Treffer 1 - 16 von 16 für Suche 'Drepper, Michael D', Suchdauer: 1,48s Treffer weiter einschränken
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    A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD von Renton, Alan E., Majounie, Elisa, Waite, Adrian, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James, Murray, Alex, Pearson, Justin, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek, Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel M., Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw R., Tienari, Pentti J., Traynor, Bryan J.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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    Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data von Saez-Atienzar, Sara, Souza, Cleide dos Santos, Chia, Ruth, Burciu, Camelia, Gibbs, J. Raphael, Jones, Ashley, Dewan, Ramita, Pensato, Viviana, Corrado, Lucia, van Vugt, Joke J.F.A., van Rheenen, Wouter, Camu, William, Cusi, Daniele, Ding, Jinhui, Drepper, Carsten, Drory, Vivian E., Gerhard, Glenn, Gibbs, J. Raphael, Gibson, Summer B., Hardy, John, Landers, John E., Guissart, Claire, MacGowan, Daniel JL, Mouzat, Kevin, Myllykangas, Liisa, Pulst, Stefan M., Ravits, John M., Renton, Alan E., Rogaeva, Ekaterina, Salvi, Erika, Scholz, Sonja W., Tienari, Pentti J., Valori, Miko, Van Damme, Philip, Zinman, Lorne, Barberis, Marco, Bersano, Enrica, Bisogni, Giulia, Canale, Fabrizio, Carrera, Paola, Casale, Federico, Colletti, Tiziana, Conforti, Francesca L., Ferrarese, Carlo, Greco, Lucia, La Bella, Vincenzo, Marrosu, Maria Giovanna, Messina, Sonia, Moglia, Cristina, Passaniti, Carla, Petrelli, Cristina, Petrucci, Antonio, Russo, Massimo, Salvi, Fabrizio, Santarelli, Marialuisa, Sideri, Riccardo, Vasta, Rosario, Zucchi, Elisabetta, Ticozzi, Nicola, Tiloca, Cinzia, Peverelli, Silvia, Taroni, Franco, Pensato, Viviana, Castellotti, Barbara, Comi, Giacomo P., Corrado, Lucia, Sorarù, Gianni, Corcia, Philippe, Vourc'h, Patrick, Gotkine, Marc, Drory, Vivian, Berg, Leonard H., Andersen, Peter, Tiloca, Cinzia, Verde, Federico, Al Khleifat, Ahmad, Piccinelli, Stefano Cotti, Padovani, Alessandro, Calvo, Andrea, Canosa, Antonio, Lunetta, Christian, Cardinali, Patrizio, Scarpini, Elio, Comi, Giacomo P., Pinter, Giuseppe Lauria, Taroni, Franco, Bella, Eleonora Dalla, Adeleye, Adelani, McGrath Martinez, Elisa, Soltis, Anthony R., Sukumar, Gauthaman, Viollet, Coralie, McLaughlin, Russell, Sorarù, Gianni, Ratti, Antonia, Doucet-O’Hare, Tara, Nath, Avindra, Siciliano, Gabriele, Glass, Jonathan D., Ferraiuolo, Laura

    Veröffentlicht in Cell genomics

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    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot M, McLaughlin, Russell L, Diekstra, Frank P, Pulit, Sara L, van der Spek, Rick A.A, Võsa, Urmo, de Jong, Simone, Robinson, Matthew R, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs H.P, Koppers, Max, Blokhuis, Anna M, Sproviero, William, Jones, Ashley R, Kenna, Kevin P, van Eijk, Kristel R, Harschnitz, Oliver, Schellevis, Raymond D, Brands, William J, Medic, Jelena, Menelaou, Androniki, Vajda, Alice, Ticozzi, Nicola, Lin, Kuang, Rogelj, Boris, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Grošelj, Leja Dolenc, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel A, Staats, Kim A, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M, Trojanowski, John Q, Elman, Lauren, McCluskey, Leo, Basak, A. Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A.M, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre G, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke M, van der Kooi, Anneke J

    Veröffentlicht in Nature Genetics

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