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Analysis of the Molecular Pathogenesis of Cardiomyopathy-Causing cTnT Mutants I79N,          ΔE96, and ΔK210
Myofilament Calcium De-Sensitization and Contractile Uncoupling Prevent Pause-Triggered          Ventricular Tachycardia in Mouse Hearts with Chronic Myocardial Infarction
Absence of Myocardial Thyroid Hormone Inactivating Deiodinase Results in Restrictive          Cardiomyopathy in Mice
Kallikrein 6 is a Novel Molecular Trigger of Reactive Astrogliosis
Collagen XIV Is Important for Growth and Structural Integrity of the Myocardium
Pharmacokinetic Properties of 2(nd)-Generation Fibroblast Growth Factor-1 Mutants for          Therapeutic Application
Experimental Support for the Evolution of Symmetric Protein Architecture from a Simple          Peptide Motif
Expression and Function of the Kallikrein-Related Peptidase 6 in the Human Melanoma          Microenvironment
Myosin Cross-Bridges Do Not Form Precise Rigor Bonds in Hypertrophic Heart Muscle          Carrying Troponin T Mutations
Cardiac Troponin Mutations and Restrictive Cardiomyopathy
Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T          Mutation
X-ray Structure and Biophysical Properties of Rabbit Fibroblast Growth Factor 1
Engineering an Improved Crystal Contact Across a Solvent-Mediated Interface of Human          Fibroblast Growth Factor 1
Functional Effects of a Restrictive-Cardiomyopathy-Linked Cardiac Troponin I Mutation          (R145W) in Transgenic Mice
Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients with          Dilated Cardiomyopathy
S(1)' and S(2)' Subsite Specificities of Human Plasma Kallikrein and Tissue Kallikrein          1 for the Hydrolysis of Peptides Derived from the Bradykinin Domain of Human          Kininogen
Protease-Activated Receptor Dependent and Independent Signaling by Kallikreins 1 and 6          in CNS Neuron and Astroglial Cell Lines
Substrate Specificity of Human Kallikreins 1 and 6 Determined by Phage Display
Kallikreins are Associated with Secondary Progressive Multiple Sclerosis and Promote          Neurodegeneration
Molecular and Functional Characterization of Novel Hypertrophic Cardiomyopathy          Susceptibility Mutations in TNNC1-encoded Troponin C
Myofilament Ca2+ Sensitization Causes Susceptibility to Cardiac Arrhythmia in          Mice
Mutagenesis of the Crystal Contact of Acidic Fibroblast Growth Factor