Role of the Slow Sodium Channel in Hereditary Cardiomyopathy-Reference-Cited by-同舟云学术

Role of the Slow Sodium Channel in Hereditary Cardiomyopathy

Published:1996 Issue: Volume: Page:109-125
ISSN:0166-9842
Container-title:Developments in Cardiovascular Medicine
language:
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Author:

Bkaily Ghassan,Jasmin Gaétan,Jacques Danielle,Proschek Libuse

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4613-1235-2_8.pdf

Reference49 articles.

1. Jasmin G, Pasternac A, Bkaily G, Proschek L. 1991. Modulation of calcium channels in the management of cardiomyopathies. In Hurwitz L, Partridge D, Leach J (eds.), Calcium Channels: Their Properties, Functions, Regulation and Clinical Relevance. CRC Press: Boca Raton, FL, pp. 295–307.

2. Bkaily G, Jacques D, Yamamoto T, Sculptoreanu A, Payet MD, Sperelakis N. 1988. Three types of slow inward Na+ currents as distinguished by melittin in 3-day-old embryonic heart. Can J Physiol Pharmacol 66:1017–1022.

3. Bkaily G, Peyrow M, Yamamoto T, Sculptoreanu A, Jacques D, Sperelakis N. 1988. Measurements of macroscopic Ca2+, Na+ and K+ currents in single heart and rabbit aortic cells. Mol Cell Biochem 80:59–72.

4. Bkaily G, Jacques D, Sculptoreanu A, Yamamoto T, Carrier D, Vigneault D, Sperelakis N. 1991. Apamin, a highly potent blocker of the TTX- and Mn2+ insensitive fast transient Na+ current in young embryonic heart. J Mol Cell Cardiol 23:25–39.

5. Sperelakis N. 1980. Changes in membrane electrical properties during development of the heart. In Zipes DP, Bailey JC, Elharrar V (eds.), Slow Inward Current and Cardiac Arrhythmias. Martinus Nijhoff: Boston, pp. 221–262.

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