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Plos One|August 27, 2009
Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overloadAnna N Panek, Maximilian G Posch, Natalia Alenina, et al.
American Journal of Hypertension|January 3, 2007
The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathyRalph Telgmann, Bassam A Harb, Cemil Ozcelik, et al.
Disease Models & Mechanisms|October 9, 2020
Identification of <i>MYOM2</i> as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the <i>Drosophila</i> heartEmilie Auxerre-Plantié, Tanja Nielsen, Marcel Grunert, et al.
Journal of Medical Genetics|January 18, 2011
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practiceSiv Fokstuen, Analia Munoz, Paola Melacini, et al.
European Journal of Human Genetics : EJHG|March 7, 2013
Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathyRoberta Roncarati, Chiara Viviani Anselmi, Peter Krawitz, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 20, 2004
Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cellsSebastian E Kirschner, Edgar Becker, Massimo Antognozzi, et al.
Archives of Medical Science : AMS|May 18, 2016
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathiesAndreas Perrot, Pavol Tomasov, Eric Villard, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 28, 2005
Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathyAndreas Perrot, Hajo Schmidt-Traub, Bernard Hoffmann, et al.
European Heart Journal|September 9, 2010
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial DiseasesPhilippe Charron, Michael Arad, Eloisa Arbustini, et al.
Plos One|December 24, 2011
Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defectsMaximilian G Posch, Stephan Waldmuller, Melanie Müller, et al.
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