The Human T-Lymphotropic Virus Type 1 Tax Protein Inhibits Nonsense-Mediated mRNA Decay by Interacting with INT6/EIF3E and UPF1 von MOCQUET, Vincent, NEUSIEDLER, Julia, CIMINALE, Vincenzo, JALINOT, Pierre, RENDE, Francesca, CLUET, David, ROBIN, Jean-Philippe, TERME, Jean-Michel, DUE DODON, Madeleine, WITTMANN, Jürgen, MORRIS, Christelle, LE HIR, Herve

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Ribosome dynamics and mRNA turnover, a complex relationship under constant cellular scrutiny von Morris, Christelle, Cluet, David, Ricci, Emiliano P.

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Human INT6/eIF3e is required for nonsense-mediated mRNA decay von Morris, Christelle, Wittmann, Jürgen, Jäck, Hans-Martin, Jalinot, Pierre

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INT6/EIF3E Interacts with ATM and Is Required for Proper Execution of the DNA Damage Response in Human Cells von MORRIS, Christelle, TOMIMATSU, Nozomi, RICHARD, Derek J, CLUET, David, BURMA, Sandeep, KUM KHANNA, Kum, JALINOT, Pierre

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Decreased expression of the translation factor eIF3e induces senescence in breast cancer cells via suppression of PARP1 and activation of mTORC1 von Morris, Christelle, Durand, Sébastien, Jalinot, Pierre

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Silencing of human Int-6 impairs mitosis progression and inhibits cyclin B-Cdk1 activation von Morris, Christelle, Jalinot, Pierre

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INT6/EIF3E Controls the RNF8-Dependent Ubiquitylation Pathway and Facilitates DNA Double-Strand Break Repair in Human Cells von Morris, Christelle, Tomimatsu, Nozomi, Burma, Sandeep, Jalinot, Pierre

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INT6EIF3E Controls the RNF8-Dependent Ubiquitylation Pathway and Facilitates DNA Double-Strand Break Repair in Human Cells von Morris, Christelle, Tomimatsu, Nozomi, Burma, Sandeep, Jalinot, Pierre

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The HTLV-1 Tax protein inhibits nonsense-mediated mRNA decay by interacting with INT6/EIF3E and UPF1 von Mocquet, Vincent, Neusiedler, Julia, Rende, Francesca, Terme, Jean-Michel, Morris, Christelle, Wittman, Jürgen, Duc Dodon, Madeleine, Ciminale, Vincenzo, Jalinot, Pierre

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INT6 interacts with MIF4GD/SLIP1 and is necessary for efficient histone mRNA translation von Neusiedler, Julia, Mocquet, Vincent, Limousin, Taran, Ohlmann, Theophile, Morris, Christelle, Jalinot, Pierre

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The Human Protein HSPC021 Interacts with Int-6 and Is Associated with Eukaryotic Translation Initiation Factor 3 von Morris-Desbois, Christelle, Réty, Stéphane, Ferro, Myriam, Garin, Jérôme, Jalinot, Pierre

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Nonsense-mediated mRNA decay inhibition by HTLV-1 Tax protein von Mocquet, Vincent, Neusiedler, Julia, Rende, Francesca, Cluet, David, Robin, Jean-Philippe, Terme, Jean-Michel, Duc-Dodon, Madeleine, Morris, Christelle, Le Hir, Hervé, Ciminale, Vincenzo, Jalinot, Pierre

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Interaction between the Ret finger protein and the Int-6 gene product and co-localisation into nuclear bodies von Morris-Desbois, C, Bochard, V, Reynaud, C, Jalinot, P

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The human protein HSPC021 interacts with Int-6 and is associated with the translation initiation factor eIF3 von Morris-Desbois, Christelle, Rety, S., Ferro, M., Garin, J., Jalinot, Pierre

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Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study von Forgetta, Vincenzo, Keller-Baruch, Julyan, Forest, Marie, Durand, Audrey, Bhatnagar, Sahir, Kemp, John P, Nethander, Maria, Evans, Daniel, Morris, John A, Kiel, Douglas P, Rivadeneira, Fernando, Johansson, Helena, Harvey, Nicholas C, Mellström, Dan, Karlsson, Magnus, Cooper, Cyrus, Evans, David M, Clarke, Robert, Kanis, John A, Orwoll, Eric, McCloskey, Eugene V, Ohlsson, Claes, Pineau, Joelle, Leslie, William D, Greenwood, Celia M T, Richards, J Brent

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Efficacy of Selpercatinib in RET-Altered Thyroid Cancers von Wirth, Lori J, Sherman, Eric, Robinson, Bruce, Solomon, Benjamin, Kang, Hyunseok, Lorch, Jochen, Worden, Francis, Brose, Marcia, Patel, Jyoti, Leboulleux, Sophie, Godbert, Yann, Barlesi, Fabrice, Morris, John C, Owonikoko, Taofeek K, Tan, Daniel S.W, Gautschi, Oliver, Weiss, Jared, de la Fouchardière, Christelle, Burkard, Mark E, Laskin, Janessa, Taylor, Matthew H, Kroiss, Matthias, Medioni, Jacques, Goldman, Jonathan W, Bauer, Todd M, Levy, Benjamin, Zhu, Viola W, Lakhani, Nehal, Moreno, Victor, Ebata, Kevin, Nguyen, Michele, Heirich, Dana, Zhu, Edward Y, Huang, Xin, Yang, Luxi, Kherani, Jennifer, Rothenberg, S. Michael, Drilon, Alexander, Subbiah, Vivek, Shah, Manisha H, Cabanillas, Maria E

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KCTD7‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature von Yoganathan, Sangeetha, Whitney, Robyn, Thomas, Maya, Danda, Sumita, Chettali, Akbar Mohamed, Prasad, Asuri N., Farhan, Sali M. K., AlSowat, Daad, Abukhaled, Musaad, Aldhalaan, Hesham, Gowda, Vykuntaraju K., Kinhal, Uddhava V., Bylappa, Arun Y., Konanki, Ramesh, Lingappa, Lokesh, Parchuri, Bindu Madhavi, Appendino, Juan P., Scantlebury, Morris H., Cunningham, Jessie, Hadjinicolaou, Aristides, El Achkar, Christelle Moufawad, Kamate, Mahesh, Menon, Ramshekhar N., Jose, Manna, Riordan, Gillian, Kannan, Lakshminarayanan, Jain, Vivek, Manokaran, Ranjith Kumar, Chau, Vann, Donner, Elizabeth J., Costain, Gregory, Minassian, Berge A., Jain, Puneet

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Dependence on the Pyrimidine Biosynthetic Enzyme DHODH Is a Synthetic Lethal Vulnerability in Mutant KRAS-Driven Cancers von Koundinya, Malvika, Sudhalter, Judith, Courjaud, Albane, Lionne, Bruno, Touyer, Gaetan, Bonnet, Luc, Menguy, Isabelle, Schreiber, Isabelle, Perrault, Christelle, Vougier, Stephanie, Benhamou, Brigitte, Zhang, Bailin, He, Timothy, Gao, Qiang, Gee, Patricia, Simard, Daniel, Castaldi, M. Paola, Tomlinson, Ronald, Reiling, Stephan, Barrague, Matthieu, Newcombe, Richard, Cao, Hui, Wang, Yanjun, Sun, Fangxian, Murtie, Joshua, Munson, Mark, Yang, Eric, Harper, David, Bouaboula, Monsif, Pollard, Jack, Grepin, Claudine, Garcia-Echeverria, Carlos, Cheng, Hong, Adrian, Francisco, Winter, Christopher, Licht, Stuart, Cornella-Taracido, Ivan, Arrebola, Rosalia, Morris, Aaron

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BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients von Engel, Camille, Valence, Stéphanie, Delplancq, Geoffroy, Maroofian, Reza, Accogli, Andrea, Agolini, Emanuele, Alkuraya, Fowzan S, Baglioni, Valentina, Bagnasco, Irene, Becmeur-Lefebvre, Mathilde, Bertini, Enrico, Borggraefe, Ingo, Brischoux-Boucher, Elise, Bruel, Ange-Line, Brusco, Alfredo, Bubshait, Dalal K, Cabrol, Christelle, Cilio, Maria Roberta, Cornet, Marie-Coralie, Coubes, Christine, Danhaive, Olivier, Delague, Valérie, Denommé-Pichon, Anne-Sophie, Di Giacomo, Marilena Carmela, Doco-Fenzy, Martine, Engels, Hartmut, Cremer, Kirsten, Gérard, Marion, Gleeson, Joseph G, Heron, Delphine, Goffeney, Joanna, Guimier, Anne, Harms, Frederike L, Houlden, Henry, Iacomino, Michele, Kaiyrzhanov, Rauan, Kamien, Benjamin, Karimiani, Ehsan Ghayoor, Kraus, Dror, Kuentz, Paul, Kutsche, Kerstin, Lederer, Damien, Massingham, Lauren, Mignot, Cyril, Morris-Rosendahl, Déborah, Nagarajan, Lakshmi, Odent, Sylvie, Ormières, Clothilde, Partlow, Jennifer Neil, Pasquier, Laurent, Penney, Lynette, Philippe, Christophe, Piccolo, Gianluca, Poulton, Cathryn, Putoux, Audrey, Rio, Marlène, Rougeot, Christelle, Salpietro, Vincenzo, Scheffer, Ingrid, Schneider, Amy, Srivastava, Siddharth, Straussberg, Rachel, Striano, Pasquale, Valente, Enza Maria, Venot, Perrine, Villard, Laurent, Vitobello, Antonio, Wagner, Johanna, Wagner, Matias, Zaki, Maha S, Zara, Federizo, Lesca, Gaetan, Yassaee, Vahid Reza, Miryounesi, Mohammad, Hashemi-Gorji, Farzad, Beiraghi, Mehran, Ashrafzadeh, Farah, Galehdari, Hamid, Walsh, Christopher, Novelli, Antonio, Tacke, Moritz, Sadykova, Dinara, Maidyrov, Yerdan, Koneev, Kairgali, Shashkin, Chingiz, Capra, Valeria, Zamani, Mina, Van Maldergem, Lionel, Burglen, Lydie, Piard, Juliette

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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses von Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J

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