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Towards therapies for muscular dystrophies : targeting TGF-beta and myostatin signalling to improve muscle quality and development of reliable outcome measures for preclinical mouse models
Developing an antisense oligonucleotide treatment for Spinocerebellar Ataxia Type 3
Developing tissue specific antisense oligonucleotide-delivery to refine treatment for Duchenne muscular dystrophy
NOTCH3 cysteine correction : developing a rational therapeutic approach for CADASIL
Identification of therapeutic targets and antisense oligonucleotide mediated exon skipping based therapies in arthritis
Optimising antisense oligonucleotide-mediated exon skipping for Duchenne muscular dystrophy
From signal transduction to targeted therapy : interference with TGF-_ and myostatin signaling for Duchenne muscular dystrophy
Development of an anitsense-mediated exon skipping therapy for Duchenne Muscular Dystrophy.
