Mohamed Chahine
Affiliations: | Universite Laval (Canada) |
Area:
Medical Biophysics, General Biophysics, Neuroscience BiologyGoogle:
"Mohamed Chahine"Mean distance: 53433
Children
Sign in to add trainee| Isabelle Deschenes | grad student | Universite Laval (Canada) | |
| Kausalia Vijayaragavan | grad student | 2004 | Universite Laval (Canada) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Chapotte-Baldacci CA, Pierre M, Djemai M, et al. (2023) Biophysical properties of Na1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells. Scientific Reports. 13: 20685 |
| Pierre M, Djemai M, Chapotte-Baldacci CA, et al. (2023) Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels. Frontiers in Physiology. 14: 1258318 |
| Plumereau Q, Ebdalla A, Poulin H, et al. (2022) De novo Y1460C missense variant in Na1.1 impedes the pore region and results in epileptic encephalopathy. Scientific Reports. 12: 17182 |
| Gamal El-Din TM, Zimmer T, Chahine M. (2022) Editorial: Structure Related Druggability of Voltage-Gated Sodium and Calcium Ion-Channels to Treat Diseases. Frontiers in Pharmacology. 13: 947511 |
| Yang XR, Ginjupalli VKM, Theriault O, et al. (2022) -related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects. Journal of Neurophysiology. 127: 1388-1397 |
| Hui JB, Silva JCH, Pelaez MC, et al. (2022) NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis. Eneuro. 9 |
| Pierre M, Djemai M, Poulin H, et al. (2021) Na1.5 knockout in iPSCs: a novel approach to study Na1.5 variants in a human cardiomyocyte environment. Scientific Reports. 11: 17168 |
| Plumereau Q, Theriault O, Pouliot V, et al. (2021) Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State. Cjc Open. 3: 256-266 |
| Poulin H, Mercier A, Djemai M, et al. (2021) iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities. Scientific Reports. 11: 2500 |
| Poulin H, Chahine M. (2021) R1617Q epilepsy mutation slows Na 1.6 sodium channel inactivation and increases the persistent current and neuronal firing. The Journal of Physiology |