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Mapping the Gbetagamma-binding sites in GIRK1 and GIRK2 subunits of the G protein-activated K+ channelIdentification of the structural determinant responsible for the phosphorylation of G-protein activated potassium channel 1 by cAMP-dependent protein kinaseSubunit stoichiometry of heterologously expressed G-protein activated inwardly rectifying potassium channels analysed by fluorescence intensity ratio measurement.The GIRK1 brain variant GIRK1d and its functional impact on heteromultimeric GIRK channels.Isoform diversity and modulation of sodium channels by protein kinases.Four and a half LIM protein 1C (FHL1C): a binding partner for voltage-gated potassium channel K(v1.5).Single channel analysis of the regulation of GIRK1/GIRK4 channels by protein phosphorylation.Tolperisone: a typical representative of a class of centrally acting muscle relaxants with less sedative side effects.Piezo1 forms mechanosensitive ion channels in the human MCF-7 breast cancer cell line.Overexpression of KCNJ3 gene splice variants affects vital parameters of the malignant breast cancer cell line MCF-7 in an opposing manner.Critical evaluation of KCNJ3 gene product detection in human breast cancer: mRNA in situ hybridisation is superior to immunohistochemistry.IK.ACh activation by arachidonic acid occurs via a G-protein-independent pathway mediated by the GIRK1 subunit.Inhibition of an inwardly rectifying K+ channel by G-protein alpha-subunits.Influence of Lentiviral β-Synuclein Overexpression in the Hippocampus of a Transgenic Mouse Model of Alzheimer's Disease on Amyloid Precursor Protein Metabolism and Pathology.KCNJ3 is a new independent prognostic marker for estrogen receptor positive breast cancer patientsCloning and characterisation of GIRK1 variants resulting from alternative RNA editing of the KCNJ3 gene transcript in a human breast cancer cell line.S-nitrosation controls gating and conductance of the alpha 1 subunit of class C L-type Ca(2+) channels.Molecular basis of the facilitation of the heterooligomeric GIRK1/GIRK4 complex by cAMP dependent protein kinase.G protein-gated inwardly rectifying potassium channels are targets for volatile anesthetics.Mechanism of modulation of single sodium channels from skeletal muscle by the beta 1-subunit from rat brain.Single-channel properties of α3β4, α3β4α5 and α3β4β2 nicotinic acetylcholine receptors in mice lacking specific nicotinic acetylcholine receptor subunits.The sensitivity of G protein-activated K+ channels toward halothane is essentially determined by the C terminus.Serotonin and protein kinase C modulation of a rat brain inwardly rectifying K+ channel expressed in xenopus oocytes.Voltage clamping of Xenopus laevis oocytes utilizing agarose-cushion electrodes.Inhibition of the fast sodium inward current in ventricular cardiomyocytes of rats and guinea pigs by a novel potent sodium channel blocking agent.Tumor host relations. VI. Is alpha-ketoglutarate a tumor marker? Association with tumor extent in humans--correlation with tumor size in rats.Distribution and localization of a G protein-coupled inwardly rectifying K+ channel in the rat.Protein kinase A reduces voltage-dependent Na+ current in Xenopus oocytes.The TTX metabolite 4,9-anhydro-TTX is a highly specific blocker of the Na(v1.6) voltage-dependent sodium channel.Domain specialization in voltage-dependent Na+ and Ca2+ channels.Emerging role(s) of G-protein alpha-subunits in the gating of GIRKs.The cardiac acetylcholine-activated, inwardly rectifying K+-channel subunit GIRK1 gives rise to an inward current induced by free oxygen radicals.Ion permeation through a G-protein activated (GIRK1/GIRK5) inwardly rectifying potassium channel.A C-terminal peptide of the GIRK1 subunit directly blocks the G protein-activated K+ channel (GIRK) expressed in Xenopus oocytes.Modulation of the human cardiac sodium channel alpha-subunit by cAMP-dependent protein kinase and the responsible sequence domain.Modulation of cardiac sodium channel isoform by cyclic AMP dependent protein kinase does not depend on phosphorylation of serine 1504 in the cytosolic loop interconnecting transmembrane domains III and IV.Level of expression controls modes of gating of a K+ channel.Molecular mechanism of protein kinase C modulation of sodium channel alpha-subunits expressed in Xenopus oocytes.Incorporation of a voltage sensitive pore from guinea pig heart mitochondria into Black lipid membranes and characterization of electrical properties.An optically controlled probe identifies lipid-gating fenestrations within the TRPC3 channel.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Wolfgang Schreibmayer
@ast
Wolfgang Schreibmayer
@en
Wolfgang Schreibmayer
@es
Wolfgang Schreibmayer
@nl
Wolfgang Schreibmayer
@sl
type
label
Wolfgang Schreibmayer
@ast
Wolfgang Schreibmayer
@en
Wolfgang Schreibmayer
@es
Wolfgang Schreibmayer
@nl
Wolfgang Schreibmayer
@sl
prefLabel
Wolfgang Schreibmayer
@ast
Wolfgang Schreibmayer
@en
Wolfgang Schreibmayer
@es
Wolfgang Schreibmayer
@nl
Wolfgang Schreibmayer
@sl
P106
P1153
7003509660
P21
P31
P496
0000-0002-4631-7922