檢索結果 - Devoy, Anny

Genomically humanised mice: technologies and promise 由 Devoy, Anny, Bunton-Stasyshyn, Rosie KA, Tybulewicz, Victor L.J., Smith, Andrew J.H., Fisher, Elizabeth M.C.

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Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes 由 Sleigh, James N., Tosolini, Andrew P., Gordon, David, Devoy, Anny, Fratta, Pietro, Fisher, Elizabeth M.C., Talbot, Kevin, Schiavo, Giampietro

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Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions() 由 Fratta, Pietro, Collins, Toby, Pemble, Sally, Nethisinghe, Suran, Devoy, Anny, Giunti, Paola, Sweeney, Mary G., Hanna, Michael G., Fisher, Elizabeth M.C.

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The phase separation-dependent FUS interactome reveals nuclear and cytoplasmic function of liquid–liquid phase separation 由 Reber, Stefan, Jutzi, Daniel, Lindsay, Helen, Devoy, Anny, Mechtersheimer, Jonas, Levone, Brunno Rocha, Domanski, Michal, Bentmann, Eva, Dormann, Dorothee, Mühlemann, Oliver, Barabino, Silvia M L, Ruepp, Marc-David

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Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis 由 Fratta, Pietro, Charnock, James, Collins, Toby, Devoy, Anny, Howard, Robin, Malaspina, Andrea, Orrell, Richard, Sidle, Katie, Clarke, Jan, Shoai, Maryam, Lu, Ching-hua, Hardy, John, Plagnol, Vincent, Fisher, Elizabeth M C

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Regulation of Postsynaptic Function by the Dementia-Related ESCRT-III Subunit CHMP2B 由 Chassefeyre, Romain, Martínez-Hernández, José, Bertaso, Federica, Bouquier, Nathalie, Blot, Béatrice, Laporte, Marine, Fraboulet, Sandrine, Couté, Yohann, Devoy, Anny, Isaacs, Adrian M., Pernet-Gallay, Karin, Sadoul, Rémy, Fagni, Laurent, Goldberg, Yves

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Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis 由 Jutzi, Daniel, Campagne, Sébastien, Schmidt, Ralf, Reber, Stefan, Mechtersheimer, Jonas, Gypas, Foivos, Schweingruber, Christoph, Colombo, Martino, von Schroetter, Christine, Loughlin, Fionna E., Devoy, Anny, Hedlund, Eva, Zavolan, Mihaela, Allain, Frédéric H.-T., Ruepp, Marc-David

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Depletion of 26S Proteasomes in Mouse Brain Neurons Causes Neurodegeneration and Lewy-Like Inclusions Resembling Human Pale Bodies 由 Bedford, Lynn, Hay, David, Devoy, Anny, Paine, Simon, Powe, Des G., Seth, Rashmi, Gray, Trevor, Topham, Ian, Fone, Kevin, Rezvani, Nooshin, Mee, Maureen, Soane, Tim, Layfield, Robert, Sheppard, Paul W., Ebendal, Ted, Usoskin, Dmitry, Lowe, James, Mayer, R. John

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Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice 由 Devoy, Anny, Kalmar, Bernadett, Stewart, Michelle, Park, Heesoon, Burke, Beverley, Noy, Suzanna J, Redhead, Yushi, Humphrey, Jack, Lo, Kitty, Jaeger, Julian, Mejia Maza, Alan, Sivakumar, Prasanth, Bertolin, Cinzia, Soraru, Gianni, Plagnol, Vincent, Greensmith, Linda, Acevedo Arozena, Abraham, Isaacs, Adrian M, Davies, Benjamin, Fratta, Pietro, Fisher, Elizabeth M C

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C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins 由 Mizielinska, Sarah, Grönke, Sebastian, Niccoli, Teresa, Ridler, Charlotte E., Clayton, Emma L., Devoy, Anny, Moens, Thomas, Norona, Frances E., Woollacott, Ione O.C., Pietrzyk, Julian, Cleverley, Karen, Nicoll, Andrew J., Pickering-Brown, Stuart, Dols, Jacqueline, Cabecinha, Melissa, Hendrich, Oliver, Fratta, Pietro, Fisher, Elizabeth M.C., Partridge, Linda, Isaacs, Adrian M.

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FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation 由 Birsa, Nicol, Ule, Agnieszka M., Garone, Maria Giovanna, Tsang, Brian, Mattedi, Francesca, Chong, P. Andrew, Humphrey, Jack, Jarvis, Seth, Pisiren, Melis, Wilkins, Oscar G., Nosella, Micheal L., Devoy, Anny, Bodo, Cristian, de la Fuente, Rafaela Fernandez, Fisher, Elizabeth M. C., Rosa, Alessandro, Viero, Gabriella, Forman-Kay, Julie D., Schiavo, Giampietro, Fratta, Pietro

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FUS ALS-causative mutations impair FUS autoregulation and splicing factor networks through intron retention 由 Humphrey, Jack, Birsa, Nicol, Milioto, Carmelo, McLaughlin, Martha, Ule, Agnieszka M, Robaldo, David, Eberle, Andrea B, Kräuchi, Rahel, Bentham, Matthew, Brown, Anna-Leigh, Jarvis, Seth, Bodo, Cristian, Garone, Maria G, Devoy, Anny, Soraru, Gianni, Rosa, Alessandro, Bozzoni, Irene, Fisher, Elizabeth M C, Mühlemann, Oliver, Schiavo, Giampietro, Ruepp, Marc-David, Isaacs, Adrian M, Plagnol, Vincent, Fratta, Pietro

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Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion() 由 Fratta, Pietro, Polke, James M., Newcombe, Jia, Mizielinska, Sarah, Lashley, Tammaryn, Poulter, Mark, Beck, Jon, Preza, Elisavet, Devoy, Anny, Sidle, Katie, Howard, Robin, Malaspina, Andrea, Orrell, Richard W., Clarke, Jan, Lu, Ching-Hua, Mok, Kin, Collins, Toby, Shoaii, Maryam, Nanji, Tina, Wray, Selina, Adamson, Gary, Pittman, Alan, Renton, Alan E., Traynor, Bryan J., Sweeney, Mary G., Revesz, Tamas, Houlden, Henry, Mead, Simon, Isaacs, Adrian M., Fisher, Elizabeth M.C.

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Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models 由 Devoy, Anny, Price, Georgia, De Giorgio, Francesca, Bunton-Stasyshyn, Rosie, Thompson, David, Gasco, Samanta, Allan, Alasdair, Codner, Gemma F., Nair, Remya R., Tibbit, Charlotte, McLeod, Ross, Ali, Zeinab, Noda, Judith, Marrero-Gagliardi, Alessandro, Brito-Armas, José M., Williams, Chloe, Öztürk, Muhammet M., Simon, Michelle, O'Neill, Edward, Bryce-Smith, Sam, Harrison, Jackie, Atkins, Gemma, Corrochano, Silvia, Stewart, Michelle, Gilthorpe, Jonathan D., Teboul, Lydia, Acevedo-Arozena, Abraham, Fisher, Elizabeth M.C., Cunningham, Thomas J.

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Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models 由 Devoy, Anny, Price, Georgia, De Giorgio, Francesca, Bunton-Stasyshyn, Rosie, Thompson, David, Gasco, Samanta, Allan, Alasdair, Codner, Gemma F., Nair, Remya R., Tibbit, Charlotte, McLeod, Ross, Ali, Zeinab, Noda, Judith, Marrero-Gagliardi, Alessandro, Brito-Armas, José M., Williams, Chloe, Öztürk, Muhammet M., Simon, Michelle, O’Neill, Edward, Bryce-Smith, Sam, Harrison, Jackie, Atkins, Gemma, Corrochano, Silvia, Stewart, Michelle, Gilthorpe, Jonathan D., Teboul, Lydia, Acevedo-Arozena, Abraham, Fisher, Elizabeth M.C., Cunningham, Thomas J.

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