Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD von MCCLOREY, G, MOULTON, H. M, IVERSEN, P. L, FLETCHER, S, WILTON, S. D

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The Influence of Antisense Oligonucleotide Length on Dystrophin Exon Skipping von Harding, P L, Fall, A M, Honeyman, K, Fletcher, S, Wilton, S D

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Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle von Gebski, Bianca L., Mann, Chrisopher J., Fletcher, Susan, Wilton, Stephen D.

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Co-regulation of survival of motor neuron and Bcl-xL expression: Implications for neuroprotection in spinal muscular atrophy von Anderton, R.S, Price, L.L, Turner, B.J, Meloni, B.P, Mitrpant, C, Mastaglia, F.L, Goh, C, Wilton, S.D, Boulos, S

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The emperor's new dystrophin: finding sense in the noise von Wilton, S.D, Veedu, R.N, Fletcher, S

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The Regrowth of Axons within Tissue Defects in the CNS Is Promoted by Implanted Hydrogel Matrices That Contain BDNF and CNTF Producing Fibroblasts von Loh, N.K., Woerly, S., Bunt, S.M., Wilton, S.D., Harvey, A.R.

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Massive Idiosyncratic Exon Skipping Corrects the Nonsense Mutation in Dystrophic Mouse Muscle and Produces Functional Revertant Fibers by Clonal Expansion von Lu, Q. L., Morris, G. E., Wilton, S. D., Ly, T., O. V. Artem'yeva, Strong, P., Partridge, T. A.

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Enhanced in vivo delivery of antisense oligonucleotides to restore dystrophin expression in adult mdx mouse muscle von Wells, K.E., Fletcher, S., Mann, C.J., Wilton, S.D., Wells, D.J.

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A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy von Laing, Nigel G, Akkari, Patrick A, Love, Donald R, Watkins, Hugh, Wilton, Stephen D, Dorosz, Shellie, Kneebone, Chris, White, Sue, Haan, Eric, Boundy, Karyn, Blumbergs, Peter

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Use of polymerase chain reaction for rapid diagnosis of tuberculosis von COUSINS, DV, WILTON, SD, FRANCIS, BR, GOW, BL

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Autosomal dominant distal myopathy : linkage to chromosome 14 von LAING, N. G, LAING, B. A, MEREDITH, C, WILTON, S. D, ROBBINS, P, HONEYMAN, K, DOROSZ, S, KOZMAN, H, MASTAGLIA, F. L, KAKULAS, B. A

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Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy von Tan, P., Briner, J., Boltshauser, E., Davis, M.R., Wilton, S.D., North, K., Wallgren-Pettersson, C., Laing, N.G.

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Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy von Mastaglia, F L, Nowak, K J, Stell, R, Phillips, B A, Edmondston, J E, Dorosz, S M, Wilton, S D, Hallmayer, J, Kakulas, B A, Laing, N G

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A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinoma von Stirnweiss, A, McCarthy, K, Oommen, J, Crook, M L, Hardy, K, Kees, U R, Wilton, S D, Anazodo, A, Beesley, A H

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Induced dystrophin exon skipping in human muscle explants von McClorey, G., Fall, A.M., Moulton, H.M., Iversen, P.L., Rasko, J.E., Ryan, M., Fletcher, S., Wilton, S.D.

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Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy von Mann, Christopher J., Honeyman, Kaite, McClorey, Graham, Fletcher, Sue, Wilton, Stephen D.

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Bandstab: A PCR-Based Alternative to Cloning PCR Products von Wilton, Steve D, Lim, Lynnette, Dye, Danielle, Laing, Nigel

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Dystrophin gene transcripts skipping the mdx mutation von Wilton, Stephen D., Dye, Danielle E., Laing, Nigel G.

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Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides von Wilton, Stephen D, Lloyd, Frances, Carville, Kylie, Fletcher, Sue, Honeyman, Kaite, Agrawal, Sudhir, Kole, Ryszard

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A splice-site mutation causing ovine McArdle's disease von Tan, P, Allen, J.G, Wilton, S.D, Akkari, P.A, Huxtable, C.R, Laing, N.G

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