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Allosteric nature of P2X receptor activation probed by photoaffinity labelling

British journal of pharmacology, 2012-11, Vol.167 (6), p.1301-1310

2012

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Electrophysiology: Basics, Methods, Modern Approaches and Applications

Second edition., 2022

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Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X receptor antagonist

Neuropharmacology, 2005-03, Vol.48 (3), p.461-468

2005

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The suramin analogue NF279 is a novel and potent antagonist selective for the P2X(1) receptor

Neuropharmacology, 2000-08, Vol.39 (11), p.2044-2053

2000

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Roles of Individual N-Glycans for ATP Potency and Expression of the Rat P2X1 Receptor

The Journal of biological chemistry, 2000-10, Vol.275 (43), p.33542-33547

2000

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P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels

The EMBO journal, 1998-06, Vol.17 (11), p.3016-3028

1998

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Electrophysiology: Basics, Modern Approaches and Applications

1, 2016

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The suramin analog 4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis (carbonylimino)))tetra-kis-benzenesulfonic acid (NF110) potently blocks P2X3 receptors: subtype selectivity is determined by location of sulfonic acid groups

Molecular pharmacology, 2006-06, Vol.69 (6), p.2058-2067

2006

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A Functional P2X7 Splice Variant with an Alternative Transmembrane Domain 1 Escapes Gene Inactivation in P2X7 Knock-out Mice

The Journal of biological chemistry, 2009-09, Vol.284 (38), p.25813-25822

2009

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Awareness of Crime-Relevant Information and the Guilty Knowledge Test

Journal of applied psychology, 1992-02, Vol.77 (1), p.55-59

1992

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Blue Native Page as a Useful Method for the Analysis of the Assembly of Distinct Combinations of Nicotinic Acetylcholine Receptor Subunits

Journal of receptors and signal transduction, 1999, Vol.19 (1-4), p.493-507

1999

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Novel ligands for P2 receptor subtypes in innervated tissues

Progress in brain research, 1999, Vol.120, p.107

1999

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Evolving view of quaternary structures of ligand-gated ion channels

Progress in brain research, 1999, Vol.120, p.61-80

1999

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Novel properties of the depolarization-induced endogenous sodium conductance in the Xenopus laevis oocyte

Pflügers Archiv, 1999-05, Vol.437 (6), p.917-924

Rettinger, J

1999

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The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor

Neuropharmacology, 2000-10, Vol.39 (11), p.2044-2053

2000

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NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors

Naunyn-Schmiedeberg's archives of pharmacology, 2001-09, Vol.364 (3), p.285-290

2001

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Characteristics of Na +/K +-ATPase mediated proton current in Na +- and K +-free extracellular solutions. Indications for kinetic similarities between H +/K +-ATPase and Na +/K +-ATPase

Biochimica et biophysica acta, 1996-07, Vol.1282 (2), p.207-215

Rettinger, Jürgen

1996

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Desensitization Masks Nanomolar Potency of ATP for the P2X1 Receptor

The Journal of biological chemistry, 2004-02, Vol.279 (8), p.6426-6433

2004

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The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X1 receptors

European journal of pharmacology, 2000-01, Vol.387 (3), p.R19-R21

2000

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NF279: a novel potent and selective antagonist of P2X receptor-mediated responses

European journal of pharmacology, 1998-05, Vol.350 (1), p.R5-R6

1998

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Roles of Individual N-Glycans for ATP Potency and Expression of the Rat P2X sub(1) Receptor

The Journal of biological chemistry, 2000-10, Vol.275 (43), p.33542-33547

2000

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Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X sub(1) receptor antagonist

Neuropharmacology, 2005-03, Vol.48 (3), p.461-468

2005

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Monomeric and Dimeric Byproducts are the Principal Functional Elements of Higher Order P2X1 Concatamers

Molecular pharmacology, 2003-01, Vol.63 (1), p.243-252

2003

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The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X(1) receptors

European journal of pharmacology, 2000-01, Vol.387 (3), p.R19-R21

2000

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Voltage-dependent inhibition of the Na +,K + pump by tetraethylammonium

Biochimica et biophysica acta, 1998-07, Vol.1372 (2), p.289-300

1998

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Allosteric nature of P2X receptor activation probed by photoaffinity labelling

Electrophysiology: Basics, Methods, Modern Approaches and Applications

Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X receptor antagonist

The suramin analogue NF279 is a novel and potent antagonist selective for the P2X(1) receptor

Roles of Individual N-Glycans for ATP Potency and Expression of the Rat P2X1 Receptor

P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels

Electrophysiology: Basics, Modern Approaches and Applications

The suramin analog 4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis (carbonylimino)))tetra-kis-benzenesulfonic acid (NF110) potently blocks P2X3 receptors: subtype selectivity is determined by location of sulfonic acid groups

A Functional P2X7 Splice Variant with an Alternative Transmembrane Domain 1 Escapes Gene Inactivation in P2X7 Knock-out Mice

Awareness of Crime-Relevant Information and the Guilty Knowledge Test

Blue Native Page as a Useful Method for the Analysis of the Assembly of Distinct Combinations of Nicotinic Acetylcholine Receptor Subunits

Novel ligands for P2 receptor subtypes in innervated tissues

Evolving view of quaternary structures of ligand-gated ion channels

Novel properties of the depolarization-induced endogenous sodium conductance in the Xenopus laevis oocyte

The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor

NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors

Characteristics of Na +/K +-ATPase mediated proton current in Na +- and K +-free extracellular solutions. Indications for kinetic similarities between H +/K +-ATPase and Na +/K +-ATPase

Desensitization Masks Nanomolar Potency of ATP for the P2X1 Receptor

The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X1 receptors

NF279: a novel potent and selective antagonist of P2X receptor-mediated responses

Roles of Individual N-Glycans for ATP Potency and Expression of the Rat P2X sub(1) Receptor

Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X sub(1) receptor antagonist

Monomeric and Dimeric Byproducts are the Principal Functional Elements of Higher Order P2X1 Concatamers

The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X(1) receptors

Voltage-dependent inhibition of the Na +,K + pump by tetraethylammonium

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