28 results on '"Carrier, Lucie"'
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2. Targeting the population for gene therapy with MYBPC3
3. Mechanistic role of the CREB-regulated transcription coactivator 1 in cardiac hypertrophy
4. Comparison of the effects of a truncating and a missense MYBPC3 mutation on contractile parameters of engineered heart tissue
5. The E3 ubiquitin ligase Asb2β is downregulated in a mouse model of hypertrophic cardiomyopathy and targets desmin for proteasomal degradation
6. Modelling LMNA-cardiomyopathy with patient-specific human iPSC-derived engineered heart tissue and a partial rescue by gene replacement therapy
7. A human CRYABR120G Desmin-related cardiomyopathy cellular model
8. Modelling aberrant microtubule De-/Tyrosination in HiPSC-derived engineered heart tissues
9. Functional characterisation of a patient-derived laminopathy model in human engineered heart tissues recapitulates fibrosis and mechanical decoupling defect
10. Investigating the molecular disease mechanisms of the human p.G592R PRKD1 mutation in human induced pluripotent stem cell-derived cardiomyocytes
11. Ubiquitin-proteasome system and hereditary cardiomyopathies
12. Contractile abnormalities and altered drug response in engineered heart tissue from Mybpc3-targeted knock-in mice
13. Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice
14. Enhanced myofilament responsiveness upon β-adrenergic stimulation in post-infarct remodeled myocardium
15. Cardiac myosin-binding protein C in hypertrophic cardiomyopathy: Mechanisms and therapeutic opportunities
16. Investigation of ventricular arrhythmia mechanisms in hypertrophic cardiomyopathy in mice and men
17. Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties
18. Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy
19. Decreased phosphorylation levels of cardiac myosin-binding protein-C in human and experimental heart failure
20. Postnatal Isl1+ progeny can be purified and cultivated from Isl1-Cre/R26-YFP mice
21. Targeted inactivation of the murine cardiac myosin-binding protein C gene leads to hypertrophic cardiomyopathy
22. Human cardiac myosin-binding protein C frameshift mutations result in marked decrease of protein expression
23. Genomic Organisation, Alternative Splicing and Polymorphisms of the Human Cardiac Troponin T Gene
24. The Influence of the Angiotensin I Converting Enzyme Genotype in Familial Hypertrophic Cardiomyopathy Varies with the Disease Gene Mutation
25. Linkage analysis of adrenoceptor genes to familial hypertrophic cardiomyopathy
26. Familial hypertrophic cardiomyopathy: Analysis of several medium-size families with highly informative markers
27. Exclusion of desmin gene involvement in hypertrophic cardiomyopathy in several French families
28. Postnatal Isl1 + progeny can be purified and cultivated from Isl1-Cre/R26-YFP mice
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