Projects per year
Search results
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Active
Development of CRISPR/Cas Genome Editing as a Treatment for Ataxia Telangiectasia
1/11/17 → 11/03/24
Project: Research
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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. & Popplewell, L.
1/09/21 → 31/08/22
Project: Research
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Plants and Minerals in Byzantine Popular Pharmacy. A New Multidisciplinary Approach
1/11/19 → 31/10/22
Project: Other
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Universal Microdystrophin (MD) Gene Therapy Clinical Trial for DMD (UNITE-DMD)
Dickson, G., Popplewell, L. & Malerba, A.
1/07/17 → 30/06/21
Project: Other
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Enhancement of antisense oligonucleotide-mediated exon skipping as a therapy for Duchenne muscular dystrophy
Popplewell, L.
6/02/17 → 5/02/20
Project: Research
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Development of cell-penetrating peptide-conjugated antisense oligonucleotides for the treatment of fascioscapulohumeral muscular dystrophy
Popplewell, L. & Dickson, G.
1/10/16 → 30/09/19
Project: Other
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In vivo activity assessment of four AAV OPMD clinical constructs – PhasesI&II
1/09/16 → 31/07/17
Project: Other
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Development of genome editing surgery with applicability to all DMD patients
Popplewell, L.
1/07/16 → 31/12/16
Project: Research
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Prediction of drug cocktails with anti-trypanosomal effect
Eng & Phys Sci Res Council EPSRC
1/06/16 → 31/03/17
Project: Research
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Inducing Immune-Tolerance to AAV Vector Capsid for Gene Therapy of Duchenne Muscular Dystrophy
1/10/15 → 31/08/20
Project: Research
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Research Programme towards a Phase 1 / 2 Clinical trial of Microdystrophin Gene Therapy
11/11/14 → 10/03/16
Project: Research
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Towards a clinical trial for Oculopharyngeal Muscular Dystrophy (OPMD)
Association Francais contre les Myopathies
1/07/14 → 30/06/19
Project: Research
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Optimization of micro-dystrophin gene therapy for Duchenne muscular dystrophy (MD-AAV)
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
1/01/14 → 30/06/15
Project: Research
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Correction of Duchenne Muscular Dystrophy Mutations using Endonuclease-Mediated Genome Surgery
1/10/13 → 30/09/14
Project: Research
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Vectorisation of Chondroitinase for therapy in spinal cord injury
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., Paccanaro, A. & Papdi, C.
1/05/13 → 30/04/15
Project: Research
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Gene Surgery for Duchenne Muscular Dystrophy(DMD)
Dickson, G. & Yáñez-Muñoz, R. J.
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., Bogre, L. & Horvath, B.
1/03/13 → 28/02/15
Project: Research
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Pathophysiology and therapeutic approaches in Oculoparyngeal Muscular Dystropy (OPMD)
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
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
1/02/11 → 31/01/14
Project: Research
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Meganuclease-Enhance Genome Correction Therapy for Duchenne Muscular Dystrophy
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., Broadstock, M. & Yáñez-Muñoz, R. J.
1/10/09 → 1/07/13
Project: Research