134 results on '"Lacampagne, Alain"'
Search Results
2. Personalized medicine in the dish to prevent calcium leak associated with short-coupled polymorphic ventricular tachycardia in patient-derived cardiomyocytes
3. Three-vessel coronary infusion of cardiosphere-derived cells for the treatment of heart failure with preserved ejection fraction in a pre-clinical pig model
4. Early Myocardial Dysfunction and Benefits of Cardiac Treatment in Young X-Linked Duchenne Muscular Dystrophy Mice
5. Enhanced Mitochondrial Calcium Uptake Suppresses Atrial Fibrillation Associated With Metabolic Syndrome
6. LIX1-mediated changes in mitochondrial metabolism control the fate of digestive mesenchyme-derived cells
7. Use of speckle tracking echocardiography to detect late anthracycline-induced cardiotoxicity in childhood cancer: A prospective controlled cross-sectional study
8. Correction: “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?
9. Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy
10. Stabilizing Ryanodine Receptors Improves Left Ventricular Function in Juvenile Dogs With Duchenne Muscular Dystrophy
11. State-of-the-Art Differentiation Protocols for Patient-Derived Cardiac Pacemaker Cells
12. Colchicine to prevent sympathetic denervation after acute myocardial infarction: the COLD-MI trial
13. Heart graft preservation technics and limits: an update and perspectives
14. Aberrant mitochondrial dynamics contributes to diaphragmatic weakness induced by mechanical ventilation
15. Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods
16. “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?
17. Generation of patient-specific induced pluripotent stem cell lines with Type 2 Long QT Syndrome and the KCNH2 c.379C > T pathogenic variant
18. IP3 receptor orchestrates maladaptive vascular responses in heart failure
19. Le récepteur de la ryanodine, un acteur central dans les désordres multi-systémiques associés à l'insuffisance cardiaque.
20. Diastolic Cardiomyopathy Secondary to Experimentally Induced Exacerbated Emphysema
21. Impact of ciguatoxins on human cardiac and neuronal physiology
22. Ryanodine receptor dysfunction causes senescence and fibrosis in Duchenne dilated cardiomyopathy
23. Role of neuronal ryanodine receptor type 2 in cardiogenic dementia
24. Modeling and drug screening of inherited short-coupled polymorphic ventricular tachycardia using patient derived tissue
25. Neuro-cardiac organ-on-a-chip using patient specific induced pluripotent stem cells and microfluidic devices
26. Functional remodeling of the mitochondrial Ca2+ uniporter complex in metabolic cardiomyopathy
27. Modelling neuro-cardiac disorders using patient-specific iPSC and CRISPR/Cas9 technologies
28. Impact of Neurons on Patient-Derived Cardiomyocytes Using Organ-On-A-Chip and iPSC Biotechnologies
29. Impact of neurons on patient derived-cardiomyocytes using organ-on-a-chip and iPSC biotechnologies
30. Heart failure-induced cognitive dysfunction is mediated by intracellular Ca2+leak through ryanodine receptor type 2
31. Neuro-cardiac organ-a-chip using patient specific induced pluripotent stem cells and microfluidic devices
32. Role of oxidation of excitation-contraction coupling machinery in age-dependent loss of muscle function in Caenorhabditis elegans
33. Combined in silico model of cardiac electrophysiological activity and modulation by the autonomic nervous system
34. Electrophysiological characterization of hiPSC-derived cardiac pacemaker cells from CPVT bradycardia-associated patients
35. Three-dimensional genome architecture in cardiac muscle cells: Pathophysiological implications in dilated cardiomyopathy caused by mutations in A/C lamins- and dystrophin-encoding gene
36. Heart and mind at risk: Decoding channel disruptions in the food poisoning enigma
37. Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy.
38. Author response: Role of oxidation of excitation-contraction coupling machinery in age-dependent loss of muscle function in Caenorhabditis elegans
39. Generation of catecholaminergic polymorphic ventricular tachycardia patient-specific induced pluripotent stem cell line
40. Colchicine: protection of the brain beyond the heart?
41. LIX1 controls digestive mesenchyme-derived cell fate decision by regulating cristae organization in mitochondria
42. Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy
43. Role of oxidation of excitation-contraction coupling machinery in age-dependent loss of muscle function in C. elegans
44. Skeletal Ryanodine Receptors Are Involved in Impaired Myogenic Differentiation in Duchenne Muscular Dystrophy Patients
45. Dedicated Wearable Sensitive Strain Sensor, Based on Carbon Nanotubes, for Monitoring the Rat Respiration Rate
46. Design, Fabrication, and In-Vivo Characterization of Strain Sensors Based on 1D Nanomaterials for Health Monitoring Wearable Devices
47. Shear Wave Elastography, a New Tool for Diaphragmatic Qualitative Assessment: A Translational Study
48. Modeling neuro-cardiac disorders using patient-specific iPSC and CRISPR/Cas9 technologies
49. Kaempferol activates the mitochondrial calcium uniporter complex in a CA2+-dependent manner: Implication of MICU1 subunits
50. Assessment of left ventricular dyssynchrony by speckle tracking echocardiography in children with duchenne muscular dystrophy.
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