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Analysis of the Molecular Pathogenesis of Cardiomyopathy-Causing cTnT Mutants I79N,          ΔE96, and ΔK210
Absence of Myocardial Thyroid Hormone Inactivating Deiodinase Results in Restrictive          Cardiomyopathy in Mice
Myosin Cross-Bridges Do Not Form Precise Rigor Bonds in Hypertrophic Heart Muscle          Carrying Troponin T Mutations
Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T          Mutation
Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients with          Dilated Cardiomyopathy
Functional Effects of a Restrictive-Cardiomyopathy-Linked Cardiac Troponin I Mutation          (R145W) in Transgenic Mice
Molecular and Functional Characterization of Novel Hypertrophic Cardiomyopathy          Susceptibility Mutations in TNNC1-encoded Troponin C