Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
about
Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromesPerspective: a dynamics-based classification of ventricular arrhythmiasEffects on repolarization using dynamic QT interval monitoring in long-QT patients following left cardiac sympathetic denervation.A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study.Optical mapping of optogenetically shaped cardiac action potentialsEssential role of the zinc finger transcription factor Casz1 for mammalian cardiac morphogenesis and developmentInherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective.Hydrogen Sulfide Targets the Cys320/Cys529 Motif in Kv4.2 to Inhibit the Ito Potassium Channels in Cardiomyocytes and Regularizes Fatal Arrhythmia in Myocardial Infarction.Non-invasive phenotyping and drug testing in single cardiomyocytes or beta-cells by calcium imaging and optogenetics.Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosityGenetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.Genotype- and phenotype-guided management of congenital long QT syndrome.The heart and potassium: a banana republic.Calmodulin in a heartbeat.Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.Cardiac Delayed Rectifier Potassium Channels in Health and Disease.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Short QTc interval in males with klinefelter syndrome-influence of CAG repeat length, body composition, and testosterone replacement therapy.Human pluripotent stem cell models of cardiac disease: from mechanisms to therapies.Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report.Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndromeArrhythmia risk in long QT syndrome: beyond the disease-causative mutation.Wiring the developing heart: a serious matter for adulthood.Sculpting ion channel functional expression with engineered ubiquitin ligases.Cardiac Potassium Channels: Physiological Insights for Targeted Therapy.Cancer drugs and QT prolongation: weighing risk against benefit.
P2860
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P2860
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@en
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@nl
type
label
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@en
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@nl
prefLabel
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@en
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@nl
P2860
P356
P1476
Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.
@en
P2093
John R Giudicessi
Michael J Ackerman
P2860
P304
P356
10.1038/NRCARDIO.2012.3
P407
P577
2012-01-31T00:00:00Z