Michael, García-Arencibia, Moisés, Nuber, Silke, Schlaudraff, Falk, Liss, Birgit, Fernández-Ruiz, Javier, Gerlach, Manfred, Wüllner, Ullrich, Lüddens, Hartmut, Calabresi, Paolo, Auburger, Georg, Gispert, Suzana

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Erratum to: Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naïve Parkinson's disease patients von Bedarf, J R, Hildebrand, F, Coelho, L P, Sunagawa, S, Bahram, M, Goeser, F, Bork, P, Wüllner, U

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A genome-wide association study in multiple system atrophy von Sailer, Anna, Scholz, Sonja W, Nalls, Michael A, Schulte, Claudia, Federoff, Monica, Price, T Ryan, Lees, Andrew, Ross, Owen A, Dickson, Dennis W, Mok, Kin, Mencacci, Niccolo E, Schottlaender, Lucia, Chelban, Viorica, Ling, Helen, OʼSullivan, Sean S, Wood, Nicholas W, Traynor, Bryan J, Ferrucci, Luigi, Federoff, Howard J, Mhyre, Timothy R, Morris, Huw R, Deuschl, Günther, Quinn, Niall, Widner, Hakan, Albanese, Alberto, Infante, Jon, Bhatia, Kailash P, Poewe, Werner, Oertel, Wolfgang, Höglinger, Günter U, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Ferreira, Joaquim, Tolosa, Eduardo, Bloem, Bastiaan R, Rascol, Olivier, Meissner, Wassilios G, Hardy, John A, Revesz, Tamas, Holton, Janice L, Gasser, Thomas, Wenning, Gregor K, Singleton, Andrew B, Houlden, Henry

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MODULATING THE FLASH EFFECT ON A CELLULAR LEVEL FOR VARIABLE OXYGEN LEVELS von Jansen, J., Knoll, J., Milewski, K., Wüllner, A., Hanley, R., Aversa, I., Pagliari, F., Tirinato, L., Seco, J.

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EPD074 - MODULATING THE FLASH EFFECT ON A CELLULAR LEVEL FOR VARIABLE OXYGEN LEVELS von Jansen, J., Knoll, J., Milewski, K., Wüllner, A., Hanley, R., Aversa, I., Pagliari, F., Tirinato, L., Seco, J.

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No association of GBA mutations and multiple system atrophy von Srulijes, K., Hauser, A. -K., Guella, I., Asselta, R., Brockmann, K., Schulte, C., Soldà, G., Cilia, R., Maetzler, W., Schols, L., Wenning, G. K., Poewe, W., Barone, P., Wüllner, U., Oertel, W., Berg, D., Goldwurm, S., Gasser, T.

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SNCA variants are associated with increased risk for multiple system atrophy von Scholz, Sonja W., Houlden, Henry, Schulte, Claudia, Sharma, Manu, Li, Abi, Berg, Daniela, Melchers, Anna, Paudel, Reema, Gibbs, J. Raphael, Simon-Sanchez, Javier, Paisan-Ruiz, Coro, Bras, Jose, Ding, Jinhui, Chen, Honglei, Traynor, Bryan J., Arepalli, Sampath, Zonozi, Ryan R., Revesz, Tamas, Holton, Janice, Wood, Nick, Lees, Andrew, Oertel, Wolfgang, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Illig, Thomas, Riess, Olaf, Fernandez, Hubert H., Rodriguez, Ramon L., Okun, Michael S., Poewe, Werner, Wenning, Gregor K., Hardy, John A., Singleton, Andrew B., Gasser, Thomas

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Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3) von Hübener, Jeannette, Weber, Jonasz Jeremiasz, Richter, Claudia, Honold, Lisa, Weiss, Andreas, Murad, Fabronia, Breuer, Peter, Wüllner, Ullrich, Bellstedt, Peter, Paquet-Durand, Francois, Takano, Jiro, Saido, Takaomi C, Riess, Olaf, Nguyen, Huu Phuc

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Peroxisome proliferator-activated receptor gamma agonists protect cerebellar granule cells from cytokine-induced apoptotic cell death by inhibition of inducible nitric oxide syntha... von Heneka, Michael T, L. Feinstein, Douglas, Galea, Elena, Gleichmann, Marc, Wüllner, Ullrich, Klockgether, Thomas

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Inflammatory Genes Are Upregulated in Expanded Ataxin-3-Expressing Cell Lines and Spinocerebellar Ataxia Type 3 Brains von Evert, Bernd O, Vogt, Ina R, Kindermann, Claudia, Ozimek, Lucia, de Vos, Rob A. I, Brunt, Ewout R. P, Schmitt, Ina, Klockgether, Thomas, Wullner, Ullrich

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mRNA-Expression of ERα, ERβ, and PR in Clonal Stem Cell Cultures Obtained from Human Endometrial Biopsies von Kiesel, L., Wüllner, S., Braun, J., Schüring, A. N., Gotte, Martin

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The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group von Kamm, C., Healy, D. G., Quinn, N. P., Wüllner, U., Moller, J. C., Schols, L., Geser, F., Burk, K., Børglum, A. D., Pellecchia, M. T., Tolosa, E., del Sorbo, F., Nilsson, C., Bandmann, O., Sharma, M., Mayer, P., Gasteiger, M., Haworth, A., Ozawa, T., Lees, A. J., Short, J., Giunti, P., Holinski-Feder, E., Illig, T., Wichmann, H. E., Wenning, G. K., Wood, N. W., Gasser, T.

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Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features von Synofzik, Matthis, Beetz, Christian, Bauer, Claudia, Bonin, Michael, Sanchez-Ferrero, Elena, Schmitz-Hübsch, Tanja, Wüllner, Ullrich, Nägele, Thomas, Riess, Olaf, Schöls, Ludger, Bauer, Peter

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Neurobeachin: A Protein Kinase A-Anchoring, beige/Chediak-Higashi Protein Homolog Implicated in Neuronal Membrane Traffic von Wang, Xiaolu, Herberg, Friedrich W, Laue, Michael M, Wullner, Christiane, Hu, Bin, Petrasch-Parwez, Elisabeth, Kilimann, Manfred W

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Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy von LINNEBANK, M, KEMP, S, SCHLEGEL, U, SCHMIDT, S, KLOCKGETHER, T, WÜLLNER, U, WANDERS, R. J. A, KLEIJER, W. J, VAN DER STERRE, M. L. T, GÄRTNER, J, FLIESSBACH, K, SEMMLER, A, SOKOLOWSKI, P, KÖHLER, W

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Rapamycin alleviates toxicity of different aggregate-prone proteins von Berger, Zdenek, Ravikumar, Brinda, Menzies, Fiona M., Oroz, Lourdes Garcia, Underwood, Benjamin R., Pangalos, Menelas N., Schmitt, Ina, Wullner, Ullrich, Evert, Bernd O., O'Kane, Cahir J., Rubinsztein, David C.

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Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds von Bauer, Peter, Stevanin, Giovanni, Beetz, Christian, Synofzik, Matthis, Schmitz-Hübsch, Tanja, Wüllner, Ullrich, Berthier, Eric, Ollagnon-Roman, Elisabeth, Riess, Olaf, Forlani, Sylvie, Mundwiller, Emeline, Durr, Alexandra, Schöls, Ludger, Brice, Alexis

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