Search Results - Rettinger, Günter

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  1. 1
    The “80 Joule Criterion” reconsidered today

    The “80 Joule Criterion” reconsidered today by Rettinger, Günter

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  2. 2
    P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels

    P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels by Nicke, Annette, Bäumert, Hans G., Rettinger, Jürgen, Eichele, Annette, Lambrecht, Günter, Mutschler, Ernst, Schmalzing, Günther

    Published in The EMBO journal
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  3. 3
    Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist

    Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist by Rettinger, Jürgen, Braun, Kirsten, Hochmann, Henrike, Kassack, Matthias U, Ullmann, Heiko, Nickel, Peter, Schmalzing, Günther, Lambrecht, Günter

    Published in Neuropharmacology
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  4. 4
    The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor

    The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor by RETTINGER, J, SCHMALZING, G, DAMER, S, MÜLLER, G, NICKEL, P, LAMBRECHT, G

    Published in Neuropharmacology
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  5. 5
    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

    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... by Hausmann, Ralf, Rettinger, Jürgen, Gerevich, Zoltan, Meis, Sabine, Kassack, Matthias U., Illes, Peter, Lambrecht, Günter, Schmalzing, Günther

    Published in Molecular pharmacology
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  6. 6
    NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors

    NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors by Braun, K, Rettinger, J, Ganso, M, Kassack, M, Hildebrandt, C, Ullmann, H, Nickel, P, Schmalzing, G, Lambrecht, G

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  7. 7
    The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X1 receptors

    The novel pyridoxal-5'-phosphate derivative PPNDS potently antagonizes activation of P2X1 receptors by LAMBRECHT, G, RETTINGER, J, MUTSCHLER, E, BÄUMERT, H. G, CZECHE, S, DAMER, S, GANSO, M, HILDEBRANDT, C, NIEBEL, B, SPATZ-KÜMBEL, G, SCHMALZING, G

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  8. 8
    NF279: a novel potent and selective antagonist of P2X receptor-mediated responses

    NF279: a novel potent and selective antagonist of P2X receptor-mediated responses by Damer, Susanne, Niebel, Beate, Czeche, Sittah, Nickel, Peter, Ardanuy, Ursula, Schmalzing, Günther, Rettinger, Jürgen, Mutschler, Ernst, Lambrecht, Günter

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  9. 9
    Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X 1 receptor antagonist

    Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X 1 receptor antagonist by Rettinger, Jürgen, Braun, Kirsten, Hochmann, Henrike, Kassack, Matthias U., Ullmann, Heiko, Nickel, Peter, Schmalzing, Günther, Lambrecht, Günter

    Published in Neuropharmacology
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  10. 10
    The suramin analogue NF279 is a novel and potent antagonist selective for the P2X 1 receptor

    The suramin analogue NF279 is a novel and potent antagonist selective for the P2X 1 receptor by Rettinger, Jürgen, Schmalzing, Günther, Damer, Susanne, Müller, Gregor, Nickel, Peter, Lambrecht, Günter

    Published in Neuropharmacology
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  11. 11
    NF449: a subnanomolar potency antagonist at recombinant rat P2X 1 receptors

    NF449: a subnanomolar potency antagonist at recombinant rat P2X 1 receptors by Braun, Kirsten, Rettinger, Jürgen, Ganso, Matthias, Kassack, Matthias, Hildebrandt, Caren, Ullmann, Heiko, Nickel, Peter, Schmalzing, Günther, Lambrecht, Günter

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  12. 12
    The novel pyridoxal-5′-phosphate derivative PPNDS potently antagonizes activation of P2X 1 receptors

    The novel pyridoxal-5′-phosphate derivative PPNDS potently antagonizes activation of P2X 1 receptors by Lambrecht, Günter, Rettinger, Jürgen, Bäumert, Hans G, Czeche, Sittah, Damer, Susanne, Ganso, Matthias, Hildebrandt, Caren, Niebel, Beate, Spatz-Kümbel, Gerhard, Schmalzing, Günther, Mutschler, Ernst

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