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dc.contributor.authorArintaya Phrommintikulen_US
dc.contributor.authorNipon Chattipakornen_US
dc.date.accessioned2018-09-11T08:59:42Z-
dc.date.available2018-09-11T08:59:42Z-
dc.date.issued2006-09-20en_US
dc.identifier.issn01675273en_US
dc.identifier.other2-s2.0-33748446380en_US
dc.identifier.other10.1016/j.ijcard.2005.11.106en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33748446380&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61822-
dc.description.abstractCalcium (Ca2+) plays an important role as a messenger in the excitation-contraction coupling process of the myocardium. It is stored in the sarcoplasmic reticulum (SR) and released via a calcium release channel called the ryanodine receptor. Cardiac ryanodine receptor (RyR2) controls Ca2+release, which is essential for cardiac contractility. There are several molecules which bind and regulate the function of RyR2 including calstabin2, calmodulin, protein kinase A (PKA), phosphatase, sorcin and calsequestrin. Alteration of RyR2 and associated molecules can cause functional and/or structural changes of the heart, leading to heart failure and sudden cardiac death. In this review, the alteration of RyR2 and its regulatory proteins, and its roles in heart failure and sudden cardiac death, are discussed. Evidence of a possible novel therapy targeting RyR2 and its associated regulatory proteins, currently proposed by investigators, is also included in this article. © 2006 Elsevier Ireland Ltd. All rights reserved.en_US
dc.subjectMedicineen_US
dc.titleRoles of cardiac ryanodine receptor in heart failure and sudden cardiac deathen_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Cardiologyen_US
article.volume112en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsFaculty of Medicine, Thammasat Universityen_US
Appears in Collections:CMUL: Journal Articles

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