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Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels

Nature, 2008-04, Vol.452 (7190), p.1007-1011

2008

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Regulation of cell function by methionine oxidation and reduction

The Journal of physiology, 2001-02, Vol.531 (1), p.1-11

2001

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Haem can bind to and inhibit mammalian calcium-dependent Slo1 BK channels

Nature, 2003-10, Vol.425 (6957), p.531-535

2003

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Bilirubin oxidation end products directly alter K channels important in the regulation of vascular tone

Journal of cerebral blood flow and metabolism, 2011-01, Vol.31 (1), p.102-112

2011

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Three methionine residues located within the regulator of conductance for K+ (RCK) domains confer oxidative sensitivity to large-conductance Ca2+-activated K+ channels

The Journal of physiology, 2006-03, Vol.571 (2), p.329-348

2006

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CO-independent modification of K+ channels by tricarbonyldichlororuthenium(II) dimer (CORM-2)

European journal of pharmacology, 2017-11, Vol.815, p.33-41

2017

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Studies into Slo1 K+ channels and their ligand docosahexaenoic acid in murine sepsis to delineate off-target effects of immunonutrition

Life sciences (1973), 2018-06, Vol.203, p.112-120

2018

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Calcium channel characteristics conferred on the sodium channel by single mutations

Nature (London), 1992-04, Vol.356 (6368), p.441-443

1992

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Characterization of an eag-like potassium channel in human neuroblastoma cells

The Journal of physiology, 1998-04, Vol.508 (1), p.49-56

1998

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The amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl) benzofuran (KB130015) opens large-conductance Ca2+-activated K+ channels and relaxes vascular smooth muscle

European journal of pharmacology, 2007-01, Vol.555 (2-3), p.185-193

2007

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Impact of higher-order heme degradation products on hepatic function and hemodynamics

Journal of hepatology, 2017-08, Vol.67 (2), p.272-281

2017

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Cysteine 723 in the C‐linker segment confers oxidative inhibition of hERG1 potassium channels

The Journal of physiology, 2010-08, Vol.588 (16), p.2999-3009

2010

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Molecular determinants for the subtype specificity of μ-conotoxin SIIIA targeting neuronal voltage-gated sodium channels

Neuropharmacology, 2011-07, Vol.61 (1), p.105-111

2011

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Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons

Pharmacological research, 2014-09, Vol.87, p.80-86

2014

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A novel µ‐conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors

British journal of pharmacology, 2012-07, Vol.166 (5), p.1654-1668

2012

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Mechanism and molecular basis for the sodium channel subtype specificity of µ‐conopeptide CnIIIC

British journal of pharmacology, 2012-10, Vol.167 (3), p.576-586

2012

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The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism

European journal of pharmacology, 2010-04, Vol.632 (1), p.52-59

2010

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Carbon monoxide and outcome of stroke—A dream CORM true?

Critical care medicine, 2012-02, Vol.40 (2), p.687-688

2012

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Ca2+‐activated K+ channels in human melanoma cells are up‐regulated by hypoxia involving hypoxia‐inducible factor‐1α and the von Hippel‐Lindau protein

The Journal of physiology, 2006-03, Vol.571 (2), p.349-359

2006

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Gene polymorphisms in the heme degradation pathway and outcome of severe human sepsis

Shock (Augusta, Ga.), 2012-11, Vol.38 (5), p.459-465

2012

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Inactivation properties of voltage-gated K + channels altered by presence of β-subunit

Nature (London), 1994-05, Vol.369 (6478), p.289-294

1994

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Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels

FEBS letters, 2001-02, Vol.490 (1-2), p.49-53

2001

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dOr83b-Receptor or Ion Channel?

Annals of the New York Academy of Sciences, 2009-07, Vol.1170 (1), p.164-167

2009

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Inhibition of hEAG1 and hERG1 potassium channels by clofilium and its tertiary analogue LY97241

British journal of pharmacology, 2003-01, Vol.138 (1), p.161-171

2003

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Functional consequences of methionine oxidation of hERG potassium channels

Biochemical pharmacology, 2007-09, Vol.74 (5), p.702-711

2007

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Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels

Regulation of cell function by methionine oxidation and reduction

Haem can bind to and inhibit mammalian calcium-dependent Slo1 BK channels

Bilirubin oxidation end products directly alter K channels important in the regulation of vascular tone

Three methionine residues located within the regulator of conductance for K+ (RCK) domains confer oxidative sensitivity to large-conductance Ca2+-activated K+ channels

CO-independent modification of K+ channels by tricarbonyldichlororuthenium(II) dimer (CORM-2)

Studies into Slo1 K+ channels and their ligand docosahexaenoic acid in murine sepsis to delineate off-target effects of immunonutrition

Calcium channel characteristics conferred on the sodium channel by single mutations

Characterization of an eag-like potassium channel in human neuroblastoma cells

The amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl) benzofuran (KB130015) opens large-conductance Ca2+-activated K+ channels and relaxes vascular smooth muscle

Impact of higher-order heme degradation products on hepatic function and hemodynamics

Cysteine 723 in the C‐linker segment confers oxidative inhibition of hERG1 potassium channels

Molecular determinants for the subtype specificity of μ-conotoxin SIIIA targeting neuronal voltage-gated sodium channels

Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons

A novel µ‐conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors

Mechanism and molecular basis for the sodium channel subtype specificity of µ‐conopeptide CnIIIC

The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism

Carbon monoxide and outcome of stroke—A dream CORM true?

Ca2+‐activated K+ channels in human melanoma cells are up‐regulated by hypoxia involving hypoxia‐inducible factor‐1α and the von Hippel‐Lindau protein

Gene polymorphisms in the heme degradation pathway and outcome of severe human sepsis

Inactivation properties of voltage-gated K + channels altered by presence of β-subunit

Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels

dOr83b-Receptor or Ion Channel?

Inhibition of hEAG1 and hERG1 potassium channels by clofilium and its tertiary analogue LY97241

Functional consequences of methionine oxidation of hERG potassium channels

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