Zobrazeno 1 - 10
of 241
pro vyhledávání: '"G Hanft"'
Autor:
Carrillo, Elba D.1 (AUTHOR) elcarrillo@cinvestav.mx, Alvarado, Juan A.1 (AUTHOR), Hernández, Ascención1 (AUTHOR), Lezama, Ivonne1 (AUTHOR), García, María C.1 (AUTHOR), Sánchez, Jorge A.1 (AUTHOR) jsanchez@cinvestav.mx
Publikováno v:
International Journal of Molecular Sciences. Oct2024, Vol. 25 Issue 19, p10798. 13p.
Publikováno v:
ResearcherID
This paper reviews recent studies that have aimed to establish the relative bioavailability of a new oral formulation of meloxicam, and to evaluate its safety and efficacy in a clinical setting. For the bioavailability study, 16 healthy volunteers we
Publikováno v:
European Journal of Clinical Pharmacology. 40:373-378
The effects of a single dose of 2 mg/kg amrinone (60 min constant rate IV infusion) have been assessed in a double-blind, placebo-controlled, within-subject cross-over study in six healthy volunteers. Combined impedance cardiography, phonocardiograph
Publikováno v:
American Journal of Noninvasive Cardiology. 5:115-120
Ten healthy males were profiled noninvasively by impedance cardiography, electrocardiography, and phonocardiography 1 h before and up to 8 h after administration of an investigational PDE III phosphodiesterase inhibitor (SK & F 94836). The study was
Publikováno v:
Journal of Cardiovascular Pharmacology. 15:S8-S16
Urapidil and three derivatives with hypotensive properties (5-acetyl-, 5-formyl-, 5-methylurapidil) bind selectively to 5-HT receptors of the 5-HT1A subtype and to alpha 1-adrenoceptors labeled by [3H]8-OH-DPAT and [3H]prazosin, respectively. Binding
Autor:
E M, Lemmel, W, Bolten, R, Burgos-Vargas, P, Platt, M, Nissilä, D, Sahlberg, O, Björneboe, H, Baumgartner, J P, Valat, P, Franchimont, E, Bluhmki, G, Hanft, M, Distel
Publikováno v:
The Journal of rheumatology. 24(2)
To evaluate the efficacy and safety of meloxicam, a new acidic enolic nonsteroidal anti-inflammatory drug, at doses of 7.5 and 15 mg once daily in patients with rheumatoid arthritis (RA).Meloxicam 15 and 7.5 mg daily was administered for 21 days in t
Autor:
G. Hanft, Natasha B. Leighl, Steve Gyorffy, Quincy Chu, Scott A. Laurie, D. Trommeshauser, Peter M. Ellis, Gerd Munzert
Publikováno v:
Journal of Clinical Oncology. 26:8115-8115
8115 Background: BI 2536 is a novel, highly selective, potent inhibitor of Polo-like kinase 1 (Plk1), a key regulator of mitotic progression. BI 2536 has demonstrated favorable tolerability and ant...
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 341(4)
We used novel highly subtype-selective antagonists to study whether alpha 1A- and/or alpha 1B-adrenoceptors mediate the stimulation of inositol phosphate generation by noradrenaline in rat cerebral cortex. Phentolamine (10 microM) and prazosin (100 n
Publikováno v:
Fine Focus. Spring2024, Vol. 10, p74-89. 16p.
Autor:
Wunnoo, Suttiwan1,2,3 (AUTHOR), Lorenzo-Leal, Ana C.3 (AUTHOR), Voravuthikunchai, Supayang P.1,2 (AUTHOR), Bach, Horacio3 (AUTHOR) hbach@mail.ubc.ca
Publikováno v:
PLoS ONE. 10/20/2023, Vol. 18 Issue 10, p1-14. 14p.