Humanising the mouse genome piece by piece von Zhu, Fei, Nair, Remya R., Fisher, Elizabeth M. C., Cunningham, Thomas J.

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A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome von Wiseman, Frances K., Al-Janabi, Tamara, Hardy, John, Karmiloff-Smith, Annette, Nizetic, Dean, Tybulewicz, Victor L. J., Fisher, Elizabeth M. C., Strydom, André

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Is SOD1 loss of function involved in amyotrophic lateral sclerosis? von SACCON, Rachele A, BUNTON-STASYSHYN, Rosie K. A, FISHER, Elizabeth M. C, FRATTA, Pietro

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Association of Dementia With Mortality Among Adults With Down Syndrome Older Than 35 Years von Hithersay, Rosalyn, Startin, Carla M, Hamburg, Sarah, Mok, Kin Y, Hardy, John, Fisher, Elizabeth M. C, Tybulewicz, Victor L. J, Nizetic, Dean, Strydom, André

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Mouse models of aneuploidy to understand chromosome disorders von Tosh, Justin, Tybulewicz, Victor, Fisher, Elizabeth M. C.

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Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia von Fratta, Pietro, Poulter, Mark, Lashley, Tammaryn, Rohrer, Jonathan D., Polke, James M., Beck, Jon, Ryan, Natalie, Hensman, Davina, Mizielinska, Sarah, Waite, Adrian J., Lai, Mang-Ching, Gendron, Tania F., Petrucelli, Leonard, Fisher, Elizabeth M. C., Revesz, Tamas, Warren, Jason D., Collinge, John, Isaacs, Adrian M., Mead, Simon

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Correlation of clinical and molecular features in spinal bulbar muscular atrophy von Fratta, Pietro, Nirmalananthan, Niranjanan, Masset, Luc, Skorupinska, Iwona, Collins, Toby, Cortese, Andrea, Pemble, Sally, Malaspina, Andrea, Fisher, Elizabeth M.C, Greensmith, Linda, Hanna, Michael G

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C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins von 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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Down syndrome—recent progress and future prospects von Wiseman, Frances K., Alford, Kate A., Tybulewicz, Victor L.J., Fisher, Elizabeth M.C.

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Cytoplasmic dynein heavy chain: the servant of many masters von Schiavo, Giampietro, Greensmith, Linda, Hafezparast, Majid, Fisher, Elizabeth M.C

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Species-Specific Transcription in Mice Carrying Human Chromosome 21 von Wilson, Michael D, Barbosa-Morais, Nuno L, Schmidt, Dominic, Conboy, Caitlin M, Vanes, Lesley, Tybulewicz, Victor L.J, Fisher, Elizabeth M.C, Tavaré, Simon, Odom, Duncan T

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SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments von Joyce, Peter I., Fratta, Pietro, Fisher, Elizabeth M. C., Acevedo-Arozena, Abraham

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Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease von Filimonenko, Maria, Stuffers, Susanne, Raiborg, Camilla, Yamamoto, Ai, Malerød, Lene, Fisher, Elizabeth M.C, Isaacs, Adrian, Brech, Andreas, Stenmark, Harald, Simonsen, Anne

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Endosomal structure and APP biology are not altered in a preclinical mouse cellular model of Down syndrome von Cannavo, Claudia, Cleverley, Karen, Maduro, Cheryl, Mumford, Paige, Moulding, Dale, Fisher, Elizabeth M C, Wiseman, Frances K

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Maternal iron deficiency perturbs embryonic cardiovascular development in mice von Kalisch-Smith, Jacinta I., Ved, Nikita, Szumska, Dorota, Munro, Jacob, Troup, Michael, Harris, Shelley E., Rodriguez-Caro, Helena, Jacquemot, Aimée, Miller, Jack J., Stuart, Eleanor M., Wolna, Magda, Hardman, Emily, Prin, Fabrice, Lana-Elola, Eva, Aoidi, Rifdat, Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Mohun, Timothy J., Lakhal-Littleton, Samira, De Val, Sarah, Giannoulatou, Eleni, Sparrow, Duncan B.

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Genetic analysis of the cytoplasmic dynein subunit families von Pfister, K Kevin, Shah, Paresh R, Hummerich, Holger, Russ, Andreas, Cotton, James, Annuar, Azlina Ahmad, King, Stephen M, Fisher, Elizabeth M C

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NMJ-Analyser identifies subtle early changes in mouse models of neuromuscular disease von Mejia Maza, Alan, Jarvis, Seth, Lee, Weaverly Colleen, Cunningham, Thomas J., Schiavo, Giampietro, Secrier, Maria, Fratta, Pietro, Sleigh, James N., Fisher, Elizabeth M. C., Sudre, Carole H.

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Rodent models in Down syndrome research: impact and future opportunities von Herault, Yann, Delabar, Jean M, Fisher, Elizabeth M C, Tybulewicz, Victor L J, Yu, Eugene, Brault, Veronique

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Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations von Urwin, Hazel, Authier, Astrid, Nielsen, Jorgen E., Metcalf, Daniel, Powell, Caroline, Froud, Kristina, Malcolm, Denise S., Holm, Ida, Johannsen, Peter, Brown, Jeremy, Fisher, Elizabeth M.C., van der Zee, Julie, Bruyland, Marc, Van Broeckhoven, Christine, Collinge, John, Brandner, Sebastian, Futter, Clare, Isaacs, Adrian M.

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point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice von Becker, Esther B.E, Oliver, Peter L, Glitsch, Maike D, Banks, Gareth T, Achilli, Francesca, Hardy, Andrea, Nolan, Patrick M, Fisher, Elizabeth M.C, Davies, Kay E

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