Search Results - "Romey, G"
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TREK-1, a K+ channel involved in neuroprotection and general anesthesia
Published in The EMBO journal (07-07-2004)“…TREK‐1 is a two‐pore‐domain background potassium channel expressed throughout the central nervous system. It is opened by polyunsaturated fatty acids and…”
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2
Mechanisms underlying excitatory effects of group I metabotropic glutamate receptors via inhibition of 2P domain K+ channels
Published in The EMBO journal (15-10-2003)“…Group I metabotropic glutamate receptors (mGluRs) are implicated in diverse processes such as learning, memory, epilepsy, pain and neuronal death. By…”
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3
Cloning, functional expression and brain localization of a novel unconventional outward rectifier K+ channel
Published in The EMBO journal (16-12-1996)“…Human TWIK‐1, which has been cloned recently, is a new structural type of weak inward rectifier K+ channel. Here we report the structural and functional…”
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4
TWIK‐1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure
Published in The EMBO journal (01-03-1996)“…A new human weakly inward rectifying K+ channel, TWIK‐1, has been isolated. This channel is 336 amino acids long and has four transmembrane domains. Unlike…”
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5
p11, an annexin II subunit, an auxiliary protein associated with the background K+ channel, TASK-1
Published in The EMBO journal (02-09-2002)“…TASK‐1 belongs to the 2P domain K+ channel family and is the prototype of background K+ channels that set the resting membrane potential and tune action…”
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6
Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
Published in The EMBO journal (01-09-1997)“…Mutations in the delayed rectifier K+ channel subunit KvLQT1 have been identified as responsible for both Romano–Ward (RW) and Jervell and Lange‐Nielsen (JLN)…”
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7
Genomic and Functional Characteristics of Novel Human Pancreatic 2P Domain K+ Channels
Published in Biochemical and biophysical research communications (23-03-2001)“…We isolated three novel 2P domain K+ channel subunits from human. The first two subunits, TALK-1 and TALK-2, are distantly related to TASK-2. Their genes form…”
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8
PP2A-Bγ subunit and KCNQ2 K+ channels in bipolar disorder
Published in The pharmacogenomics journal (01-04-2007)“…Many bipolar affective disorder (BD) susceptibility loci have been identified but the molecular mechanisms responsible for the disease remain to be elucidated…”
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9
The bee venom peptide tertiapin underlines the role of I(KACh) in acetylcholine-induced atrioventricular blocks
Published in British journal of pharmacology (01-10-2000)“…Acetylcholine (ACh) is an important neuromodulator of cardiac function that is released upon stimulation of the vagus nerve. Despite numerous reports on…”
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10
Effects of a mosquitocidal toxin on a mammalian epithelial cell line expressing its target receptor
Published in Cellular microbiology (01-09-2005)“…Summary The spread of diseases transmitted by Anopheles and Culex mosquitoes, such as malaria and West Nile fever, is a growing concern for human health…”
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11
Susceptibility of Cloned K+Channels to Reactive Oxygen Species
Published in Proceedings of the National Academy of Sciences - PNAS (05-12-1995)“…Free radical-induced oxidant stress has been implicated in a number of physiological and pathophysiological states including ischemia and reperfusion-induced…”
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12
Heterologous Multimeric Assembly Is Essential for K+ Channel Activity of Neuronal and Cardiac G-Protein-Activated Inward Rectifiers
Published in Biochemical and biophysical research communications (17-07-1995)“…The family of G-protein-activated inward-rectifiers K+ channels presently comprise at least 3 cloned members called GIRK1, GIRK2 and GIRK3. A close structural…”
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13
Calcicludine, A Venom Peptide of the Kunitz-Type Protease Inhibitor Family, is a Potent Blocker of High-Threshold Ca2+Channels with a High Affinity for L-Type Channels in Cerebellar Granule Neurons
Published in Proceedings of the National Academy of Sciences - PNAS (01-02-1994)“…Calcicludine (CaC) is a 60-amino acid polypeptide from the venom of Dendroaspis angusticeps. It is structurally homologous to the Kunitz-type protease…”
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14
Mice display sex differences in halothane-induced polymorphic ventricular tachycardia
Published in Circulation (New York, N.Y.) (23-07-2002)“…Molecularly engineered mice are extensively used as models of cardiovascular diseases, yet little is known about sex differences in the electrophysiology of…”
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15
Cloning, expression, pharmacology and regulation of a delayed rectifier K+ channel in mouse heart
Published in The EMBO journal (01-10-1991)“…Neonatal mouse cardiac poly(A)+ mRNA microinjection into Xenopus oocytes directed the expression of a delayed rectifier K+ current. A cDNA encoding this…”
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16
PP2A-Bgamma subunit and KCNQ2 K+ channels in bipolar disorder
Published in The pharmacogenomics journal (01-04-2007)“…Many bipolar affective disorder (BD) susceptibility loci have been identified but the molecular mechanisms responsible for the disease remain to be elucidated…”
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17
Cloning, functional expression, and regulation of two K+ channels in human T lymphocytes
Published in The Journal of biological chemistry (25-04-1992)“…Low stringency screening of a Jurkat cDNA library with a rat brain K+ channel (RCK1) probe has resulted in the isolation of HLK3, a voltage-gated K+ channel…”
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18
Vasopressin Modulates the Spontaneous Electrical Activity in Aortic Cells (Line A7r5) by Acting on Three Different Types of Ionic Channels
Published in Proceedings of the National Academy of Sciences - PNAS (01-12-1988)“…A7r5 smooth muscle (aorta) cells have a spontaneous electrical activity. Application of vasopressin produces a hyperpolarization accompanied by an interruption…”
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19
Effects of a new class of calcium antagonists, SR33557 (fantofarone) and SR33805, on neuronal voltage-activated Ca++ channels
Published in The Journal of pharmacology and experimental therapeutics (01-12-1994)“…SR33557 (fantofarone) and SR33805 are structurally novel calcium antagonists that bind selectively to the alpha 1-subunit of the L-type Ca++ channel at a site…”
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20
Apamin as a Selective Blocker of the Calcium-Dependent Potassium Channel in Neuroblastoma Cells: Voltage-Clamp and Biochemical Characterization of the Toxin Receptor
Published in Proceedings of the National Academy of Sciences - PNAS (01-02-1982)“…This paper describes the interaction of apamin, a bee venom neurotoxin, with the mouse neuroblastoma cell membrane. Voltage-clamp analyses have shown that…”
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