Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2010-4-30
pubmed:abstractText
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is caused by a single point mutation in a well-defined region of the cardiac type 2 ryanodine receptor (RyR)2. However, the underlying mechanism by which a single mutation in such a large molecule produces drastic effects on channel function remains unresolved.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-10069797, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-10512814, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-10766778, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-10830164, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-11814342, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-11861212, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-12837242, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-15322274, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-15890976, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-15967847, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-16157601, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-16339485, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-16391617, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-16825580, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-16873551, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-17234966, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-17452324, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-17606610, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-18006488, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-18483626, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-18755143, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-19096022, http://linkedlifedata.com/resource/pubmed/commentcorrection/20224043-19460614
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1524-4571
pubmed:author
pubmed:issnType
Electronic
pubmed:day
30
pubmed:volume
106
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1413-24
pubmed:dateRevised
2011-7-28
pubmed:meshHeading
pubmed-meshheading:20224043-Animals, pubmed-meshheading:20224043-Caffeine, pubmed-meshheading:20224043-Calcium Signaling, pubmed-meshheading:20224043-Cells, Cultured, pubmed-meshheading:20224043-Cyclic AMP-Dependent Protein Kinases, pubmed-meshheading:20224043-Disease Models, Animal, pubmed-meshheading:20224043-Epinephrine, pubmed-meshheading:20224043-Excitation Contraction Coupling, pubmed-meshheading:20224043-Genotype, pubmed-meshheading:20224043-Isoproterenol, pubmed-meshheading:20224043-Membrane Potentials, pubmed-meshheading:20224043-Mice, pubmed-meshheading:20224043-Mice, Inbred C57BL, pubmed-meshheading:20224043-Mice, Transgenic, pubmed-meshheading:20224043-Myocardial Contraction, pubmed-meshheading:20224043-Myocytes, Cardiac, pubmed-meshheading:20224043-Peptide Fragments, pubmed-meshheading:20224043-Phenotype, pubmed-meshheading:20224043-Phosphorylation, pubmed-meshheading:20224043-Physical Exertion, pubmed-meshheading:20224043-Point Mutation, pubmed-meshheading:20224043-Protein Conformation, pubmed-meshheading:20224043-Protein Structure, Tertiary, pubmed-meshheading:20224043-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:20224043-Sarcoplasmic Reticulum, pubmed-meshheading:20224043-Structure-Activity Relationship, pubmed-meshheading:20224043-Tachycardia, Ventricular, pubmed-meshheading:20224043-Time Factors
pubmed:year
2010
pubmed:articleTitle
Catecholaminergic polymorphic ventricular tachycardia is caused by mutation-linked defective conformational regulation of the ryanodine receptor.
pubmed:affiliation
Department of Medicine and Clinical Science, Division of Cardiology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi, 755-8505, Japan.
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