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1 ripheral nerve block or spinal clonidine, an alpha2-adrenergic agonist.
2 o assess anesthetic depth in the presence of alpha2-adrenergic agonists.
3  guanine nucleotide-sensitive binding of the alpha2-adrenergic agonist, [3H]UK-14,304.
4 ta-blockers, 4.01 (CrI, 0.48 to 7.43); 1995: alpha2-adrenergic agonists, 5.64 (CrI, 1.73 to 9.50); 19
5     In this review the authors will focus on alpha2-adrenergic agonists, a new class of sedative/anal
6                    Our findings suggest that alpha2-adrenergic agonists act via a Gi family member on
7 as to investigate the effects of a selective alpha2-adrenergic agonist, alpha-methylnorepinephrine (a
8                                The selective alpha2-adrenergic agonist, alphaMNE, was as effective as
9                                              Alpha2-adrenergic agonists also reduced stimulation of E
10  that Muller cells are unique in response to alpha2-adrenergic agonists and imply a role for Muller c
11 0 microM NE or 62% by 2 microM UK-14,304, an alpha2-adrenergic agonist, and reduced 63% by 10 microM
12                                              Alpha2 adrenergic agonists are used in the anesthetic ma
13                                          The alpha2-adrenergic agonists are unique.
14        Incubation with norepinephrine or the alpha2-adrenergic agonist BHT 920 also caused dose-depen
15 romoter (Thy1-CFP mice) to determine how the alpha2-adrenergic agonist brimonidine influences loss of
16 Similar actions were evoked by the selective alpha2 adrenergic agonist clonidine.
17 mg/kg i.p.) after chronic treatment with the alpha2-adrenergic agonist clonidine (200 microg/kg per d
18     We therefore examined the effects of the alpha2-adrenergic agonist clonidine on mean arterial pre
19 amezole to rats chronically treated with the alpha2-adrenergic agonist clonidine triggers a powerful
20 onist, phenylephrine (PHE; 0.5 mg/kg BW), an alpha2-adrenergic agonist, clonidine (CLON; 0.6 mg/kg BW
21 pha2-adrenergic receptors because a specific alpha2-adrenergic agonist could substitute for epinephri
22 ions of loss of consciousness (LOC) with the alpha2-adrenergic agonist dexmedetomidine and return of
23 inoimidazolidines including analogues of the alpha2 adrenergic agonist drug clonidine is elaborated.
24 viously, we found that sedation induced with alpha2-adrenergic agonists (e.g., dexmedetomidine) and s
25 nd atomoxetine than for the extended-release alpha2-adrenergic agonists guanfacine or clonidine (no s
26                We examine the effects of the alpha2 adrenergic agonist, guanfacine HCl, on responses
27                                              Alpha2-adrenergic agonists have specific and selective e
28 gonists and imply a role for Muller cells in alpha2-adrenergic agonist-induced photoreceptor protecti
29                          Dexmedetomidine, an alpha2 adrenergic agonist, is a useful sedative but can
30                          Dexmedetomidine, an alpha2-adrenergic agonist, is not approved by the Food a
31 es of this work were to study the effects of alpha2-adrenergic agonists on the inflammatory response
32                          Dexmedetomidine, an alpha2-adrenergic agonist, produces sedation and reduces
33 i.m. treatment with xylazine or UK14304, two alpha2-adrenergic agonists, reduced neutrophil migration
34               Immune modulation by selective alpha2-adrenergic agonists represents a novel, to our kn
35 ults indicate that systemically administered alpha2-adrenergic agonists selectively activate ERKs in
36 raarterial hindlimb infusion of the specific alpha2-adrenergic agonist UK 14,304 during KATP channel
37                Epinephrine and the selective alpha2-adrenergic agonist UK14304 reduced insulin secret
38 ood flows by its alpha1 (alpha1) and alpha2 (alpha2)-adrenergic agonist vasopressor actions.
39                                              Alpha2-adrenergic agonists xylazine and clonidine were a