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1 sts, like clonidine, are very different from betaxolol.
2 tion of [Ca2+]i was significantly reduced by betaxolol.
3 I-118,551, but not the beta-1 AR antagonist, betaxolol.
4 antagonist alprenolol or the inverse agonist betaxolol.
5 terenol in the order timolol > propranolol > betaxolol.
6 1.85; 3.13), brinzolamide 2.42 (1.62; 3.23), betaxolol 2.24 (1.59; 2.88), and unoprostone 1.91 (1.15;
10 d from 6.19 to 23.53 microM, indicating that betaxolol acts as a non-competitive inhibitor of glutama
11 experiments provide supporting evidence that betaxolol acts in a manner consistent with preventing re
14 energic antagonist timolol, propranolol, and betaxolol also inhibited Na+, K+, Cl- cotransport stimul
15 he mean IOP for the experimental eyes in the betaxolol and apraclonidine groups was lower than that i
16 he experimental eyes of animals administered betaxolol and apraclonidine were 29 +/- 7 and 29 +/- 4 m
18 the beta1 and beta2 NE receptor antagonists betaxolol and ICI 118551 or vehicle into the CeA or BNST
21 ta are consistent with previous reports that betaxolol and other beta-adrenergic blockers may exert i
22 sent study, we examined the effectiveness of betaxolol and other beta-adrenergic blockers on glutamat
23 s study, the beta(2)- (ICI-18551), beta(1)- (betaxolol) and mixed beta(1)/beta(2)- (timolol, metipran
24 ge-clamp conditions was reduced by 50 microM betaxolol, and the difference current-voltage (I-V) rela
25 to block the sympathetic nervous system and betaxolol as a control agent in independent test session
26 ctiveness of flunarizine with nifedipine and betaxolol at reducing the influx of calcium or sodium.
28 an alpha1-(prazosin) and beta1-adrenoceptor (betaxolol) blocker but not by a selective 5-HT1A blocker
31 AM beta2-adrenoceptor levels, treatment with betaxolol did not significantly alter levels of the G pr
33 of inhibitory potency is (s)(-)-propranolol>betaxolol>>timolol, with average IC(50) of 78.05, 235.7
35 medications (prednisolone acetate [generic], betaxolol HCl [Betoptic; Alcon Laboratories Inc., Fort W
36 the selective beta1-adrenoceptor antagonist betaxolol hydrochloride (30 microM), the facilitating ef
38 g seeking on ED1, and WAY100635/GR127935 and betaxolol/ICI-118 551 were each partially effective.
39 lls are long (15-35 minutes for 20-50 microM betaxolol), indicative of modulation through slow bioche
41 he aim of the study was to determine whether betaxolol is a neuroprotective agent and can therefore s
42 te that the up-regulation of the receptor by betaxolol is likely to reflect an increase in translatio
45 a either to argon laser trabeculoplasty plus betaxolol (n = 129) or to no immediate treatment (n = 12
46 ons of either artificial tears (n = 6), 0.5% betaxolol (n = 5), or 0.5% apraclonidine (n = 5) were de
50 s GR127935 (5-HT1A/1B receptor antagonists), betaxolol plus ICI-118 551 (beta1 and beta2 antagonists)
53 ls harboring the CAM beta2-adrenoceptor with betaxolol resulted in a large (4-7-fold within 24 hr) up
55 eta2-adrenoceptor required concentrations of betaxolol similar to those needed to cause half-maximal
60 to alprenolol, and a much smaller effect of betaxolol was produced in cells expressing the wild-type
63 current-voltage (I-V) relation (I(Control)-I(betaxolol)) was N-shaped and AP5-sensitive, characterist
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