Search Results - "ACHARFI, Said" :: K.UTB vyhledávací portál

Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome

by Deschênes, Dominic, Acharfi, Said, Pouliot, Valerie, Hegele, Robert, Krahn, Andrew, Daleau, Pascal, Chahine, Mohamed
Published in Canadian journal of physiology and pharmacology (01.02.2003)

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Expression and Intracellular Localization of an SCN5A Double Mutant R1232W/T1620M Implicated in Brugada Syndrome

by Baroudi, Ghayath, Acharfi, Said, Larouche, Chantal, Chahine, Mohamed
Published in Circulation research (11.01.2002)

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A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia

by CHANG, Chien-Chih, ACHARFI, Said, WU, Mei-Hwan, CHIANG, Fu-Tien, WANG, Jou-Kou, SUNG, Tseng-Chen, CHAHINE, Mohamed
Published in Cardiovascular research (01.11.2004)

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The C‐terminal region as a modulator of rNa v 1.7 and rNa v 1.8 expression levels

by Vijayaragavan, Kausalia, Acharfi, Said, Chahine, Mohamed
Published in FEBS letters (13.02.2004)

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The C-terminal region as a modulator of rNa v1.7 and rNa v1.8 expression levels

by Vijayaragavan, Kausalia, Acharfi, Said, Chahine, Mohamed
Published in FEBS letters (2004)

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A novel mutation in SCN5A, delQKP 1507–1509, causing long QT syndrome: : Role of Q1507 residue in sodium channel inactivation

by Keller, Dagmar I., Acharfi, Said, Delacrétaz, Etienne, Benammar, Nawal, Rotter, Martin, Pfammatter, Jean-Pierre, Fressart, Véronique, Guicheney, Pascale, Chahine, Mohamed
Published in Journal of molecular and cellular cardiology (01.12.2003)

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