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1 phy was performed with [(3)H]MK-3207 (a CGRP receptor antagonist).
2 gnaling pathway rather than as a competitive receptor antagonist.
3 ory bulb with a broad-spectrum noradrenergic receptor antagonist.
4 ione peroxidase 1 mice with an interleukin-1 receptor antagonist.
5 RP pathway was shown in skin by using a CGRP receptor antagonist.
6 es, such as interleukin (IL)-10 and the IL-1 receptor antagonist.
7 nd the tone change were prevented by an NMDA receptor antagonist.
8 her a D1 dopamine receptor or NMDA glutamate receptor antagonist.
9 effects of LSD are fully blocked by a 5-HT2A receptor antagonist.
10 free media or in the presence of an estrogen receptor antagonist.
11 intranasal corticosteroid over a leukotriene receptor antagonist.
12 with either a glial toxin or an adenosine A1 receptor antagonist.
13 neurons that could be blocked by a nicotinic receptor antagonist.
14 clinical trials of anifrolumab, a type I IFN-receptor antagonist.
15 he presence of 4 mum SCH23390, a dopamine D1 receptor antagonist.
16 a novel anti-angiogenic small-molecule CysLT receptor antagonist.
17 kedly ameliorated by treatment with a CysLT1 receptor antagonist.
18 nted by icatibant, a clinically available B2 receptor antagonist.
19 following administration of a dopamine D2/3 receptor antagonist.
20 3 potentiation was also blocked by ryanodine receptor antagonist.
21 ch was partially rescued by VPC23109, an S1P receptor antagonist.
22 decreased by addition of C1-inhibitor or B1 receptor-antagonist.
23 hymocyte globulin (r-ATG), and interleukin-2 receptor-antagonist.
24 ockers, beta-blockers, and mineralocorticoid-receptor antagonists.
25 l-4-carboxamide derivatives developed as CB1 receptor antagonists.
26 sisted in the presence of glutamate and GABA receptor antagonists.
27 al effects that are unaffected by endothelin receptor antagonists.
28 tor antagonist CGS15943, but not by A1 or A3 receptor antagonists.
29 use it was abolished by ionotropic glutamate receptor antagonists.
30 epression-like symptoms, than other dopamine receptor antagonists.
31 generate more potent, selective melanocortin receptor antagonists.
32 neuron stimulation and resistant to dopamine receptor antagonists.
33 ventrolateral medulla (RVLM) using selective receptor antagonists.
34 heir use in preparing potential kappa opioid receptor antagonists.
35 , long-acting beta-agonists, and leukotriene receptor antagonists.
36 ment associated with non-TARP-dependent AMPA receptor antagonists.
37 playing low internalization, as expected for receptor antagonists.
38 neffective by either nicotinic or muscarinic receptor antagonists.
39 ol drinking, and its sensitivity to dopamine receptor antagonists.
40 d for the development of adenosine human (h) receptor antagonists.
41 n was stratified by baseline use of dopamine receptor antagonists.
42 es is blocked by AM251, a cannabinoid type 1 receptors antagonist.
44 herally restricted, potent, competitive NMDA receptor antagonist 1l by a structure-activity study of
45 pective phase I/II study to evaluate the sst receptor antagonist (68)Ga-OPS202 ((68)Ga-NODAGA-JR11; N
46 ro pharmacological characterization of 5-HT6 receptor antagonist 7 indicates high affinity and select
47 th augmented concentrations of interleukin-1 receptor antagonist, a key anti-inflammatory protein.
48 mpounds include selective serotonin (5-HT)2C receptor antagonists, a 5-HT4 receptor agonist, a 5-HT7
49 r agonist, a 5-HT7 receptor antagonist, NMDA receptor antagonists, a TREK-1 receptor antagonist, mGlu
50 ion was found for current use of histamine-2-receptor antagonists (adjusted OR, 1.82; 95% CI, 0.89-3.
52 effects of PGE2-G were prevented by EP1/EP2 receptor antagonist AH-6809 but not the EP4 antagonist O
54 onism of orexin receptors with a dual orexin receptor antagonist, almorexant, normalizes the augmente
56 bo or a single low dose (50 mg) of the D2/D3 receptor antagonist amisulpride, which is believed to in
57 st cancer, we demonstrate here that the IL-1 receptor antagonist anakinra abrogates IL-22 production
58 n acute-phase hsCRP production with the IL-1 receptor antagonist anakinra and the IL-6 receptor block
59 ory effect on IL-1beta secretion by the IL-1 receptor antagonist anakinra in phagocytes of patients w
60 that administration of IL-1 (interleukin-1) receptor antagonist (anakinra) could inhibit the inflamm
62 Furthermore, administration of the IL-1beta receptor antagonist, anakinra, efficiently decreased nit
64 n inverse relationship between interleukin 1 receptor antagonist and colony-stimulating factor 1, col
65 The summation was amplified by a D2-like receptor antagonist and experiments with mice with targe
66 nflammatory markers (increased interleukin-1 receptor antagonist and lower monocyte and neutrophil re
67 emmed from the upregulation of interleukin-1 receptor antagonist and suppression of MDSC-promoting cy
69 ents in PRRT include the use of somatostatin receptor antagonists and alpha-emitting radionuclides, w
70 l effects of ketamine were abolished by AMPA receptor antagonists and mimicked by the AMPA-positive a
71 cells with two different neurokinin-1 (NK-1) receptor antagonists and siRNA inhibits TNF secretion by
72 ide formulations, mTOR inhibitors, and GLP-1 receptor antagonists) and surgical therapies (eg, laparo
73 g [(11)C]raclopride (a weak competitive D2/3 receptor antagonist), and dopamine release using [(11)C]
75 (ARBs), beta blockers, and mineralocorticoid receptor antagonists, and advanced device therapies.
76 ion immunosuppression was with interleukin-2 receptor antagonists, and antithymocyte globulin in high
77 ed corticosteroids (ICSs), daily leukotriene receptor antagonists, and as-needed ICS treatment coadmi
78 hen cells were treated with the neurokinin 1 receptor antagonist aprepitant before SP stimulation.
79 zed trial of the ability of the neurokinin-1 receptor antagonist aprepitant to reduce symptoms in pat
80 oint because numerous metabotropic glutamate receptor antagonists are available, many of which have b
84 inophen metabolite AM 404 and of cannabinoid receptor antagonists as well as data from tissue-specifi
86 ne and its potential interactions with P2Y12 receptor antagonists, as well as on the central issue of
87 se, early treatment of adenosine diphosphate receptor antagonists at presentation, older age, female
90 Therefore, we developed and optimized P2Y4 receptor antagonists based on an anthraquinone scaffold.
92 covery of potent and selective adenosine A2A receptor antagonists bearing substituted 1-methylcyclohe
93 cktail of WAY100635 plus GR127935 (5-HT1A/1B receptor antagonists), betaxolol plus ICI-118 551 (beta1
100 A receptor antagonist, or CGP 35348, a GABAB receptor antagonist, blocked the antinociceptive activit
102 design of subunit-selective competitive NMDA receptor antagonists by identifying a cavity for ligand
103 To do so, we infused a selective GABAB(1a) receptor antagonist, CGP 36216, intracerebroventricularl
105 This effect was prevented by a pan-adenosine receptor antagonist CGS15943, but not by A1 or A3 recept
107 gainst NLRP3, recombinant IL-1beta, and IL-1 receptor antagonist confirmed the role of NLRP3 inflamma
109 cells, which was blocked by NMDA and mGluR1 receptor antagonists, converting mitral cell responses t
112 1 receptor antagonist losartan, the oxytocin receptor antagonist desGly-NH2 , d(CH2 )5 [D-Tyr(2) ,Thr
113 increase in social behaviors, while a 5-HT1A receptor antagonist did not alter affiliative vocalizati
115 reatment with naloxone, non-selective opioid receptor antagonist, did not affect the effect of l-THP.
116 5, 10, or 15 mg/kg), a nonspecific adenosine receptor antagonist, dose-dependently and at high doses
117 previously reported that memantine, an NMDA receptor antagonist, enhanced two biomarkers of early au
119 ere pretreated with vehicle solution, a PAC1 receptor antagonist (experiment 2), or a PACAP agonist (
121 we bilaterally implanted the potent androgen receptor antagonist flutamide in two key brain regions t
122 otherapy; and the addition of a neurokinin 1 receptor antagonist for adults who receive carboplatin a
123 ition and Patient Outcomes (PLATO), Thrombin Receptor Antagonist for Clinical Event Reduction in Acut
124 s of this trial, the first evaluating a CRF1 receptor antagonist for the treatment of PTSD, combined
126 cation (proton pump inhibitors or histamine2 receptor antagonists for >6 months) or secondary antiref
127 ion of TNF secretion from DCs is reversed by receptor antagonists for EP2 and EP4, indicating PGE2 ac
128 combined with other negative trials of CRF1 receptor antagonists for major depressive disorder, gene
129 erapy (proton pump inhibitors or histamine-2-receptor antagonists) for patients with IPF, in the abse
130 naldemedine, a peripherally acting mu-opioid receptor antagonist, for the treatment of opioid-induced
133 ction in arteries from males, whereas the TP receptor antagonist GR32191B inhibited the PVAT-induced
134 oke volume) was improved in the neurokinin-1 receptor antagonist group during the first 6 hours of se
135 urther that a selective and potent mu-opioid receptor antagonist (GSK1521498) reduced both alcohol se
137 osis in pre-clinical models and histamine H2 receptor antagonist (H2RA) use may improve symptoms in p
139 sociated with PPIs compared with histamine-2 receptor antagonists (H2RAs) in privately insured adults
140 roton pump inhibitors (PPIs) and histamine-2 receptor antagonists (H2RAs) suppress gastric acid produ
141 roton pump inhibitors (PPIs) and histamine-2 receptor antagonists (H2RAs) suppress gastric acid produ
147 the N-methyl-d-aspartate class of glutamate receptor antagonists have been shown to be effective adj
150 ntiemetic agents (serotonin and neurokinin-1 receptor antagonists) have increased efficacy but are ex
151 ketamine, an N-methyl-D-aspartate glutamate receptor antagonist, have not been fully elucidated.
152 PGE2-mediated cervical ripening or (ii) EP2 receptor antagonists, HDAC4 inhibitors, and 15-PGDH acti
153 teric neurons was inhibited by the nicotinic receptor antagonists hexamethonium and dihydro-beta-eryt
155 en a chlorine atom of the new class of 5-HT6 receptor antagonists identified herein and a backbone ca
156 lly, the NR2B-selective N-methyl-D-aspartate receptor antagonists ifenprodil and CP-101,606 blocked c
158 yte production of the natural inhibitor IL-1 receptor antagonist (IL-1Ra) and shifts production towar
159 of IL-1 is tightly regulated by the specific receptor antagonist (IL-1Ra) and the decoy receptor IL-1
160 the anti-inflammatory cytokine interleukin-1 receptor antagonist (IL-1Ra) secretion in LPS-activated
161 s of C-reactive protein (CRP), interleukin-1 receptor antagonist (IL-1Ra), and soluble interleukin-6
164 ukin [IL]-1 beta [IL-1beta], rs1143623; IL-1 receptor antagonist [IL-1ra], rs4251961; IL-10, rs180087
165 We compared sequences of IL-1beta and IL-1 receptor antagonist (IL1RN), which is an IL-1beta homolo
166 added to ICSs with or without a leukotriene receptor antagonist in a phase III trial in adolescent p
167 support clinical efficacy of a bradykinin B2 receptor antagonist in ACE inhibitor-associated angioede
169 heres and vascular endothelial growth factor receptor antagonist in polystyrene microspheres (PE) + t
171 so support an expanded role for neurokinin 1 receptor antagonists in patients who are treated with ch
172 ng kinetics is useful for selecting new hCB1 receptor antagonists in the early phases of drug discove
174 evaluated the novel compound, ABT-436, a V1b receptor antagonist, in alcohol-dependent participants i
175 amined the role of LOTUS, an endogenous Nogo receptor antagonist, in promoting functional recovery an
176 omy or treating female mice with an estrogen receptor antagonist increased mortality, indicating a pr
177 hetized rats pretreated with intrathecal A2A receptor antagonist injections before mASH (PaO2 = 40-54
178 oral intake of caffeine, a potent adenosine receptor antagonist, interferes with acupuncture analges
179 tial immune markers, including interleukin 1 receptor antagonist, interferon gamma-inducible protein
180 icroinjection of ICI 174,864, a delta-opioid receptor antagonist, into the rVLM of EA-treated CIH rat
184 e with this, we show that gabazine, a GABA-A receptor antagonist, is antihyperalgesic in primed mice
185 injectable formulation of the full mu-opioid receptor antagonist, is effective for the prevention of
186 have such properties-tachykinin neurokinin 3 receptor antagonists-is proposed as a way of reducing ca
187 ntrally available, potent, and specific P2X7 receptor antagonist JNJ-47965567 (30 mg/kg) significantl
189 ke partial agonist properties; like the NMDA receptor antagonist ketamine GLYX-13 produces rapid anti
190 -anesthetic dose of the N-methyl-D-aspartate receptor antagonist ketamine may work to correct these n
193 yr(2) ,Thr(4) ]OVT, the ionotropic glutamate receptor antagonist kynurenate or the GABAA antagonist b
194 of the glia-derived N-methyl-D-aspartic acid receptor antagonist kynurenic acid (KYNA) have consisten
195 ects whereas subeffective doses of the DA D2 receptor antagonist, L-741,626, rescued cocaine's abilit
196 d social anxiety disorder, suggest that CRF1 receptor antagonists lack efficacy as monotherapy agents
197 pretreatment with the angiotensin II type 1 receptor antagonist losartan, the oxytocin receptor anta
198 -type natriuretic peptide, mineralocorticoid receptor antagonists, low voltage, ineligibility for che
199 2C receptor agonist, WAY163909, and a 5-HT2A receptor antagonist, M100907, given alone and in combina
200 agonist, NMDA receptor antagonists, a TREK-1 receptor antagonist, mGluR antagonists and (2R,6R)-HNK.
201 d by bacterial endotoxin LPS or progesterone receptor antagonist mifepristone more often than current
203 NTERPRETATION: Treatment with a neurokinin 3 receptor antagonist (MLE4901) could be practice changing
204 ed the effectiveness of an oral neurokinin 3 receptor antagonist (MLE4901) on menopausal hot flushes.
205 through infusions of the mGluR7 presynaptic receptor antagonist MMPIP had no effect on performance.
209 (ARB), beta-blockers (BB), mineralocorticoid receptor antagonists (MRA), and angiotensin receptor-nep
210 lines recommend the use of mineralocorticoid receptor antagonists (MRAs) for selected patients with s
212 roinjected BDNF or the highly selective TrkB receptor antagonist [N2-2-2-oxoazepan-3-yl amino] carbon
213 aloxone, the non-opioid isomer of the opioid receptor antagonist (-)-naloxone, in infection-associate
215 tagonists, a 5-HT4 receptor agonist, a 5-HT7 receptor antagonist, NMDA receptor antagonists, a TREK-1
216 nistration of OrxA+/-DynA+/-the kappa-opioid receptor antagonist nor-binaltorphimine (NorBNI) under e
217 ng with ecdysone signaling using an ecdysone receptor antagonist or knocking down the ecdysone recept
218 enol were weaned off post-LT, and endothelin receptor antagonist or phosphodiesterase type 5 inhibito
219 e treatment, which was blocked by the sigma1-receptor antagonist or various nitric oxide synthase blo
220 ceptor antagonist), R-propranolol (5-HT1A/1B receptor antagonist), or racemic propranolol in both mal
221 ng N-t-Boc-Met-Leu-Phe, a nonselective AnxA1 receptor antagonist, or by using an anti-AnxA1 neutraliz
222 dministration of either bicuculline, a GABAA receptor antagonist, or CGP 35348, a GABAB receptor anta
224 dicates that radiolabeled somatostatin (sst) receptor antagonists perform better than agonists in det
226 es of drugs are now available-ie, endothelin receptor antagonists, phosphodiesterase-5 inhibitors, so
228 letion, via treatment of mice with the CSF-1 receptor antagonist PLX5622, and abrogated neuronal-micr
229 o-neutralizing Abs and the class A scavenger receptor antagonist polyinosinic acid inhibited phagocyt
230 nercept (TNFalpha inhibitor), anakinra (IL-1 receptor antagonist), prednisone (NFkappaB translocation
231 ine, a nonselective muscarinic acetylcholine receptor antagonist, produces rapid antidepressant effec
232 d that administration of the beta-adrenergic receptor antagonist propranolol before memory retrieval,
234 S-propranolol (beta-adrenergic and 5-HT1A/1B receptor antagonist), R-propranolol (5-HT1A/1B receptor
236 Application of D-AP5, but not the purinergic receptor antagonist RB2, blocks the NMDA-induced Kir act
237 Macrophage depletion or injection of an IL1 receptor antagonist reduced ileal inflammation in SHIP-n
239 of GFAP and MMP-9 and a purinergic ATP (P2) receptor antagonist reduction in calcium response identi
240 demonstrate that such specific anti-cytokine receptor antagonists represent a new class of drugs that
244 mice and in WT mice treated with an insulin receptor antagonist, revealing metabolic control of expr
245 as evidenced by application of glutamatergic receptor antagonists, reversibly inhibiting glutamate-in
246 WIN55212 inhibition was reversed by the CB1 receptor antagonist rimonabant in naive rats but not in
247 Accordingly, local injection of the CB1 receptor antagonist rimonabant into the rostral ventrome
249 ndomized Study of the Selective A1 Adenosine Receptor Antagonist Rolofylline for Patients Hospitalize
250 Randomized Study of the Selective Adenosine Receptor Antagonist Rolofylline for Patients Hospitalize
253 However, microinjection of the progesterone receptor antagonist, RU486, into the AVPV reversed the p
258 mphetamine seeking, using selective dopamine receptor antagonists (SCH39166 or raclopride) and the Da
260 eatment of the RVLM with the vasopressin V1a receptor antagonist, SR 49059 (-1 +/- 1 mmHg; 1.1 +/- 1.
261 dyskinesia results from exposure to dopamine receptor antagonists, such as typical and atypical antip
262 effect could also be induced by a nicotinic receptor antagonist, suggesting that xenobiotic exposure
263 l ligation and puncture sepsis (neurokinin-1 receptor antagonist survival = 79% vs vehicle = 54%).
265 ine (hyoscine) is a muscarinic acetylcholine receptor antagonist that has traditionally been used to
266 s a potent intravenous adenosine diphosphate-receptor antagonist that in the CHAMPION trials reduced
268 Leu-NH2 ((68)Ga-RM2) is a synthetic bombesin receptor antagonist that targets gastrin-releasing pepti
269 migraine in humans and the efficacy of CGRP receptor antagonists that evidently do no penetrate the
270 formation for the discovery of adenosine A2A receptor antagonists that have potential to treat multip
271 ull mutations with complete absence of IL-36 receptor antagonist (the two previously unreported mutat
273 tnatal development and investigated two IL-1 receptor antagonists, the competitive inhibitor anakinra
274 ogues, and peripherally restricted mu-opiate receptor antagonists, the latter a major advance in the
276 tinal bleeding, and prior use of histamine-2 receptor antagonist therapy (hazard ratio, 1.08; 95% con
280 ose involving N-methyl-D-aspartate glutamate receptor antagonists, to illustrate principles of networ
282 ce, >/=60 ml per minute), the vasopressin V2-receptor antagonist tolvaptan slowed the growth in total
286 on alcohol-related behaviors, and on opioid receptor antagonist treatments, have been inconsistent.
287 expression of a thyroid-stimulating hormone receptor antagonist (TSHAntag), which competitively inhi
289 sin-converting enzyme inhibitors/angiotensin receptor antagonists, use of beta-blocker, and smoking c
290 uman recombinant form of the endogenous IL-1 receptor antagonist used to treat rheumatoid arthritis,
292 pped at least 7 days before the study and H2 receptor antagonists were stopped for at least 24 hours
295 hr-Cys)-dTyr-NH2)), a novel radiolabeled sst receptor antagonist with a high affinity for the sst2 re
296 Ketamine is a potent N-methyl-D-aspartate receptor antagonist with a potentially novel mechanism o
297 to test the hypothesis that a bradykinin B2 receptor antagonist would shorten time-to-resolution fro
298 , and that ketamine (an N-methyl-D-aspartate receptor antagonist) would reduce or block this response
299 ot previously seen for amino acid-based AMPA receptor antagonists, X-ray crystal structures of both e
300 tagonist (antalarmin), and alpha2-adrenergic receptor antagonist (yohimbine; used as a pharmacologica
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