Treffer 1 - 20 von 57 für Suche 'Menden, Thomas J', Suchdauer: 1,22s Treffer weiter einschränken
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    The Marine Microbial Eukaryote Transcriptome Sequencing Project (MMETSP): illuminating the functional diversity of eukaryotic life in the oceans through transcriptome sequencing von Keeling, Patrick J, Burki, Fabien, Wilcox, Heather M, Allam, Bassem, Allen, Eric E, Amaral-Zettler, Linda A, Armbrust, E Virginia, Archibald, John M, Bharti, Arvind K, Bell, Callum J, Beszteri, Bank, Bidle, Kay D, Cameron, Connor T, Campbell, Lisa, Caron, David A, Cattolico, Rose Ann, Collier, Jackie L, Coyne, Kathryn, Davy, Simon K, Deschamps, Phillipe, Dyhrman, Sonya T, Edvardsen, Bente, Gates, Ruth D, Gobler, Christopher J, Greenwood, Spencer J, Guida, Stephanie M, Jacobi, Jennifer L, Jakobsen, Kjetill S, James, Erick R, Jenkins, Bethany, John, Uwe, Johnson, Matthew D, Juhl, Andrew R, Kamp, Anja, Katz, Laura A, Kiene, Ronald, Kudryavtsev, Alexander, Leander, Brian S, Lin, Senjie, Lovejoy, Connie, Lynn, Denis, Marchetti, Adrian, McManus, George, Nedelcu, Aurora M, Menden-Deuer, Susanne, Miceli, Cristina, Mock, Thomas, Montresor, Marina, Moran, Mary Ann, Murray, Shauna, Nadathur, Govind, Nagai, Satoshi, Ngam, Peter B, Palenik, Brian, Pawlowski, Jan, Petroni, Giulio, Piganeau, Gwenael, Posewitz, Matthew C, Rengefors, Karin, Romano, Giovanna, Rumpho, Mary E, Rynearson, Tatiana, Schilling, Kelly B, Schroeder, Declan C, Simpson, Alastair G B, Slamovits, Claudio H, Smith, David R, Smith, G Jason, Smith, Sarah R, Sosik, Heidi M, Stief, Peter, Theriot, Edward, Twary, Scott N, Umale, Pooja E, Vaulot, Daniel, Wawrik, Boris, Wheeler, Glen L, Wilson, William H, Xu, Yan, Zingone, Adriana, Worden, Alexandra Z

    Veröffentlicht in PLoS biology

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    Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy von Tucci, Arianna, Cipriani, Valentina, Demidov, German, Rocca, Clarissa, Senderek, Jan, Butryn, Michaela, Lam, Tanya, Cali, Elisa, Vestito, Letizia, Maroofian, Reza, Deininger, Natalie, Rautenberg, Maren, Admard, Jakob, Bartels, Claudius, Horvath, Rita, Chinnery, Patrick F., Tiet, May Yung, Hewamadduma, Channa, Tofaris, George K., Ambrose, J.C., Arumugam, P., Baple, E.L., Bleda, M., Boardman-Pretty, F., Boissiere, J.M., Boustred, C.R., Brittain, H., Caulfield, M.J., Craig, C.E.H., Daugherty, L.C., Devereau, A., Elgar, G., Foulger, R.E., Fowler, T., Furió-Tarí, P., Hackett, J.M., Halai, D., Hamblin, A., Henderson, S., Holman, J.E., Ibáñez, K., Jackson, R., Jones, L.J., Kasperaviciute, D., Kayikci, M., Lahnstein, L., Lawson, K., Leigh, S.E.A., Leong, I.U.S., Maleady-Crowe, F., Mason, J., McDonagh, E.M., Moutsianas, L., Mueller, M., Odhams, C.A., Patch, C., Perez-Gil, D., Pullinger, J., Rahim, T., Riesgo-Ferreiro, P., Rogers, T., Ryten, M., Sawant, K., Scott, R.H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K.R., Spooner, W., Stevens, H.E., Stuckey, A., Sultana, R., Thomas, E.R.A., Tucci, A., Watters, S.A., Welland, M.J., Williams, E., Zarowiecki, M., Wood, Nicholas W., Hayer, Stefanie N., Bender, Friedemann, Menden, Benita, Cordts, Isabell, Klein, Katrin, Krauss, Joachim K., Blahak, Christian, Strom, Tim M., Sturm, Marc, van de Warrenburg, Bart, Lerche, Holger, Maček, Boris, Ossowski, Stephan, Timmann, Dagmar, Wolf, Marc E., Smedley, Damian, Riess, Olaf, Schöls, Ludger, Houlden, Henry, Haack, Tobias B., Hengel, Holger

    Veröffentlicht in Genetics in medicine

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