Investigating dysfunctional RNA processing in TDP-43 mouse mutants
Sivakumar, P, Humphrey, J, Ule, A, Bodo, C, Emmett, W, Ricketts, T, Oliveira, H, Wang, E, Housman, D, Greensmith, L, Buratti, E, Baralle, F, Plagnol, V, Acevedo-Arozena, A, Fisher, E.M.C, Fratta, P
Published in Neuromuscular disorders : NMD (01.03.2017)
Published in Neuromuscular disorders : NMD (01.03.2017)
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Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment
Rogers, D C, Fisher, E M, Brown, S D, Peters, J, Hunter, A J, Martin, J E
Published in Mammalian genome (01.10.1997)
Published in Mammalian genome (01.10.1997)
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P16 Investigating novel mutant mouse models of motor neuron disease
McGoldrick, P, Dick, J, Ricketts, T, Joyce, P, Fratta, P, Acevedo-Arozena, A, Fisher, E.M.C, Greensmith, L
Published in Neuromuscular disorders : NMD (2011)
Published in Neuromuscular disorders : NMD (2011)
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MND05 - Dissecting TDP-43 gain- and loss-of-function in neurodegeneration
Sivakumar, P., Humphrey, J., Lo, K., Ricketts, T., Oliveira, H., Kalmar, B., Wang, E., Housman, D., Baralle, F., Greensmith, L., Buratti, E., Plagnol, V., Fisher, E.M.C., Arozena, A.A., Fratta, P.
Published in Neuromuscular disorders : NMD (01.04.2018)
Published in Neuromuscular disorders : NMD (01.04.2018)
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Dissecting TDP-43 gain- and loss-of-function in neurodegeneration
Sivakumar, P., Humphrey, J., Lo, K., Ricketts, T., Oliveira, H., Kalmar, B., Wang, E., Housman, D., Baralle, F., Greensmith, L., Buratti, E., Plagnol, V., Fisher, E.M.C., Arozena, A.A., Fratta, P.
Published in Neuromuscular disorders : NMD (01.04.2018)
Published in Neuromuscular disorders : NMD (01.04.2018)
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Hippocampal circuit dysfunction in the Tc1 mouse model of Down syndrome
Witton, Jonathan, Padmashri, Ragunathan, Zinyuk, Larissa E, Popov, Victor I, Kraev, Igor, Line, Samantha J, Jensen, Thomas P, Tedoldi, Angelo, Cummings, Damian M, Tybulewicz, Victor L J, Fisher, Elizabeth M C, Bannerman, David M, Randall, Andrew D, Brown, Jonathan T, Edwards, Frances A, Rusakov, Dmitri A, Stewart, Michael G, Jones, Matt W
Published in Nature neuroscience (01.09.2015)
Published in Nature neuroscience (01.09.2015)
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MN13 - Investigating dysfunctional RNA processing in TDP-43 mouse mutants
Sivakumar, P., Humphrey, J., Ule, A., Bodo, C., Emmett, W., Ricketts, T., Oliveira, H., Wang, E., Housman, D., Greensmith, L., Buratti, E., Baralle, F., Plagnol, V., Acevedo-Arozena, A., Fisher, E.M.C., Fratta, P.
Published in Neuromuscular disorders : NMD (01.03.2017)
Published in Neuromuscular disorders : NMD (01.03.2017)
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Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome
De Vita, S, Canzonetta, C, Mulligan, C, Delom, F, Groet, J, Baldo, C, Vanes, L, Dagna-Bricarelli, F, Hoischen, A, Veltman, J, Fisher, E M C, Tybulewicz, V L J, Nizetic, D
Published in Oncogene (18.11.2010)
Published in Oncogene (18.11.2010)
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A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS
Wills, A-M, Cronin, S, Slowik, A, Kasperaviciute, D, Van Es, M A, Morahan, J M, Valdmanis, P N, Meininger, V, Melki, J, Shaw, C E, Rouleau, G A, Fisher, E M C, Shaw, P J, Morrison, K E, Pamphlett, R, Van den Berg, L H, Figlewicz, D A, Andersen, P M, Al-Chalabi, A, Hardiman, O, Purcell, S, Landers, J E, Brown, Jr, R H
Published in Neurology (07.07.2009)
Published in Neurology (07.07.2009)
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Chromosome 3 linked frontotemporal dementia (FTD-3)
Gydesen, S, Brown, J M, Brun, A, Chakrabarti, L, Gade, A, Johannsen, P, Rossor, M, Thusgaard, T, Grove, A, Yancopoulou, D, Spillantini, M G, Fisher, E M C, Collinge, J, Sorensen, S A
Published in Neurology (26.11.2002)
Published in Neurology (26.11.2002)
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The Frequency and Position of Alu Repeats in cDNAs, as Determined by Database Searching
Yulug, Isik G., Yulug, Aydin, Fisher, Elizabeth M.C.
Published in Genomics (San Diego, Calif.) (10.06.1995)
Published in Genomics (San Diego, Calif.) (10.06.1995)
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Mapping TNNC1, the gene that encodes cardiac troponin I in the human and the mouse
BERMINGHAM, N, HERNANDEZ, D, BALFOUR, A, GILMOUR, F, MARTIN, J. E, FISHER, E. M. C
Published in Genomics (San Diego, Calif.) (10.12.1995)
Published in Genomics (San Diego, Calif.) (10.12.1995)
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The DAD1 protein, whose defect causes apoptotic cell death, maps to human chromosome 14
Ylug, Isik G., See, Chee Gee, Fisher, Elizabeth M.C.
Published in Genomics (San Diego, Calif.) (20.03.1995)
Published in Genomics (San Diego, Calif.) (20.03.1995)
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The SHB Adaptor Protein Maps to Human Chromosome 9
Yulug, Isik G., Hillermann, Renate, Fisher, Elizabeth M.C.
Published in Genomics (San Diego, Calif.) (01.12.1994)
Published in Genomics (San Diego, Calif.) (01.12.1994)
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The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus
BERMINGHAM, N. A, MARTIN, J. E, FISHER, E. M. C
Published in Genomics (San Diego, Calif.) (01.03.1996)
Published in Genomics (San Diego, Calif.) (01.03.1996)
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