Cardiac α-actin over-expression therapy in dominant ACTA1 disease. by Ravenscroft, G, McNamara, E, Griffiths, L, Papadimitriou, J, Hardeman, E, Bakker, A, Davies, K, Laing, N, Nowak, K

Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies. by Ravenscroft, G, Jackaman, C, Bringans, S, Papadimitriou, J, Griffiths, L, McNamara, E, Bakker, A, Davies, K, Laing, N, Nowak, K

Mouse models of dominant ACTA1 disease recapitulate human disease and provide insight into therapies by Ravenscroft, G, Jackaman, C, Bringans, S, Papadimitriou, J, Griffiths, L, McNamara, E, Bakker, A, Davies, K, Laing, N, Nowak, K

Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression by Ravenscroft, G, Jackaman, C, Sewry, C, McNamara, E, Squire, SE, Potter, A, Papadimitriou, J, Griffiths, L, Bakker, A, Davies, K, Laing, N, Nowak, K

Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression. by Ravenscroft, G, Jackaman, C, Sewry, C, McNamara, E, Squire, SE, Potter, A, Papadimitriou, J, Griffiths, L, Bakker, A, Davies, K, Laing, N, Nowak, K

A mutant skeletal muscle alpha-actin gene, fused to enhanced green fluorescent protein (EGFP) produces a unique myopathic mouse model by Nowak, K, Ravenscroft, G, Jackaman, C, Lim, E, Sewry, C, Potter, A, Squire, S, Fisher, R, Baker, E, Feng, J, Marston, S, Fabian, V, Morling, P, Bakker, A, Griffiths, L, Papadimitriou, J, Davies, K, Laing, N

Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin. by Nowak, K, Ravenscroft, G, Jackaman, C, Filipovska, A, Davies, S, Lim, E, Squire, SE, Potter, A, Baker, E, Clément, S, Sewry, C, Fabian, V, Crawford, K, Lessard, J, Griffiths, L, Papadimitriou, J, Shen, Y, Morahan, G, Bakker, A, Davies, K, Laing, N