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Cell Death & Disease|November 2, 2021
"Ryanopathies" and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?Yvonne Sleiman, Alain Lacampagne, Albano C MeliInternational Journal of Molecular Sciences|September 14, 2024
Differentiation of Sinoatrial-like Cardiomyocytes as a Biological Pacemaker ModelYvonne Sleiman, Jean-Baptiste Reisqs, Mohamed BoutjdirBiorxiv : the Preprint Server for Biology|May 25, 2026
Modeling Sympathetic Neuro-Cardiac Interactions in a hiPSC-Based Microphysiological SystemJean-Baptiste Reisqs, Yvonne Sleiman, Mohamed BoutjdirBiomedicines|June 26, 2025
Role of Cav1.3 Channels in Brain-Heart Interactions: An Unexpected JourneyJean-Baptiste Reisqs, Yvonne Sleiman, Michael Cupelli, et al.Stem Cell Research|November 17, 2024
Generation of an iPSC cell line (VANYHHi001-A) from a patient with cardiac arrythmias carrying CACNA1D, SCN5A, and DSP variantsYvonne Sleiman, Jean-Baptiste Reisqs, Reina Bianca Tan, et al.International Journal of Molecular Sciences|July 15, 2026
Impact of CaV1.3 L-Type Calcium Channels on Arrhythmogenesis in CancerLianlen Joy Go Distor, Yvonne Sleiman, Jean-Baptiste Reisqs, et al.Cells|May 13, 2026
C-Terminus of Cav1.3 L-Type Ca2+ Channel Upregulates Its Own Gene ExpressionYvonne Sleiman, Ujala Srivastava, Jean-Baptiste Reisqs, et al.Journal of Personalized Medicine|February 25, 2023
Spironolactone as a Potential New Treatment to Prevent Arrhythmias in Arrhythmogenic Cardiomyopathy Cell ModelJean-Baptiste Reisqs, Adrien Moreau, Yvonne Sleiman, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|October 18, 2024
Calcium handling abnormalities increase arrhythmia susceptibility in DMSXL myotonic dystrophy type 1 miceMichael Cupelli, Vamsi Krishna Murthy Ginjupalli, Jean-Baptiste Reisqs, et al.Frontiers in Physiology|October 9, 2023
Electrophysiological basis of cardiac arrhythmia in a mouse model of myotonic dystrophy type 1Vamsi Krishna Murthy Ginjupalli, Michael Cupelli, Jean-Baptiste Reisqs, et al.Pageof 2