Electrochemical reaction of CO2 to CO on a catalyst coated cation exchange membrane enabled by ammonium proton shuttling von Reinisch, D, Reichbauer, T, Vetter, K M, Martić, N, Mayrhofer, K J J, Schmid, G

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Evolution of nitrogen concentration and ammonia production in N2-seeded H-mode discharges at ASDEX Upgrade von Drenik, A., Laguardia, L., McDermott, R., Meisl, G., Neu, R., Oberkofler, M., Pawelec, E., Pitts, R.A., Potzel, S., Pütterich, T., Reichbauer, T., Rohde, V., Seibt, M., De Temmerman, G., Zaplotnik, R.

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Electrochemical reaction of CO to CO on a catalyst coated cation exchange membrane enabled by ammonium proton shuttling von Reinisch, D, Reichbauer, T, Vetter, K. M, Marti, N, Mayrhofer, K. J. J, Schmid, G

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Electrochemical reaction of CO 2 to CO on a catalyst coated cation exchange membrane enabled by ammonium proton shuttling von Reinisch, D., Reichbauer, T., Vetter, K. M., Martić, N., Mayrhofer, K. J. J., Schmid, G.

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Evolution of nitrogen concentration and ammonia production in N 2 -seeded H-mode discharges at ASDEX Upgrade von Drenik, A., Laguardia, L., McDermott, R., Meisl, G., Neu, R., Oberkofler, M., Pawelec, E., Pitts, R.A., Potzel, S., Pütterich, T., Reichbauer, T., Rohde, V., Seibt, M., De Temmerman, G., Zaplotnik, R.

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Link between divertor conditions and high-field-side/low-field-side midplane density profiles in H-mode plasmas at ASDEX Upgrade von Guimarais, L., Silva, C., Bernert, M., Brida, D., Cavedon, M., Conway, G.D., Drenik, A., Gil, L., Reichbauer, T., Reimold, F., Santos, J., Seliunin, E., Silva, A., Stroth, U., Vicente, J., Wolfrum, E.

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Evaluation of the plasma hydrogen isotope content by residual gas analysis at JET and AUG von Drenik, A, Alegre, D, Brezinsek, S, De Castro, A, Kruezi, U, Oberkofler, M, Panjan, M, Primc, G, Reichbauer, T, Resnik, M, Rohde, V, Seibt, M, Schneider, P A, Wauters, T, Zaplotnik, R

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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications von Rattay, Tim W, Lindig, Tobias, Baets, Jonathan, Smets, Katrien, Deconinck, Tine, Söhn, Anne S, Hörtnagel, Konstanze, Eckstein, Kathrin N, Wiethoff, Sarah, Reichbauer, Jennifer, Döbler-Neumann, Marion, Krägeloh-Mann, Ingeborg, Auer-Grumbach, Michaela, Plecko, Barbara, Münchau, Alexander, Wilken, Bernd, Janauschek, Marc, Giese, Anne-Katrin, De Bleecker, Jan L, Ortibus, Els, Debyser, Martine, Lopez de Munain, Adolfo, Pujol, Aurora, Bassi, Maria Teresa, D'Angelo, Maria Grazia, De Jonghe, Peter, Züchner, Stephan, Bauer, Peter, Schöls, Ludger, Schüle, Rebecca

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Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia von Wagner, Matias, Osborn, Daniel P. S., Gehweiler, Ina, Nagel, Maike, Ulmer, Ulrike, Bakhtiari, Somayeh, Amouri, Rim, Boostani, Reza, Hentati, Faycal, Hockley, Maryam M., Hölbling, Benedikt, Schwarzmayr, Thomas, Karimiani, Ehsan Ghayoor, Kernstock, Christoph, Maroofian, Reza, Müller-Felber, Wolfgang, Ozkan, Ege, Padilla-Lopez, Sergio, Reich, Selina, Reichbauer, Jennifer, Darvish, Hossein, Shahmohammadibeni, Neda, Tafakhori, Abbas, Vill, Katharina, Zuchner, Stephan, Kruer, Michael C., Winkelmann, Juliane, Jamshidi, Yalda, Schüle, Rebecca

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia von Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78) von Estrada-Cuzcano, Alejandro, Martin, Shaun, Chamova, Teodora, Synofzik, Matthis, Timmann, Dagmar, Holemans, Tine, Andreeva, Albena, Reichbauer, Jennifer, De Rycke, Riet, Chang, Dae-In, van Veen, Sarah, Samuel, Jean, Schöls, Ludger, Pöppel, Thorsten, Mollerup Sørensen, Danny, Asselbergh, Bob, Klein, Christine, Zuchner, Stephan, Jordanova, Albena, Vangheluwe, Peter, Tournev, Ivailo, Schüle, Rebecca

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Ag2Cu2O3 – a catalyst template material for selective electroreduction of CO to C2+ products von Martić, Nemanja, Reller, Christian, Macauley, Chandra, Löffler, Mario, Reichert, Andreas M, Reichbauer, Thomas, Kim-Marie Vetter, Schmid, Bernhard, McLaughlin, David, Leidinger, Paul, Reinisch, David, Vogl, Christoph, Mayrhofer, Karl J J, Katsounaros, Ioannis, Schmid, Günter

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Morphological tuning of membrane processing by temporal proton-metal cation substitution in perfluorosulfonic acid membranes von Vetter, Kim-Marie, Reichbauer, Thomas, Martić, Nemanja, Reinisch, David, Hinrichsen, Olaf, Schmid, Günter

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Assessment of nitrogen fluence from the divertor plasma in nitrogen seeded discharges von Reichbauer, Thomas, Drenik, Aleksander, McDermott, Rachael, Rohde, Volker

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Electrical energy input efficiency limitations in CO2‐to‐CO electrolysis and attempts for improvement von Reichbauer, Thomas, Schmid, Bernhard, Vetter, Kim‐Marie, Reinisch, David, Martić, Nemanja, Reller, Christian, Grasruck, Alexander, Dorta, Romano, Schmid, Günter

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Motor protein mutations cause a new form of hereditary spastic paraplegia von Caballero Oteyza, Andrés, Battaloğlu, Esra, Ocek, Levent, Lindig, Tobias, Reichbauer, Jennifer, Rebelo, Adriana P, Gonzalez, Michael A, Zorlu, Yasar, Ozes, Burcak, Timmann, Dagmar, Bender, Benjamin, Woehlke, Günther, Züchner, Stephan, Schöls, Ludger, Schüle, Rebecca

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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia von Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S, Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmüller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A, Stirnberg, Rüdiger, Sturm, Marc, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan, Heilmann-Heimbach, Stefanie, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Brüstle, Oliver, Klopstock, Thomas, Mathews, Katherine D, Shy, Michael E, de Jonghe, Peter, Chinnery, Patrick F, Horvath, Rita, Kohlhase, Jürgen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schöls, Ludger, Nürnberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo, Schüle, Rebecca

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Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46) von Sultana, Saki, Reichbauer, Jennifer, Schüle, Rebecca, Mochel, Fanny, Synofzik, Matthis, van der Spoel, Aarnoud C.

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Generation of two iPSC lines derived from two unrelated patients with Gaucher disease von Nagel, Maike, Reichbauer, Jennifer, Böhringer, Judith, Schelling, Yvonne, Krägeloh-Mann, Inge, Schüle, Rebecca, Ulmer, Ulrike

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Electrical energy input efficiency limitations in CO 2 ‐to‐CO electrolysis and attempts for improvement von Reichbauer, Thomas, Schmid, Bernhard, Vetter, Kim‐Marie, Reinisch, David, Martić, Nemanja, Reller, Christian, Grasruck, Alexander, Dorta, Romano, Schmid, Günter

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