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Publications by M. J. Tyska
Single-Molecule Mechanics of R403Q Cardiac Myosin Isolated From the Mouse Model of Familial Hypertrophic Cardiomyopathy
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
Related publications
The R403Q Myosin Mutation Implicated in Familial Hypertrophic Cardiomyopathy Causes Disorder at the Actomyosin Interface
Myosin Phosphorylation-Mediated Rescue of Cardiac Function in Familial Hypertrophic Cardiomyopathy
Biophysical Journal
Biophysics
Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.
Journal of Medical Genetics
Genetics
Diastolic Dysfunction and Altered Energetics in the alphaMHC403/+ Mouse Model of Familial Hypertrophic Cardiomyopathy.
Journal of Clinical Investigation
Medicine
Myosin Binding Protein C: Structural Abnormalities in Familial Hypertrophic Cardiomyopathy
Cell Research
Cell Biology
Molecular Biology
Hypertrophic Cardiomyopathy R403Q Mutation in Rabbit Β-Myosin Reduces Contractile Function at the Molecular and Myofibrillar Levels
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Impact of Hypertrophic Cardiomyopathy Mutations on the Cardiac Myosin Super-Relaxed State
Biophysical Journal
Biophysics
The Effect of Regulatory Light Chain Phosphorylation on Myosin Bearing Familial Hypertrophic Cardiomyopathy-Linked Mutations
Biophysical Journal
Biophysics
Functional Analysis of the Mutations in the Human Cardiac Beta-Myosin That Are Responsible for Familial Hypertrophic Cardiomyopathy. Implication for the Clinical Outcome.
Journal of Clinical Investigation
Medicine