M. Eltze

发表

In vitro and in vivo uroselectivity of B8805-033, an antagonist with high affinity at prostatic α1A- vs. α1B- and α1D-adrenoceptors

M. Michel, P. Hein, K. Sanders, 2001, Naunyn-Schmiedeberg's Archives of Pharmacology.

Functional characterization of muscarinic autoreceptors in rat and human neocortex

J. Zentner, T. Feuerstein, R. Jackisch, 2009, Journal of neurochemistry.

Contraction of guinea-pig gallbladder: muscarinic M3 or M4 receptors?

M. Eltze, H. König, B. Ullrich, 1997, European journal of pharmacology.

Glibenclamide is a competitive antagonist of cromakalim, pinacidil and RP 49356 in guinea-pig pulmonary artery.

M. Eltze, 1989, European journal of pharmacology.

Zardaverine: a cyclic AMP specific PDE III/IV inhibitor.

C. Schudt, S. Winder, M. Eltze, 1991, Agents and actions. Supplements.

The affinity, selectivity and biological activity of telenzepine enantiomers.

N. Birdsall, R. Boer, C. Schudt, 1989, European journal of pharmacology.

Muscarinic M1- and M2-receptors mediating opposite effects on neuromuscular transmission in rabbit vas deferens.

M. Eltze, 1988, European journal of pharmacology.

Montelukast exerts no acute direct effect on NO synthases.

A. Wendel, R. Lucas, J. Hamacher, 2007, Pulmonary pharmacology & therapeutics.

Celecoxib dilates guinea-pig coronaries and rat aortic rings and amplifies NO/cGMP signaling by PDE5 inhibition.

A. Hatzelmann, M. Kömhoff, T. Klein, 2007, Cardiovascular research.

Investigations on the mode of action of a new antihypertensive drug, urapidil, in the isolated rat vas deferens.

M. Eltze, 1979, European journal of pharmacology.

External ATP antagonizes the effect of potassium channel openers in guinea-pig ventricular papillary muscle.

P. Illés, M. Eltze, A. Bott, 1992, European journal of pharmacology.

Affinity profile at α1- and α2-adrenoceptor subtypes and in vitro cardiovascular actions of (+)-boldine

M. Michel, M. Eltze, B. Ullrich, 2002 .

In vivo efficacy in airway disease models of roflumilast, a novel orally active PDE4 inhibitor.

J. Barsig, D. Bundschuh, A. Hatzelmann, 2001, The Journal of pharmacology and experimental therapeutics.

Pathways involved in muscarinic M1 and M2 receptor stimulation in rabbit vas deferens.

M. Eltze, 1994, European journal of pharmacology.

In Vivo Characterization of the Novel Imidazopyridine BYK191023 [2-[2-(4-Methoxy-pyridin-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridine], a Potent and Highly Selective Inhibitor of Inducible Nitric-Oxide Synthase

R. Schermuly, M. Lehner, J. Barsig, 2006, Journal of Pharmacology and Experimental Therapeutics.

Involvement of muscarinic M2 and M3, but not of M1 and M4 receptors in vagally stimulated contractions of rabbit bronchus/trachea.

M. Galvan, M. Eltze, 1994, Pulmonary pharmacology.

Characterization of vascular P2 purinoceptors in the rat isolated perfused kidney.

M. Eltze, B. Ullrich, 1996, European journal of pharmacology.

Pharmacological evidence for selective inhibition of gastric acid secretion by telenzepine, a new antimuscarinic drug.

W. Simon, C. Schudt, M. Eltze, 1985, European journal of pharmacology.

Specificity of the substituted benzimidazole B 823-08: a prodrug for gastric proton pump inhibition.

C. Schudt, K. Heintze, M. Eltze, 1987, Pharmacology.

Affinity and selectivity of biperiden enantiomers for muscarinic receptor subtypes.

M. Eltze, V. Figala, 1988, European journal of pharmacology.

Biotransformation of urapidil: metabolites in serum and urine and their biological activity in vitro and in vivo.

K. Sanders, M. Eltze, N. Kolassa, 1984, Archives internationales de pharmacodynamie et de therapie.

Characterization of muscarinic receptors mediating vasodilation in rat perfused kidney.

E. Mutschler, R. Tacke, U. Moser, 1993, European journal of pharmacology.

The sulphoxide moiety of substituted benzimidazoles is essential for inhibition of parietal cell K+/H+‐ATPase

K. Sewing, W. Beil, C. Schudt, 1986, British journal of pharmacology.

Affinity profiles of pizotifen, ketotifen and other tricyclic antimuscarinics at muscarinic receptor subtypes M1, M2 and M3.

E. Mutschler, G. Lambrecht, M. Eltze, 1992, European journal of pharmacology.

Affinity profiles of BTM-1086 and BTM-1041 at muscarinic receptor subtypes and at H1- and alpha 1-receptors.

E. Mutschler, G. Lambrecht, R. Boer, 1989, European journal of pharmacology.

Vasodilatation elicited by 5-HT1A receptor agonists in constant-pressure-perfused rat kidney is mediated by blockade of alpha 1A-adrenoceptors.

K. Sanders, R. Boer, M. Eltze, 1991, European journal of pharmacology.

Multiple mechanisms of action: the pharmacological profile of budipine.

M. Eltze, 1999, Journal of neural transmission. Supplementum.

Stereoselective inhibition of thromboxane-induced coronary vasoconstriction by 1,4-dihydropyridine calcium channel antagonists.

H. Boss, K. Sanders, W. Ulrich, 1990, Chirality.

Telenzepine inhibits electrically-stimulated, acetylcholine plus histamine-mediated acid secretion in the mouse isolated stomach by blockade of M1 muscarine receptors

R. Boer, M. Eltze, W. Kromer, 2004, Naunyn-Schmiedeberg's Archives of Pharmacology.

Characterization of the α1-adrenoceptor subtype mediating contraction of guinea-pig spleen

M. Eltze, 1994 .

The adrenoceptor agonist, SDZ NVI 085, discriminates between α1A- and α1B-adrenoceptor subtypes in vas deferens, kidney and aorta of the rat

R. Boer, M. Eltze, 1992 .

Evidence that α1B-adrenoceptors are involved in noradrenaline-induced contractions of rat tail artery

H. Pertz, S. Jähnichen, M. Eltze, 2004 .

Affinity of the Miotic Drug, Dapiprazole, at α1‐Adrenoceptor Subtypes A, B and D

M. Eltze, 1997 .

Failure of AH11110A to functionally discriminate between α1-adrenoceptor subtypes A, B and D or between α1- and α2-adrenoceptors

M. Eltze, H. König, B. Ullrich, 2001 .

Buspirone functionally discriminates tissues endowed with alpha1-adrenoceptor subtypes A, B, D and L.

M. Eltze, H. König, B. Ullrich, 1999, European journal of pharmacology.

Evidence that alpha(1B)-adrenoceptors are involved in noradrenaline-induced contractions of rat tail artery.

H. Pertz, S. Jähnichen, M. Eltze, 2004, European journal of pharmacology.

Affinity profile at alpha(1)- and alpha(2)-adrenoceptor subtypes and in vitro cardiovascular actions of (+)-boldine.

M. Michel, M. Eltze, B. Ullrich, 2002, European Journal of Pharmacology.

In vitro and in vivo uroselectivity of B8805-033, an antagonist with high affinity at prostatic alpha1A- vs. alpha1B- and alpha1D-adrenoceptors.

M. Michel, P. Hein, K. Sanders, 2001, Naunyn-Schmiedeberg's archives of pharmacology.

Functional evidence that alpha-1B adrenoceptors are involved in noradrenaline-induced contraction of rat tail artery

S. Jaêhnichen, H. Pertz, M. Eltze, 2003 .

Functional evidence for an α1B-adrenoceptor mediating contraction of the mouse spleen

M. Eltze, 1996 .

In functional experiments, risperidone is selective, not for the B, but for the A subtype of alpha 1-adrenoceptors.

M. Eltze, 1996, European journal of pharmacology.

Functional evidence for an alpha 1B-adrenoceptor mediating contraction of the mouse spleen.

M. Eltze, 1996, European journal of pharmacology.

Is phosphodiesterase inhibition a relevant bronchospasmolytic principle?

C. Schudt, M. Eltze, R. Beume, 1989, Agents and actions. Supplements.

Cytoplasmic changes in level and distribution of glucose-6-phosphatase activities from rat liver during diethylnitrosamine-induced carcinogenesis.

R. Jackisch, A. Jung, M. Eltze, 1977, Chemico-Biological Interactions.

The Novel Imidazopyridine 2-[2-(4-Methoxy-pyridin-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridine (BYK191023) Is a Highly Selective Inhibitor of the Inducible Nitric-Oxide Synthase

Susanne Strand, S. Strand, M. Lehner, 2006, Molecular Pharmacology.

The Novel Imidazopyridine BYK 191023 is a Highly Selective Inhibitor of the Inducible Nitric Oxide Synthase

S. Strand, M. Lehner, J. Strassner, 2005 .

The effects of prodipine and budipine on 14C-5-hydroxytryptamine uptake and release by human blood platelets.

M. Eltze, 1980, Arzneimittel-Forschung.

Telenzepine enantiomers block muscarinic M1-receptors with opposite kinetics.

M. Eltze, 1990, European journal of pharmacology.

Assessment of selectivity of muscarinic antagonists for M1 and M2 receptors in rabbit isolated vas deferens.

M. Eltze, 1988, Pharmacology.

Stimulation by McN-A-343 and blockade by telenzepine of acid secretion in the mouse isolated stomach at histamine-liberating cells

W. Simon, M. Eltze, W. Kromer, 1989, Naunyn-Schmiedeberg's Archives of Pharmacology.

The Novel Imidazopyridine 2-[2-(4-Methoxy-pyridin-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridine (BYK191023) Is a Highly Selective Inhibitor of the Inducible Nitric-Oxide Synthase

S. Strand, M. Lehner, J. Strassner, 2006, Molecular Pharmacology.