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M. Chahine, Blanchet, J., Chemaly, A. El, and Bois, P., [A channel without pore? The primary structure of a proton permeable channel is finally revealed]., Med Sci (Paris), vol. 22, no. 11, pp. 930-1, 2006.
E. Herbert and Chahine, M., Clinical aspects and physiopathology of Brugada syndrome: review of current concepts., Can J Physiol Pharmacol, vol. 84, no. 8-9, pp. 795-802, 2006.
H. Huang, Zhao, J., Barrane, F. - Z., Champagne, J., and Chahine, M., Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes., Can J Cardiol, vol. 22, no. 4, pp. 309-13, 2006.
D. I. Keller, Huang, H., Zhao, J., Frank, R., Suarez, V., Delacrétaz, E., Brink, M., Osswald, S., Schwick, N., and Chahine, M., A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation., Cardiovasc Res, vol. 70, no. 3, pp. 521-9, 2006.
G. Baroudi, Qu, Y., Ramadan, O., Chahine, M., and Boutjdir, M., Protein kinase C activation inhibits Cav1.3 calcium channel at NH2-terminal serine 81 phosphorylation site., Am J Physiol Heart Circ Physiol, vol. 291, no. 4, pp. H1614-22, 2006.
S. Poelzing, Forleo, C., Samodell, M., Dudash, L., Sorrentino, S., Anaclerio, M., Troccoli, R., Iacoviello, M., Romito, R., Guida, P., Chahine, M., Pitzalis, M., and Deschênes, I., SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene., Circulation, vol. 114, no. 5, pp. 368-76, 2006.
K. Vijayaragavan, Acharfi, S., and Chahine, M., The C-terminal region as a modulator of rNa(v)1.7 and rNa(v)1.8 expression levels., FEBS Lett, vol. 559, no. 1-3, pp. 39-44, 2004.
P. Chevrier, Vijayaragavan, K., and Chahine, M., Differential modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by the local anesthetic lidocaine., Br J Pharmacol, vol. 142, no. 3, pp. 576-84, 2004.
D. - J. Shin, Jang, Y., Park, H. - Y., Lee, J. Eun, Yang, K., Kim, E., Bae, Y., Kim, J., Kim, J., Kim, S. Soon, Lee, M. Hyoung, Chahine, M., and Yoon, S. Kim, Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome., J Hum Genet, vol. 49, no. 10, pp. 573-8, 2004.
G. Baroudi, Napolitano, C., Priori, S. G., Del Bufalo, A., and Chahine, M., Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome., Can J Cardiol, vol. 20, no. 4, pp. 425-30, 2004.
K. Vijayaragavan, Boutjdir, M., and Chahine, M., Modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by protein kinase A and protein kinase C., J Neurophysiol, vol. 91, no. 4, pp. 1556-69, 2004.
C. - C. Chang, Acharfi, S., Wu, M. - H., Chiang, F. - T., Wang, J. - K., Sung, T. - C., and Chahine, M., A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia., Cardiovasc Res, vol. 64, no. 2, pp. 268-78, 2004.
M. Chahine, Pilote, S., Pouliot, V., Takami, H., and Sato, C., Role of arginine residues on the S4 segment of the Bacillus halodurans Na+ channel in voltage-sensing., J Membr Biol, vol. 201, no. 1, pp. 9-24, 2004.
K. Vijayaragavan, Powell, A. J., Kinghorn, I. J., and Chahine, M., Role of auxiliary beta1-, beta2-, and beta3-subunits and their interaction with Na(v)1.8 voltage-gated sodium channel., Biochem Biophys Res Commun, vol. 319, no. 2, pp. 531-40, 2004.
D. Deschênes, Acharfi, S., Pouliot, V., Hegele, R., Krahn, A., Daleau, P., and Chahine, M., Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome., Can J Physiol Pharmacol, vol. 81, no. 2, pp. 129-34, 2003.
M. E. O'Leary, Digregorio, M., and Chahine, M., Closing and inactivation potentiate the cocaethylene inhibition of cardiac sodium channels by distinct mechanisms., Mol Pharmacol, vol. 64, no. 6, pp. 1575-85, 2003.
M. Chahine, Sculptoreanu, A., and Varma, D. R., Modulation of L-type Ca2+ channels in neonatal rat heart by a novel Ca2+ channel agonist., Can J Physiol Pharmacol, vol. 81, no. 2, pp. 135-41, 2003.
N. - S. Mok, Priori, S. G., Napolitano, C., Chan, N. - Y., Chahine, M., and Baroudi, G., A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia., J Cardiovasc Electrophysiol, vol. 14, no. 4, pp. 407-11, 2003.
D. I. Keller, Acharfi, S., Delacrétaz, E., Benammar, N., Rotter, M., Pfammatter, J. Pierre, Fressart, V., Guicheney, P., and Chahine, M., A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation., J Mol Cell Cardiol, vol. 35, no. 12, pp. 1513-21, 2003.
M. Chahine, Pathophysiology of Brugada syndrome., J Cardiovasc Electrophysiol, vol. 14, no. 11, pp. 1257-8; author reply 1258, 2003.

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