Biblio

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2022
Benichou SAit, Jauvin D, De Serres-Bérard T, Pierre M, Ling KK, C Bennett F, Rigo F, Gourdon G, Chahine M, Puymirat J. Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1. Gene Ther. 2022;.
Sun BB, Kurki MI, Foley CN, Mechakra A, Chen C-Y, Marshall E, Wilk JB, Chahine M, Chevalier P, Christé G, Palotie A, Daly MJ, Runz H. Genetic associations of protein-coding variants in human disease. Nature. 2022;603(7899):95-102.
Hui JB, Silva JCesar Hern, Pelaez MCarmen, Sévigny M, Venkatasubramani JPriya, Plumereau Q, Chahine M, Proulx CD, Sephton CF, Dutchak PA. NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis. eNeuro. 2022;9(2).
Chahine M, Fontaine JM, Boutjdir M. Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death. J Am Heart Assoc. 2022;11(6):e023446.
2021
De Serres-Bérard T, Pierre M, Chahine M, Puymirat J. Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy. Neurobiol Dis. 2021;160:105532.
Herbert E, Fournier D, Al-Shaqha WMohammed, Chahine M. The myocardial and neuronal infectivity of SARS-CoV-2 and detrimental outcomes. Can J Physiol Pharmacol. 2021;99(11):1128-1136.
Pierre M, Djemai M, Poulin H, Chahine M. Na1.5 knockout in iPSCs: a novel approach to study Na1.5 variants in a human cardiomyocyte environment. Sci Rep. 2021;11(1):17168.
2019
Poulin H, Martineau L, Racine V, Puymirat J, Chahine M. Differentiation of lymphoblastoid-derived iPSCs into functional cardiomyocytes, neurons and myoblasts. Biochem Biophys Res Commun. 2019;516(1):222-228.
Kadala A, Charreton M, Charnet P, Cens T, Rousset M, Chahine M, Vaissière BE, Collet C. Voltage-gated sodium channels from the bees Apis mellifera and Bombus terrestris are differentially modulated by pyrethroid insecticides. Sci Rep. 2019;9(1):1078.