Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-3-9
pubmed:abstractText
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a familial arrhythmic syndrome caused by mutations in genes encoding the calcium-regulation proteins cardiac ryanodine receptor (RyR2) or calsequestrin-2 (CASQ2). Mechanistic studies indicate that CPVT is mediated by diastolic Ca(2+) overload and increased Ca(2+) leak through the RyR2 channel, implying that treatment targeting these defects might be efficacious in CPVT.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1540-8167
pubmed:author
pubmed:copyrightInfo
© 2010 Wiley Periodicals, Inc.
pubmed:issnType
Electronic
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
316-24
pubmed:meshHeading
pubmed-meshheading:20807279-Adrenergic beta-Antagonists, pubmed-meshheading:20807279-Animals, pubmed-meshheading:20807279-Anti-Arrhythmia Agents, pubmed-meshheading:20807279-Calcium Channel Blockers, pubmed-meshheading:20807279-Calcium Signaling, pubmed-meshheading:20807279-Calsequestrin, pubmed-meshheading:20807279-Diltiazem, pubmed-meshheading:20807279-Disease Models, Animal, pubmed-meshheading:20807279-Electrocardiography, pubmed-meshheading:20807279-Gene Knock-In Techniques, pubmed-meshheading:20807279-Magnesium, pubmed-meshheading:20807279-Mice, pubmed-meshheading:20807279-Mice, Knockout, pubmed-meshheading:20807279-Mutation, pubmed-meshheading:20807279-Myocytes, Cardiac, pubmed-meshheading:20807279-Propranolol, pubmed-meshheading:20807279-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:20807279-Sarcoplasmic Reticulum, pubmed-meshheading:20807279-Tachycardia, Ventricular, pubmed-meshheading:20807279-Time Factors, pubmed-meshheading:20807279-Verapamil
pubmed:year
2011
pubmed:articleTitle
Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutation.
pubmed:affiliation
Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural