31 results on '"Blair, Cheavar A"'
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2. Dual-protein patterning to investigate effects of cell-cell adhesions on hiPSC-CM maturity
3. The polyamine spermidine enhances contractile function and sarcomere dynamics post-doxorubicin treatment
4. Sarcomere length affects Ca2+ sensitivity of contraction in ischemic but not non-ischemic myocardium
5. The Length-Dependent Increase in Ca 2+-Sensitivity of Contraction is Eliminated in Myocardium from Patients with Non-Ischemic Heart Failure
6. Insights into single hiPSC-derived cardiomyocyte phenotypes and maturation using ConTraX, an efficient pipeline for tracking contractile dynamics
7. Titin-truncating mutations associated with dilated cardiomyopathy alter length-dependent activation and its modulation via phosphorylation
8. Heart Failure in Humans Reduces Contractile Force in Myocardium From Both Ventricles
9. Mechanobiology Assays with Applications in Cardiomyocyte Biology and Cardiotoxicity
10. Engineering the Microenvironment for Heart Muscle Cell Mechanobiology
11. Engineering hiPSC cardiomyocyte in vitro model systems for functional and structural assessment
12. Diabetes with Heart Failure Increases Methylglyoxal Modifications in the Sarcomere Which Inhibit Function
13. Diabetes with heart failure increases methylglyoxal modifications in the sarcomere, which inhibit function
14. Author Correction: Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
15. Sex Specific Differences in Cardiac Fibrosis
16. Methylglyoxal Modifications are Elevated in the Myofilament of Diabetic Cardiomyopathy Patients and Reduce Myofilament Function
17. Length-Dependent Activation is Reduced in Myocardium from Patients with Non-ischemic Heart Failure
18. Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
19. No Difference in Myosin Kinetics and Spatial Distribution of the Lever Arm in the Left and Right Ventricles of Human Hearts
20. Abstract 227: Skinned Myocardial Strips From Non-failing and Failing Human Hearts Produce More Force at Physiological Temperature
21. Omecamtiv Mecarbil Enhances the Duty Ratio of Human β-Cardiac Myosin Resulting in Increased Calcium Sensitivity and Slowed Force Development in Cardiac Muscle
22. Maximal Force Increases at Physiological Temperature in Myocardial Strips from Non-Failing and Failing Human Hearts
23. Engineered Troponins Modulate the Ca 2+ Sensitivity of the Failing Human Myocardium
24. Impact of Para-Nitroblebbistatin on Human Beta-Cardiac Myosin at the Molecular and Tissue Levels
25. Modulating Beta-Cardiac Myosin Function at the Molecular and Tissue Levels
26. A Protocol for Collecting Human Cardiac Tissue for Research
27. Myocardium From the Left and Right Ventricles of Human Hearts Have Similar Mechanical Properties
28. Omecamtiv Mecarbil Enhances Actin Affinity and Slows Force Production in Human β-Cardiac Myosin
29. Myocardium from the Left and Right Ventricles of Human Hearts have Similar Mechanical Properties
30. Faculty Opinions recommendation of Identification of micro-RNA networks in end-stage heart failure because of dilated cardiomyopathy.
31. Faculty Opinions recommendation of Regulation of connective tissue growth factor gene expression and fibrosis in human heart failure.
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