Accumulation and degradation of Em proteins in Arabidopsis thaliana: evidence for post-transcriptional controls by Bies, Natacha, Aspart, Lorette, Carles, Christel, Gallois, Patrick, Delseny, Michel

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Late Embryogenesis Abundant (LEA) protein gene regulation during Arabidopsis seed maturation by Delseny, Michel, Bies-Etheve, Natacha, Carles, Christel, Hull, Gillian, Vicient, Carlos, Raynal, Monique, Grellet, Françoise, Aspart, Lorette

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Accumulation and degradation of Em proteins in Arabidopsis thaliana: evidence for post-transcriptional controls by Bies, Natacha, Aspart, Lorette, Carles, Christel, Gallois, Patrick, Delseny, Michel

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Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases by Zurek, Birte, Ellwanger, Kornelia, Vissers, Lisenka E L M, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, de Voer, Richarda M, Laurie, Steven, Matalonga, Leslie, Gilissen, Christian, Ossowski, Stephan, 't Hoen, Peter A C, Vitobello, Antonio, Schulze-Hentrich, Julia M, Riess, Olaf, Brunner, Han G, Brookes, Anthony J, Rath, Ana, Bonne, Gisèle, Gumus, Gulcin, Verloes, Alain, Hoogerbrugge, Nicoline, Evangelista, Teresinha, Harmuth, Tina, Swertz, Morris, Spalding, Dylan, Hoischen, Alexander, Beltran, Sergi, Graessner, Holm

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In-Situ Synthesis and Characterization of Nanocomposites in the Si-Ti-N and Si-Ti-C Systems by Balestrat, Maxime, Lale, Abhijeet, Bezerra, André Vinícius Andrade, Proust, Vanessa, Awin, Eranezhuth Wasan, Machado, Ricardo Antonio Francisco, Carles, Pierre, Kumar, Ravi, Gervais, Christel, Bernard, Samuel

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Optically selective SiC-based nanocomposite objects derived from titanium and boron-modified polycarbosilanes by Balestrat, Maxime, Cheype, Maxime, Carles, Pierre, Deschanels, Xavier, Soum-Glaude, Audrey, Gervais, Christel, Rossignol, Fabrice, Pradeilles, Nicolas, Bernard, Samuel

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Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease by Chartier-Harlin, Marie-Christine, Dachsel, Justus C., Vilariño-Güell, Carles, Lincoln, Sarah J., Leprêtre, Frédéric, Hulihan, Mary M., Kachergus, Jennifer, Milnerwood, Austen J., Tapia, Lucia, Song, Mee-Sook, Le Rhun, Emilie, Mutez, Eugénie, Larvor, Lydie, Duflot, Aurélie, Vanbesien-Mailliot, Christel, Kreisler, Alexandre, Ross, Owen A., Nishioka, Kenya, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Melrose, Heather L., Behrouz, Bahareh, Keeling, Brett H., Bacon, Justin A., Hentati, Emna, Williams, Lindsey, Yanagiya, Akiko, Sonenberg, Nahum, Lockhart, Paul J., Zubair, Abba C., Uitti, Ryan J., Aasly, Jan O., Krygowska-Wajs, Anna, Opala, Grzegorz, Wszolek, Zbigniew K., Frigerio, Roberta, Maraganore, Demetrius M., Gosal, David, Lynch, Tim, Hutchinson, Michael, Bentivoglio, Anna Rita, Valente, Enza Maria, Nichols, William C., Pankratz, Nathan, Foroud, Tatiana, Gibson, Rachel A., Hentati, Faycal, Dickson, Dennis W., Destée, Alain, Farrer, Matthew J.

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Solving unsolved rare neurological diseases-a Solve-RD viewpoint by Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E, Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis

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Tuning of the high temperature behaviour of Si–C–N ceramics via the chemical crosslinking of poly(vinylmethyl-co-methyl)silazanes with controlled borane contents by Wynn, Mélanie, Lopez-Ferber, David, Viard, Antoine, Fonblanc, Diane, Schmidt, Marion, Rossignol, Fabrice, Carles, Pierre, Chollon, Georges, Gervais, Christel, Bernard, Samuel

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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing by Yaldiz, Burcu, Kucuk, Erdi, Hampstead, Juliet, Hofste, Tom, Pfundt, Rolph, Corominas Galbany, Jordi, Rinne, Tuula, Yntema, Helger G, Hoischen, Alexander, Nelen, Marcel, Gilissen, Christian

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An interconnected data infrastructure to support large-scale rare disease research by Johansson, Lennart F, Laurie, Steve, Spalding, Dylan, Gibson, Spencer, Ruvolo, David, Thomas, Coline, Piscia, Davide, de Andrade, Fernanda, Been, Gerieke, Bijlsma, Marieke, Brunner, Han, Cimerman, Sandi, Dizjikan, Farid Yavari, Ellwanger, Kornelia, Fernandez, Marcos, Freeberg, Mallory, van de Geijn, Gert-Jan, Kanninga, Roan, Maddi, Vatsalya, Mehtarizadeh, Mehdi, Neerincx, Pieter, Ossowski, Stephan, Rath, Ana, Roelofs-Prins, Dieuwke, Stok-Benjamins, Marloes, van der Velde, K Joeri, Veal, Colin, van der Vries, Gerben, Wadsley, Marc, Warren, Gregory, Zurek, Birte, Keane, Thomas, Graessner, Holm, Beltran, Sergi, Swertz, Morris A, Brookes, Anthony J

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Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses by Demidov, German, Yaldiz, Burcu, Garcia-Pelaez, José, de Boer, Elke, Schuermans, Nika, Van de Vondel, Liedewei, Paramonov, Ida, Johansson, Lennart F., Musacchia, Francesco, Benetti, Elisa, Bullich, Gemma, Sablauskas, Karolis, Beltran, Sergi, Gilissen, Christian, Hoischen, Alexander, Ossowski, Stephan, de Voer, Richarda, Lohmann, Katja, Oliveira, Carla, Topf, Ana, Vissers, Lisenka E. L. M., Laurie, Steven

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