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1 as associated with diuretic, natriuretic and hypotensive effects.
2 nal biochemical phenotype that exerts potent hypotensive effects.
3 ation related through negative inotropic and hypotensive effects.
4 leads to the best results in terms of ocular hypotensive effect and safety.
5 SC, at a dose selected for lack of long-term hypotensive effects at baseline).
6 the mechanism(s) responsible for this ocular hypotensive effect has not been established.
7                        We defined the portal hypotensive effect in rat models of sinusoidal PHT and t
8 ned by activation of vagal afferents and the hypotensive effect may be secondary to a reduction of ca
9 d mice, O-1918 dose-dependently inhibits the hypotensive effect of abn-cbd but not the hypotensive ef
10                                          The hypotensive effect of alpha2 agonists was completely abs
11      The aim of this work was to analyse the hypotensive effect of amaranth protein/peptides on spont
12 ribution of TRPV(1) receptors to the in vivo hypotensive effect of anandamide is equivocal.
13 on of icatibant significantly attenuated the hypotensive effect of captopril (maximal decrease in mea
14 uggest a link between the estrogen-dependent hypotensive effect of chronically administered ethanol a
15 abolished the bradycardia and attenuated the hypotensive effect of endomorphin 1.
16 aneous pellet, 14.2 microg/day) restored the hypotensive effect of ethanol to a level similar to that
17 action is involved in the estrogen-dependent hypotensive effect of ethanol.
18                                          The hypotensive effect of inhaled Y-27632 on hypoxic PH was
19           In EP2-/- mice, the characteristic hypotensive effect of intravenous PGE2 infusion was abse
20 B2-receptor antagonist, had no effect on the hypotensive effect of kallistatin yet it abolished the b
21           These data indicate that the early hypotensive effect of latanoprost in the mouse eye is as
22                                  The initial hypotensive effect of spinal anaesthesia is caused by a
23 n and counteracted the clinically beneficial hypotensive effect of stimulating alpha2a receptors in t
24 reported findings that ethanol abolishes the hypotensive effect of the alpha(2)-adrenoceptor agonist
25 he hypotensive effect of abn-cbd but not the hypotensive effect of the CB(1) receptor agonist (-)-11-
26                        To compare the ocular hypotensive effects of 15-keto latanoprost (KL) with the
27 rdiovascular regulation, which contribute to hypotensive effects of acupuncture.
28 e cardioprotective, bronchoconstrictive, and hypotensive effects of adenosine.
29 c receptor (alpha2A-AR) is necessary for the hypotensive effects of clonidine and other sympathoinhib
30 irs the diuretic and natriuretic but not the hypotensive effects of D(1)-like agonist stimulation.
31                           The early and late hypotensive effects of endotoxin were attenuated with 20
32 hypothesis that a greater attenuation of the hypotensive effects of losartan would be observed in rat
33 ons were independently lesioned, the chronic hypotensive effects of the AT(1) receptor blocker losart
34 the LHA or PAG with lidocaine attenuates the hypotensive effects produced by electrical stimulation o
35 no greater attenuation of losartan's chronic hypotensive effects than animals with lesion of either t
36            In addition to their sedative and hypotensive effect, their curare-like activity and struc
37                                          The hypotensive effects were observed within 3 wk after the