Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD by Guiraud, S, Edwards, B, Squire, S, Moir, L, Berg, A, Babbs, A, Ramadan, N, Wood, M, Davies, K

Identification of new chemical compounds with upregulate utrophin for the therapy of Duchenne muscular dystrophy by Fairclough, R, Squire, SE, Potter, A, Powell, D, Davies, S, Bataille, C, Wynne, G, Russell, A, Davies, K

A 1-day extreme rainfall event in Tasmania: process evaluation and long tail attribution by Tozer, CR, Risbey, JS, Grose, MR, Monselesan, DP, Squire, DT, Black, AS, Richardson, D, Sparrow, SN, Li, S, Wallom, D

Crystallographic snapshots of sulfur insertion by lipoyl synthase by Lanz, Nicholas D., Lee, Kyung-Hoon, Booker, Squire J., McLaughlin, Martin I., Goldman, Peter John, Drennan, Catherine L.

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X-ray structure of an AdoMet radical activase reveals an anaerobic solution for formylglycine posttranslational modification by Goldman, Peter J., McLaughlin, Martin I., Drennan, Catherine L., Grove, Tyler L., Sites, Lauren A., Booker, Squire J.

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Crystal structure of the C1 domain of cardiac myosin binding protein-C: implications for hypertrophic cardiomyopathy. by Govada, L, Carpenter, L, da Fonseca, P, Helliwell, JR, Rizkallah, P, Flashman, E, Chayen, N, Redwood, C, Squire, J

Micro-utrophin improves cardiac and skeletal muscle function of severely affected D2/mdx mice by Kennedy, T, Guiraud, S, Edwards, B, Squire, S, Moir, L, Babbs, A, Odom, G, Golebiowski, D, Schneider, J, Chamberlain, J, Davies, K

A specific and rapid neural signature for parental instinct. by Kringelbach, M, Lehtonen, A, Squire, S, Harvey, A, Craske, MG, Holliday, I, Green, A, Aziz, T, Hansen, P, Cornelissen, P, Stein, A

Mutating the tight-dimer interface of dihydrodipicolinate synthase disrupts the enzyme quaternary structure: toward a monomeric enzyme. by Pearce, F, Dobson, R, Weber, A, Lane, L, McCammon, MG, Squire, M, Perugini, M, Jameson, G, Robinson, C, Gerrard, J

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

Second-generation compound for the modulation of utrophin in the therapy of DMD by Guiraud, S, Squire, S, Edwards, B, Chen, H, Burns, D, Shah, N, Babbs, A, Davies, S, Wynne, G, Russell, A, Elsey, D, Wilson, F, Tinsley, J, Davies, K

Structural basis for non-radical catalysis by TsrM, a radical SAM methylase by Knox, Hayley L, Chen, Percival Yang-Ting, Blaszczyk, Anthony J, Mukherjee, Arnab, Grove, Tyler L, Schwalm, Erica L, Wang, Bo, Drennan, Catherine L, Booker, Squire J

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Structural basis for non-radical catalysis by TsrM, a radical SAM methylase by Knox, Hayley L, Chen, Percival Yang-Ting, Blaszczyk, Anthony J, Mukherjee, Arnab, Grove, Tyler L, Schwalm, Erica L, Wang, Bo, Drennan, Catherine L, Booker, Squire J.

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Daily treatment with SMTC1100, a novel small molecule utrophin upregulator, dramatically reduces the dystrophic symptoms in the mdx mouse. by Tinsley, J, Fairclough, R, Storer, R, Wilkes, F, Potter, A, Squire, SE, Powell, D, Cozzoli, A, Capogrosso, R, Lambert, A, Wilson, F, Wren, S, De Luca, A, Davies, K

New orally available compounds which modulate utrophin expression for the therapy of Duchenne muscular dystrophy (DMD) by Fairclough, R, Guiraud, S, Squire, SE, Babbs, A, Edward, B, Shah, N, Bracchi, A, Wilson, F, Horne, G, Robinson, N, Araujo, N, Hewings, D, Vuorinen, A, Davies, S, Wynne, G, Russell, A, Tinsley, J, Davies, 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

Risk Related to Pre–Diabetes Mellitus and Diabetes Mellitus in Heart Failure With Reduced Ejection Fraction by Kristensen, S, Preiss, D, Jhund, P, Squire, I, Cardoso, J, Merkely, B, Martinez, F, Starling, R, Desai, A, Lefkowitz, M, Rizkala, A, Rouleau, J, Shi, V, Solomon, S, Swedberg, K, Zile, M, McMurray, J, Packer, M

Synthesis of SMT022357 enantiomers and in vivo evaluation in a Duchenne muscular dystrophy mouse model by Babbs, A, Berg, A, Chatzopoulou, M, Davies, K, Davies, S, Edwards, B, Elsey, D, Emer, E, Figuccia, A, Fletcher, A, Guiraud, S, Harriman, S, Moir, L, Robinson, N, Rowley, J, Russell, A, Squire, S, Thomson, J, Tinsley, J, Wilson, F, Wynne, G

Chemical proteomics and phenotypic profiling identifies the aryl hydrocarbon receptor as a molecular target of the utrophin modulator ezutromid by Wilkinson, IVL, Perkins, KJ, Dugdale, H, Moir, L, Vuorinen, A, Chatzopoulou, M, Squire, SE, Monecke, S, Lomow, A, Geese, M, Charles, PD, Burch, P, Tinsley, JM, Wynne, GM, Davies, SG, Wilson, FX, Rastinejad, F, Mohammed, S, Davies, KE, Russell, AJ