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Annals of Neurology|January 13, 2018
Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3)Barbara Joureau, Josine Marieke de Winter, Stefan Conijn, et al.
Circulation|December 12, 2007
Diastolic stiffness of the failing diabetic heart: importance of fibrosis, advanced glycation end products, and myocyte resting tensionLoek van Heerebeek, Nazha Hamdani, M Louis Handoko, et al.
Cardiovascular Research|May 16, 2013
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathyE Rosalie Witjas-Paalberends, Nicoletta Piroddi, Kelly Stam, et al.
American Journal of Respiratory and Critical Care Medicine|August 9, 2017
Diaphragm Atrophy and Weakness in the Absence of Mitochondrial Dysfunction in the Critically IllMarloes van den Berg, Pleuni E Hooijman, Albertus Beishuizen, et al.
Cardiovascular Research|May 20, 2014
Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutationsE Rosalie Witjas-Paalberends, Ahmet Güçlü, Tjeerd Germans, et al.
American Journal of Respiratory and Critical Care Medicine|March 12, 2015
Diaphragm muscle fiber weakness and ubiquitin-proteasome activation in critically ill patientsPleuni E Hooijman, Albertus Beishuizen, Christian C Witt, et al.
Annals of Neurology|April 14, 2016
Mutation-specific effects on thin filament length in thin filament myopathyJosine M de Winter, Barbara Joureau, Eun-Jeong Lee, et al.
Circulation Research|March 20, 2013
Perturbed length-dependent activation in human hypertrophic cardiomyopathy with missense sarcomeric gene mutationsVasco Sequeira, Paul J M Wijnker, Louise L A M Nijenkamp, et al.
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