Variability and comparability of testing procedures for PEMFC stacks and modules regarding performance aspects von Harms, Corinna, Nürnberg, Katrin, Jungmann, Thomas, Köhrmann, Frank, Dyck, Alexander

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Dysfunction of the MDM2/p53 axis is linked to premature aging von Lessel, Davor, Wu, Danyi, Trujillo, Carlos, Ramezani, Thomas, Lessel, Ivana, Alwasiyah, Mohammad K, Saha, Bidisha, Hisama, Fuki M, Rading, Katrin, Goebel, Ingrid, Schütz, Petra, Speit, Günter, Högel, Josef, Thiele, Holger, Nürnberg, Gudrun, Nürnberg, Peter, Hammerschmidt, Matthias, Zhu, Yan, Tong, David R, Katz, Chen, Martin, George M, Oshima, Junko, Prives, Carol, Kubisch, Christian

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SepT, a novel protein specific to multicellular cyanobacteria, influences peptidoglycan growth and septal nanopore formation in Anabaena sp. PCC 7120 von Velázquez-Suárez, Cristina, Springstein, Benjamin L, Nieves-Morión, Mercedes, Helbig, Andreas O, Kieninger, Ann-Katrin, Maldener, Iris, Nürnberg, Dennis J, Stucken, Karina, Luque, Ignacio, Dagan, Tal, Herrero, Antonia

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Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis von Hildebrandt, Friedhelm, Treier, Mathias, Attanasio, Massimo, Uhlenhaut, N Henriette, Sousa, Vitor H, O'Toole, John F, Otto, Edgar, Anlag, Katrin, Klugmann, Claudia, Treier, Anna-Corina, Helou, Juliana, Sayer, John A, Seelow, Dominik, Nürnberg, Gudrun, Becker, Christian, Chudley, Albert E, Nürnberg, Peter

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Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects von Baasanjav, Sevjidmaa, Al-Gazali, Lihadh, Hashiguchi, Taishi, Mizumoto, Shuji, Fischer, Bjoern, Horn, Denise, Seelow, Dominik, Ali, Bassam R., Aziz, Samir A.A., Langer, Ruth, Saleh, Ahmed A.H., Becker, Christian, Nürnberg, Gudrun, Cantagrel, Vincent, Gleeson, Joseph G., Gomez, Delphine, Michel, Jean-Baptiste, Stricker, Sigmar, Lindner, Tom H., Nürnberg, Peter, Sugahara, Kazuyuki, Mundlos, Stefan, Hoffmann, Katrin

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy von Geier, Christian, Gehmlich, Katja, Ehler, Elisabeth, Hassfeld, Sabine, Perrot, Andreas, Hayess, Katrin, Cardim, Nuno, Wenzel, Katrin, Erdmann, Bettina, Krackhardt, Florian, Posch, Maximilian G., Bublak, Angelika, Nägele, Herbert, Scheffold, Thomas, Dietz, Rainer, Chien, Kenneth R., Spuler, Simone, Fürst, Dieter O., Nürnberg, Peter, Özcelik, Cemil

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar

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Transcriptional diversity during lineage commitment of human blood progenitors von Chen, Lu, Kostadima, Myrto, Martens, Joost H. A., Canu, Giovanni, Garcia, Sara P., Turro, Ernest, Downes, Kate, Macaulay, Iain C., Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert B. G., Astle, William J., Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C., Consortium, BRIDGE, Choudry, Fizzah A., Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N., Jansen, Joop H., Favier, Rémi, Fenech, Matthew E., Foad, Nicola, Freson, Kathleen, van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M., Kerstens, Hindrik H. D., Kooner, Jaspal S., Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A., Richardson, David, Sammut, Stephen J., Slodkowicz, Greg, Tamuri, Asif U., Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J., Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H., Stunnenberg, Hendrik G., Frontini, Mattia, Rendon, Augusto

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CNSC-38. CHARACTERIZATION OF THE FUNCTIONAL RELEVANCE OF INTRA- AND INTERTUMORAL NETWORKS IN PRIMARY BREAST CANCER von Nürnberg, Christina, Schrenk-Siemens, Katrin, Würth, Roberto, Trumpp, Andreas, Mayer, Chanté, Karreman, Matthia, Pan, Chenchen, Wick, Wolfgang, Winkler, Frank

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Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment von Schulte-Schrepping, Jonas, Reusch, Nico, Paclik, Daniela, Baßler, Kevin, Schlickeiser, Stephan, Krammer, Tobias, Brumhard, Sophia, Bonaguro, Lorenzo, Wendisch, Daniel, Grasshoff, Martin, Beckstette, Michael, Pecht, Tal, Saglam, Adem, Dietrich, Oliver, Mei, Henrik E., Schulz, Axel R., Conrad, Claudia, Kunkel, Désirée, Vafadarnejad, Ehsan, Xu, Cheng-Jian, Herbert, Miriam, Drews, Anna, Thibeault, Charlotte, Pfeiffer, Moritz, Hippenstiel, Stefan, Hocke, Andreas, Müller-Redetzky, Holger, Heim, Katrin-Moira, Bosquillon de Jarcy, Laure, Stegemann, Miriam, Glösenkamp, Christoph R., Volk, Hans-Dieter, Wyler, Emanuel, Georg, Philipp, Schneider, Maria, Dang-Heine, Chantip, Neuwinger, Nick, Kappert, Kai, Corman, Victor, Raabe, Jan, Kaiser, Kim Melanie, Rieke, Gereon, Meisel, Christian, Ulas, Thomas, Becker, Matthias, Drosten, Christian, Suttorp, Norbert, Kurth, Florian, Schultze, Joachim L., Aschenbrenner, Anna C., Li, Yang, Nattermann, Jacob, Saliba, Antoine-Emmanuel, Sander, Leif Erik, Angelov, Angel, Bals, Robert, Bartholomäus, Alexander, Becker, Anke, Bonifacio, Ezio, Clavel, Thomas, Colome-Tatche, Maria, Diefenbach, Andreas, Dilthey, Alexander, Fischer, Nicole, Förstner, Konrad, Hain, Torsten, Hummel, Michael, Janssen, Stefan, Kallies, René, Kehr, Birte, Keller, Andreas, Kim-Hellmuth, Sarah, Klein, Christoph, Korbel, Jan O., Landthaler, Markus, Li, Yang, Ludwig, Kerstin, Marz, Manja, McHardy, Alice, Mertes, Christian, Nöthen, Markus, Nürnberg, Peter, Ohler, Uwe, Ossowski, Stephan, Overmann, Jörg, Peter, Silke, Pfeffer, Klaus, Rajewsky, Nikolaus, Ralser, Markus, Saliba, Antoine-Emmanuel, Schulte, Eva-Christina, Schultze, Joachim L., Sczyrba, Alexander, Stoye, Jens, Theis, Fabian, Vogel, Jörg, von Kleist, Max, Walker, Andreas, Walter, Jörn, Wieczorek, Dagmar

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Laminin-α4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells von KNOLL, Ralph, POSTEL, Ruben, KUBE, Dieter, KNOLL, Gudrun, SCHÄFER, Katrin, HAYASHI, Takeharu, HOLM, Torbjorn, KIMURA, Akinori, SCHORK, Nicholas, MOHAMMAD REZA TOLIAT, NÜRNBERG, Peter, SCHULTHEISS, Heinz-Peter, JIANMING WANG, SCHAPER, Wolfgang, SCHAPER, Jutta, BOS, Erik, DEN HERTOG, Jeroen, VAN EEDEN, Fredericus J. M, PETERS, Peter J, HASENFUSS, Gerd, CHIEN, Kenneth R, BAKKERS, Jeroen, KRÄTZNER, Ralph, HENNECKE, Gerrit, VACARU, Andrei M, VAKEEL, Padmanabhan, SCHUBERT, Cornelia, MURTHY, Kenton, RANA, Brinda K

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Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas von Spier, Isabel, Holzapfel, Stefanie, Altmüller, Janine, Zhao, Bixiao, Horpaopan, Sukanya, Vogt, Stefanie, Chen, Sophia, Morak, Monika, Raeder, Susanne, Kayser, Katrin, Stienen, Dietlinde, Adam, Ronja, Nürnberg, Peter, Plotz, Guido, Holinski‐Feder, Elke, Lifton, Richard P., Thiele, Holger, Hoffmann, Per, Steinke, Verena, Aretz, Stefan

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A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site von Nürnberg, Sylvia T., Rendon, Augusto, Smethurst, Peter A., Paul, Dirk S., Voss, Katrin, Thon, Jonathan N., Lloyd-Jones, Heather, Sambrook, Jennifer G., Tijssen, Marloes R., Italiano, Joseph E., Deloukas, Panos, Gottgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H.

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Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible von Hildebrandt, Friedhelm, Hinkes, Bernward, Wiggins, Roger C, Gbadegesin, Rasheed, Vlangos, Christopher N, Seelow, Dominik, Nürnberg, Gudrun, Garg, Puneet, Verma, Rakesh, Chaib, Hassan, Hoskins, Bethan E, Ashraf, Shazia, Becker, Christian, Hennies, Hans Christian, Goyal, Meera, Wharram, Bryan L, Schachter, Asher D, Mudumana, Sudha, Drummond, Iain, Kerjaschki, Dontscho, Waldherr, Rüdiger, Dietrich, Alexander, Ozaltin, Fatih, Bakkaloglu, Aysin, Cleper, Roxana, Basel-Vanagaite, Lina, Pohl, Martin, Griebel, Martin, Tsygin, Alexey N, Soylu, Alper, Müller, Dominik, Sorli, Caroline S, Bunney, Tom D, Katan, Matilda, Liu, Jinhong, Attanasio, Massimo, O'Toole, John F, Hasselbacher, Katrin, Mucha, Bettina, Otto, Edgar A, Airik, Rannar, Kispert, Andreas, Kelley, Grant G, Smrcka, Alan V, Gudermann, Thomas, Holzman, Lawrence B, Nürnberg, Peter

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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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Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genes von Blume, Felix, Kirsten, Holger, Ahnert, Peter, Chakraborty, Trinad, Gross, Arnd, Horn, Katrin, Toliat, Mohammad Reza, Nürnberg, Peter, Westenfelder, Eva-Maria, Goepel, Wolfgang, Scholz, Markus

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Mutations in GMPPA Cause a Glycosylation Disorder Characterized by Intellectual Disability and Autonomic Dysfunction von Koehler, Katrin, Malik, Meera, Mahmood, Saqib, Gießelmann, Sebastian, Beetz, Christian, Hennings, J. Christopher, Huebner, Antje K., Grahn, Ammi, Reunert, Janine, Nürnberg, Gudrun, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Mumtaz, Rizwan, Babovic-Vuksanovic, Dusica, Basel-Vanagaite, Lina, Borck, Guntram, Brämswig, Jürgen, Mühlenberg, Reinhard, Sarda, Pierre, Sikiric, Alma, Anyane-Yeboa, Kwame, Zeharia, Avraham, Ahmad, Arsalan, Coubes, Christine, Wada, Yoshinao, Marquardt, Thorsten, Vanderschaeghe, Dieter, Van Schaftingen, Emile, Kurth, Ingo, Huebner, Angela, Hübner, Christian A.

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Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients von König, Katharina, Peifer, Martin, Fassunke, Jana, Ihle, Michaela A., Künstlinger, Helen, Heydt, Carina, Stamm, Katrin, Ueckeroth, Frank, Vollbrecht, Claudia, Bos, Marc, Gardizi, Masyar, Scheffler, Matthias, Nogova, Lucia, Leenders, Frauke, Albus, Kerstin, Meder, Lydia, Becker, Kerstin, Florin, Alexandra, Rommerscheidt-Fuss, Ursula, Altmüller, Janine, Kloth, Michael, Nürnberg, Peter, Henkel, Thomas, Bikár, Sven-Ernö, Sos, Martin L., Geese, William J., Strauss, Lewis, Ko, Yon-Dschun, Gerigk, Ulrich, Odenthal, Margarete, Zander, Thomas, Wolf, Jürgen, Merkelbach-Bruse, Sabine, Buettner, Reinhard, Heukamp, Lukas C.

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STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly von Kakar, Naseebullah, Ahmad, Jamil, Morris-Rosendahl, Deborah J., Altmüller, Janine, Friedrich, Katrin, Barbi, Gotthold, Nürnberg, Peter, Kubisch, Christian, Dobyns, William B., Borck, Guntram

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Mutations in Bone Morphogenetic Protein Receptor 1B Cause Brachydactyly Type A2 von Lehmann, Katarina, Seemann, Petra, Stricker, Sigmar, Sammar, Marai, Meyer, Birgit, Süring, Katrin, Majewski, Frank, Tinschert, Sigrid, Grzeschik, Karl-Heinz, Müller, Dietmar, Knaus, Petra, Nürnberg, Peter, Mundlos, Stefan

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