AAAAAA

   
Results: 1-25 | 26-50 | 51-56
Results: 1-25/56
P2X(1) AND P2X(3) RECEPTORS FORM STABLE TRIMERS - A NOVEL STRUCTURAL MOTIF OF LIGAND-GATED ION CHANNELS
Authors: NICKE A BAUMERT HG RETTINGER J EICHELE A LAMBRECHT G MUTSCHLER E SCHMALZING G
Citation: A. Nicke et al., P2X(1) AND P2X(3) RECEPTORS FORM STABLE TRIMERS - A NOVEL STRUCTURAL MOTIF OF LIGAND-GATED ION CHANNELS, EMBO journal, 17(11), 1998, pp. 3016-3028
NEURONAL P2X-LIKE RECEPTORS MEDIATE CHOLINERGIC CONTRACTION VIA POSTJUNCTIONAL MUSCARINIC M-3-RECEPTORS IN GUINEA-PIG ILEAL LONGITUDINAL SMOOTH-MUSCLE
Authors: CZECHE S NIEBEL B MUTSCHLER E LAMBRECHT G
Citation: S. Czeche et al., NEURONAL P2X-LIKE RECEPTORS MEDIATE CHOLINERGIC CONTRACTION VIA POSTJUNCTIONAL MUSCARINIC M-3-RECEPTORS IN GUINEA-PIG ILEAL LONGITUDINAL SMOOTH-MUSCLE, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 78-78
AFFINITY OF THE ANTIPARKINSONIAN DRUG, BUDIPINE, AT NATIVE MUSCARINICM-1-M-3 AND HUMAN RECOMBINANT M1-M5 RECEPTORS
Authors: KEIM C MUTSCHLER E LAMBRECHT G ELTZE M
Citation: C. Keim et al., AFFINITY OF THE ANTIPARKINSONIAN DRUG, BUDIPINE, AT NATIVE MUSCARINICM-1-M-3 AND HUMAN RECOMBINANT M1-M5 RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 79-79
DETERMINATION OF THE QUATERNARY STRUCTURE OF LIGAND-GATED ION CHANNELS BY BLUE NATIVE POLYACRYLAMIDE-GEL ELECTROPHORESIS
Authors: NICKE A RETTINGER J EICHELE A LAMBRECHT G MUTSCHLER E SCHMALZING G
Citation: A. Nicke et al., DETERMINATION OF THE QUATERNARY STRUCTURE OF LIGAND-GATED ION CHANNELS BY BLUE NATIVE POLYACRYLAMIDE-GEL ELECTROPHORESIS, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 115-115
NF279 AND NF031, NEW SELECTIVE P2X-RECEPTOR ANTAGONISTS
Authors: DAMER S NIEBEL B NICKEL P ARDANUY U MUTSCHLER E LAMBRECHT G
Citation: S. Damer et al., NF279 AND NF031, NEW SELECTIVE P2X-RECEPTOR ANTAGONISTS, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 122-122
M-2 RECEPTOR-BINDING OF THE SELECTIVE ANTAGONIST AF-DX-384 - POSSIBLEINVOLVEMENT OF THE COMMON ALLOSTERIC SITE
Authors: TRANKLE C ANDRESEN I LAMBRECHT G MOHR K
Citation: C. Trankle et al., M-2 RECEPTOR-BINDING OF THE SELECTIVE ANTAGONIST AF-DX-384 - POSSIBLEINVOLVEMENT OF THE COMMON ALLOSTERIC SITE, Molecular pharmacology, 53(2), 1998, pp. 304-312
NF279 - A NOVEL POTENT AND SELECTIVE ANTAGONIST OF P2X RECEPTOR-MEDIATED RESPONSES
Authors: DAMER S NIEBEL B CZECHE S NICKEL P ARDANUY U SCHMALZING G RETTINGER J MUTSCHLER E LAMBRECHT G
Citation: S. Damer et al., NF279 - A NOVEL POTENT AND SELECTIVE ANTAGONIST OF P2X RECEPTOR-MEDIATED RESPONSES, European journal of pharmacology, 350(1), 1998, pp. 5-6
QUANTITATIVE COLORIMETRIC AND GAS-CHROMATOGRAPHIC DETERMINATION OF ARECAIDINE PROPARGYL ESTER
Authors: LANGER K LAMBRECHT G MOSER U MUTSCHLER E KREUTER J
Citation: K. Langer et al., QUANTITATIVE COLORIMETRIC AND GAS-CHROMATOGRAPHIC DETERMINATION OF ARECAIDINE PROPARGYL ESTER, Journal of chromatography B. Biomedical sciences and applications, 692(2), 1997, pp. 345-350
THROMBOLYSIS IN CENTRAL SPLANCHNIC THROMBOSIS
Authors: DEMEY HE LAMBRECHT G MOORKENS G MICHIELSEN P VANDENENDE J BOSSAERT LL
Citation: He. Demey et al., THROMBOLYSIS IN CENTRAL SPLANCHNIC THROMBOSIS, Journal of intensive care medicine, 12(5), 1997, pp. 269-275
METHYLMETHACRYLATE SULFOPROPYLMETHACRYLATE COPOLYMER NANOPARTICLES FOR DRUG-DELIVERY - PART II - ARECAIDINE PROPARGYL ESTER AND PILOCARPINELOADING AND IN-VITRO RELEASE
Authors: LANGER K STIENEKER F LAMBRECHT G MUTSCHLER E KREUTER J
Citation: K. Langer et al., METHYLMETHACRYLATE SULFOPROPYLMETHACRYLATE COPOLYMER NANOPARTICLES FOR DRUG-DELIVERY - PART II - ARECAIDINE PROPARGYL ESTER AND PILOCARPINELOADING AND IN-VITRO RELEASE, International journal of pharmaceutics, 158(2), 1997, pp. 211-217
METHYLMETHACRYLATE SULFOPROPYLMETHACRYLATE COPOLYMER NANOPARTICLES FOR DRUG-DELIVERY - PART III - EVALUATION AS DRUG-DELIVERY SYSTEM FOR OPHTHALMIC APPLICATIONS
Authors: LANGER K MUTSCHLER E LAMBRECHT G MAYER D TROSCHAU G STIENEKER F KREUTER J
Citation: K. Langer et al., METHYLMETHACRYLATE SULFOPROPYLMETHACRYLATE COPOLYMER NANOPARTICLES FOR DRUG-DELIVERY - PART III - EVALUATION AS DRUG-DELIVERY SYSTEM FOR OPHTHALMIC APPLICATIONS, International journal of pharmaceutics, 158(2), 1997, pp. 219-231
CHARACTERIZATION OF POSTJUNCTIONAL MUSCARINIC RECEPTORS MEDIATING CONTRACTION IN RAT ANOCOCCYGEUS MUSCLE
Authors: WEISER M MUTSCHLER E LAMBRECHT G
Citation: M. Weiser et al., CHARACTERIZATION OF POSTJUNCTIONAL MUSCARINIC RECEPTORS MEDIATING CONTRACTION IN RAT ANOCOCCYGEUS MUSCLE, Naunyn-Schmiedeberg's archives of pharmacology, 356(5), 1997, pp. 671-677
EVIDENCE FOR MUSCARINIC M-4 RECEPTORS MEDIATING NONADRENERGIC NONCHOLINERGIC RELAXATIONS IN RABBIT ANOCOCCYGEUS MUSCLE
Authors: GROSS J MUTSCHLER E LAMBRECHT G
Citation: J. Gross et al., EVIDENCE FOR MUSCARINIC M-4 RECEPTORS MEDIATING NONADRENERGIC NONCHOLINERGIC RELAXATIONS IN RABBIT ANOCOCCYGEUS MUSCLE, Naunyn-Schmiedeberg's archives of pharmacology, 356(4), 1997, pp. 505-516
PD102807 - A NOVEL M-4-SELECTIVE MUSCARINIC ANTAGONIST
Authors: GROSS J AUGELLISZAFRAN CE CZECHE S FRIEBE T JAEN JC PENVOSEYI JR SCHWARZ RD MUTSCHLER E LAMBRECHT G
Citation: J. Gross et al., PD102807 - A NOVEL M-4-SELECTIVE MUSCARINIC ANTAGONIST, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 62-62
CONTRACTILE RESPONSES TO MUSCARINIC AGONISTS IN RAT ANOCOCCYGEUS MUSCLE ARE MEDIATED BY POSTJUNCTIONAL M-3 RECEPTORS
Authors: WEISER M WAELBROECK M LAMBRECHT G MUTSCHLER E
Citation: M. Weiser et al., CONTRACTILE RESPONSES TO MUSCARINIC AGONISTS IN RAT ANOCOCCYGEUS MUSCLE ARE MEDIATED BY POSTJUNCTIONAL M-3 RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 67-67
STEREOSELECTIVE INTERACTION OF GLYCOPYRRONIUM BROMIDE WITH 4 MUSCARINIC RECEPTOR SUBTYPES
Authors: CZECHE S ELGERT M NOE C WAELBROECK M MUTSCHLER E LAMBRECHT G
Citation: S. Czeche et al., STEREOSELECTIVE INTERACTION OF GLYCOPYRRONIUM BROMIDE WITH 4 MUSCARINIC RECEPTOR SUBTYPES, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 68-68
INVESTIGATION OF THE QUATERNARY STRUCTURE OF THE P2X(1) RECEPTOR USING BIFUNCTIONAL PPADS ANALOGS AS CROSS-LINKERS
Authors: NICKE A BAUMERT HG SPATZKUMBEL G EICHELE A LAMBRECHT G MUTSCHLER E SCHMALZING G
Citation: A. Nicke et al., INVESTIGATION OF THE QUATERNARY STRUCTURE OF THE P2X(1) RECEPTOR USING BIFUNCTIONAL PPADS ANALOGS AS CROSS-LINKERS, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 106-106
BIOSYNTHESIS AND ASSEMBLY OF RAT P2X(1), P2X(2) AND P2X(3) RECEPTORS
Authors: EICHELE A NICKE A MUTSCHLER M LAMBRECHT G SCHMALZING G
Citation: A. Eichele et al., BIOSYNTHESIS AND ASSEMBLY OF RAT P2X(1), P2X(2) AND P2X(3) RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 107-107
STEREOSELECTIVE INTERACTION OF P-FLUORO-TRIHEXYPHENIDYL AND ITS METHIODIDE WITH 4 MUSCARINIC RECEPTOR SUBTYPES
Authors: LAMBRECHT G PFAFF O AASEN AJ SJO P MUTSCHLER E WAELBROECK M
Citation: G. Lambrecht et al., STEREOSELECTIVE INTERACTION OF P-FLUORO-TRIHEXYPHENIDYL AND ITS METHIODIDE WITH 4 MUSCARINIC RECEPTOR SUBTYPES, Life sciences, 60(13-14), 1997, pp. 8-8
ANTIMUSCARINIC PROPERTIES OF THE STEREOISOMERS OF GLYCOPYRRONIUM BROMIDE
Authors: CZECHE S ELGERT M NOE C WAELBROECK M MUTSCHLER E LAMBRECHT G
Citation: S. Czeche et al., ANTIMUSCARINIC PROPERTIES OF THE STEREOISOMERS OF GLYCOPYRRONIUM BROMIDE, Life sciences, 60(13-14), 1997, pp. 9-9
FUNCTIONAL-CHARACTERIZATION OF PD102807 - A NOVEL M(4)-SELECTIVE MUSCARINIC ANTAGONIST
Authors: GROSS J AUGELLISZAFRAN CE CZECHE S FRIEBE T JAEN JC PENVOSEYI JR SCHWARZ RD MUTSCHLER E LAMBRECHT G
Citation: J. Gross et al., FUNCTIONAL-CHARACTERIZATION OF PD102807 - A NOVEL M(4)-SELECTIVE MUSCARINIC ANTAGONIST, Life sciences, 60(13-14), 1997, pp. 12-12
FUNCTIONAL-CHARACTERIZATION OF POSTJUNCTIONAL MUSCARINIC RECEPTORS INRAT ANOCOCCYGEUS MUSCLE
Authors: WEISER M WAELBROECK M LAMBRECHT G MUTSCHLER E
Citation: M. Weiser et al., FUNCTIONAL-CHARACTERIZATION OF POSTJUNCTIONAL MUSCARINIC RECEPTORS INRAT ANOCOCCYGEUS MUSCLE, Life sciences, 60(13-14), 1997, pp. 61-61
VASOCONSTRICTOR RESPONSES VIA P2X-RECEPTORS ARE SELECTIVELY ANTAGONIZED BY NF023 IN RABBIT ISOLATED AORTA AND SAPHENOUS ARTERY
Authors: ZIYAL R ZIGANSHIN AU NICKEL P ARDANUY U MUTSCHLER E LAMBRECHT G BURNSTOCK G
Citation: R. Ziyal et al., VASOCONSTRICTOR RESPONSES VIA P2X-RECEPTORS ARE SELECTIVELY ANTAGONIZED BY NF023 IN RABBIT ISOLATED AORTA AND SAPHENOUS ARTERY, British Journal of Pharmacology, 120(5), 1997, pp. 954-960
DESIGN AND PHARMACOLOGY OF SELECTIVE P-2-PURINOCEPTOR ANTAGONISTS
Authors: LAMBRECHT G
Citation: G. Lambrecht, DESIGN AND PHARMACOLOGY OF SELECTIVE P-2-PURINOCEPTOR ANTAGONISTS, Journal of autonomic pharmacology, 16(6), 1996, pp. 341-344
PHARMACOLOGICAL DISCRIMINATION BETWEEN ENANTIOMERIC GERMANES BY MUSCARINIC RECEPTORS - A STUDY ON GERMANIUM SILICON BIOISOSTERISM/
Authors: TACKE R REICHEL D JONES PG HOU X WAELBROECK M GROSS J MUTSCHLER E LAMBRECHT G
Citation: R. Tacke et al., PHARMACOLOGICAL DISCRIMINATION BETWEEN ENANTIOMERIC GERMANES BY MUSCARINIC RECEPTORS - A STUDY ON GERMANIUM SILICON BIOISOSTERISM/, Journal of organometallic chemistry, 521(1-2), 1996, pp. 305-323
Risultati: 1-25 | 26-50 | 51-56