P10 Utrophin modulators to treat Duchenne Muscular Dystrophy (DMD): Future clinical trial plans for SMT C1100 and biomarker development programme
Tinsley, J.M, Bracchi, A, Wilson, F.X, Horne, G, Robinson, N, Fairclough, R.J, Davies, K.E
Published in Neuromuscular disorders : NMD (01.03.2014)
Published in Neuromuscular disorders : NMD (01.03.2014)
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P.13.14 Future clinical and biomarker development for SMTC1100, the first utrophin modulator to enter clinical trials for Duchenne Muscular Dystrophy (DMD)
Tinsley, J.M, Robinson, N, Wilson, F.X, Horne, G, Fairclough, R.J, Davies, K.E
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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P13 New orally available compounds which modulate utrophin expression for the therapy of Duchenne muscular dystrophy (DMD)
Fairclough, R.J, Squire, S.E, Araujo, N, Vuorinen, A, Davies, S.G, Wynne, G.M, Russell, A.J, Davies, K.E
Published in Neuromuscular disorders : NMD (01.03.2014)
Published in Neuromuscular disorders : NMD (01.03.2014)
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T.O.3 Tricyclo-DNA: A promising chemistry for the synthesis of antisense molecules for splice-switching approaches in DMD
Goyenvalle, A, Babbs, A, Avril, A, Griffiths, G, Dugovic, B, Davies, K.E, Leumann, C, Garcia, L
Published in Neuromuscular disorders : NMD (01.10.2012)
Published in Neuromuscular disorders : NMD (01.10.2012)
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P.20.8 AAV genome loss from dystrophic mouse muscles during AAV-U7snRNA-mediated exon skipping therapy
Hir, M. Le, Goyenvalle, A, Peccate, C, Précigout, G, Davies, K.E, Voit, T, Garcia, L, Lorain, S
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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P3.02 AAV-U7snRNA mediated multi exon-skipping for Duchenne muscular dystrophy
Goyenvalle, A, Babbs, A, Garcia, L, Davies, K.E
Published in Neuromuscular disorders : NMD (01.10.2010)
Published in Neuromuscular disorders : NMD (01.10.2010)
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A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets
Poustka, A, Davies, K.E, Lorenz, B, Korn, B, Drezner, M.K, O'Riordan, J.L.H, Pannetier, S, Rowe, P.S.N, Summerfield, T, Nesbitt, T, Meindl, A, Lehrach, H, Strom, T.M, Popowska, E, Mountford, R, Cagnoli, B, Mohnike, K.L, Hanauer, A, Reinhardt, R, Read, A.P, Econs, M.J, Murken, J, de Jong, P, Goulding, J.N, Hennig, S, Meitinger, T, Oudet, C, Francis, F, Pronicka, E
Published in Nature genetics (01.10.1995)
Published in Nature genetics (01.10.1995)
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G.P.89
Fairclough, R.J, Guiraud, S, Squire, S.E, Babbs, A, Edward, B, Shah, N, Bracchi, A, Wilson, F.X, Horne, G, Robinson, N, Araujo, N, Hewings, D.S, Vuorinen, A, Davies, S.G, Wynne, G.M, Russell, A.J, Tinsley, J, Davies, K.E
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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P06 AAV-U7snRNA mediated multi exon-skipping for Duchenne muscular dystrophy
Goyenvalle, A, Babbs, A, Wright, J, Garcia, L, Davies, K.E
Published in Neuromuscular disorders : NMD (2011)
Published in Neuromuscular disorders : NMD (2011)
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O01 Identification of new chemical compounds with upregulate utrophin for the therapy of Duchenne muscular dystrophy
Fairclough, R.J, Squire, S.E, Potter, A.C, Powell, D.S, Davies, S.G, Bataille, C.J.R, Wynne, G.M, Russell, A.J, Davies, K.E
Published in Neuromuscular disorders : NMD (01.03.2012)
Published in Neuromuscular disorders : NMD (01.03.2012)
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Stromal cell-derived receptor 2 and cytochrome b561 are functional ferric reductases
Vargas, J.D., Herpers, B., McKie, A.T., Gledhill, S., McDonnell, J., van den Heuvel, M., Davies, K.E., Ponting, C.P.
Published in Biochimica et biophysica acta (23.09.2003)
Published in Biochimica et biophysica acta (23.09.2003)
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P23 Assessing the effects of exercise-induced stress on the Fiona mouse model
Bareja, A, Fairclough, R.J, Potter, A, Powell, D, Squire, S, Davies, K.E
Published in Neuromuscular disorders : NMD (2010)
Published in Neuromuscular disorders : NMD (2010)
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O.24 Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies
Ravenscroft, G, Jackaman, C, Bringans, S, Papadimitriou, J.M, Griffiths, L.M, McNamara, E, Bakker, A.J, Davies, K.E, Laing, N.G, Nowak, K.J
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
Knight, S.J.L., Flannery, A.V., Hirst, M.C., Campbell, L., Christodoulou, Z., Phelps, S.R., Pointon, J., Middleton-Price, H.R., Barnicoat, A., Pembrey, M.E., Holland, J., Oostra, B.A., Bobrow, M., Davies, K.E.
Published in Cell (16.07.1993)
Published in Cell (16.07.1993)
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T.P.3.03 TREAT-NMD-Activity 7: Accelerate preclinical phase of new therapeutic treatment development
Willmann, R, Rüegg, M.A, Fairclough, R, Davies, K.E, Possekel, S, Meier, T
Published in Neuromuscular disorders : NMD (01.10.2008)
Published in Neuromuscular disorders : NMD (01.10.2008)
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