20 results on '"Recalde, Alice"'
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2. Inhibition of EPAC1 signaling pathway alters atrial electrophysiology and prevents atrial fibrillation
3. Regional Differences in Ca2+ Signaling and Transverse-Tubules across Left Atrium from Adult Sheep
4. Critical Link between Calcium Regional Heterogeneity and Atrial Fibrillation Susceptibility in Sheep Left Atria
5. Regional Differences in Ca 2+ Signaling and Transverse-Tubules across Left Atrium from Adult Sheep.
6. BH4 Increases nNOS Activity and Preserves Left Ventricular Function in Diabetes
7. Inducibility, but not stability, of atrial fibrillation is increased by NOX2 overexpression in mice
8. PO-01-171 ROLE OF THE EXCHANGE PROTEIN ACTIVATED BY CAMP (EPAC) IN ATRIAL ELECTROPHYSIOLOGY AND ATRIAL FIBRILLATION MECHANISMS
9. Pharmacological activation of exchange protein directly activated by cAMP 1 (EPAC1) increases action potential duration in mouse atrial myocytes
10. Mutual Regulation of Epicardial Adipose Tissue and Myocardial Redox State by PPAR-gamma/Adiponectin Signalling
11. Mutual Regulation of Epicardial Adipose Tissue and Myocardial Redox State by PPAR-gamma/Adiponectin Signalling
12. 154 Myocardial nox2 activity regulates atrial fibrillation susceptibility
13. Up-regulation of miR-31 in human atrial fibrillation begets the arrhythmia by depleting dystrophin and neuronal nitric oxide synthase
14. Tetrahydrobiopterin Protects Against Hypertrophic Heart Disease Independent of Myocardial Nitric Oxide Synthase Coupling
15. Mutual Regulation of Epicardial Adipose Tissue and Myocardial Redox State by PPAR-γ/Adiponectin Signalling
16. Loss of Myocardial nNOS Mediated by Upregulation of miR-31 in Human Atria Contributes to Begetting of Atrial Fibrillation
17. Tetrahydrobiopterin Protects Against Hypertrophic Heart Disease Independent of Myocardial Nitric Oxide Synthase Coupling.
18. Inhibition of Prolyl Hydroxylase Domain Proteins Promotes Therapeutic Revascularization
19. Abstract 5448: Regulatory T Cells Control Post-Ischemic Neovascularization
20. P119. Direct measurements of NOS3, BH4 level and NO bioavailability in vascular tissue
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