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Circulation Research|July 4, 2009
Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiencySteven Marston, O'Neal Copeland, Adam Jacques, et al.
Circulation Research|February 28, 2002
Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathyEdward Blair, Charles Redwood, Marisa de Jesus Oliveira, et al.
Nature Communications|July 21, 2026
Comprehensive biophysical and structural profiling of alpha-actinin-2 variants reveals mechanistic diversity in hypertrophic cardiomyopathyMaya Noureddine, Halina Mikolajek, Nathan Cowieson, et al.
Journal of Molecular Biology|April 1, 2008
Crystal structure of the C1 domain of cardiac myosin binding protein-C: implications for hypertrophic cardiomyopathyLata Govada, Liz Carpenter, Paula C A da Fonseca, et al.
Journal of Molecular and Cellular Cardiology Plus|May 9, 2023
Low expression of the K280N TNNT2 mutation is sufficient to increase basal myofilament activation in human hypertrophy cardiomyopathyVasco Sequeira, Lili Wang, Paul J M Wijnker, et al.
Journal of Molecular and Cellular Cardiology|July 6, 2010
Investigation of a transgenic mouse model of familial dilated cardiomyopathyWeihua Song, Emma Dyer, Daniel Stuckey, et al.
Molecular Therapy. Nucleic Acids|June 19, 2017
Evaluation of MYBPC3 trans-Splicing and Gene Replacement as Therapeutic Options in Human iPSC-Derived CardiomyocytesMaksymilian Prondzynski, Elisabeth Krämer, Sandra D Laufer, et al.
Circulation. Heart Failure|October 13, 2017
Activation of Autophagy Ameliorates Cardiomyopathy in Mybpc3-Targeted Knockin MiceSonia R Singh, Antonia T L Zech, Birgit Geertz, et al.
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