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1 s increased by treatment with IL-4 or a beta-adrenergic receptor antagonist.
2 phages were prevented by propranolol, a beta-adrenergic receptor antagonist.
3 further inhibited by yohimbine, an alpha(2A)-adrenergic receptor antagonist.
4 ion of PI 3-kinase in the presence of a beta adrenergic receptor antagonist.
5 response was blocked by prazosin, an alpha 1-adrenergic receptor antagonist.
6 imes increased by treatment with IL-4 or a B-adrenergic receptor antagonist.
7 observed in control EAE mice treated with B1 adrenergic receptor antagonist.
8 nonmotor symptoms of PD that were rescued by adrenergic receptor antagonists.
9 ents with current or previous use of alpha-1 adrenergic receptor antagonists.
10 alterations of affinity values for selective adrenergic receptor antagonists.
12 c hyperplasia is commonly treated with alpha-adrenergic-receptor antagonists (alpha-blockers) or 5alp
14 ritical poisoning from benzodiazepines, beta-adrenergic receptor antagonists (also known as beta-bloc
16 rtan (10 mg/kg b.wt) nor prazosin, an alpha1 adrenergic receptor antagonist, at doses of 5 microg/5 m
20 patients have shown that treatment with beta-adrenergic receptor antagonists (betaB) improves cardiac
23 anolol or nadolol or the alpha1- + beta1,2,3-adrenergic receptor antagonist carvedilol before or afte
24 riment examined whether prazosin, an alpha 1-adrenergic receptor antagonist, could attenuate NMDA-ind
25 ression, but pre-exposure to timolol, a beta-adrenergic receptor antagonist, delayed this effect.
26 agonist, or propranolol, a nonselective beta-adrenergic receptor antagonist, delivered by osmotic pum
27 prevented with either LTCC blockers or beta-adrenergic receptor antagonists, demonstrating a proxima
34 ceptor antagonist phentolamine nor the beta2-adrenergic receptor antagonist ICI 118, 551 antagonized
35 s repeated after administration of the beta2-adrenergic receptor antagonist ICI 118,551 (0.2 mg/kg).
36 al peritonitis with dopexamine and the beta2-adrenergic receptor antagonist ICI 118,551 (n = 4), ceca
39 is before and during infusion of the alpha 2-adrenergic receptor antagonist idazoxan (1.0 microgram.k
41 responses can be inhibited by alpha and beta-adrenergic receptor antagonists implying a bacterial rec
42 Most clinical studies have shown that beta-adrenergic receptor antagonists improve long-term surviv
43 ls testing rho-kinase inhibitors and alpha2c-adrenergic receptors antagonists in vasospastic conditio
46 cocktail of alpha(1)-, beta(1)-, and beta(2)-adrenergic receptor antagonists into the mPFC prior to e
48 action for several compounds, including the adrenergic receptor antagonist JP1302, which we show dis
52 hen compared with users of tamsulosin, an a1 adrenergic receptor antagonist of a different class that
54 ecursor, or with S(-) pindolol, a 5HT1A/beta adrenergic receptor antagonist or with LY206130, a more
55 h saline, phentolamine, a nonselective alpha-adrenergic receptor antagonist, or propranolol, a nonsel
56 effect was completely reversed by the alpha-adrenergic receptor antagonist phentolamine (i.p. and i.
57 4 h or by intravenous infusion of the alpha-adrenergic receptor antagonist phentolamine for only 30
58 the SPGN terminal, because neither the alpha-adrenergic receptor antagonist phentolamine nor the beta
62 l fear conditioning, injections of the alpha-adrenergic receptor antagonist prazosin (1.0 or 3.0 mg/k
63 urrent to 5.9 nM, and addition of the alpha1-adrenergic receptor antagonist prazosin did not cause an
64 tions in MA but not in MV while the alpha(1)-adrenergic receptor antagonist, prazosin (0.1 microm), b
67 Thy-1 mRNA levels were prevented by the beta-adrenergic receptor antagonist propranolol (10 microM).
68 30 mug) or vehicle (Experiment 1), the beta-adrenergic receptor antagonist propranolol (2 mug) or ve
69 ocked the effects of NA on Ito, but the beta-adrenergic receptor antagonist propranolol (20 microM) d
73 lthy participants were administered the beta-adrenergic receptor antagonist propranolol or a placebo
74 t, treatment before hemorrhage with the beta-adrenergic receptor antagonist propranolol was associate
77 ubjected to the nonselective (beta1 + beta2) adrenergic receptor antagonists propranolol or nadolol o
78 bsence of a alpha2-agonist (clonidine), beta-adrenergic receptor antagonist (propranolol), and beta(1
81 ctivity was completely blocked by the alpha2-adrenergic receptor antagonist rauwolscine and by Clostr
83 ic receptor antagonist) and prazosin (alpha1-adrenergic receptor antagonist) reduced female but not m
87 ystment was inhibited by addition of beta(1)-adrenergic receptor antagonist to cells that were stimul
88 ies is also enhanced by administering a beta-adrenergic receptor antagonist to mice housed at 22 degr
90 xed beta(1)/beta(2)- (timolol, metipranolol) adrenergic receptor antagonists were all shown to attenu
91 an melanocyte cell cultures with the alpha-2 adrenergic receptor antagonist yohimbine results in a ma
92 1 (CRF1) antagonist (antalarmin), and alpha2-adrenergic receptor antagonist (yohimbine; used as a pha
93 overflow for MA was enhanced by the alpha(2)-adrenergic receptor antagonist, yohimbine (1.0 microm),