Loratadine blockade of K(+) channels in human heart: comparison with terfenadine under physiological conditions
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Dog left ventricular midmyocardial myocytes for assessment of drug-induced delayed repolarization: short-term variability and proarrhythmic potential.Identification of novel small molecule modulators of K2P18.1 two-pore potassium channel.hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds.Drug-induced torsades de pointes and implications for drug development.Predicting QT prolongation in humans during early drug development using hERG inhibition and an anaesthetized guinea-pig model.Prediction of hERG Liability - Using SVM Classification, Bootstrapping and Jackknifing.
P2860
Loratadine blockade of K(+) channels in human heart: comparison with terfenadine under physiological conditions
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2000 nî lūn-bûn
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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Loratadine blockade of K(+) ch ...... under physiological conditions
@ast
Loratadine blockade of K(+) ch ...... under physiological conditions
@en
Loratadine blockade of K(+) ch ...... under physiological conditions
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type
label
Loratadine blockade of K(+) ch ...... under physiological conditions
@ast
Loratadine blockade of K(+) ch ...... under physiological conditions
@en
Loratadine blockade of K(+) ch ...... under physiological conditions
@nl
prefLabel
Loratadine blockade of K(+) ch ...... under physiological conditions
@ast
Loratadine blockade of K(+) ch ...... under physiological conditions
@en
Loratadine blockade of K(+) ch ...... under physiological conditions
@nl
P1476
Loratadine blockade of K(+) ch ...... under physiological conditions
@en
P2093
Crumb WJ Jr
P304
P407
P577
2000-01-01T00:00:00Z