Mutations in tropomyosin that cause DCM, affect cooperativity of cardiac muscle thin filaments by Marston, S, Mirza, M, Robinson, P, Kremneva, E, Levitsky, D, Redwood, C, EL-Mezgueldi, M

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

Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation by Messer, A, Bayliss, C, El-Mezgueldi, M, Redwood, C, Ward, D, Leung, M, Papadaki, M, Dos Remedios, C, Marston, S

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