18 results on '"Carrier, Lucie"'
Search Results
2. Nitro-fatty acids suppress ischemic ventricular arrhythmias by preserving calcium homeostasis
3. Phosphomimetic cardiac myosin-binding protein C partially rescues a cardiomyopathy phenotype in murine engineered heart tissue
4. Cardiomyopathy phenotypes in human-induced pluripotent stem cell-derived cardiomyocytes—a systematic review
5. Gene therapy strategies in the treatment of hypertrophic cardiomyopathy
6. The embryological basis of subclinical hypertrophic cardiomyopathy
7. Knock-out of nexilin in mice leads to dilated cardiomyopathy and endomyocardial fibroelastosis
8. Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice
9. FHL2 expression and variants in hypertrophic cardiomyopathy
10. Sexual dimorphic response to exercise in hypertrophic cardiomyopathy-associated MYBPC3-targeted knock-in mice
11. MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correction
12. Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue
13. The miRNA-212/132 family regulates both cardiac hypertrophy and cardiomyocyte autophagy
14. Defective proteolytic systems in Mybpc3-targeted mice with cardiac hypertrophy
15. Erratum to: How do MYBPC3 mutations cause hypertrophic cardiomyopathy?
16. Adrenergic stress reveals septal hypertrophy and proteasome impairment in heterozygous Mybpc3-targeted knock-in mice
17. Identification of two novel mutations in the ventricular regulatory myosin light chain gene ( MYL2 ) associated with familial and classical forms of hypertrophic cardiomyopathy
18. Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.