Projects per year
Search results
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Active
Building translational capacity in WA; Establishing the tools needed to develop treatments for Australian children with muscle disease.
Taylor, R. (Investigator 01), Ravenscroft, G. (Investigator 02), Clayton, J. (Investigator 03), Kuznetsova, I. (Investigator 04), Elaskalani, O. (Investigator 05), Endersby, R. (Investigator 06) & Forrest, A. (Investigator 07)
Stan Perron Charitable Foundation
2/07/23 → 4/07/27
Project: Research
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Finished
WA Near-miss Awards: Ideas Grants 2021
Taylor, R. (Investigator 01)
Department of Health (Western Australia)
1/07/22 → 30/06/23
Project: Research
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Testing novel genetic therapies for ACTA1 nemaline myopathy (NEM3) – harnessing patient cells
Laing, N. (Investigator 01), Nowak, K. (Investigator 02), Ravenscroft, G. (Investigator 03), Taylor, R. (Investigator 04) & Clayton, J. (Investigator 05)
A Foundation Building Strength Inc
5/08/20 → 4/08/22
Project: Research
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Evaluating an allele-specific genetic therapy for congenital myopathy caused by dominant mutations in the skeletal muscle actin (ACTA1) gene
Nowak, K. (Investigator 01), Laing, N. (Investigator 02) & Taylor, R. (Investigator 03)
Association Francaise contre les Myopathies (AFM)
30/05/18 → 30/11/19
Project: Research
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Evaluating gene therapy for McArdle's disease using a mouse model
Laing, N. (Investigator 01), Nowak, K. (Investigator 02) & Taylor, R. (Investigator 03)
Muscular Dystrophy Association of America
1/02/17 → 31/07/18
Project: Research