Biblio
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Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1. Gene Ther. 2022;.
. Genetic associations of protein-coding variants in human disease. Nature. 2022;603(7899):95-102.
. NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis. eNeuro. 2022;9(2).
. Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death. J Am Heart Assoc. 2022;11(6):e023446.
. Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy. Neurobiol Dis. 2021;160:105532.
. The myocardial and neuronal infectivity of SARS-CoV-2 and detrimental outcomes. Can J Physiol Pharmacol. 2021;99(11):1128-1136.
. Na1.5 knockout in iPSCs: a novel approach to study Na1.5 variants in a human cardiomyocyte environment. Sci Rep. 2021;11(1):17168.
. Differentiation of lymphoblastoid-derived iPSCs into functional cardiomyocytes, neurons and myoblasts. Biochem Biophys Res Commun. 2019;516(1):222-228.
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