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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.
43 udy of the broad-acting ionotropic glutamate receptor antagonist 1a.
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.
51                            Mineralocorticoid receptor antagonists administered at high doses may reli
52  effects of PGE2-G were prevented by EP1/EP2 receptor antagonist AH-6809 but not the EP4 antagonist O
53                                       The FP receptor antagonist AL8810 attenuated the PVAT-induced c
54 onism of orexin receptors with a dual orexin receptor antagonist, almorexant, normalizes the augmente
55 terneurons or locally introducing DA or GABA receptor antagonists alters kinship preference.
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
61 eved a complete response to recombinant IL-1 receptor antagonist (anakinra).
62  Furthermore, administration of the IL-1beta receptor antagonist, anakinra, efficiently decreased nit
63                   Pretreatment with a 5-HT2A receptor antagonist and a 5-HT2C receptor agonist attenu
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
68                                         5-HT receptor antagonists and agonists were given as drug pre
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]
74                             Losartan, an AT1 receptor antagonist, and inhibitors of either mitogen-ac
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
81             Traditionally, G protein-coupled receptor antagonists are classified as competitive or no
82                         Ionotropic glutamate receptor antagonists are valuable tool compounds for stu
83 nd support the further investigation of NMDA receptor antagonists as a possible PTHS treatment.
84 inophen metabolite AM 404 and of cannabinoid receptor antagonists as well as data from tissue-specifi
85 ed telmisartan, a widely used angiotensin II receptor antagonist, as a potent inhibitor.
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
88            Here, we show that the muscarinic receptor antagonist, atropine, eliminated the effect of
89                       Type 2 and 3 serotonin receptor antagonists attenuated serotonin's potentiation
90   Therefore, we developed and optimized P2Y4 receptor antagonists based on an anthraquinone scaffold.
91           Unilateral injections of the sigma receptor antagonist BD-1063 prior to METH administration
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
94                                   The NPY Y1 receptor antagonist BIBO3304 completely abolished NPY ef
95            This effect was blocked by the Y1 receptor antagonist BIBO3304 trifluoroacetate (2 nmol/2
96 ther analyzed the response of NS to the GABA receptor antagonist bicuculline.
97 acetate (2 nmol/2 microl), but not by the Y2 receptor antagonist BIIE0246 (2 nmol/2 microl).
98 cant neutrophil chemotactic effect, and a B1 receptor antagonist blocked this effect.
99                                     Estrogen receptor antagonists blocked the synergistic increase in
100 A receptor antagonist, or CGP 35348, a GABAB receptor antagonist, blocked the antinociceptive activit
101 or, which was dose-dependently blocked by DA receptor antagonists, but enhanced by cocaine.
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
104 longer detectable in the presence of a GABAb receptor antagonist CGP52432.
105 This effect was prevented by a pan-adenosine receptor antagonist CGS15943, but not by A1 or A3 recept
106                  Consistently, the histamine receptor antagonist chlorpheniramine potently inhibited
107 gainst NLRP3, recombinant IL-1beta, and IL-1 receptor antagonist confirmed the role of NLRP3 inflamma
108            There are currently numerous NMDA receptor antagonists containing a variety of chemical gr
109  cells, which was blocked by NMDA and mGluR1 receptor antagonists, converting mitral cell responses t
110       This process is inhibited by chemokine receptor antagonists (CoRAs) that block Env-receptor int
111 eatment of non-obese diabetic mice with a Y1 receptor antagonist delays the onset of diabetes.
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
114                            GABA or glutamate receptor antagonists did not block the ethanol effect.
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
118        Importantly, treatment with the GLP-1 receptor antagonist exendin 9-39 abolished the observed
119 ere pretreated with vehicle solution, a PAC1 receptor antagonist (experiment 2), or a PACAP agonist (
120  was blocked by pretreatment with the apelin receptor antagonist, F13A (0 +/- 1 mmHg; P < 0.01).
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
125                      Suvorexant is an orexin receptor antagonist for treatment of insomnia.
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
131         Notably, administration of a ghrelin receptor antagonist further reduced blood glucose levels
132  a fluorinated analogue of G protein-coupled receptor antagonist (GPR91).
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
136       One-week treatment with a histamine H1 receptor antagonist (H1RA) ameliorated the glucose intol
137 osis in pre-clinical models and histamine H2 receptor antagonist (H2RA) use may improve symptoms in p
138 indications, we examined associations for H2 receptor antagonists (H2RAs) as a secondary aim.
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
142         Treatment with estrogen and androgen receptor antagonists had opposite effects on Lep transcr
143 r effect was blocked by the dopamine D2-like receptor antagonist haloperidol.
144 , the compounds behave like the known sigma1 receptor antagonist haloperidol.
145                            No selective P2Y4 receptor antagonist has been described so far.
146                 Recently, laropiprant, a DP1 receptor antagonist, has been used in combination with n
147  the N-methyl-d-aspartate class of glutamate receptor antagonists have been shown to be effective adj
148                                   Endothelin receptor antagonists have emerged as a novel treatment f
149            Interestingly, dopamine D1 and D2 receptor antagonists have opposite effects on plasticity
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
154                                       The B2 receptor antagonist icatibant is approved for treatment
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
157          Here we have shown that a new CXCR4 receptor antagonist IgG1 antibody (PF-06747143) binds st
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
162 ntiinflammatory molecules, specifically IL-1 receptor antagonist (IL-1Ra).
163       Mice were treated acutely with an IL-1 receptor antagonist (IL-1Ra; 100 mg/kg, s.c.) or vehicle
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
168 nthesis of an A2-subtype selective adenosine receptor antagonist in only two steps.
169 heres and vascular endothelial growth factor receptor antagonist in polystyrene microspheres (PE) + t
170                      TRA2P-TIMI 50 (Thrombin Receptor Antagonist in Secondary Prevention of Atherothr
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
173 ticotropin-releasing factor receptor 1 (CRF1 receptor) antagonist in adult women with PTSD.
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
181                                           H3 receptor antagonists/inverse agonists also may be useful
182 y pain, which was antagonized by CB1 and CB2 receptor antagonists/inverse agonists.
183                               The endothelin receptor antagonist is among the most effective agents f
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
188        Nalmefene is a micro and delta opioid receptor antagonist, kappa opioid receptor partial agoni
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
191 ulfonate) represents the most selective P2Y4 receptor antagonist known to date.
192                  Orthosteric beta-adrenergic receptor antagonists, known as beta-blockers, are amongs
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
202 artially blocked by the N-methyl-d-aspartate receptor antagonist MK-801.
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.
206                               While need for receptor antagonist (MRA) MRA after diagnosis suggests t
207 in patients treated with a mineralocorticoid receptor antagonist (MRA).
208                            Mineralocorticoid receptor antagonists (MRA) improve outcome in the settin
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
211                        The mineralocorticoid receptor antagonists (MRAs) spironolactone and eplerenon
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
214           OT coadministered with a mu-opioid receptor antagonist, naloxone, invoked a supralinear enh
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
223           Acute CeA infusions with the PACAP receptor antagonist PACAP(6-38) blocked chronic constric
224 dicates that radiolabeled somatostatin (sst) receptor antagonists perform better than agonists in det
225 intravenous infusion of the alpha-adrenergic receptor antagonist phentolamine for only 30 min.
226 es of drugs are now available-ie, endothelin receptor antagonists, phosphodiesterase-5 inhibitors, so
227 ine or serotonin, was prevented by the GABAA receptor antagonist picrotoxin.
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,
233                            Anakinra, an IL-1 receptor antagonist protein, inhibited BAL TH2/TH17 cell
234 S-propranolol (beta-adrenergic and 5-HT1A/1B receptor antagonist), R-propranolol (5-HT1A/1B receptor
235              In contrast, the dopamine D2/D3 receptor antagonist raclopride reduced the seeking of ch
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
238           Suvorexant, a dual (OX1/2R) orexin receptor antagonist, reduced cocaine-evoked premature re
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
241                                  A mu opioid receptor antagonist restored GABA currents in D2-, but n
242            Moreover, selective NPY2 and NPY5 receptor antagonists restored vascular integrity and lim
243         Interestingly, 1 mum sulpiride, a D2 receptor antagonist, restored tLTP.
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
248          Here, we show that the adenosine A1 receptor antagonist rolofylline (KW-3902) is alleviating
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
251                       Moreover, progesterone receptor antagonist RU-486 partially reversed the effect
252                                 Progesterone receptor antagonist RU-486 were further applied.
253  However, microinjection of the progesterone receptor antagonist, RU486, into the AVPV reversed the p
254                          We used the insulin receptor antagonist S961 to induce severe insulin resist
255 nge or short term treatment with the insulin receptor antagonist S961.
256                     Pretreatment with the D1 receptor antagonist SCH-23390 before optical VTA stimula
257                                     The D1/5 receptor antagonist SCH23390 had no effect on instrument
258 mphetamine seeking, using selective dopamine receptor antagonists (SCH39166 or raclopride) and the Da
259                    However, the neurokinin-1 receptor antagonist significantly reduced both circulati
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%).
264      A selective TARP gamma-8-dependent AMPA receptor antagonist (TDAA) is an innovative approach to
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
267              Cangrelor is an intravenous ADP receptor antagonist that leads to potent and reversible
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
272                       As cimetidine is an H2 receptor antagonist, the authors hypothesize that this a
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
275           We then tested TRPV1, EP2, and EP4 receptor antagonists: The EP2 antagonist was the most ef
276 tinal bleeding, and prior use of histamine-2 receptor antagonist therapy (hazard ratio, 1.08; 95% con
277                                    The P2Y12 receptor antagonist ticagrelor has been shown to be clin
278             Administration of a neurokinin-1-receptor antagonist to block substance P signaling elimi
279       In addition, focal application of GABA receptor antagonists to sensory ganglia triggered or exa
280 ose involving N-methyl-D-aspartate glutamate receptor antagonists, to illustrate principles of networ
281                       The oral vasopressin-2 receptor antagonist tolvaptan causes aquaresis in patien
282 ce, >/=60 ml per minute), the vasopressin V2-receptor antagonist tolvaptan slowed the growth in total
283 d after administration of the vasopressin V2 receptor antagonist tolvaptan.
284 n life-long improved visual function in IL-1 receptor antagonist-treated OIR animals.
285                                 Neurokinin-1 receptor antagonist treatment did not prevent the sepsis
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
288                                  Vasopressin receptor antagonists, urea, and loop diuretics serve thi
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,
291                      Using RNA silencing and receptor antagonists, we demonstrated that OR51E2 activa
292 pped at least 7 days before the study and H2 receptor antagonists were stopped for at least 24 hours
293          Ketamine is an N-methyl-D-aspartate receptor antagonist, which on administration produces fa
294 zines 4 and 5 were reported to be pan opioid receptor antagonists, while 6 was a MOR agonist.
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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