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Cardiac Troponin Mutations and Restrictive Cardiomyopathy
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
Functional Effects of a Restrictive-Cardiomyopathy-Linked Cardiac Troponin I Mutation          (R145W) in Transgenic Mice
Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T          Mutation
Molecular and Functional Characterization of Novel Hypertrophic Cardiomyopathy          Susceptibility Mutations in TNNC1-encoded Troponin C
Myosin Cross-Bridges Do Not Form Precise Rigor Bonds in Hypertrophic Heart Muscle          Carrying Troponin T Mutations
Myofilament Ca2+ Sensitization Causes Susceptibility to Cardiac Arrhythmia in          Mice
Myofilament Calcium De-Sensitization and Contractile Uncoupling Prevent Pause-Triggered          Ventricular Tachycardia in Mouse Hearts with Chronic Myocardial Infarction
Collagen XIV Is Important for Growth and Structural Integrity of the Myocardium
Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients with          Dilated Cardiomyopathy