614 results on '"Wehrens, Xander H. T."'
Search Results
2. Blocking p38γ/δ, a molecular cardiac defibrillator
3. Speg interactions that regulate the stability of excitation-contraction coupling protein complexes in triads and dyads
4. Mouse models of spontaneous atrial fibrillation
5. Role of Ca2+ in healthy and pathologic cardiac function: from normal excitation–contraction coupling to mutations that cause inherited arrhythmia
6. A mechanistic LNK between inflammation and atrial fibrillation?
7. Junctophilin-2 Regulates Mitochondrial Metabolism.
8. Mechanisms underlying pathological Ca2+ handling in diseases of the heart
9. Altered myocardial lipid regulation in junctophilin-2-associated familial cardiomyopathies.
10. Long-term efficacy and safety of cardiac genome editing for catecholaminergic polymorphic ventricular tachycardia
11. Paracrine signalling by cardiac calcitonin controls atrial fibrogenesis and arrhythmia
12. Endothelial cell dysfunction: the culprit for cardiac denervation in aging?
13. The Role of Non-coding RNAs in Ischemic Myocardial Reperfusion Injury
14. Genome Editing and Cardiac Arrhythmias
15. Nuclear localization of a novel calpain-2 mediated junctophilin-2 C-terminal cleavage peptide promotes cardiomyocyte remodeling
16. Nonsense Variant PRDM16-Q187X Causes Impaired Myocardial Development and TGF-β Signaling Resulting in Noncompaction Cardiomyopathy in Humans and Mice.
17. Leaky RyR2 channels unleash a brainstem spreading depolarization mechanism of sudden cardiac death
18. Correction to: mechanisms underlying pathological Ca2+ handling in diseases of the heart
19. Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
20. Regulation of Ryanodine Receptor Ca2+ Release by Macromolecular Complexes
21. Ryanodine Receptor Dysfunction in Heart Failure and Arrhythmias
22. Evolution of the Ryanodine Receptor Gene Family
23. A microtubule-connexin-43 regulatory link suppresses arrhythmias and cardiac fibrosis in Duchenne muscular dystrophy mice
24. Ca2+ Release Channels (Ryanodine Receptors) and Arrhythmogenesis
25. Role of Ca2+ in healthy and pathologic cardiac function: from normal excitation–contraction coupling to mutations that cause inherited arrhythmia
26. Mouse models of spontaneous atrial fibrillation
27. Pitx2-microRNA pathway that delimits sinoatrial node development and inhibits predisposition to atrial fibrillation
28. An improved reporter identifies ruxolitinib as a potent and cardioprotective CaMKII inhibitor.
29. Common disease-promoting signalling pathways in heart failure and atrial fibrillation: putative underlying mechanisms and potential therapeutic consequences
30. The role of junctophilin proteins in cellular function
31. Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation
32. Genetic inhibition of PKA phosphorylation of RyR2 prevents dystrophic cardiomyopathy
33. Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification
34. Calmodulin Kinase II Is Required for Fight or Flight Sinoatrial Node Physiology
35. In-depth characterization of a mouse model of postoperative atrial fibrillation
36. Mice with the R176Q Cardiac Ryanodine Receptor Mutation Exhibit Catecholamine-Induced Ventricular Tachycardia and Cardiomyopathy
37. Inhibition of the Anti-Apoptotic Bcl-2 Family by BH3 Mimetics Sensitize the Mitochondrial Permeability Transition Pore Through Bax and Bak
38. Gut microbiota: a key regulator of ageing-associated atrial fibrillation?
39. Stabilization of Cardiac Ryanodine Receptor Prevents Intracellular Calcium Leak and Arrhythmias
40. Analysis of Calstabin2 (FKBP12.6)-Ryanodine Receptor Interactions: Rescue of Heart Failure by Calstabin2 in Mice
41. Ryanodine Receptor/Calcium Release Channel PKA Phosphorylation: A Critical Mediator of Heart Failure Progression
42. In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia
43. Role of Ca2+ in healthy and pathologic cardiac function: from normal excitation–contraction coupling to mutations that cause inherited arrhythmia.
44. Cardiac function, structural, and electrical remodeling by microgravity exposure.
45. Phosphorylation-Dependent Interactome of Ryanodine Receptor Type 2 in the Heart
46. Irisin: A Promising Target for Ischemia-Reperfusion Injury Therapy
47. Genetic inhibition of nuclear factor of activated T-cell c2 prevents atrial fibrillation in CREM transgenic mice
48. Genetic inhibition of nuclear factor of activated T-cell c2 prevents atrial fibrillation in CREM transgenic mice.
49. Prolonged β-adrenergic stimulation disperses ryanodine receptor clusters in cardiomyocytes and has implications for heart failure.
50. Efficacy of RyR2 inhibitor EL20 in induced pluripotent stem cell‐derived cardiomyocytes from a patient with catecholaminergic polymorphic ventricular tachycardia
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