Characterization of mSelB, a novel mammalian elongation factor for selenoprotein translation von Fagegaltier, Delphine, Hubert, Nadia, Yamada, Kenichiro, Mizutani, Takaharu, Carbon, Philippe, Krol, Alain

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Structural analysis of new local features in SECIS RNA hairpins von Fagegaltier, D, Lescure, A, Walczak, R, Carbon, P, Krol, A

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A Genome-Wide Survey of Sexually Dimorphic Expression of Drosophila miRNAs Identifies the Steroid Hormone-Induced miRNA let-7 as a Regulator of Sexual Identity von Fagegaltier, Delphine, König, Annekatrin, Gordon, Assaf, Lai, Eric C, Gingeras, Thomas R, Hannon, Gregory J, Shcherbata, Halyna R

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endogenous siRNA pathway is involved in heterochromatin formation in Drosophila von Fagegaltier, Delphine, Bougé, Anne-Laure, Berry, Bassam, Poisot, Émilie, Sismeiro, Odile, Coppée, Jean-Yves, Théodore, Laurent, Voinnet, Olivier, Antoniewski, Christophe

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Minotaur is critical for primary piRNA biogenesis von Vagin, Vasily V, Yu, Yang, Jankowska, Anna, Luo, Yicheng, Wasik, Kaja A, Malone, Colin D, Harrison, Emily, Rosebrock, Adam, Wakimoto, Barbara T, Fagegaltier, Delphine, Muerdter, Felix, Hannon, Gregory J

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X chromosome sites autonomously recruit the dosage compensation complex in Drosophila males von Fagegaltier, Delphine, Baker, Bruce S

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Distinctive features in the SelB family of elongation factors for selenoprotein synthesis. A glimpse of an evolutionary complexified translation apparatus von Fagegaltier, Delphine, Carbon, Philippe, Krol, Alain

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The selenocysteine insertion sequence binding protein SBP is different from the Y-box protein dbpB von Fagegaltier, Delphine, Hubert, Nadia, Carbon, Philippe, Krol, Alain

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TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A von Brown, A.L., Wilkins, O.G., Keuss, M.J., Hill, S.E., Zanovello, M., Lee, W.C., Bampton, A., Lee, F.C.Y., Masino, L., Qi, Y.A., Bryce-Smith, S., Gatt, A., Hallegger, M., Fagegaltier, D., Phatnani, H., Newcombe, J., Gustavsson, E.K., Seddighi, S., Reyes, J.F., Coon, S.L., Ramos, D., Schiavo, G., Fisher, E.M.C., Raj, T., Secrier, M., Lashley, T., Ule, J., Buratti, E., Humphrey, J., Ward, M.E., Fratta, P.

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism von Conlon, E.G., Fagegaltier, D., Agius, P., Davis-Porada, J., Gregory, J., Hubbard, I., Kang, K., Kim, D., Phatnani, H., Shneider, N.A., Manley, J.L.

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism von Conlon, EG, Fagegaltier, D, Agius, P, Davis-Porada, J, Gregory, J, Hubbard, I, Kang, K, Kim, D, Phatnani, H, Shneider, NA, Manley, JL

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Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia von Prudencio, M, Humphrey, J, Pickles, S, Brown, A-L, Hill, SE, Kachergus, J, Shi, J, Heckman, M, Spiegel, M, Cook, C, Song, Y, Yue, M, Daughrity, L, Carlomagno, Y, Jansen-West, K, Fernandez De Castro, C, DeTure, M, Koga, S, Wang, Y-C, Sivakumar, P, Bodo, C, Candalija, A, Talbot, K, Selvaraj, BT, Burr, K, Chandran, S, Newcombe, J, Lashley, T, Hubbard, I, Catalano, D, Kim, D, Propp, N, Fennessey, S, Fagegaltier, D, Phatnani, H, Secrier, M, Fisher, EM, Oskarsson, B, van Blitterswijk, M, Rademakers, R, Graff-Radford, NR, Boeve, B, Knopman, DS, Petersen, R, Josephs, K, Thompson, EA, Raj, T, Ward, ME, Dickson, D, Gendron, TF, Fratta, P, Petrucelli, L

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Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia von Tam, OH, Rozhkov, NV, Shaw, R, Kim, D, Hubbard, I, Fennessey, S, Propp, N, Fagegaltier, D, Harris, BT, Ostrow, LW, Phatnani, H, Ravits, J, Dubnau, J, Hammell, MG, Kwan, J, Sareen, D, Broach, JR, Simmons, Z, Arcila-Londono, X, Lee, EB, Van Deerlin, VM, Shneider, NA, Fraenkel, E, Baas, F, Zaitlen, N, Berry, JD, Malaspina, A, Fratta, P, Cox, GA, Thompson, LM, Finkbeiner, S, Dardiotis, E, Miller, TM, Chandran, S, Pal, S, Hornstein, E, MacGowan, DJ, Heiman-Patterson, T, Patsopoulos, NA, Butovsky, O, Nath, A, Bowser, R, Harms, M, Aronica, E, Poss, M, Phillips-Cremins, J, Crary, J, Atassi, N, Lange, DJ, Adams, DJ, Stefanis, L, Gotkine, M, Baloh, R, Babu, S, Raj, T, Paganoni, S, Shalem, O, Smith, C, Zhang, B

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From RNA Structure to the Identification of New Genes : The Example of selenoproteins von Lescure, Alain, Gautheret, Daniel, Fagegaltier, Delphine, Carbon, Philippe, Krol, Alain

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195 - Procédures d’aide à la régulation à l’attention des permanenciers auxiliaires de régulation médicale dans un SAMU-centre 15 : étude préliminaire de faisabilité von Cahun-Giraud, S., Dolveck, F., Templier, F., Goddet, N.S., Fagegaltier, D., Chauvin, M., Fletcher, D., Baer, M.

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TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A von Brown, Anna-Leigh, Wilkins, Oscar G., Keuss, Matthew J., Hill, Sarah E., Zanovello, Matteo, Lee, Weaverly Colleen, Bampton, Alexander, Lee, Flora C. Y., Masino, Laura, Qi, Yue A., Bryce-Smith, Sam, Gatt, Ariana, Hallegger, Martina, Fagegaltier, Delphine, Phatnani, Hemali, Newcombe, Jia, Gustavsson, Emil K., Seddighi, Sahba, Reyes, Joel F., Coon, Steven L., Ramos, Daniel, Schiavo, Giampietro, Fisher, Elizabeth M. C., Raj, Towfique, Secrier, Maria, Lashley, Tammaryn, Ule, Jernej, Buratti, Emanuele, Humphrey, Jack, Ward, Michael E., Fratta, Pietro

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Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia von Tam, Oliver H., Rozhkov, Nikolay V., Shaw, Regina, Kim, Duyang, Hubbard, Isabel, Fennessey, Samantha, Propp, Nadia, Phatnani, Hemali, Kwan, Justin, Sareen, Dhruv, Broach, James R., Simmons, Zachary, Arcila-Londono, Ximena, Lee, Edward B., Van Deerlin, Vivianna M., Shneider, Neil A., Fraenkel, Ernest, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Berry, James D., Malaspina, Andrea, Fratta, Pietro, Cox, Gregory A., Thompson, Leslie M., Finkbeiner, Steve, Dardiotis, Efthimios, Miller, Timothy M., Chandran, Siddharthan, Pal, Suvankar, Hornstein, Eran, MacGowan, Daniel J., Heiman-Patterson, Terry, Hammell, Molly G., Patsopoulos, Nikolaos.A., Butovsky, Oleg, Dubnau, Joshua, Nath, Avindra, Bowser, Robert, Harms, Matt, Aronica, Eleonora, Poss, Mary, Phillips-Cremins, Jennifer, Crary, John, Atassi, Nazem, Lange, Dale J., Adams, Darius J., Stefanis, Leonidas, Gotkine, Marc, Baloh, Robert, Babu, Suma, Raj, Towfique, Paganoni, Sabrina, Shalem, Ophir, Smith, Colin, Zhang, Bin, Harris, Brent T., Fagegaltier, Delphine, Harris, Brent T., Ostrow, Lyle W., Phatnani, Hemali, Ravits, John, Dubnau, Josh, Gale Hammell, Molly

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism von Conlon, Erin G, Fagegaltier, Delphine, Agius, Phaedra, Davis-Porada, Julia, Gregory, James, Hubbard, Isabel, Kang, Kristy, Kim, Duyang, Phatnani, Hemali, Shneider, Neil A, Manley, James L

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Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE von Roy, Sushmita, Ernst, Jason, Kharchenko, Peter V, Kheradpour, Pouya, Negre, Nicolas, Eaton, Matthew L, Landolin, Jane M, Bristow, Christopher A, Ma, Lijia, Lin, Michael F, Washietl, Stefan, Arshinoff, Bradley I, Ay, Ferhat, Meyer, Patrick E, Robine, Nicolas, Washington, Nicole L, Di Stefano, Luisa, Berezikov, Eugene, Brown, Christopher D, Candeias, Rogerio, Carlson, Joseph W, Carr, Adrian, Jungreis, Irwin, Marbach, Daniel, Sealfon, Rachel, Tolstorukov, Michael Y, Will, Sebastian, Alekseyenko, Artyom A, Artieri, Carlo, Booth, Benjamin W, Brooks, Angela N, Dai, Qi, Davis, Carrie A, Duff, Michael O, Feng, Xin, Gorchakov, Andrey A, Gu, Tingting, Henikoff, Jorja G, Kapranov, Philipp, Li, Renhua, MacAlpine, Heather K, Malone, John, Minoda, Aki, Nordman, Jared, Okamura, Katsutomo, Perry, Marc, Powell, Sara K, Riddle, Nicole C, Sakai, Akiko, Samsonova, Anastasia, Sandler, Jeremy E, Schwartz, Yuri B, Sher, Noa, Spokony, Rebecca, Sturgill, David, van Baren, Marijke, Wan, Kenneth H, Yang, Li, Yu, Charles, Feingold, Elise, Good, Peter, Guyer, Mark, Lowdon, Rebecca, Ahmad, Kami, Andrews, Justen, Berger, Bonnie, Brenner, Steven E, Brent, Michael R, Cherbas, Lucy, Elgin, Sarah C.R, Gingeras, Thomas R, Grossman, Robert, Hoskins, Roger A, Kaufman, Thomas C, Kent, William, Kuroda, Mitzi I, Orr-Weaver, Terry, Perrimon, Norbert, Pirrotta, Vincenzo, Posakony, James W, Ren, Bing, Russell, Steven, Cherbas, Peter, Graveley, Brenton R, Lewis, Suzanna, Micklem, Gos, Oliver, Brian, Park, Peter J, Celniker, Susan E, Henikoff, Steven, Karpen, Gary H, Lai, Eric C, MacAlpine, David M, Stein, Lincoln D, White, Kevin P, Kellis, Manolis

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Retromer dysfunction in amyotrophic lateral sclerosis von Pérez-Torres, Eduardo J., Utkina-Sosunova, Irina, Mishra, Vartika, Barbuti, Peter, De Planell-Saguer, Mariangels, Dermentzaki, Georgia, Geiger, Heather, Basile, Anna O., Robine, Nicolas, Fagegaltier, Delphine, Politi, Kristin A., Rinchetti, Paola, Jackson-Lewis, Vernice, Harms, Matthew, Phatnani, Hemali, Lotti, Francesco, Przedborski, Serge

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