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Publications by Benjamin Seebohm
Familial Hypertrophic Cardiomyopathy: Unequal Expression of Mutant and Wildtype Myosin in Individual Myocytes as Trigger for Functional Impairment of the Heart?
Biophysical Journal
Biophysics
Familial Hypertrophic Cardiomyopathy: Functional Variance Among Individual Cardiomyocytes as a Trigger of FHC-phenotype Development
Frontiers in Physiology
Physiology
Related publications
Independent Stochastic Burst-Like Transcription of Mutant and Wildtype Alleles as Mechanism for Cell-To-Cell Functional Imbalance in Hypertrophic Cardiomyopathy
Biophysical Journal
Biophysics
Myosin Phosphorylation-Mediated Rescue of Cardiac Function in Familial Hypertrophic Cardiomyopathy
Biophysical Journal
Biophysics
Myosin Binding Protein C: Structural Abnormalities in Familial Hypertrophic Cardiomyopathy
Cell Research
Cell Biology
Molecular Biology
Fluorescence Lifetime of Actin in the Familial Hypertrophic Cardiomyopathy Transgenic Heart†
Biochemistry
Biochemistry
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
An Abnormal Ca2+ Response in Mutant Sarcomere Protein–mediated Familial Hypertrophic Cardiomyopathy
Journal of Clinical Investigation
Medicine
The Effect of Regulatory Light Chain Phosphorylation on Myosin Bearing Familial Hypertrophic Cardiomyopathy-Linked Mutations
Biophysical Journal
Biophysics
The R403Q Myosin Mutation Implicated in Familial Hypertrophic Cardiomyopathy Causes Disorder at the Actomyosin Interface
