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Science

Muscle TissueEngineeringMicroscopyGreen Fluorescent ProteinBiomedical Engineering +17

Spectrum of Mutations in Long-QT Syndrome Genes

Igor Splawski, Jiaxiang Shen, Katherine W. Timothy, +8

Circulation

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Ludwig Thierfelder, Hugh Watkins, Calum A. MacRae, +5

Cell

Cardiac MuscleCardiomyopathyFamilial Hypertrophic CardiomyopathyPathologyMedicine +3

Cardiac troponin T is essential in sarcomere assembly and cardiac contractility

Amy J. Sehnert, Anja Huq, Brant M. Weinstein, +3

Nature Genetics

MechanobiologyCardiac MuscleCardiomyopathyPhysiologyCardiac Troponin T +6

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

Igor Splawski, Katherine W. Timothy, Niels Decher, +5

Proceedings of the National Academy of Sciences

Mutations affecting the formation and function of the cardiovascular system in the zebrafish embryo

Didier Y. R. Stainier, Bernadette Fouquet, Jau‐Nian Chen, +12

Development

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

Brenda Gerull, Michael Gramlich, J. Atherton, +9

Nature Genetics

Cardiac MuscleCardiomyopathyHeart FailureDevelopmental BiologyGenetics +4

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Karl Poetter, He Jiang, Shahin Hassanzadeh, +7

Nature Genetics

Mitochondrial MyopathyCardiac MuscleCardiomyopathyMolecular PhysiologyRegulatory Light Chains +9

Mutations affecting the cardiovascular system and other internal organs in zebrafish

Jau‐Nian Chen, Pascal Haffter, Jörg Odenthal, +12

Development

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

Sabine Klaassen, Susanne Probst, Erwin Oechslin, +13

Circulation