Modulation of thin filament activation by breakdown or isoform switching of thin filament proteins: physiological and pathological implications. by Marston, S, Redwood, C

New mechanisms and concepts for cardiac-resynchronization therapy. by Neubauer, S, Redwood, C

Alpha-tropomyosin mutations in inherited cardiomyopathies. by Redwood, C, Robinson, P

The E117K mutation in β-tropomyosin disturbs concerted conformational changes of actomyosin in muscle fibers. by Karpicheva, O, Redwood, C, Borovikov, Y

Hypertrophic and dilated cardiomyopathycausing mutations of troponin and alpha-tropomyosin have opposite effects on thin filament calcium binding by Robinson, P, Watkins, H, Redwood, C

A revised method of troponin exchange in permeabilised cardiac trabeculae using vanadate: functional consequences of a HCM-causing mutation in troponin I. by Preston, L, Watkins, H, Redwood, C

Functional investigation of beta-tropomyosin mutations that cause congenital skeletal myopathies by Piers, A, Robinson, P, Redwood, C

[Effect of mutation Arg9lGly on the thermal stability of beta-tropomyosin] by Nevzorov, I, Redwood, C, Levitskiĭ, D

Effect of mutation Arg91Gly on the thermal stability of β-tropomyosin by Nevzorov, I, Redwood, C, Levitsky, D

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy. by Elliott, K, Watkins, H, Redwood, C

DCM troponin C mutant Gly159Asp blunts the response to troponin phosphorylation. by Preston, L, Ashley, C, Redwood, C

Localization of the binding site of the C-terminal domain of cardiac myosin-binding protein-C on the myosin rod. by Flashman, E, Watkins, H, Redwood, C

Altered inhibitory and troponin C-binding activities in cardiac troponin I mutants known to cause hypertrophic cardiomyopathy by Elliott, K, Watkins, H, Redwood, C

Using fluorescence emission spectroscopy to asses the Ca2+ affinity of reconstituted troponin and thin filaments containing cardiomyopathy causing mutations of troponin and alpha-t... by Robinson, P, Watkins, H, Redwood, C

Localization of a novel N-terminal cardiac MyBP-C binding site on myosin rod by King, K, Watkins, H, Redwood, C

Inherited cardiomyopathies. by Watkins, H, Ashrafian, H, Redwood, C

Stability of two beta-tropomyosin isoforms: effects of mutation Arg91Gly. by Nevzorov, I, Redwood, C, Levitsky, D

Inherited cardiomyopathies. by Watkins, H, Ashrafian, H, Redwood, C

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy. by Blair, E, Redwood, C, Watkins, H

Mutations in fast skeletal troponin I, troponin T and beta-tropomyosin that cause distal arthrogryposis all enhance thin filament activation by Robinson, P, Altin, E, Redwood, C