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Screening of Epilepsy-Linked Gabaa Receptor Mutants for Assembly Defects

Biophysical journal, 2020-02, Vol.118 (3), p.580a-580a

2020

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Electrophysiological and Biochemical Characterization of the Human P2X7B Receptor Inxenopus Laevisoocytes

Biophysical journal, 2021-02, Vol.120 (3), p.209a-210a

2021

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Localization of the gate and selectivity filter of the full-length P2X7 receptor

Proceedings of the National Academy of Sciences - PNAS, 2017-03, Vol.114 (11), p.E2156-E2165

2017

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Heterotrimeric concatamers of ionotropic P2X4 and P2X7 receptors

Biophysical journal, 2022-02, Vol.121 (3), p.245a-245a

2022

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Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia

Biophysical journal, 2021-02, Vol.120 (3), p.339a-340a

2021

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Identification of residues involved in homotrimeric assembly of the human P2X4 receptor by simulations and site-directed mutagenesis

Biophysical journal, 2023-02, Vol.122 (3), p.459a-460a

2023

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Point Mutations of P2X7 Receptors

Biophysical journal, 2020-02, Vol.118 (3), p.582a-582a

2020

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Key sites for P2X receptor function and multimerization: overview of mutagenesis studies on a structural basis

Current medicinal chemistry, 2015-01, Vol.22 (7), p.799

2015

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Trophic activity of a naturally occurring truncated isoform of the P2X7 receptor

The FASEB journal, 2010-09, Vol.24 (9), p.3393-3404

2010

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Dihydropyridines Potentiate ATP-Induced Currents Mediated by the Full-Length Human P2X5 Receptor

Molecules (Basel, Switzerland), 2022-03, Vol.27 (6), p.1846

2022

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The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel

Nature communications, 2018-04, Vol.9 (1), p.1354-18, Article 1354

2018

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TMEM16A(a)/anoctamin-1 Shares a Homodimeric Architecture with CLC Chloride Channels

Molecular & cellular proteomics, 2011-02, Vol.10 (2), p.S1-S11

2011

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Gallic Acid Alleviates Neuropathic Pain Behaviors in Rats by Inhibiting P2X7 Receptor-Mediated NF-κB/STAT3 Signaling Pathway

Frontiers in pharmacology, 2021-08, Vol.12, p.680139-680139

2021

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Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Nav1.7 channel mutation

British journal of pharmacology, 2020-10, Vol.177 (19), p.4481-4496

2020

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Interaction of Purinergic P2X4 and P2X7 Receptor Subunits

Frontiers in pharmacology, 2017-11, Vol.8, p.860-860

2017

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The β Subunit Determines the Ligand Binding Properties of Synaptic Glycine Receptors

Neuron (Cambridge, Mass.), 2005-03, Vol.45 (5), p.727-739

2005

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Role of the Cytoplasmatic M3-M4 Loop for the Homopentameric Assembly of a Chimeric Nicotinic Alpha 7 Receptor

Biophysical journal, 2019-02, Vol.116 (3), p.393a-394a

2019

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Biochemical and Functional Evidence for Homodimerization of Voltage-Gated Sodium Channels (Navs)

Biophysical journal, 2019-02, Vol.116 (3), p.312a-312a

2019

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Flexible subunit stoichiometry of functional human P2X2/3 heteromeric receptors

Neuropharmacology, 2015-12, Vol.99, p.115-130

2015

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Homodimeric anoctamin-1, but not homodimeric anoctamin-6, is activated by calcium increases mediated by the P2Y1 and P2X7 receptors

Pflügers Archiv, 2015-10, Vol.467 (10), p.2121-2140

2015

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The effect of anions on the human P2X7 receptor

Biochimica et biophysica acta, 2011-12, Vol.1808 (12), p.2913-2922

2011

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Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor

Frontiers in pharmacology, 2023-03, Vol.14, p.1120360-1120360

2023

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Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaine

Pflügers Archiv, 2018-12, Vol.470 (12), p.1787-1801

2018

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An intramembrane aromatic network determines pentameric assembly of Cys-loop receptors

Nature structural & molecular biology, 2010-01, Vol.17 (1), p.90

2010

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Discovery of Potent Competitive Antagonists and Positive Modulators of the P2X2 Receptor

Journal of medicinal chemistry, 2011-02, Vol.54 (3), p.817-830

2011

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Screening of Epilepsy-Linked Gabaa Receptor Mutants for Assembly Defects

Electrophysiological and Biochemical Characterization of the Human P2X7B Receptor Inxenopus Laevisoocytes

Localization of the gate and selectivity filter of the full-length P2X7 receptor

Heterotrimeric concatamers of ionotropic P2X4 and P2X7 receptors

Dissection of P2X4 and P2X7 Receptor Current Components in BV-2 Microglia

Identification of residues involved in homotrimeric assembly of the human P2X4 receptor by simulations and site-directed mutagenesis

Point Mutations of P2X7 Receptors

Key sites for P2X receptor function and multimerization: overview of mutagenesis studies on a structural basis

Trophic activity of a naturally occurring truncated isoform of the P2X7 receptor

Dihydropyridines Potentiate ATP-Induced Currents Mediated by the Full-Length Human P2X5 Receptor

The ASIC3/P2X3 cognate receptor is a pain-relevant and ligand-gated cationic channel

TMEM16A(a)/anoctamin-1 Shares a Homodimeric Architecture with CLC Chloride Channels

Gallic Acid Alleviates Neuropathic Pain Behaviors in Rats by Inhibiting P2X7 Receptor-Mediated NF-κB/STAT3 Signaling Pathway

Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Nav1.7 channel mutation

Interaction of Purinergic P2X4 and P2X7 Receptor Subunits

The β Subunit Determines the Ligand Binding Properties of Synaptic Glycine Receptors

Role of the Cytoplasmatic M3-M4 Loop for the Homopentameric Assembly of a Chimeric Nicotinic Alpha 7 Receptor

Biochemical and Functional Evidence for Homodimerization of Voltage-Gated Sodium Channels (Navs)

Flexible subunit stoichiometry of functional human P2X2/3 heteromeric receptors

Homodimeric anoctamin-1, but not homodimeric anoctamin-6, is activated by calcium increases mediated by the P2Y1 and P2X7 receptors

The effect of anions on the human P2X7 receptor

Diclofenac and other non-steroidal anti-inflammatory drugs (NSAIDs) are competitive antagonists of the human P2X3 receptor

Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaine

An intramembrane aromatic network determines pentameric assembly of Cys-loop receptors

Discovery of Potent Competitive Antagonists and Positive Modulators of the P2X2 Receptor

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