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Circulation. Heart Failure|October 8, 2009
Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscleEmma C Dyer, Adam M Jacques, Anita C Hoskins, et al.Cardiovascular Research|October 26, 2012
Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin TChristopher R Bayliss, Adam M Jacques, Man-Ching Leung, et al.Cardiovascular Research|April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathyAdam M Jacques, Natalia Briceno, Andrew E Messer, et al.Scientific Reports|November 3, 2017
Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genesPetr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.Scientific Reports|September 26, 2018
Author Correction: Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genesPetr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.Journal of Muscle Research and Cell Motility|January 14, 2009
Myofilament dysfunction in cardiac disease from mice to menNazha Hamdani, Monique de Waard, Andrew E Messer, et al.Pageof 3