Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Van Meel Jacques"'
Autor:
Hauf, Silke, Cole, Richard W., LaTerra, Sabrina, Zimmer, Christine, Schnapp, Gisela, Walter, Rainer, Heckel, Armin, van Meel, Jacques, Rieder, Conly L., Peters, Jan-Michael
Publikováno v:
The Journal of Cell Biology, 2003 Apr . 161(2), 281-294.
Externí odkaz:
https://www.jstor.org/stable/1621574
Autor:
Dengg, Marlene, van Meel, Jacques C.A. *
Publikováno v:
In Journal of Pharmacological and Toxicological Methods 2004 50(3):209-214
Publikováno v:
European Journal of Pharmacology. 218:35-41
Two new nonpeptide angiotensin II (AII) receptor antagonists, 4'-[(2-n-butyl-6-cyclohexylaminocarbonylamino-benzimidazole-1-yl)-methyl] biphenyl-2-carboxylic acid (BIBS 39) and 2-n-butyl-1-[4-(6-carboxy-2,5-dichlorobenzoylamino)-benzyl]-6-N-(methylam
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 351(6)
Recent data show that UD-CG 212 in nanomolar concentrations increases myofibrillar Ca++ responsiveness of chemically skinned cardiac preparations in the presence of elevated inorganic phosphate. We studied the effects of UD-CG 212 on cell shortening
Publikováno v:
European journal of pharmacology, 262(3), 247-253. Elsevier
The role of endothelium in angiotensin II-induced contractions of the rabbit aorta and the mechanism involved were investigated. Destruction of the endothelium significantly shifted the concentration-response curve for angiotensin II to the left in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9107a8c25fafc3e7e6a8abfebf8ecaf
https://pure.amc.nl/en/publications/endotheliumdependent-nitric-oxidemediated-inhibition-of-angiotensin-iiinduced-contractions-in-rabbit-aorta(9fd0ca2e-e256-45ea-b379-eb338a2a5519).html
https://pure.amc.nl/en/publications/endotheliumdependent-nitric-oxidemediated-inhibition-of-angiotensin-iiinduced-contractions-in-rabbit-aorta(9fd0ca2e-e256-45ea-b379-eb338a2a5519).html
Autor:
Robert M. Haigh, Van Meel Jacques
Publikováno v:
European journal of pharmacology. 247(3)
Mastoparan preferentially activates the G protein Gi in transmembrane signalling pathways. In heart tissue Gi couples receptors to negative inotropy so we have examined the effect of mastoparan on contractility in cardiac myocytes electrically stimul
Autor:
Michel Pairet, Henri Doods, Willi Dr Diederen, Marco Turconi, Wolfgang Wienen, Van Meel Jacques, Robert M. Haigh
Publikováno v:
European journal of pharmacology. 233(2-3)
The 5-HT4 receptor antagonist action of DAU 6285 was investigated in vivo in anesthetized pigs. DAU 6285 (0.3–3 mg/kg i.v.) dose dependently antagonized 5-hydroxytryptamine (5-HT)-induced tachycardiac responses. In contrast, the 5-HT3 receptor anta
Publikováno v:
Hypertension (0194911X); 1983 Supplement2, Vol. 5, pII-8-II-18, 11p
Publikováno v:
Journal of Cardiovascular Pharmacology; Jul/Aug1983, Vol. 5 Issue 4, p580-585, 6p
Autor:
Timmermans, Pieter B. M. W. M., de Jonge, Adriaan, van Meel, Jacques C. A., Mathy, Marie-Jeanne, van Zwieten, Pieter A.
Publikováno v:
Journal of Cardiovascular Pharmacology; Jan/Feb1983, Vol. 5 Issue 1, p1-11, 11p