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Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.
Biliczki P, Girmatsion Z, Brandes RP, Harenkamp S, Pitard B, Charpentier F, Hébert TE, Hohnloser SH, Baró I, Nattel S, Ehrlich JR. Biliczki P, et al. Among authors: baro i. Heart Rhythm. 2009 Dec;6(12):1792-801. doi: 10.1016/j.hrthm.2009.08.009. Epub 2009 Aug 13. Heart Rhythm. 2009. PMID: 19959132
KCNQ1 K+ channel-mediated cardiac channelopathies.
Loussouarn G, Baró I, Escande D. Loussouarn G, et al. Among authors: baro i. Methods Mol Biol. 2006;337:167-83. doi: 10.1385/1-59745-095-2:167. Methods Mol Biol. 2006. PMID: 16929947
Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology.
Le Bouter S, Demolombe S, Chambellan A, Bellocq C, Aimond F, Toumaniantz G, Lande G, Siavoshian S, Baró I, Pond AL, Nerbonne JM, Léger JJ, Escande D, Charpentier F. Le Bouter S, et al. Among authors: baro i. Circ Res. 2003 Feb 7;92(2):234-42. doi: 10.1161/01.res.0000053185.75505.8e. Circ Res. 2003. PMID: 12574152
77 results