Projects per year
Projects
- 49 Finished
Search results
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Finished
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Identifying metabolic signatures of pathology in muscle and blood to identify biomarkers of oculopharyngeal muscular dystrophy.
Snowden, S. (PI) & Popplewell, L. (CoI)
1/09/21 → 31/08/22
Project: Research
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Plants and Minerals in Byzantine Popular Pharmacy. A New Multidisciplinary Approach
Zipser, B. (PI) & Scott, A. C. (CoI)
1/11/19 → 31/10/22
Project: Research
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Development of CRISPR/Cas Genome Editing as a Treatment for Ataxia Telangiectasia
Yáñez-Muñoz, R. J. (PI)
1/11/17 → 11/03/25
Project: Research
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In vivo evaluation of muscle specific synthetic promoters
Dickson, G. (PI)
1/08/17 → 30/04/18
Project: Research
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Universal Microdystrophin (MD) Gene Therapy Clinical Trial for DMD (UNITE-DMD)
Dickson, G. (PI), Popplewell, L. (CoI) & Malerba, A. (Researcher)
1/07/17 → 30/06/21
Project: Research
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Enhancement of antisense oligonucleotide-mediated exon skipping as a therapy for Duchenne muscular dystrophy
Popplewell, L. (PI)
6/02/17 → 5/02/20
Project: Research
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Genome Editing in Muscle Stem Cells for Duchenne Muscular Dystrophy
Dickson, G. (PI)
1/02/17 → 31/01/18
Project: Research
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Development of cell-penetrating peptide-conjugated antisense oligonucleotides for the treatment of fascioscapulohumeral muscular dystrophy
Popplewell, L. (PI) & Dickson, G. (CoI)
1/10/16 → 30/09/19
Project: Research
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In vivo activity assessment of four AAV OPMD clinical constructs – Phases I & II
Dickson, G. (PI)
1/09/16 → 31/07/17
Project: Research
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Development of genome editing surgery with applicability to all DMD patients
Popplewell, L. (PI)
1/07/16 → 31/12/16
Project: Research
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Prediction of drug cocktails with anti-trypanosomal effect
Paccanaro, A. (PI)
Eng & Phys Sci Res Council EPSRC
1/06/16 → 31/03/17
Project: Research
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An investigation into the role of Rp131 and regulation of ribosome biogenesis in the pathogenesis of Duchenne muscular dystrophy implications for novel therapeutic strategies
Popplewell, L. (PI)
Neurological Foundation of New Zealand
1/04/16 → 31/03/18
Project: Research
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The UK Spinal Muscular Atrophy Research Consortium
Yáñez-Muñoz, R. J. (PI)
1/01/16 → 3/03/20
Project: Research
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Enhancement of splicing efficiency between trans-spliced DMD AAV vectors for the production of full-length fully functional dystrophin protein
Dickson, G. (PI)
1/01/16 → 1/01/17
Project: Research
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Development of broadly applicable combinatorial genome editing and antisense therapies for Duchenne muscular dystrophy addressing dystrophin deficiency, muscle wasting and muscle fibrosis
Popplewell, L. (PI)
1/10/15 → 30/09/16
Project: Research
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Inducing Immune-Tolerance to AAV Vector Capsid for Gene Therapy of Duchenne Muscular Dystrophy
Dickson, G. (PI)
1/10/15 → 31/08/20
Project: Research
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Second generation hyper-active micro-dystrophin AAV vectors for Duchenne muscular dystrophy gene therapy
Dickson, G. (PI)
1/10/15 → 30/09/18
Project: Research
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Stage 2 study on DNA-directed RNAi for the treatment of OPMd
Dickson, G. (PI)
1/09/15 → 31/08/16
Project: Research
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Bilateral NSF/BIO-BBSRC - Translational landscape to link cell growth with proliferation in the root meristem
Bogre, L. (PI) & Paccanaro, A. (PI)
Biotechnology and Biological Sciences Research Council BBSRC
1/07/15 → 30/06/18
Project: Research
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Research Programme towards a Phase 1 / 2 Clinical trial of Microdystrophin Gene Therapy
Dickson, G. (PI)
11/11/14 → 10/03/16
Project: Research
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Towards a clinical trial for Oculopharyngeal Muscular Dystrophy (OPMD)
Dickson, G. (PI)
Association Francais contre les Myopathies
1/07/14 → 30/06/19
Project: Research
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Multi-level analysis of the evolution of cooperative behaviour in social insects Marie Curie Fellow – Dr Fabio Manfredini
Brown, M. J. F. (PI) & Paccanaro, A. (CoI)
1/04/14 → 31/03/16
Project: Research
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Optimization of micro-dystrophin gene therapy for Duchenne muscular dystrophy (MD-AAV)
Dickson, G. (PI)
6/01/14 → 5/01/16
Project: Research
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Destructive Exon Skipping of Myostatin mRNA with and without Open Reading Frame Rescue of Dystrophin
Dickson, G. (PI)
1/01/14 → 30/06/15
Project: Research
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Development of dual/triple transpliced AAV vectors to restore quasi/full length dystrophin variants to muscle
Dickson, G. (PI)
1/10/13 → 30/09/16
Project: Research
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Correction of Duchenne Muscular Dystrophy Mutations using Endonuclease-Mediated Genome Surgery
Dickson, G. (PI)
1/10/13 → 30/09/14
Project: Research
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Vectorisation of Chondroitinase for therapy in spinal cord injury
Yáñez-Muñoz, R. J. (PI)
International Spinal Research Trust
1/10/13 → 30/09/15
Project: Research
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MAPK signalling network to adapt leaf growth to drought conditions
Bogre, L. (PI), Paccanaro, A. (CoI) & Papdi, C. (CoI)
1/05/13 → 30/04/15
Project: Research
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Gene Surgery for Duchenne Muscular Dystrophy(DMD)
Dickson, G. (PI) & Yáñez-Muñoz, R. J. (CoI)
Association Francais contre les Myopathies
1/04/13 → 31/03/15
Project: Research
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Inference of RBR network and dynamic RBR complexes during leaf development
Paccanaro, A. (PI), Bogre, L. (CoI) & Horvath, B. (CoI)
1/03/13 → 28/02/15
Project: Research
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Phase I/IIa clinical trial in Duchenne muscular dystrophy using systematically delivered morpholino antisense oligomer to skip exon 53.
Dickson, G. (PI)
1/11/12 → 31/10/15
Project: Research
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Long-term follow-up of transgene expression in vivo in mouse motor neurons after intra-uterine injection
Yáñez-Muñoz, R. J. (PI)
The Spinal Muscular Atrophy Trust
1/04/12 → 30/06/12
Project: Research
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Pathophysiology and therapeutic approaches in Oculoparyngeal Muscular Dystropy (OPMD)
Dickson, G. (PI)
Association Francais contre les Myopathies
1/05/11 → 30/04/13
Project: Research
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Advances in oligonucleotide-mediated exon skipping for DMD and related disorders
Dickson, G. (PI)
Association Francais contre les Myopathies
1/04/11 → 31/03/15
Project: Research
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Advanced antisense oligonucleotide technology for Exon skipping in Duchenne Muscular Dystrophy
Dickson, G. (PI)
1/02/11 → 31/01/14
Project: Research
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Meganuclease-Enhance Genome Correction Therapy for Duchenne Muscular Dystrophy
Dickson, G. (PI)
Association Francais contre les Myopathies
1/04/10 → 31/03/12
Project: Research
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Integration-deficient lentiviral vectors delivering neurotrophic factors for gene therapy of Parkinson’s disease
Lu-Nguyen, N. (Student), Broadstock, M. (Fellow) & Yáñez-Muñoz, R. J. (PI)
1/10/09 → 1/07/13
Project: Research