Publications

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Filtres: Author is Mohamed Chahine  [Enlever les filtres]
2023
S. Zaveri, Qu, Y. Sarah, Chahine, M., et Boutjdir, M., « Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death. », Front Cardiovasc Med, vol. 10, p. 1253479, 2023.
C. - A. Chapotte-Baldacci, Jauvin, D., et Chahine, M., « Generation of control iPSC lines CBRCULi008-A and CBRCULi009-A derived from lymphoblastoid cell lines. », Stem Cell Res, vol. 71, p. 103168, 2023.
D. Jauvin, Pierre, M., Boutjdir, M., Puymirat, J., et Chahine, M., « Generation of four myotonic dystrophy type 1 patient iPSC lines (CBRCULi002-A, CBRCULi003-A, CBRCULi004-A, CBRCULi005-A) and a control (CBRCULi001-A) derived from lymphoblastoids cell lines. », Stem Cell Res, vol. 67, p. 103037, 2023.
M. Chahine, Jauvin, D., Pierre, M., Puymirat, J., et Boutjdir, M., « Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A). », Stem Cell Res, vol. 71, p. 103148, 2023.
M. Djemai, Cupelli, M., Boutjdir, M., et Chahine, M., « Optical Mapping of Cardiomyocytes in Monolayer Derived from Induced Pluripotent Stem Cells. », Cells, vol. 12, nᵒ 17, 2023.
S. Zaveri, Srivastava, U., Qu, Y. Sarah, Chahine, M., et Boutjdir, M., « Pathophysiology of Ca1.3 L-type calcium channels in the heart. », Front Physiol, vol. 14, p. 1144069, 2023.
2022
S. Ait Benichou, Jauvin, D., De Serres-Bérard, T., Pierre, M., Ling, K. K., C Bennett, F., Rigo, F., Gourdon, G., Chahine, M., et Puymirat, J., « Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1. », Gene Ther, vol. 29, nᵒ 12, p. 698-709, 2022.
R. Sheta, Teixeira, M., Idi, W., Pierre, M., Jacquet, Ade Rus, Emond, V., Zorca, C. E., Vanderperre, B., Durcan, T. M., Fon, E. A., Calon, F., Chahine, M., et Oueslati, A., « Combining NGN2 programming and dopaminergic patterning for a rapid and efficient generation of hiPSC-derived midbrain neurons. », Sci Rep, vol. 12, nᵒ 1, p. 17176, 2022.
Q. Plumereau, Ebdalla, A., Poulin, H., Appendino, J. Pablo, Scantlebury, M. H., Au, P. Yee Billie, et Chahine, M., « De novo Y1460C missense variant in Na1.1 impedes the pore region and results in epileptic encephalopathy. », Sci Rep, vol. 12, nᵒ 1, p. 17182, 2022.
T. M. Gamal El-Din, Zimmer, T., et Chahine, M., « Editorial: Structure Related Druggability of Voltage-Gated Sodium and Calcium Ion-Channels to Treat Diseases. », Front Pharmacol, vol. 13, p. 947511, 2022.
S. Ait Benichou, Jauvin, D., De Serres-Bérard, T., Bennett, F., Rigo, F., Gourdon, G., Boutjdir, M., Chahine, M., et Puymirat, J., « Enhanced Delivery of Ligand-Conjugated Antisense Oligonucleotides (C16-HA-ASO) Targeting Dystrophia Myotonica Protein Kinase Transcripts for the Treatment of Myotonic Dystrophy Type 1. », Hum Gene Ther, vol. 33, nᵒ 15-16, p. 810-820, 2022.
B. B. Sun, Kurki, M. I., Foley, C. N., Mechakra, A., Chen, C. - Y., Marshall, E., Wilk, J. B., Chahine, M., Chevalier, P., Christé, G., Palotie, A., Daly, M. J., et Runz, H., « Genetic associations of protein-coding variants in human disease. », Nature, vol. 603, nᵒ 7899, p. 95-102, 2022.
J. B. Hui, Silva, J. Cesar Hern, Pelaez, M. Carmen, Sévigny, M., Venkatasubramani, J. Priya, Plumereau, Q., Chahine, M., Proulx, C. D., Sephton, C. F., et Dutchak, P. A., « NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis. », eNeuro, vol. 9, nᵒ 2, 2022.
M. Chahine, Fontaine, J. M., et Boutjdir, M., « Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death. », J Am Heart Assoc, vol. 11, nᵒ 6, p. e023446, 2022.
T. De Serres-Bérard, Benichou, S. Ait, Jauvin, D., Boutjdir, M., Puymirat, J., et Chahine, M., « Recent Progress and Challenges in the Development of Antisense Therapies for Myotonic Dystrophy Type 1. », Int J Mol Sci, vol. 23, nᵒ 21, 2022.
X. - R. Yang, Ginjupalli, V. Krishna Mu, Thériault, O., Poulin, H., Appendino, J. Pablo, Au, P. Yee Billie, et Chahine, M., « -related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects. », J Neurophysiol, vol. 127, nᵒ 5, p. 1388-1397, 2022.

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