Erratum: How do MYBPC3 mutations cause hypertrophic cardiomyopathy? (Journal of Muscle Research and Cell Motility DOI 10.1007/s10974-011-9268-3) by Marston, S, Copeland, O, Gehmlich, K, Schlossarek, S, Carrier, L

How do MYBPC3 mutations cause hypertrophic cardiomyopathy? by Marston, S, Copeland, O, Gehmlich, K, Schlossarek, S, Carrier, L, Carrrier, L

Evidence for haploinsufficiency as the mechanism of action of MyBP-C mutations that cause HCM by Carballo, S, Copeland, O, Jacques, A, Livesey, K, Redwood, C, Watkins, H, Marston, S

Direct evidence in man for haploinsufficiency as the mechanism of action of myosin-binding protein C mutations that cause hypertrophic cardiomyopathy by Carballo, S, Copeland, O, Livesey, K, Jacques, A, McKenna, W, Redwood, C, Marston, S, Watkins, H

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency. by Marston, S, Copeland, O, Jacques, A, Livesey, K, Tsang, V, McKenna, W, Jalilzadeh, S, Carballo, S, Redwood, C, Watkins, H

Two DCM mutations in cardiac tropomyosin alter thin filament function by different mechanisms by Marston, S, Mirza, M, Copeland, O, Robinson, P, Redwood, C, Levitsky, D, Kremneva, E, Nikolaieva, O, EL-Mezgueldi, M

The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments. by Mirza, M, Robinson, P, Kremneva, E, Copeland, O, Nikolaeva, O, Watkins, H, Levitsky, D, Redwood, C, El-Mezgueldi, M, Marston, S

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T. by Bayliss, C, Jacques, A, Leung, M, Ward, D, Redwood, C, Gallon, C, Copeland, O, McKenna, W, Dos Remedios, C, Marston, S, Messer, A

A post-MI power struggle: adaptations in cardiac power occur at the sarcomere level alongside MyBP-C and RLC phosphorylation by Toepfer, Christopher N., Sikkel, Markus B., Caorsi, Valentina, Vydyanath, Anupama, Torre, Iratxe, Copeland, O'Neal, Lyon, Alexander R., Marston, Steven B., Luther, Pradeep K., Macleod, Kenneth T., West, Timothy G., Ferenczi, Michael Alan

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Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse. by Song, W, Dyer, E, Stuckey, D, Copeland, O, Leung, M, Bayliss, C, Messer, A, Wilkinson, R, Tremoleda, J, Schneider, MD, Harding, SE, Redwood, C, Clarke, K, Nowak, K, Monserrat, L, Wells, D, Marston, S