29 results on '"Carrier, Lucie"'
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2. RNA Editing Holds Promise for Hypertrophic Cardiomyopathy Therapy.
3. Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy.
4. Depletion of Vasohibin 1 Speeds Contraction and Relaxation in Failing Human Cardiomyocytes.
5. Activation of Autophagy Ameliorates Cardiomyopathy in Mybpc3-Targeted Knockin Mice.
6. Making Sense of Inhibiting Nonsense in Hypertrophic Cardiomyopathy.
7. Perturbed Length-Dependent Activation in Human Hypertrophic Cardiomyopathy With Missense Sarcomeric Gene Mutations.
8. GSK3β Phosphorylates Newly Identified Site in the Proline-Alanine-Rich Region of Cardiac Myosin-Binding Protein C and Alters Cross-Bridge Cycling Kinetics in Human.
9. Aldosterone Inhibits Antifibrotic Factors in Mouse Hypertensive Heart.
10. Localization of Islet-1-Positive Cells in the Healthy and Infarcted Adult Murine Heart.
11. Contractile Dysfunction Irrespective of the Mutant Protein in Human Hypertrophic Cardiomyopathy With Normal Systolic Function.
12. The ubiquitin-proteasome system in cardiomyopathies.
13. Effects of Chronic Atrial Fibrillation on Active and Passive Force Generation in Human Atrial Myofibrils.
14. Nonsense-Mediated mRNA Decay and Ubiquitin—Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice.
15. Prevention of Myofilament Dysfunction by β-Blocker Therapy in Postinfarct Remodeling.
16. Cardiac Myosin-Binding Protein C Is Required for Complete Relaxation in Intact Myocytes.
17. Exclusion of Cardiac Myosin Heavy Chain and Actin Gene Involvement in Hypertrophic Cardiomyopathy of Several French Families.
18. Expression of the Sarcomeric Actin Isogenes in the Rat Heart With Development and Senescence.
19. Familial Hypertrophic Cardiomyopathy.
20. Cardiac Myosin Binding Protein C Gene Is Specifically Expressed in Heart During Murine and Human Development.
21. Organization and Sequence of Human Cardiac Myosin Binding Protein C Gene (MYBPC3) and Identification of Mutations Predicted to Produce Truncated Proteins in Familial Hypertrophic Cardiomyopathy.
22. Abstract 15559: Genetic Characterization of a Large Pediatric Cardiomyopathy Cohort Reveals Novel Variants in Half of Patients.
23. Abstract 15434: Characterization of Novel Modifiers of Cardiac Hypertrophy Derived From an Integrated Analysis of Whole Genome Dna-Methylation and Transcription.
24. Chronic Activation of Tubulin Tyrosination Improves Heart Function.
25. EGFR/IGF1R Signaling Modulates Relaxation in Hypertrophic Cardiomyopathy.
26. Prevention of myofilament dysfunction by beta-blocker therapy in postinfarct remodeling.
27. Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction.
28. Molecular determinants of altered Ca2+ handling in human chronic atrial fibrillation.
29. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
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