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Human-induced pluripotent stem cell-derived cardiomyocytes exhibit temporal changes in phenotype

American journal of physiology. Heart and circulatory physiology, 2013-09, Vol.305 (6), p.H913-H922

2013

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Mallotoxin is a novel human ether-a-go-go-related gene (hERG) potassium channel activator

The Journal of pharmacology and experimental therapeutics, 2006-11, Vol.319 (2), p.957-962

2006

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2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic Acid (PD-307243) Causes Instantaneous Current through Human Ether-a-go-go-Related Gene Potassium Channels

Molecular pharmacology, 2008-03, Vol.73 (3), p.639-651

2008

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Functional TRPV4 channels and an absence of capsaicin-evoked currents in freshly-isolated, guinea-pig urothelial cells

Channels (Austin, Tex.), 2009-05, Vol.3 (3), p.156-160

2009

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1-[1-Hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone, a potent and highly selective small molecule blocker of the large-conductance voltage-gated and calcium-dependent K+ channel

The Journal of pharmacology and experimental therapeutics, 2008-10, Vol.327 (1), p.168-177

2008

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The discovery of potent blockers of the canonical transient receptor channels, TRPC3 and TRPC6, based on an anilino-thiazole pharmacophore

Bioorganic & medicinal chemistry letters, 2013-09, Vol.23 (17), p.4979-4984

2013

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Characterizing the role of Thr352 in the inhibition of the large conductance Ca2+-activated K+ channels by 1-[1-hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone

The Journal of pharmacology and experimental therapeutics, 2010-08, Vol.334 (2), p.402

2010

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Ca2+ Channel Inactivation in Small Mesenteric Arteries of WKY and SHR

American journal of hypertension, 2008-04, Vol.21 (4), p.406-412

2008

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Augmented calcium currents in mesenteric artery branches of the spontaneously hypertensive rat

Hypertension (Dallas, Tex. 1979), 1995-12, Vol.26 (6), p.1060-1064

1995

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Ca Channel Inactivation in Small Mesenteric Arteries of WKY and SHR

American journal of hypertension, 2008-04, Vol.21 (4), p.406-412

2008

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Characterizing the Role of Thr352 in the Inhibition of the Large Conductance Ca 2+ -Activated K + Channels by 1-[1-Hexyl-6-(methyloxy)-1 H -indazol-3-yl]-2-methyl-1-propanone

The Journal of pharmacology and experimental therapeutics, 2010-08, Vol.334 (2), p.402-409

2010

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2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nico tini c Acid (PD-307243) Causes Instantaneous Current through Human Ether-a-go-go-Related Gene Potassium Channels

Molecular pharmacology, 2008-03, Vol.73 (3), p.639-651

2008

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Effects of Age on Ca2+ Currents in Small Mesenteric Artery Myocytes From Wistar-Kyoto and Spontaneously Hypertensive Rats

Hypertension (Dallas, Tex. 1979), 1997-06, Vol.29 (6), p.1329-1336

1997

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A multicenter, inpatient, phase 2, double-blind, placebo-controlled dose-ranging study of LY2140023 monohydrate in patients with DSM-IV schizophrenia

Journal of clinical psychopharmacology, 2011-06, Vol.31 (3), p.349-355

2011

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Automation System of Intellectual Activity on Creating Programs in the Language of Logical Programming

Smart Education and e-Learning 2018, p.67-77

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Novel phosphonated poly(1,3,4-oxadiazole)s: Synthesis in ionic liquid and characterization

Reactive & functional polymers, 2008, Vol.68 (1), p.208-224

2008

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Novel phosphonated poly(1,3,4-oxadiazole)s : Synthesis in ionic liquid and characterization

Reactive & functional polymers, 2008, Vol.68 (1), p.208-224

2008

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Human-induced pluripotent stem cell-derived cardiomyocytes exhibit temporal changes in phenotype

Mallotoxin is a novel human ether-a-go-go-related gene (hERG) potassium channel activator

2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic Acid (PD-307243) Causes Instantaneous Current through Human Ether-a-go-go-Related Gene Potassium Channels

Functional TRPV4 channels and an absence of capsaicin-evoked currents in freshly-isolated, guinea-pig urothelial cells

1-[1-Hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone, a potent and highly selective small molecule blocker of the large-conductance voltage-gated and calcium-dependent K+ channel

The discovery of potent blockers of the canonical transient receptor channels, TRPC3 and TRPC6, based on an anilino-thiazole pharmacophore

Characterizing the role of Thr352 in the inhibition of the large conductance Ca2+-activated K+ channels by 1-[1-hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone

Ca2+ Channel Inactivation in Small Mesenteric Arteries of WKY and SHR

Augmented calcium currents in mesenteric artery branches of the spontaneously hypertensive rat

Ca Channel Inactivation in Small Mesenteric Arteries of WKY and SHR

Characterizing the Role of Thr352 in the Inhibition of the Large Conductance Ca 2+ -Activated K + Channels by 1-[1-Hexyl-6-(methyloxy)-1 H -indazol-3-yl]-2-methyl-1-propanone

2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nico tini c Acid (PD-307243) Causes Instantaneous Current through Human Ether-a-go-go-Related Gene Potassium Channels

Effects of Age on Ca2+ Currents in Small Mesenteric Artery Myocytes From Wistar-Kyoto and Spontaneously Hypertensive Rats

An orally active TRPV4 channel blocker prevents and resolves pulmonary edema induced by heart failure

A multicenter, inpatient, phase 2, double-blind, placebo-controlled dose-ranging study of LY2140023 monohydrate in patients with DSM-IV schizophrenia

Automation System of Intellectual Activity on Creating Programs in the Language of Logical Programming

Novel phosphonated poly(1,3,4-oxadiazole)s: Synthesis in ionic liquid and characterization

Novel phosphonated poly(1,3,4-oxadiazole)s : Synthesis in ionic liquid and characterization

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