Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-7-26
pubmed:abstractText
Inherited arrhythmias can be caused by mutations in the cardiac ryanodine receptor (RyR2). The cellular source of these arrhythmias is unknown. Isolated RyR2(R4496C) mouse ventricular myocytes display arrhythmogenic activity related to spontaneous Ca(2+) release during diastole. On the other hand, recent whole-heart epicardial and endocardial optical mapping data demonstrate that ventricular arrhythmias in the RyR2(R4496C) mouse model of catecholaminergic polymorphic ventricular tachycardia (CPVT) originate in the His-Purkinje system, suggesting that Purkinje cells, and not ventricular myocytes, may be the cellular source of arrhythmogenic activity. The relative effect of the RyR2(R4496C) mutation on calcium homeostasis in ventricular myocytes versus Purkinje cells is unknown.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-10700450, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-11157710, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-11208676, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-11509449, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-12093772, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-12106942, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-12169647, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-12618230, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-15194464, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-15322274, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-15890976, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-15947247, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-16825580, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-17119150, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-17429038, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-17872467, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-19096022, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-19939742, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-5645545, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-7074728, http://linkedlifedata.com/resource/pubmed/commentcorrection/20538074-7867192
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1556-3871
pubmed:author
pubmed:copyrightInfo
Copyright 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1122-8
pubmed:dateRevised
2011-8-3
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Purkinje cell calcium dysregulation is the cellular mechanism that underlies catecholaminergic polymorphic ventricular tachycardia.
pubmed:affiliation
Center for Arrhythmia Research, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48108, USA. toddherr@umich.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural