about
Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversityMechanisms of pharmacological rescue of trafficking-defective hERG mutant channels in human long QT syndromeGene regulatory networks in cardiac conduction system developmentComputational methods in drug discoveryA common polymorphism associated with antibiotic-induced cardiac arrhythmiaAnion transport in heartA structural basis for drug-induced long QT syndromeADMET evaluation in drug discovery. 12. Development of binary classification models for prediction of hERG potassium channel blockageDynamin, encoded by shibire, is central to cardiac function.Risk of death in the long QT syndrome when a sibling has died.Molecular advances in cardiac and cardiovascular disease.Sodium channel carboxyl-terminal residue regulates fast inactivation.Review of microbial infections and the immune response to cardiac antigens.Novel Bayesian classification models for predicting compounds blocking hERG potassium channels.Life and death of a cardiac myocyte: principles of cellular biology.Safety pharmacology of DW-224a, a novel fluoroquinolone antibiotic agent.The whole genome sequence of coxsackievirus B3 MKP strain leading to myocarditis and its molecular phylogenetic analysis.Early identification of risk factors for sudden cardiac death.The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.Modelling and imaging cardiac repolarization abnormalities.Computational biology in the study of cardiac ion channels and cell electrophysiology.A noninvasive imaging modality for cardiac arrhythmiasCurrent perspectives on laboratory markers for the assessment of cardiovascular disease and myocardial damageSingle-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome.Localization of atherosclerosis susceptibility loci to chromosomes 4 and 6 using the Ldlr knockout mouse modelThe link between abnormal calcium handling and electrical instability in acquired long QT syndrome--Does calcium precipitate arrhythmic storms?RXRalpha overexpression in cardiomyocytes causes dilated cardiomyopathy but fails to rescue myocardial hypoplasia in RXRalpha-null fetuses.Molecular correlates of altered expression of potassium currents in failing rabbit myocardium.Stroke pharmacogenomics.Genetics of ischemic stroke, stroke-related risk factors, stroke precursors and treatments.Targeting the energy guardian AMPK: another avenue for treating cardiomyopathy?Interactions at human ether-à-go-go-related gene channels.Molecular diagnostics for cardiovascular disease.Effects of levobupivacaine, ropivacaine and bupivacaine on HERG channels: stereoselective bupivacaine block.Electrophysiological safety of DW-286a, a novel fluoroquinolone antibiotic agent.Computer model of action potential of mouse ventricular myocytes.Genetic and pharmacological identification of ion channels central to the Drosophila cardiac pacemaker.New approaches for identifying antiarrhythmic drug targets.Association of Apolipoprotein E Polymorphism and Concentration with Serum Lipids and Apo-lipoprotein Level in the Chinese fromShanghaiLinking a genetic defect to its cellular phenotype in a cardiac arrhythmia
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Molecular genetic insights into cardiovascular disease.
@en
type
label
Molecular genetic insights into cardiovascular disease.
@en
prefLabel
Molecular genetic insights into cardiovascular disease.
@en
P1433
P1476
Molecular genetic insights into cardiovascular disease.
@en
P2093
Keating MT
Sanguinetti MC
P304
P356
10.1126/SCIENCE.272.5262.681
P407
P577
1996-05-01T00:00:00Z