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Publications by Risto-Pekka Pölönen
Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Orα-Tropomyosin Mutation for Hypertrophic Cardiomyopathy
Stem Cells International
Cell Biology
Molecular Biology
Simultaneous Recordings of Action Potentials and Calcium Transients From Human Induced Pluripotent Stem Cell Derived Cardiomyocytes
Biology Open
Biochemistry
Agricultural
Genetics
Molecular Biology
Biological Sciences
Related publications
Myosin Binding Protein C: Structural Abnormalities in Familial Hypertrophic Cardiomyopathy
Cell Research
Cell Biology
Molecular Biology
Beta-Myosin Heavy Chain (Β-Mhc) and Myosin Binding Protein C (MyBP-C) Genes Mutation in Bangladeshi Hypertrophic Cardiomyopathy Patients: A Genotype-Phenotype Correlation
Canadian Journal of Biotechnology
Impact of Human Beta-Cardiac Myosin Mutation Implicated in Both Hypertrophic and Dilated Cardiomyopathy
Biophysical Journal
Biophysics
A Dilated Cardiomyopathy Troponin C Mutation Lowers Contractile Force by Reducing Strong Myosin-Actin Binding
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Novel Α-Tropomyosin Mutation (D55N) Associated With Familial Dilated Cardiomyopathy Increases Tropomyosin Binding to Actin
Biophysical Journal
Biophysics
Variable Cardiac Myosin Binding Protein-C Expression in the Myofilaments Due to MYBPC3 Mutations in Hypertrophic Cardiomyopathy
Journal of Molecular and Cellular Cardiology
Cardiovascular Medicine
Molecular Biology
Cardiology
Impact of Hypertrophic Cardiomyopathy Mutations and the Role of Myosin Binding Protein-C on the Sequestered State of Myosin
Biophysical Journal
Biophysics
The R403Q Myosin Mutation Implicated in Familial Hypertrophic Cardiomyopathy Causes Disorder at the Actomyosin Interface
Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.
Journal of Medical Genetics
Genetics
