Search Results - "Baumert, Hans G." :: K.UTB vyhledávací portál

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
Published in European journal of pharmacology (01.01.2000)

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Inhibitory action of PPADS on relaxant responses to adenine nucleotides or electrical field stimulation in guinea‐pig taenia coli and rat duodenum

by Windscheif, Ursula, Pfaff, Otmar, Ziganshin, Airat U., Hoyle, Charles H.V., Baumert, Hans G., Mutschler, Ernst, Burastock, Geoffrey, Lambrecht, Gunter
Published in British journal of pharmacology (01.08.1995)

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P2 receptor antagonist PPADS inhibits mesangial cell proliferation in experimental mesangial proliferative glomerulonephritis

by Rost, Sylvia, Daniel, Christoph, Schulze-Lohoff, Eckhard, Bäumert, Hans G., Lambrecht, Günter, Hugo, Christian
Published in Kidney international (01.11.2002)

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PPADS, a novel functionally selective antagonist of P2 purinoceptor-mediated responses

by Lambrecht, G, Friebe, T, Grimm, U, Windscheif, U, Bungardt, E, Hildebrandt, C, Bäumert, H G, Spatz-Kümbel, G, Mutschler, E
Published in European journal of pharmacology (07.07.1992)

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PPADS selectively antagonizes P2X‐purinoceptor‐mediated responses in the rabbit urinary bladder

by Ziganshin, Airat U., Hoyle, Charles H.V., Bo, Xuenong, Lambrecht, Günter, Mutschler, Ernst, Bäumert, Hans G., Burnstock, Geoffrey
Published in British journal of pharmacology (01.12.1993)

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Selective antagonism by PPADS at P2X‐purinoceptors in rabbit isolated blood vessels

by Ziganshin, Airat U., Hoyle, Charles H.V., Lambrecht, Günter, Mutschler, Ernst, Bäumert, Hans G., Burnstock, Geoffrey
Published in British journal of pharmacology (01.03.1994)

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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 (01.06.1998)

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The novel heteromeric bivalent ligand SB9 potently antagonizes P2Y1 receptor-mediated responses

by Lambrecht, Günter, Ganso, Matthias, Bäumert, Hans G, Spatz-Kümbel, Gerhard, Hildebrandt, Caren, Braun, Kirsten, Mutschler, Ernst
Published in Journal of the autonomic nervous system (03.07.2000)

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Vasoconstrictor and vasodilator responses to various agonists in the rat perfused mesenteric arterial bed: selective inhibition by PPADS of contractions mediated via P 2x ‐purinoceptors

by Windscheif, Ursula, Ralevic, Vera, Bäumert, Hans G., Mutschler, Ernst, Lambrecht, Günter, Burnstock, Geoffrey
Published in British journal of pharmacology (01.11.1994)

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Selective antagonism by PPADS at P 2X ‐purinoceptors in rabbit isolated blood vessels

by Ziganshin, Airat U., Hoyle, Charles H.V., Lambrecht, Günter, Mutschler, Ernst, Bäumert, Hans G., Burnstock, Geoffrey
Published in British journal of pharmacology (01.03.1994)

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Vasoconstrictor and vasodilator responses to various agonists in the rat perfused mesenteric arterial bed: selective inhibition by PPADS of contractions mediated via P2x‐purinoceptors

by Windscheif, Ursula, Ralevic, Vera, Bäumert, Hans G., Mutschler, Ernst, Lambrecht, Günter, Burnstock, Geoffrey
Published in British journal of pharmacology (01.11.1994)

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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
Published in European journal of pharmacology (2000)

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Identification of a cross‐linked double‐peptide from the catalytic site of the Ca 2+ ‐ATPase of sarcoplasmic reticulum formed by the Ca 2+ ‐ and pH‐dependent reaction with ATP γ P ‐imidazolidate

by Gutowski-Eckel, Zeynep, Mann, Karlheinz, Bäumert, Hans G.
Published in FEBS letters (21.06.1993)

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Identification of a cross-linked double-peptide from the catalytic site of the Ca(2+)-ATPase of sarcoplasmic reticulum formed by the Ca(2+)- and pH-dependent reaction with ATP gamma P-imidazolidate

by Gutowski-Eckel, Z, Mann, K, Bäumert, H G
Published in FEBS letters (21.06.1993)

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Characterization of the prejunctional muscarinic receptors mediating inhibition of evoked release of endogenous noradrenaline in rabbit isolated vas deferens

by Grimm, U, Fuder, H, Moser, U, Bümert, H G, Mutschler, E, Lambrecht, G
Published in Naunyn-Schmiedeberg's archives of pharmacology (01.01.1994)

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Identification of a cross-linked double-peptide from the catalytic site of the Ca2+-ATPase of sarcoplasmic reticulum formed by the Ca2+- and pH-dependent reaction with ATP γP-imidazolidate

by Gutowski-Eckel, Zeynep, Mann, Karlheinz, Bäumert, Hans G.
Published in FEBS letters (21.06.1993)

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PPADS selectively antagonizes P 2X ‐purinoceptor‐mediated responses in the rabbit urinary bladder

by Ziganshin, Airat U., Hoyle, Charles H.V., Bo, Xuenong, Lambrecht, Günter, Mutschler, Ernst, Bäumert, Hans G., Burnstock, Geoffrey
Published in British journal of pharmacology (01.12.1993)

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