H. Batink

发表

The interaction between methylene blue and the cholinergic system

M. Pfaffendorf, T. Bruning, H. Batink, 1997, British journal of pharmacology.

Pharmacologic characterization in vitro and in vivo of iodine 123-labeled derivatives of the β-adrenoceptor antagonist CGP 12177, designed for the imaging of cardiac β-receptors

E. A. Royen, G. Somsen, M. Pfaffendorf, 1996, Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology.

Thyroid hormone modulates inotropic responses, α-adrenoceptor density and catecholamine concentrations in the rat heart

M. Pfaffendorf, H. Batink, P. Zwieten, 1996, Naunyn-Schmiedeberg's Archives of Pharmacology.

Cardiac sympathetic neuronal function in left ventricular volume and pressure overload.

K. Lie, E. V. van Royen, G. Somsen, 1996, Cardiovascular research.

The lens proteins of a marine invertebrate Octopus vulgaris.

H. Batink, A. Dohrn, W. F. Bon, 1967, Biochimica et biophysica acta.

Cardiac iodine-123 metaiodobenzylguanidine uptake in animals with diabetes mellitus and/or hypertension

K. D. de Bruin, E. A. Royen, G. Somsen, 1996, European Journal of Nuclear Medicine.

Beta-andrenoceptors in the hearts of diabetic-hypertensive rats: radioligand binding and functional experiments.

M. Pfaffendorf, H. Batink, P. V. van Zwieten, 1997, Blood pressure.

Characterization of flufylline, fluprofylline, ritanserin, butanserin and R 56413 with respect to in‐vivo α1‐, α2‐ and 5‐HT2‐receptor antagonism and in‐vitro affinity for α1‐, α2‐ and 5‐HT2‐receptors: comparison with ketanserin

E. Boddeke, H. Batink, M. Thoolen, 1986 .

Characterization of flufylline, fluprofylline, ritanserin, butanserin and R 56413 with respect to in-vivo alpha 1-,alpha 2- and 5-HT2-receptor antagonism and in-vitro affinity for alpha 1-,alpha 2- and 5-HT2-receptors: comparison with ketanserin.

E. Boddeke, H. Batink, P. V. van Zwieten, 1986, The Journal of pharmacy and pharmacology.

Development of radioligands for the imaging of cardiac beta-adrenoceptors using SPECT. Part II: Pharmacological characterization in vitro and in vivo of new 123I-labeled beta-adrenoceptor antagonists.

E. V. van Royen, G. Somsen, M. Pfaffendorf, 1997, Nuclear medicine and biology.

Synthesis and in vitro and in vivo characteristics of an iodinated analogue of the beta-adrenoceptor antagonist carazolol.

E. V. van Royen, G. Somsen, M. Pfaffendorf, 1996, Journal of medicinal chemistry.

Angiotensin II-induced increase in slowly exchanging 45Ca2+ in relation to contractile responses of rat and guinea-pig aorta

H. Batink, P. A. Zwieten, P. Heiningen, 1991, Naunyn-Schmiedeberg's Archives of Pharmacology.

Possible mechanism of the negative inotropic effect of α1‐adrenoceptor agonists in rat isolated left atria after exposure to free radicals

M. Michel, M. Pfaffendorf, H. Batink, 1998, British journal of pharmacology.

Thyroid status affects the rat cardiac beta-adrenoceptor system transiently and time-dependently.

M. Michel, M. Pfaffendorf, H. Batink, 1998, Journal of autonomic pharmacology.

Comparative physicochemical investigations on the lens proteins of fishes.

H. Batink, A. Dohrn, W. F. Bon, 1968, Experimental eye research.

Discrimination by N-ethylmaleimide between the chronotropic and inotropic response to muscarinic receptor stimulation in rat atrium

H. Batink, H. Doods, P. A. Zwieten, 1986, Naunyn-Schmiedeberg's Archives of Pharmacology.

Correlation between the affinity for [3H]mianserin-labelled receptors in brain and antagonism of the serotonin pressor response in pithed rats.

P. Timmermans, H. Batink, P. V. van Zwieten, 1983, Biochemical pharmacology.

Hypotensive activity of serotonin antagonists; correlation with alpha 1-adrenoceptor and serotonin receptor blockade.

P. Timmermans, H. Batink, P. V. van Zwieten, 1983, Life sciences.

Postsynaptic alpha 1- and alpha 2-adrenoceptor blocking properties of (dihydro)quinidine and (dihydro)quinine.

P. Timmermans, J. V. van Meel, H. Batink, 1983, Arzneimittel-Forschung.

Lack of relationship between intrinsic activity and susceptibility of pressor responses to blockade by nifedipine among the α2 agonists B-HT 920 and B-HT 958

P. Timmermans, B. Wilffert, H. Batink, 1984, Naunyn-Schmiedeberg's Archives of Pharmacology.

Interference of enantiomers of lofexidine with alpha-adrenoceptors.

P. Timmermans, B. Wilffert, H. Batink, 1985, Archives internationales de pharmacodynamie et de therapie.

Quantitative relationships between alpha-adrenergic activity and binding affinity of alpha-adrenoceptor agonists and antagonists.

P. Timmermans, B. Wilffert, H. Batink, 1984, Journal of medicinal chemistry.

Abstracts of papers Pharmacological meeting

N. Ramsey, J. M. Ree, M. Danhof, 1985, Pharmaceutisch Weekblad.

Probing the selectivity of allosteric modulators of muscarinic receptors at other G-protein-coupled receptors.

K. Mohr, C. Tränkle, M. Pfaffendorf, 2000, Journal of autonomic pharmacology.

Reduced muscarinic cholinoceptor density and sensitivity in various models of experimental cardiac hypertrophy.

M. Pfaffendorf, H. Batink, P. V. van Zwieten, 1995, Journal of autonomic pharmacology.

Reactive oxygen species potentiate the negative inotropic effect of cardiac M2-muscarinic receptor stimulation

M. Pfaffendorf, H. Batink, P. V. van Zwieten, 2001, Naunyn-Schmiedeberg's Archives of Pharmacology.

Analysis of the displaceable binding of the hypotensive drug R 28935 in rat brain.

P. Timmermans, H. Batink, P. V. van Zwieten, 1982, Biochemical pharmacology.

Specific binding of threo 1-{1-[2-(1,4-benzo-dioxane-2-yl)-2-hydroxyethyl] 4-piperidyl}-2-benzimidazolinone (R 29814), to rat brain membranes

P. Timmermans, H. Batink, P. A. Zwieten, 1982, Neuropharmacology.

Hypotensive properties of benzodioxane derivatives structurally related to R 28935. Comparison of activity with some receptor affinities.

P. Timmermans, H. Batink, P. V. van Zwieten, 1982, Archives internationales de pharmacodynamie et de therapie.

The interaction between methylene blue and the cholinergic system

H. Batink, T. Bruning, Martin Pfaffendorf, 1997, British journal of pharmacology.